Zhou Zhengrong, Meyerhoff Mark E
Department of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109-1055, USA.
Biomacromolecules. 2005 Mar-Apr;6(2):780-9. doi: 10.1021/bm049462l.
A series of new nitric oxide (NO) releasing copolymers have been prepared by covalently anchoring alkyldiamine side chains onto a polymethacrylate-based polymer backbone, followed by NO addition to form the desired pendant diazeniumdiolate structures. The resulting diazeniumdiolated copolymers were characterized via UV spectroscopy, and their proton-driven decomposition to release NO was also examined by UV and FTIR as well as chemiluminescence. Polymers with up to 22.1 mol % of incorporated amine sites that can be converted to corresponding diazeniumdiolates could be prepared, and such polymers release up to 0.94 micromol/mg of NO. Further, novel NO releasing polymeric coatings were formulated by doping one of the new polymethacrylate-based NO donors within inert polymeric matrixes. Biodegradable poly(lactide-co-glycolide) was employed as a film additive to greatly prolong the NO release of such coatings by continuously generating protons within the organic phase of the polymeric films, thereby driving decomposition of the diazeniumdiolates.
通过将烷基二胺侧链共价锚定在聚甲基丙烯酸酯基聚合物主链上,随后添加一氧化氮(NO)以形成所需的侧挂二氮烯二醇盐结构,制备了一系列新型的一氧化氮释放共聚物。通过紫外光谱对所得的二氮烯二醇盐共聚物进行了表征,并且还通过紫外光谱、傅里叶变换红外光谱以及化学发光法研究了它们由质子驱动分解以释放一氧化氮的情况。可以制备出胺位点掺入量高达22.1摩尔%且可转化为相应二氮烯二醇盐的聚合物,此类聚合物可释放高达0.94微摩尔/毫克的一氧化氮。此外,通过将一种新型的聚甲基丙烯酸酯基一氧化氮供体掺入惰性聚合物基质中,配制出了新型的一氧化氮释放聚合物涂层。可生物降解的聚(丙交酯-共-乙交酯)被用作薄膜添加剂,通过在聚合物薄膜的有机相中持续产生质子,从而驱动二氮烯二醇盐的分解,极大地延长了此类涂层的一氧化氮释放时间。