肺癌
肺癌的治疗
阿霉素
肺
癌症
靶向治疗
医学
体内
癌症研究
药物输送
不利影响
靶向给药
药理学
化疗
肿瘤科
材料科学
药品
内科学
生物
纳米技术
生物技术
作者
Ya‐Ping He,Ting Xiong,Siyu He,Hongyu Sun,Chenxi Huang,Xiaohong Ren,Li Wu,Laurence H. Patterson,Jiwen Zhang
标识
DOI:10.1002/adfm.202004550
摘要
Abstract Lung cancer is a serious threat to human health with the highest morbidity and mortality; metastatic lung cancer accounts for a majority of cancer‐related deaths. Hence, there is considerable interest in developing efficient lung‐targeted drug delivery systems to improve overall survival and quality of life of lung cancer patients. Based on the lung‐targeting characteristics of cubic crosslinked cyclodextrin metal–organic framework (CDF) nanoparticles, this study shows the synthesis of a nanoplatform using RGD‐functionalized CDF to co‐deliver low‐molecular‐weight heparin (LMWH) and doxorubicin (DOX) for treatment of lung cancer. Rational design of the DOX‐loaded RGD‐CDF‐LMWH nanoplatform (RCLD) is carried out. RCLD nanoparticles are efficiently targeted to lung tumors following intravenous administration; RCLD accumulation in the lung is 5.8 times greater than that in the liver. Moreover, RCLD inhibits migration and invasion of cancer cells in vitro and significantly diminishes lung tumor nodule count and area of spread in human A549 and murine B16F10 lung cancer models in vivo. Furthermore, RCLD does not show serum enzyme or histopathologic indicators of tissue damage or adverse hematologic effects. Therefore, the multiple antitumor activities of this novel RCLD nanoplatform, alongside its safety profile for normal tissues, strongly support its use for targeted treatment of lung cancer.
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