JP5803850B2 - Sterilization aid and sterilization method - Google Patents

Description

  The present invention relates to a sterilization aid and a sterilization method used in a sterilization room of a sterilization apparatus to promote the sterilization effect of a lumen of an object to be sterilized.

As a method of sterilizing medical instruments used in medical treatment, there is a method of sterilizing using hydrogen peroxide gas. If the object to be sterilized is, for example, scissors, the surface may be sterilized. However, if the object to be sterilized is an endoscope or an injection needle, the object to be sterilized has a complex-shaped lumen, so the lumen is also sterilized. There is a need to.
The following techniques are disclosed as techniques for enhancing the sterilization effect of a lumen having a constant internal volume.

  Prior art document 1 includes an adapter unit that connects a container in which a sterilant is charged and an object to be sterilized having a lumen. By decompressing the sterilization chamber (chamber), the vapor of the sterilant is covered from the container. A technique for flowing into the lumen of a sterilized body is disclosed.

  In prior art document 2, it consists of an adapter part that connects an empty container and an object to be sterilized with a lumen. A technique is disclosed in which the sterilant vapor flows from the chamber into the lumen of the body to be sterilized by increasing the pressure.

Japanese Patent Laid-Open No. 64-049563 JP 2001-204799 A

  However, the prior art documents have the following problems.

In the techniques of Prior Art Documents 1 and 2, the sterilization effect cannot be obtained unless the adapter part and the object to be sterilized are in close contact with each other, and there is a risk of sterilization failure due to the adapter part coming off during sterilization.
Furthermore, since the adapter portion is in intimate contact with the object to be sterilized, there is a problem that the object to be sterilized and the intimate part cannot be sterilized.

Furthermore, since this adapter part seals one opening of the lumen, another opening other than the adapter part is essential for discharging the vapor of the sterilizing agent from the lumen or for flowing into the lumen. Therefore, it can be used only for an object to be sterilized having a lumen having at least two openings, and there is a great restriction on the object to be used.
Against this background, in the medical field, there is no structural restriction on the lumen of an object to be sterilized such as the number of openings, and there is a demand for a sterilization aid that can be reused at low cost and can reduce sterilization defects. .
It is an object of the present invention to provide a mechanism that can enhance the effect of sterilizing a lumen of a sterilization target without being subjected to structural restrictions on the sterilization target such as the shape of a lumen portion into which a sterilization aid is inserted. And

The present invention relates to a sterilization aid used when sterilizing an object to be sterilized having a lumen in a sterilization chamber, a container capable of storing a predetermined amount of sterilizing agent, and the lumen of the object to be sterilized When the sterilization chamber is depressurized by being inserted into the insertion tube, an opening for introducing a sterilant stored in the container into the inner side of the lumen is provided in the insertion portion; When the insertion tube is inserted into the lumen of the article to be sterilized and the sterilization chamber is decompressed, the sterilizing agent introduced into the inner side of the lumen is inserted into the lumen. In order to discharge from the mouth, an insertion diameter of the insertion tube is provided, and when the insertion tube is inserted from the insertion port into the lumen of the sterilized object, one end of the container is bent in the direction of gravity. At least a part of the insertion tube is made of a flexible material, One end of the insertion tube reaches near the back side, which is one end of the container, and the sterilization chamber is decompressed, so that the sterilizing agent accumulated on the back side, which is one end of the container, Moving from one end to the opening inserted into the lumen of the article to be sterilized, and releasing the sterilizing agent stored in the container from the opening to the inner side of the lumen ;
Further comprising an adhesion preventing part that prevents the insertion tube from closing and closing when inserting the insertion tube into the lumen;
The adhesion preventing part, the insertion opening and rods not to close contact with the container the sterilant and wherein Rukoto a free space can be discharged.

The insertion tube may have an insertion diameter so that a maximum diameter of the insertion tube is smaller than a minimum diameter of the insertion port .

In addition, when sterilizing an object to be sterilized that is open at one end of the lumen that is not the insertion port, a position near one third of the length of the lumen from the insertion port, and the insertion The sterilization process is performed such that the distal end of the insertion tube is located between the mouth and a position in the vicinity of a half of the length of the lumen.

Further, when the insertion tube into the lumen is depressurized the sterilization chamber is inserted only one end of the previous SL lumen is opened in the vicinity one-half of the inner chamber long from the insertion port The sterilization process is performed such that the distal end of the insertion tube is located behind the position at a distance of.

Also, the shape in the container end of the insertion tube to the back side near the container has reached is characterized by a bowl-shaped.

According to the present invention, it is possible to provide a mechanism capable of enhancing the sterilization effect of the lumen of the sterilization target without being subjected to structural restrictions of the sterilization target such as the shape of the lumen portion into which the sterilization aid is inserted. It becomes.

It is the figure which looked at the external appearance of the sterilizer by which the sterilization auxiliary tool of this invention is used from the front. It is a figure which shows an example of the structure of the hardware of the sterilizer by which the sterilization auxiliary tool of this invention is used. It is a figure which shows an example of the screen displayed on the display part 102 of the sterilizer 100. FIG. It is a figure which shows an example of each process of the sterilization process by the sterilization auxiliary tool of this invention by a sterilizer. It is a figure which shows an example of the detailed process of the sterilization process shown to S111 of FIG. It is a figure which shows an example of the detailed process of the pre-sterilization process shown to S501 of FIG. It is a figure which shows an example of the detailed process of the sterilization process shown to S502 of FIG. It is a figure which shows an example of the detailed process of the ventilation process shown to S503 of FIG. It is a figure which shows an example of the detailed process of the sterilization discharge | emission process shown to S114 of FIG. Concentration furnace 208 of sterilizer 100, valve (V1) 211, valve (V3) 212, valve (V4) 213, metering tube 214, valve (V2) 215, vaporizer 216, valve (V5) 217, valve (V9) 227 is a diagram illustrating an example of a block configuration diagram according to a hardware configuration of 227; FIG. It is a block diagram which shows an example of the sterilization assistance tool concerning this invention. It is a block diagram which shows an example of the sterilization assistance tool concerning this invention. It is a figure which shows arrangement | positioning in the case of using the sterilization assistance tool concerning this invention. It is a figure which shows arrangement | positioning in the case of using the sterilization assistance tool concerning this invention.

A sterilization apparatus used with the sterilization aid of the present invention will be described below with reference to the drawings.
<Description of FIG. 1>
First, the external appearance of the sterilization apparatus used with the sterilization auxiliary tool of the present invention will be described with reference to FIG.
FIG. 1 is a front view of the appearance of a sterilizer.

  100 is a sterilization measure used with the sterilization aid of the present invention, 101 is a cartridge mounting door, 102 is a display unit, 103 is a printing unit 103, and 104 is a sterilization chamber. It is a door.

The cartridge mounting door 101 is a door for mounting a cartridge which is a container filled with a sterilizing agent (hydrogen peroxide or hydrogen peroxide solution liquid). When the cartridge mounting door 101 is opened, there is a cartridge mounting location, and the user can mount the cartridge there.
The display unit 102 is a display screen of a touch panel such as a liquid crystal display.
The printing unit 103 is a printer that prints a history of sterilization processing and printing results on printing paper, and appropriately prints a history of sterilization processing and printing results on printing paper.

  The sterilization chamber door 104 is a door for placing an object to be sterilized in a sterilization chamber in order to sterilize an object to be sterilized (object to be sterilized) such as a medical instrument. When the door 104 of the sterilization chamber is opened, there is a sterilization chamber. The object to be sterilized can be put in the sterilization chamber by closing the door 104 of the sterilization chamber.

The sterilization chamber is a casing having a predetermined capacity. The pressure in the sterilization chamber can be maintained from atmospheric pressure to vacuum pressure. Further, the temperature in the sterilization chamber is maintained within a predetermined range during the sterilization process.
<Description of FIG. 2>
Next, an example of the hardware configuration of the sterilizer will be described with reference to FIG.
FIG. 2 is a diagram illustrating an example of a hardware configuration of the sterilizer.

The sterilization apparatus 100 includes an arithmetic processing unit (MPU or the like) 201, a display unit 102, a printing unit 103, a lock operation control unit 202, an extraction needle operation control unit 203, a sterilization chamber door 101, and a liquid sensor 204. , Cartridge 205, RF-ID reader / writer 206, liquid feed rotary pump 207, concentrating furnace 208, air feed pressurizing pump 209, intake HEPA filter 210, valve (V1) 211, valve (V3) 212, valve (V4) 213, metering tube 214, valve (V2) 215, vaporizer 216, valve (V5) 217, valve (V9) 227, valve (V7) 226, , A sterilization chamber (also referred to as a vacuum chamber) 219, an air feed vacuum pump 220, an exhaust HEPA filter 221, a sterilant decomposer 222, a liquid feed rotary pump 223, and an exhaust evaporation furnace And a 24.
An arithmetic processing unit (MPU or the like) 201 performs arithmetic processing and controls each hardware constituting the sterilization apparatus 100.
The display unit 102, the printing unit 103, and the door 101 of the sterilization chamber have already been described with reference to FIG.

  The lock operation control unit 202 is a unit that performs the operation of locking and unlocking the cartridge mounting door 101. By locking the cartridge mounting door 101, the cartridge mounting door 101 is prevented from being opened, and the cartridge mounting door 101 is opened. By unlocking the mounting door 101, the cartridge mounting door 101 can be opened.

  The cartridge 205 is a sealed container filled with a sterilizing agent (hydrogen peroxide or a hydrogen peroxide solution liquid). An RF-ID storage medium is provided below the cartridge 205. The storage medium includes a serial number as information for identifying the cartridge, the date of manufacture of the cartridge, and the first cartridge. The date and time (first use date and time) used in the sterilizer and the remaining amount of the sterilant filled in the cartridge are stored.

