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CN101957363A - Sample treatment fluid for latex immunoturbidimetry detection - Google Patents

Sample treatment fluid for latex immunoturbidimetry detection Download PDF

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Publication number
CN101957363A
CN101957363A CN2010102787066A CN201010278706A CN101957363A CN 101957363 A CN101957363 A CN 101957363A CN 2010102787066 A CN2010102787066 A CN 2010102787066A CN 201010278706 A CN201010278706 A CN 201010278706A CN 101957363 A CN101957363 A CN 101957363A
Authority
CN
China
Prior art keywords
sample treatment
treatment solution
buffering agent
latex immunoturbidimetry
ionics
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN2010102787066A
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Chinese (zh)
Inventor
吕军
赵世鹏
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NANJING KABO BIOTECHNOLOGY CO Ltd
Original Assignee
NANJING KABO BIOTECHNOLOGY CO Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NANJING KABO BIOTECHNOLOGY CO Ltd filed Critical NANJING KABO BIOTECHNOLOGY CO Ltd
Priority to CN2010102787066A priority Critical patent/CN101957363A/en
Publication of CN101957363A publication Critical patent/CN101957363A/en
Pending legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The invention relates to sample treatment fluid for latex immunoturbidimetry detection, which comprises triglycercide ethoxylate, a nonionic surfactant, glucan (20 thousands) and a buffer. The invention solves the problem that latex immunoturbidimetry can not be adopted for detection because the sample treatment fluid in the traditional reagent has poor effect of eliminating high-degree chyle or turbidity phenomenon of a sample.

Description

The latex immunoturbidimetry detects uses sample treatment solution
Technical field
The invention belongs to the medical science detection and use the sample treatment solution field, particularly relate to a kind of latex immunoturbidimetry detection sample treatment solution.
Technical background
The detectable of latex immunoturbidimetry is widely used in the clinical examination field detecting the immunoassays of antigen in the sample or antibody.But when running into the clinical sample of height chyle or muddiness, the sample treatment solution in the available reagent is bad for the height chyle or the turbid phenomenon elimination effect of sample, thereby causes can't adopting the latex immunoturbidimetry to detect because of the sample blank value is too high.
Summary of the invention
The purpose of this invention is to provide a kind of latex immunoturbidimetry and detect the sample change clarification of using sample treatment solution, described sample preparation liquid can make height chyle or muddiness.Solved clinically and eliminated the bad problem that can't adopt the latex immunoturbidimetry to detect of effect for the height chyle or the turbid phenomenon of sample because of the sample treatment solution in the available reagent.
To achieve these goals, the technical solution used in the present invention is: the latex immunoturbidimetry detects and uses sample treatment solution, comprises following composition: ethoxylated triglycerides, non-ionics, glucosan 20,000, buffering agent.Its hydrophilic hydrophobic balance value of described ethoxylated triglycerides is 6.Described non-ionics is Qu Latong 100 or polysorbas20.Described buffering agent is any one in phosphate buffer, 4-hydroxyethyl piperazine ethanesulfonic acid damping fluid, 2-sign indicating number quinoline ethyl sulfonic acid damping fluid, the trishydroxymethylaminomethane hydrochloride buffer.The content that the latex immunoturbidimetry detects with each composition of sample treatment solution is: the buffering agent of (1) 0.3~3% ethoxylated triglycerides, (2) 0.05~3% non-ionics, glucosan 20,000, (4) 0.02~0.5mol/L of (3) 0.02~2%.
Chyle or muddiness easily become when increasing because of the hdl particle that is rich in triglyceride in the blood plasma, the present invention has added ethoxylated triglycerides in sample preparation liquid, ethoxylated triglycerides can dissolve the hdl particle that is rich in triglyceride, makes sample to be checked become clarification.When the hydrophilic hydrophobic balance value of ethoxylated triglycerides is 6, content be 0.3~3% o'clock better.But independent ethoxylated triglycerides can not be dissolved in the buffering agent, therefore needs to add at least a non-ionic surfactant and promotes its dissolving.Non-ionics can be Qu Latong 100 or polysorbas20, and its content is neither to influence the latex immunoturbidimetry at 0.05~3% o'clock to measure and 0.3~3% ethoxylated triglycerides can be dissolved fully again.Glucosan 20,000 in the sample preparation liquid also works to quicken the ethoxylated triglycerides dissolving, content be 0.02~2% o'clock better.Buffering agent is any one in phosphate buffer, 4-hydroxyethyl piperazine ethanesulfonic acid damping fluid, 2-sign indicating number quinoline ethyl sulfonic acid damping fluid, the trishydroxymethylaminomethane hydrochloride buffer, the pH value of sample treatment solution can be controlled in 6~8 the scope, content is advisable with 0.02~0.5mol/L, is beneficial to the carrying out of latex immunoturbidimetry reaction.
The advantage that latex immunoturbidimetry from the above of the present invention detects with sample treatment solution is that sample preparation liquid can make height chyle or muddy sample become clarification, has solved problems of the prior art.
Embodiment
The latex immunoturbidimetry detects and uses sample treatment solution, and comprise following composition: (1) 1%, hydrophilic hydrophobic balance value is 6 ethoxylated triglycerides, (2) 0.1% polysorbas20, (3) 0.04% glucosan 20,000, the phosphate buffer of (4) 0.05mol/L.
Get the piarhemia sample and the normal blood of 20 μ L muddinesses respectively, each adds 800 μ L sample preparation liquid and mixes, after leaving standstill 10 seconds, detect the background level of two samples with the specific protein analyser, the result shows that two background levels are identical, i.e. Hun Zhuo piarhemia sample clarification fully after sample preparation liquid is handled.

