Yadav Umakant, Mishra Himanshu, Singh Vimal, Kashyap Sunayana, Srivastava Anchal, Yadav Sanjay, Saxena Preeti S
ACS Biomater Sci Eng. 2019 Sep 9;5(9):4511-4521. doi: 10.1021/acsbiomaterials.9b00227. Epub 2019 Jul 30.
The advances in the arena of biomedical engineering enable us to fabricate novel biomaterials that provide a suitable platform for rapid bone regeneration. Herein, we have investigated the in vitro and in vivo osteogenic differentiation, proliferation, and bone regeneration capability of molybdenum disulfide nanosheets (MoSNSs) reinforced HAP nanocomposite scaffolds. The MG-63 cells were incubated with HAP and HAP/MoSNSs nanocomposite and followed for various cellular activities. The cells incubated with HAP@2 shows higher cell adhesion, cell proliferation, and alkaline phosphatase activity (ALP) in contrast to HAP. The in vivo and in vitro results of the increased ALP level confirm that HAP@2 promotes osteogenic differentiation. This improved osteogenesis was validated with upregulation of osteogenic marker viz. transcription factor, RUNX-2 (∼34 fold), collagen-1 (∼15 fold), osteopontin (∼11 fold), osteocalcin (∼20 fold), and bone morphogenetic protein-2 (∼12 fold) after 12 week postimplantation in comparison to drilled. The X-ray imaging demonstrates that HAP@2 implants promote rapid osteogenesis and bioresorbability than HAP and drilled. The outcomes of the present study provide a promising tool for the regeneration of bone deformities, without using any external growth factor.
生物医学工程领域的进展使我们能够制造出新型生物材料,为快速骨再生提供合适的平台。在此,我们研究了二硫化钼纳米片(MoSNSs)增强的羟基磷灰石(HAP)纳米复合支架在体外和体内的成骨分化、增殖及骨再生能力。将MG-63细胞与HAP及HAP/MoSNSs纳米复合材料共同培养,并观察各种细胞活性。与HAP相比,用HAP@2培养的细胞表现出更高的细胞黏附、细胞增殖及碱性磷酸酶(ALP)活性。ALP水平升高的体内和体外结果证实HAP@2促进成骨分化。这种改善的成骨作用通过成骨标志物的上调得到验证,即与钻孔组相比,植入12周后转录因子RUNX-2(约34倍)、胶原蛋白-1(约15倍)、骨桥蛋白(约11倍)、骨钙素(约20倍)和骨形态发生蛋白-2(约12倍)上调。X射线成像显示,与HAP和钻孔组相比,HAP@2植入物促进更快的骨生成和生物可吸收性。本研究结果为骨畸形的再生提供了一种有前景 的工具,无需使用任何外部生长因子。