Literature DB >> 19670338

Drug impurity profiling by capillary electrophoresis/mass spectrometry using various ionization techniques.

Paul Hommerson1, Amjad M Khan, Tony Bristow, Mark W Harrison, Gerhardus J de Jong, Govert W Somsen.   

Abstract

Capillary electrophoresis/mass spectrometry (CE/MS) is predominantly carried out using electrospray ionization (ESI). Recently, atmospheric pressure chemical ionization (APCI) and atmospheric pressure photoionization (APPI) have become available for CE/MS. With the VUV lamp turned off, the APPI source may also be used for CE/MS by thermospray ionization (TSI). In the present study the suitability of ESI, APCI, APPI and TSI for drug impurity profiling by CE/MS in the positive ion mode is evaluated. The drugs carbachol, lidocaine and proguanil and their potential impurities were used as test compounds, representing different molecular polarities. A background electrolyte of 100 mM acetic acid (pH 4.5) provided baseline separation of nearly all impurities from the respective drugs. APPI yielded both even- and odd-electron ions, whereas the other ionization techniques produced even-electron ions only. In-source fragmentation was more pronounced with APCI and APPI than with ESI and TSI, which was most obvious for proguanil and its impurities. In general, ESI and TSI appeared the most efficient ionization techniques for impurities that are charged in solution achieving detection limits of 100 ng/mL (full-scan mode). APPI and APCI showed a lower efficiency, but allowed ionization of low and high polarity analytes, although quaternary ammonium compounds (e.g. carbachol) could not be detected. Largely neutral compounds, such as the lidocaine impurity 2,6-dimethylaniline, could not be detected by TSI, and yielded similar detection limits (500 ng/mL) for ESI, APPI and APCI. In many cases, impurity detection at the 0.1% (w/w) level was possible when 1 mg/mL of parent drug was injected with at least one of the CE/MS systems. Overall, the tested CE/MS systems provide complementary information as illustrated by the detection and identification of an unknown impurity in carbachol. Copyright (c) 2009 John Wiley & Sons, Ltd.

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Year:  2009        PMID: 19670338     DOI: 10.1002/rcm.4206

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  4 in total

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Authors:  Jun He; Shahab A Shamsi
Journal:  Electrophoresis       Date:  2011-04-18       Impact factor: 3.535

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4.  Proteomics as a Quality Control Tool of Pharmaceutical Probiotic Bacterial Lysate Products.

Authors:  Günter Klein; Joost P Schanstra; Janosch Hoffmann; Harald Mischak; Justyna Siwy; Kurt Zimmermann
Journal:  PLoS One       Date:  2013-06-19       Impact factor: 3.240

  4 in total

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