Claims (9)

1. the latex immunoturbidimetry detects and uses sample treatment solution, it is characterized in that comprising following composition: ethoxylated triglycerides, non-ionics, glucosan 20,000, buffering agent.
2. detect according to the described latex immunoturbidimetry of claim 1 and use sample treatment solution, it is characterized in that its hydrophilic hydrophobic balance value of described ethoxylated triglycerides is 6.
3. use sample treatment solution according to claim 1 or 2 described latex immunoturbidimetries detections, it is characterized in that described non-ionics is Qu Latong 100 or polysorbas20.
4. use sample treatment solution according to claim 1 or 2 described latex immunoturbidimetries detections, it is characterized in that described buffering agent is any one in phosphate buffer, 4-hydroxyethyl piperazine ethanesulfonic acid damping fluid, 2-sign indicating number quinoline ethyl sulfonic acid damping fluid, the trishydroxymethylaminomethane hydrochloride buffer.
5. detect according to the described latex immunoturbidimetry of claim 3 and use sample treatment solution, it is characterized in that described buffering agent is any one in phosphate buffer, 4-hydroxyethyl piperazine ethanesulfonic acid damping fluid, 2-sign indicating number quinoline ethyl sulfonic acid damping fluid, the trishydroxymethylaminomethane hydrochloride buffer.
6. detect according to claim 1 or 2 described latex immunoturbidimetries and use sample treatment solution, it is characterized in that the content of each composition is: the buffering agent of (1) 0.3~3% ethoxylated triglycerides, (2) 0.05~3% non-ionics, glucosan 20,000, (4) 0.02~0.5mol/L of (3) 0.02~2%.
7. detect according to the described latex immunoturbidimetry of claim 3 and use sample treatment solution, it is characterized in that the content of each composition is: the buffering agent of (1) 0.3~3% ethoxylated triglycerides, (2) 0.05~3% non-ionics, glucosan 20,000, (4) 0.02~0.5mol/L of (3) 0.02~2%.
8. detect according to the described latex immunoturbidimetry of claim 4 and use sample treatment solution, it is characterized in that the content of each composition is: the buffering agent of (1) 0.3~3% ethoxylated triglycerides, (2) 0.05~3% non-ionics, glucosan 20,000, (4) 0.02~0.5mol/L of (3) 0.02~2%.
9. detect according to the described latex immunoturbidimetry of claim 5 and use sample treatment solution, it is characterized in that the content of each composition is: the buffering agent of (1) 0.3~3% ethoxylated triglycerides, (2) 0.05~3% non-ionics, glucosan 20,000, (4) 0.02~0.5mol/L of (3) 0.02~2%.
CN2010102787066A 2010-09-13 2010-09-13 Sample treatment fluid for latex immunoturbidimetry detection Pending CN101957363A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010102787066A CN101957363A (en) 2010-09-13 2010-09-13 Sample treatment fluid for latex immunoturbidimetry detection

