Wang Huiyong, Bussy Ugo, Chung-Davidson Yu-Wen, Li Weiming
Department of Fisheries and Wildlife, Room 13 Natural Resources Building, 480 Wilson Road, Michigan State University, East Lansing, MI 48824, USA.
Department of Fisheries and Wildlife, Room 13 Natural Resources Building, 480 Wilson Road, Michigan State University, East Lansing, MI 48824, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Jan 15;1009-1010:170-8. doi: 10.1016/j.jchromb.2015.12.030. Epub 2015 Dec 21.
This study aims to provide a rapid, sensitive and precise UPLC-MS/MS method for target steroid quantitation in biological matrices. We developed and validated an UPLC-MS/MS method to simultaneously determine 16 steroids in plasma and tissue samples. Ionization sources of Electrospray Ionization (ESI) and Atmospheric Pressure Chemical Ionization (APCI) were compared in this study by testing their spectrometry performances at the same chromatographic conditions, and the ESI source was found up to five times more sensitive than the APCI. Different sample preparation techniques were investigated for an optimal extraction of steroids from the biological matrices. The developed method exhibited excellent linearity for all analytes with regression coefficients higher than 0.99 in broad concentration ranges. The limit of detection (LOD) was from 0.003 to 0.1ng/mL. The method was validated according to FDA guidance and applied to determine steroids in sea lamprey plasma and tissues (fat and testes) by the developed method.
本研究旨在提供一种快速、灵敏且精确的超高效液相色谱-串联质谱(UPLC-MS/MS)方法,用于生物基质中目标类固醇的定量分析。我们开发并验证了一种UPLC-MS/MS方法,可同时测定血浆和组织样品中的16种类固醇。本研究通过在相同色谱条件下测试电喷雾电离(ESI)和大气压化学电离(APCI)这两种电离源的光谱性能进行比较,发现ESI源的灵敏度比APCI源高五倍。研究了不同的样品制备技术,以从生物基质中最佳提取类固醇。所开发的方法对所有分析物均表现出优异的线性,在较宽浓度范围内回归系数高于0.99。检测限(LOD)为0.003至0.1ng/mL。该方法根据美国食品药品监督管理局(FDA)指南进行了验证,并应用所开发的方法测定海七鳃鳗血浆和组织(脂肪和睾丸)中的类固醇。