Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Environmental Health Sciences, University of Michigan, Ann Arbor, MI 48109, USA.
Acta Biomater. 2019 May;90:112-121. doi: 10.1016/j.actbio.2019.04.021. Epub 2019 Apr 10.
Nitric oxide (NO) releasing polymers have been widely applied as biomaterials for a variety of biomedical implants and devices. However, the chemical leaching of NO donors and their byproduct species is almost always observed during the application of polymers doped with NO donors, unless the donor is covalently linked to the polymer. Herein, we report the first NO releasing poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) fluorinated copolymer prepared by incorporating a fluorinated S-nitrosothiol as the NO donor. Under physiological conditions, the resulting polymeric films can release NO for 16 days. Importantly, due to both fluorine-fluorine and electrostatic charge interactions between the fluorinated NO donor and the PVDF-HFP copolymer, the total chemical leaching of the fluorinated NO donor and its disulfide product after 9 day was only 0.6% (mol%) of the initial amount of NO donor loaded into the film. These new NO release PVDF-HFP films exhibit antimicrobial and anti-biofilm activities against both Gram positive S. aureus and Gram negative P. aeruginosa strains. The NO-releasing PVDF-HFP polymer can also be coated on Teflon tubing to release NO under physiological conditions for extended time periods. This NO-releasing PVDF-HFP copolymer with greatly reduced chemical leaching could help enhance the biocompatibility and antimicrobial activity of various biomedical devices. STATEMENT OF SIGNIFICANCE: Fluoropolymers have been widely used in creating various biomedical implants and devices. However, nitric oxide (NO) release fluoropolymers have not been well studied to date. Additionally, in the application of biomaterials doped with NO donors, a significant amount of NO donors and their byproducts almost always leach into aqueous environment. We now report an NO releasing poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) fluoropolymer by incorporating a new fluorinated S-nitrosothiol. The NO release can last for 16 days under physiological conditions. The total chemical leaching was determined to be only 0.6 mol% of the initial S-nitrosothiol loaded. As expected, significant antimicrobial/anti-biofilm activities of the NO release PVDF-HFP film were observed against Gram positive S. aureus and Gram negative P. aeruginosa bacterial strains.
一氧化氮(NO)释放聚合物已被广泛用作各种生物医学植入物和设备的生物材料。然而,在应用掺杂有 NO 供体的聚合物时,几乎总是会观察到 NO 供体及其副产物的化学浸出,除非供体与聚合物共价连接。在此,我们报告了首例通过掺入氟化 S-亚硝硫醇作为 NO 供体制备的一氧化氮释放聚(偏二氟乙烯-共-六氟丙烯)(PVDF-HFP)氟化共聚物。在生理条件下,所得聚合物薄膜可在 16 天内释放 NO。重要的是,由于氟化 NO 供体与 PVDF-HFP 共聚物之间的氟-氟和静电电荷相互作用,在 9 天后,氟化 NO 供体及其二硫化物产物的总化学浸出量仅为初始加载到薄膜中的 NO 供体量的 0.6%(摩尔%)。这些新型 NO 释放的 PVDF-HFP 薄膜对革兰氏阳性菌金黄色葡萄球菌和革兰氏阴性菌铜绿假单胞菌均表现出抗菌和抗生物膜活性。NO 释放的 PVDF-HFP 聚合物还可以涂覆在特氟龙管上,在生理条件下延长时间释放 NO。这种化学浸出大大减少的 NO 释放 PVDF-HFP 共聚物有助于提高各种生物医学设备的生物相容性和抗菌活性。
氟聚合物已广泛用于制造各种生物医学植入物和设备。然而,迄今为止,对一氧化氮(NO)释放氟聚合物的研究还不够充分。此外,在应用掺杂有 NO 供体的生物材料时,大量的 NO 供体及其副产物几乎总是会浸出到水相环境中。我们现在通过掺入一种新的氟化 S-亚硝硫醇报告了一种一氧化氮释放的聚(偏二氟乙烯-共-六氟丙烯)(PVDF-HFP)氟聚合物。在生理条件下,NO 的释放可持续 16 天。总化学浸出量被确定仅为初始加载的 S-亚硝硫醇的 0.6%mol%。正如预期的那样,NO 释放的 PVDF-HFP 薄膜对革兰氏阳性菌金黄色葡萄球菌和革兰氏阴性菌铜绿假单胞菌的抗菌/抗生物膜活性显著。