Stabilizer-free poly(lactide-co-glycolide) nanoparticles for multimodal biomedical probes

被引:138
作者
Cheng, Fong-Yu [6 ]
Wang, Saprina Ping-Hsien [1 ,2 ]
Su, Chio-Hao [5 ,6 ]
Tsai, Tsung-Liu [4 ]
Wu, Ping-Ching [4 ]
Shieh, Dar-Bin [3 ,4 ]
Chen, Jyh-Horng [5 ]
Hsieh, Patrick Ching-Ho [1 ,2 ]
Yeh, Chen-Sheng [6 ]
机构
[1] Natl Cheng Kung Univ, Inst Clin Med & Biomed Engn, Tainan 704, Taiwan
[2] Natl Cheng Kung Univ, Dept Surg, Tainan 704, Taiwan
[3] Natl Cheng Kung Univ, Inst Oral Med, Tainan 701, Taiwan
[4] Natl Cheng Kung Univ, Inst Basic Med Sci, Tainan 701, Taiwan
[5] Natl Taiwan Univ, Dept Elect Engn, Interdisciplinary MRI MRS Lab, Taipei 106, Taiwan
[6] Natl Cheng Kung Univ, Dept Chem, Tainan 701, Taiwan
基金
美国国家科学基金会;
关键词
PLGA; nanoparticles; drug delivery; nuclear localization signal; MRI;
D O I
10.1016/j.biomaterials.2008.01.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Apart from the reported PLGA submicro- and microspheres with broad size distribution, we have successfully developed a methodology using nanoprecipitation to prepare different sizes of PLGA nanoparticles with narrow size distributions. The newly developed PLGA nanoparticles could be readily modified with hydrophilic biomaterials on their surface and entrap hydrophobic drugs into their interiors. The encapsulation of FITC inside PLGA nanoparticles displayed a controlled release of drug system. The surfaces of the FITC entrapped PLGA nanoparticles were conjugated with quantum dots to serve as bimodal imaging probes. For nuclear transport, combination of nuclear localization signal (NLS) and PLGA nanoparticles, PLGA nanoparticles could successfully enter into HeLa cells nuclei. From tissue uptake results, PLGA nanoparticles had more uptaken by brain and liver than other tissues. The iron oxide nanoparticles-conjugated PLGA nanoparticle showed high efficiency of relaxivities r2 and could be used as the powerful magnetic resonance imaging (MRI) agents. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2104 / 2112
页数:9
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