中国药学杂志2024,Vol.59Issue(6) :555-558.DOI:10.11669/cpj.2024.06.012

新型冠状病毒灭活疫苗抗原含量检测能力验证

Laboratory Proficiency Testing for Antigen Content of Inactived COVID-19 Vaccines

徐康维 郭君贞 高晓明 鲁旭 权娅茹 项新华 李长贵
中国药学杂志2024,Vol.59Issue(6) :555-558.DOI:10.11669/cpj.2024.06.012

新型冠状病毒灭活疫苗抗原含量检测能力验证

Laboratory Proficiency Testing for Antigen Content of Inactived COVID-19 Vaccines

徐康维 1郭君贞 2高晓明 1鲁旭 1权娅茹 1项新华 1李长贵1
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作者信息

  • 1. 中国食品药品检定研究院,北京 102629
  • 2. 山东省食品药品检验研究院,济南 250101
  • 折叠

摘要

目的 开展新型冠状病毒灭活疫苗抗原含量检测能力验证,对参加实验室检测能力进行评价.方法 对能力验证用新型冠状病毒灭活疫苗样品进行均匀性和稳定性检验,采用冷链运输方式将新型冠状病毒灭活疫苗样品、参考品及检测试剂盒分发至各参加实验室.考察鉴别试验、抗原含量检测和实验室内变异3项指标.结果 能力验证样品的均匀性和稳定性符合要求,共有14家实验室参加本次能力验证并按要求报告结果,各实验室3项指标考核结果均为满意.结论 参加本次能力验证的我国省级药检机构及灭活疫苗生产企业具有较好的新型冠状病毒灭活疫苗检测能力和质控水平.

Abstract

OBJECTIVE To evaluate the capacity of laboratories which participate in the proficiency testing of antigen content in-actived COVID-19 vaccines.METHODS Samples of inactived COVID-19 vaccines for proficiency testing were tested for uniformity and stability,and was distributed together with reference and test kits to participating laboratories by cold chain transportation.Three indexes were evaluated:differential test,antigen content detection and laboratory variation.RESULTS The uniformity and stability of the proficiency test samples met the requirements.A total of 14 laboratories participated in this proficiency test and reported the re-sults as required,and the assessment results of three indicators by each laboratory all satisfactory.CONCLUSION China's provin-cial drug testing institutions and inactivated vaccine manufacturers participating in this proficiency test have good detection capabilities and quality control levels for inactived COVID-19 vaccines.

关键词

新型冠状病毒灭活疫苗/酶联免疫吸附试验/能力验证

Key words

inactived COVID-19 vaccine/ELISA/proficiency testing

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基金项目

国家科技重大专项(2018ZX09738-005)

国家科技重大专项(2018ZX09737-003)

北京市自然科学基金(L192009)

出版年

2024
中国药学杂志
中国药学会

中国药学杂志

CSTPCD北大核心
影响因子:0.957
ISSN:1001-2494
参考文献量13
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