Literature DB >> 22519368

Isotopic labeling of metabolites in drug discovery applications.

Jacobo Iglesias1, Lekha Sleno, Dietrich A Volmer.   

Abstract

Understanding the metabolic and pharmacokinetic fate of a drug in humans is a key factor in its development and registration, as well as in the elaboration of new therapeutic agents. To carry out these studies, stable isotope labeling techniques have been effectively used by drug metabolism scientists and toxicologists in order to gain better understanding of the drugs' disposition, bioavailability and toxicity in in vivo studies. Among the different analytical techniques used, mass spectrometry (MS) coupled to separation techniques has become the detection method of choice due to its high sensitivity and selectivity. In vitro quantification of metabolite levels in biofluids by MS is often difficult if a proper internal standard is not available due to the inherent problems associated with the technique (e.g. chromatographic coelutions, ion suppression, low reproducibility etc.). Stable isotope coding approaches alleviate these drawbacks and allow comparative drug metabolomics studies similarly to the differential proteomic techniques developed in the last decade. This review describes a selection of methodological improvements in the use of stable isotopes labeling in combination with MS to detect drug metabolites. In the first part of the paper, the application of labeled compounds to study the absorption, distribution, metabolism, excretion and toxicology of drugs (ADMET) in addition to the elucidation of metabolic pathways is presented. In the second part, recent developments of stable isotope coded tags for the in vitro relative metabolite quantification in biofluids are presented.

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Year:  2012        PMID: 22519368     DOI: 10.2174/138920012803341357

Source DB:  PubMed          Journal:  Curr Drug Metab        ISSN: 1389-2002            Impact factor:   3.731


  3 in total

1.  Untargeted profiling of tracer-derived metabolites using stable isotopic labeling and fast polarity-switching LC-ESI-HRMS.

Authors:  Bernhard Kluger; Christoph Bueschl; Nora Neumann; Romana Stückler; Maria Doppler; Alexander W Chassy; Andrew L Waterhouse; Justyna Rechthaler; Niklas Kampleitner; Gerhard G Thallinger; Gerhard Adam; Rudolf Krska; Rainer Schuhmacher
Journal:  Anal Chem       Date:  2014-11-17       Impact factor: 6.986

2.  Less Cytotoxic Protoflavones as Antiviral Agents: Protoapigenone 1'-O-isopropyl ether Shows Improved Selectivity Against the Epstein-Barr Virus Lytic Cycle.

Authors:  Máté Vágvölgyi; Gábor Girst; Norbert Kúsz; Sándor B Ötvös; Ferenc Fülöp; Judit Hohmann; Jean-Yves Servais; Carole Seguin-Devaux; Fang-Rong Chang; Michael S Chen; Li-Kwan Chang; Attila Hunyadi
Journal:  Int J Mol Sci       Date:  2019-12-12       Impact factor: 5.923

Review 3.  Metabolomics in infectious diseases and drug discovery.

Authors:  Vivian Tounta; Yi Liu; Ashleigh Cheyne; Gerald Larrouy-Maumus
Journal:  Mol Omics       Date:  2021-06-14
  3 in total

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