Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN 55905, USA.
Semin Reprod Med. 2012 Jun;30(3):182-90. doi: 10.1055/s-0032-1311520. Epub 2012 May 14.
The quality of in vitro culture conditions is a key component of a successful clinical embryology laboratory. Many, but not all, supplies used in the embryology laboratory are screened by the supplier with a bioassay. Embryology laboratories use a variety of approaches to verify the quality of mineral oil, protein, and disposables before clinical use; however, a best practice has not been determined. Some laboratories test every supply, even those already screened by the supplier, whereas other laboratories perform as little testing as possible. Despite screening by the supplier, recent reports of embryo toxicity, specifically with mineral oil, highlight that the integrity of the supply system has gaps. This review describes current bioassay quality control testing and discusses how it applies to screening of products with documented lot-to-lot variation.
体外培养条件的质量是临床胚胎学实验室成功的关键组成部分。许多(但不是全部)胚胎学实验室使用的供应品都经过供应商的生物测定筛选。胚胎学实验室在临床使用前使用各种方法来验证矿物油、蛋白质和一次性用品的质量;然而,尚未确定最佳实践。一些实验室测试每一种供应品,甚至是那些已经经过供应商筛选的供应品,而其他实验室则尽可能少地进行测试。尽管经过供应商筛选,但最近有关矿物油等胚胎毒性的报告强调,供应系统的完整性存在差距。本综述描述了当前的生物测定质量控制测试,并讨论了如何将其应用于具有记录的批间变化的产品筛选。