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Rapid Commun Mass Spectrom. 2010 Feb;24(3):309-14. doi: 10.1002/rcm.4390.
The present work describes the methodology and investigates the performance of desorption electrospray ionization (DESI) combined with a triple quadrupole mass spectrometer for the quantitation of small drug molecules in human plasma. Amoxepine, atenolol, carbamazepine, clozapine, prazosin, propranolol and verapamil were selected as target analytes while terfenadine was selected as the internal standard common to each of the analytes. Protein precipitation of human plasma using acetonitrile was utilized for all samples. Limits of detection were determined for all analytes in plasma and shown to be in the range 0.2-40 ng/mL. Quantitative analysis of amoxepine, prazosin and verapamil was performed over the range 20-7400 ng/mL and shown to be linear in all cases with R(2) >0.99. In most cases, the precision (relative standard deviation) and accuracy (relative error) of each method were less than or equal to 20%, respectively. The performance of the combined techniques made it possible to analyze each sample in 15 s illustrating DESI tandem mass spectrometry (MS/MS) as powerful tool for the quantitation of analytes in deproteinized human plasma.
本工作描述了一种方法,并考察了解吸电喷雾电离(DESI)与三重四极杆质谱联用对人血浆中小药物分子定量的性能。阿莫西汀、阿替洛尔、卡马西平、氯氮平、哌唑嗪、普萘洛尔和维拉帕米被选为目标分析物,而特非那定被选为每个分析物共有的内标。所有样品均采用乙腈对人血浆进行蛋白沉淀。所有分析物在血浆中的检测限均为 0.2-40ng/mL。阿莫西汀、哌唑嗪和维拉帕米的定量分析在 20-7400ng/mL 范围内进行,所有情况下均呈线性,相关系数(R(2))大于 0.99。在大多数情况下,每种方法的精密度(相对标准偏差)和准确度(相对误差)均小于或等于 20%。该联合技术的性能使得可以在 15 秒内分析每个样品,表明 DESI 串联质谱(MS/MS)是对去蛋白人血浆中分析物进行定量的有力工具。