Formulation Development, Physicochemical Characterization and In Vitro-In Vivo Drug Release of Vaginal Films
Language English Country Netherlands Media print
Document type Journal Article
PubMed
26564015
DOI
10.2174/1570162x14666151113123040
PII: CHR-EPUB-71822
Knihovny.cz E-resources
- MeSH
- Administration, Intravaginal MeSH
- Chemical Phenomena MeSH
- Dideoxynucleosides administration & dosage pharmacokinetics MeSH
- Rabbits MeSH
- Anti-HIV Agents administration & dosage pharmacokinetics MeSH
- Dosage Forms * MeSH
- Drug Carriers administration & dosage chemistry MeSH
- Drug Compounding * MeSH
- Drug Liberation * MeSH
- Animals MeSH
- Check Tag
- Rabbits MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- abacavir MeSH Browser
- Dideoxynucleosides MeSH
- Anti-HIV Agents MeSH
- Dosage Forms * MeSH
- Drug Carriers MeSH
PURPOSE: The purpose of this study was formulation and optimization of vaginal film formulation containing abacavir (ABC), a potent nucleoside reverse transcriptase inhibitor. METHODS: Vaginal films were prepared by solvent evaporation method using hydroxypropyl methylcellulose (HPMC) blended with polyvinyl pyrrolidone (PVP). Various physicochemical parameters of the prepared films such as drug content, thickness, tensile strength, percentage elongation at break, drug polymer interaction, swelling capacity, folding endurance, bio-adhesion, pH, and moisture content were evaluated with morphological studies. In vitro release study and in vivo release study were also performed. RESULTS: Films exhibited favorable physicochemical properties. The in vitro study showed that HPMC-PVP combination can control the release of abacavir through vaginal films with higher amount of PVP in the formulation resulting in an enhanced drug release rate. During the in vivo study in rabbits, systemic absorption of the drug was noted and the films remained intact for long in vagina without causing any sort of irritations. CONCLUSION: Thus, in a nutshell, the findings of our experimental work indicate that such films can be considered as a novel drug carrier system for the treatment of AIDS and other sexually transmitted diseases (STDs), and are suitable for local as well as systemic effects.
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