  The extraction needle operation control unit 203 is a unit that operates the extraction needle to puncture the extraction needle (injection needle) for aspirating the sterilizing agent in the cartridge from the top of the cartridge.

  That is, when an extraction needle (injection needle) for aspirating the sterilizing agent in the cartridge is inserted from the upper part of the cartridge, the extraction needle (injection needle) is directed toward the cartridge and operated to be lowered from the upper part of the cartridge. Thus, the extraction needle (injection needle) can be inserted from the top of the cartridge. When the extraction needle (injection needle) is removed from the cartridge, the extraction needle (injection needle) can be removed from the cartridge by operating to raise the extraction needle (injection needle) above the cartridge.

  The liquid sensor 204 is a device that detects whether the liquid sterilizing agent in the cartridge 205 passes through a pipe (conduit) connected to the liquid feed rotary pump 207 and the liquid feed rotary pump 223 from the extraction needle (injection needle). It is. Specifically, it is possible to detect whether a sterilant passes through the tube from a spectrum obtained by irradiating the tube with infrared rays.

  The RF-ID reader / writer 206 is a device that can read the serial number, the date of manufacture, the date of first use, and the remaining amount of sterilant from the RF-ID provided on the lower side of the cartridge 205. Further, the device can write the date and time of initial use and the remaining amount of sterilizing agent from the RF-ID reader / writer 206 to the RF-ID provided on the lower side of the cartridge 205. The RF-ID reader / writer 206 is installed at the lower part of the cartridge mounting location behind the cartridge mounting door 101, and reads the RF-ID provided on the lower side of the cartridge 205. Data such as the date and time of first use and the remaining amount of sterilant can be written in the RF-ID.

  The liquid feed rotary pump 207 is electrically connected to the concentrating furnace 208 via a conduit, and is electrically connected to the liquid sensor 204 via a conduit. The liquid feed rotary pump 207 is a device that sucks the liquid sterilant in the cartridge 205 with a pump and sends the sterilant through a conduit to the concentration furnace 208. Further, the liquid feeding rotary pump 207 can suck a predetermined amount of the sterilizing agent from the cartridge 205 in cooperation with the liquid sensor 204.

  The concentrating furnace 208 is electrically connected to the liquid feeding rotary pump 207, the air feeding and pressurizing pump 209, the measuring pipe 214, the exhaust HEPA filter 221, and the measuring pipe 214 through conduits. As will be described later with reference to FIG. 10, the concentrating furnace 208 heats the sterilizing agent fed from the liquid feed rotary pump 207 through the conduit using a heater, and evaporates (vaporizes) moisture contained in the sterilizing agent to sterilize. Concentrate the agent. Further, the vaporized water is pushed out to the conduit connected to the exhaust HEPA filter 221 by the air sent through the conduit from the pneumatic pressurizing pump 209 and exhausted from the concentration furnace 208. Further, a valve (1) 211 is provided between the conduit between the measuring pipe 214 and the concentrating furnace 208.

  The air pressure pressurizing pump 209 is electrically connected to the concentrating furnace 208, the intake HEPA filter 210, and a conduit. The air feed pressurization pump 209 is a device that conducts the outside air (air) of the sterilizer 100 through the intake HEPA filter 210 through a conduit with the intake HEPA filter 210 and sends it to the concentrating furnace 208.

  The intake HEPA filter 210 is electrically connected to each other by a pneumatic pressure pump 209, a sterilization chamber 219, a vaporization furnace 216, and a conduit. The inhalation HEPA filter 210 filters dust, dust, germs, and the like in the outside air (air) outside the sterilization apparatus 100 with a HEPA (High Efficiency Particulate Air Filter) filter to clean the air. Then, the cleaned air is sent to the concentrating furnace 208 through a conduit by an air feeding and pressure pump 209. Further, the purified air is conducted through a conduit with the vaporizing furnace 216 and sent to the vaporizing furnace 216, or conducted through a conduit with the sterilization chamber 219 and sent into the sterilization chamber 219. That is, the intake HEPA filter 210 is electrically connected to the outside air (air) outside the sterilizer 100. Therefore, a conduit between the air feed pressurization pump 209 and the intake HEPA filter 210, a conduit between the sterilization chamber 219 and the intake HEPA filter 210, and between the vaporizer 216 and the intake HEPA filter 210 are provided. The conduit is in communication with outside air (air) via the intake HEPA filter 210.

  A valve (V9) 227 is provided in the conduit between the intake HEPA filter 210 and the vaporizing furnace 216. A valve (V 7) 226 is provided in the conduit between the intake HEPA filter 210 and the sterilization chamber 219.

  The valve (V1) 211 is a valve provided in a conduit between the concentrating furnace 208 and the metering pipe 214, and enables conduction by a conduit between the concentrating furnace 208 and the metering pipe 214 by opening the valve. The valve is closed so that the conduit between the concentrating furnace 208 and the metering pipe 214 cannot be connected by closing the valve.

  The valve (V3) 212 is a valve provided in a conduit between the metering tube 214 and the sterilization chamber 219. By opening the valve, the conduit between the metering tube 214 and the sterilization chamber 219 can be connected. The valve is closed so that the connection between the metering tube 214 and the sterilization chamber 219 is disabled. Further, this valve is provided in the vicinity of the measuring pipe 214, and is provided at a position closer to the measuring pipe 214 than at least a valve (V4) described later.

  The valve (V4) 213 is a valve provided in a conduit between the metering tube 214 and the sterilization chamber 219. By opening the valve, the conduit between the metering tube 214 and the sterilization chamber 219 can be connected. The valve is closed so that the connection between the metering tube 214 and the sterilization chamber 219 is disabled. Further, this valve is provided near the sterilization chamber 219, and is provided at a position closer to the sterilization chamber 210 than at least a valve (V3) described later.

In this embodiment, the valve (V4) 213 and the valve (V3) 213 are opened and closed to enable or disable the conduit between the measuring tube and the sterilization chamber. Whether to open or close one of the valve (V4) 213 and valve (V3) 213 enables or disables the conduit between the measuring tube and the sterilization chamber. Also good.
The measuring pipe 214 is connected by a conduit between the concentrating furnace 208, the vaporizing furnace 216, and the sterilization chamber 219.

When the valve (V1) 211 is opened, the sterilizing agent flows into the measuring pipe 214 from the concentrating furnace 208, and when the valve (V3) 212 and the valve (V4) 213 are opened, the metering pipe 214 is unnecessary from the cartridge 205. This is a device that removes unnecessary air flowing in from the inside of the concentration furnace 208 by the measuring tube 214. Details of the measuring tube 214 will be described later with reference to FIG.

  The valve (V2) 215 is a valve provided in a conduit between the metering pipe 214 and the vaporizing furnace 216. By opening the valve, the conduit between the metering pipe 214 and the vaporizing furnace 216 can be connected. And the valve is closed to disable conduction by a conduit between the metering pipe 214 and the vaporizing furnace 216.

The vaporizing furnace 216 is electrically connected by conduits between the measuring pipe 214, the intake HEPA filter 210, and the sterilization chamber 219. The vaporizing furnace 216 is an application example of a vaporizing chamber.
The vaporizing furnace 216 is a device that vaporizes the sterilant by being depressurized by the pneumatic vacuum pump 220.

  The valve (V5) 217 is a valve provided in a conduit between the vaporizing furnace 216 and the sterilization chamber 219. By opening the valve, conduction by the conduit between the vaporizing furnace 216 and the sterilization chamber 219 is possible. And the valve is closed to disable conduction by a conduit between the vaporizing furnace 216 and the sterilization chamber 219.

  The valve (V9) 227 is a valve provided in a conduit between the vaporizer 216 and the intake HEPA filter 210, and is opened by the conduit between the vaporizer 216 and the intake HEPA filter 210. This is a valve that enables conduction and closes the valve to disable conduction by a conduit between the vaporizing furnace 216 and the intake HEPA filter 210. That is, the valve (V9) 227 is a valve that can open and close the conduction between the vaporizing furnace 216 and the outside air (atmosphere).

  The valve (V7) 226 is a valve provided in a conduit between the sterilization chamber 219 and the intake HEPA filter 210. By opening the valve, the valve (V7) 226 is formed by a conduit between the sterilization chamber 219 and the intake HEPA filter 210. It is a valve that enables conduction and closes the valve to disable conduction by a conduit between the sterilization chamber 219 and the intake HEPA filter 210. That is, the valve (V7) 226 is a valve that can open and close the connection between the sterilization chamber 219 and the outside air (atmosphere).

  The sterilization chamber (also referred to as a vacuum chamber) 219 is a casing having a predetermined capacity for sterilizing an object to be sterilized such as a medical instrument as described with reference to FIG. The pressure in the sterilization chamber can be maintained from atmospheric pressure to vacuum pressure. Further, the temperature in the sterilization chamber is maintained within a predetermined range during the sterilization process. Further, a pressure sensor is provided in the sterilization chamber 219, and the pressure (atmospheric pressure) in the sterilization chamber 219 can be measured by the pressure sensor. The sterilization apparatus 100 determines whether the pressure (atmospheric pressure) in the sterilization chamber 219 or the like is a predetermined atmospheric pressure using the atmospheric pressure in the sterilization chamber 219 measured by the pressure sensor.

The air feed vacuum pump 220 is provided in the sterilization chamber 219, the vaporizer 216, the metering tube 214, the conduit between the metering tube 214 and the vaporizer 216, the conduit between the vaporizer 216 and the sterilization chamber 219, The gas in the space in the conduit between the measuring tube 214 and the sterilization chamber 219 is sucked, and the pressure in each space is reduced to a vacuum state (a state filled with a gas having a pressure lower than atmospheric pressure). Device.
The pneumatic vacuum pump 220 is connected to the sterilization chamber 219 by a conduit, and is connected to the exhaust HEPA filter 221 by a conduit.

