CN104561230B - A kind of medical science detects the preparation of sputum sample homogeneity method and reagent - Google Patents

A kind of medical science detects the preparation of sputum sample homogeneity method and reagent Download PDF

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Publication number
CN104561230B
CN104561230B CN201510031792.3A CN201510031792A CN104561230B CN 104561230 B CN104561230 B CN 104561230B CN 201510031792 A CN201510031792 A CN 201510031792A CN 104561230 B CN104561230 B CN 104561230B
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digestive system
sputum
sputum sample
preparation
phlegm
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CN104561230A (en
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燕启江
郭周萍
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SICHUAN KINGMED DIAGNOSTICS CENTER CO Ltd
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SICHUAN KINGMED DIAGNOSTICS CENTER CO Ltd
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Abstract

A kind of medical science detects the preparation of sputum sample homogeneity method and reagent.The invention provides a kind of novel phlegm Digestive system meeting clinical detection, by N-acetyl-L-cysteine 0.2% (w/v), trypsinase 0.1% (w/v), trolamine 0.4% (w/v), Repone K 0.2% (w/v), potassium primary phosphate 1.5% (w/v), phosphoric acid hydrogen dimethylamino 0.2% (w/v), sterilized water solvent composition.

Description

A kind of medical science detects the preparation of sputum sample homogeneity method and reagent
Technical field
The invention provides a kind of novel phlegm Digestive system meeting clinical detection, it can effective homogeneity sputum, protects the bacterium in sputum injury-free simultaneously, is conducive to the further analysis to sputum sample.
Background technology
Generally adopt nature expectoration method and suction sputum method to collect sputum sample clinically, the sputum sample obtained like this has obvious nonuniformity, and the distribution of the compositions such as bacterium is very uneven.Along with the development of medical test and the raising of Good Laboratory control overflow, the pre-treatment of sample is subject to increasing attention.Observe according to routine work, it is general higher that sputum specimen cultivates positive rate, but clinical coincidence rate is unsatisfactory, often occurs detecting actual pathogenic bacterium in sputum and mislead the situation of clinical diagnosis and treatment.
At present, cultivate to clinical sputum specimen bacteria distribution the commodity phlegm Digestive system used both at home and abroad and mainly produce Sputasol (Liquid) SR0233 by OXOID company of Britain, its composition comprises dithiothreitol (DTT), sodium-chlor, Repone K, Sodium phosphate dibasic, potassium primary phosphate etc.In addition, actual clinical detects or uses trypsinase, Chymotrypsin etc. to digest the way of sputum in experiment in addition.
Although had above-mentioned phlegm Digestive system and digestion method for the detection of sputum specimen, clinical practice result has shown, in the homogeneity performance of these Digestive systems and protection sample, the ability of bacterium is still weak.
Summary of the invention
Through large quantity research and comparison, contriver finds that the major cause of the problems referred to above is that the composition of viscous protein in the cracking such as dithiothreitol (DTT), proteolytic enzyme sputum also has infringement to multiple bacterium thalline, and when these material concentrations are lower, homogeneity effect has deficiency.Inventor has devised a kind of novel phlegm Digestive system meeting clinical detection, the viscous protein matter in cracking sputum is carried out with the N-acetyl-L-cysteine of low concentration and trypsinase combination, and be aided with the lower trolamine of sequestrant toxic to eliminate the detrimentally affect of heavy metal to bacterium, good homogeneity effect can be obtained while guarantee is to the low infringement of the bacterium of sputum.
On the one hand, the invention provides a kind of phlegm Digestive system, its composition comprises N-acetyl-L-cysteine.
Further, this phlegm Digestive system is made up of following ingredients:
Sterilized water solvent.
Again further, this phlegm Digestive system is made up of following ingredients:
Sterilized water solvent.
On the other hand, the invention provides the application of phlegm Digestive system of the present invention in the clinical sputum sample detection kit of preparation.
On the other hand, present invention also offers a kind of sputum sample homogeneity method, use phlegm Digestive system process sputum sample provided by the invention.
Embodiment
The preparation of 1 phlegm Digestive system of the present invention and contrast phlegm Digestive system and use
The preparation of phlegm Digestive system of the present invention
Phlegm Digestive system of the present invention is prepared according to following ingredients list:
Sterilized water solvent.
The bottle phlegm Digestive system made being packed as 10ml/ part is kept in 4 DEG C of refrigerators as stock solution.During use, every 10ml stock solution adds sterilized water 90ml and is mixed with working fluid.In sputum, add equivalent working fluid, digest 20 minutes, 10000rpm/min, centrifugal 5min in 37 DEG C of water-baths, taking precipitate is for microbial culture or be used as DNA extraction.
Contrast Digestive system 1: commercially available Sputasol (Liquid) SR0233 (OXOID), using method illustratively.
The trypsinase normal saline solution of contrast Digestive system 2:0.1% (w/v), in sputum, add equivalent Digestive system during use, digest 20 minutes in 37 DEG C of water-baths, 10000rpm/min, centrifugal 5min, taking precipitate is for microbial culture or be used as DNA extraction.
Contrast Digestive system 3:0.1% (w/v) N-acetyl-L-cysteine normal saline solution, in sputum, add equivalent Digestive system during use, digest 20 minutes in 37 DEG C of water-baths, 10000rpm/min, centrifugal 5min, taking precipitate is for microbial culture or be used as DNA extraction.
Contrast Digestive system 4: the phlegm Digestive system in Chinese patent application No. 201110126201.2 embodiments 1, using method is by the record in this application specification sheets.
2 various phlegm Digestive system digestion effects compare
2.1 homogeneity effects
Get 1 part, suction sputum sample, wash 3 times to remove the respiratory tract normal microflora on sputum surface with 40ml stroke-physiological saline solution.According to the digestion of method described in embodiment 1 sputum.Digested sputum be divided into 10 equal portions be inoculated in the dull and stereotyped and chocolate of blood agar, Mai Kangkai dull and stereotyped on, be placed in 35 DEG C of CO 2cultivate in incubator.Distinguish bacterial classification class by colonial morphology and microscopy after 3 days, record the bacterium species number that every portion of sputum is turned out on three kinds of flat boards.Result is as follows:
1 kind 2 kinds 3 kinds Be greater than 3 kinds
Phlegm Digestive system of the present invention 0 1 7 2
Contrast Digestive system 1 1 3 4 2
Contrast Digestive system 2 2 1 5 2
Contrast Digestive system 3 5 2 3 0
Contrast Digestive system 4 2 4 3 1
Visible in the sputum sample of phlegm Digestive system digestion of the present invention, in each part, bacterium species number is comparatively close, has 70% to be in same interval (3 kinds), significantly better than contrast phlegm Digestive system.
The protected effect of bacterium in 2.2 pairs of samples
100 parts, nature expectoration sample, washs 3 times to remove the respiratory tract normal microflora on sputum surface with 20ml stroke-physiological saline solution.According to the digestion of method described in embodiment 1 sputum.The sputum of digestion is inoculated in the dull and stereotyped and chocolate of blood agar, Mai Kangkai dull and stereotyped on, be placed in 35 DEG C of CO 2cultivate in incubator.Bacterial classification class is distinguished by colonial morphology and microscopy, the bacterium species number that the sputum recording often kind of method process is turned out on three kinds of flat boards after 3 days.Result is as follows:
1 kind 2 kinds 3 kinds Be greater than 3 kinds
Phlegm Digestive system of the present invention 3 29 51 17
Contrast Digestive system 1 24 24 43 9
Contrast Digestive system 2 30 27 40 3
Contrast Digestive system 3 16 31 45 8
Contrast Digestive system 4 28 19 43 10
Result shows that the bacterial classification class that phlegm Digestive system of the present invention digestion sputum specimen obtains is obviously many compared with contrast Digestive system, demonstrates phlegm Digestive system of the present invention less to the infringement of bacterium in sample.
Above-described embodiment proves, the novel phlegm Digestive system meeting clinical detection of the present invention is by carrying out the viscous protein matter in cracking sputum with the N-acetyl-L-cysteine of low concentration and trypsinase combination, and be aided with the lower trolamine of sequestrant toxic to eliminate the detrimentally affect of heavy metal to bacterium, good homogeneity effect can be obtained while guarantee is to the low infringement of the bacterium in sputum.There is situation in that can react bacterium in sputum more accurately for clinical detection, effectively reduces misdiagnosis rate.

