Chemo-biologic combinatorial drug delivery using folate receptor-targeted dendrimer nanoparticles for lung cancer treatment

被引:97
作者
Amreddy, Narsireddy [1 ,4 ]
Babu, Anish [1 ,4 ]
Panneerselvam, Janani [1 ,4 ]
Srivastava, Akhil [1 ,4 ]
Muralidharan, Ranganayaki [1 ,4 ]
Chen, Allshine [2 ]
Zhao, Yan D. [2 ,4 ]
Munshi, Anupama [3 ,4 ]
Ramesh, Rajagopal [1 ,4 ,5 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Biostat & Epidemiol, Oklahoma City, OK 73104 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Radiat Oncol, Oklahoma City, OK 73104 USA
[4] Univ Oklahoma, Hlth Sci Ctr, Stephenson Canc Ctr, Oklahoma City, OK 73104 USA
[5] Univ Oklahoma, Hlth Sci Ctr, Grad Program Biomed Sci, Oklahoma City, OK 73104 USA
基金
美国国家卫生研究院;
关键词
Lung cancer; Dendrimer; FRA; CDDP; HuR siRNA; VIVO PHOTODYNAMIC THERAPY; BINDING PROTEIN; OVARIAN-CANCER; IN-VIVO; POSTTRANSCRIPTIONAL REGULATION; PAMAM DENDRIMER; MESSENGER-RNA; GENE DELIVERY; HUR; CISPLATIN;
D O I
10.1016/j.nano.2017.11.010
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Co-administration of functionally distinct anti-cancer agents has emerged as an efficient strategy in lung cancer treatment. However, a specially designed drug delivery system is required to co-encapsulate functionally different agents, such as a combination of siRNA and chemotherapy, for targeted delivery. We developed a folic acid (FA)-conjugated polyamidoamine dendrimer (Den)-based nanoparticle (NP) system for co-delivery of siRNA against HuR mRNA (HuR siRNA) and cis-diamine platinum (CDDP) to folate receptor-alpha (FRA)-overexpressing H1299 lung cancer cells. The co-delivery of HuR siRNA and CDDP using the FRA-targeted NP had a significantly greater therapeutic effect than did individual therapeutics. Further, the FRA-targeted NP exhibited improved cytotoxicity compared to non-targeted NP against lung cancer cells. Finally, the NP showed negligible toxicity towards normal MRC9 lung fibroblast cells. Thus, the present study demonstrates FRA-targeted Den nanoparticle system as a suitable carrier for targeted co-delivery of siRNA and chemotherapy agents in lung cancer cells. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:373 / 384
页数:12
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