School of Life Science and Technology, Harbin Institute of Technology, 150080 Harbin, China.
Division of Glycoscience, Department of Chemistry, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH, Royal Institute of Technology, AlbaNova University Center, 106 91 Stockholm, Sweden.
Biomater Sci. 2022 Mar 29;10(7):1821-1830. doi: 10.1039/d2bm00076h.
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. and 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.
破骨细胞 (OC) 异常是骨质疏松症的关键机制 (OP)。OC 经历了从单核细胞到功能的多个过程。不同的药物针对 OC 的不同发育阶段;然而,几乎没有合适的药物靶向递药系统存在。因此,我们设计了两种双靶向纳米颗粒,以针对不同功能阶段的 OC。使用 OC 前体高表达的降钙素基因相关肽受体 (CGRPR) 和在成熟 OC 功能的骨吸收陷窝中筛选出的特异性 TRAP 肽,分别构建了两种双靶向纳米颗粒。随后,纳米颗粒与透明质酸 (HA) 接枝,HA 特异性结合 OC 表面的 CD44。 和 实验表明,两种纳米颗粒对 OC 均具有明显的靶向作用。这表明,针对 OC 不同功能期设计的双靶向纳米颗粒可以很好地靶向相应的 OC,并进一步促进用于治疗 OP 的药物的更精确递送。