Caffeic acid-coated multifunctional magnetic nanoparticles for the treatment and bimodal imaging of tumours

被引:26
|
作者
Lee, Jun [1 ]
Kim, Kyoung Sub [2 ]
Na, Kun [2 ]
机构
[1] Gyeonggi Acad Foreign Languages, 30,105 105 Gosan Ro, Uiwang Si 437010, Gyeonggi Do, South Korea
[2] Catholic Univ Korea, Dept Biotechnol, Ctr Photomed, 43 Jibong Ro, Bucheon Si 420743, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Tumour theranostic; Iron oxide nanoparticles; MRI contrast agent; Photodynamic therapy; Tumour-target ligand; IRON-OXIDE NANOPARTICLES; PHOTODYNAMIC THERAPY; DRUG-DELIVERY; CANCER-THERAPY; SOLID TUMOR; CELLS; MICROENVIRONMENT; NANOCARRIERS; PLATFORM; AGENTS;
D O I
10.1016/j.jphotobiol.2016.03.058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accurate theragnosis of tumour is essential for improving the life rate of tumour patients. Superparamagnetic iron oxide nanoparticles (SPIONs) have been used as both diagnostic and therapeutic agents. However, their application is often limited because of a lack of water solubility, lack of cancer treatment efficacy, and ineffective targeting of tumour cells. In this report, a double ligand (caffeic acid-polyethylene glycol-folic acid; FA-PEG-CA, caffeic acid-polyethylene glycol-pheophorbide-a; PheoA-PEG-CA) coated iron oxide nanoparticle has been fabricated that overcomes the limitations of conventional SPION. Photosensitizer and tumour targeting ligands were coated on SPION using a ligand-substitution method. We confirmed the successful substitution of oleic acid ligands with FA-PEG-CA and PheoA-PEG-CA ligands by FT-IR spectroscopy. The caffeic acid coated iron oxide nanoparticles (CAMNPs) also demonstrated high water solubility in an aqueous environment and folate-mediated active tumour targeting. The water solubility of CAMNPs was evaluated by DLS measurement and TEM images. The cytotoxicity of CAMNPs increased two-fold in MDA-MB-231 cells at a laser irradiation condition. The fabricated CAMNPs retained their ability to function as both MRI diagnostic and tumour-selective therapeutic agents. These results suggest that these efficient characteristics of CAMNPs can be incorporated into applications, thus enhancing the efficacy of clinical cancer treatment. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:210 / 216
页数:7
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