FORMULATION AND EVALUATION OF SILODOSIN BUCCAL FILM

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Autor principal: Bhargavi Patel1*, Bhakti Shah2, Dr. Shailesh T. Prajapati 3
Formato: Recurso digital
Lenguaje:inglés
Publicado: Zenodo 2026
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author Bhargavi Patel1*, Bhakti Shah2, Dr. Shailesh T. Prajapati 3
author_facet Bhargavi Patel1*, Bhakti Shah2, Dr. Shailesh T. Prajapati 3
contents <p class="Default"><strong><span>Objective:</span></strong><em><span> </span></em><span>The objective of this research work was to formulate and evaluate buccal film containing Silodosin by enhancement of Permeability by preparing inclusion complex of Silodosin with ꞵ-CD and to increase patient compliance which is useful in the treatment of Hyperplasia.<span>  </span><strong>Materials and Methods</strong>: In this research, the method used to prepare buccal films was solvent casting. ꞵ-CD inclusion complex with silodosin in 1:1 ratio to increase permeability of drug. 3<sup>2</sup> Full Factorial design was used for optimization by selecting two independent factors –concentration of film forming agent (HPMC E5)-X I and concentration of plasticizer (Propylene glycol)-X II and their effect on Disintegration time- (R I), and % drug release- (R II). Optimization of factorial batches was done using Design Expert 13 software. <strong>Result</strong>: Best results were obtained in Batch F1 in which HPMC E5 was 150mg and Propylene glycol was 1ml with 31.4 seconds of disintegration time and 99.1 % cumulative drug release at 15 minutes. Check point batch shows 34.74 seconds of disintegration time 97.09 % cumulative drug release. A 1 month accelerated Short term stability study was done on prepared films and it is stable for 1 month. <strong>Conclusion</strong>: Buccal film containing Silodosin were formulated using HPMC E5 as a film forming and Propylene glycol as a plasticizer by solvent casting method. Hence, from the results it was concluded that faster disintegration and faster drug release can be achieved by the buccal film of Silodosin.</span></p>
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publishDate 2026
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spellingShingle FORMULATION AND EVALUATION OF SILODOSIN BUCCAL FILM
Bhargavi Patel1*, Bhakti Shah2, Dr. Shailesh T. Prajapati 3
<p class="Default"><strong><span>Objective:</span></strong><em><span> </span></em><span>The objective of this research work was to formulate and evaluate buccal film containing Silodosin by enhancement of Permeability by preparing inclusion complex of Silodosin with ꞵ-CD and to increase patient compliance which is useful in the treatment of Hyperplasia.<span>  </span><strong>Materials and Methods</strong>: In this research, the method used to prepare buccal films was solvent casting. ꞵ-CD inclusion complex with silodosin in 1:1 ratio to increase permeability of drug. 3<sup>2</sup> Full Factorial design was used for optimization by selecting two independent factors –concentration of film forming agent (HPMC E5)-X I and concentration of plasticizer (Propylene glycol)-X II and their effect on Disintegration time- (R I), and % drug release- (R II). Optimization of factorial batches was done using Design Expert 13 software. <strong>Result</strong>: Best results were obtained in Batch F1 in which HPMC E5 was 150mg and Propylene glycol was 1ml with 31.4 seconds of disintegration time and 99.1 % cumulative drug release at 15 minutes. Check point batch shows 34.74 seconds of disintegration time 97.09 % cumulative drug release. A 1 month accelerated Short term stability study was done on prepared films and it is stable for 1 month. <strong>Conclusion</strong>: Buccal film containing Silodosin were formulated using HPMC E5 as a film forming and Propylene glycol as a plasticizer by solvent casting method. Hence, from the results it was concluded that faster disintegration and faster drug release can be achieved by the buccal film of Silodosin.</span></p>
title FORMULATION AND EVALUATION OF SILODOSIN BUCCAL FILM
url https://doi.org/10.5281/zenodo.19885451