Do gastrointestinal transit parameters influence the pharmacokinetics of gefitinib?
Wilson, C. G. and O'Mahony, B. and Connolly, S. M. and Cantarini, M. V. and Farmer, M.R. and Dickinson, P.A. and Smith, R. P. and Swaisland, H.C. (2009) Do gastrointestinal transit parameters influence the pharmacokinetics of gefitinib? International Journal of Pharmaceutics, 376 (1-2). pp. 7-12. ISSN 1873-3476 (https://doi.org/10.1016/j.ijpharm.2009.04.008)
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The selective EGFR tyrosine kinase inhibitor, gefitinib has been shown to be active against certain human carcinomas. It had been noted that a proportion of volunteers consistently had lower gefitinib exposure following oral administration. The shape of the elimination profile in this subset was also different, showing a monophasic elimination pattern rather than the biphasic pattern observed in the majority of subjects. A gamma scintigraphic study was conducted to examine the relationship of gastrointestinal transit and drug absorption in a cohort of rapid clearance subjects (n = 5) and normal profile volunteers (n = 7). The fasted volunteer panel received a 250 mg gefitinib tablet labelled with [111In]–DTPA together with 240 mL [99mTc]-labelled water. The rapid clearance cohorts were shown to have a faster mean gastric emptying T90 (37 min vs 74 min) and shorter small intestinal transit time (156 min vs 204 min), resulting in an earlier colonic arrival time (181 min vs 244 min). Mean plasma Cmax was lower (99.2 ng/mL vs 116 ng/mL) and AUC almost half in the rapid clearance group (2162 ± 81 ngh/mL vs 4996 ± 64 ngh/mL). These data suggest that gastrointestinal transit parameters play a role in the differences in the rapid clearance profile group, also contributing to the biphasic to monophasic switch. However, historical data show, at the recommended dose of 250 mg/day steady-state plasma concentrations adequate for clinical benefit are achieved in patients with non-small cell lung cancer.
ORCID iDs
Wilson, C. G. ORCID: https://orcid.org/0000-0002-4211-7907, O'Mahony, B., Connolly, S. M., Cantarini, M. V., Farmer, M.R., Dickinson, P.A., Smith, R. P. and Swaisland, H.C.;-
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Item type: Article ID code: 34794 Dates: DateEvent6 July 2009Published14 April 2009Published OnlineSubjects: Medicine > Pharmacy and materia medica Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences > Pharmaceutical SciencesDepositing user: Pure Administrator Date deposited: 19 Oct 2011 17:35 Last modified: 16 Nov 2024 19:23 URI: https://strathprints.strath.ac.uk/id/eprint/34794