Formulation and Characterization of Minoxidil Oral Thin Film

Objective: The primary aim of the current investigation was to formulate and assess immediate-release oral thin films of minoxidil, with the goal of increasing the bioavailability of the medication and accelerating its onset of action, thereby enhancing patient adherence. Methods: Using a film-forming polymer such as hydroxypropyl methylcellulose, the solvent evaporation method was used to create instantrelease oral thin films of minoxidil. Results: A number of physicochemical characteristics, such as drug content, in vitro drug release, folding endurance, tensile strength, thickness and weight change, were assessed for the films. Since the formed films F1-F9 were immediately wetted by the dissolving medium, no variations in the in vitro dissolution of the drug were observed. For the F8 formulations, the drug release was almost 94%. Conclusion: The current formulation uses mouth-dissolved films that have a quick start of action to deliver medication properly and have good therapeutic efficacy when taken orally.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-08-29
DOI
https://doi.org/10.5281/zenodo.17461988
Primary Topic
Advanced Drug Delivery Systems
Type
article
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article

Formulation and Characterization of Minoxidil Oral Thin Film

Zenodo (CERN European Organization for Nuclear Research)
Advanced Drug Delivery Systems
article

Formulation and Characterization of Minoxidil Oral Thin Film

article en

Abstract

Objective: The primary aim of the current investigation was to formulate and assess immediate-release oral thin films of minoxidil, with the goal of increasing the bioavailability of the medication and accelerating its onset of action, thereby enhancing patient adherence. Methods: Using a film-forming polymer such as hydroxypropyl methylcellulose, the solvent evaporation method was used to create instantrelease oral thin films of minoxidil. Results: A number of physicochemical characteristics, such as drug content, in vitro drug release, folding endurance, tensile strength, thickness and weight change, were assessed for the films. Since the formed films F1-F9 were immediately wetted by the dissolving medium, no variations in the in vitro dissolution of the drug were observed. For the F8 formulations, the drug release was almost 94%. Conclusion: The current formulation uses mouth-dissolved films that have a quick start of action to deliver medication properly and have good therapeutic efficacy when taken orally.

Zenodo (CERN European Organization for Nuclear Research)
Government of West Bengal (IN)
Openalex Percentile: Top 57%
Advanced Drug Delivery Systems
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