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

被引:2
|
作者
Ma, Tingting [1 ]
Liu, Donglai [1 ]
Lyu, Keliang [1 ,2 ]
Gao, Tingting [1 ,2 ]
Shi, Dawei [1 ]
Zhao, Lanqing [1 ]
Shen, Shu [1 ]
Tian, Yabin [1 ]
Xu, Sihong [1 ,3 ]
Zhou, Haiwei [1 ,3 ]
机构
[1] Natl Inst Food & Drug Control, Inst Vitro Diagnost Control, Div Vitro Diagnost Infect Dis 2, Beijing 100050, Peoples R China
[2] Shandong Univ Technol, Sch Life Sci & Med, Zibo 255049, Peoples R China
[3] 2 Tiantan Xili, Beijing 100050, Peoples R China
关键词
SARS-CoV-2; Antigen detection kit; National reference panel; Quality standard;
D O I
10.1016/j.bsheal.2023.10.002
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
To develop a national reference panel for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) anti-gen detection kit and establish a quality standard. The cultures of SARS-CoV-2 and other pathogens were col-lected 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 sam-ples, 20 negative samples, 1 repetitive sample, and 1 lower detection limit sample. The stability and homogene-ity 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 x 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 eval-uation and post-marketing quality supervision in China. (c) 2023 Chinese Medical Association Publishing House. Published by Elsevier BV. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:326 / 330
页数:5
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