Self-assembled nanoparticles based on a cationic conjugated polymer/hyaluronan-cisplatin complex as a multifunctional platform for simultaneous tumor-targeting cell imaging and drug delivery

被引:17
|
作者
Huang, Yan-Qin [1 ,2 ]
Zhang, Rui [3 ]
Zhao, Yong-Kang [1 ,2 ]
Chen, Hao [1 ,2 ]
Jiang, Rong-Cui [1 ,2 ]
Liu, Xing-Fen [1 ,2 ]
Fan, Qu-Li [1 ,2 ]
Wang, Lian-Hui [1 ,2 ]
Huang, Wei [1 ,2 ,4 ,5 ]
机构
[1] Nanjing Univ Posts & Telecommun, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, KLOEID, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, IAM, Nanjing 210023, Jiangsu, Peoples R China
[3] Southeast Univ, Zhongda Hosp, Dept Ophthalmol, Nanjing 211189, Jiangsu, Peoples R China
[4] Nanjing Tech Univ, NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Key Lab Flexible Elect KLOFE, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[5] Nanjing Tech Univ, NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, IAM, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
SENSITIVE FLUORESCENCE DETECTION; TRIBLOCK COPOLYMERS; HYALURONAN; EFFICIENT; CANCER; GRAPHENE; NANOCARRIERS; AGGREGATION; PACLITAXEL;
D O I
10.1039/c6nj04128k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multifunctional therapeutic systems that can realize simultaneous tumor-targeting imaging and drug delivery are highly desired to improve the therapeutic efficacy of conventional chemotherapy. Herein, we described a novel nanoparticle system prepared by electrostatic and hydrophobic self-assembly of a cationic conjugated polymer, PFEP, and anionic hyaluronan (HA) conjugated with the model anticancer drug cisplatin (CDDP). PFEP exhibited high fluorescence quantum yield, good photostability and low cytotoxity to meet the essential requests for cell imaging. HA is a natural glycosaminoglycan that possesses high specific affinity for the CD44 receptor overexpressed on surfaces of various cancer cells. The 20.2% CDDP-loaded PFEP/HA-CDDP complex nanoparticles (PHCNPs) were observed to comprise a compact hydrophobic inner core and a hydrophilic HA shell, and exhibit smaller size and better dispersity in aqueous solution than HA-CDDP nanoparticles (HCNPs) with the same drug loading content. Moreover, the fluorescence of PHCNPs was almost quenched due to the increased torsional conformation and aggregation of PFEP in the compact inner core. After PHCNPs were taken up by the target cancer cells through the specific HA-CD44 binding, HA was hydrolyzed by overexpressed hyaluronidase (HAase) in the cancer cells, which destroyed the nanoparticles, resulting in fluorescence recovery from PFEP and the release of CDDP. In vitro drug release studies also confirmed the HAase-promoted sustained CDDP release of PHCNPs. Therefore, tumor-targeting drug release and distribution in cells can be monitored by the recovered fluorescence signals. Furthermore, in vitro cytotoxicity studies demonstrated that the PHCNPs showed evident selective cytotoxicity, thereby leading to reduced side effects in normal cells. Therefore, the studies of conjugated polymers in multifunctional therapeutic system may offer a promising approach for improving the therapeutic efficacy of chemotherapy.
引用
收藏
页码:4998 / 5006
页数:9
相关论文
共 23 条
  • [21] Multifunctional TPP-PEG-biotin self-assembled nanoparticle drug delivery-based combination therapeutic approach for co-targeting of GRP78 and lysosome
    Purushothaman, Baskaran
    Lee, Jeongmin
    Hong, Sera
    Song, Joon Myong
    JOURNAL OF NANOBIOTECHNOLOGY, 2020, 18 (01)
  • [22] Multifunctional TPP-PEG-biotin self-assembled nanoparticle drug delivery-based combination therapeutic approach for co-targeting of GRP78 and lysosome
    Baskaran Purushothaman
    Jeongmin Lee
    Sera Hong
    Joon Myong Song
    Journal of Nanobiotechnology, 18
  • [23] A tumor-targeting near-infrared laser-triggered drug delivery system based on GO@Ag nanoparticles for chemo-photothermal therapy and X-ray imaging
    Shi, Jinjin
    Wang, Lei
    Zhang, Jing
    Ma, Rou
    Gao, Jun
    Liu, Yan
    Zhang, Chaofeng
    Zhang, Zhenzhong
    BIOMATERIALS, 2014, 35 (22) : 5847 - 5861