Abstract
A balance between pharmacological activity, safety and drug metabolism and pharmacokinetics (DMPK) at-tributes determines the fate of a new chemical entity (NCE) in drug discovery. Because of the increased number of NCEsrequiring DMPK evaluation, several in vitro higher-throughput screens and counter screens designed to evaluate DMPKattributes have been introduced in drug discovery. The DMPK screens evaluate NCEs for potential absorption, metabo-lism, drug-drug interactions, brain penetration, protein binding and pharmacokinetics. Higher-throughput analytical meth-odologies for the determination of either a common end product of a screen or the parent compound (and/or possible me-tabolites) are essential for successful DMPK screens. Because of its speed, sensitivity and specificity, liquid chromatogra-phy-tandem mass spectrometry (LC-MS/MS) has become the technology of choice for sample analysis. In this review,several in vitro screening assays that we employ in drug discovery are discussed with an e mphasis on LC-MS/MS role inaccelerating them.
Keywords: LC-MS/MS, MUX, DMPK screens, drug discovery, in vitro assays, matrix effect, higher-throughput analysis
Current Drug Metabolism
Title: Utility of Mass Spectrometry for In-Vitro ADME Assays
Volume: 7 Issue: 5
Author(s): Inhou Chu and Amin A.Nomeir
Affiliation:
Keywords: LC-MS/MS, MUX, DMPK screens, drug discovery, in vitro assays, matrix effect, higher-throughput analysis
Abstract: A balance between pharmacological activity, safety and drug metabolism and pharmacokinetics (DMPK) at-tributes determines the fate of a new chemical entity (NCE) in drug discovery. Because of the increased number of NCEsrequiring DMPK evaluation, several in vitro higher-throughput screens and counter screens designed to evaluate DMPKattributes have been introduced in drug discovery. The DMPK screens evaluate NCEs for potential absorption, metabo-lism, drug-drug interactions, brain penetration, protein binding and pharmacokinetics. Higher-throughput analytical meth-odologies for the determination of either a common end product of a screen or the parent compound (and/or possible me-tabolites) are essential for successful DMPK screens. Because of its speed, sensitivity and specificity, liquid chromatogra-phy-tandem mass spectrometry (LC-MS/MS) has become the technology of choice for sample analysis. In this review,several in vitro screening assays that we employ in drug discovery are discussed with an e mphasis on LC-MS/MS role inaccelerating them.
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Cite this article as:
Chu Inhou and A.Nomeir Amin, Utility of Mass Spectrometry for In-Vitro ADME Assays, Current Drug Metabolism 2006; 7 (5) . https://dx.doi.org/10.2174/138920006777697954
DOI https://dx.doi.org/10.2174/138920006777697954 |
Print ISSN 1389-2002 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5453 |
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