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010102787066A CN101957363A (en) 2010-09-13 2010-09-13 Sample treatment fluid for latex immunoturbidimetry detection

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CN101957363A true CN101957363A (en) 2011-01-26

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102628868A (en) * 2011-12-30 2012-08-08 北京九强生物技术股份有限公司 Latex enhanced immunoturbidimetry kit for detection of asymmetric dimethylarginine content
CN103698525A (en) * 2014-01-09 2014-04-02 北京万泰德瑞诊断技术有限公司 Latex immunoturbidimetry pepsinogen I detection kit for eliminating chyle interference
CN105067815A (en) * 2015-09-16 2015-11-18 浙江凯成生物科技有限公司 Kit for measuring pepsinogen I/II content of human serum

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CN1507564A (en) * 2001-12-27 2004-06-23 ���µ�����ҵ��ʽ���� Method for measuring immune response and kit for measuring immune response used in the method
CN1545420A (en) * 2001-08-20 2004-11-10 ˹��ά˹��ҽҩ���޹�˾ Topical composition, topical composition precursor, and methods for manufacturing and using
CN101266244A (en) * 2007-03-15 2008-09-17 爱芙乐赛制药株式会社 Settlement inhibiting method of tiny particle for binding reactive substance and the reagent

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JPS582660A (en) * 1981-06-30 1983-01-08 Chugai Pharmaceut Co Ltd Immunological reagent
JPS59220646A (en) * 1983-05-30 1984-12-12 Green Cross Corp:The Aqueous solvent for aggregation test
JPS6125062A (en) * 1984-07-13 1986-02-03 Nitsusui Seiyaku Kk Measurement of aso value by immunonephelometry
CN1372144A (en) * 2001-02-19 2002-10-02 奥林匹斯诊断有限公司 Reagent for eliminating biological specimen turbidness
CN1545420A (en) * 2001-08-20 2004-11-10 ˹��ά˹��ҽҩ���޹�˾ Topical composition, topical composition precursor, and methods for manufacturing and using
CN1507564A (en) * 2001-12-27 2004-06-23 ���µ�����ҵ��ʽ���� Method for measuring immune response and kit for measuring immune response used in the method
CN101266244A (en) * 2007-03-15 2008-09-17 爱芙乐赛制药株式会社 Settlement inhibiting method of tiny particle for binding reactive substance and the reagent

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102628868A (en) * 2011-12-30 2012-08-08 北京九强生物技术股份有限公司 Latex enhanced immunoturbidimetry kit for detection of asymmetric dimethylarginine content
CN102628868B (en) * 2011-12-30 2014-09-17 北京九强生物技术股份有限公司 Latex enhanced immunoturbidimetry kit for detection of asymmetric dimethylarginine content
CN103698525A (en) * 2014-01-09 2014-04-02 北京万泰德瑞诊断技术有限公司 Latex immunoturbidimetry pepsinogen I detection kit for eliminating chyle interference
CN103698525B (en) * 2014-01-09 2015-10-14 北京万泰德瑞诊断技术有限公司 Latex immunoturbidimetry pepsinogen I detection kit for eliminating chyle interference
CN105067815A (en) * 2015-09-16 2015-11-18 浙江凯成生物科技有限公司 Kit for measuring pepsinogen I/II content of human serum

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Application publication date: 20110126