Evolution of gold nanoparticle clusters in living cells studied by sectional dark-field optical microscopy and chromatic analysis.

J Biophotonics

Department of Engineering and System Science, National Tsing-Hua University, , No. 101, Sec. 2, Kuang-Fu Road, Hsinchu, Taiwan, 30013, R.O.C.

Published: July 2016

AI Article Synopsis

  • The study uses dark-field optical microscopy and chromatic analysis to observe how gold nanoparticle (Au NP) clusters change color during endocytosis, reflecting their dynamic behavior in living cells.
  • Au NP clusters are categorized into four groups during the endocytic process; large clusters increase in late endosomes over time, while smaller clusters fluctuate due to vesicle fusion and fission.
  • The efficiency of Au NP uptake is higher in cancer cells (75%) compared to normal cells (50%), indicating that cancer cells not only take up nanoparticles more effectively but also remove them quicker.

Article Abstract

The evolution of gold nanoparticle (Au NP) clusters in living cells are studied by using sectional dark-field optical microscopy and chromatic analysis approach. During endocytosis, Au NP clusters undergo fantastic color changes, from green to yellow-orange due to the plasmonic coupling effect. Analysis of brightness/hue values of the dark-field images helps estimate the numbers of Au NPs in the clusters. The Au NP clusters were further categorized into four groups within the endocytosis. As the results, the late endosomes had increased number of large Au NP clusters with time, while clustered numbers in secondary and tertiary groups were first increased and then decreased due to the fusion and fission of the endocytic vesicles. The time constants and cluster numbers for different groups are fitted by using an integrated rate equation, and show a positive correlation with the size of the Au NP cluster. The efficiency of Au NP uptake is only about 50% for normal cells, while 75% for cancer cells. Compared to normal cells, cancer cells show a larger number in uptake, while faster rate in removal. The propose method helps the kinetic study of endocytosed nanoparticles in physiological conditions.

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Source
http://dx.doi.org/10.1002/jbio.201500182DOI Listing

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