  The exhaust HEPA filter 221 is electrically connected to the pneumatic vacuum pump 220 by a conduit. The exhaust HEPA filter 221 is electrically connected to the exhaust evaporation furnace 224 by a conduit. Further, the exhaust HEPA filter 221 is electrically connected to the sterilizing agent decomposing apparatus 222 by a conduit. Further, the exhaust HEPA filter 221 is connected to the concentration furnace 208 by a conduit.

  The exhaust HEPA filter 221 removes the gas sucked from the inside of the sterilization chamber 219 by the air feed vacuum pump 220 from dust, dust, germs, etc. in the gas sent from the conduit between the air feed vacuum pump 220 and the like. Filter with a High Efficiency Particulate Air Filter (HEPA) filter to clean the aspirated gas. The cleaned gas passes through a conduit between the sterilant decomposer 222 and the exhaust HEPA filter 221, and is sent to the sterilizer decomposer 222. The sterilant decomposer 222 removes the sterilant contained in the gas. The molecules are decomposed, and the decomposed molecules are released out of the sterilizer 100.

  Further, the exhaust HEPA filter 221 cleans the gas exhausted from the concentration furnace 208 through a conduit between the concentration furnace 208 and the exhaust HEPA filter 221. This gas is water that has been vaporized by superheating the sterilant in the concentrating furnace 208, but contains a small amount of sterilant. Therefore, this gas passes through a conduit between the sterilant decomposer 222 and the exhaust HEPA filter 221. To the sterilizing agent decomposing apparatus 222. Then, the sterilizing agent decomposition apparatus 222 decomposes the molecules of the sterilizing agent contained in the gas, and releases the decomposed molecules out of the sterilizing apparatus 100.

  Further, the exhaust HEPA filter 221 cleans the vaporized sterilizing agent sent from the exhaust evaporation furnace 224 through the conduit between the exhaust evaporation furnace 224 and the exhaust HEPA filter 221. Then, the cleaned sterilizing agent (gas) passes through a conduit between the sterilizing agent decomposing apparatus 222 and the exhaust HEPA filter 221 and is sent to the sterilizing agent decomposing apparatus 222, and the sterilizing agent decomposing apparatus 222 converts the gas into the gas. The molecule | numerator of the sterilizing agent contained is decomposed | disassembled and the molecule | numerator after decomposition | disassembly is discharge | released out of the sterilizer 100. FIG.

  The sterilizing agent decomposing apparatus 222 is connected by a conduit between the exhaust HEPA filter 221. The sterilizing agent decomposing apparatus 222 decomposes the molecules of the sterilizing agent contained in the gas sent from the conduit between the sterilizing agent decomposing apparatus 222 and the exhaust HEPA filter 221 and sterilizes the molecules generated by the decomposition. Release out of device 100.

For example, when the sterilizing agent is hydrogen peroxide or a hydrogen peroxide solution, the sterilizing agent decomposing apparatus 222 can decompose vaporized hydrogen peroxide into water and oxygen using manganese dioxide as a catalyst. Device.
The liquid feed rotary pump 223 is electrically connected to the exhaust evaporation furnace 224 via a conduit, and is electrically connected to the liquid sensor 204 via a conduit.

The liquid feed rotary pump 223 sucks all the liquid sterilizing agent in the cartridge 205 by the pump, and sends all the sterilizing agent sent through the conduit between the liquid sensor 204 and the liquid feed rotary pump 223 to the liquid feed. This is a device for sending to the exhaust evaporation furnace 224 through a conduit between the rotary pump 223 and the exhaust evaporation furnace 224.
The exhaust evaporation furnace 224 is electrically connected to the liquid feed rotary pump 223 by a conduit, and is electrically connected to the exhaust HEPA filter 221 by an conduit.

The exhaust evaporation furnace 224 heats all the liquid sterilizing agents in the cartridge 205 sent through a conduit between the liquid feed rotary pump 223 and the exhaust evaporation furnace 224 by a heater provided in the exhaust evaporation furnace 224. Vaporize all of the sterilant. The vaporized sterilizing agent is sent to the exhaust HEPA filter 221 through a conduit between the exhaust HEPA filter 221 and the exhaust evaporation furnace 224.
<Description of FIG. 4>
Next, an example of each process of the sterilization process by the sterilizer according to the present embodiment will be described with reference to FIG.
Each step (process) shown in FIG. 4 is performed by controlling the operation of each device in the sterilization apparatus by the arithmetic processing unit 201 of the sterilization apparatus 100.
FIG. 4 is a diagram illustrating an example of each step of sterilization processing by the sterilization apparatus according to the present embodiment.

  When the sterilizer 100 is turned on, first, the RF-ID reader / writer 206 reads data from the RF-ID (storage medium) provided on the lower side of the cartridge 205 (step S101).

  In step S101, the data read from the RF-ID (storage medium) includes a serial number as information for identifying the cartridge, the date of manufacture of the cartridge, and the date and time when the cartridge was first used in the sterilizer. (First use date and time) and the remaining amount of sterilant filled in the cartridge. That is, an RF-ID (storage medium) provided in the cartridge 205 stores in advance a serial number, date of manufacture, date of first use, and remaining amount of sterilant.

  Next, when it is determined in step S101 that data has been read from the RF-ID (step S102: YES), the sterilizer 100 determines that a cartridge is installed at the cartridge mounting location in the sterilizer 100. Then, the cartridge mounting door 101 is locked (step S103).

  Then, the sterilizer 100 determines whether or not there is a predetermined amount of sterilizing agent for one sterilization in the cartridge. Specifically, it is determined whether or not the remaining amount of the sterilizing agent acquired from the RF-ID is larger than a predetermined amount for one sterilization. That is, when it is determined that the remaining amount of the sterilizing agent is larger than the predetermined amount for one sterilization, there is a predetermined amount of the sterilizing agent for one sterilization in the cartridge (a sufficient sterilization process can be performed). (Step S104: YES), the process of step S105 is performed. On the other hand, if it is determined that the remaining amount of the sterilizing agent is less than a predetermined amount (for example, 8 ml) for one sterilization, there is no predetermined amount of the sterilizing agent for one sterilization in the cartridge (sufficient sterilization). It is determined that the process cannot be executed (step S104: NO), and the process of step S112 is performed.

  In step S105, the sterilizer 100 determines whether a predetermined period (for example, 13 months) has elapsed from the date of manufacture of the cartridge acquired from the RF-ID.

If it is determined that a predetermined period has elapsed since the date of manufacture (step S105: YES), it is determined that sufficient sterilization processing cannot be performed, and the process of step S112 is performed. On the other hand, when it is determined that the predetermined period has not elapsed since the date of manufacture (step S105: NO), it is determined that sufficient sterilization processing can be performed, and the process of step S106 is performed.
In step S106, the sterilizer 100 determines whether a predetermined period (for example, two weeks) has elapsed from the first use date and time acquired from the RF-ID.

If it is determined that a predetermined period (for example, two weeks) has elapsed from the first use date and time acquired from the RF-ID (step S106: YES), it is determined that sufficient sterilization processing cannot be performed. Then, the process of step S112 is performed. On the other hand, when it is determined that a predetermined period (for example, two weeks) has not elapsed (step S106: NO), it is determined that sufficient sterilization processing can be performed, and the process of step S107 is performed.
The sterilizer 100 displays a sterilization start screen (301 in FIG. 3) on the display unit 102 in step S107.
FIG. 3 is a diagram illustrating an example of a screen displayed on the display unit 102 of the sterilization apparatus 100.

  On the sterilization start screen 301, a “sterilization start button” is displayed. The “sterilization start button” 302 in the sterilization start screen 301 displayed in step S107 can be pressed (activated) by the user.

  Then, when the “sterilization start button” 302 is pressed by the user (step S108: YES), the sterilization apparatus 100 displays a sterilization mode selection screen (303 in FIG. 3) on the display unit 102.

  The sterilization mode selection screen 303 displays a “mode for concentrating and sterilizing sterilizing agents” button 304 and a “mode for sterilizing without concentrating sterilizing agents” button 305.

  The sterilizer 100 accepts selection of either the “mode for sterilizing and sterilizing the sterilizing agent” button 304 or the “mode for sterilizing without concentrating the sterilizing agent” button 305 from the user (step S110). The sterilization process (step S111) according to the mode of the selected button is performed. Details of the sterilization process (step S111) will be described later with reference to FIG.

Thus, it becomes possible to switch and use the sterilization processing mode with one sterilization apparatus in accordance with a user instruction. That is, when the “concentrate sterilant and sterilize” button 304 is pressed by the user, the sterilant is concentrated and sterilized, and the “mode sterilize without concentrating sterilant” button 305 is displayed. If pressed, sterilization is performed without concentrating the sterilant.
Then, when the sterilization process (step S111) ends, the sterilizer 100 returns the process to step S110.

  The sterilizer 100 displays a sterilization start screen (301 in FIG. 3) on the display unit 102 in step S112. However, the “sterilization start button” 302 in the sterilization start screen (301 in FIG. 3) displayed in step S112 is displayed so as not to be pressed by the user (the “sterilization start button” 302 is not active). . Therefore, it is possible to prevent the user from receiving an instruction to start the sterilization process.

  Then, the sterilizer 100 determines from the serial number acquired from the RF-ID in step S101 whether or not the cartridge installed at the cartridge mounting location has already been subjected to the sterilizing agent discharge processing ( Step S113). Specifically, the memory (storage unit) in the sterilization apparatus 100 stores a serial number for identifying a cartridge that has already been subjected to the sterilizing agent discharge process, and the serial number acquired from the RF-ID in step S101 is stored in the memory (storage unit). By determining whether or not the serial number stored in the memory (storage unit) matches, the cartridge currently attached to the sterilization apparatus 100 is a cartridge that has already been subjected to the sterilizing agent discharge process. It is determined whether or not.

