Establishment and application of national reference panels for SARS-CoV-2 antigen detection kit

IF 3.5 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Tingting Ma , Donglai Liu , Keliang Lyu , Tingting Gao , Dawei Shi , Lanqing Zhao , Shu Shen , Yabin Tian , Sihong Xu , Haiwei Zhou
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引用次数: 0

Abstract

To develop a national reference panel for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen detection kit and establish a quality standard. The cultures of SARS-CoV-2 and other pathogens were collected to establish a national reference panel for SARS-CoV-2 antigen detection. The stability and homogeneity of the reference panel were evaluated. Based on World Health Organization (WHO) guidance and nucleic acid quantitative results, a quality standard reference panel was established. Currently, three generations of SARS-CoV-2 antigen national reference materials with batch numbers 370095–202001, 370095–202202, and 370095–202203 have been successfully established. These national reference panels comprised 8 positive samples, 20 negative samples, 1 repetitive sample, and 1 lower detection limit sample. The stability and homogeneity of the reference panel meet the requirements. The quality standards are as follows: the positive and negative coincidence rates are 8/8 and 20/20, respectively. The 10 test results of the medium and low-concentration repetitive reference materials should be positive, and the color rendering should be uniform (or the coefficient of variance should not be higher than 20.0%). The lower detection limit should be at least 5 × 105 U/mL (equivalent to copies/mL), and higher concentrations above the lower detection limit must be positive. A national reference panel for the SARS-CoV-2 antigen detection kit has been established. As the standard of SARS-CoV-2 antigen reagents, the reference panel has played a crucial role in the pre-marketing quality evaluation and post-marketing quality supervision in China.

建立和应用国家 SARS-CoV-2 抗原检测试剂盒参考面板
开发严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)抗原检测试剂盒的国家参考试剂盒,并制定质量标准。收集 SARS-CoV-2 和其他病原体的培养物,建立 SARS-CoV-2 抗原检测国家参考试剂盒。对参考面板的稳定性和同质性进行了评估。根据世界卫生组织(WHO)的指导意见和核酸定量结果,建立了质量标准参考板。目前,已成功建立了三代 SARS-CoV-2 抗原国家参考材料,批号分别为 370095-202001、370095-202202 和 370095-202203。这些国家参考样本包括 8 份阳性样本、20 份阴性样本、1 份重复样本和 1 份检测下限样本。参比板的稳定性和均一性均符合要求。质量标准如下:阳性和阴性重合率分别为 8/8 和 20/20。中、低浓度重复性参比物的 10 次检测结果均应为阳性,显色均匀(或方差系数不高于 20.0%)。检测下限应至少为 5 × 105 U/mL(相当于拷贝数/毫升),高于检测下限的浓度必须为阳性。SARS-CoV-2 抗原检测试剂盒的国家参考面板已经建立。作为SARS-CoV-2抗原试剂的标准,参比架在我国SARS-CoV-2试剂上市前的质量评价和上市后的质量监管中发挥了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biosafety and Health
Biosafety and Health Medicine-Infectious Diseases
CiteScore
7.60
自引率
0.00%
发文量
116
审稿时长
66 days
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