Wei Junchao, Liu Aixue, Chen Lei, Zhang Peibiao, Chen Xuesi, Jing Xiabin
State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
Macromol Biosci. 2009 Jul 7;9(7):631-8. doi: 10.1002/mabi.200800324.
The surface modification of hydroxyapatite (HA) nanoparticles by the ring opening polymerization (ROP) of gamma-benzyl-L-glutamate N-carboxyanhydride (BLG-NCA) was proposed to prepare the poly(gamma-benzyl-L-glutamate) (PBLG)-grafted HA nanoparticles (PBLG-g-HA) for the first time. HA nanoparticles were firstly treated by 3-aminopropylthriethoxysilane (APS) and then the terminal amino groups of the modified HA particles initiated the ROP of BLG-NCA to obtain PBLG-g-HA. The process was monitored by XPS and FT-IR. The surface grafting amounts of PBLG on HA ranging from 12.1 to 43.1% were characterized by thermal gravimetric analysis (TGA). The powder X-ray diffraction (XRD) analysis confirmed that the ROP only underwent on the surface of HA nanoparticles without changing its bulk properties. The SEM measurement showed that the PBLG-g-HA hybrid could form an interpenetrating net structure in the self-assembly process. The PBLG-g-HA hybrid could maintain higher colloid stability than the pure HA nanoparticles. The in vitro cell cultures suggested the cell adhesion ability of PBLG-g-HA was much higher than that of pure HA.
首次提出通过γ-苄基-L-谷氨酸N-羧酸酐(BLG-NCA)的开环聚合(ROP)对羟基磷灰石(HA)纳米颗粒进行表面改性,以制备聚(γ-苄基-L-谷氨酸)(PBLG)接枝的HA纳米颗粒(PBLG-g-HA)。首先用3-氨丙基三乙氧基硅烷(APS)处理HA纳米颗粒,然后改性HA颗粒的末端氨基引发BLG-NCA的ROP以获得PBLG-g-HA。通过XPS和FT-IR监测该过程。通过热重分析(TGA)表征了PBLG在HA上的表面接枝量,范围为12.1%至43.1%。粉末X射线衍射(XRD)分析证实ROP仅在HA纳米颗粒表面发生,而没有改变其本体性质。SEM测量表明,PBLG-g-HA杂化物在自组装过程中可以形成互穿网络结构。PBLG-g-HA杂化物比纯HA纳米颗粒具有更高的胶体稳定性。体外细胞培养表明,PBLG-g-HA的细胞粘附能力远高于纯HA。