  If it is determined that the cartridge currently attached to the sterilization apparatus 100 has already been subjected to the sterilizing agent discharge process (step S113: YES), the process of step S115 is performed. On the other hand, when it is determined that the cartridge has not been subjected to the sterilizing agent discharge process (step S113: NO), the entire remaining amount of the liquid sterilizing agent remaining in the cartridge is sucked and all the sterilizing agents are removed. A sterilizing agent discharge process (step S114) that is decomposed and released to the outside of the sterilizer 100 is performed, and then the process of step S115 is performed. Details of the sterilant discharge process in step S114 will be described later with reference to FIG.

When the process of step S114 is performed, the serial number read in step S101 is stored in the memory (storage unit) in the sterilization apparatus 100 as the serial number for identifying the cartridge that has already been subjected to the sterilizing agent discharge process.
In step 115, the sterilizer 100 unlocks the cartridge mounting door 101.

If it is determined in step S102 that data could not be read from the RF-ID in step S101 (step S102: NO), the sterilizer 100 has a cartridge installed at the cartridge mounting location in the sterilizer 100. It is determined that there is no cartridge attachment request screen (not shown) (step S116).
An “OK” button 1102 is displayed on the cartridge attachment request screen 1101.

Then, the sterilizer 100 determines whether the “OK” button 1102 on the cartridge attachment request screen 1101 has been pressed by the user (step S117). If the “OK” button 1102 is pressed (YES), the cartridge mounting request screen 1101 is displayed. The door 101 is unlocked (step S118), and the process returns to step S101. On the other hand, when the “OK” button 1102 is not pressed (NO), the cartridge attachment request screen 1101 is continuously displayed.
The unlocking and locking process of the cartridge mounting door 101 is performed by an operation by the lock operation control unit 202.
<Description of FIG. 5>
Next, an example of detailed processing of the sterilization processing shown in S111 of FIG. 4 will be described using FIG.
FIG. 5 is a diagram showing an example of detailed processing of the sterilization processing shown in S111 of FIG.
Each process (process) shown in FIG. 5 is performed by controlling the operation of each apparatus in the sterilization apparatus by the arithmetic processing unit 201 of the sterilization apparatus 100.

  First, in step S501, the sterilizer 100 operates the pneumatic vacuum pump 220, sucks the gas in the sterilization chamber 219, and reduces the atmospheric pressure in the sterilization chamber 219 to a predetermined atmospheric pressure (45 Pascals). Process. Detailed processing of the pre-sterilization process will be described later with reference to FIG.

  In step S502, the sterilization apparatus 100 performs a sterilization process of sterilizing an object to be sterilized by putting a sterilizing agent in the sterilization chamber 219. Detailed processing of the sterilization process will be described later with reference to FIG.

Next, in step S503, the sterilizer 100 performs a ventilation process for removing the sterilant contained in the sterilization chamber 219 and the vaporizing furnace 216. Detailed processing of the ventilation process will be described later with reference to FIG.
<Description of FIG. 6>
Next, an example of detailed processing of the pre-sterilization process shown in S501 of FIG. 5 will be described using FIG.
FIG. 6 is a diagram showing an example of detailed processing of the pre-sterilization process shown in S501 of FIG.
Each process (process) shown in FIG. 6 is performed by controlling the operation of each apparatus in the sterilization apparatus by the arithmetic processing unit 201 of the sterilization apparatus 100.
First, the sterilizer 100 operates the pneumatic vacuum pump 220 to start a process of sucking the gas in the sterilization chamber 219 (step S601).

  In step S602, the sterilization apparatus 100 determines whether the pressure (atmospheric pressure) in the sterilization chamber 219 has been reduced to a predetermined atmospheric pressure (45 Pascals). Specifically, it is determined whether the pressure (atmospheric pressure) in the sterilization chamber 219 measured by a pressure sensor provided in the sterilization chamber 219 is reduced to a predetermined atmospheric pressure (45 Pascals).

  If it is determined in step S602 that the pressure (atmospheric pressure) in the sterilization chamber 219 has not been reduced to a predetermined atmospheric pressure (45 Pascals) (NO), the pneumatic vacuum pump 220 is continuously operated to sterilize the chamber 219. And the pressure (atmospheric pressure) in the sterilization chamber 219 is reduced. In the present invention, the sterilization chamber 219 is installed with a sterilization aid insertion portion, which will be described later with reference to FIG. Therefore, in accordance with the decompression of the sterilization chamber of the sterilization apparatus by this treatment, the inside of the container 1101 (described later) of the sterilization aid is also decompressed (corresponding to the decompression process of the present invention).

On the other hand, if it is determined in step S602 that the pressure (atmospheric pressure) in the sterilization chamber 219 has been reduced to a predetermined atmospheric pressure (45 Pascals) (YES), the pneumatic vacuum pump 220 is continuously operated to sterilize. The gas in the chamber 219 is sucked and the process of step S502 is started.
<Explanation of FIG. 7>
Next, an example of detailed processing of the sterilization process shown in S502 of FIG. 5 will be described using FIG.
FIG. 7 is a diagram showing an example of detailed processing of the sterilization process shown in S502 of FIG.
Each process (process) shown in FIG. 7 is performed by controlling the operation of each apparatus in the sterilization apparatus by the arithmetic processing unit 201 of the sterilization apparatus 100.

  First, the sterilizer 100 opens the valve (V5) 217, and conducts the conduit between the sterilization chamber 219 and the vaporizing furnace 216 (step S701). Thereby, since the gas in the sterilization chamber 219 is currently sucked and depressurized by the pneumatic vacuum pump 220, depressurization in the sterilization chamber 219 and in the vaporizing furnace 216 is started (step S702).

Then, in step S110, the sterilizer 100 determines which one of the “mode for sterilizing and sterilizing the sterilant” button 304 and the “mode for sterilizing without sterilizing agent” button 305 is pressed (step S110). S703). If it is determined that the “mode for sterilizing and sterilizing” button 304 is pressed (YES), the process of step S704 is performed, and the “mode for sterilizing without concentrating sterilizing agent” button 305 is pressed. If it is determined (NO), the process of step S728 is performed.
Here, first, a case where the “mode for sterilizing and sterilizing sterilizing agent” button 304 is pressed (when sterilizing agent is concentrated and sterilized) will be described.

  In step S704, the sterilizer 100 operates the liquid feed rotary pump 207 to suck out a predetermined amount (2 milliliters) of the sterilizing agent in the cartridge 205. Then, the sucked predetermined amount of sterilizing agent is put into the concentration furnace 208. The predetermined amount of the sterilizing agent sucked out here is an amount that can saturate the space in the sterilization chamber 219 with the sterilizing agent.

  In step S705, the sterilizer 100 writes the remaining amount of the sterilizing agent remaining in the cartridge 205 in the RF-ID of the cartridge 205 attached to the cartridge attachment location. Specifically, a value obtained by subtracting a predetermined amount (2 milliliters) sucked from the cartridge 205 in step S704 from the remaining amount of the sterilant in the cartridge 205 read in step S101 is stored in the RF-ID.

  In addition, the sterilization apparatus 100 determines that the cartridge is not used this time when the first use date and time (date and time when the cartridge is first used in the sterilization apparatus) read from the RF-ID in step S101 does not include information indicating the date and time. Judged to be used for the first time in a sterilizer. Thus, only when it is determined that the cartridge is used for the first time in the sterilizer, the current date and time information is also written in the RF-ID.

  Next, since the sterilizer 100 heats the heater provided in the concentration furnace 208 whenever the sterilization apparatus 100 is powered on, the sterilant placed in the concentration furnace 208 in step S704 is Heated by the heat of the heater, the moisture contained in the sterilant in the concentration furnace 208 is evaporated (step S706).

  That is, when the sterilizing agent is a hydrogen peroxide solution (also referred to as an aqueous hydrogen peroxide solution), the heater provided in the concentration furnace 208 is specifically heated at 80 degrees here. Thereby, water can be mainly evaporated (vaporized), and the sterilizing agent can be concentrated.

  Next, in step S707, the sterilizer 100 determines whether a predetermined time (6 minutes) has elapsed since the sterilizing agent was added to the concentration furnace 208 in step S704. If it is determined that a predetermined time has elapsed since the sterilizing agent was put into the concentration furnace 208 (YES), the process of step S708 is performed. On the other hand, if a predetermined time has not elapsed since the sterilizing agent was put into the concentrating furnace 208 (NO), the sterilizing agent is continuously put in the concentrating furnace 208 and the sterilizing agent is subsequently concentrated.

  Next, in step S708, the sterilizer 100 determines whether the atmospheric pressure in the sterilization chamber 219 and the vaporization furnace 216 has been reduced to a predetermined atmospheric pressure (500 Pascals).

  When the pressure in the sterilization chamber 219 and in the vaporization furnace 216 is reduced to a predetermined pressure (YES), the sterilizer 100 determines that the valve (V3) 212 and the valve (V4) 213 in step S709. Are opened for a predetermined time (the valve (V3) 212 and the valve (V4) 213 are opened for a predetermined time (3 seconds) and the valve (V3) 212 and the valve (V4) 213 are closed)). The pressure is reduced. On the other hand, when the pressure in the sterilization chamber 219 and the vaporization furnace 216 is not reduced to a predetermined pressure (NO), the sterilant is continuously concentrated.

In step S710, the sterilizer 100 then opens the valve (V3) 212 and the valve (V4) 213 for a predetermined time and closes the valve (V3) 212 and the valve (V4) 213 in step S709. When the valve (V1) is opened for a predetermined time (3 seconds), the atmospheric pressure in the measuring tube 214 is lower than the atmospheric pressure in the concentrating furnace 208 (external). It is sucked in (step S710). Here, by opening and closing the valve (V1) for a predetermined time, the sterilant contained in the concentrating furnace 208 is sucked into the measuring tube 214. Here, not only the sterilizing agent but also the air in the concentration furnace 208 is sucked into the measuring tube 214 together.
After that, the inside of the sterilization chamber 219 is continuously depressurized by the pneumatic vacuum pump 220.

