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使用常规基质辅助激光解吸/电离飞行时间质谱系统快速同时定量测定不同的小分子药物。

Rapid simultaneous quantitative determination of different small pharmaceutical drugs using a conventional matrix-assisted laser desorption/ionization time-of-flight mass spectrometry system.

机构信息

Cluster of Excellence Macromolecular Complexes, Institute of Pharmaceutical Chemistry, Goethe University Frankfurt, Max-von-Laue-Str. 9, 60438 Frankfurt, Germany.

出版信息

Rapid Commun Mass Spectrom. 2009 Nov;23(22):3555-62. doi: 10.1002/rcm.4283.

DOI:10.1002/rcm.4283
PMID:19844965
Abstract

The present study establishes a simple, rapid and sensitive method for the simultaneous quantification of different small pharmaceutical drugs using a matrix-assisted laser desorption/ionization source (MALDI) coupled with a time-of-flight (TOF) mass analyzer. Neither time-consuming sample preparation, nor special target plates, isotopically labelled internal standards or other extra equipment are necessary. A simple standard dried-droplet preparation with the common matrix alpha-cyano-4-hydroxycinnamic acid (CHCA) was used. The background signals of CHCA in the low-mass region did not pose the presumed problem, because the sensitivity, resolution and mass accuracy of a modern MALDI-TOF MS system is sufficient to overcome this difficulty. Four experiments were performed in order to verify the quantification method. First, ten different phenothiazines were quantified in the range of 5-2000 nM (1-880 ng/mL). A good precision (relative standard deviation (RSD) 4.4-9.3%), linearity (R2 >0.99) and accuracy (error 4.7-11%) was obtained in all cases. Additionally, simultaneous quantification of these ten phenothiazines was carried out in human plasma without prior chromatographic separation in the range of 2-1750 ng/mL yielding good linearity, precision and accuracy (mean RSD 7.6%; R2 >0.99, mean error 8.0%). Accordingly, a quantitative analysis of ten chemically and pharmaceutically unrelated drugs was performed in the same way. A comparable linearity (R2 >0.99), precision (mean RSD 7.6%) and accuracy (mean error 8.3%) was obtained in the range of 5-2000 nM. Finally, the prazosin content of a commercial tablet was directly determined without further purification steps.

摘要

本研究建立了一种简单、快速、灵敏的方法,用于使用基质辅助激光解吸/电离源(MALDI)与飞行时间(TOF)质谱仪同时定量不同的小分子药物。既不需要耗时的样品制备,也不需要特殊的靶板、同位素标记的内标或其他额外的设备。使用了一种简单的标准干液滴制备方法,使用常见的基质α-氰基-4-羟基肉桂酸(CHCA)。CHCA 在低质量区域的背景信号不会造成假设的问题,因为现代 MALDI-TOF MS 系统的灵敏度、分辨率和质量精度足以克服这一困难。进行了四项实验以验证定量方法。首先,在 5-2000 nM(1-880 ng/mL)范围内定量了十种不同的吩噻嗪。在所有情况下,均获得了良好的精密度(相对标准偏差(RSD)4.4-9.3%)、线性(R2>0.99)和准确性(误差 4.7-11%)。此外,无需色谱分离即可在 2-1750 ng/mL 范围内对人血浆中的这十种吩噻嗪进行同时定量,得到了良好的线性、精密度和准确性(平均 RSD 7.6%;R2>0.99,平均误差 8.0%)。因此,以相同的方式对十种化学和药物上无关的药物进行了定量分析。在 5-2000 nM 的范围内,获得了相当的线性(R2>0.99)、精密度(平均 RSD 7.6%)和准确性(平均误差 8.3%)。最后,直接对市售片剂中的普萘洛尔含量进行了测定,无需进一步的纯化步骤。

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