1. Department of Engineering and System Science, National Tsing‐Hua University, Hsinchu, Taiwan, R.O.C.;2. Research Center for Applied Sciences, Academia Sinica, Nankang, Taipei, Taiwan, R.O.C.;3. Department of Biochemical Science and Technology, National Taiwan University, Taipei, R.O.C.;4. Institute of Biophotonics, National Yang‐Ming University, Taipei, Taiwan, R.O.C.
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.
