Manganese oxide and docetaxel co-loaded fluorescent polymer nanoparticles for dualmodal imaging and chemotherapy of breast cancer

被引:56
作者
Abbasi, Azhar Z. [1 ]
Prasad, Preethy [1 ]
Cai, Ping [1 ]
He, Chunsheng [1 ]
Foltz, Warren D. [2 ]
Amini, Mohammad Ali [1 ]
Gordijo, Claudia R. [1 ]
Rauth, Andrew M. [3 ]
Wu, Xiao Yu [1 ]
机构
[1] Univ Toronto, Leslie L Dan Fac Pharm, Adv Pharmaceut & Drug Delivery Lab, Toronto, ON M5S 3M2, Canada
[2] Princess Margaret Hosp, Dept Radiat Oncol, STTARR Innovat Ctr, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Dept Med Biophys, Div Radiat Oncol, Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
关键词
Multifunctional nanoparticles; Manganese oxide; Cancer; Dual modal imaging; Drug delivery; MRI CONTRAST; DRUG-RELEASE; MULTIDRUG-RESISTANCE; AGENTS; RELAXIVITY; BLOOD;
D O I
10.1016/j.jconrel.2015.04.020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multifunctional nanoparticles (NPs) have found important applications in diagnosis, chemotherapy, and image-guided surgery of tumors. In this work, we have developed polymeric theranostic NPs (PTNPs) containing the anticancer drug docetaxel (DTX), a fluorescent dye, and magnetic manganese oxide (MnO) NPs for dual modal imaging and chemotherapy. PTNPs similar to 150 nm in diameter were synthesized by co-loading hydrophobic DTX and MnO NPs similar to 5 nm in diameter, into the matrix of a fluorescent dye-labeled amphiphilic polymer. The PTNPs enabled high loading efficiency and sustained in vitro release of DTX. Energy-dependent cellular uptake and extended cytoplasmic retention of the PTNPs in MDA-MB-231 human breast cancer cells were observed by fluorescence microscopy examination. DTX-loaded PTNPs exhibited higher cytotoxicity than free DTX with a 3 to 4.4-fold decrease in drug dose required for 50% cell growth inhibition. The hydrophilic backbone of the amphiphilic polymer improved the fluidity of PTNPs which enhanced the longitudinal relaxivity (r(1)) of loaded MnO NPs by 2.7-fold with r(1) = 2.4 mM(-1) s(-1). Whole body fluorescence imaging (FI) and magnetic resonance imaging (MRI) showed significant accumulation and prolonged retention of PTNPs in orthotopic MDA-MB-231 breast tumors. These results suggest that the newamphiphilic polymer-based PTNP system, able to simultaneously deliver a poorly soluble anticancer drug, enhance MRI contrast, and stain tumor tissue by fluorescence, is a good candidate for cancer theranostic applications. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:186 / 196
页数:11
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