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一种用于慢性神经应用的长期可控原位递送多种抗炎因子的双层微流控系统。

A Dual-layered Microfluidic System for Long-term Controlled In Situ Delivery of Multiple Anti-inflammatory Factors for Chronic Neural Applications.

作者信息

Frey Laura, Bandaru Praveen, Zhang Yu Shrike, O'Kelly Kevin, Khademhosseini Ali, Shin Su Ryon

机构信息

Biomaterials Innovation Research Center, Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02139, USA.

出版信息

Adv Funct Mater. 2018 Mar 21;28(12). doi: 10.1002/adfm.201702009. Epub 2017 Sep 20.

Abstract

We report the development of a microfluidic system capable of repeated infusions of anti-inflammatory factors post-implantation for use as a coating for neural probes. This system consists of a microchannel in a thin gelatin methacryloyl (GelMA)-polyethylene glycol (PEG) composite hydrogel surrounded by a porous polydimethylsiloxane (PDMS) membrane, where the hydrogel can be dried to increase the stiffness for easy insertion. Reswelling allowed us to perfuse interleukin (IL)-4 and dexamethasone (DEX) as anti-inflammatory factors through the channel with minimal burst release and significant amounts of IL-4 were observed to release for up to 96 hr post-infusion. Repeated injections of IL-4 increased the ratio of prohealing M2 proinflammatory M1 phenotypes of macrophages encapsulated in the hydrogel by six fold compared with a single injection, over a 2-week period. These repeated infusions also significantly downregulated the expression of inflammatory markers tumor necrosis factor (TNF)-α and IL-6 in astrocytes encapsulated in hydrogel. To demonstrate the system as a coating of neural probe for applications, we further fabricated a prototype device, where a thin dual-layered microfluidic system was integrated onto a metal probe. Such a drug delivery system could help reduce the formation of a glial scar around neural probes.

摘要

我们报告了一种微流体系统的开发情况,该系统能够在植入后重复注入抗炎因子,用作神经探针的涂层。该系统由一个微通道组成,该微通道位于薄的甲基丙烯酰化明胶(GelMA)-聚乙二醇(PEG)复合水凝胶中,并被多孔聚二甲基硅氧烷(PDMS)膜包围,水凝胶可以干燥以增加硬度以便于插入。再水化使我们能够通过通道灌注白细胞介素(IL)-4和地塞米松(DEX)作为抗炎因子,且突发释放最小,观察到大量的IL-4在注入后长达96小时内释放。与单次注射相比,在两周的时间内,重复注射IL-4使包裹在水凝胶中的巨噬细胞的促愈合M2与促炎M1表型的比例增加了六倍。这些重复注入还显著下调了包裹在水凝胶中的星形胶质细胞中炎症标志物肿瘤坏死因子(TNF)-α和IL-6的表达。为了证明该系统作为神经探针涂层的应用,我们进一步制造了一个原型装置,其中一个薄的双层微流体系统被集成到一个金属探针上。这种药物递送系统有助于减少神经探针周围胶质瘢痕的形成。

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