In situ time-resolved X-ray diffraction study of evolution of nanohydroxyapatite particles in physiological solution

被引:2
作者
Rau, J. V. [1 ]
Generosi, A. [1 ]
Ferro, D. [2 ]
Minozzi, F. [3 ]
Paci, B. [1 ]
Albertini, V. Rossi [1 ]
Dolci, G. [3 ]
Barinov, S. M. [4 ]
机构
[1] CNR, Ist Struttura Mat, I-00133 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Chim, CNR, Ist Studio Mat Nanostrutturati, I-00185 Rome, Italy
[3] Univ Roma La Sapienza, Dipartimento Sci Odontostomatol, I-00161 Rome, Italy
[4] Russian Acad Sci, Baikov Inst Met & Mat Sci, Moscow 119991, Russia
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2009年 / 29卷 / 04期
关键词
Nanohydroxyapatite; Dental and bone filling material; Phase transformations; Crystallite size evolution; X-ray diffraction; HYDROXYAPATITE NANOPARTICLES; BONE; CRYSTALLINITY; PHASE;
D O I
10.1016/j.msec.2008.09.035
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nanosized hydroxyapatite (nano-HA) is known to be of enhanced biological efficacy, being used in medical events as a mix with physiological solution, saline or patient's blood before the application. This study is aimed at the investigation of the time evolution of both phase composition and particle size of nano-HA in aqueous (isotonic 0.9% NaCl) solution. An energy-dispersive X-ray diffraction method, allowing the real time rapid data collection was employed. The X-ray amorphous component of initial powder was shown to convert fully into the crystalline hydroxyapatite (HA), the characteristic crystallization time being of approximately 25 min. The initial crystallite average size (approximately 35 nm) was enlarged by a factor of about 4 within the first 100 min after mixing the powder with the physiological solution and no more structural changes were detected during the following period. The sigmoidal kinetics of the HA crystal growth was evidenced. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1140 / 1143
页数:4
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