Characterization and Evaluation of the Cytotoxicity of Pregabalin Gels for Oral Application

Author:

Xavier Gabriela Monteiro Barbosa1ORCID,Ferreira Lindalva Maria de Meneses Costa2ORCID,Passos Marcele Fonseca3ORCID,Rodrigues Ana Paula Drummond4,Franco Felipe Tuji de Castro4,Silva Cecy Martins1ORCID,Silva Júnior José Otávio Carréra5ORCID,Ribeiro-Costa Roseane Maria2ORCID,Araújo Jesuína Lamartine Nogueira1

Affiliation:

1. School of Dentistry, Federal University of Pará, Belém 66075-110, PA, Brazil

2. Laboratory of Pharmaceutical Nanotechnology, College of Pharmacy, Federal University of Pará, Belém 66075-110, PA, Brazil

3. Biotechnology School, Federal University of Pará, Belém 66075-110, PA, Brazil

4. Electron Microscopy Laboratory, Evandro Chagas Institute, Belém 66093-020, PA, Brazil

5. Laboratory of Pharmaceutical and Cosmetic R&D, College of Pharmacy, Federal University of Pará, Belém 66075-110, PA, Brazil

Abstract

The efficacy of pregabalin in pain treatment has led to the search for new formulations for its use through different routes of administration. This study aimed to prepare, characterize, and evaluate the cytotoxicity of pregabalin (PG) gels for topical application in the oral cavity. Solutions with three different concentrations of PG were prepared and added to a 1.0% carbopol gel base. Thermal analyses (TG and DSC) and FTIR were performed on the gel and pure pregabalin. Stability (preliminary and accelerated) and rheology studies were also conducted on the gels. Cytotoxicity was evaluated in human gingival fibroblasts in the following groups: WG (1.0% carbopol gel base), PG2G (2.0% pregabalin gel), PG5G (5.0% pregabalin gel), and PG10G (10% pregabalin gel). A transparent and homogeneous gel with a pH of 6 was obtained. The formulations showed stability, and the different drug concentrations did not influence the product’s characteristics. None of the tested groups showed cytotoxicity for the analyzed cells. The pregabalin gels exhibited favorable and non-toxic characteristics for human gingival fibroblasts in vitro. Therefore, this product may be a promising therapeutic alternative for topical application in the oral mucosa.

Publisher

MDPI AG

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