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IMMULITE 2000 XPi孕酮检测法在绵羊血清定量分析中的分析验证

Analytical Validation of the IMMULITE 2000 XPi Progesterone Assay for Quantitative Analysis in Ovine Serum.

作者信息

Jones Kristi L, Megahed Ameer A, Diehl Brittany N, Chan Ann M, Hernández Oscar, Cabrera Catalina, Bittar João H J

机构信息

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.

出版信息

Animals (Basel). 2022 Dec 14;12(24):3534. doi: 10.3390/ani12243534.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e7/9774115/e00b7a5077aa/animals-12-03534-g001.jpg

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