| Literature DB >> 27855337 |
Yitong Wang1, Jian Yang2, Hongmei Liu3, Xinyu Wang1, Zhengjie Zhou1, Quan Huang2, Dianwen Song2, Xiaopan Cai2, Lin Li2, Kaili Lin4, Jianru Xiao2, Peifeng Liu5, Qiang Zhang6, Yiyun Cheng7.
Abstract
The treatment of bone tumors is a challenging problem due to the inefficient delivery of therapeutics to bone and the bone microenvironment-associated tumor resistance to chemo- and radiotherapy. Here, we developed a bone-targeted nanoparticle, aspartate octapeptide-modified dendritic platinum-copper alloy nanoparticle (Asp-DPCN), for photothermal therapy (PTT) of bone tumors. Asp-DPCN showed much higher affinity toward hydroxyapatite and bone fragments than the non-targeted DPCN in vitro. Furthermore, Asp-DPCN accumulated more efficiently around bone tumors in vivo, and resulted in a higher temperature in bone tumors during PTT. Finally, Asp-DPCN-mediated PTT not only efficiently depressed the tumor growth but also significantly reduced the osteoclastic bone destruction. Our study developed a promising therapeutic approach for the treatment of bone tumors. Copyright ÂEntities:
Keywords: Bone targeting; Bone tumor; Osteoclastic bone resorption; Photothermal therapy
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Year: 2016 PMID: 27855337 DOI: 10.1016/j.biomaterials.2016.11.010
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479