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过敏原特异性IgE抗体定量检测试剂的性能验证 被引量:3

Performance verification for allergen specific IgE antibody quantitative detection reagents
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摘要 目的对某品牌过敏原IgE抗体定量检测试剂进行性能验证。方法参考美国临床和实验室标准协会(clinical and laboratory standards institute,CLSI)及中华人民共和国医药行业标准YY/T 1581-2018的相关文件,对符博克TM过敏原IgE抗体定量检测试剂进行准确度、检出限、线性、重复性、批间差、特异性验证,并与ImmunoCAP系统检测结果进行一致性评价。结果该试剂批内变异系数(CV)<10%,批间CV<20%,与WHO 11/234标准品的相对偏差<15%,回收率为85%~115%,检出限≤0.35 IU/mL,稀释线性相关系数>0.99,对总IgE浓度>60 IU/mL的样本、IgA浓度>700μg/mL的样本、IgM浓度>500μg/mL的样本、IgG浓度>7000μg/mL的样本的测定浓度均不高于检出限(0.35 IU/mL)。与ImmunoCAP系统进行方法学比对,屋尘螨、粉尘螨、屋尘、艾蒿、鸡蛋、牛奶6个项目Kappa值均>0.75。结论该过敏原特异性IgE抗体的定量检测试剂具有良好的准确度、检出限、线性、重复性、批间差、特异性,与ImmunoCAP系统具有较高的一致性,具备临床推广价值。 Objective To verify the performance of a brand of allergen IgE antibody quantitative detection reagents.Methods According to the relevant documents of Clinical and Laboratory Standards Institute(CLSI)and pharmaceutical industry standards of the People′s Republic of China YY/T 1581-2018,the accuracy,detection limit,linearity,repeatability,inter-assay variation and specificity of HOBTM allergen IgE antibody quantitative detection reagents were verified,and the consistency was evaluated by comparing with the results of the ImmunoCAP system.Results The intra-assay coefficients of variation(CV),inter-assay CV,recovery,detection limit and linear correlation coefficient of the reagents were<10%,<20%,85%-115%,≤0.35 IU/mL and>0.99,respectively.The relative deviation between the reagents and WHO 11/234 standard mateirals was below 15%.When the samples with total IgE>60 IU/mL,IgA>700μg/mL,IgM>500μg/mL or IgG>7000μg/mL were detected by the reagents,the concentrations of allergen specific IgE antibody were not higher than the detection limit(0.35 IU/mL).Compared with the ImmunoCAP system,the Kappa values of 6 items,including dermatophagoides pteronyssinus,dermatophagoides farinae,house dust,mugwort,egg and milk,were higher than 0.75.Conclusion HOBTM allergen specific IgE antibody quantitative detection reagents have good accuracy,detection limit,linearity,repeatability,inter-assay variation and specificity,and have high consistency with the ImmunoCAP system,indicating that they have clinical application value.
作者 杜文胜 朱杰华 潘丽 黎兵 何应中 陈莉 黄俊琼 DU Wensheng;ZHU Jiehua;PAN Li;LI Bing;HE Yingzhong;CHEN Li;HUANG Junqiong(Department of Medical Laboratory, Affiliated Hospital of Zunyi Medical University, Zunyi 563003, Guizhou;Department of Clinical Laboratory, Yuxi People′s Hospital, Yuxi 653100, Yunnan, China)
出处 《临床检验杂志》 CAS 2020年第11期810-814,共5页 Chinese Journal of Clinical Laboratory Science
关键词 过敏原 IGE抗体 定量检测 性能验证 allergen IgE antibody quantitative detection performance verification
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