| Literature DB >> 20347138 |
Jin Hee Maeng1, Don-Haeng Lee, Kyung Hee Jung, You-Han Bae, In-Suh Park, Seok Jeong, Yong-Sun Jeon, Chang-Koo Shim, Wooyoung Kim, Jungahn Kim, Jeongmi Lee, Yoon-Mi Lee, Ji-Hee Kim, Won-Hong Kim, Soon-Sun Hong.
Abstract
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 (Fe(3)O(4)) 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. 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 groups in the rat and rabbit models, respectively. Furthermore, YCC-DOX showed higher MRI sensitivity comparable to a conventional MRI contrast agent (Resovist), 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. (c) 2010. Published by Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20347138 DOI: 10.1016/j.biomaterials.2010.02.068
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479