Claims (4)

1. a phlegm Digestive system, is made up of following ingredients:
2. the phlegm Digestive system of claim 1, is made up of following ingredients:
3. the phlegm Digestive system of claim 1 or 2 is in the application preparing clinical sputum sample detection kit.
4. a sputum sample homogeneity method, uses the phlegm Digestive system process sputum sample of claim 1 or 2.
CN201510031792.3A 2015-01-22 2015-01-22 A kind of medical science detects the preparation of sputum sample homogeneity method and reagent Expired - Fee Related CN104561230B (en)

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Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105274185A (en) * 2015-11-16 2016-01-27 南京邦博生物技术有限公司 Sputum treating liquid for detecting Mycobacterium tuberculosis
CN105506085A (en) * 2015-12-28 2016-04-20 北京澳利文生物科技有限公司 Treating method for viscous fluid specimen
CN107400695B (en) * 2017-03-06 2018-03-06 李齐 A kind of sputum sample homogeneity method and the reagent used
CN106967778B (en) * 2017-03-27 2018-04-06 南京邦博生物技术有限公司 A kind of quick sputum dissolving preserves liquid
CN106868090B (en) * 2017-03-28 2020-09-29 王绪友 Sputum treatment method for medical examination
CN110964842B (en) * 2019-12-31 2023-11-03 广州金域医学检验集团股份有限公司 Sample processing reagent for detecting mycobacterium tuberculosis nucleic acid, kit and mycobacterium tuberculosis nucleic acid amplification method
CN111238893B (en) * 2020-01-19 2023-05-23 湖北泰康医疗设备有限公司 Extraction method of humoral cells for detecting lung cancer
CN112345319B (en) * 2020-09-29 2024-05-17 郑州安图生物工程股份有限公司 Digestion method of sputum sample
CN112345318B (en) * 2020-09-29 2024-05-17 郑州安图生物工程股份有限公司 Compound phlegm digestive juice

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
三种细菌培养痰标本预处理方法学评价;桂勇;《中国现代医生》;20101031;第50卷(第28期);第101页第1.2节 *

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