CN1834233A - Preservative fluid for exfoliative cell - Google Patents

Preservative fluid for exfoliative cell Download PDF

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Publication number
CN1834233A
CN1834233A CN 200610017591 CN200610017591A CN1834233A CN 1834233 A CN1834233 A CN 1834233A CN 200610017591 CN200610017591 CN 200610017591 CN 200610017591 A CN200610017591 A CN 200610017591A CN 1834233 A CN1834233 A CN 1834233A
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China
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parts
preservative fluid
edta
ethylene diamine
diamine tetraacetate
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CN 200610017591
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Chinese (zh)
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CN100500835C (en
Inventor
张展
李肖甫
贾莉婷
敬明辉
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李肖甫
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Priority to CNB2006100175919A priority Critical patent/CN100500835C/en
Publication of CN1834233A publication Critical patent/CN1834233A/en
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Abstract

This invention discloses a preservation solution of exfoliated cells, which is composed of (by volume parts): methanol or ethanol 40-60, phosphate buffer solution or trihydroxymethyl aminomethane/HCl buffer solution 20-40, formaldehyde or acetone 5-10, and ethylenediamine tetraacetic acid dipotassium or Ethylenediamine tetraacetic acid disodium 5-10. This invention can reduce the cost of TCT consumable material by using inexpensive raw materials, and can reduce the consumption of consumable materials and time used on retreatment of the samples. This invention can keep the fixation of cells in reset conditions.

