Preparation and Characterization of CdSe/ZnS Quantum Dots Encapsulated in Poly(ethylene glycol)-b-Poly(D,L-lactide) Micelle Nanoparticles

被引:13
作者
Lee, Joohyeon [1 ]
Im, Jeong Hyuk [2 ]
Huh, Kang Moo [2 ]
Lee, Yong-kyu [3 ]
Shin, Heungsoo [1 ]
机构
[1] Hanyang Univ, Coll Engn, Dept Bioengn, Seoul 133791, South Korea
[2] Chungnam Natl Univ, Dept Polymer Sci & Engn, Taejon 305764, South Korea
[3] Chungju Natl Univ, Dept Biol & Chem Engn, Chungbuk 380702, South Korea
关键词
PEG-PLA; Micelle; Quantum Dots; Imaging; Drug Delivery Carrier; BLOCK COPOLYMERIC MICELLE; LIVE CELLS; PEG; CORE; DELIVERY; GLYCOL); SHELL; MICELLIZATION; INDOMETHACIN; NANOSPHERES;
D O I
10.1166/jnn.2010.1736
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The final goal of this study is to develop multi-functional organic/inorganic hybrid nanoparticles, which can be utilized as biomedical imaging probes and drug delivery carriers. As an initial step toward this goal, we encapsulated CdSe/ZnS quantum dots (QDs) into poly(ethylene glycol)-b-poly(D,L-lactide) (PEG-PLA) micelles using a solid dispersion method. The size and fluorescent intensity of QDs encapsulated in PEG-PLA micelles depended on the amount of incorporated QDs. For example, when the amount of QDs increased from 0.1 to 1.0 mu g, the mean diameter increased from 24.2 +/- 6.0 to 211.2 +/- 6.5 nm and the fluorescent intensity changed from 10.2 +/- 1.0 to 469.9 +/- 15.6 (RFU). Stability studies showed that the size and zeta-potential (ZP) of QDs encapsulated in PEG-PLA micelles (QEMs) did not change significantly in response to a change in pH conditions or under a 10% serum condition. We also tested the cytotoxicity and cellular uptake of the QEMS. The viability of HeLa cells treated with micelles for 24 h was 80 similar to 100% in various concentration ranges of micelles. Confocal laser scanning microscopic images showed that the QEMs penetrated into the cells, particularly into the cytosolic compartments. Our results suggest that the QEMs may be a promising multi-functional nanocarrier for biomedical imaging and drug delivery.
引用
收藏
页码:487 / 496
页数:10
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