Wo Yaqi, Brisbois Elizabeth J, Wu Jianfeng, Li Zi, Major Terry C, Mohammed Azmath, Wang Xianglong, Colletta Alessandro, Bull Joseph L, Matzger Adam J, Xi Chuanwu, Bartlett Robert H, Meyerhoff Mark E
Department of Chemistry, Department of Surgery, University of Michigan Medical Center, Department of Environmental Health Sciences, and Department of Biomedical Engineering, University of Michigan , Ann Arbor, Michigan 48109, United States.
ACS Biomater Sci Eng. 2017 Mar 13;3(3):349-359. doi: 10.1021/acsbiomaterials.6b00622. Epub 2017 Jan 22.
Nitric oxide (NO) has many important physiological functions, including its ability to inhibit platelet activation and serve as potent antimicrobial agent. The multiple roles of NO in vivo have led to great interest in the development of biomaterials that can deliver NO for specific biomedical applications. Herein, we report a simple solvent impregnation technique to incorporate a nontoxic NO donor, -nitroso--acetylpenicillamine (SNAP), into a more biocompatible biomedical grade polymer, CarboSil 20 80A. The resulting polymer-crystal composite material yields a very stable, long-term NO release biomaterial. The SNAP impregnation process is carefully characterized and optimized, and it is shown that SNAP crystal formation occurs in the bulk of the polymer after solvent evaporation. LC-MS results demonstrate that more than 70% of NO release from this new composite material originates from the SNAP embedded CarboSil phase, and not from the SNAP species leaching out into the soaking solution. Catheters prepared with CarboSil and then impregnated with 15 wt % SNAP provide a controlled NO release over a 14 d period at physiologically relevant fluxes and are shown to significantly reduce long-term (14 day) bacterial biofilm formation against and in a CDC bioreactor model. After 7 h of catheter implantation in the jugular veins of rabbit, the SNAP CarboSil catheters exhibit a 96% reduction in thrombus area (0.03 ± 0.01 cm/catheter) compared to the controls (0.84 ± 0.19 cm/catheter) ( = 3). These results suggest that SNAP impregnated CarboSil can become an attractive new biomaterial for use in preparing intravascular catheters and other implanted medical devices.
一氧化氮(NO)具有许多重要的生理功能,包括抑制血小板活化的能力以及作为强效抗菌剂的作用。NO在体内的多种作用引发了人们对开发能够为特定生物医学应用递送NO的生物材料的浓厚兴趣。在此,我们报告了一种简单的溶剂浸渍技术,将无毒的NO供体——亚硝基乙酰青霉胺(SNAP)掺入生物相容性更好的生物医学级聚合物CarboSil 20 80A中。所得的聚合物 - 晶体复合材料产生了一种非常稳定、长期释放NO的生物材料。对SNAP浸渍过程进行了仔细的表征和优化,结果表明在溶剂蒸发后,SNAP晶体在聚合物本体中形成。液相色谱 - 质谱(LC - MS)结果表明,这种新型复合材料释放的NO中超过70%源自嵌入CarboSil相的SNAP,而非从浸泡溶液中浸出的SNAP物种。用CarboSil制备然后浸渍15 wt% SNAP的导管在生理相关通量下可在14天内实现可控的NO释放,并在疾病控制与预防中心(CDC)生物反应器模型中显示出能显著减少针对金黄色葡萄球菌和大肠杆菌的长期(14天)细菌生物膜形成。在将导管植入兔颈静脉7小时后,与对照组(0.84 ± 0.19 cm²/导管)相比,SNAP - CarboSil导管的血栓面积减少了96%(0.03 ± 0.01 cm²/导管)(n = 3)。这些结果表明,浸渍了SNAP的CarboSil可能成为一种有吸引力的新型生物材料,用于制备血管内导管和其他植入式医疗设备。