Description

Exfoliated cell preservative fluid
Technical field
The present invention relates to a kind ofly, especially relate to a kind of exfoliated cell preservative fluid.
Background technology
Preservation liquid (the PreserveCyt of the present new Bai Shi of the U.S. (Tinpreper TCT) manufacturer production TMSlution) be and the supporting patent reagent of its machine Tinpreper-2000, shortcoming: 1. cost an arm and a leg.2. flocks occurs after placing for some time for courageous and upright sample, operate the computer easy obstruction filtering net, cause film-making epithelial cell amount to reduce, therefore need to handle sample with Glacial acetic acid again and can go up machine.3. for the iuntercellular nucleus of piling up phenomenon appears increasing.
Summary of the invention
Purpose of the present invention just is that preserving the existing problem of liquid with regard to above-mentioned TCT improves: make it and can 1. reduce cost greatly.2. reduce flocculent precipitate, equal amount of bleeding and TCT preserve the liquid phase ratio.3. strengthen cell fixation, reduce nucleus and increase phenomenon.Thereby provide a kind of exfoliated cell preservative fluid of with low cost, better effects if.
Purpose of the present invention can realize by following measure:
The present invention is composed of the following components substantially, by volume part meter: 5 parts~10 parts of 40 parts~60 parts of methyl alcohol or ethanol, phosphate buffered saline buffer or 20 parts~40 parts of Tutofusin tris hydrochloride buffers, formaldehyde or 5 parts~10 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.
EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40% among the present invention.EDTA-2K or disodium ethylene diamine tetraacetate preferred concentration are 10%.Certainly, also can adopt other suitable concentration.One-tenth is grouped into and also includes hemolytic agent, and hemolytic agent is cyaniding high ferro or bromo 16 alkyl Trimethylamine 99s, also can be other suitable hemolytic agents.
The present invention makes it to have following advantage owing to adopt above-mentioned prescription:
1, at first can reduce the price of TCT consumptive material, because above-mentioned starting material are common biochemical reagents, cost is low. and secondly can reduce and go out the dissatisfied rate of blood specimen for the first time, reduce the consumption and the waste of time of the consumptive material handle sample again and brought. because penetration power forces cell fixation abundant, keep cell fixing under virgin state as far as possible.
Import Tnpreper TCT protects liquid Protection liquid of the present invention
Hemoglobin absorption degree cell aggregation amount sample disposal rate behind the courageous and upright sample floss of the price 30 μ l haemolysis 60 yuan/person-portion many more than 0.19 11.8% 10 yuan/person-portion few 0.27 few 4.8%
Hemolytic agent: HiCN (cyaniding high ferro/bromo 16 alkyl Trimethylamine 99s
2,1. reduce cost greatly.2. reduce flocculent precipitate, equal amount of bleeding and TCT preserve the liquid phase ratio.3. strengthen cell fixation, reduce nucleus and increase phenomenon.
Embodiment
The present invention does with detailed description below in conjunction with drawings and Examples:
Embodiment 1, the present invention are grouped into by following one-tenth substantially, by volume part is counted: methyl alcohol or ethanol (concentration 95-100%, as follows) 5 parts of 40 parts, phosphate buffered saline buffer or 20 parts of Tutofusin tris hydrochloride buffers (Tris/HCl damping fluid, as follows), formaldehyde or 5 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.More than each constituent concentration can adopt conventional concentration (as follows).
EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40% among the present invention, and preferred concentration is 10%.One-tenth is grouped into and also includes hemolytic agent, and hemolytic agent is cyaniding high ferro or bromo 16 alkyl Trimethylamine 99s, also can be other suitable hemolytic agents.Hemolytic agent by volume part is 5 parts.
Embodiment 2,
The present invention is grouped into by following one-tenth substantially, meter by volume part: 7 parts of 25 parts of 45 parts of methyl alcohol or ethanol, phosphate buffered saline buffer or Tutofusin tris hydrochloride buffers (Tris/HCl damping fluid, as follows), formaldehyde or 7 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.
EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40% among the present invention, and preferred concentration is 10%.One-tenth is grouped into and also includes hemolytic agent, and hemolytic agent is cyaniding high ferro or bromo 16 alkyl Trimethylamine 99s, also can be other suitable hemolytic agents.Hemolytic agent by volume part is 8 parts.
Embodiment 3,
The present invention is grouped into by following one-tenth substantially, meter by volume part: 8 parts of 30 parts of 50 parts of methyl alcohol or ethanol, phosphate buffered saline buffer or Tutofusin tris hydrochloride buffers (Tris/HCl damping fluid, as follows), formaldehyde or 8 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.
EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40% among the present invention, and preferred concentration is 10%.One-tenth is grouped into and also includes hemolytic agent, and hemolytic agent is cyaniding high ferro or bromo 16 alkyl Trimethylamine 99s, also can be other suitable hemolytic agents.Hemolytic agent by volume part is 15 parts.
Embodiment 4,
The present invention is grouped into by following one-tenth substantially, meter by volume part: 9 parts of 35 parts of 55 parts of methyl alcohol or ethanol, phosphate buffered saline buffer or Tutofusin tris hydrochloride buffers (Tris/HCl damping fluid, as follows), formaldehyde or 9 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.
EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40% among the present invention, and preferred concentration is 10%.
Embodiment 5,
The present invention is grouped into by following one-tenth substantially, meter by volume part: 10 parts of 40 parts of 60 parts of methyl alcohol or ethanol, phosphate buffered saline buffer or Tutofusin tris hydrochloride buffers (Tris/HCl damping fluid, as follows), formaldehyde or 10 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.
EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40% among the present invention, and preferred concentration is 10%.
In the mentioned component parameter value of each component can be as required in its value range value arbitrarily.

Claims (6)

