摘要
探讨罗氏cobas e801电化学发光免疫定量分析仪进行项目游离前列腺特异性抗原(fPSA)检测方法的精密度、正确度、可报告范围等分析性能。参照卫健委行业标准WS/T 492-2016验证fPSA精密度,采用卫健委行业标准WS/T 408-2012验证fPSA线性区间。研究发现,罗氏cobas e801电化学发光免疫定量分析仪检测fPSA分析性能结果均符合相关行业标准要求,能为临床提供更准确可靠的检测结果。
Explore the precision,accuracy,reportable range,and other analytical performance of the Roche Cobas e801 Electrochemiluminescence Immunoassay Quantitative Analyzer for project fPSA detection methods.Verify the precision of fPSA according to the industry standard WS/T 492-2016 of the Ministry of Health;The fPSA linear interval was validated using the industry standard WS/T408-2012 of the Ministry of Health.Research has found that the performance results of Roche Cobas e801 electrochemical luminescence immunoassay quantitative analyzer in detecting fPSA meet the requirements of relevant industry standards,providing more accurate and reliable detection results for clinical practice.
作者
韦入翠
吴海婴
范林
龙玉成
WEI Rucai;WU Haiying;FAN Lin;LONG Yucheng(Xingyi People’s Hospital,Xingyi,Guizhou 562400)
出处
《科技与健康》
2023年第8期35-37,共3页
Technology and Health
