Li Xian, Chen Xiaofeng, Miao Guohou, Liu Hui, Mao Cong, Yuan Guang, Liang Qiming, Shen Xiongjun, Ning Chengyun, Fu Xiaoling
School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China.
J Mater Chem B. 2014 Oct 28;2(40):7045-7054. doi: 10.1039/c4tb00883a. Epub 2014 Sep 15.
Mesoporous bioactive glasses (MBGs) can be used as carriers for biomolecule delivery with improved functions. Although there are a great number of studies on drug delivery by MBGs, until now little work has been done to investigate the DNA gene transfection effect of MBGs. In this study, radial mesoporous bioactive glasses (rMBGs) were prepared by sol-gel process combined with a micro-emulsion method. The surface was further modified by amino groups in order to improve its affinity for DNA. Our study showed that rMBGs have good apatite-forming ability and cellular biocompatibility. In addition, rMBGs can enter cells in a time- and dose-dependent manner, and mainly localize in the cytoplasm. Agarose gel electrophoresis demonstrated that pOA-EGFP (containing the osteoactivin and the green fluorescent protein fusion gene) can be completely absorbed and protected from DNase I degradation by the aminated rMBGs. Additionally, the plasmid can be successfully expressed in cells transfected by rMBGs.
介孔生物活性玻璃(MBGs)可用作具有改进功能的生物分子递送载体。尽管关于MBGs用于药物递送已有大量研究,但迄今为止,关于MBGs的DNA基因转染效果的研究却很少。在本研究中,通过溶胶 - 凝胶法结合微乳液法制备了径向介孔生物活性玻璃(rMBGs)。为了提高其对DNA的亲和力,对其表面进行了氨基修饰。我们的研究表明,rMBGs具有良好的磷灰石形成能力和细胞生物相容性。此外,rMBGs能够以时间和剂量依赖性方式进入细胞,并且主要定位于细胞质中。琼脂糖凝胶电泳表明,pOA - EGFP(包含骨激活素和绿色荧光蛋白融合基因)能够被胺化的rMBGs完全吸收并免受DNase I降解。此外,该质粒能够在由rMBGs转染的细胞中成功表达。