Matrix effects in metabolite quantification for MIST assessment: the impact of phospholipid removal and HPLC column particle size
Author:
Affiliation:
1. Waters Corporation, Chemistry Applied Technology, 34 Maple Street, Milford, MA 01757, USA
2. Department of Drug Metabolism & Pharmacokinetics, Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, USA
Abstract
Publisher
Future Science Ltd
Subject
Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry
Link
http://www.future-science.com/doi/pdf/10.4155/bio.13.330
Reference18 articles.
1. US FDA. Guidance for Industry: Safety Testing of Drug Metabolites.www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM079266.pdf
2. ICH. Guidance on Nonclinical Safety Studies for the Conduct of Human Clinical Trials and Marketing Authorization for Pharmaceuticals. (2009).www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Multidisciplinary/M3_R2/Step4/M3_R2__Guideline.pdf
3. Challenges and solutions to metabolites in safety testing: impact of the International Conference on Harmonization M3(R2) guidance
4. Approaches to the Assessment of Stable and Chemically Reactive Drug Metabolites in Early Clinical Trials
5. Determination of Exposure Multiples of Human Metabolites for MIST Assessment in Preclinical Safety Species without Using Reference Standards or Radiolabeled Compounds
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