Multifunctional doxorubicin loaded superparamagnetic iron oxide nanoparticles for chemotherapy and magnetic resonance imaging in liver cancer

被引:280
作者
Maeng, Jin Hee [2 ]
Lee, Don-Haeng [2 ]
Jung, Kyung Hee [1 ]
Bae, You-Han [2 ,3 ]
Park, In-Suh [1 ]
Jeong, Seok [1 ]
Jeon, Yong-Sun [1 ]
Shim, Chang-Koo [4 ]
Kim, Wooyoung [4 ]
Kim, Jungahn [5 ]
Lee, Jeongmi [6 ]
Lee, Yoon-Mi [7 ]
Kim, Ji-Hee [7 ]
Kim, Won-Hong [1 ]
Hong, Soon-Sun [1 ]
机构
[1] Inha Univ, Sch Med, Inchon 400712, South Korea
[2] Utah Inha DDS Inst, Inchon 406840, South Korea
[3] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84108 USA
[4] Seoul Natl Univ, Coll Pharm, Natl Res Lab Transporters Targeted Drug Design, Seoul 151742, South Korea
[5] Kyung Hee Univ, Dept Chem, Seoul 130701, South Korea
[6] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, South Korea
[7] Youl Chon Chem Co Ltd, Seoul 156709, South Korea
关键词
Drug delivery; Doxorubicin; Liver cancer; Magnetic resonance imaging; Nanoparticles; RECEPTOR-MEDIATED ENDOCYTOSIS; FOLATE-RECEPTOR; IN-VIVO; HEPATOCELLULAR-CARCINOMA; POLYMERIC MICELLE; CONTRAST AGENTS; DRUG-DELIVERY; TUMOR-MODEL; VX2; TUMOR; ALPHA;
D O I
10.1016/j.biomaterials.2010.02.068
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
To develop a drug delivery system with enhanced efficacy and minimized adverse effects, we synthesized a novel polymeric nanoparticles, (YCC-DOX) composed of poly (ethylene oxide)-trimellitic anhydride chloride-folate (PEO-TMA-FA), doxorubicin (DOX) and superparamagnetic iron oxide (Fe3O4) and folate. The efficacy of the nanoparticles was evaluated in rats and rabbits with liver cancer, in comparison with free-DOX (FD) and a commercial liposome drug, DOXIL(R). YCC-DOX showed the anticancer efficacy and specifically targeted folate receptor (FR)-expressing tumors, thereby increasing the bioavailability and efficacy of DOX. The relative tumor volume of the YCC-DOX group was decreased two- and four-fold compared with the FD and DOXIL(R) groups in the rat and rabbit models, respectively. Furthermore, YCC-DOX showed higher MRI sensitivity comparable to a conventional MRI contrast agent (Resovist(R)), even in its lower iron content. In the immunohistochemical analysis, YCC-DOX group showed the lower expression of CD34 and Ki-67, markers of angiogenesis and cell proliferation, respectively, while apoptotic cells were significantly rich in the YCC-DOX group in terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. These results indicate that YCC-DOX is a promising candidate for treating liver cancer and monitoring the progress of the cancer using MRI. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4995 / 5006
页数:12
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