Gutowska A, Bae Y H, Jacobs H, Mohammad F, Mix D, Feijen J, Kim S W
Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City 84108, USA.
J Biomed Mater Res. 1995 Jul;29(7):811-21. doi: 10.1002/jbm.820290705.
Biomer/poly(N-isopropylacrylamide)/[poly(NiPAAm)] thermosensitive polymer blends were prepared and their application as heparin-releasing polymer coatings for the prevention of surface-induced thrombosis was examined. The advantage of using poly (NiPAAm)-based coatings as heparin-releasing polymers is based on the unique temperature-dependent swelling of these materials. At room temperature, i.e., below the lower critical solution temperature (LCST) of poly (NiPAAm), the Biomer/(poly(NiPAAm) coatings are highly swollen. The high swelling enables fast loading of hydrophilic macromolecules (e.g., heparin) into the coating by a solution sorption technique. At a body temperature, i.e., above the LCST of poly (NiPAAm) the coatings are in a deswollen state and the absorbed macromolecules may be slowly released from a dense coating via a diffusion controlled mechanism. Biomer/poly(NiPAAm) coatings were obtained by blending and coprecipitation of the two linear polymers, Biomer and (poly(NiPAAm). The structure and water-swelling properties of the coatings were examined. Significant differences in water swelling at room temperature (RT) and 37 degrees C were observed as a result of the thermosensitivity of poly (NiPAAm). The surface structure of the coatings in dry and swollen states at RT and 37 degrees C was examined by scanning electron microscopy. Heparin was loaded into the coatings via a solution sorption at room temperature. Kinetic studies of heparin loading demonstrated that maximum loading was obtained within 1 h. The in vitro (37 degrees C) release profiles were characterized by a rapid initial release due to the squeezing effect of the collapsing polymer network, followed by a slower release phase controlled by heparin diffusion through the dense coating. The short-term antithrombogenicity of intravenous polyurethane catheters coated with heparin-releasing Biomer/poly(NiPAAm) thermosensitive coating was evaluated in a canine animal model. The results show that the heparin release from Biomer/poly(NiPAAm)-coated surfaces resulted in a significant reduction of thrombus formation on test surfaces in contact with venous blood as compared to control surfaces.
制备了生物聚合物/聚(N-异丙基丙烯酰胺)/[聚(N-异丙基丙烯酰胺)]热敏聚合物共混物,并研究了其作为肝素释放聚合物涂层在预防表面诱导血栓形成方面的应用。使用基于聚(N-异丙基丙烯酰胺)的涂层作为肝素释放聚合物的优势在于这些材料独特的温度依赖性溶胀特性。在室温下,即低于聚(N-异丙基丙烯酰胺)的低临界溶液温度(LCST)时,生物聚合物/(聚(N-异丙基丙烯酰胺)涂层高度溶胀。这种高溶胀性使得通过溶液吸附技术能够将亲水性大分子(如肝素)快速载入涂层中。在体温下,即高于聚(N-异丙基丙烯酰胺)的LCST时,涂层处于去溶胀状态,被吸收的大分子可能通过扩散控制机制从致密涂层中缓慢释放出来。生物聚合物/聚(N-异丙基丙烯酰胺)涂层是通过将两种线性聚合物生物聚合物和(聚(N-异丙基丙烯酰胺))共混和共沉淀而获得的。研究了涂层的结构和水溶胀性能。由于聚(N-异丙基丙烯酰胺)的热敏性,在室温(RT)和37℃下观察到水溶胀存在显著差异。通过扫描电子显微镜检查了涂层在RT和37℃下干燥和溶胀状态的表面结构。在室温下通过溶液吸附将肝素载入涂层中。肝素载入的动力学研究表明,在1小时内可达到最大载入量。体外(37℃)释放曲线的特征是,由于聚合物网络塌陷的挤压效应,最初会快速释放,随后是由肝素通过致密涂层扩散控制的较慢释放阶段。在犬类动物模型中评估了涂有肝素释放生物聚合物/聚(N-异丙基丙烯酰胺)热敏涂层的静脉内聚氨酯导管的短期抗血栓形成性。结果表明,与对照表面相比,生物聚合物/聚(N-异丙基丙烯酰胺)涂层表面释放的肝素导致与静脉血接触的测试表面上血栓形成显著减少。