Department of Molecular Pathobiology, New York University, New York, 10010, USA; Department of Neuroscience and Physiology, Neuroscience Institute, New York University, New York, 10010, USA.
Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, 3052, Australia.
Biomaterials. 2022 Jun;285:121536. doi: 10.1016/j.biomaterials.2022.121536. Epub 2022 Apr 28.
Soft polymer nanoparticles designed to disassemble and release an antagonist of the neurokinin 1 receptor (NKR) in endosomes provide efficacious yet transient relief from chronic pain. These micellar nanoparticles are unstable and rapidly release cargo, which may limit the duration of analgesia. We examined the efficacy of stable star polymer nanostars containing the NKR antagonist aprepitant-amine for the treatment of chronic pain in mice. Nanostars continually released cargo for 24 h, trafficked through the endosomal system, and disrupted NKR endosomal signaling. After intrathecal injection, nanostars accumulated in endosomes of spinal neurons. Nanostar-aprepitant reversed mechanical, thermal and cold allodynia and normalized nociceptive behavior more efficaciously than free aprepitant in preclinical models of neuropathic and inflammatory pain. Analgesia was maintained for >10 h. The sustained endosomal delivery of antagonists from slow-release nanostars provides effective and long-lasting reversal of chronic pain.
设计用于在内体中解体和释放神经激肽 1 受体 (NKR) 拮抗剂的软聚合物纳米颗粒为慢性疼痛提供了有效但短暂的缓解。这些胶束纳米颗粒不稳定,并且迅速释放货物,这可能会限制镇痛的持续时间。我们研究了含有 NKR 拮抗剂阿瑞匹坦-胺的稳定星形聚合物纳米星用于治疗小鼠慢性疼痛的功效。纳米星持续释放货物 24 小时,通过内体系统运输,并破坏 NKR 内体信号。鞘内注射后,纳米星在脊髓神经元的内体中积累。纳米星-阿瑞匹坦比游离阿瑞匹坦更有效地逆转神经病理性和炎性疼痛的临床前模型中的机械、热和冷感觉过敏,并使痛觉正常化。镇痛作用持续时间超过 10 小时。从缓释纳米星中持续递送来拮抗药可有效且持久地逆转慢性疼痛。