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基于原子转移自由基聚合的水凝胶控制释放外泌体。

Controlled Release of Exosomes Using Atom Transfer Radical Polymerization-Based Hydrogels.

机构信息

Department of Biomedical Engineering and Engineering Research Accelerator, Carnegie Mellon University, 5000 Forbes Avenue, Pittsburgh, Pennsylvania 15213, United States.

Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.

出版信息

Biomacromolecules. 2022 Apr 11;23(4):1713-1722. doi: 10.1021/acs.biomac.1c01636. Epub 2022 Mar 18.

Abstract

Exosomes are 30-200 nm sized extracellular vesicles that are increasingly recognized as potential drug delivery vehicles. However, exogenous exosomes are rapidly cleared from the blood upon intravenous delivery, which limits their therapeutic potential. Here, we report bioactive exosome-tethered poly(ethylene oxide)-based hydrogels for the localized delivery of therapeutic exosomes. Using cholesterol-modified DNA tethers, the lipid membrane of exosomes was functionalized with initiators to graft polymers in the presence of additional initiators and crosslinker using photoinduced atom transfer radical polymerization (ATRP). This strategy of tethering exosomes within the hydrogel network allowed their controlled release over a period of 1 month, which was much longer than physically entrapped exosomes. Exosome release profile was tuned by varying the crosslinking density of the polymer network and the use of photocleavable tethers allowed stimuli-responsive release of exosomes. The therapeutic potential of the hydrogels was assessed by evaluating the osteogenic potential of bone morphogenetic protein 2-loaded exosomes on C2C12 and MC3T3-E1 cells. Thus, ATRP-based exosome-tethered hydrogels represent a tunable platform with improved efficacy and an extended-release profile.

摘要

外泌体是 30-200nm 大小的细胞外囊泡,越来越多地被认为是有潜力的药物传递载体。然而,外源性外泌体在静脉给药后会迅速从血液中清除,这限制了它们的治疗潜力。在这里,我们报告了生物活性的外泌体连接的聚(氧化乙烯)基水凝胶,用于局部递送治疗性外泌体。使用胆固醇修饰的 DNA 接头,在外泌体的脂质膜上用引发剂进行功能化,在额外的引发剂和交联剂存在下使用光诱导原子转移自由基聚合(ATRP)接枝聚合物。这种在水凝胶网络中连接外泌体的策略允许它们在 1 个月的时间内进行控制释放,这比物理包埋的外泌体释放时间长得多。通过改变聚合物网络的交联密度和使用光可裂解的接头来调节外泌体的释放曲线,允许对外泌体进行刺激响应性释放。通过评估负载骨形态发生蛋白 2 的外泌体对 C2C12 和 MC3T3-E1 细胞的成骨潜力来评估水凝胶的治疗潜力。因此,基于 ATRP 的外泌体连接的水凝胶代表了一种具有改善功效和延长释放曲线的可调平台。

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