Synthesis methods for nanosized hydroxyapatite with diverse structures

被引:1408
作者
Sadat-Shojai, Mehdi [1 ]
Khorasani, Mohammad-Taghi [1 ]
Dinpanah-Khoshdargi, Ehsan [1 ]
Jamshidi, Ahmad [1 ]
机构
[1] IPPI, Tehran, Iran
关键词
Hydroxyapatite; Calcium phosphate; Nanoparticles; Bioceramics; Bone; ALPHA-TRICALCIUM PHOSPHATE; MECHANOCHEMICAL-HYDROTHERMAL SYNTHESIS; SINGLE-CRYSTAL HYDROXYAPATITE; SOLUTION COMBUSTION SYNTHESIS; ULTRASONIC SPRAY-PYROLYSIS; SOL-GEL SYNTHESIS; NANOCRYSTALLINE CALCIUM HYDROXYAPATITE; FLUORIDE-SUBSTITUTED HYDROXYAPATITE; CARBONATE-CONTAINING HYDROXYAPATITE; SPHERICAL NANO-HYDROXYAPATITE;
D O I
10.1016/j.actbio.2013.04.012
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Hydroxyapatite (HAp) is the major mineral constituent of vertebrate bones and teeth. It has been well documented that HAp nanoparticles can significantly increase the biocompatibility and bioactivity of man-made biomaterials. Over the past decade, HAp nanoparticles have therefore increasingly been in demand, and extensive efforts have been devoted to develop many synthetic routes, involving both scientifically and economically new features. Several investigations have also been made to determine how critical properties of HAp can be effectively controlled by varying the processing parameters. With such a wide variety of methods for the preparation of HAp nanoparticles, choosing a specific procedure to synthesize a well-defined powder can be laborious; accordingly, in the present review, we have summarized all the available information on the preparation methodologies of HAp, and highlighted the inherent advantages and disadvantages involved in each method. This article is focused on nanosized HAp, although recent articles on microsized particles, especially those assembled from nanoparticles and/or nanocrystals, have also been reviewed for comparison. We have also provided several scientific figures and discussed a number of critical issues and challenges which require further research and development. (C) 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7591 / 7621
页数:31
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