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Design and evaluation of bilayer floating tablets of captopril

ZIYAUR RAHMAN
MUSHIR ALI
RK KHAR


Puni tekst: engleski pdf 82 Kb

str. 49-57

preuzimanja: 7.753

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Sažetak

The objective of the present investigation was to develop a bilayer-floating tablet (BFT) for captopril using direct compression technology. HPMC, K-grade and effervescent mixture of citric acid and sodium bicarbonate formed the floating layer. The release layer contained captopril and various polymers such as HPMC-K15M, PVP-K30 and Carbopol 934p, alone or in combination with the drug. The floating behavior and in vitro dissolution studies were carried out in a USP 23 apparatus 2 in simulated gastric fluid (without enzyme, pH 1.2). Final formulation released approximately 95% drug in 24 h in vitro, while the floating lag time was 10 min and the tablet remained floatable throughout all studies. Final formulation followed the Higuchi release model and showed no significant change in physical appearance, drug content, floatability or in vitro dissolution pattern after storage at 45 oC/75% RH for three months. Placebo formulation containing barium sulphate in the release layer administered to human volunteers for in vivo X-ray studies showed that BFT had significantly increased the gastric residence time.

Ključne riječi

bilayer floating tablet; HPLC; Higuchi, X-ray

Hrčak ID:

4564

URI

https://hrcak.srce.hr/4564

Datum izdavanja:

1.1.2006.

Podaci na drugim jezicima: hrvatski

Posjeta: 9.798 *