Tumoral Acidic pH-Responsive cis-Diaminodichloroplatinum-Incorporated Cy5.5-PEG-g-A-HA Nanoparticles for Targeting Delivery of CDDP against Cervical Cancer

被引:32
作者
Cheng, Cui [1 ]
Meng, Yabin [1 ]
Zhang, Zhihong [1 ]
Li, Ya [1 ]
Zhang, Qiqing [1 ]
机构
[1] Fuzhou Univ, Inst Biomed & Pharmaceut Technol, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
cervical cancer; CDDP; aldehyde hyaluronic acid; selective targeting; antitumor efficiency; HYALURONIC-ACID; IN-VITRO; CISPLATIN COMPLEX; DRUG; CELLS; OVARIAN; IDENTIFICATION; ACCUMULATION; THERAPEUTICS; FLUORESCENCE;
D O I
10.1021/acsami.8b07425
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Cisplatin (CDDP) has been considered as one of the most effective anticancer drugs against cervical cancer, but the lack of selectivity of CDDP to tumor tissues often leads to serious toxic side effects. In this study, CDDP-incorporated CyS.S-PEG-g-A-HA nanoparticles were prepared to endue CDDP the ability to selectively target tumors and fluorescence imaging in vivo. The nanoparticles exhibited a spherical shape with particle sizes between 216.4 and 281.5 nm and had a pH and Cl- concentration dependence on controlled and sustained CDDP release, which was favorable for nanoparticles to release more drugs at acidic tumor microenvironment. Cell biology experiments demonstrated that the nanoparticles had good biocompatibility and tumor targeting; the nanoparticles could selectively bind and internalize into HeLa cells and induce apoptosis, but lead cytotoxicity on NIH3T3 cells. What is more, the nanoparticles could be clearly fluorescent-imaged in vivo and showed effective accumulation at the tumor site. Antitumor test in vivo displayed that the nanoparticles had good antitumor efficiency and low systemic toxicity which improved the life quality of mice. Hence, the CDDP-incorporated Cy5.5-PEG-g-A-HA nanoparticles were a potential delivery system for targeting delivery of CDDP against cervical cancer.
引用
收藏
页码:26882 / 26892
页数:11
相关论文
共 40 条
[21]  
Liu Y., 2017, COLLOID SURFACE, V159, pS96
[22]   Validation of eGFP fluorescence intensity for testing in vitro cytotoxicity according to ISO 10993-5 [J].
Miller, Felicitas ;
Hinze, Ulf ;
Chichkov, Boris ;
Leibold, Wolfgang ;
Lenarz, Thomas ;
Paasche, Gerrit .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2017, 105 (04) :715-722
[23]   Improving Drug Potency and Efficacy by Nanocarrier-Mediated Subcellular Targeting [J].
Murakami, Mami ;
Cabral, Horacio ;
Matsumoto, Yu ;
Wu, Shourong ;
Kano, Mitsunobu R. ;
Yamori, Takao ;
Nishiyama, Nobuhiro ;
Kataoka, Kazunori .
SCIENCE TRANSLATIONAL MEDICINE, 2011, 3 (64)
[24]   Prevention and treatment of chemotherapy-induced peripheral neuropathy [J].
Piccolo, Jennifer ;
Kolesar, Jill M. .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2014, 71 (01) :19-25
[25]   Anticancer therapeutics: Targeting macromolecules and nanocarriers to hyaluronan or CD44, a hyaluronan receptor [J].
Platt, Virginia M. ;
Szoka, Francis C., Jr. .
MOLECULAR PHARMACEUTICS, 2008, 5 (04) :474-486
[26]   Prevention of chemotherapy-induced peripheral neuropathy: a matter of personalized treatment? [J].
Postma, T. J. ;
Reijneveld, J. C. ;
Heimans, J. J. .
ANNALS OF ONCOLOGY, 2013, 24 (06) :1424-1426
[27]   The antitumor effect of folic acid conjugated-Auricularia auricular polysaccharide-cisplatin complex on cervical carcinoma cells in nude mice [J].
Qiu, Junqiang ;
Zhang, Hua ;
Wang, Zhenyu ;
Liu, Didi ;
Liu, Shumin ;
Han, Wei ;
Regenstein, Joe M. ;
Geng, Lin .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 107 :2180-2189
[28]   Synthesis of PEGylated hyaluronic acid for loading dichloro(1,2-diaminocyclohexane)platinum(II) (DACHPt) in nanoparticles for cancer treatment [J].
Quan, Xiu-Quan ;
Rang, Lin ;
Yin, Xue-Zhe ;
Jin, Zhe-Hu ;
Gao, Zhong-Gao .
CHINESE CHEMICAL LETTERS, 2015, 26 (06) :695-699
[29]   Sheddable coatings for long-circulating nanoparticles [J].
Romberg, Birgit ;
Hennink, Wim E. ;
Storm, Gert .
PHARMACEUTICAL RESEARCH, 2008, 25 (01) :55-71
[30]   Cisplatin-Induced Formation of Biocompatible and Biodegradable Polypeptide-Based Vesicles for Targeted Anticancer Drug Delivery [J].
Shirbin, Steven J. ;
Ladewig, Katharina ;
Fu, Qiang ;
Klimak, Molly ;
Zhang, Xiaoqing ;
Duan, Wei ;
Qiao, Greg G. .
BIOMACROMOLECULES, 2015, 16 (08) :2463-2474