CN103882089A - High-flux microorganism detecting method for qinglu tincture - Google Patents
High-flux microorganism detecting method for qinglu tincture Download PDFInfo
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- CN103882089A CN103882089A CN201210560914.4A CN201210560914A CN103882089A CN 103882089 A CN103882089 A CN 103882089A CN 201210560914 A CN201210560914 A CN 201210560914A CN 103882089 A CN103882089 A CN 103882089A
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Abstract
The invention belongs to the technical field of microorganisms. The objective of the invention is to provide a microorganism limit detecting method of a qinglu tincture so as to facilitate research in medical science and biology. By membrane filtration, microorganisms are fully intercepted by a filtration membrane, and are washed with a proper amount of interference-free washing liquid so as to remove interference of a sample to be detected, and therefore the detection of the microorganism limit can be accurately performed. The using amount of the washing liquid is critical. Excessive washing can impair bacteria and is not conductive to growth, thus influencing the recovery rate. In addition, excessive washing will damage the filtration membrane so that the pore diameter is changed and the experiment results are influenced. Otherwise, insufficient washing cannot completely eliminate the antibacterial function of the sample, so that the accuracy of the experiment results cannot be guaranteed.
Description
Technical field
The invention belongs to biological technical field, relate to a kind of method of clear dew tincture limit test of microbe, contribute to the research to microorganism from now on of medical science and biology aspect.
Background technology
Clear dew tincture has more reasonably used the traditional Chinese medical science to take stopgap measures and has consolidated, and enriching yin wets one's whistle, clearing heat and detoxicating diagnosis and treatment based on an overall analysis of the illness and the patient's condition.Balloonflower root in prescription, Radix Glycyrrhizae clearing throat medicine carrying are up, join the Fructus Aurantii lifting mechanism of qi of regulating the flow of vital energy.The tuber of dwarf lilyturf, asparagus fern, the stem of noble dendrobium, the dried rhizome of rehmannia, cultivated land the is nourishing Yin and clearing heat anti-inflammatory that wets one's whistle.Full side reaches enriching yin and wets one's whistle, clearing heat and detoxicating (relieve sore throat).Treating acute and chronic pharyngitis, laryngeal edema.This product smell side perfume (or spice) is pure, good mouthfeel, and suitable patient takes, and has no untoward reaction, is clinical treatment acute and chronic pharyngitis, laryngeal edema good medicine.
Limit test of microbe genealogy of law test procedure specifies that sterilization preparation and raw material thereof, auxiliary material are subject to the method for microbial contamination degree, is also important means and the foundation with raw material, auxiliary material, equipment, utensil, technical process, environment and operator's sanitary condition of evaluating manufacturing enterprise.Inspection item comprises microbiological contamination amount and Control bacteria examination.
Summary of the invention
The clear tincture that reveals is made up of Chinese medicines such as balloonflower root, the stem of noble dendrobium, the dried immature fruit of citron orange, the dried rhizome of rehmannia, Radix Glycyrrhizae, cultivated land, the tuber of dwarf lilyturf and asparagus ferns, has treatment pharyngalgia, coughs and breathe heavily and heat-clearing toxin-expelling functions, occurs a small amount of precipitation after placing, on quality effect without impact.The clear tincture that reveals contains 15% ethanol, and low alcohol environment has interference to microorganism growth, can affect the accuracy of test-results.Test shows, measuring according to a conventional method its rate of recovery is only 50% ~ 60%, undesirable (should be more than 70%).By adopting membrane-filter procedure to measure, can reduce the impact of ethanol on test-results.
Embodiment
1, the supernatant liquor that test liquid is prepared sample thief adds diluent and makes test liquid.
2, bacterium solution preparation is prepared escherichia coli, streptococcus aureus, subtilis, Candida albicans and black-koji mould bacterium liquid by two methods of Chinese Pharmacopoeia version in 2005, and another compound concentration is 10 ~ 100cfu/ml escherichia coli liquid.
3, get test liquid and add in filter through membrane filtration post-flush, in washing fluid the last time, add escherichia coli, streptococcus aureus, subtilis bacterium liquid or Candida albicans and black-koji mould bacterium liquid, filter.Take out filter membrane, bacterium faces up and is affixed on nutrient agar or Rose Bengal Sodium nutrient agar, cultivates.2 plates of the parallel preparation of every strain test organisms, counting.
embodiment 1
1, test liquid is prepared supernatant liquor 10 ml of sample thief, adds diluent to 100ml, makes 1 10 test liquids.
