He Ren, Zewen Wu, Jingxuan Li, Nan Zhang, Coo Yee Nah, Jiexin Li, Jingyu Zhang, Jonathan F. Lovell, Liyun Zhang, Yumiao Zhang
{"title":"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)","authors":"He Ren, Zewen Wu, Jingxuan Li, Nan Zhang, Coo Yee Nah, Jiexin Li, Jingyu Zhang, Jonathan F. Lovell, Liyun Zhang, Yumiao Zhang","doi":"10.1002/bmm2.12132","DOIUrl":null,"url":null,"abstract":"<p>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.\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":100191,"journal":{"name":"BMEMat","volume":"2 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bmm2.12132","citationCount":"0","resultStr":"{\"title\":\"A biomimetic, triggered-release micelle formulation of methotrexate and celastrol controls collagen-induced arthritis in mice (4/2024)\",\"authors\":\"He Ren, Zewen Wu, Jingxuan Li, Nan Zhang, Coo Yee Nah, Jiexin Li, Jingyu Zhang, Jonathan F. Lovell, Liyun Zhang, Yumiao Zhang\",\"doi\":\"10.1002/bmm2.12132\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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.\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure></p>\",\"PeriodicalId\":100191,\"journal\":{\"name\":\"BMEMat\",\"volume\":\"2 4\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bmm2.12132\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMEMat\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/bmm2.12132\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMEMat","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bmm2.12132","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.