Effects of silica and calcium levels in nanobioglass ceramic particles on osteoblast proliferation

被引:38
作者
Moorthi, A. [1 ]
Parihar, P. R. [1 ]
Saravanan, S. [1 ]
Vairamani, M. [1 ]
Selvamurugan, N. [1 ]
机构
[1] SRM Univ, Sch Bioengn, Dept Biotechnol, Kattankulathur 603203, Tamil Nadu, India
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2014年 / 43卷
关键词
Bioglass ceramic; Calcium; Silica; Cell proliferation; Cyclins; Osteoblasts; TISSUE ENGINEERING APPLICATIONS; ANTIMICROBIAL ACTIVITY; COMPOSITE SCAFFOLDS; CHITOSAN SCAFFOLDS; IN-VITRO; BONE; CELLS; DIFFERENTIATION; BIOGLASS(R); EXPRESSION;
D O I
10.1016/j.msec.2014.07.040
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
At nanoscale, bioglass ceramic (nBGC) particles containing calcium oxide (lime), silica and phosphorus pentoxide promote osteoblast proliferation. However, the role of varied amounts of calcium and silica present in nBGC particles on osteoblast proliferation is not yet completely known. Hence, the current work was aimed at synthesizing two different nBGC particles with varied amounts of calcium oxide and silica, nBGC-1: SiO2:CaO:P2O5; mol% similar to 70:25:5 and nBGC-2: SiO2:CaO:P2O5; mol% similar to 64:31:5, and investigating their role on osteoblast proliferation. The synthesized nBGC particles were characterized by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) studies. They exhibited their size at nanoscale and were non-toxic to human osteoblastic cells (MG-63). The nBGC-2 particles were found to have more effect on stimulation of osteoblast proliferation and promoted entering of more cells into G2/M cell cycle phase compared to nBGC-1 particles. There was a differential expression of cyclin proteins in MG-63 cells by nBGC-1 and nBGC-2 treatments, and the expression of cyclin B1 and E proteins was found to be more by nBGC-2 treatment. Thus, these results provide us a new insight in understanding the design of various nBGC particles by altering their ionic constituents with desirable biological properties thereby supporting bone augmentation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:458 / 464
页数:7
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