Biorelevant in-vitro performance testing of orally administered dosage forms
Authors:
- 1 July 2012
- journal article
- review article
- Published by Oxford University Press (OUP) in Journal of Pharmacy and Pharmacology
- Vol. 64 (7) , 919-930
Abstract
Objectives: This review focuses on the evolution and current status of biorelevant media and hydrodynamics, and discusses the usefulness of biorelevant performance testing in the evaluation of specific dosage form related lumenal processes. Key findings: During the last 15 years our knowledge of the gastrointestinal environment (including the lower gut) has improved dramatically and biorelevant media composition and, to a lesser extent, biorelevant hydrodynamics, have been refined. Biorelevant dissolution/release testing is useful for the evaluation of formulation and food effects on plasma levels after administration of immediate release dosage forms containing low solubility compounds and after administration of extended release products. Lumenal disintegration times of immediate release dosage forms and the bile acid sequestering activity of resins in the lumen can also be successfully forecasted with biorelevant in vitro testing. Summary: Biorelevant in-vitro performance testing is an important tool for evaluating intralumenal dosage form performance. Since the formulation of new active pharmaceutical ingredients for oral delivery is more challenging than ever before, efforts to improve the predictability of biorelevant tests are expected to continue.Keywords
This publication has 80 references indexed in Scilit:
- Biorelevant Media to Simulate Fluids in the Ascending Colon of Humans and Their Usefulness in Predicting Intracolonic Drug SolubilityPharmaceutical Research, 2010
- Estimating drug solubility in the gastrointestinal tractAdvanced Drug Delivery Reviews, 2007
- Parallel Monitoring of Plasma and Intraluminal Drug Concentrations in Man After Oral Administration of Fosamprenavir in the Fasted and Fed StatePharmaceutical Research, 2007
- Impact of the intragastric location of extended release tablets on food interactionsJournal of Controlled Release, 2005
- In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution mediaEuropean Journal of Pharmaceutical Sciences, 2005
- The use of biopharmaceutic classification of drugs in drug discovery and development: current status and future extensionJournal of Pharmacy and Pharmacology, 2005
- Dissolution Testing as a Prognostic Tool for Oral Drug Absorption: Immediate Release Dosage FormsPharmaceutical Research, 1998
- A new approach for direct in vivo dissolution studies of poorly soluble drugs.Pharmaceutical Research, 1997
- Upper Gastrointestinal pH in Seventy-Nine Healthy, Elderly, North American Men and WomenPharmaceutical Research, 1993
- Upper Gastrointestinal (GI) pH in Young, Healthy Men and WomenPharmaceutical Research, 1990