共 38 条
Optically Traceable Solid Lipid Nanoparticles Loaded with siRNA and Paclitaxel for Synergistic Chemotherapy with In situ Imaging
被引:86
作者:
Bae, Ki Hyun
[1
]
Lee, Jeong Yu
[2
]
Lee, Soo Hyeon
[1
]
Park, Tae Gwan
[1
]
Nam, Yoon Sung
[1
,2
,3
]
机构:
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, KAIST Inst NanoCentury KINC & BioCentury KIB, Taejon 305701, South Korea
关键词:
theranostics;
cancer therapy;
solid lipid nanoparticles;
quantum dots;
paclitaxel;
siRNA;
CANCER-CELLS;
INTRACELLULAR DELIVERY;
QUANTUM DOTS;
CO-DELIVERY;
APOPTOTIC CELLS;
ANTICANCER DRUG;
CELLULAR UPTAKE;
INDUCTION;
COMPLEXES;
BCL-2;
D O I:
10.1002/adhm.201200338
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Here, we report quantum dot-incorporating solid lipid nanoparticles (SLNs) for anticancer theranostics with synergistic therapeutic effects of paclitaxel-siRNA combination. The natural components of a low-density lipoprotein (LDL) are reconstituted to produce LDL-mimetic SLNs having a stable core/shell nanostructure incorporating quantum dots and paclitaxel within the lipid shell while anionic siRNA molecules are electrostatically complexed with the outer surface of SLNs. The produced SLN/siRNA complexes efficiently deliver both of paclitaxel and Bcl-2 targeted siRNA into human lung carcinoma cells and exhibit synergistic anticancer activities by triggering caspase-mediated apoptosis as determined by median effect plot analysis. Moreover, the strong fluorescence from quantum dots within SLNs enables in situ visualization of intracellular translocation of SLNs into cancer cells. Our study suggests that LDL-mimetic SLNs can be utilized as a multifunctional and optically traceable nanocarrier for efficient anticancer theranostics.
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页码:576 / 584
页数:9
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