Multifunctional Carboxymethyl Cellulose-Based Magnetic Nanovector as a Theragnostic System for Folate Receptor Targeted Chemotherapy, Imaging, and Hyperthermia against Cancer

被引:82
作者
Sivakumar, Balasubramanian [1 ]
Aswathy, Ravindran Girija [1 ]
Nagaoka, Yutaka [1 ]
Suzuki, Masashi [1 ]
Fukuda, Takahiro [1 ]
Yoshida, Yasuhiko [1 ]
Maekawa, Toru [1 ]
Sakthikumar, Dasappan Nair [1 ]
机构
[1] Toyo Univ, Grad Sch Interdisciplinary New Sci, Bio Nano Elect Res Ctr, Kawagoe, Saitama, Japan
关键词
DRUG-DELIVERY; QUANTUM DOTS; CELL-DEATH; NANOPARTICLES; FUNCTIONALIZATION; MICROSPHERES; DISPERSION; PROTEINS;
D O I
10.1021/la305048m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A multifunctional biocompatible nanovector based on magnetic nanoparticle and carboxymethyl cellulose (CMC) was developed. The nanoparticles have been characterized using TEM, SEM, DLS, FT-IR spectra, VSM, and TGA studies. We found that the synthesized carboxymethyl cellulose magnetic nanoparticles (CMC MNPs) were spherical in shape with an average size of 150 nm having low aggregation and superparamagnetic properties. We found that the folate-tagged CMC MNPs were delivered to cancer cells by a folate-receptor-mediated endocytosis mechanism. 5-FU was encapsulated as a model drug for delivering cytotoxicity, and we could demonstrate the sustained release of 5-FU. It was also observed that the FITC-labeled CMC MNPs could effectively enter cells, and the fate of nanoparticles was tracked with Lysotracker. The CMC MNPs could induce significant cell death when an alternating magnetic field was applied. These results indicate that the multifunctional CMC MNPs possess a high drug loading efficiency and high biocompatibility and with low cell cytotoxicity and can be considered to be promising candidates for CMC-based targeted drug delivery, cellular imaging, and magnetic hypertherrnia (MHT).
引用
收藏
页码:3453 / 3466
页数:14
相关论文
共 46 条
[1]   Controlled Cell Death by Magnetic Hyperthermia: Effects of Exposure Time, Field Amplitude, and Nanoparticle Concentration [J].
Asin, L. ;
Ibarra, M. R. ;
Tres, A. ;
Goya, G. F. .
PHARMACEUTICAL RESEARCH, 2012, 29 (05) :1319-1327
[2]  
Aswathy RG., 2012, J Biomater Nanobiotechnol, V3, P254, DOI [DOI 10.4236/jbnb.2012.322031, DOI 10.4236/JBNB.2012.322031]
[3]  
Berry C. C., 2002, J PHYS D, V36, pR167
[4]   Polymeric nanoparticle-encapsulated curcumin (nanocurcumin"): A novel strategy for human cancer therapy" [J].
Bisht S. ;
Feldmann G. ;
Soni S. ;
Ravi R. ;
Karikar C. ;
Maitra A. ;
Maitra A. .
Journal of Nanobiotechnology, 5 (1)
[5]   Characterisation of carboxymethyl cellulose and polyacrylamide graft copolymer [J].
Biswal, DR ;
Singh, RP .
CARBOHYDRATE POLYMERS, 2004, 57 (04) :379-387
[6]   Preparation of 5-fluorouracil-poly(L-lactide) microparticles using solution-enhanced dispersion by supercritical CO2 [J].
Chen, Ai-Zheng ;
Pu, Xi-Ming ;
Kang, Yun-Qing ;
Liao, Li ;
Yao, Ya-Dong ;
Yin, Guang-Fu .
MACROMOLECULAR RAPID COMMUNICATIONS, 2006, 27 (15) :1254-1259
[7]   Novel thermosensitive 5-fluorouracil-cyclotriphosphazene conjugates: Synthesis, thermosensitivity, degradability, and in vitro antitumor activity [J].
Cho, YW ;
Lee, JR ;
Song, SC .
BIOCONJUGATE CHEMISTRY, 2005, 16 (06) :1529-1535
[8]   Monodisperse magnetic nanoparticles for biodetection, imaging, and drug delivery: a versatile and evolving technology [J].
Dave, Shivang R. ;
Gao, Xiaohu .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2009, 1 (06) :583-609
[9]   Evaluation of nano- and microparticle uptake by the gastrointestinal tract [J].
Delie, F .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 34 (2-3) :221-233
[10]   Development of biodegradable co-poly(D,L-lactic/glycolic acid) microspheres for the controlled release of 5-FU by the spray drying method [J].
Fu, YJ ;
Shyu, SS ;
Su, FH ;
Yu, PC .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2002, 25 (04) :269-279