Noninvasive monitoring of orthotopic glioblastoma therapy response using RGD-conjugated iron oxide nanoparticles

被引:97
作者
Zhang, Fan [2 ]
Huang, Xinglu [1 ]
Zhu, Lei [1 ,3 ]
Guo, Ning [3 ]
Niu, Gang [1 ]
Swierczewska, Magdalena [1 ]
Lee, Seulki [1 ]
Xu, Hong [4 ]
Wang, Andrew Y. [4 ]
Mohamedali, Khalid A. [5 ]
Rosenblum, Michael G. [5 ]
Lu, Guangming [2 ]
Chen, Xiaoyuan [1 ,3 ]
机构
[1] NIBIB, Lab Mol Imaging & Nanomed LOMIN, NIH, Bethesda, MD 20892 USA
[2] Nanjing Univ, Dept Radiol, Nanjing Jinling Hosp, Clin Sch,Med Coll, Nanjing 210002, Jiangsu, Peoples R China
[3] Xiamen Univ, Ctr Mol Imaging & Translat Med, Sch Publ Hlth, Xiamen 361005, Peoples R China
[4] Ocean NanoTech LLC, Springdale, AR 72764 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77230 USA
基金
美国国家科学基金会;
关键词
Magnetic resonance imaging (MRI); Iron oxide nanoparticles (IONPs); RGD peptides; Tumor targeting; Therapy response; RESONANCE-IMAGING CONTRAST; TUMOR ANGIOGENESIS; IN-VIVO; INTEGRIN ALPHA(V)BETA(3); MALIGNANT GLIOMA; DELIVERY; BARRIER;
D O I
10.1016/j.biomaterials.2012.04.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Noninvasive imaging techniques have been considered important strategies in the clinic to monitor tumor early response to therapy. In the present study, we applied RGD peptides conjugated to iron oxide nanoparticles (IONP-RGD) as contrast agents in magnetic resonance imaging (MRI) to noninvasively monitor the response of a vascular disrupting agent VEGF(121)/rGel in an orthotopic glioblastoma model. RGD peptides were firstly coupled to IONPs coated with a crosslinked PEGylated amphiphilic triblock copolymer. In vitro binding assays confirmed that cellular uptake of particles was mainly dependent on the interaction between RGD and integrin alpha(v)beta(3) of human umbilical vein endothelial cells (HUVEC). The tumor targeting of IONP-RGD was observed in an orthotopic U87 glioblastoma model. Finally, noninvasive monitoring of the tumor response to VEGF(121)/rGel therapy at early stages of treatment was successfully accomplished using IONP-RGD as a contrast agent for MRI, a superior method over common anatomical approaches which are based on tumor size measurements. This preclinical study can accelerate anticancer drug development and promote clinical translation of nanoprobes. Published by Elsevier Ltd.
引用
收藏
页码:5414 / 5422
页数:9
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