No abstract

Biologically mineralized tissues are well recognized for their unusual crystal morphologies and hierarchically organized composite structures. The soluble acidic macromolecules associated with biominerals are thought to play an important role in modulating the mineral morphology. Our in vitro studies, which use acidic polypeptide additives to modify crystal growth of calcium-based minerals, have demonstrated a crystallization mechanism that proceeds via a liquid-phase mineral precursor. Various features of the crystals produced via this mechanism, such as "extruded" mineral fibers and mineralized collagen composites, have led us to propose the hypothesis that an amorphous, liquid-phase precursor could play a fundamental role in the morphogenesis of calcium-based biominerals. Although in vivo evidence of this process remains to be determined, we demonstrate crystallization features that mimic bone and dental enamel and suggest that this process could be relevant to biomineralization in both vertebrates and invertebrates.

Biologically mineralized tissues are well recognized for their unusual crystal morphologies and hierarchically organized composite structures. The soluble acidic macromolecules associated with biominerals are thought to play an important role in modulating the mineral morphology. Our in vitro studies, which use acidic polypeptide additives to modify crystal growth of calcium-based minerals, have demonstrated a crystallization mechanism that proceeds via a liquid-phase mineral precursor. Various features of the crystals produced via this mechanism, such as "extruded" mineral fibers and mineralized collagen composites, have led us to propose the hypothesis that an amorphous, liquid-phase precursor could play a fundamental role in the morphogenesis of calcium-based biominerals. Although in vivo evidence of this process remains to be determined, we demonstrate crystallization features that mimic bone and dental enamel and suggest that this process could be relevant to biomineralization in both vertebrates and invertebrates.

We have investigated the transport properties of nanopore alumina membranes that were rendered hydrophobic by functionalization with octadecyltrimethoxysilane (ODS). The pores in these ODS-modified membranes are so hydrophobic that they are not wetted by water. Nevertheless, nonionic molecules can be transported from an aqueous feed solution on one side of the membrane, through the dry nanopores, and into an aqueous receiver solution on the other side. The transport mechanism involves Langmuir-type adsorption of the permeating molecule onto the ODS layers lining the pore walls, followed by solid-state diffusion along these ODS layers; we have measured the diffusion coefficients associated with this transport process. We have also investigated the transport properties of membranes prepared by filling the ODS-modified pores with the water-immiscible (hydrophobic) liquid mineral oil. In this case the transport mechanism involves solvent extraction of the permeating molecule into the mineral oil subphase confined with the pores, followed by solution-based diffusion through this liquid subphase. Because of this different transport mechanism, the supported-liquid membranes show substantially better transport selectivity than the ODS-modified membranes that contain no liquid subphase.