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Manipulation Of Drug Release Behaviors Of Chitosan-based Orthopedic Nano-composites By Paa-coated Cdha Nanoparticles

机译:PAA涂层CDHA纳米粒子用壳聚糖基整体纳米复合材料的药物释放行为的操纵

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It is known that the release behavior of polymeric delivery system is strongly influenced by polymer crystallinity, plasticization, glass transition temperature and swelling extent which are further affected by the existence of nano-fillers. However, the roles of nano-fillers in current researches were inconsistent [1 - 3], which was primarily due to the various interfacial interaction strength between fillers and polymeric matrices [4]. In order to clarify the role of the filler-polymer interaction on the drug release behaviors of Chitosan/Calcium deficient hydroxyapatite (CS/CDHA) nano-composite, implantable PAA (poly acrylic acid) was employed instead of highly toxic silane as a physical coupling agent to enhance chitosan-CDHA interfacial interaction via electrostatic force. Although PAA has been reported to improve the mechanical properties of chitosan/HAp composite [5], studies on the effects of PAA-coated CDHA nano-crystals on the drug release behaviors of chitosan/CDHA nano-composites were not available.
机译:众所周知,聚合物递送系统的释放行为受到聚合物结晶度,塑化,玻璃化转变温度和膨胀程度的强烈影响,其进一步受纳米填料的存在影响。然而,纳米填料在当前研究中的作用是不一致的[1-3],其主要是由于填料和聚合物基质之间的各种界面相互作用强度[4]。为了阐明填料 - 聚合物相互作用对壳聚糖/缺乏羟基磷灰石(CS / CDHA)纳米复合材料的药物释放行为,采用可植入PAA(聚丙烯酸)而不是高度毒性硅烷作为物理耦合通过静电力提高壳聚糖-CDHA界面相互作用的剂。据报道,虽然据报道了PAA改善了壳聚糖/ HAP复合材料的机械性能[5],但不能研究对PAA涂覆的CDHA纳米晶体对壳聚糖/ CDHA纳米复合材料的药物释放行为的影响。

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