An improved method for the quantitative measurement of the angiotensin-converting enzyme inhibitor lisinopril in human plasma is presented. The assay is based on gas chromatography/negative ion chemical ionization mass spectrometry. The method involves solid phase extraction on C18 sorbent and deriv
Mass spectrometry for enzyme assays and inhibitor screening: An emerging application in pharmaceutical research
โ Scribed by Kenneth D. Greis
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 628 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0277-7037
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โฆ Synopsis
Abstract
Robust methods that monitor enzyme activity and inhibitor potency are crucial to drug discovery and development. Over the past 20 years, mass spectrometric methods have increasingly been used to measure enzyme activity and kinetics. However, for rapid screening of inhibitory compounds, various forms of fluorescence and chemiluminscence readout have continued to dominate the market. As the sensitivity, speed, and miniaturization of mass spectrometry methods continue to advance, opportunities to couple mass spectrometry with screening will continue to come to the forefront. To appreciate the tremendous potential for MSโbased screening assays, it becomes necessary to understand the current state of capabilities in this arena. Thus, this review is intended to capture how mass spectrometry for studying enzymes activity has progressed from simple qualitative questions (i.e., is the product detected?) to quantitative measures of enzyme activity and kinetics and then as a tool for rapidly screening inhibitory compounds as an alternative to current methods of high throughput drug screening. ยฉ 2007 Wiley Periodicals, Inc., Mass Spec Rev
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