Pulmonary Targeting Crosslinked Cyclodextrin Metal-Organic Frameworks for Lung Cancer Therapy

被引:55
|
作者
He, Yaping [1 ,2 ]
Xiong, Ting [1 ,3 ]
He, Siyu [1 ,4 ]
Sun, Hongyu [1 ,4 ]
Huang, Chenxi [1 ]
Ren, Xiaohong [1 ]
Wu, Li [1 ]
Patterson, Laurence H. [5 ]
Zhang, Jiwen [1 ,4 ,6 ]
机构
[1] Chinese Acad Sci, Ctr Drug Delivery Syst, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Pharm, Zhengzhou 450052, Peoples R China
[3] Jiangxi Univ Tradit Chinese Med, Key Lab Modern Preparat TCM, Minist Educ, Nanchang 330004, Jiangxi, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Univ Bradford, Fac Life Sci, Inst Canc Therapeut, Bradford BD7 1DP, W Yorkshire, England
[6] Natl Inst Food & Drug Control, NMPA Key Lab Qual Res & Evaluat Pharmaceut Excipi, Beijing 100050, Peoples R China
关键词
cancer therapy; cyclodextrin frameworks; low-molecular-weight heparin; lung-targeting carriers; RGD peptide; DELIVERY-SYSTEMS; PROTEIN CORONA; DRUG-DELIVERY; NANOPARTICLES; MICROSPHERES; POLYMER; DOXORUBICIN; METASTASIS; STABILITY; INTEGRINS;
D O I
10.1002/adfm.202004550
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
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页数:13
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