Biocomposite for Prolonged Release of Water-Soluble Drugs

Author:

Meirelles Lyghia M. A.1,de Melo Barbosa Raquel12ORCID,de Almeida Júnior Renato Ferreira3,Machado Paula Renata Lima3,Perioli Luana4ORCID,Viseras César25ORCID,Raffin Fernanda Nervo1ORCID

Affiliation:

1. Laboratory of Drug Development, Department of Pharmacy, Federal University of Rio Grande do Norte, Natal 59012-570, Brazil

2. Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, Campus de Cartuja s/n, University of Granada, 18071 Granada, Spain

3. Immunology Laboratory, Pharmacy Faculty, Federal University of Rio Grande do Norte, Natal 59010-180, Brazil

4. Department of Pharmaceutic Science, University of Perugia, 06123 Perugia, Italy

5. Andalusian Institute of Earth Sciences, CSIC-University of Granada, Av. de Las Palmeras 4, 18100 Armilla, Spain

Abstract

This study aimed to develop a prolonged-release system based on palygorskite and chitosan, which are natural ingredients widely available, affordable, and accessible. The chosen model drug was ethambutol (ETB), a tuberculostatic drug with high aqueous solubility and hygroscopicity, which is incompatible with other drugs used in tuberculosis therapy. The composites loaded with ETB were obtained using different proportions of palygorskite and chitosan through the spray drying technique. The main physicochemical properties of the microparticles were determined using XRD, FTIR, thermal analysis, and SEM. Additionally, the release profile and biocompatibility of the microparticles were evaluated. As a result, the chitosan–palygorskite composites loaded with the model drug appeared as spherical microparticles. The drug underwent amorphization within the microparticles, with an encapsulation efficiency greater than 84%. Furthermore, the microparticles exhibited prolonged release, particularly after the addition of palygorskite. They demonstrated biocompatibility in an in vitro model, and their release profile was influenced by the proportion of inputs in the formulation. Therefore, incorporating ETB into this system offers improved stability for the administered product in the initial tuberculosis pharmacotherapy dose, minimizing its contact with other tuberculostatic agents in the treatment, as well as reducing its hygroscopicity.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior-Brazil

Publisher

MDPI AG

Subject

Pharmaceutical Science

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