Inhibiting Friction-Induced Exogenous Adhesion via Robust Lubricative Core-Shell Nanofibers for High-Quality Tendon Repair.

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xin Cao, Jinghua Li, Weijie Zhai, Bowen Zhou, Hao Lin, Yi Wang
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引用次数: 0

Abstract

Friction is the trigger cause for excessive exogenous adhesion, leading to the poor self-repair of the tendon. To address this problem, we developed electrospun dual-functional nanofibers with surface robust superlubricated performance and bioactive agent delivery to regulate healing balance by reducing exogenous adhesion and promoting endogenous healing. Coaxial electrospinning and our previous developed in situ robust nanocoating growth techniques were employed to create the lubricative/repairable core-shell structured nanofibrous membrane (L/R-NM). The L/R-NM shell featured a robust coating of the zwitterionic PMPC polymer for strong hydration lubrication to resist exogenous healing. The core could achieve sustained platelet-rich plasma release to promote endogenous healing. Friction tests and cell experiments confirmed L/R-NM's prominent lubricating properties and antiadhesive performance in vitro. Rat tendon injury model evaluation indicated that L/R-NM effectively promotes high-quality tendon repair by inhibiting friction-induced exogenous adhesion and promoting endogenous healing. Therefore, we believe that L/R-NM will open a unique novel horizon for tendon repair.

通过坚固的润滑核壳纳米纤维抑制摩擦诱导的外源性粘连用于高质量肌腱修复。
摩擦是外源性粘连过多的触发原因,导致肌腱自我修复能力差。为了解决这一问题,我们开发了具有表面强大的超润滑性能和生物活性剂递送功能的静电纺双功能纳米纤维,通过减少外源性粘连和促进内源性愈合来调节愈合平衡。同轴静电纺丝和我们之前开发的原位坚固的纳米涂层生长技术被用于制造润滑/可修复的核壳结构纳米纤维膜(L/R-NM)。L/R-NM外壳具有坚固的两性离子PMPC聚合物涂层,具有强水化润滑作用,可抵抗外源愈合。核心可以实现持续的富血小板血浆释放,以促进内源性愈合。摩擦试验和细胞实验证实了L/R-NM具有良好的体外润滑性能和抗粘接性能。大鼠肌腱损伤模型评价表明,L/R-NM通过抑制摩擦诱导的外源性粘连,促进内源性愈合,有效促进高质量肌腱修复。因此,我们相信L/R-NM将为肌腱修复开辟一个独特的新领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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