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Biomimetic layer-by-layer templates for calcium phosphate biomineralization

机译:用于磷酸钙生物矿化的仿生层层模板

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摘要

Carboxylated, sulfated and/or phosphorylated surfaces are admitted as potential optimal templates for biomimetic deposition of calcium phosphate (CaP) coatings in view of improving implants' osseointegration. Layer-by-layer films were built up consisting of anionic chondroitin sulfate (ChS), a biological carboxylated and sulfated polysaccharide and cationic poly(l-lysine) (PLL). The films were used as soft matrices to immobilize a model phosphoprotein, phosvitin (PhV). The respective roles of ChS, PLL and PhV terminal layers on the heterogeneous nucleation kinetics and the structure of CaP deposits obtained from supersaturated solutions were inspected. Critical supersaturation ratios and induction times preceding heterogeneous nucleation were precisely determined and interpreted within the framework of classical nucleation theory in order to derive the effective interfacial energies of CaP crystals. It was found that the potency of terminal layers toward CaP nucleation increased in the order: PLL < ChS < PhV. Beyond a supersaturation threshold, PhV-terminated films exerted unique influence on the nucleation kinetics, maintaining the induction time at a constant value owing to conformational change of the PhV molecules upon calcium bridging. Promisingly, all films templated the deposition of thin (a few micrometer thick) uniform coatings of octacalcium phosphate and possibly hydroxyapatite, the two most relevant biological phases of CaP.
机译:考虑到改善植入物的骨整合,羧化,硫酸化和/或磷酸化的表面被认为是用于仿生沉积磷酸钙(CaP)涂层的潜在最佳模板。建立了由硫酸软骨素(ChS),生物羧化硫酸盐多糖和阳离子聚(1-赖氨酸)(PLL)组成的逐层薄膜。该膜用作软基质以固定模型磷蛋白磷光蛋白(PhV)。检查了ChS,PLL和PhV末端层在非均相成核动力学中的各自作用以及从过饱和溶液中获得的CaP沉积物的结构。在经典成核理论的框架内,精确确定和解释了非均相成核之前的临界过饱和率和诱导时间,以便得出CaP晶体的有效界面能。发现端子层对CaP成核的效力按以下顺序增加:PLL

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