Development of Poly (Methyl vinyl ether-alt-maleic acid) Microneedles for Transdermal Delivery of Atorvastatin Calcium

Author:

Castañeda Pablo S.1ORCID,Domínguez Delgado Clara L.2ORCID,Cruz Isabel M.R.3,Contreras Luz M.M.4,Trinidad Eva M.M.5ORCID,Cervantes Miriam L.1ORCID,Escobar-Chávez José J.1ORCID

Affiliation:

1. Unidad de Investigacion Multidisciplinaria. Laboratorio 12: Sistemas transdermicos, Facultad de Estudios Superiores Cuautitlan-Universidad Nacional Autonoma de Mexico (FESC-UNAM), Carretera Cuautitlan Teoloyucan km 2.5, San Sebastian Xhala C.P. 54714, Cuautitlan Izcalli, Mexico

2. College of Pharmacy, The University of Texas at Austin, 2409 West University Avenue, PHR 4.214, Austin, Texas 78712, United States

3. Unidad de Investigacion y Ensenanza, Hospital Regional de Alta Especialidad de Zumpango, Autopista Zumpango-Jilotzingo # 400, Barrio de Santiago 2a seccion, C.P. 55600, Zumpango, Mexico

4. Departamento de Sistemas Biologicos, Universidad Autonoma Metropolitana-Xochimilco, Calzada del Hueso 1100, Colonia Villa Quietud, C.P. 04960, Ciudad de Mexico, United States

5. Area Academica de Medicina, Universidad Autonoma del Estado de Hidalgo, Circuito ex-Hacienda de la Concepcion, Lote 17, San Juan Tilcuautla, Municipio de San Agustin Tlaxiaca, C.P. 42160, Estado de Hidalgo, Mexico

Abstract

Aims: Biodegradable polymeric microneedles containing atorvastatin calcium were developed in order to improve the percutaneous absorption of the drug, useful for the treatment of hypercholesterolemia. Background: The use of physical enhancers like microneedles have shown good results to increase the delivery of drugs through the skin, the use of microneedles has very important advantages for transdermal drug delivery, for example, they are painless, easy to use and safe, they increase time interval of drug activity, dose, and reductions in adverse reactions, they also offer, the facility to remove the system instantly of the skin. Objective: Develop polymer microneedles loaded with a calcium atorvastatin and evaluate them by Differential Scanning Calorimetry (DSC), Scanning Electron Microscopy (SEM), bioadhesion, postwetting- bioadhesion, breaking strength, drug release test and in vitro percutaneous absorption studies to demonstrate the use of microneedles atorvastatin is able to cross the skin. Methods: The microneedles were made with poly (methyl vinyl ether-alt-maleic acid) as biodegradable polymer using the technique of casting in solution in a mold. After solidification these microneedles were characterized by Differential Scanning Calorimetry (DSC), Scanning Electron Microscopy (SEM), bioadhesion, post-wetting-bioadhesion, breaking strength, drug release test and in vitro percutaneous absorption studies. Results: In general, the performances were satisfactory for optimal formulation in terms of DSC with no interactions between drug and excipients, SEM shows microneedles with a conical shape, bioadhesion of 1570 g.f, post wetting-bioadhesion of 1503.4 g.f, breaking strength of 1566.7g.f that is sufficient to disrupt Stratum corneum, good drug release and a flux of 33.4 μg/cm2*h with a tLag of 15.14 h for the in vitro percutaneous absorption. Conclusion: The results indicate that it is possible to generate microneedles to increase the percutaneous absorption of calcium atorvastatin transdermally, with the potential to be used as an alternative to the oral route for the treatment of dyslipidemias.

Funder

CONACyT

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science,Biotechnology

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