Real-time and label-free monitoring of nanoparticle cellular uptake using capacitance-based assays

被引:8
|
作者
Lee, Rimi [1 ]
Jo, Dong Hyun [2 ,3 ]
Chung, Sang J. [4 ]
Na, Hee-Kyung [1 ]
Kim, Jeong Hun [2 ,3 ,5 ]
Lee, Tae Geol [1 ,6 ]
机构
[1] Korea Res Inst Stand & Sci Daejeon, Ctr Nanobio Measurement, Daejeon, South Korea
[2] Seoul Natl Univ Hosp, Clin Res Inst, Fight Angiogenesis Related Blindness FARB Lab, Seoul, South Korea
[3] Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea
[4] Dongguk Univ, Coll Nat Sci, Dept Chem, 26 Pil Dong 3 Ga, Seoul, South Korea
[5] Seoul Natl Univ, Dept Ophthalmol, Coll Med, Seoul, South Korea
[6] Univ Sci & Technol, Dept Nanosci, Daejeon, South Korea
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
新加坡国家研究基金会;
关键词
ENDOCYTOSIS; PERMEABILITY; CELLS;
D O I
10.1038/srep33668
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nanoparticles have shown great potential as vehicles for the delivery of drugs, nucleic acids, and therapeutic proteins; an efficient, high-throughput screening method to analyze nanoparticle interaction with the cytomembrane would substantially improve the efficiency and accuracy of the delivery. Here, we developed a capacitance sensor array that monitored the capacitance values of nanoparticle-treated cells in a real-time manner, without the need for labeling. Upon cellular uptake of the nanoparticles, a capacitance peak was observed at a low frequency (e.g., 100 Hz) as a function of time based on zeta potential changes. In the high frequency region (e.g., 15-20 kHz), the rate of decreasing capacitance slowed as a function of time compared to the cell growth control group, due to increased cytoplasm resistance and decreased membrane capacitance and resistance. The information provided by our capacitance sensor array will be a powerful tool for scientists designing nanoparticles for specific purposes.
引用
收藏
页数:10
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