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体外受精实验室的质量控制:人类精子存活研究的应用

Quality control in an in-vitro fertilization laboratory: use of human sperm survival studies.

作者信息

Critchlow J D, Matson P L, Newman M C, Horne G, Troup S A, Lieberman B A

机构信息

Regional IVF Unit, St Mary's Hospital, Manchester.

出版信息

Hum Reprod. 1989 Jul;4(5):545-9. doi: 10.1093/oxfordjournals.humrep.a136942.

Abstract

A bioassay procedure is described for quality control testing of various disposable items used in routine IVF procedures. This bioassay is performed over 4 days and uses the survival of human sperm in vitro at room temperature to assess which products are suitable for use. New products were tested for cytotoxicity using a general screening method and subsequent batches of every suitable item tested to detect interbatch variation. Products were considered suitable or unsuitable for use depending upon a calculated sperm survival index. Two main types of product were found to be cytotoxic, namely certain brands of syringe and surgical gloves, the common feature of both being the presence of rubber components. The bioassay was also used to investigate further the cytotoxic effect of the powdered and starch-free surgical gloves. The cytotoxic substances from both types of surgical glove were readily transferred to an embryo replacement catheter by touch, and washing of the gloves reduced this effect only moderately. The bioassay has proved inexpensive and convenient but more importantly it has been invaluable for detecting potential sources of cytotoxicity before they are introduced into a standard IVF protocol.

摘要

本文描述了一种生物测定方法,用于对常规体外受精(IVF)程序中使用的各种一次性物品进行质量控制测试。该生物测定在4天内完成,利用室温下人类精子在体外的存活情况来评估哪些产品适合使用。使用通用筛选方法对新产品进行细胞毒性测试,并对每一种合适产品的后续批次进行测试,以检测批次间差异。根据计算得出的精子存活指数,判断产品是否适合使用。发现有两种主要类型的产品具有细胞毒性,即某些品牌的注射器和手术手套,两者的共同特征是都含有橡胶成分。该生物测定还用于进一步研究无粉无淀粉手术手套的细胞毒性作用。两种手术手套中的细胞毒性物质都很容易通过接触转移到胚胎移植导管上,清洗手套只能适度降低这种影响。事实证明,该生物测定成本低廉且操作方便,但更重要的是,在潜在的细胞毒性来源被引入标准IVF方案之前,它对于检测这些来源具有不可估量的价值。

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