Discovery pharmaceutics—Challenges and opportunities
- 1 June 2006
- journal article
- review article
- Published by Springer Nature in The AAPS Journal
- Vol. 8 (2), E402-E408
- https://doi.org/10.1007/bf02854912
Abstract
Most pharmaceutical companies are now evaluating compounds for druglike properties early in the discovery process. The data generated at these early stages allow upfront identification of potential development challenges and thus selection of the best candidates for lead nomination. Most often, lead nomination candidates are selected based on pharmacological and toxicological data. However, many drugs in development suffer from poor biopharmaceutical properties due to suboptimal physiochemical parameters. The poor biopharmaceutical properties often lead to extended timelines and a higher cost of developing the compounds. To avoid these problems and choose the best compounds from a biopharmaceutical perspective, physicochemical parameters such as solubility, lipophilicity, and stability need to be evaluated as early as possible. Furthermore, the preformulation approaches used to evaluate the compounds for their pharmacokinetic and toxicological properties need to be optimized. This minireview summarizes some of the parameters and approaches that can be used to evaluate compounds in the early stages of drug discovery.Keywords
This publication has 27 references indexed in Scilit:
- ICH guidance in practice: establishment of inherent stability of secnidazole and development of a validated stability-indicating high-performance liquid chromatographic assay methodJournal of Pharmaceutical and Biomedical Analysis, 2004
- Impact of solid state properties on developability assessment of drug candidatesAdvanced Drug Delivery Reviews, 2004
- Prediction of Precipitation-Induced Phlebitis: A Statistical Validation of an In Vitro ModelJournal of Pharmaceutical Sciences, 2003
- General pharmaceutics—The new physical pharmacyJournal of Pharmaceutical Sciences, 2003
- Development of validated stability-indicating assay methods—critical reviewJournal of Pharmaceutical and Biomedical Analysis, 2002
- Stabilization of Pharmaceuticals to Oxidative DegradationPharmaceutical Development and Technology, 2002
- Chemical reactivity in solid-state pharmaceuticals: formulation implicationsAdvanced Drug Delivery Reviews, 2001
- Predictive strategy for the rapid structure elucidation of drug degradantsJournal of Pharmaceutical and Biomedical Analysis, 1996
- Effect of pH on Injection PhlebitisJournal of Pharmaceutical Sciences, 1995
- Automated analytical systems for drug development studies. I — A system for the determination of drug stabilityJournal of Pharmaceutical and Biomedical Analysis, 1994