TY - GEN
T1 - Cationic colloidal gold assisting delivery of macromolecular fluoresceins into target CHO-K1 cells by focused femtosecond laser
AU - Li, Zheng
AU - Zhang, Zhenxi
AU - Qu, Xiaochao
AU - Wang, Jing
AU - Hüttmann, Gereon
PY - 2007
Y1 - 2007
N2 - We describe a new method for delivering macromolecules into the target cells based on light-absorbing cationic colloidal gold nanoparticles that are irradiated by focused femtosecond laser pulses. Cationic colloidal 15nm gold particles which were made by conjugation with poly-L-Lysine, were attached on the anionic sites, especially on the membrane, of CHOK1 cells because of their strong positive charge at physiological pH. Target cells labeled with cationic gold nanoparticles were imaged under two-photon fluorescence microscopy, and lifetime images of the same targets were taken by TCSPC technique in order to verify the fluorescence of the marker and the luminescence of the gold particles. A macromolecular 10k Dalton fluorescein isothiocyanate dextran (FITC-D), was added into the sample and the focused femtosecond laser of two-photon fluorescence microscopy was employed to scan the target cells layer by layer. Typical laser power level used in biological imaging is about 3-5 mW. Here the laser power of scanning was below 5 mW in order to prevent photochemical damage of the fs-pulses alone and to localize effects to the nanoparticles on a nano-scale. After scanning the target cells under stack mode, macromolecular fluoresceins surrounding the cells was observed to cross the membrane and to diffuse in the cytoplasma. Comparing with the images before scanning, the two-photon fluorescence and fluorescence lifetime images revealed the delivery of FITC-D into target cells.
AB - We describe a new method for delivering macromolecules into the target cells based on light-absorbing cationic colloidal gold nanoparticles that are irradiated by focused femtosecond laser pulses. Cationic colloidal 15nm gold particles which were made by conjugation with poly-L-Lysine, were attached on the anionic sites, especially on the membrane, of CHOK1 cells because of their strong positive charge at physiological pH. Target cells labeled with cationic gold nanoparticles were imaged under two-photon fluorescence microscopy, and lifetime images of the same targets were taken by TCSPC technique in order to verify the fluorescence of the marker and the luminescence of the gold particles. A macromolecular 10k Dalton fluorescein isothiocyanate dextran (FITC-D), was added into the sample and the focused femtosecond laser of two-photon fluorescence microscopy was employed to scan the target cells layer by layer. Typical laser power level used in biological imaging is about 3-5 mW. Here the laser power of scanning was below 5 mW in order to prevent photochemical damage of the fs-pulses alone and to localize effects to the nanoparticles on a nano-scale. After scanning the target cells under stack mode, macromolecular fluoresceins surrounding the cells was observed to cross the membrane and to diffuse in the cytoplasma. Comparing with the images before scanning, the two-photon fluorescence and fluorescence lifetime images revealed the delivery of FITC-D into target cells.
KW - Cationic colloidal gold
KW - Femtosecond laser
KW - Fluorescence lifetime image
KW - Plasma membrane permeability
KW - Two-photon fluorescence microscopy
UR - https://www.scopus.com/pages/publications/84898804046
M3 - 会议稿件
AN - SCOPUS:84898804046
SN - 9780819467713
T3 - Optics InfoBase Conference Papers
BT - European Conference on Biomedical Optics, ECBO 2007
PB - Optical Society of America
T2 - European Conference on Biomedical Optics, ECBO 2007
Y2 - 17 June 2007 through 17 June 2007
ER -