  Therefore, the atmospheric pressure in the sterilization chamber 219 is lower than the atmospheric pressure in the measuring tube. Specifically, the atmospheric pressure in the sterilization chamber 219 is 400 Pa, and the atmospheric pressure in the measuring tube is a value of atmospheric pressure (101325 Pa). The reason why the pressure in the measuring tube rises to near atmospheric pressure is that not only the sterilizing agent but also the air in the concentrating furnace 208 is sucked into the measuring tube 214 together.

  Next, in step S711, the sterilizer 100 opens the valve (V3) 212 and the valve (V4) 213 for a predetermined time (3 seconds), and sterilizes the air in the measuring tube (not including the liquid sterilant). Sucked into chamber 219. That is, here, when the valve (V3) 212 and the valve (V4) 213 are opened and the predetermined time has elapsed, the valve (V3) 212 and the valve (V4) 213 are closed.

  Next, the sterilizer 100 determines whether the pressure in the sterilization chamber 219 and the vaporization furnace 216 has been reduced to a predetermined pressure (80 Pa), and when it is determined that the pressure has been reduced (step S712). The valve (V5) 217 is closed (step S713).

Then, the sterilizer 100 opens the valve (V2) 215 (step S714). As a result, the sterilizing agent in the measuring tube 214 is sucked into the vaporizing furnace 216 and vaporized in the vaporizing furnace 216.
Here, the sterilizing agent is vaporized in the vaporizer as a molecular cluster.

  The inside of the sterilization chamber has a volume larger than that of the vaporizing furnace, and in the vaporizing furnace, the sterilizing agent is vaporized as a molecular cluster. This is because the volume of the vaporizing furnace is smaller than that in the sterilization chamber, and the distance between the molecules of the sterilant in the sterilization chamber is so close that molecular clusters are easily formed due to intermolecular forces.

Also at this time, the pneumatic vacuum pump 220 continues to suck the gas in the sterilization chamber 219 and depressurize the interior of the sterilization chamber 219. The atmospheric pressure rises in the vaporizing furnace 216 into which the sterilizing agent in the measuring tube 214 has been sucked.
That is, the atmospheric pressure in the vaporizing furnace 216 is higher than the atmospheric pressure in the sterilization chamber 219.

Next, the sterilizer 100 determines whether or not the atmospheric pressure in the sterilization chamber 219 is reduced to a predetermined atmospheric pressure (50 Pa) and a predetermined time has elapsed since the valve (V2) 215 was opened in step S714 ( Step S715), when the pressure in the sterilization chamber 219 is reduced to a predetermined pressure (50 Pa), and a predetermined time has elapsed since the valve (V2) 215 was opened in Step S714 (YES), the pneumatic vacuum The suction (evacuation) in the sterilization chamber 219 by the pump 220 is stopped (step S716), and the valve (V5) 217 is opened (step S717). As a result, the vaporized sterilizing agent diffuses into the sterilization chamber 219, and the object to be sterilized can be sterilized. That is, this process corresponds to an injection process in which a sterilant is injected into the sterilization chamber of the sterilization apparatus after the decompression process.
This diffuses because the atmospheric pressure (50 Pa) in the sterilization chamber 219 is lower than the atmospheric pressure in the vaporization furnace 216.
Here, the sterilizing agent that diffuses further subdivides the molecular clusters in the vaporization furnace, so that the sterilizing agent can be further diffused into the sterilization chamber, and the sterilization effect can be enhanced.
In addition, it becomes possible to effectively sterilize a fine lumen of an object to be sterilized.

  In step S717, it is determined whether a predetermined time has elapsed since the valve (V5) 217 was opened. If it is determined that a predetermined time (330 seconds) has elapsed since the valve (V5) 217 was opened. (Step S718: YES), the valve (V9) 227 is opened (Step S719).

  Thereby, since the atmospheric pressure in the vaporizing furnace 216 and the sterilization chamber 219 is lower than the atmospheric pressure outside the sterilizing apparatus 100, the outside air (air) outside the sterilizing apparatus 100 that has been cleaned with the intake HEPA filter is removed. And is sucked into the vaporizing furnace 216. Then, the sterilizing agent filled in the vaporizing furnace 216 as a gas and the sterilizing agent adhering to the inner surface of the vaporizing furnace 216 are sent into the sterilization chamber 219 by the air sent into the vaporizing furnace 216. The sterilization effect on the object to be sterilized in the sterilization chamber 219 is enhanced. That is, for example, this enhances the sterilization effect on a portion that is difficult to sterilize, such as the back of a thin tube to be sterilized.

In step S719, the sterilizer 100 opens the valve (V7) 226 after a predetermined time (15 seconds) has elapsed since opening the valve (V9) 227, and is further cleaned by the intake HEPA filter 210. Further, outside air (air) outside the sterilization apparatus 100 is sucked into the sterilization chamber 219. This is because the atmospheric pressure inside the sterilization chamber 219 and the vaporizing furnace 216 is lower than the atmospheric pressure outside the sterilization apparatus 100, so the outside air (air) outside the sterilization apparatus 100 is sucked into the sterilization chamber 219.
Thereby, the sterilization effect | action about the parts which are hard to sterilize, such as the backs, such as a thin tube to be sterilized, increases.

  Next, the sterilizer 100 determines whether the inside of the sterilization chamber 219 and the inside of the vaporizing furnace 216 have increased to atmospheric pressure, and when it is determined that the pressure has increased to atmospheric pressure (step S721: YES), the valve (V2) 215 is closed.

  Next, the sterilizer 100 closes the valve (V7) 226 (step S723), and resumes the suction (evacuation) in the sterilization chamber 219 by the pneumatic vacuum pump 220 (step S724). Thereby, the outside air (air) outside the sterilization apparatus 100 cleaned by the intake HEPA filter 210 is sucked into the vaporizing furnace 216. The sterilizing agent filled as a gas in the vaporizing furnace 216 and the sterilizing agent adhering to the inner surface of the vaporizing furnace 216 are further transferred into the sterilization chamber 219 by the air sent into the vaporizing furnace 216. It is sent.

  As a result, the sterilization effect on a portion that is difficult to sterilize such as the back of a thin tube to be sterilized is enhanced, and the sterilizing agent in the vaporizing furnace 216 can be effectively reduced.

  The sterilizer 100 then closes the valve (V9) 227 after a predetermined time (15 seconds) after resuming the suction (evacuation) in the sterilization chamber 219 by the pneumatic vacuum pump 220 in step S724 (step S724). S725).

  At this time, suction (evacuation) in the sterilization chamber 219 is continuously performed by the pneumatic vacuum pump 220. In step S725, the sterilization chamber 219 and the vaporization furnace 216 are sealed, and the sterilization chamber 219 and The inside of the vaporizing furnace 216 is depressurized (step S726).

  Next, the sterilizer 100 determines whether or not the process from step S702 to step S726 has been executed a predetermined number of times (for example, 4 times) (step S727). If it is determined that the process has been executed (YES), the process proceeds to step S503. Process. On the other hand, if it is determined that the processing from step S702 to step S726 has not been executed a predetermined number of times, the processing after step S702 is performed again. As described above, by performing the processing from step S702 to step S726 a predetermined number of times, the effect of the sterilization effect on the object to be sterilized is increased, and the object to be sterilized can be sufficiently sterilized.

  Next, a case where it is determined in step S703 that the “mode for sterilization without concentrating sterilant” button 305 is pressed (when sterilization is performed without concentrating sterilant) will be described.

  When it is determined in step S703 that the “mode for sterilization without concentrating sterilizing agent” button 305 is pressed (NO), the sterilizer 100 determines that the pressure in the sterilization chamber 219 and the vaporization furnace 216 is a predetermined pressure ( It is determined whether the pressure has been reduced to 1000 Pa) (step S728).

When it is determined that the pressure in the sterilization chamber 219 and the vaporization furnace 216 is reduced to a predetermined pressure (100 Pa) (step S728: YES), the sterilizer 100 operates the liquid feeding rotary pump 207. Then, a predetermined amount (2 ml) of the sterilant in the cartridge 205 is sucked. Then, the sucked predetermined amount of sterilizing agent is put into the concentration furnace 208 (step S729).
The predetermined amount of the sterilizing agent sucked out here is an amount that can saturate the space in the sterilization chamber 219 with the sterilizing agent.

  Next, in step S730, the sterilizer 100 writes the remaining amount of the sterilizing agent remaining in the cartridge 205 in the RF-ID of the cartridge 205 attached to the cartridge attachment location. Specifically, a value obtained by subtracting a predetermined amount (2 milliliters) sucked from the cartridge 205 in step S729 from the remaining amount of the sterilant in the cartridge 205 read in step S101 is stored in the RF-ID.

In addition, in step S730, the sterilizer 100 does not include information indicating the date and time in the first use date and time (date and time when the cartridge was first used in the sterilizer) read from the RF-ID in step S101. This time, it is determined that the cartridge has been used for the first time in the sterilizer. Thus, only when it is determined that the cartridge is used for the first time in the sterilizer, the current date and time information is also written in the RF-ID.
And if the sterilizer 100 performs the process of step S730, it will perform the process after step S709 already demonstrated.

  In step S728, when the inside of the sterilization chamber 219 reaches 1000 Pa, the suction of the sterilant is started in step S729, and when the sterilant is completely sucked in step S729, the pressure falls below 500 Pa.

