JOURNAL OF THE CZECH PHARMACEUTICAL SOCIETY AND THE SLOVAK PHARMACEUTICAL SOCIETY

Čes. slov. farm. 1999, 48(5):214-217

In vitro determination of verapamil hydrochloride tablet dissolution

A. Štambergová, Z. Ulbrichová, J. Šedivý, T. Sechser
Pracoviště klinické farmakologie Institutu klinické a experimentální medicíny, Praha

Three different products containing 240 mg of verapamil hydrochloride in a coated tablet withsustained release were compared using the blinded dissolution test. The amount of the activesubstance released from the tablet and its dynamics differed significantly with all three productsafter 3 hours of dissolution. With product C (Isoptin SR, a proprietary product manufactured byKnoll), 92,2 % of the active substance was released after seven hours. With generic products A andB, the amounts were higher and lower, respectively. The dynamics of release of the active substancewas linear only with the proprietary product. Irregular and non-linear rates of active substancerelease from the tablet may result in clinically suboptimal efficacy and safety of generic products.

Keywords: dissolution test; verapamil; sustained release; UV spectrophotometry

Published: May 1, 1999  Show citation

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Štambergová A, Ulbrichová Z, Šedivý J, Sechser T. In vitro determination of verapamil hydrochloride tablet dissolution. Čes. slov. farm. 1999;48(5):214-217.
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