Biodegradable devices for medical applications should be with an appropriate degradation rate for satisfying the various requirements of bone healing. In this study, composite materials of polylactic acid (PLA)/stearic acid-modified magnesium oxide (MgO) with a 1 wt% were prepared through blending extrusion, and the effects of the MgO shapes on the composites’ properties in in vitro and in vivo degradation were investigated. The results showed that the long-term degradation behaviors of the composite samples depended significantly on the filler shape. The degradation of the composites is accelerated by the increase in the water uptake rate of the PLA matrix and the composite containing the MgO nanoparticles was influenced more severely by the enhanced hydrophilicity. Furthermore, the pH value of the phosphate buffer solution (PBS) was obviously regulated by the dissolution of MgO through the neutralization of the acidic product of the PLA degradation. In addition, the improvement of the in vivo degrading process of the composite illustrated that the PLA/MgO materials can effectively regulate the degradation of the PLA matrix as well as raise its bioactivity, indicating the composites for utilization as a biomedical material matching the different requirements for bone-related repair.

In this study, composite films of stearic acid–modified magnesium oxide whiskers (Sa–w-MgO)/poly-l-lactic acid (PLLA) were prepared through solution casting, and the in vitro degradation properties and cytocompatibility of the composites with different whisker contents were investigated. The results showed that the degradation behavior of the composite samples depended significantly on the whisker content, and the degradation rate increased with the addition of MgO content. Furthermore, the degradation of the composites with higher contents of whiskers was influenced more severely by the hydrophilicity and pH value, leading to more final weight loss, but the decomposition rate decreased gradually. Furthermore, the pH value of the phosphate buffer solution (PBS) was obviously regulated by the dissolution of MgO whiskers through neutralization of the acidic product of PLLA degradation. The cytocompatibility of the composites also increased remarkably, as determined from the cell viability results, and was higher than that of PLLA at the chosen whisker content. This was beneficial for the cell affinity of the material, as it notably led to an enhanced biocompatibility of the PLLA, in favor of promoting cell proliferation, which significantly improved its bioactivity, as well.

Nanocomposites of biodegradable PLLA and magnesium oxide composite (PLLA/MgO-NPs) and surface modified magnesium oxide composite (PLLA/m-MgO-NPs) were prepared using a solution casting method. Effects of the MgO-NPs and m-MgO-NPs on the crystallization behavior and mechanical properties of the PLLA are investigated systematically. Differential scanning calorimetry (DSC) was used to characterize the melting behavior and isothermal crystallization kinetics of pure PLLA and PLLA nanocomposite samples at varying isothermal crystallization temperatures. The Avrami equation was used to calculate the half crystallization time (t_1/2) and shown that the m-MgO-NPs is a kind of better nucleating agents than MgO-NPs because it enhanced crystallization rate significantly. Polarized optical microscopy (POM) results showed the density of spherulites increased and their size decreased in PLLA/MgO-NPs and PLLA/m-MgO-NPs samples. While the large amount (1.5 wt%) of MgO-NPs could hinder the crystallization of the PLLA. α′-PLLA emerged more easily than α-PLLA. The nucleation mechanism and geometry of crystal growth of neat PLLA and PLLA nanocomposite materials were determined to be similar. Mechanical property analysis showed both MgO-NPs and m-MgO-NPs could improve greatly the tensile strength, Young's modulus and elongation at break. Especially in the case of PLLA/m-MgO-NPs, the elongation at break was increased by 8.2 times. Uniform dispersion of m-MgO-NPs, and strong interaction and binding force between m-MgO-NPs and the PLLA matrix are favorable for the large enhancement in mechanical properties of the PLLA.

The present work focuses on the preparation of poly(l–lactide)–magnesium oxide whiskers (PLLA–MgO) composites by the in-situ polymerization method for bone repair and implant. PLLA–MgO composites were evaluated using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and solid-state ¹³C and ¹H nuclear magnetic resonance spectroscopy (NMR). It was found that the whiskers were uniformly dispersed in the PLLA matrix through the interfacial interaction bonding between PLLA and MgO; thereby, the MgO whisker was found to be well-distributed in the PLLA matrix, and biocomposites with excellent interface bonding were produced. Notably, the MgO whisker has an effect on the crystallization behavior and mechanical properties; moreover, the in vivo degradation of PLLA–MgO composites could also be adjusted by MgO. These results show that the whisker content of 0.5 wt % and 1.0 wt % exhibited a prominent nucleation effect for the PLLA matrix, and specifically 1.0 wt % MgO was found to benefit the enhanced mechanical properties greatly. In addition, the improvement of the degrading process of the composite illustrated that the MgO whisker can effectively regulate the degradation of the PLLA matrix as well as raise its bioactivity. Hence, these results demonstrated the promising application of PLLA–MgO composite to serve as a biomedical material for bone-related repair.