Superparamagnetic iron oxide - Loaded poly (lactic acid)-D-α-tocopherol polyethylene glycol 1000 succinate copolymer nanoparticles as MRI contrast agent

被引:92
作者
Prashant, Chandrasekharan [1 ]
Dipak, Maity [2 ]
Yang, Chang-Tong [3 ]
Chuang, Kai-Hsiang [3 ]
Jun, Ding [2 ]
Feng, Si-Shen [1 ,4 ,5 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Fac Engn, Singapore 117576, Singapore
[2] Natl Univ Singapore, Fac Engn, Dept Mat Sci & Engn, Singapore 117574, Singapore
[3] Agcy Sci Technol & Res Singapore, Singapore Bioimaging Consortium, Lab Mol Imaging, Singapore 138667, Singapore
[4] Natl Univ Singapore, Div Bioengn, Fac Engn, Singapore 117574, Singapore
[5] Natl Univ Singapore, NUS Nanosci & Nanotechnol Initiat NUSNNI, Singapore 117581, Singapore
关键词
Biodegradable polymers; Biocompatibility; Cellular and molecular imaging; Microencapsulation; Nanoprecipitation; Nanocomposite; EMULSIFICATION-DIFFUSION TECHNIQUE; IN-VITRO; BIODEGRADABLE POLYMERS; DRUG-DELIVERY; CHEMOTHERAPY; FORMULATION; LIVER; TPGS; MINIEMULSION; PARTICLES;
D O I
10.1016/j.biomaterials.2010.03.070
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We developed a strategy to formulate supraparamagnetic iron oxides (SPIOs) in nanoparticles (NPs) of biodegradable copolymer made up of poly(lactic acid) (PLA) and D-alpha-tocopherol polyethylene glycol 1000 succinate (TPGS) for medical imaging by magnetic resonance imaging (MRI) of high contrast and low side effects. The IOs-loaded PLA TPGS NPs (IOs-PNPs) were prepared by the single emulsion method and the nanoprecipitation method. Effects of the process parameters such as the emulsifier concentration, IOs loading in the nanoparticles, and the solvent to non-solvent ratio on the IOs distribution within the polymeric matrix were investigated and the formulation was then optimized. The transmission electron microscopy (TEM) showed direct visual evidence for the well dispersed distribution of the IOs within the NPs. We further investigated the biocompatibility and cellular uptake of the IOs-PNPs in vitro with MCF-7 breast cancer cells and NIH-3T3 mouse fibroblast in close comparison with the commercial IOs imaging agent Resovist (R). MRI imaging was further carried out to investigate the biodistribution of the IOs formulated in the IOs-PNPs, especially in the liver to understand the liver clearance process, which was also made in close comparison with Resovist (R). We found that the PLA TPGS NPs formulation at the clinically approved dose of 0.8 mg Fe/kg could be cleared within 24 h in comparison with several weeks for Resovist (R). Xenograft tumor model MRI confirmed the advantages of the IOs-PNPs formulation versus Resovist (R) through the enhanced permeation and retention (EPR) effect of the tumor vasculature. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5588 / 5597
页数:10
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