Effect of silver content on the antibacterial and bioactive properties of silver-substituted hydroxyapatite

被引:77
|
作者
Lim, Poon Nian [1 ]
Teo, Erin Yiling [2 ]
Ho, Bow [3 ]
Tay, Bee Yen [4 ]
Thian, Eng San [1 ]
机构
[1] Natl Univ Singapore, Dept Mech Engn, Singapore 117576, Singapore
[2] KK Womens & Childrens Hosp, Dept Reprod Med, Singapore 229899, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol, Singapore 119757, Singapore
[4] Singapore Inst Mfg Technol, Singapore 638075, Singapore
关键词
antibacterial; bioactivity; hydroxyapatite; mesenchymal stem cell; silver; MECHANISMS; INFECTION; RELEASE; NITRATE; SURFACE; IONS; BONE;
D O I
10.1002/jbm.a.34544
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The long-term success of a biomaterial used during surgery may be compromised by infection. A possible effective solution is to make the biomaterial osteoconductive and antibacterial. A range of silver-substituted hydroxyapatite (AgHA) of up to 1.1 wt. % of Ag was synthesized. AgHA displayed a rod-like morphology of dimensions approximate to 50 nm in length and approximate to 15 nm in width. Phase-pure AgHA was demonstrated in the X-ray diffraction patterns and Fourier transform infrared spectroscopy spectra. Comparing with hydroxyaptite (HA), 0.5AgHA exhibited a 3-log reduction in the number of bacteria. Diffusion of the entrapped Ag+ ions towards the crystal structure surface was revealed by an increase of 6 at. % Ag in the X-ray photoelectron spectroscopy results. Furthermore, less than 0.5 ppm of Ag+ ions being released from 0.5AgHA into the deionized water medium was evidenced from the inductively coupled plasma mass spectrometry results. AgHA produced by co-precipitation gave rise to minimal release of Ag+ ions. It was hypothesized that the diffused surface Ag+ ions damaged the bacteria cell membrane and impede its replication. With the culturing time, significant increase in the number of human mesenchymal stem cells (p < 0.05) was demonstrated on 0.5AgHA. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 101A: 2456-2464, 2013.
引用
收藏
页码:2456 / 2464
页数:9
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