Folate-decorated chitosan/doxorubicin poly(butyl)cyanoacrylate nanoparticles for tumor-targeted drug delivery

被引:12
作者
Duan, Jinghua [2 ]
Liu, Mujun [3 ]
Zhang, Yangde [2 ]
Zhao, Jinfeng [2 ]
Pan, Yifeng [2 ]
Yang, Xiyun [1 ]
机构
[1] Cent S Univ, Sch Met Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Hepatobiliary & Enter Surg Res Ctr, Changsha 410008, Hunan, Peoples R China
[3] Cent S Univ, Sch Biol Sci & Technol, Changsha 410083, Hunan, Peoples R China
关键词
Doxorubicin; Chitosan-poly(butyl cyanoacrylate) nanoparticles; Folate receptor; Targeting drug delivery; Nanomedicine; POLY(BUTYL CYANOACRYLATE) NANOPARTICLES; CULTURED KB CELLS; PARTICLE-SIZE; RECEPTOR; DOXORUBICIN; LIPOSOMES; DISPOSITION; ADRIAMYCIN; RESISTANCE; TRANSPORT;
D O I
10.1007/s11051-012-0761-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel chitosan coated poly(butyl cyanoacrylate) (PBCA) nanoparticles loaded doxorubicin (DOX) were synthesized and then conjugated with folic acid to produce a folate-targeted drug carrier for tumor-specific drug delivery. Prepared nanoparticles were surface modified by folate for targeting cancer cells, which is confirmed by FTIR spectroscopy and characterized for shape, size, and zeta potential measurements. The size and zeta potential of prepared DOX-PBCA nanoparticles (DOX-PBCA NPs) were almost 174 +/- 8.23 nm and +23.14 +/- 4.25 mV, respectively with 46.8 +/- 3.32% encapsulation capacity. The transmission electron microscopy study revealed that preparation allowed the formation of spherical nanometric and homogeneous. Fluorescent microscopy imaging and flow cytometry analysis revealed that DOX-PBCA NPs were endocytosed into MCF-7 cells through the interaction with overexpressed folate receptors on the surface of the cancer cells. The results demonstrate that folate-conjugated DOX-PBCA NPs drug delivery system could provide increased therapeutic benefit by delivering the encapsulated drug to the folate receptor positive cancer cells.
引用
收藏
页数:9
相关论文
共 41 条
[1]   Influence of surfactants, polymer and doxorubicin loading on the anti-tumour effect of poly(butyl cyanoacrylate) nanoparticles in a rat glioma model [J].
Ambruosi, Alessandra ;
Gelperina, Svetlana ;
Khalansky, Alexander ;
Tanski, Sandra ;
Theisen, Alf ;
Kreuter, Joerg .
JOURNAL OF MICROENCAPSULATION, 2006, 23 (05) :582-592
[2]   Synthesis and characterization of poly (ethyl-2-cyanoacrylate) nanoparticles with a magnetic core [J].
Arias, JL ;
Gallardo, V ;
Gómez-Lopera, SA ;
Plaza, RC ;
Delgado, AV .
JOURNAL OF CONTROLLED RELEASE, 2001, 77 (03) :309-321
[3]   Poly n-butyl cyanoacrylate nanoparticles:: a mechanistic study of polymerisation and particle formation [J].
Behan, N ;
Birkinshaw, C ;
Clarke, N .
BIOMATERIALS, 2001, 22 (11) :1335-1344
[4]   Folate receptor-mediated gene delivery using folate-poly(ethylene glycol)-poly (L-lysine) conjugate [J].
Cho, KC ;
Kim, SH ;
Jeong, JH ;
Park, TG .
MACROMOLECULAR BIOSCIENCE, 2005, 5 (06) :512-519
[5]   POLYALKYLCYANOACRYLATE NANOPARTICLES AS DRUG CARRIER - PRESENT STATE AND PERSPECTIVES [J].
COUVREUR, P ;
VAUTHIER, C .
JOURNAL OF CONTROLLED RELEASE, 1991, 17 (02) :187-198
[6]   STUDIES ON THE INVIVO DISPOSITION OF ADRIAMYCIN IN HUMAN-TUMORS WHICH EXHIBIT DIFFERENT RESPONSES TO THE DRUG [J].
CUMMINGS, J ;
MCARDLE, CS .
BRITISH JOURNAL OF CANCER, 1986, 53 (06) :835-838
[7]  
DEVERDIERE AC, 1994, CANCER CHEMOTH PHARM, V33, P504
[8]   PARTICLE-SIZE AND SIZE DISTRIBUTION OF POLY(BUTYL-2-CYANOACRYLATE) NANOPARTICLES .1. INFLUENCE OF PHYSICOCHEMICAL FACTORS [J].
DOUGLAS, SJ ;
ILLUM, L ;
DAVIS, SS ;
KREUTER, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1984, 101 (01) :149-158
[9]   PARTICLE-SIZE AND SIZE DISTRIBUTION OF POLY(BUTYL 2-CYANOACRYLATE) NANOPARTICLES .2. INFLUENCE OF STABILIZERS [J].
DOUGLAS, SJ ;
ILLUM, L ;
DAVIS, SS .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1985, 103 (01) :154-163
[10]   Synthesis and in vitro/in vivo anti-cancer evaluation of curcumin-loaded chitosan/poly(butyl cyanoacrylate) nanoparticles [J].
Duan, Jinghua ;
Zhang, Yangde ;
Han, Shiwei ;
Chen, Yuxiang ;
Li, Bo ;
Liao, Mingmei ;
Chen, Wei ;
Deng, Xingming ;
Zhao, Jinfeng ;
Huang, Boyun .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 400 (1-2) :211-220