Evaluation of a High-Throughput Online Solid Phase Extraction鈥揟andem Mass Spectrometry System for In Vivo Bioanalytical Studies

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• 作者：Wenying Jian ; Michelle V. Romm ; Richard W. Edom ; Vaughn P. Miller ; William A. LaMarr ; Naidong Weng
• 刊名：Analytical Chemistry
• 出版年：2011
• 出版时间：November 1, 2011
• 年：2011
• 卷：83
• 期：21
• 页码：8259-8266
• 全文大小：818K
• 年卷期：v.83,no.21(November 1, 2011)
• ISSN：1520-6882

文摘

High throughput-solid phase extraction tandem mass spectrometry (HT-SPE/MS) is a fully automated system that integrates sample preparation using ultrafast online solid phase extraction (SPE) with mass spectrometry detection. HT-SPE/MS is capable of conducting analysis at a speed of 5鈥?0 s per sample, which is several fold faster than chromatographically based liquid chromatography鈥搈ass spectrometry (LC鈥揗S). Its existing applications mostly involve in vitro studies such as high-throughput therapeutic target screening, CYP450 inhibition, and transporter evaluations. In the current work, the feasibility of utilizing HT-SPE/MS for analysis of in vivo preclinical and clinical samples was evaluated for the first time. Critical bioanalytical parameters, such as ionization suppression and carry-over, were systematically investigated for structurally diverse compounds using generic SPE operating conditions. Quantitation data obtained from HT-SPE/MS was compared with those from LC鈥揗S analysis to evaluate its performance. Ionization suppression was prevalent for the test compounds, but it could be effectively managed by using a stable isotope labeled internal standard (IS). A structural analogue IS also generated data comparable to the LC鈥揗S system for a test compound, indicating matrix effects were also compensated for to some extent. Carry-over was found to be minimal for some compounds and variable for others and could generally be overcome by inserting matrix blanks without sacrificing assay efficiency due to the ultrafast analysis speed. Quantitation data for test compounds obtained from HT-SPE/MS were found to correlate well with those from conventional LC鈥揗S. Comparable accuracy, precision, linearity, and sensitivity were achieved with analysis speeds 20鈥?0-fold higher. The presence of a stable metabolite in the samples showed no impact on parent quantitation for a test compound. In comparison, labile metabolites could potentially cause overestimation of the parent concentration if the ion source conditions are not optimized to minimize in-source breakdown. However, with the use of conditions that minimized in-source conversion, accurate measurement of the parent was achieved. Overall, HT-SPE/MS exhibited significant potential for high-throughput in vivo bioanalysis.