4.5 Editorial Material

Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Enalapril

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 106, Issue 8, Pages 1933-1943

Publisher

WILEY
DOI: 10.1016/j.xphs.2017.04.019

Keywords

enalapril maleate; enalaprilat; absorption; Biopharmaceutics Classification System (BCS); permeability; regulatory science; solubility; in situ conversion

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Literature data relevant to the decision to allow a waiver of in vivo bioequivalence testing for the marketing authorization of immediate-release, solid oral dosage forms containing enalapril maleate are reviewed. Enalapril, a prodrug, is hydrolyzed by carboxylesterases to the active angiotensin-converting enzyme inhibitor enalaprilat. Enalapril as the maleate salt is shown to be highly soluble, but only 60%-70% of an orally administered dose of enalapril is absorbed from the gastrointestinal tract into the enterocytes. Consequently, enalapril maleate is a Biopharmaceutics Classification System class III substance. Because in situ conversion of the maleate salt to the sodium salt is sometimes used in production of the finished drug product, not every enalapril maleate-labeled finished product actually contains the maleate salt. Enalapril is not considered to have a narrow therapeutic index. With this background, a biowaiver-based approval procedure for new generic products or after major revisions to existing products is deemed acceptable, provided the in vitro dissolution of both test and reference preparation is very rapid (at least 85% within 15 min at pH 1.2, 4.5, and 6.8). Additionally, the test and reference product must contain the identical active drug ingredient. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.

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