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PEO-PPO diblock copolymers protect myoblasts from hypo-osmotic stressin vitro dependent on copolymer size composition andarchitecture

机译:PEO-PPO二嵌段共聚物可保护成肌细胞免受低渗压力的影响在体外取决于共聚物的大小组成和建筑

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摘要

Poloxamer 188, a triblock copolymer of poly(ethylene oxide) (PEO) and poly(propylene oxide) (PPO), protects cellular membranes from various stresses. Though numerous block copolymer variants exist, evaluation of alternative architecture, composition, and size has been minimal. Herein, cultured murine myoblasts are exposed to the stresses of hypotonic shock and isotonic recovery, and membrane integrity was evaluated by quantifying release of lactate dehydrogenase. Comparative evaluation of a systematic set of PEO-PPO diblock and PEO-PPO-PEO triblock copolymers demonstrates that the diblock architecture can be protective in vitro. Short PPO blocks hinder protection with >9 PPO units needed for protection at 150 µM and >16 units needed at 14 µM. Addition of a tert-butyl end group enhances protection at reduced concentration. When the end group and PPO length are fixed, increasing the PEO length improves protection. This systematic evaluation establishes a new in vitro screening tool for evaluating membrane-sealing amphiphiles and provides mechanistic insight to guide future copolymer design for membrane stabilization in vivo.
机译:Poloxamer 188是聚环氧乙烷(PEO)和聚环氧丙烷(PPO)的三嵌段共聚物,可保护细胞膜免受各种压力的影响。尽管存在许多嵌段共聚物变体,但对替代结构,组成和尺寸的评估却很少。在此,将培养的鼠成肌细胞暴露于低渗休克和等渗恢复的压力下,并通过定量乳酸脱氢酶的释放来评估膜的完整性。对一组系统化的PEO-PPO二嵌段共聚物和PEO-PPO-PEO三嵌段共聚物进行的比较评估表明,该二嵌段结构可以在体外起到保护作用。短的PPO块妨碍了保护,在150 µM时需要> 9个PPO单元,在14 µM时需要> 16个单元。叔丁基端基的添加在降低的浓度下增强了保护。当端基和PPO长度固定时,增加PEO长度可改善保护。这项系统的评估建立了一种新的体外筛选工具,用于评估膜密封性的两亲物,并提供了机械方面的见识,可指导未来的共聚物设计在体内稳定膜。

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