A multifunctional polyethylenimine-based nanoplatform for targeted anticancer drug delivery to tumors in vivo

被引:45
作者
Zhou, Benqing [1 ]
Zhao, Lingzhou [2 ]
Shen, Mingwu [1 ]
Zhao, Jinhua [2 ]
Shi, Xiangyang [1 ,3 ]
机构
[1] Donghua Univ, Coll Chem Chem Engn & Biotechnol, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Sch Med, Dept Nucl Med, Shanghai 200080, Peoples R China
[3] Univ Madeira, CQM, Campus Penteada, P-9000390 Funchal, Portugal
基金
中国国家自然科学基金;
关键词
ENTRAPPED GOLD NANOPARTICLES; BLOCK-COPOLYMER MICELLES; FOLIC-ACID; BRANCHED POLYETHYLENEIMINE; CONJUGATED NANOPARTICLES; HYALURONIC-ACID; BLOOD-POOL; DOXORUBICIN; DESIGN; CELLS;
D O I
10.1039/c6tb02620f
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The development of cost-effective targeted drug delivery systems for cancer chemotherapy still remains a great challenging task. Here, we describe the synthesis and characterization of multifunctional polyethylenimine (PEI) as an effective vehicle to load an anticancer drug doxorubicin (DOX) for in vivo targeted cancer therapy. In this study, PEI was sequentially conjugated with polyethylene glycol (PEG) monomethyl ether, PEGylated folic acid (FA), and fluorescein isothiocyanate (FI). This was followed by the acetylation of the remaining PEI surface amines. The formed FA-targeted multifunctional PEI (FA-mPEI) was used as a vehicle to encapsulate DOX. We show that the formed FA-mPEI/DOX complexes with each PEI encapsulating 6.9 DOX molecules are water dispersible and can sustainably release DOX in a pH-dependent manner, showing a higher release rate under acidic pH conditions than under physiological pH conditions. Furthermore, the complexes display specific therapeutic efficacy to cancer cells in vitro and a subcutaneous tumor model in vivo, and have good organ compatibility. The designed multifunctional PEI may be used as an effective vehicle for targeted cancer chemotherapy.
引用
收藏
页码:1542 / 1550
页数:9
相关论文
共 56 条
[1]   Recent advances on chitosan-based micro- and nanoparticles in drug delivery [J].
Agnihotri, SA ;
Mallikarjuna, NN ;
Aminabhavi, TM .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :5-28
[2]   Liposomal drug delivery systems: From concept to clinical applications [J].
Allen, Theresa M. ;
Cullis, Pieter R. .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (01) :36-48
[3]   Hyperbranched PEI with Various Oligosaccharide Architectures: Synthesis, Characterization, ATP Complexation, and Cellular Uptake Properties [J].
Appelhans, Dietmar ;
Komber, Hartmut ;
Quadir, Mohiuddin Abdul ;
Richter, Sven ;
Schwarz, Simona ;
van der Vlist, Jereon ;
Aigner, Achim ;
Mueller, Martin ;
Loos, Katja ;
Seidel, Juergen ;
Arndt, Karl-Friedrich ;
Haag, Rainer ;
Voit, Brigitte .
BIOMACROMOLECULES, 2009, 10 (05) :1114-1124
[4]   Folate-targeted pH-responsive calcium zoledronate nanoscale metal-organic frameworks: Turning a bone antiresorptive agent into an anticancer therapeutic [J].
Au, Kin Man ;
Satterlee, Andrew ;
Min, Yuanzeng ;
Tian, Xi ;
Kim, Young Seok ;
Caster, Joseph M. ;
Zhang, Longzhen ;
Zhang, Tian ;
Huang, Leaf ;
Wang, Andrew Z. .
BIOMATERIALS, 2016, 82 :178-193
[5]   Folate-conjugated nanoparticles as a potent therapeutic approach in targeted cancer therapy [J].
Bahrami, Behdokht ;
Mohammadnia-Afrouzi, Mousa ;
Bakhshaei, Peyman ;
Yazdani, Yaghoub ;
Ghalamfarsa, Ghasem ;
Yousefi, Mehdi ;
Sadreddini, Sanam ;
Jadidi-Niaragh, Farhad ;
Hojjat-Farsangi, Mohammad .
TUMOR BIOLOGY, 2015, 36 (08) :5727-5742
[6]   Branched polyethyleneimine modified with hyaluronic acid via a PEG spacer for targeted anticancer drug delivery [J].
Chen, Chen ;
Zhou, Benqing ;
Zhu, Xiaoyue ;
Shen, Mingwu ;
Shi, Xiangyang .
RSC ADVANCES, 2016, 6 (11) :9232-9239
[7]   Targeted CT/MR dual mode imaging of tumors using multifunctional dendrimer-entrapped gold nanoparticles [J].
Chen, Qian ;
Li, Kangan ;
Wen, Shihui ;
Liu, Hui ;
Peng, Chen ;
Cai, Hongdong ;
Shen, Mingwu ;
Zhang, Guixiang ;
Shi, Xiangyang .
BIOMATERIALS, 2013, 34 (21) :5200-5209
[8]   Dual and multi-stimuli responsive polymeric nanoparticles for programmed site-specific drug delivery [J].
Cheng, Ru ;
Meng, Fenghua ;
Deng, Chao ;
Klok, Harm-Anton ;
Zhong, Zhiyuan .
BIOMATERIALS, 2013, 34 (14) :3647-3657
[9]   Polyethylenimine-grafted copolymer of poly(L-lysine) and poly(ethylene glycol) for gene delivery [J].
Dai, Jian ;
Zou, Seyin ;
Pei, Yuanyuan ;
Cheng, Du ;
Ai, Hua ;
Shuai, Xintao .
BIOMATERIALS, 2011, 32 (06) :1694-1705
[10]   pH-responsive complexes using prefunctionalized polymers for synchronous delivery of doxorubicin and siRNA to cancer cells [J].
Dong, Da-Wen ;
Xiang, Bai ;
Gao, Wei ;
Yang, Zhen-Zhen ;
Li, Jing-Quan ;
Qi, Xian-Rong .
BIOMATERIALS, 2013, 34 (20) :4849-4859