Sotalol Permeability in Cultured-Cell, Rat Intestine, and PAMPA System

Author:

Liu Wei,Okochi Hideaki,Benet Leslie Z.,Zhai Suo-Di

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology

Reference23 articles.

1. Amidon GL, Lennernäs H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res. 1995;12:413–20.

2. Research CfDEa,U.S. Food and Drug Administration, Guidance for industry: Waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a biopharmaceutics classification system, 2000 August, http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm064964.htm . (Available from)

3. Use CfMPfH,European Medicines Agency, Guideline on the investigation of bioequivalence, 2010 January 20, http://www.ema.europa.eu/ema/pages/includes/document/open_document.jsp?webContentId=WC500070039 . (Available from)

4. Chen M-L, Amidon GL, Benet LZ, Lennernäs H, Yu LX. The BCS, BDDCS, and regulatory guidances. Pharm Res. 2011;28:1774–8.

5. Wu C-Y, Benet LZ. Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm Res. 2005;22:11–23.

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