Co-culture of BMSCs and HUVECs with simvastatin-loaded gelatin nanosphere/chitosan coating on Mg alloy for osteogenic differentiation and vasculogenesis.

Mg alloys are increasingly being investigated as a versatile and economical alternative for developing bone repair implants because of their high mechanical strength, wide availability, adjustable structure and properties. In this study, magnesium alloy WE43 is coated on both sides with gelatin nanosphere/chitosan (GNs/CTS), a coating enhanced by incorporating simvastatin (SIM). SIM-loaded GNs/CTS coated magnesium alloy can promote the osteogenic differentiation of bone mesenchymal stem cells (BMSCs). BMSCs and human umbilical vein endothelial cells (HUVECs) are co-cultured through transwell systems. The release of SIM from the coating is found to increase the secretion of chemokine and angiogenic factors from BMSCs, which promote the migration and tube formation of HUVECs, respectively. Bone morphogenetic protein secreted by HUVECs is seen to increase by the release of SIM from the coating, promoting the osteogenic differentiation of BMSCs. The secretion of chemokines from HUVECs promote the migration of BMSCs. The coated magnesium alloy substrate loaded with SIM is found to regulate the osteogenic differentiation of BMSCs. The study of the paracrine interaction between BMSCs and HUVECs proves that the applied coating promotes both osteogenic differentiation and vascularization, thus demonstrating a new approach for the design of bone repair materials based on magnesium alloys.

Influence of proteins on the corrosion behavior of a chitosan-bioactive glass coated magnesium alloy.

The current study explored the degradation behavior of a WE43 Mg alloy during immersion tests in Dulbecco's Modified Eagle's Medium (DMEM) for 3d and 7d, for a bare alloy surface as well as for samples with surface pre-treatment, and finally for samples coated with chitosan-bioactive glass. The immersion tests were conducted with and without addition of serum, to study the influence of proteins on the degradation process. Mass-loss was measured to determine the corrosion rate after 3d and 7d of immersion. The samples were analyzed by SEM with respect to their surface morphology and the chemical composition was screened by high-resolution XPS. The results demonstrate not only a significant, time-dependent influence of serum addition on the corrosion behavior of the materials studied, but noteworthy is that depending on the sample type, proteins in solution were observed to either accelerate or inhibit corrosion. These results are discussed in correlation to observed changes in surface chemistry taking place upon immersion in the absence and presence of proteins.

Electrophoretic Deposition of Bioadaptive Drug Delivery Coatings on Magnesium Alloy for Bone Repair.

Biodegradable polymer coatings on magnesium alloys are attractive, as they can provide corrosion resistance as well as additional functions for biomedical applications, e.g., drug delivery. A gelatin nanospheres/chitosan (GNs/CTS) composite coating on WE43 substrate was fabricated by electrophoretic deposition with simvastatin (SIM) loaded into the GNs. Apart from a sustained drug release over 28 days, an anticorrosion behavior of the coated WE43 substrates was confirmed by electrochemical tests. Both the degradation and corrosion rates of the coated substrate were significantly minimized in contrast to bare WE43. The cytocompatibility of the coated samples was analyzed  both quantitatively and qualitatively. Additionally, the osteogenic differentiation of MC3T3-E1 cells on SIM-containing coatings was assessed by measuring the expression of osteogenic genes and related proteins, alkaline phosphatase (ALP) activity, and extracellular matrix mineralization, showing that the SIM-loaded composite coating could upregulate the expression of osteogenic genes and related proteins, promote ALP activity, and enhance extracellular matrix mineralization. In summary, the SIM-loaded GNs/CTS composite coatings were able to enhance the corrosion resistance of the WE43 substrate and promote osteogenic activity, thus demonstrating a promising coating system for modifying the surface of magnesium alloys targeted for orthopedic applications.

Tackling Mg alloy corrosion by natural polymer coatings-A review.

The field of protective coatings for magnesium and its alloys (e.g., AZ31) using natural polymers is reviewed. Polymers utilized are broadly divided into polysaccharides and proteins. For both polymer classes examples are given focusing on coating processing and characterization. Several analysing methods reported in literature are summarized highlighting the different characterization approaches applied in different studies, which makes difficult a direct comparison of the outcomes. In most cases, the protective behavior of coatings was determined using electrochemical impedance spectroscopy or by assessing hydrogen evolution in different fluids. Mechanical tests and in vitro cell culture studies have been also carried out on selected coating systems. Overall, the results show the possibility of applying protective coatings based on natural polymers on magnesium and its alloys, however, in vivo investigations are scarce so that long-term results in relevant conditions are not yet available. A comparison with the use of synthetic polymers is presented and current challenges and areas for future research are discussed, highlighting the need for further investigations in the field, which should enable broadening the applications of Mg and Mg alloys in medicine. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2628-2641, 2016.