Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), Ikoma, Nara, Japan.
J Mater Sci Mater Med. 2010 Jan;21(1):11-9. doi: 10.1007/s10856-009-3829-7. Epub 2009 Jul 26.
Biomimetic mineralization of supramolecular scaffolds consisting of biomolecules or their analogues has received much attention recently from the viewpoint of creation of novel biomaterials. This study investigated biomimetic deposition of hydroxyapatite (HAp) on cerasomes, morphologically stable organic-inorganic hybrid vesicles. Scanning electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray diffraction studies revealed that the pristine cerasomes induced heterogeneous nucleation of HAp when they were immersed in 1.5SBF, a solution having 1.5 times higher ion concentration than that of a simulated body fluid (SBF). The HAp deposition was further accelerated when dicarboxylic and monocarboxylic acid groups were displayed on cerasome surfaces. These carboxylic acid groups are expected to enhance calcium ion binding to the cerasome surface, causing an increase of HAp nucleation sites. At lower surface concentrations on the cerasome surface, the dicarboxylic acid group is apparently more effective for HAp deposition than the monocarboxylic acid group. The resultant HAp-cerasome hybrids are useful as biocompatible materials having unique properties deriving from the lipid bilayer structure of the cerasomes.
最近,从创造新型生物材料的角度出发,人们对由生物分子或其类似物组成的超分子支架的仿生矿化给予了极大关注。本研究考察了在类脂体(形态稳定的有机-无机杂化囊泡)上仿生沉积羟基磷灰石(HAp)。扫描电子显微镜、能谱 X 射线和 X 射线衍射研究表明,当原始类脂体浸入离子浓度比模拟体液(SBF)高 1.5 倍的 1.5SBF 溶液中时,类脂体诱导了 HAp 的异质成核。当二羧酸和单羧酸基团显示在类脂体表面时,HAp 的沉积进一步加速。这些羧酸基团有望增强钙离子与类脂体表面的结合,从而增加 HAp 的成核位点。在类脂体表面较低的表面浓度下,二羧酸基团显然比单羧酸基团更有利于 HAp 的沉积。所得的 HAp-类脂体杂化物可用作具有源自类脂体双层脂质结构的独特性质的生物相容性材料。