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用于高通量评估创伤愈合和抗感染生物材料的微流控 3D 骨组织模型。

Microfluidic 3D bone tissue model for high-throughput evaluation of wound-healing and infection-preventing biomaterials.

机构信息

Chemical Engineering and Materials Science, Stevens Institute of Technology, Hoboken, NJ 07030, USA.

出版信息

Biomaterials. 2012 Feb;33(4):999-1006. doi: 10.1016/j.biomaterials.2011.10.036. Epub 2011 Nov 5.

Abstract

We report the use of a microfluidic 3D bone tissue model, as a high-throughput means of evaluating the efficacy of biomaterials aimed at accelerating orthopaedic implant-related wound-healing while preventing bacterial infection. As an example of such biomaterials, inkjet-printed micropatterns were prepared to contain antibiotic and biphasic calcium phosphate (BCP) nanoparticles dispersed in a poly(D,L-lactic-co-glycolic) acid matrix. The micropatterns were integrated with a microfluidic device consisting of eight culture chambers. The micropatterns immediately and completely killed Staphylococcus epidermidis upon inoculation, and enhanced the calcified extracellular matrix production of osteoblasts. Without antibiotic elution, bacteria rapidly proliferated to result in an acidic microenvironment which was detrimental to osteoblasts. These results were used to demonstrate the tissue model's potential in: (i) significantly reducing the number of biomaterial samples and culture experiments required to assess in vitro efficacy for wound-healing and infection prevention and (ii) in situ monitoring of dynamic interactions of biomaterials with bacteria as wells as with tissue cells simultaneously.

摘要

我们报告了使用微流控 3D 骨组织模型作为高通量手段来评估旨在加速骨科植入物相关伤口愈合同时预防细菌感染的生物材料的功效。作为此类生物材料的一个例子,喷墨打印了微图案以包含抗生素和双相磷酸钙(BCP)纳米颗粒分散在聚(D,L-乳酸-co- 乙醇酸)基质中。微图案与由八个培养室组成的微流控装置集成在一起。微图案在接种时立即完全杀死表皮葡萄球菌,并增强成骨细胞的钙化细胞外基质产生。没有抗生素洗脱,细菌迅速增殖导致酸性微环境对成骨细胞有害。这些结果用于证明组织模型在以下方面的潜力:(i)显著减少评估伤口愈合和感染预防的体外功效所需的生物材料样品和培养实验的数量,以及(ii)原位监测生物材料与细菌以及组织细胞的动态相互作用。

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