Impact of Particle Size of Acyclovir Loaded Mucoadhesive Microcapsules on Drug Release Characteristics
Giri IC*, Ramanunny AK
Department of Pharmacy, Suresh Gyan Vihar University, Jaipur-302017, Rajasthan. India
Received: 1st Aug, 2024; Revised: 19th Nov, 2024; Accepted: 2nd Dec, 2024; Available Online: 25th Dec, 2024
ABSTRACT
This study focuses on the preparation and evaluation of prolonged-release acyclovir (ACV)-loaded mucoadhesive microcapsules using the emulsion solvent evaporation technique with sodium CMC as a mucoadhesive and rate-retarding polymer. The microcapsules exhibited a high yield (92.67–97.85%), drug entrapment efficiency (72.79–92.17%), and mucoadhesion (62–73%). Particle size ranged between 250 µm (F1) and 302 µm (F4), increasing with polymer concentration. In vitro drug release studies conducted in pH 1.2 phosphate buffer revealed an inverse relationship between polymer concentration and release rate. Smaller microcapsules (F1) demonstrated faster drug release (95% in 12 hours), while larger microcapsules (F4) showed sustained release (55% in 12 hours). These insights underscore the importance of optimizing particle size to achieve desired therapeutic outcomes. This study provides valuable data for the development of tailored microcapsule formulations, improving the efficacy and compliance of ACV therapy.
Keywords: Acyclovir, microcapsules, particle size, drug release, mucoadhesion
How to cite this article: Giri IC, Ramanunny AK. Impact of Particle Size of Acyclovir Loaded Mucoadhesive Microcapsules on Drug Release Characteristics. International Journal of Drug Delivery Technology. 2024;14(4):2108-13 doi: 10.25258/ijddt.14.4.23
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