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使用解吸电喷雾电离和与正交加速飞行时间质谱仪相连的双离子源对药物样品进行极性切换精确质量测量。

Polarity switching accurate mass measurement of pharmaceutical samples using desorption electrospray ionization and a dual ion source interfaced to an orthogonal acceleration time-of-flight mass spectrometer.

作者信息

Williams Jonathan P, Lock Richard, Patel Vibhuti J, Scrivens James H

机构信息

Department of Biological Sciences, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK.

出版信息

Anal Chem. 2006 Nov 1;78(21):7440-5. doi: 10.1021/ac0609125.

Abstract

A novel approach for the rapid, accurate mass analysis of pharmaceutical solid, liquid, and cream formulations using desorption electrospray ionization (DESI) is described. The method is based on polarity switching and real-time accurate mass measurement in an orthogonal acceleration time-of-flight mass spectrometer fitted with a dual-inlet electrospray ion source. Infusion of a reference compound into one inlet provides a single-point "lock mass" for accurate mass measurement. The other inlet sprays solvent at the sample being investigated using DESI. Minimal sample preparation was required. Results demonstrate the ability to acquire simultaneously positive and negative accurate mass DESI data within the same acquisition, thus negating the need for repeat analysis in each ion mode. In this paper, drugs that preferentially ionize in a particular mode depending on their physiochemical properties are presented. Mass accuracy to within 2 mTh was obtained for all drugs sampled.

摘要

本文描述了一种使用解吸电喷雾电离(DESI)对药物固体、液体和乳膏制剂进行快速、准确质量分析的新方法。该方法基于在配备双入口电喷雾离子源的正交加速飞行时间质谱仪中进行极性切换和实时准确质量测量。将参考化合物注入一个入口可提供用于准确质量测量的单点“锁定质量”。另一个入口使用DESI向被研究的样品喷射溶剂。所需的样品制备极少。结果表明能够在同一采集中同时获取正离子和负离子准确质量的DESI数据,从而无需在每种离子模式下进行重复分析。本文展示了根据其物理化学性质在特定模式下优先电离的药物。对所有采样药物均获得了±2 mTh以内的质量准确度。

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