A multifunctional biodegradable brush polymer-drug conjugate for paclitaxel/gemcitabine co-delivery and tumor imaging

被引:17
|
作者
Sun, Haotian [1 ]
Yan, Lingyue [2 ]
Chang, Michael Yu Zarng [2 ]
Carter, Kevin A. [2 ]
Zhang, Runsheng [1 ]
Slyker, Leigh [1 ]
Lovell, Jonathan F. [2 ]
Wu, Yun [2 ]
Cheng, Chong [1 ]
机构
[1] Univ Buffalo State Univ New York, Dept Chem & Biol Engn, Buffalo, NY 14260 USA
[2] Univ Buffalo State Univ New York, Dept Biomed Engn, Buffalo, NY 14260 USA
来源
NANOSCALE ADVANCES | 2019年 / 1卷 / 07期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
NAB-PACLITAXEL; CANCER-THERAPY; GEMCITABINE; NANOPARTICLE; PLATFORM; NANOCAPSULES; DOXORUBICIN; MICELLES; RELEASE; PRODRUG;
D O I
10.1039/c9na00282k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A multifunctional biodegradable brush polymer-drug conjugate (BPDC) is developed for the co-delivery of hydrophobic paclitaxel (PTX) and hydrophilic gemcitabine (GEM) chemotherapeutics, as well as a tumor imaging agent. A novel ternary copolymer of conventional, acetylenyl-functionalized and allyl-functionalized lactides is prepared to serve as the backbone precursor of the BPDC. Acetylenyl groups of the copolymer are then reacted with azide-functionalized poly(ethylene glycol) (PEG) and cyanine5.5, a fluorescent probe, via azide-alkyne click reactions. Subsequently, the allyl groups of the yielded PEG-grafted brush polymer are used to covalently link PTX and GEM onto the backbone via thiol-ene click reactions. The resulting BPDC exhibits an average hydrodynamic diameter of 111 nm. Sustained and simultaneous release of PTX and GEM from the BPDC is observed in phosphate buffered saline, with the release of PTX showing sensitivity under mildly acidic conditions. In vitro studies using MIA PaCa-2 human pancreatic cancer cells illustrate the cellular uptake and cytotoxicity of the BPDC. In vivo, the BPDC undergoes long blood circulation and tumor accumulation, and enables optical tumor imaging. Further development and testing are warranted for multifunctional conjugated brush polymer systems that integrate combination chemotherapy and imaging.
引用
收藏
页码:2761 / 2771
页数:11
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