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3D 打印聚吡咯微针阵列用于电子控制经颅药物释放。

3D-Printed Polypyrrole Microneedle Arrays for Electronically Controlled Transdural Drug Release.

机构信息

Department of Bioengineering, University of Washington, Seattle, 98195-5061, Washington, United States.

Department of Neurological Surgery, University of Washington, Seattle 98104-2499, Washington, United States.

出版信息

ACS Biomater Sci Eng. 2022 Apr 11;8(4):1544-1553. doi: 10.1021/acsbiomaterials.1c01305. Epub 2022 Mar 16.

Abstract

After the spinal cord injury, inflammation and cytotoxicity cause further damage to neural cells. The progression of this secondary injury might be reduced by the administration of anti-inflammatory drugs. To allow the local delivery of such drugs while minimizing dural opening, we have created a polypyrrole (PPy)-coated microneedle array using a microscale three-dimensional (3D) printing technology that facilitates electronically controlled encapsulation and the transdural release of drugs. PPy microneedles demonstrated an electronically controlled release of steroid dexamethasone (Dexa) in a novel in vitro transdural model and in vivo. The biological activity of the device was then tested by the electronic release of Dexa into an in vitro model of neuroinflammation, using activated microglia. Following electrically activated Dexa release, inflammation was reduced, as demonstrated by a decrease in nitric oxide and proinflammatory cytokines Il-6 and MCP-1. These results demonstrate the feasibility of PPy-coated microneedles for the transdural delivery of anti-inflammatory drugs to the central nervous system.

摘要

脊髓损伤后,炎症和细胞毒性会导致神经细胞进一步受损。通过给予抗炎药物可以减轻这种继发性损伤的进展。为了在最小化硬脑膜开口的情况下允许局部递送此类药物,我们使用微尺度三维(3D)打印技术创建了一种聚吡咯(PPy)涂层的微针阵列,该技术可实现电子控制封装和药物经硬脑膜释放。PPy 微针在新颖的体外经硬脑膜模型和体内模型中证明了类固醇地塞米松(Dexa)的电子控制释放。然后,通过使用激活的小胶质细胞将 Dexa 电子释放到神经炎症的体外模型中,测试了该装置的生物学活性。电激活的 Dexa 释放后,炎症减轻,一氧化氮和促炎细胞因子 Il-6 和 MCP-1 的减少证明了这一点。这些结果表明 PPy 涂层的微针可用于将抗炎药物经硬脑膜递送到中枢神经系统。

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