2, bacterium solution preparation escherichia coli, streptococcus aureus, subtilis, Candida albicans and black-koji mould bacterium liquid are all by two method preparations of Chinese Pharmacopoeia version in 2005, concentration is 50 ~ 100cfu/ml, and another compound concentration is 10 ~ 100cfu/m l escherichia coli liquid.
3, getting 1 10 test liquid 1ml adds in the filter that 50ml diluent is housed, after membrane filtration, rinse 3 times, each 100ml, in washing fluid the last time, respectively add 50 ~ 100cfu/ml escherichia coli, streptococcus aureus, subtilis bacterium liquid or Candida albicans and the black-koji mould bacterium liquid of 1ml, filter.Take out filter membrane, bacterium faces up and is affixed on nutrient agar or Rose Bengal Sodium nutrient agar, puts respectively 30 ~ 35 DEG C and cultivates 48 h or put 23 ~ 28 DEG C and cultivate 72h.2 plates of the parallel preparation of every strain test organisms.Press Chinese Pharmacopoeia version method for counting colonies counting in 2005.
Claims (4)
1. a clear method of revealing tincture limit test of microbe, is characterized in that: realize by following steps: the supernatant liquor that (1) test liquid is prepared sample thief adds diluent and makes test liquid; (2) bacterium solution preparation is prepared escherichia coli, streptococcus aureus, subtilis, Candida albicans and black-koji mould bacterium liquid by two methods of Chinese Pharmacopoeia version in 2005, and another compound concentration is 10 ~ 100cfu/ml escherichia coli liquid; (3) get test liquid and add in filter through membrane filtration post-flush, in washing fluid the last time, add escherichia coli, streptococcus aureus, subtilis bacterium liquid or Candida albicans and black-koji mould bacterium liquid, filter; Take out filter membrane, bacterium faces up and is affixed on nutrient agar or Rose Bengal Sodium nutrient agar, cultivates; 2 plates of the parallel preparation of every strain test organisms, counting.
2. cell as claimed in claim 1 breeding method altogether, is characterized in that: supernatant liquor 10 ml of step (1) sample thief, add diluent to 100ml, and make 1 10 test liquids.
3. cell as claimed in claim 1 breeding method altogether, it is characterized in that: step (2) escherichia coli, streptococcus aureus, subtilis, Candida albicans and black-koji mould bacterium liquid are all by two method preparations of Chinese Pharmacopoeia version in 2005, concentration is 50 ~ 100cfu/ml, and another compound concentration is 10 ~ 100cfu/m l escherichia coli liquid.
4. cell as claimed in claim 1 breeding method altogether, it is characterized in that: step (3) is got 1 10 test liquid 1ml and added in the filter that 50ml diluent is housed, after membrane filtration, rinse 3 times, each 100ml, in washing fluid the last time, respectively add 50 ~ 100cfu/ml escherichia coli, streptococcus aureus, subtilis bacterium liquid or Candida albicans and the black-koji mould bacterium liquid of 1ml, filter; Take out filter membrane, bacterium faces up and is affixed on nutrient agar or Rose Bengal Sodium nutrient agar, puts respectively 30 ~ 35 DEG C and cultivates 48 h or put 23 ~ 28 DEG C and cultivate 72h; 2 plates of the parallel preparation of every strain test organisms; Press Chinese Pharmacopoeia version method for counting colonies counting in 2005.
Priority Applications (1)
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CN201210560914.4A CN103882089A (en) | 2012-12-21 | 2012-12-21 | High-flux microorganism detecting method for qinglu tincture |
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CN201210560914.4A CN103882089A (en) | 2012-12-21 | 2012-12-21 | High-flux microorganism detecting method for qinglu tincture |
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CN103882089A true CN103882089A (en) | 2014-06-25 |
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CN201210560914.4A Pending CN103882089A (en) | 2012-12-21 | 2012-12-21 | High-flux microorganism detecting method for qinglu tincture |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107095968A (en) * | 2017-04-24 | 2017-08-29 | 许昌学院 | A kind of anti-haze effervescent tablet of relieving sore-throat clearing lung-heat and preparation method thereof |
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2012
- 2012-12-21 CN CN201210560914.4A patent/CN103882089A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107095968A (en) * | 2017-04-24 | 2017-08-29 | 许昌学院 | A kind of anti-haze effervescent tablet of relieving sore-throat clearing lung-heat and preparation method thereof |
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Application publication date: 20140625 |