Literature DB >> 11002275

Applications of hyphenated LC-MS techniques in pharmaceutical analysis.

J Ermer1, M Vogel.   

Abstract

In pharmaceutical analysis, ie the analytical development and quality control of drug substances and dosage forms, mass spectrometry (MS) combined with chromatographic separation is perhaps the most powerful technique for the monitoring, characterization and identification of impurities. The addition of further dimensions to chromatographic separations by hyphenated techniques offers unique possibilities of efficiently supporting pharmaceutical development and ensuring the quality and safety of pharmaceuticals. However, the ionization process in MS involves some characteristics which have to be recognized and taken into account for an appropriate application as well as the evaluation of the results. Chromatographic method development and validation can be supported very effectively by MS detection, eg in the investigation of coelution and peak purity. Chiral amino acid analysis is largely facilitated by the mass-specific detection of the derivatized amino acid enantiomers, which ignores all other interfering substance peaks. Examples are presented for the use of LC-MS-MS fragmentation and high-resolution MS in the structural elucidation of degradation products and impurities. LC-MS is systematically applied to monitor impurity profiles during pharmaceutical development and scaling up and supports the safety evaluation of batches used in clinical studies. Copyright 2000 John Wiley & Sons, Ltd.

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Year:  2000        PMID: 11002275     DOI: 10.1002/1099-0801(200010)14:6<373::AID-BMC29>3.0.CO;2-S

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  6 in total

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2.  Liquid Chromatography-High Resolution Mass Spectrometry for Peptide Drug Quality Control.

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Review 4.  Current and potential applications of simultaneous DSC-FTIR microspectroscopy for pharmaceutical analysis.

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5.  Identification of process related trace level impurities in the actinide decorporation agent 3,4,3-LI(1,2-HOPO): Nozzle-skimmer fragmentation via ESI LC-QTOFMS.

Authors:  Nagender R Panyala; Manuel Sturzbecher-Hoehne; Rebecca J Abergel
Journal:  J Pharm Biomed Anal       Date:  2014-08-12       Impact factor: 3.935

Review 6.  Adaptation of high-throughput screening in drug discovery-toxicological screening tests.

Authors:  Paweł Szymański; Magdalena Markowicz; Elżbieta Mikiciuk-Olasik
Journal:  Int J Mol Sci       Date:  2011-12-29       Impact factor: 5.923

  6 in total

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