Nanospheres-Incorporated Implantable Hydrogel as a Trans-Tissue Drug Delivery System

被引:98
作者
Ding, Dan [1 ,2 ]
Zhu, Zhenshu [1 ,2 ]
Li, Rutian [3 ,4 ]
Li, Xiaolin [3 ,4 ]
Wu, Wei [1 ,2 ]
Jiang, Xiqun [1 ,2 ]
Liu, Baorui [3 ,4 ]
机构
[1] Nanjing Univ, Coll Chem & Chem Engn, Lab Mesoscop Chem, Nanjing 210008, Peoples R China
[2] Nanjing Univ, Coll Chem & Chem Engn, Dept Polymer Sci & Engn, Nanjing 210008, Peoples R China
[3] Nanjing Univ, Ctr Comprehens Canc, Drum Tower Hosp, Sch Med, Nanjing 210008, Peoples R China
[4] Nanjing Univ, Clin Canc Inst, Nanjing 210008, Peoples R China
基金
中国国家自然科学基金;
关键词
polymer nanoparticles; polymer hydrogel; drug delivery; peritumoral chemotherapy; antitumor effect; BIODEGRADABLE GELATIN HYDROGEL; METAL COMPLEX MICELLE; HERPES-SIMPLEX-VIRUS; IN-VIVO; CANCER-THERAPY; SOLID TUMORS; SUSTAINED-RELEASE; CARBON NANOTUBES; POLYMER IMPLANTS; NUDE-MICE;
D O I
10.1021/nn102138u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The objective of this study is to investigate the anticancer efficacy of a drug delivery system comprised of gelatin hydrogel (Jelly) containing cisplatin (CDDP)-loaded gelatin/poly(acrylic acid) nanoparticles by peritumoral implantation and to compare the treatment response between the implantation administration of the jelly and intravenous (i.v.) administration of the nanoparticles. It is found that the implantation, of the jelly containing CDDP-loaded nanoparticles on tumor tissue exhibited significantly superior efficacy in impeding tumor growth and prolonging the lifetime of mice than that of i.v. Injection of CDDP-loaded nanoparticles in a murine hepatoma H(22) cancer model. An in vivo biodistribution, assay performed on tumor-bearing mice demonstrated that the jelly implant caused much higher concentration and retention of CDDP In tumor and lower CDDP accumulation in nontarget organs than that of i.v. injected nanoparticles. Immunohistochemical analysis demonstrated that the nanoparticles from the jelly can be distributed in tumor tissue not only by their diffusion but also by the vasculature in the implantation region into tumor interior, enabling CDDP to efficiently reach more viable cells of tumor compared with i.v. injected nanoparticles. Thus, nanoparticles for peritumoral chemotherapy are promising for higher treatment efficacy due to increased tumor-to-normal organ drug uptake ratios and Improved drug penetration in tumors.
引用
收藏
页码:2520 / 2534
页数:15
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