Developing Mg-Zn-Fish Bone Derived Hydroxyapatite Composites for Biomedical Applications: In vitro Degradation Studies

The study of magnesium (Mg) based biomaterials has emerged as a potential research area in recent times. Controlling the rapid corrosion and improving the implant-tissue interface kinetics for better tissue regeneration are the prime interests behind developing novel Mg-based composites. In the current work, the metal matrix composites of Mg-Zn, dispersed with nano-hydroxyapatite derived from fish bones (fHA), were produced by powder metallurgy route. The powders were mixed with the help of ball milling in the presence of ethanol and then sintered at 440 °C. From the microstructural studies, micro-lamellar morphology was noticed for the sintered compacts due to the flake-like morphology of the milled powders. The sintered compacts were then subjected to in vitro biodegradation studies in simulated conditions for one week. From the results, the presence of fHA was found to be highly influential in increasing the rate of mineral deposition on the surface of the composites. These higher mineral depositions protected the surface of the composites from further degradation. The results demonstrate that adding fHA to Mg accelerates biomineralization and controls degradation, leading to better implant-tissue interactions.

Shock growth of ice crystal near equilibrium melting pressure under dynamic compression

Crystal growth is governed by an interplay between macroscopic driving force and microscopic interface kinetics at the crystal–liquid interface. Unlike the local equilibrium growth condition, the interplay becomes blurred under local nonequilibrium, which raises many questions about the nature of diverse crystal growth and morphological transitions. Here, we systematically control the growth condition from local equilibrium to local nonequilibrium by using an advanced dynamic diamond anvil cell (dDAC) and generate anomalously fast growth of ice VI phase with a morphological transition from three- to two-dimension (3D to 2D), which is called a shock crystal growth. Unlike expected, the shock growth occurs from the edges of 3D crystal along the (112) crystal plane rather than its corners, which implies that the fast compression yields effectively large overpressure at the crystal–liquid interface, manifesting the local nonequilibrium condition. Molecular dynamics (MD) simulation reproduces the faster growth of the (112) plane than other planes upon applying large overpressure. Moreover, the MD study reveals that the 2D shock crystal growth originates from the similarity of the interface structure between water and the (112) crystal plane under the large overpressure. This study provides insight into crystal growth under dynamic compressions, which makes a bridge for the unknown behaviors of crystal growth between under static and dynamic pressure conditions.