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Cyclic Polymer Grafts That Lubricate and Protect Damaged Cartilage

机译:润滑和保护受损软骨的环状聚合物移植物

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摘要

Tissue-reactive graft copolymers were designed to protect the cartilage against enzymatic degradation and restore its lubrication properties during the early stages of osteoarthritis (OA). The copolymers feature a poly(glutamic acid) (PGA) backbone bearing hydroxybenzaldehyde (HBA) functions and cyclic poly(2-methyl-2-oxazoline) (PMOXA) side chains. PGA-PMOXA-HBA species chemisorb on the degraded tissue via Schiff bases and expose the biopassive and lubricious PMOXA cyclic grafts at the interface. The smaller hydrodynamic radius by cyclic PMOXA side chains coupled to the intrinsic absence of chain ends generate denser and more lubricious films on cartilage when compared to those produced by copolymers bearing linear PMOXA. Topology effects demonstrate how the introduction of cyclic polymers within tissue-reactive copolymers substantially improve their tribological and biopassive properties, suggesting a plethora of possible applications for cyclic macromolecules in biomaterials formulations.
机译:设计组织反应接枝共聚物以保护软骨免受酶促降解,并在骨关节炎(OA)的早期阶段恢复其润滑性质。共聚物具有含有羟基苯甲醛(HBA)功能的聚(谷氨酸)(PGA)骨架(HBA)功能和环状聚(2-甲基-2-恶唑啉)(PMOXA)侧链。 PGA-PMOXA-HBA物种通过Schiff碱基在降解组织上进行化学isb,暴露在界面处暴露生物分配和润滑的Pmoxa循环移植物。与通过轴承线性PMOXA产生的共聚物产生的那些相比,循环pmoxa侧链通过环状PmOxa侧链的循环pmoxa侧链产生较小的循环末端链。拓扑效果表明如何在组织反应性共聚物中引入循环聚合物的引入显着改善其摩擦学和生物分析性质,表明循环大分子在生物材料制剂中可能的应用。

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