Bigi A, Boanini E, Gazzano M, Rubini K, Torricelli P
Dipartimento di Chimica "G. Ciamician" and ISOF-CNR, via Selmi 2, 40126 Bologna, Italy.
Biomed Mater Eng. 2004;14(4):573-9.
The direct synthesis of hydroxyapatite-poly-L-aspartic acid (HA-PASP) nanocrystals has been carried out in presence of increasing amounts of PASP in solution up to 56 mmol/l. WAXS, TEM, TGA, IR and chemical analyses were used to characterize the structure, morphology and composition of the products. PASP is quantitatively incorporated into HA crystals, provoking a reduction of the coherent length of the crystalline domains. Furthermore, composite crystals display a greater length/width ratio with respect to the control HA crystals, and show a remarkable trend towards aggregation. The broadening of the X-ray diffraction reflections indicate a reduction of the coherent length along the long dimension 002 and the cross section 310 of the apatite crystals. The comparison between the morphological and structural data allows to suggest a specific interaction between PASP and HA structure.
在溶液中存在的聚天冬氨酸(PASP)量不断增加直至56 mmol/l的情况下,已经进行了羟基磷灰石-聚-L-天冬氨酸(HA-PASP)纳米晶体的直接合成。采用广角X射线散射(WAXS)、透射电子显微镜(TEM)、热重分析(TGA)、红外光谱(IR)和化学分析来表征产物的结构、形态和组成。PASP被定量地掺入到HA晶体中,导致晶畴相干长度减小。此外,复合晶体相对于对照HA晶体表现出更大的长径比,并显示出明显的聚集趋势。X射线衍射反射的展宽表明沿磷灰石晶体的长轴002和横截面310方向的相干长度减小。形态学和结构数据之间的比较表明PASP与HA结构之间存在特定的相互作用。