As described above, after the pressure in the sterilization chamber 219 and in the vaporization furnace 216 is reduced to a predetermined pressure (1000 Pascals) at which the pressure reduction in the measuring tube 214 is started, the sucked-in predetermined amount of the sterilizing agent is concentrated. In the furnace 208, the measuring tube 214 can be immediately depressurized in step S709. After that, in step S710, the sterilizing agent in the concentrating furnace 208 is put in the measuring tube, so that the measuring tube 214 is immediately sterilized from the concentrating furnace 208. It becomes possible to put the agent. That is, the sterilizing agent can be put into the measuring tube 214 without being concentrated in the concentration furnace 208.
<Description of FIG. 8>
Next, an example of detailed processing of the ventilation process shown in S503 of FIG. 5 will be described with reference to FIG.
FIG. 8 is a diagram showing an example of detailed processing of the ventilation process shown in S503 of FIG.
Each process (process) shown in FIG. 8 is performed by controlling the operation of each apparatus in the sterilization apparatus by the arithmetic processing unit 201 of the sterilization apparatus 100.
First, the sterilizer 100 opens the valve V (7) 226 (step S801).
Then, the sterilizer 100 continues the suction (evacuation) in the sterilization chamber 219 by the pneumatic vacuum pump 220 (step S802).

  In step S802, when a predetermined time has elapsed after the suction (evacuation) in the sterilization chamber 219 by the pneumatic vacuum pump 220 is started, the valve V (7) 226 is closed (step S804), and the pneumatic vacuum pump Suction (evacuation) in the sterilization chamber 219 by 220 is performed. Thereby, the inside of the sterilization chamber 219 is depressurized.

  Next, when the inside of the sterilization chamber 219 is depressurized to a predetermined atmospheric pressure (50 Pa) (step S806: YES), the sterilizer 100 opens the valve V (7) 226 (step S807). As a result, the outside air (air) outside the sterilization apparatus 100 cleaned by the intake HEPA filter 210 is sucked into the sterilization chamber 219. This is because the air pressure inside the sterilization chamber 219 is lower than the air pressure outside the sterilization device 100, so that outside air (air) outside the sterilization device 100 is sucked into the sterilization chamber 219.

Then, the sterilizer 100 determines whether the atmospheric pressure in the sterilization chamber 219 has increased to atmospheric pressure, and if it is determined that the atmospheric pressure in the sterilization chamber 219 has increased to atmospheric pressure (step S808: YES), It is determined whether the processing from step S804 to step S808 has been performed a predetermined number of times (for example, 4 times) (step S809). If the processing from step S804 to step S808 has been performed a predetermined number of times (for example, 4 times) (YES), The valve V (7) 226 is closed (step S810), and the ventilation process ends.
On the other hand, if the processing from step S804 to step S808 has not been performed a predetermined number of times (for example, 4 times) (NO), the processing from step S804 is performed again.

Thereby, the sterilizing agent adhering to the surface in the sterilization chamber 219 and the sterilizing agent remaining as a gas in the sterilization chamber 219 are sucked by the pneumatic vacuum pump 220. The sucked gas (including the sterilizing agent) passes through the exhaust HEPA filter 221, the sterilizing agent is decomposed by the sterilizing agent decomposing apparatus 222, and the decomposed molecules are released to the outside.
<Description of FIG. 9>
Next, an example of detailed processing of the sterilization discharge processing shown in S114 of FIG. 4 will be described using FIG.
FIG. 9 is a diagram showing an example of detailed processing of the sterilization discharge processing shown in S114 of FIG.
Each process (process) shown in FIG. 8 is performed by controlling the operation of each apparatus in the sterilization apparatus by the arithmetic processing unit 201 of the sterilization apparatus 100.

  First, the sterilizer 100 sucks all the liquid sterilizing agent in the cartridge 205 by the liquid feed rotary pump 223 and sends it all through the conduit between the liquid sensor 204 and the liquid feed rotary pump 223. The sterilizing agent is sent into the exhaust evaporator 224 through a conduit between the liquid feed rotary pump 223 and the exhaust evaporator 224 (step S901).

  The sterilization apparatus 100 is configured so that all the liquid sterilizing agents (sterilizing agents stored in the exhaust evaporation furnace 224) are sent by the exhaust evaporation furnace 224 through the conduit between the liquid feed rotary pump 223 and the exhaust evaporation furnace 224. Is heated by a heater provided in the exhaust evaporation furnace 224 to vaporize all of the sterilant. The vaporized sterilizing agent is sent to the exhaust HEPA filter 221 through a conduit between the exhaust HEPA filter 221 and the exhaust evaporation furnace 224 (step S902).

  Here, the heater provided in the exhaust evaporation furnace 224 is heated to a temperature higher than the boiling point of the sterilant (hydrogen peroxide) (the boiling point of hydrogen peroxide is 141 degrees). Therefore, all of the sterilizing agent is vaporized by the exhaust evaporation furnace 224.

  Then, the sterilizer 100 cleans the vaporized sterilant sent through the conduit between the exhaust evaporation furnace 224 and the exhaust HEPA filter 221 with the exhaust HEPA filter 221, (Containing the agent) passes through the conduit between the sterilant decomposer 222 and the exhaust HEPA filter 221 and is sent to the sterilizer decomposer 222.

The sterilizing agent decomposing apparatus 222 decomposes the molecules of the sterilizing agent contained in the gas sent from the conduit between the sterilizing agent decomposing apparatus 222 and the exhaust HEPA filter 221, and generates molecules generated by decomposing. Is released out of the sterilizer 100 (step S903).
<Description of FIG. 10>

  Next, using FIG. 10, the concentration furnace 208, the valve (V1) 211, the valve (V3) 212, the valve (V4) 213, the metering tube 214, the valve (V2) 215 of the sterilizer 100 according to this embodiment, A block configuration related to the hardware configuration of the vaporizing furnace 216, the valve (V5) 217, and the valve (V9) 227 will be described.

FIG. 10 shows a concentration furnace 208, a valve (V1) 211, a valve (V3) 212, a valve (V4) 213, a measuring pipe 214, a valve (V2) 215, a vaporizer 216, a valve of the sterilization apparatus 100 according to the present embodiment. It is a figure which shows an example of the block block diagram which concerns on the hardware constitutions of (V5) 217 and valve | bulb (V9) 227.
In the hardware shown in FIG. 10, the same reference numerals are assigned to the same hardware as the hardware shown in FIG.

  In step S704 and step S729, the liquid feeding rotary pump 207 is operated to suck a predetermined amount (2 milliliters) of the sterilizing agent in the cartridge 205, and the sucked predetermined amount of the sterilizing agent is put into the concentration furnace 208.

In step S706, as shown in FIG. 10, the concentrating furnace 208 is provided with a heater at the bottom of the concentrating furnace 208, and the sterilizing agent is heated by the heat of the heater. When the sterilizing agent is an aqueous hydrogen peroxide solution, water is vaporized by the heat of the heater. The vaporized water is pushed out by the air fed through the conduit from the pneumatic pressurizing pump 209 to the conduit connected to the exhaust HEPA filter 221 and exhausted from the concentration furnace 208. Thereby, a sterilant (hydrogen peroxide aqueous solution) is concentrated.
As described with reference to FIG. 7, the sterilizing agent in the concentration furnace 208 enters the measuring tube 215 in step S <b> 710.
As shown in FIG. 10, the measuring pipe 215 includes a straight pipe portion 1001 and a branch pipe portion 1002.
The straight pipe portion 1001 is a straight tubular portion. The pipe of the straight pipe portion 1001 is arranged in the direction of gravity.
Further, the branch pipe portion 1002 is a tubular portion extending in a branch shape from an intermediate portion or an upper portion of the straight pipe portion 1001.
The straight pipe part 1001 is installed so that the axis of the straight pipe part and the axis of the branch pipe part 1002 are perpendicular to each other.

Because of this configuration, the sterilizing agent that has entered from the concentration furnace 208 is configured to accumulate in the straight tube portion 1001 in the measuring tube 215. A portion where the sterilant is collected in the straight pipe portion 1001 is referred to as a sterilant reservoir portion 1003.
That is, the sterilant reservoir 1003 has a sufficient space for the sterilant entering from the concentration furnace 208 to enter.

  Therefore, the sterilant that has entered from the concentration furnace 208 is accumulated in the sterilant reservoir 1003, and the air that has entered from the concentration furnace 208 together with the sterilant is a space other than the sterilant space that has accumulated in the sterilant reservoir 1003. It will be full. That is, the space other than the space for the sterilizing agent is a space in the branch pipe portion 1002, and is a space communicating with the space in the branch pipe portion 1002, and therefore, in step S711, the valve (V3) 212 and the valve (V4) By opening 213, the air is sucked into the sterilizer 219.

  Then, by opening the valve (V9) in step S714, the sterilant accumulated in the sterilant reservoir 1003 is sucked into the vaporizing furnace 216 and vaporized. As shown in FIG. 10, the liquid sterilizing agent enters the vaporizing furnace 216 from the upper part of the vaporizing furnace 216, so that the sterilizing agent is easily vaporized.

Further, a conduit between the intake HEPA filter 210 and the vaporizing furnace 216 is provided at the upper part of the vaporizing furnace 216 as shown in FIG. Therefore, when the valve (V9) is opened in step S719, air (outside air) passes from the upper part of the vaporization furnace 216 to the sterilization chamber 219 at the lower part of the vaporization furnace 216, and thus sterilization that has adhered to the inside of the vaporization furnace 216. It becomes easy to remove the agent and the vaporized sterilant in the vaporizing furnace 216 in a wide range, and more of the removed sterilant can flow into the sterilization chamber 219.
<Description of FIG. 11>
Next, an example of the sterilization aid 13 according to the present invention will be described using the configuration diagram of FIG.

  The sterilization aid of the present invention is applied to sterilization of a medical device having a long and narrow lumen 10. Such medical devices include devices having lumens such as catheters and tubes, and devices such as gastrocameras.

