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Effect of Penetration Enhancers and Safety on the Transdermal Delivery of Apremilast in Skin.
Sarango-Granda, Paulo; Espinoza, Lupe Carolina; Díaz-Garrido, Natalia; Alvarado, Helen; Rodríguez-Lagunas, María J; Baldomá, Laura; Calpena, Ana.
Afiliación
  • Sarango-Granda P; Department of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, 08028 Barcelona, Spain.
  • Espinoza LC; Institute of Nanoscience and Nanotechnology (IN2UB), University of Barcelona, 08028 Barcelona, Spain.
  • Díaz-Garrido N; Departamento de Química, Universidad Técnica Particular de Loja, Loja 1101608, Ecuador.
  • Alvarado H; Institute of Nanoscience and Nanotechnology (IN2UB), University of Barcelona, 08028 Barcelona, Spain.
  • Rodríguez-Lagunas MJ; Departamento de Química, Universidad Técnica Particular de Loja, Loja 1101608, Ecuador.
  • Baldomá L; Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Sciences, University of Barcelona, 08028 Barcelona, Spain.
  • Calpena A; Institute of Biomedicine of the University of Barcelona (IBUB), Sant Joan de Déu Research Institute, 08028 Barcelona, Spain.
Pharmaceutics ; 14(5)2022 May 07.
Article en En | MEDLINE | ID: mdl-35631597
ABSTRACT
The poor water solubility of apremilast (APR) is the main impediment to the penetration of the drug through the skin barrier. The objective of this study was to evaluate the permeability of APR in different solutions enriched with penetration promoters in ex vivo samples of human skin, and additionally assess its tolerance in vivo. To this end, APR solutions with 5% promoter were developed, and the drug's ability to penetrate human abdominal skin samples was evaluated; the coefficients of permeability, cumulated amounts permeated, and flow were some of the parameters evaluated; likewise, the in vitro and in vivo tolerance of the solutions was evaluated. The results obtained showed that the solutions containing squalene as a promoter improved the penetration of APR compared to the other promoters evaluated; in the same way, on an in vitro scale in HaCaT cells, the promoters were not toxic, finding a cell viability greater than 80% at the different dilutions evaluated. In the in vivo tests carried out with the solution that presented the best results (APR-Squalene solution), it was observed that it does not cause irritation or erythema on the skin after its colorimetric and histological evaluation of the dorsal region of rats after its application. Squalene becomes an excellent candidate to improve the permeability of the drug in the case of the development of a topical formulation; in addition, it was confirmed that this penetration enhancer is neither toxic nor irritating when in contact with the skin in in vivo tests.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Aspecto: Implementation_research Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Aspecto: Implementation_research Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article País de afiliación: España