TY - GEN
T1 - Multiphoton fluorescence lifetime imaging of Karpas 299 cells using ACT1 antibody conjugated gold nanoparticles
AU - Qu, Xiaochao
AU - Norbert, Koop
AU - Li, Zheng
AU - Wang, Jing
AU - Zhang, Zhenxi
AU - Hüttmann, Gereon
PY - 2007
Y1 - 2007
N2 - Due to the unique optical properties, gold nanoparticles (NPs) can play a useful role in biological cellular imaging as biological probes. Using multiphoton microscopy and fluorescence lifetime imaging (FLIM) system, we recorded the images of Karpas 299 cells incubated without, or with gold NPs, and ACTl antibodies conjugated with gold NPs. From the FLIM, we can easily discriminate the difference among different experiment conditions due to the distinct lifetime between cells and gold NPs. Our results present that nonconjugated gold NPs are accumulated inside cells, but conjugated gold NPs bind homogeneously and specifically to the surface of cancer cells. For single Karpas 299 cells, the signal is very week when the excitation power is about 10mw; while the power is approximately 28 mw, a very sharp cell imaging can be obtained. For the Karpas 299 incubated with ACT1 conjugated gold NPs, while the excitation power is 10mw, gold NPs have clear fluorescence signal so that the profile of cells can be detected; Signal of gold NPs is very strong when the power arrived in 20mw. These results suggest that the multiphoton lifetime imaging of antibody conjugated gold NPs can support a useful method in diagnosis of cancer.
AB - Due to the unique optical properties, gold nanoparticles (NPs) can play a useful role in biological cellular imaging as biological probes. Using multiphoton microscopy and fluorescence lifetime imaging (FLIM) system, we recorded the images of Karpas 299 cells incubated without, or with gold NPs, and ACTl antibodies conjugated with gold NPs. From the FLIM, we can easily discriminate the difference among different experiment conditions due to the distinct lifetime between cells and gold NPs. Our results present that nonconjugated gold NPs are accumulated inside cells, but conjugated gold NPs bind homogeneously and specifically to the surface of cancer cells. For single Karpas 299 cells, the signal is very week when the excitation power is about 10mw; while the power is approximately 28 mw, a very sharp cell imaging can be obtained. For the Karpas 299 incubated with ACT1 conjugated gold NPs, while the excitation power is 10mw, gold NPs have clear fluorescence signal so that the profile of cells can be detected; Signal of gold NPs is very strong when the power arrived in 20mw. These results suggest that the multiphoton lifetime imaging of antibody conjugated gold NPs can support a useful method in diagnosis of cancer.
KW - Fluorescence lifetime imaging
KW - Gold nanoparticles
KW - Karpas 299 cells
KW - Multiphoton microscopy
UR - https://www.scopus.com/pages/publications/36248993967
U2 - 10.1117/12.728239
DO - 10.1117/12.728239
M3 - 会议稿件
AN - SCOPUS:36248993967
SN - 081946774X
SN - 9780819467744
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Confocal, Multiphoton, and Nonlinear Microscopic Imaging III
PB - SPIE
T2 - Confocal, Multiphoton, and Nonlinear Microscopic Imaging III
Y2 - 19 June 2007 through 21 June 2007
ER -