甲氨蝶呤和雷公藤红素的仿生触发释放胶束制剂控制胶原诱导的小鼠关节炎(4/2024)

BMEMat Pub Date : 2024-12-25 DOI:10.1002/bmm2.12132
He Ren, Zewen Wu, Jingxuan Li, Nan Zhang, Coo Yee Nah, Jiexin Li, Jingyu Zhang, Jonathan F. Lovell, Liyun Zhang, Yumiao Zhang
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引用次数: 0

摘要

在这篇编号10.1002/bmm2.12104的文章中,任和、吴泽文、张丽云、张玉淼及其合作者设计了一种名为CeViM-micelle@B的抗风湿病纳米颗粒。制备了甲氨蝶呤偶联Pluronic F127胶束,包封抗炎剂Celastrol (Cel)和稳定剂维生素K (VK),并将其包被b细胞膜。使用CeViM-micelle@B可显著增加病理性滑膜关节的药物蓄积,有效抑制免疫细胞活化,有效防止骨和软骨的侵蚀。这种新的纳米平台具有下一代靶向类风湿性关节炎治疗的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A biomimetic, triggered-release micelle formulation of methotrexate and celastrol controls collagen-induced arthritis in mice (4/2024)

A biomimetic, triggered-release micelle formulation of methotrexate and celastrol controls collagen-induced arthritis in mice (4/2024)

In this article number 10.1002/bmm2.12104, He Ren, Zewen Wu, Liyun Zhang, Yumiao Zhang and their co-authors designed an antirheumatic nanoparticle termed CeViM-micelle@B. A methotrexate-conjugated Pluronic F127 micelle was developed to encapsulate anti-inflammatory agent Celastrol (Cel) and the stabilizer Vitamin K (VK), which was further coated by B-cell membrane. The use of CeViM-micelle@B significantly increased drug accumulation at pathological synovial joints, potently inhibited immune cell activation, and effectively prevented erosion of bone and cartilage. This new nanoplatform holds potential for the next-generation targeted rheumatoid arthritis therapy.

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