A new multifunctional monticellite-ciprofloxacin scaffold: Preparation, bioactivity, biocompatibility, and antibacterial properties

被引:49
作者
Bakhsheshi-Rad, H. R. [1 ,2 ]
Chen, X. B. [3 ]
Ismail, A. F. [4 ]
Aziz, M. [4 ]
Hamzah, E. [2 ]
Najafinezhad, A. [1 ]
机构
[1] Islamic Azad Univ, Adv Mat Res Ctr, Dept Mat Engn, Najafabad Branch, Najafabad, Iran
[2] Univ Teknol Malaysia, Dept Mat Mfg & Ind Engn, Fac Mech Engn, Johor Baharu 81310, Johor, Malaysia
[3] Univ Saskatchewan, Dept Mech Engn, Coll Engn, Saskatoon, SK, Canada
[4] Univ Teknol Malaysia, Adv Membrane Technol Res Ctr AMTEC, Johor Baharu 81310, Johor, Malaysia
关键词
Monticellite scaffold; Space holder; Bioactivity; Antibacterial properties; Biocompatibility; MECHANICAL-PROPERTIES; DRUG-RELEASE; IN-VITRO; COMPOSITE SCAFFOLDS; MAGNESIUM-SILICATE; CERAMIC SCAFFOLDS; BONE; FABRICATION; CYTOCOMPATIBILITY; DEGRADABILITY;
D O I
10.1016/j.matchemphys.2018.09.054
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This work prepared novel monticellite-ciprofloxacin (Mon-CPFX) scaffolds with different concentrations of CPFX (0, 1, 3, and 6%) via the space holder method. The Mon-CPFX scaffolds had a compressive strength of 1 +/- 0.1 MPa, porosity of 81-83%, and pore size of 300-420 mu m. The formation of hydroxyapatite on the Mon-CPFX scaffold surfaces was observed after soaking in simulated body fluid (SBF) solution for 28 d, with a Ca/P atomic ratio of 1.62 indicating high apatite formation ability. Antibacterial tests indicated the antibacterial effect of Mon-CPFX scaffolds is strongly related to the CPFX concentration; the greatest bacterial inhibition was observed for the scaffold containing 6% CPFX. Furthermore, an MTT assay illustrated that Mon scaffold loading with up to 3% CPFX resulted in higher cell viability, cell proliferation, and attachment than for scaffolds containing 6% CPFX. This particular novel type of multifunctional Mon-CPFX scaffold could be considered for bone infection treatment owing to its suitable compressive strength along with excellent bioactivity, antibacterial performance, and biocompatibility.
引用
收藏
页码:118 / 131
页数:14
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