CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, 100190, China.
Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, 100010, China.
Adv Sci (Weinh). 2023 Oct;10(28):e2302586. doi: 10.1002/advs.202302586. Epub 2023 Aug 9.
A nano-enabled drug delivery acupuncture technology (nd-Acu) is developed that is based on traditional acupuncture needles where the stainless-steel surface is designed to deliver various payload molecules. To create the nd-Acu platform, an electrochemistry procedure is used to attach methyl salicylate-modified cyclodextrin in which the sugar rings allow the encapsulation of structurally defined single or multiple payload molecules via an inclusion complexation process. Drug loading and release profile are first studied using fluorescent dyes abiotically and at intact animal level. nd-Acu allows more efficient dye loading and time-dependent release compared to pristine needles without cyclodextrin modification. Subsequently, a proof-of-principle efficacy study is conducted using the platform to load a local anesthetic, lidocaine, for the treatment of knee osteoarthritis (KOA) in mice. It is demonstrated that lidocaine-laden nd-Acu can effectively alleviate pain, reduce inflammation, and slow down KOA development biochemically and histologically. Hypothesis-driven and proteomic approaches are utilized to investigate the working mechanisms of lidocaine nd-Acu, indicating that the therapeutic outcome is attributed to the in vivo modulation of the HMGB1/TLR4 signaling pathway. The study also obtained preliminary evidence suggesting the involvement of mitochondria as well as small GTPase such as cdc42 during the treatment by lidocaine nd-Acu.
一种基于传统针灸针的纳米增强药物输送针灸技术(nd-Acu)被开发出来,该技术的不锈钢表面设计用于输送各种有效载荷分子。为了创建 nd-Acu 平台,使用电化学程序将甲基水杨酸酯修饰的环糊精附着在针上,其中糖环允许通过包合络合过程封装结构定义的单个或多个有效载荷分子。首先使用荧光染料在非生物和完整动物水平上研究药物负载和释放特性。与没有环糊精修饰的原始针相比,nd-Acu 允许更有效地负载染料和时间依赖性释放。随后,使用该平台进行了一项局部麻醉药利多卡因治疗膝骨关节炎(KOA)的原理验证疗效研究。结果表明,载有利多卡因的 nd-Acu 可以有效缓解疼痛、减轻炎症,并从生化和组织学上减缓 KOA 的发展。研究人员采用假设驱动和蛋白质组学方法来研究利多卡因 nd-Acu 的作用机制,表明治疗效果归因于体内对 HMGB1/TLR4 信号通路的调节。该研究还获得了初步证据,表明在利多卡因 nd-Acu 治疗过程中涉及线粒体以及小 GTP 酶如 cdc42。