Optimisation of the controlled release of valsartan via cellulose acetate butyrate and poly(butylene succinate) microspheres: Influence of formulation conditions

This study investigates the formulation of valsartan-loaded cellulose acetate butyrate (CAB) microspheres, prepared via solvent evaporation microencapsulation, to evaluate their in vitro release behavior and the influence of formulation parameters. The study examined the effects of stirring speed, stabilizers and matrix materials on particle size and drug release. Increasing stirring speed reduced particle size but also led to higher valsartan loss, reducing encapsulation efficiency. Using the surfactant polylactic acid resulted in smooth, spherical and porous microspheres that enhanced controlled release. In contrast, using Tween 80 led to irregular particles with rough surfaces and larger pores that accelerated drug release. Including poly(butylene succinate) in the matrix resulted in smaller microparticles forming and a significantly higher rate of valsartan release. These findings emphasize the importance of optimizing formulation parameters and excipients to control drug release characteristics and enhance drug delivery system performance.

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Publication Details

Journal
Journal of the Serbian Chemical Society
Published
2025-01-01
DOI
https://doi.org/10.2298/jsc250521068b
Primary Topic
Advanced Drug Delivery Systems
Type
article
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article

Optimisation of the controlled release of valsartan via cellulose acetate butyrate and poly(butylene succinate) microspheres: Influence of formulation conditions

Youssef Ramli, Haouaria Merine, Aissa Bouharaoua
Journal of the Serbian Chemical Society
Advanced Drug Delivery Systems
article

Optimisation of the controlled release of valsartan via cellulose acetate butyrate and poly(butylene succinate) microspheres: Influence of formulation conditions

Youssef Ramli, Haouaria Merine, Aissa Bouharaoua
article en

Abstract

This study investigates the formulation of valsartan-loaded cellulose acetate butyrate (CAB) microspheres, prepared via solvent evaporation microencapsulation, to evaluate their in vitro release behavior and the influence of formulation parameters. The study examined the effects of stirring speed, stabilizers and matrix materials on particle size and drug release. Increasing stirring speed reduced particle size but also led to higher valsartan loss, reducing encapsulation efficiency. Using the surfactant polylactic acid resulted in smooth, spherical and porous microspheres that enhanced controlled release. In contrast, using Tween 80 led to irregular particles with rough surfaces and larger pores that accelerated drug release. Including poly(butylene succinate) in the matrix resulted in smaller microparticles forming and a significantly higher rate of valsartan release. These findings emphasize the importance of optimizing formulation parameters and excipients to control drug release characteristics and enhance drug delivery system performance.

Journal of the Serbian Chemical SocietyVol. 90(11)
Mohammed V University (MA), Université Djilali de Sidi Bel Abbès (DZ)
Openalex Percentile: Top 79%
Advanced Drug Delivery Systems
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Optimisation of the controlled release of valsartan via cellulose acetate butyrate and poly(butylene succinate) microspheres: Influence of formulation conditions — Youssef Ramli, Haouaria Merine, et al. · Journal of the Serbian Chemical Society (2025) | TGRS Research Map | TGRS