Jones Kristi L, Megahed Ameer A, Diehl Brittany N, Chan Ann M, Hernández Oscar, Cabrera Catalina, Bittar João H J
Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.
Department of Animal Medicine (Internal Medicine), Faculty of Veterinary Medicine, Benha University, Moshtohor-Toukh, Kalyobiya 13736, Egypt.
Animals (Basel). 2022 Dec 14;12(24):3534. doi: 10.3390/ani12243534.
Monitoring circulating progesterone (P4) concentration is an important component of basic and applied reproduction research and clinical settings. IMMULITE® 2000 XPi (Siemens) is a newly upgraded fully automated immunoassay system marketed for human use to measure concentrations of different analytes including P4. Our objective was therefore to characterize the analytical performance of the IMMULITE® 2000 XPi P4 immunoassay across the reportable range in ovine serum. This validation of analytical performance included determining (1) linearity, (2) precision through within-run, and between-run coefficient of variation (CV) calculations, (3) accuracy through bias calculations for spiking-recovery bias and interlaboratory (range and average based) bias for two laboratories across the reportable range (0.2−40 ng/mL). The average within-run and between-run precision (CV%) across the reportable range of the IMMULITE® 2000 XPi P4 immunoassay for serum P4 concentration were both <5%, ranging between 2−8%. The average Observed Total Analytic Error (TEo) reported here for serum P4 concentration across the reportable range was ~30%, ranging from 14.8−59.4%, regardless of the considered bias. Based on these data we conclude that the automated IMMULITE® 2000 XPi P4 immunoassay provides a precise, accurate, reliable, and safe method for measuring P4 concentration ovine serum.
监测循环孕酮(P4)浓度是基础生殖研究、应用生殖研究及临床环境中的一个重要组成部分。IMMULITE® 2000 XPi(西门子公司)是一种新升级的全自动免疫分析系统,用于人体检测包括P4在内的不同分析物的浓度。因此,我们的目标是在绵羊血清的可报告范围内,对IMMULITE® 2000 XPi P4免疫分析的分析性能进行表征。这种分析性能验证包括确定:(1)线性;(2)通过批内和批间变异系数(CV)计算来确定精密度;(3)通过加标回收率偏差计算以及两个实验室在可报告范围(0.2 - 40 ng/mL)内的实验室间偏差(基于范围和平均值)计算来确定准确度。IMMULITE® 2000 XPi P4免疫分析在血清P4浓度可报告范围内的平均批内和批间精密度(CV%)均<5%,范围在2 - 8%之间。无论考虑何种偏差,此处报告的血清P4浓度在可报告范围内的平均观察总分析误差(TEo)约为30%,范围为14.8 - 59.4%。基于这些数据,我们得出结论,自动化的IMMULITE® 2000 XPi P4免疫分析为测量绵羊血清中的P4浓度提供了一种精确、准确、可靠且安全的方法。