TY - JOUR
T1 - The influence of laser intensity activated plasmonic gold nanoparticle-generated photothermal effects on cellular morphology and viability
T2 - A real-time, long-term tracking and monitoring system
AU - Huang, Yu Chieh
AU - Lei, Kin Fong
AU - Liaw, Jiunn Woei
AU - Tsai, Shiao Wen
N1 - Publisher Copyright:
© 2019 The Royal Society of Chemistry and Owner Societies.
PY - 2019
Y1 - 2019
N2 - In this study, a microfluidic apparatus embedded with microstructures was designed and aligned with a laser and dark-field microscope for real-time, long-term observation of photothermal effects on cells. Gold nanorods (AuNRs, 10 ppm) were incubated with MG-63 human osteosarcoma cells for 3 h. Then, the cells were exposed to a continuous-wave laser at a wavelength of 830 nm for 10, 20, and 30 min at 5, 9, 14, 24, and 32 W cm-2. Subsequent changes in morphology were observed. Under different conditions, cell membrane blebbing occurred at different times, indicating that actin filaments were destroyed in large quantities and apoptosis was induced. In suitable conditions, we first induced slight cell injury by causing cytoskeletal fractures with a high-energy laser; then, the cells were irradiated with a low-energy laser at 0.3 W cm-2. We found that among cells treated with the high-energy laser, cells treated additionally with a low-energy laser showed extended viability compared with cells that did not receive the additional treatment.
AB - In this study, a microfluidic apparatus embedded with microstructures was designed and aligned with a laser and dark-field microscope for real-time, long-term observation of photothermal effects on cells. Gold nanorods (AuNRs, 10 ppm) were incubated with MG-63 human osteosarcoma cells for 3 h. Then, the cells were exposed to a continuous-wave laser at a wavelength of 830 nm for 10, 20, and 30 min at 5, 9, 14, 24, and 32 W cm-2. Subsequent changes in morphology were observed. Under different conditions, cell membrane blebbing occurred at different times, indicating that actin filaments were destroyed in large quantities and apoptosis was induced. In suitable conditions, we first induced slight cell injury by causing cytoskeletal fractures with a high-energy laser; then, the cells were irradiated with a low-energy laser at 0.3 W cm-2. We found that among cells treated with the high-energy laser, cells treated additionally with a low-energy laser showed extended viability compared with cells that did not receive the additional treatment.
UR - http://www.scopus.com/inward/record.url?scp=85067261833&partnerID=8YFLogxK
U2 - 10.1039/c9pp00054b
DO - 10.1039/c9pp00054b
M3 - 文章
C2 - 30946422
AN - SCOPUS:85067261833
SN - 1474-905X
VL - 18
SP - 1419
EP - 1429
JO - Photochemical and Photobiological Sciences
JF - Photochemical and Photobiological Sciences
IS - 6
ER -