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  • María S Aurora Prado, Martin Steppe, Marina Franco Maggi Tavares, Érika Rosa Maria Kedor-Hackmann, M. I Santoro
  • Chemistry, Medicine
  • Journal of pharmaceutical and biomedical analysis
  • 2005 (First Published: 1 February 2005)
  • Two novel analytical methodologies using capillary electrophoresis (CE) and reversed-phase high-performance liquid chromatography (RP-HPLC) for the determination of diazepam in commercial andContinue Reading
  • M. I Santoro, Nájla Mohamad Kassab, Anil Kumar Singh, Erika Rosa Maria Kedor-Hackmam
  • Chemistry, Medicine
  • Journal of pharmaceutical and biomedical analysis
  • 2006
  • The objective of this research was to develop and validate analytical methods for quantitative determination of fluoroquinolones of third generation. Simple and rapid chromatographic method wasContinue Reading
    Abstract High-performance liquid-chromatographic (HPLC) methods were validated for determination of pravastatin sodium (PS), fluvastatin sodium (FVS), atorvastatin calcium (ATC), and rosuvastatinContinue Reading
  • S A Benetton, Érika Rosa Maria Kedor-Hackmann, M. I Santoro, Valéria Matos Borges
  • Chemistry, Medicine
  • Talanta
  • 1998 (First Published: 1 November 1998)
  • Two methods are described for the determination of rifampicin and isoniazid in mixtures by visible spectrophotometry and first-derivative ultraviolet spectrophotometry. The absorbance at 475 nm inContinue Reading
  • Tatiana Tatit de Fazio, Anil Kumar Singh, Érika Rosa Maria Kedor-Hackmann, M. I Santoro
  • Chemistry, Medicine
  • Journal of pharmaceutical and biomedical analysis
  • 2007 (First Published: 1 March 2007)
  • Cleaning validation is an integral part of current good manufacturing practices in any pharmaceutical industry. Nowadays, azathioprine and several other pharmacologically potent pharmaceuticals areContinue Reading