Titlebook: LC-MS in Drug Bioanalysis; Q. Alan Xu,Timothy L. Madden Book 2012 Springer Science+Business Media, LLC 2012 Bioanalysis.LC-MS.LC-MS/MS.Liq

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书目名称LC-MS in Drug Bioanalysis影响因子(影响力)




书目名称LC-MS in Drug Bioanalysis影响因子(影响力)学科排名




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书目名称LC-MS in Drug Bioanalysis网络公开度学科排名




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书目名称LC-MS in Drug Bioanalysis被引频次学科排名




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书目名称LC-MS in Drug Bioanalysis年度引用学科排名




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书目名称LC-MS in Drug Bioanalysis读者反馈学科排名

本能

Book 2012epileptic drugs antifundal drug antimicrobial drugs antipsychotic drugs antiretroviral drugs anxiolytic/hypnotic drugs cardiac drugs drugs for addiction immunosuppressant drugs mood stabilizer drugs This book will primarily cover the various methods of validation for LC-MS techniques and applications used in modern clinical pharmacology.

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摘要记录

RAFF

Liquid Chromatography-Mass Spectrometry for the Determination of Antidepressants and Some of their used for these therapeutic drugs, as well as common chromatographic and mass spectrometric characteristics. In addition, an LC-MS/MS method for the most common antidepressants used in clinical practice is described as an example of a whole method development and validation.

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Book 2012(MS), the high performance liquid chromatography – mass spectrometry (LC-MS) analytical technique is widely used in the determination of drugs in human biological matrixes for clinical pharmacology. Specifically, LC-MS is used to analyze: anticancer drugs antidementia drugs antidepressant drugs anti

CRAB

Internal Standards for Quantitative LC-MS Bioanalysis,al standard so that analyte losses and experimental variations during sample preparation, chromatographic separation, and mass spectrometric detection could be corrected? How is the concentration of an internal standard determined? Should internal standard responses be monitored during the analysis

贪婪的人

Method Development, Validation, and Sample Analysis for Regulated Quantitative Bioanalysis Using LCt, method validation, and sample analysis including incurred sample reanalysis (ISR). Robust and rugged LC-MS/MS methods are essential in support of drug discovery, toxicology studies, and clinical trials. The development of a robust bioanalytical method requires careful consideration of many critic

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有助于

Highly Sensitive Pharmaceutical and Clinical Analysis Using Selective Solid-Phase Extraction Coupledministration and quantification of low-abundance markers in circulating systems. Nonetheless, this task is highly challenging even for a LC-MS/MS approach, due to the extremely low levels of analytes and the highly complex matrices. Here we describe a robust method for the ultrasensitive quantifica