Is the full potential of the biopharmaceutics classification system reached?

• Published in: European journal of pharmaceutical sciences Vol. 57; pp. 224 - 231
• Main Authors: Bergström, Christel A.S., Andersson, Sara B.E., Fagerberg, Jonas H., Ragnarsson, Gert, Lindahl, Anders
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 16.06.2014
• Subjects: Administration, Oral; Animals; Biopharmaceutics - methods; Biopharmaceutics classification system; Biorelevant dissolution; Computer Simulation; Dose number; Humans; Hydrogen-Ion Concentration; In silico; Intestinal Absorption; Intestines - metabolism; Models, Biological; Permeability; Pharmaceutical Preparations - administration & dosage; Pharmaceutical Preparations - chemistry; Pharmaceutical Preparations - classification; Pharmaceutical Preparations - metabolism; Pharmacokinetics; Poorly soluble; Reproducibility of Results; Solubility; Terminology as Topic; Dose number; In silico; Biorelevant dissolution; Poorly soluble; Biopharmaceutics classification system; Solubility
• ISSN: 0928-0987; 1879-0720; 1879-0720
• DOI: 10.1016/j.ejps.2013.09.010

In this paper we analyse how the biopharmaceutics classification system (BCS) has been used to date. A survey of the literature resulted in a compilation of 242 compounds for which BCS classes were reported. Of these, 183 compounds had been reported to belong to one specific BCS class whereas 59 compounds had been assigned to multiple BCS classes in different papers. Interestingly, a majority of the BCS class 2 compounds had fraction absorbed (FA) values >85%, indicating that they were completely absorbed after oral administration. Solubility was computationally predicted at pH 6.8 for BCS class 2 compounds to explore the impact of the pH of the small intestine, where most of the absorption occurs, on the solubility. In addition, the solubilization capacity of lipid aggregates naturally present in the intestine was studied computationally and experimentally for a subset of 12 compounds. It was found that all acidic compounds with FA>85% were completely dissolved in the pH of the small intestine. Further, lipids at the concentration used in fasted state simulated intestinal fluid (FaSSIF) dissolved the complete dose given of the most lipophilic (logD6.5>3) compounds studied. Overall, biorelevant dissolution media (pure buffer of intestinal pH or FaSSIF) identified that for 20 of the 29 BCS class 2 compounds with FA>85% the complete dose given orally would be dissolved. These results indicate that a more relevant pH restriction for acids and/or dissolution medium with lipids present better forecast solubility-limited absorption in vivo than the presently used BCS solubility criterion. The analysis presented herein further strengthens the discussion on the requirement of more physiologically relevant dissolution media for the in vitro solubility classification performed to reach the full potential of the BCS.