In FIG. 11, a container 1101 is a container having a predetermined internal volume. The container 1101 does not contact the container as in the prior art document 1. When the inside of the sterilization chamber (chamber) is evacuated, the inside of the container 1101 is also depressurized through the tubes (1103, 1104, 1105), so that the hydrogen peroxide solution is brought into the tubes (1103, 1104, 1105) by negative pressure. Is moved to the tip 1305, reaches the tip of the insertion portion of the tube 1103, and is then released into the lumen. Thereafter, the hydrogen peroxide solution is evaporated (vaporized) by vacuum, and the inside of the lumen is sterilized with steam.
The sterilization aid 13 sterilizes the lumen of the article 12 to be sterilized in a sterilization chamber.
The container 1101 is a container for storing a predetermined amount of the sterilizing agent 14.
The tubes (1103, 1104, 1105) are tubes that are inserted into the lumen through the insertion port of the lumen and introduce a predetermined amount of the sterilizing agent 14 from the container into the lumen.

  The sterilization auxiliary tool introduces the sterilizing agent 14 stored in the container 1101 into the lumen 10 by depressurizing the sterilization chamber, and discharges it from the insertion port 11 into which the tube is inserted, thereby sterilizing the lumen. It is for raising.

The connection unit 1102 is a connection unit that joins the container 1101 and the tubes 1104, 1105, and 1103 (referred to as an insertion unit) inserted into the lumen 10, and serves as a cap for the container 1101.
The sterilization aid of the present invention includes at least an empty container 1101 and a tube 1103 inserted into the lumen 10 of the object to be sterilized. 1104 is a steel tube extending to the bottom of the container 1101.

This is because, as shown in the lower part of FIG. 13, one end of the tube in the container needs to be extended to reach the back side (bottom part) of the container. With this mechanism, when the container is bent in the direction of gravity, it is possible to suck out the last drop of the sterilant accumulated in the back side (bottom part) of the container.
Reference numeral 1105 denotes a tube connecting the tube 1103 and the steel tube 1104, and a softer (flexible) tube than the tube 1103 is used.

The reason for this is that, as shown at the bottom of FIG. 13, when the tube 1103 is inserted into the lumen 10 of the object to be sterilized, at least a part of the tube is made of a flexible material so that one end of the container bends in the direction of gravity. This is because it needs to be configured. This mechanism allows the sterilant 14 to be collected in the direction of gravity so that no drop of sterilant remains in the container. At that time, the air 15 in the container gathers in the opposite direction of the sterilant 14.
The material of the tube 1103 is preferably PTFE.
The tube 1104 is preferably made of stainless steel.
The tube 1105 is preferably a silicon material.
The container 1101 is preferably a stainless material.
Each of the connection portions 1102 uses PTFE.

  The shape of the container in which one end of the tube reaches the back side (bottom part) 16 of the container is a mortar shape. By this mechanism, it is possible to collect and suck out the sterilant accumulated in the back side (bottom) of the container.

  The reason for this is that, as shown at the bottom of FIG. 13, one end of the tube in the container is extended to reach the back side (bottom part) of the container, so when the container is bent in the direction of gravity, This is because the sterilizing agent accumulated on the back side (bottom) in the container is collected in the suction part at one end of the tube.

To the extent that the hydrogen peroxide solution is sucked out from the container through the insertion portion by the negative pressure due to vacuum, and the other end of the insertion portion is sucked out from the other end of the insertion portion in order to release the hydrogen peroxide solution from the tip of the insertion portion. The structure has a length up to the bottom of the container. In order to extrude the hydrogen peroxide solution, a flexible material is used for a part of the insertion portion so that the bottom of the container faces in the direction of gravity. Since the hydrogen peroxide solution at the bottom of the container is completely sucked out, the bottom of the container has a mortar shape. The tube 1103 is preferably a poly-based resin such as PTFE having high chemical resistance. The other end of the tube 1104 leading to the container and the container bottom is preferably stainless steel, which is a metal with high chemical resistance so that the bottom can easily face the direction of gravity. It is desirable that the soft material (tube 1105) connecting the insertion portion is a silicon resin that is soft and has high chemical resistance.
<Description of FIG. 12>
Next, another example of the sterilization aid according to the present invention will be described with reference to the block diagram of FIG.

Similarly to FIG. 11, the sterilization aid of FIG. 12 also includes a container 1101, a tube 1103 to be inserted into the lumen 10, and a connection part 1102, although not essential. A difference from FIG. 11 is that an adhesion prevention unit 1201 is provided.
The close-contact prevention unit closes the insertion port 11 and prevents close contact when the tube is inserted into the lumen.

  The adhesion prevention unit 1201 is a prevention unit for preventing the sterilization auxiliary tool and the insertion port, which is the entrance of the outside air in the lumen of the object to be sterilized, from coming into close contact with each other. If the insertion port for the object to be sterilized comes into close contact with the container 1101 or the connection part 1102 of the sterilization aid 13, the sterilization effect of the close contact part is lowered, and it is necessary to prevent this.

FIG. 12 shows a cross-sectional view of the adhesion preventing portion 1201. The contact prevention unit 1201 is provided with a holding rod 1202 so that the insertion port (opening portion) of the sterilization object does not come into close contact with the container 1101 or the connection unit 1102 of the sterilization aid. This refill rod 1202 comes into contact with the object to be sterilized, directly contacts the sterilization aid container 1101 and the connection part 1102, and sterilization gas (steam of the sterilant 14) is not discharged from the insertion port on the contact side. It is preventing.
That is, the sterilization assisting device of the present invention includes an adhesion preventing unit for preventing the sterilization assisting device from being in close contact with the entrance (insertion port) of the lumen of the object to be sterilized.
Therefore, the adhesion prevention unit 1201 is provided with a hole (empty space) 1204 into which sterilization gas can be injected (drawn).
<Description of FIG. 13: Length of Insertion Section>
Next, the arrangement relationship (positional relationship) during the sterilization process between the sterilization aid according to the present invention and the article to be sterilized having a lumen will be described with reference to FIG.

  When the sterilization process is performed, the tube 1103 of the sterilization aid is inserted into the lumen of the article to be sterilized, and in that state, is placed in the sterilization chamber (chamber). In the upper example (external view) in FIG. 13, the sterilization object shows an arrangement relationship when both ends of the lumen are open.

When sterilizing an object to be sterilized having such a lumen shape, the lumen length 1302 (L ′) of the object to be sterilized, which is the entire length of the lumen, and the tube 1103 are used for the object to be sterilized. The length 1301 (L) inserted into the lumen is desirably in the following relationship.
Formula) L≈L '/ 3 to L' / 2

That is, when performing sterilization of an object to be sterilized in which one end 1303 of the lumen that is not the insertion port 11 is open, the position of the insertion port 11 and a third of the length of the lumen are inserted. It can be seen that sterilization may be performed after the tube 1103 is disposed so that the tip 1305 is between (range) from a position near one half of the length of the lumen.
Since the tip 1305 of the tube 1103 is open, the vapor of the sterilizing agent 14 is introduced from the tip 1305 into the lumen.
If both ends of the lumen are open, the insertion port 11 may be on either side of the both ends.
That is, the length 1301 of the tube 1103 inserted into the lumen of the object to be sterilized is about one third to about one half of the length 1302 of the lumen of the object to be sterilized.
Further, the case where the sterilizing effect is most effective and efficient is a case in which the tip 1305 is inserted at a position about one half of the length 1302 of the lumen of the sterilized object.
This ratio is obtained from the sterilization result in the following experiment.

注釈：滅菌されたケースと、滅菌されなかったケースが見受けられた。
内径１ｍｍとはチューブ１１０３の内径１４０３である。
挿入長０．７５ｍ、１．５ｍとはチューブ１１０３が被滅菌物の内腔に挿入されている長さ１３０１である。 The experimental data in Table 1 below shows the CI discoloration results when chemical indicators (CI) are placed at 30 cm intervals in the lumen 10 of a silicon tube (inner diameter 1405 is Φ6 mm, length 1302 is 3 m). . The volume of the sterilization aid container 1101 was 5 cc.
[Table 1]

Note: Some cases were sterilized and some were not sterilized.
The inner diameter 1 mm is the inner diameter 1403 of the tube 1103.
The insertion lengths 0.75 m and 1.5 m are the lengths 1301 in which the tube 1103 is inserted into the lumen of the article to be sterilized.

  According to the experimental results in Table 1, the length (insertion length) of the tube 1103 of the sterilization aid inserted into the lumen of the object to be sterilized is approximately two minutes the length of the lumen of the object to be sterilized. In the case of 1 (insertion length 1.5 m), it was confirmed that the lumen 10 was completely sterilized.

  In addition, the length (insertion length) of the tube 1103 of the sterilization aid inserted into the lumen of the object to be sterilized (insertion length) is a quarter of the length of the lumen of the object to be sterilized (insertion length 0.75 m). In some cases, sterilization was performed on a part of the insertion side, and cases where the sterilization was not performed reliably were observed.

  This is probably because the hydrogen peroxide gas (the vapor of the sterilizing agent 14) did not reach the inside of the lumen 10 sufficiently because the depth of the sterilizing agent input was shallow. Therefore, the insertion length is desirably about one half to about one third of the total length of the lumen.

注釈：十分な変色が確認出来ないケースが見受けられた。 Similarly, the experimental data in Table 2 shows that when a chemical indicator (CI) is placed at 10 cm intervals on a flexible endoscopic forceps channel (inner diameter 1405 is Φ2.5 mm, length 1302 is 1.2 m), which is an endoscope. The discoloration tendency is shown. The volume of the sterilization aid container 1101 is 5 cc.
[Table 2]

Note: There were cases where sufficient discoloration could not be confirmed.

  According to the experimental results in Table 2, the length (insertion length) inserted into the lumen of the sterilized object in the tube 1103 of the sterilization assisting tool is approximately two minutes of the length of the lumen of the sterilized object. In the case of 1 (insertion length 60 cm), it was confirmed that all were sterilized.

