Hierarchical Hybrid Coatings with Drug-Eluting Capacity for Mg Alloy Biomaterials

Author:

Nicolao-Gómez Ana1,Martínez-Campos Enrique23,Moreno Lara1ORCID,Rodríguez-Hernández Juan23,Matykina Endzhe13

Affiliation:

1. Departamento de Ingeniería Química y de Materiales, Facultad de Ciencias Químicas, Universidad Complutense, 28040 Madrid, Spain

2. Funcionalización de Polímeros (FUPOL), Instituto de Ciencia y Tecnología de Polímeros (ICTP-CSIC), 28006 Madrid, Spain

3. Unidad Asociada al ICTP-CSIC, Instituto de Química Médica (IQM-CSIC), Grupo de Síntesis Orgánica y Bioevaluación, Instituto Pluridisciplinar (UCM), Paseo de Juan XXIII 1, 28040 Madrid, Spain

Abstract

A hierarchical hybrid coating (HHC) comprising a ceramic oxide layer and two biodegradable polymeric (polycaprolactone, PCL) layers has been developed on Mg3Zn0.4Ca cast alloy in order to provide a controlled degradation rate and functionality by creating a favorable porous surface topography for cell adhesion. The inner, ceramic layer formed by plasma electrolytic oxidation (PEO) has been enriched in bioactive elements (Ca, P, Si). The intermediate PCL layer sealed the defect in the PEO layer and the outer microporous PCL layer loaded with the appropriate active molecule, thus providing drug-eluting capacity. Morphological, chemical, and biological characterizations of the manufactured coatings loaded with ciprofloxacin (CIP) and paracetamol (PAR) have been carried out. In vitro assays with cell lines relevant for cardiovascular implants and bone prosthesis (endothelial cells and premyoblasts) showed that the drug-loaded coating allows for cell proliferation and viability. The study of CIP and PAR cytotoxicity and release rate indicated that the porous PCL layer does not release concentrations detrimental to the cells. However, complete system assays revealed that corrosion behavior and increase of the pH negatively affects cell viability. H2 evolution during corrosion of Mg alloy substrate generates blisters in PCL layer that accelerate the corrosion locally in crevice microenvironment. A detailed mechanism of the system degradation is disclosed. The accelerated degradation of the developed system may present interest for its further adaptation to new cancer therapy strategies.

Funder

MCIU/AEI/FEDER, UE

Regional Government of Madrid and EU Structural Funds

Publisher

MDPI AG

Subject

General Materials Science

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