破骨细胞
化学
体内
骨吸收
透明质酸
药物输送
基因传递
体外
降钙素
受体
药理学
细胞生物学
生物化学
遗传增强
医学
生物
基因
内科学
解剖
生物技术
有机化学
作者
Bosong Zhang,Juzhi Zhao,Hongji Yan,Yufang Zhao,Hui Tian,Wang Cao,Ruiqi Wang,Jiaming Jin,Yue Chen,Chaofan Yang,Chunfeng Li,Yanwen Jiao,Kaipeng Zheng,Fuxing Zhu,Weiming Tian
出处
期刊:Biomaterials Science
[The Royal Society of Chemistry]
日期:2022-01-01
卷期号:10 (7): 1821-1830
被引量:6
摘要
Osteoclast (OC) abnormalities represent osteoporosis's critical mechanism (OP). OCs undergo multiple processes that range from monocytic to functional. Different drugs target OCs at different developmental stages; however, almost no Suitable drug-targeted delivery systems exist. Therefore, we designed two dual-targeting nanoparticles to target OCs at different functional stages. Using the calcitonin gene-related peptide receptor (CGRPR), which OC precursors highly express, and specific TRAPpeptides screened in the bone resorption lacuna, where mature OCs function, respectively, two types of dual-targeted nanoparticles were constructed. Afterwards, nanoparticles were grafted with hyaluronic acid (HA), which specifically binds to CD44 on the surface of the OCs. In vivo and in vitro experiments show that both nanoparticles have noticeable targeting effects on OCs. This suggests that dual-targeting nanoparticles designed for different functional periods of OC can be well targeted to the corresponding OC, and further promote the more precise delivery of drugs used to treat OP.
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