流式细胞仪在GLP体系下性能验证方法的建立
作者:
作者单位:

1.北京协和建昊医药技术开发有限责任公司,北京 100176; 2.中国医学科学院药物研究所新药安全评价研究中心,北京 100050

中图分类号:

R-33


Establishment of a performance verification method for flow cytometer under GLP conditions
Author:
Affiliation:

1.Beijing Union-Genius Pharmaceutical Technology Development Co., Ltd., Beijing 100176, China. 2. New Drug Safety Evaluation Center, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050

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    摘要:

    目的 建立流式细胞仪在 GLP 体系下的性能验证方法。 方法 以《YY/ T 0588-2017 流式细胞仪》行业标准为依据,在 BD FACSVerseTM流式细胞仪上建立流式细胞仪性能评价的验证方法,包括药物安全性评价中 免疫学评价常用的流式检测项目,前向角散射光和侧向角散射光分辨率、重复性、携带污染率、仪器稳定性等。 结果 BD FACSVerseTM流式细胞仪在本实验检测条件下各项性能指标均符合行业标准的技术要求。 结论 上述 性能指标验证方法准确可靠,能够满足药物安全性评价的需要,可以为流式细胞仪在GLP体系下的性能验证提供 一定的参考。

    Abstract:

    Objective To establish a method to verify the performance of a flow cytometer under GLP conditions. Methods Based on the industry standard document, YY/ T 0588 - 2017 flow cytometer, a verification method for performance evaluation of a flow cytometer was established using a BD FACSVerseTM flow cytometer, including the commonly used flow detection settings for immunological assessment in drug safety evaluation, forward angular scattering light and lateral angular scattering light resolution, repeatability, carrying pollution rateand instrument stability, among others. Results Under the test conditionsin our laboratory, the performance parameters of the BD FACSVerseTM flow cytometer were in accordance with the technical requirements of the industry standard. Conclusions The above method is accurate and reliable, and can meet the needs of drug safety evaluation. It can provide a useful reference for the performance verification of flow cytometer under GLP conditions.

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引用本文

牟文波,李 慧,安会苹,程红旭,王凤华,靳洪涛,魏金锋.流式细胞仪在GLP体系下性能验证方法的建立[J].中国比较医学杂志,2020,30(2):27~32.

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  • 收稿日期:2019-09-19
  • 在线发布日期: 2020-04-01
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