An injectable nanoparticle generator enhances delivery of cancer therapeutics

被引:234
作者
Xu, Rong [1 ,2 ]
Zhang, Guodong [1 ]
Mai, Junhua [1 ]
Deng, Xiaoyong [1 ,8 ]
Segura-Ibarra, Victor [1 ]
Wu, Suhong [1 ]
Shen, Jianliang [1 ]
Liu, Haoran [1 ]
Hu, Zhenhua [1 ]
Chen, Lingxiao [1 ]
Huang, Yi [1 ]
Koay, Eugene [1 ,3 ]
Huang, Yu [1 ,9 ]
Liu, Jun [4 ]
Ensor, Joe E. [5 ]
Blanco, Elvin [1 ]
Liu, Xuewu [1 ]
Ferrari, Mauro [1 ,6 ]
Shen, Haifa [1 ,7 ]
机构
[1] Houston Methodist Res Inst, Dept Nanomed, Houston, TX USA
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Basic Med, Dept Pharmacol, Wuhan 430074, Peoples R China
[3] Univ Texas MD Anderson Canc Ctr, Div Radiat Oncol, Houston, TX 77030 USA
[4] Univ Texas Houston, Sch Med, Dept Pathol & Lab Med, Houston, TX 77030 USA
[5] Houston Methodist Canc Ctr, Houston, TX USA
[6] Weill Cornell Med Coll, Dept Med, New York, NY USA
[7] Weill Cornell Med Coll, Dept Cell & Dev Biol, New York, NY USA
[8] Shanghai Univ, Inst Nanochem & Nanobiol, Shanghai, Peoples R China
[9] Univ S Dakota, Dept Biomed Engn, Sioux Falls, SD USA
基金
中国国家自然科学基金;
关键词
PEGYLATED LIPOSOMAL DOXORUBICIN; BREAST-CANCER; MULTIDRUG-RESISTANCE; METASTASIS; PH; VASCULATURE; PARTICLES; THERAPY; DESIGN; FUSION;
D O I
10.1038/nbt.3506
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The efficacy of cancer drugs is often limited because only a small fraction of the administered dose accumulates in tumors. Here we report an injectable nanoparticle generator (iNPG) that overcomes multiple biological barriers to cancer drug delivery. The iNPG is a discoidal micrometer-sized particle that can be loaded with chemotherapeutics. We conjugate doxorubicin to poly(l-glutamic acid) by means of a pH-sensitive cleavable linker, and load the polymeric drug (pDox) into iNPG to assemble iNPG-pDox. Once released from iNPG, pDox spontaneously forms nanometer-sized particles in aqueous solution. Intravenously injected iNPG-pDox accumulates at tumors due to natural tropism and enhanced vascular dynamics and releases pDox nanoparticles that are internalized by tumor cells. Intracellularly, pDox nanoparticles are transported to the perinuclear region and cleaved into Dox, thereby avoiding excretion by drug efflux pumps. Compared to its individual components or current therapeutic formulations, iNPG-pDox shows enhanced efficacy in MDA-MB-231 and 4T1 mouse models of metastatic breast cancer, including functional cures in 40-50% of treated mice.
引用
收藏
页码:414 / +
页数:7
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