  Moreover, the length (insertion length) inserted in the lumen of the sterilized object in the tube 1103 of the sterilization aid is one-fourth (insertion length 30 cm) of the lumen of the sterilized object. In the case, a case where the sterilization treatment was performed on a part of the insertion side and a case where the treatment was not performed reliably were observed.

  This is thought to be because the hydrogen peroxide gas did not reach the inside of the lumen 10 sufficiently because the depth of the sterilizing agent input was shallow. For this reason, the insertion length is desirably about one half of the lumen.

  That is, the sterilization aid 13 of the present invention has a length inserted in the lumen of the object to be sterilized in the tube 1103 when sterilizing the object to be sterilized with both ends of the lumen open. It can be seen that it is desirable to perform the sterilization process in a positional relationship from about one half to about one third of the length of the lumen of the object to be sterilized.

Next, when performing the sterilization process, the tube 1103 of the sterilization aid is inserted into the lumen of the article to be sterilized, and in that state, is placed in the sterilization chamber (chamber). In the lower example of FIG. 13 (cross-sectional view), the object to be sterilized shows the positional relationship when only one side of the lumen is open.
When the sterilization process is performed, the tube 1103 of the sterilization aid is inserted into the lumen of the article to be sterilized, and in that state, is placed in the sterilization chamber (chamber).

When sterilizing the object to be sterilized 12 that is open only on one side of the lumen, the length 1302 (L ′) of the object to be sterilized and the lumen of the object to be sterilized in the tube 1103 are disposed. The inserted length 1301 (L) is preferably in the following relationship.
Formula) L ≈ L '/ 2 to about L'

  That is, it is desirable that the length 1301 of the tube 1103 inserted into the lumen of the object to be sterilized is substantially the same from 50% of the length 1302 of the lumen of the object to be sterilized.

When performing sterilization of an object to be sterilized in which only one end of the lumen is open at the insertion port 11, the tube is placed on the back side from the position at a distance of about one-half of the lumen length from the insertion port 11. It can be seen that sterilization may be performed after the tip 1305 is disposed.
This ratio is obtained from the sterilization result in the following experiment.

The experimental data in Table 3 below shows the discoloration tendency when chemical indicators (CI) are placed at 10 cm intervals on a silicon dead end (one end is closed) tube (inner diameter Φ6 mm, length 1 m). ing. The volume of the sterilization aid container 1101 is 5 cc.
[Table 3]

  According to the experimental results in Table 3, the length (insertion length) inserted into the lumen of the dead-end 1304 type sterilization object in the tube 1103 of the sterilization aid is equal to the lumen of the sterilization object. It was confirmed that all cases were sterilized in cases where the length was almost the same from 80% or more of the length.

  Further, the length (insertion length) inserted into the lumen of the sterilized object in the tube 1103 of the sterilization aid is 30% of the length of the dead end type sterilized object (insertion length 30 cm). In cases where the sterilization treatment was not performed, the sterilization treatment was not reliably performed on the inner side of the lumen of the dead-end structure. It is assumed that the vaporized sterilization gas was not transmitted to the back side around the front mouth of the tube of the sterilization aid. For this reason, it has been found that it is desirable that the insertion length of the insertion portion of the sterilization auxiliary tool is approximately the same from 50% of the lumen for the object to be sterilized (bottom of FIG. 13).

  That is, when the sterilization aid of the present invention performs sterilization of an object to be sterilized that is opened only at one end of the lumen, the length inserted into the lumen of the object to be sterilized in the insertion portion is: From 50% of the length of the lumen of the article to be sterilized, it can be seen that it is desirable to perform the sterilization process in a positional relationship where the lengths are substantially the same.

As described above, when sterilizing an object to be sterilized having a lumen in a sterilization chamber of a sterilization apparatus, a container having a predetermined internal volume and an insertion inserted into the lumen 10 of the object to be sterilized In the sterilization processing method using the sterilization aid provided with a part, it is realized by the following procedure.
(1) Depressurization step of depressurizing the sterilization chamber.

(2) A discharge process in which the vapor generated by the vaporization of the sterilant 14 stored in the container is introduced into the lumen through the decompression process and discharged from the insertion port 11 into which the tube 1103 is inserted.
Furthermore, the manufacturing cost of the sterilization aid itself can be kept low, and the user can use the same sterilization aid repeatedly in the sterilization process.
Furthermore, since it is not the structure which closely_contact | adheres to a to-be-sterilized thing, it can prevent a close_contact | adherence part becoming poor sterilization.
Furthermore, it becomes possible to sterilize the article to be sterilized 12 having one insertion port 11 (dead end structure) for insertion into the lumen.
<Description of FIG. 14>
Using the sectional view of the insertion opening and the sectional view of the tube, the inner diameter and outer diameter of each are shown.

As shown in FIG. 14, the maximum inner diameter 1404 of the tube inserted from the insertion port 11 of the lumen is smaller than the minimum outer diameter 1405 of the insertion port. Since there is a gap in the smallest part of the diameter and the lumen is open even if the tube is inserted, the vapor of the sterilizing agent 14 can be discharged from the insertion port, and the vicinity of the insertion port can be sterilized. it can.
14 in FIG. 14 is a cross-sectional view of the lumen (insertion port 11 portion).
14 in FIG. 14 is a cross-sectional view of an object to be sterilized.
In FIG. 14, reference numeral 1405 denotes a minimum portion of the outer diameter of the lumen (insertion port 11 portion). For example, it is about 2.5 mm.
Reference numeral 1404 in FIG. 14 denotes the maximum portion of the outer diameter of the tube 1103. For example, it is about 2 mm.

1401 in FIG. 14 is a cavity in the tube 1103. This cavity is also communicated with the tube 1104 and the tube 1105, and the sterilant 14 in the container can be supplied to the tip 1305.
1403 in FIG. 14 is the inner diameter of the tube 1103. For example, it is about 1 mm.

10 Lumen 11 Insertion Port 12 Object to be Sterilized 13 Sterilization Aid 14 Sterilizing Agent (Hydrogen Peroxide Solution)
100 Sterilizer 219 Sterilization chamber 1101 Container 1103 tube (lumen insertion part)
1104 tube (container flexible part)
1105 tube (sterilant suction part)
1201 adhesion prevention part

Claims (6)

A sterilization aid used when sterilizing an object to be sterilized with a lumen in a sterilization chamber,
A container capable of storing a predetermined amount of sterilant;
When the sterilization chamber is decompressed after being inserted into the lumen of the article to be sterilized, an opening for introducing a sterilant stored in the container into the inner side of the lumen is provided at the insertion portion. An insertion tube provided;
With
When the insertion tube is inserted into the lumen of the article to be sterilized and the sterilization chamber is depressurized, the sterilizing agent introduced into the inner side of the lumen is discharged from the insertion port of the lumen. The insertion diameter of the insertion tube is provided as
When the insertion tube is inserted into the inner cavity of the article to be sterilized from the insertion port, at least a part of the insertion tube is made of a flexible material so that one end of the container bends in the direction of gravity.
One end of the insertion tube in the container reaches near the back side, which is one end of the container,
As the sterilization chamber is depressurized, the sterilizing agent accumulated at the back, which is one end of the container, moves from one end of the insertion tube to the opening inserted into the lumen of the sterilized object. And releasing the sterilizing agent stored in the container from the opening to the back side of the lumen ,
Further comprising an adhesion preventing part that prevents the insertion tube from closing and closing when inserting the insertion tube into the lumen;
The close-contact prevention unit includes a stick that does not allow the insertion port to be in close contact with the container and an empty space from which the sterilant can be discharged.   The sterilization aid according to claim 1, wherein an insertion diameter of the insertion tube is provided so that a maximum diameter of the insertion tube is smaller than a minimum diameter of the insertion port. When sterilizing an object to be sterilized that is open at one end of the lumen that is not the insertion port, a position near one third of the length of the lumen from the insertion port, and from the insertion port The sterilization aid according to claim 1 or 2 , wherein sterilization is performed such that the distal end of the insertion tube is between a position near one half of the length of the lumen. When the insertion tube is inserted into a lumen that is open only at one end of the lumen and the sterilization chamber is depressurized, the distance from the insertion port is about one-half of the lumen length. The sterilization auxiliary tool according to any one of claims 1 to 3 , wherein sterilization is performed such that the distal end of the insertion tube is located behind a certain position. The sterilization assist according to any one of claims 1 to 4 , wherein a shape of the container in which one end of the insertion tube reaches the back side of the container is a mortar shape. Ingredients. A container capable of storing a predetermined amount of sterilizing agent, and an insertion tube having an opening provided in the insertion portion,
When the insertion tube is inserted into the lumen of the object to be sterilized and the sterilization chamber is depressurized, the sterilizing agent introduced into the inner side of the lumen is discharged from the insertion port of the lumen. An insertion diameter is provided, and at least a part of the container is made of a flexible material so that one end of the container bends in the direction of gravity when the container is inserted from the insertion port into the lumen of the object to be sterilized. And one end in the container has reached the back side near one end of the container ,
And a sterilizing agent that further includes an adhesion preventing portion that prevents the insertion port from being closed and closed when the insertion tube is inserted into the lumen, and wherein the adhesion prevention unit does not allow the insertion port to be in close contact with the container. With empty space that can be discharged,
A sterilization method in a sterilization aid used when sterilizing an object to be sterilized having a lumen in a sterilization chamber,
A decompression step in which the sterilization aid is inserted into the lumen of the article to be sterilized to decompress the sterilization chamber;
A discharging step of introducing the sterilizing agent stored in the container into the inner side of the lumen by the pressure reducing step and discharging the sterilizing agent from the opening;
Including
As the sterilization chamber is depressurized by the depressurization step, the sterilizing agent accumulated on the back side, which is one end of the container, is inserted into the lumen of the article to be sterilized from one end of the insertion tube. A sterilization method for moving to the opening and releasing the sterilizing agent stored in the container from the opening to the inner side of the lumen.

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