Formulation And Evaluation of Oral Disintegrating Film Containing Brivaracetam

Oral disintegrating films (ODFs) are innovative drug delivery systems designed to dissolve rapidly in the oral cavity without the need for water. These films are particularly beneficial for patients who have difficulty swallowing traditional dosage forms, such as the elderly and paediatric populations. This study aims to develop ODF containing Brivaracetam were formulated using a different grade of HPMC E15 and HPMC E50 and plasticizers like polyethylene glycol and propylene glycol using solvent casting method. The formulated films were evaluated for thickness, folding endurance, weight variation, percentage elongation, drug content, in-vitro dissolution and in-vitro disintegration. The optimized formulation F4 containing HPMC E15 showed minimum disintegration time at 20 secs and highest in-vitro dissolution 98.9% within 10 mins. Stability data indicated no significant changes in parameters over time. Therefore, Formulation F4 is recognized as stable and effective. Hence oral disintegrating films represent a promising advancement in pharmaceutical formulations, offering a convenient and effective means of drug delivery. Their rapid dissolution and ease of use make them an attractive option for improving patient adherence to medication regimens.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-11-12
DOI
https://doi.org/10.5281/zenodo.14106902
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
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article

Formulation And Evaluation of Oral Disintegrating Film Containing Brivaracetam

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

Formulation And Evaluation of Oral Disintegrating Film Containing Brivaracetam

article en

Abstract

Oral disintegrating films (ODFs) are innovative drug delivery systems designed to dissolve rapidly in the oral cavity without the need for water. These films are particularly beneficial for patients who have difficulty swallowing traditional dosage forms, such as the elderly and paediatric populations. This study aims to develop ODF containing Brivaracetam were formulated using a different grade of HPMC E15 and HPMC E50 and plasticizers like polyethylene glycol and propylene glycol using solvent casting method. The formulated films were evaluated for thickness, folding endurance, weight variation, percentage elongation, drug content, in-vitro dissolution and in-vitro disintegration. The optimized formulation F4 containing HPMC E15 showed minimum disintegration time at 20 secs and highest in-vitro dissolution 98.9% within 10 mins. Stability data indicated no significant changes in parameters over time. Therefore, Formulation F4 is recognized as stable and effective. Hence oral disintegrating films represent a promising advancement in pharmaceutical formulations, offering a convenient and effective means of drug delivery. Their rapid dissolution and ease of use make them an attractive option for improving patient adherence to medication regimens.

Zenodo (CERN European Organization for Nuclear Research)
Openalex Percentile: Top 64%
Drug Solubulity and Delivery Systems
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