1, a kind of exfoliated cell preservative fluid, it is characterized in that: it is grouped into by following one-tenth substantially, by volume part meter: 5 parts~10 parts of 40 parts~60 parts of methyl alcohol or ethanol, phosphate buffered saline buffer or 20 parts~40 parts of Tutofusin tris hydrochloride buffers, formaldehyde or 5 parts~10 parts in acetone, EDTA-2K or disodium ethylene diamine tetraacetate.
2, exfoliated cell preservative fluid according to claim 1 is characterized in that: described EDTA-2K or disodium ethylene diamine tetraacetate concentration are 5%~40%.
3, exfoliated cell preservative fluid according to claim 1 and 2 is characterized in that: described EDTA-2K or disodium ethylene diamine tetraacetate preferred concentration are 10%.
4, exfoliated cell preservative fluid according to claim 1 and 2 is characterized in that: described one-tenth is grouped into that also to include hemolytic agent part be 5 parts-15 parts by volume.
5, exfoliated cell preservative fluid according to claim 4 is characterized in that: described hemolytic agent is the cyaniding high ferro.
6, exfoliated cell preservative fluid according to claim 4 is characterized in that: described hemolytic agent is bromo 16 alkyl Trimethylamine 99s.
CNB2006100175919A 2006-03-31 2006-03-31 Preservative fluid for exfoliative cell Expired - Fee Related CN100500835C (en)

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CN1834233A true CN1834233A (en) 2006-09-20
CN100500835C CN100500835C (en) 2009-06-17

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101953334A (en) * 2010-08-30 2011-01-26 南京卡博生物科技有限公司 Cell preserving fluid for liquid-based cytologic diagnosis
CN101999343A (en) * 2010-10-26 2011-04-06 深圳华大基因科技有限公司 Cell preserving fluid and preparation method and use thereof
CN102318597A (en) * 2011-08-19 2012-01-18 张雪云 Liquid-based cell preservation liquid composite and preparation method thereof
CN103120153A (en) * 2012-11-26 2013-05-29 刘召宏 Exfoliative cells preserving fluid
CN104849122A (en) * 2015-06-02 2015-08-19 蒋春亮 Long-acting tumor tissue exudate sample preservation solution
CN105994252A (en) * 2016-06-22 2016-10-12 杭州海世嘉生物科技有限公司 Liquid-based thin cell preservation liquid and preparation method thereof
CN110250160A (en) * 2019-05-31 2019-09-20 广西壮族自治区人民医院 Liquid based cell preservative fluid
CN111670896A (en) * 2020-04-28 2020-09-18 浙江大学医学院附属妇产科医院 Neutral buffer tissue fixing solution
CN114208812A (en) * 2021-12-22 2022-03-22 桂林优利特医疗电子有限公司 Liquid-based cell preservation solution

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101953334A (en) * 2010-08-30 2011-01-26 南京卡博生物科技有限公司 Cell preserving fluid for liquid-based cytologic diagnosis
CN101999343A (en) * 2010-10-26 2011-04-06 深圳华大基因科技有限公司 Cell preserving fluid and preparation method and use thereof
CN101999343B (en) * 2010-10-26 2013-11-06 深圳华大基因健康科技有限公司 Cell preserving fluid and preparation method and use thereof
CN102318597A (en) * 2011-08-19 2012-01-18 张雪云 Liquid-based cell preservation liquid composite and preparation method thereof
CN102318597B (en) * 2011-08-19 2013-04-03 张雪云 Liquid-based cell preservation liquid composite and preparation method thereof
CN103120153A (en) * 2012-11-26 2013-05-29 刘召宏 Exfoliative cells preserving fluid
CN104849122A (en) * 2015-06-02 2015-08-19 蒋春亮 Long-acting tumor tissue exudate sample preservation solution
CN105994252A (en) * 2016-06-22 2016-10-12 杭州海世嘉生物科技有限公司 Liquid-based thin cell preservation liquid and preparation method thereof
CN105994252B (en) * 2016-06-22 2019-07-02 杭州海世嘉生物科技有限公司 A kind of Thinprep pap test saves liquid and preparation method thereof
CN110250160A (en) * 2019-05-31 2019-09-20 广西壮族自治区人民医院 Liquid based cell preservative fluid
CN111670896A (en) * 2020-04-28 2020-09-18 浙江大学医学院附属妇产科医院 Neutral buffer tissue fixing solution
CN114208812A (en) * 2021-12-22 2022-03-22 桂林优利特医疗电子有限公司 Liquid-based cell preservation solution

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