破骨细胞
骨转移
唑来膦酸
骨吸收
癌症研究
体内
乳腺癌
光热治疗
癌细胞
成骨细胞
医学
肿瘤微环境
癌症
材料科学
转移
双膦酸盐
肿瘤科
骨质疏松症
化学
体外
内科学
纳米技术
生物
肿瘤细胞
受体
生物技术
生物化学
作者
Wentong Sun,Kun Ge,Yan Jin,Yu Han,Haisong Zhang,Guoqiang Zhou,Xinjian Yang,Dandan Liu,Huifang Liu,Xing‐Jie Liang,Jinchao Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-07-01
卷期号:13 (7): 7556-7567
被引量:142
标识
DOI:10.1021/acsnano.9b00097
摘要
Bone metastasis, a clinical complication of patients with advanced breast cancer, seriously reduces the quality of life. To avoid destruction of the bone matrix, current treatments focus on inhibiting the cancer cell growth and the osteoclast activity through combination therapy. Therefore, it could be beneficial to develop a bone-targeted drug delivery system to treat bone metastasis. Here, a bone-targeted nanoplatform was developed using gold nanorods enclosed inside mesoporous silica nanoparticles (Au@MSNs) which were then conjugated with zoledronic acid (ZOL). The nanoparticles (Au@MSNs-ZOL) not only showed bone-targeting ability in vivo but also inhibited the formation of osteoclast-like cells and promoted osteoblast differentiation in vitro. The combination of Au@MSNs-ZOL and photothermal therapy (PTT), triggered by near-infrared irradiation, inhibited tumor growth both in vitro and in vivo and relieved pain and bone resorption in vivo by inducing apoptosis in cancer cells and improving the bone microenvironment. This single nanoplatform combines ZOL and PTT to provide an exciting strategy for treating breast cancer bone metastasis.
科研通智能强力驱动
Strongly Powered by AbleSci AI