In Vitro Corrosion and Cytocompatibility of a Microarc Oxidation Coating and Poly(L-lactic acid) Composite Coating on Mg-1Li-1Ca Alloy for Orthopedic Implants

ACS Appl Mater Interfaces. 2016 Apr 20;8(15):10014-28. doi: 10.1021/acsami.6b00527. Epub 2016 Apr 5.

Abstract

Manipulating the degradation rate of biomedical magnesium alloys poses a challenge. The characteristics of a microarc oxidation (MAO), prepared in phytic acid, and poly(L-lactic acid) (PLLA) composite coating, fabricated on a novel Mg-1Li-1Ca alloy, were studied through field emission scanning electron microscopy (FE-SEM), electron probe X-ray microanalysis (EPMA), energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). The corrosion behaviors of the samples were evaluated via hydrogen evolution, potentiodynamic polarization and electrochemical impedance spectroscopy in Hanks' solution. The results indicated that the MAO/PLLA composite coatings significantly enhanced the corrosion resistance of the Mg-1Li-1Ca alloy. MTT and ALP assays using MC3T3 osteoblasts indicated that the MAO/PLLA coatings greatly improved the cytocompatibility, and the morphology of the cells cultured on different samples exhibited good adhesion. Hemolysis tests showed that the composite coatings endowed the Mg-1Li-1Ca alloys with a low hemolysis ratio. The increased solution pH resulting from the corrosion of magnesium could be tailored by the degradation of PLLA. The degradation mechanism of the composite coatings was discussed. The MAO/PLLA composite coating may be appropriate for applications on degradable Mg-based orthopedic implants.

Keywords: biomaterial; degradation; magnesium alloy; microarc oxidation; poly(l-lactic acid).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alloys / pharmacology*
  • Animals
  • Calcium / pharmacology
  • Cell Death / drug effects
  • Cell Differentiation / drug effects
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell Shape / drug effects
  • Coated Materials, Biocompatible / pharmacology*
  • Corrosion
  • Electrochemistry
  • Hemolysis / drug effects
  • Hydrogen / analysis
  • Hydrogen-Ion Concentration
  • Lithium / pharmacology
  • Magnesium / pharmacology
  • Mice
  • Orthopedics*
  • Oxidation-Reduction
  • Polyesters / pharmacology*
  • Prostheses and Implants*
  • Rabbits
  • Spectrometry, X-Ray Emission

Substances

  • Alloys
  • Coated Materials, Biocompatible
  • Polyesters
  • poly(lactide)
  • Hydrogen
  • Lithium
  • Magnesium
  • Calcium