研究领域
Develop methodologies to monitor the pharmacokinetics and metabolism of anticancer drugs
Perform analyses of clinical and pre-clinical samples using High Performance Liquid Chromatography and Mass Spectrometry technologies, within a Quality Management (GCLP) environment
Undertake method validation for drugs entering clinical trials, to high quality standards, for external collaborators
Apply methodologies to determine pharmacodynamic endpoints for anticancer drugs in clinical trials
近期论文
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Phillips RM, Jaffar M, Maitland DJ, Loadman PM, Shnyder SD, Steans G, Cooper PA, Race A, Patterson AV and Stratford IJ, Pharmacological and biological evaluation of a series of substituted 1,4 naphthoquinone bioreductive drugs. Biochemical Pharmacology 68: 2107-2116, 2004
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