Evaluations of cell uptake capabilities of gold nanoparticle and photosensitizer in a cell spheroid (Conference Presentation)

Author(s):  
Po-Hao Tseng ◽  
Meng Chun Low ◽  
Wei-Hsiang Hua ◽  
Jian-He Yu ◽  
Yulu He ◽  
...  
2016 ◽  
Vol 15 (2) ◽  
pp. 181-186
Author(s):  
Ming-Hao Yao ◽  
Jie Yang ◽  
Dong-Hui Zhao ◽  
Rui-Xue Xia ◽  
Rui-Mei Jin ◽  
...  

A facile method for in situ fabrication of three-dimensional gold nanoparticles micropatterns throughout a polyethylene glycol hydrogel substrate has been developed by combining photochemical synthesis of gold nanoparticles with photolithography technology.


Nanomedicine ◽  
2014 ◽  
Vol 9 (5) ◽  
pp. 607-621 ◽  
Author(s):  
Barbara Rothen-Rutishauser ◽  
Dagmar A Kuhn ◽  
Zulqurnain Ali ◽  
Michael Gasser ◽  
Faheem Amin ◽  
...  

2020 ◽  
Vol 21 (12) ◽  
pp. 4431
Author(s):  
Dylan Peukert ◽  
Ivan Kempson ◽  
Michael Douglass ◽  
Eva Bezak

Gold nanoparticle (GNP) enhanced proton therapy is a promising treatment concept offering increased therapeutic effect. It has been demonstrated in experiments which provided indications that reactive species play a major role. Simulations of the radiolysis yield from GNPs within a cell model were performed using the Geant4 toolkit. The effect of GNP cluster size, distribution and number, cell and nuclear membrane absorption and intercellular yields were evaluated. It was found that clusters distributed near the nucleus increased the nucleus yield by 91% while reducing the cytoplasm yield by 7% relative to a disperse distribution. Smaller cluster sizes increased the yield, 200 nm clusters had nucleus and cytoplasm yields 117% and 35% greater than 500 nm clusters. Nuclear membrane absorption reduced the cytoplasm and nucleus yields by 8% and 35% respectively to a permeable membrane. Intercellular enhancement was negligible. Smaller GNP clusters delivered near sub-cellular targets maximise radiosensitisation. Nuclear membrane absorption reduces the nucleus yield, but can damage the membrane providing another potential pathway for biological effect. The minimal effect on adjacent cells demonstrates that GNPs provide a targeted enhancement for proton therapy, only effecting cells with GNPs internalised. The provided quantitative data will aid further experiments and clinical trials.


Nanoscale ◽  
2017 ◽  
Vol 9 (46) ◽  
pp. 18413-18422 ◽  
Author(s):  
Marios Sotiropoulos ◽  
Nicholas T. Henthorn ◽  
John W. Warmenhoven ◽  
Ranald I. Mackay ◽  
Karen J. Kirkby ◽  
...  

A computer model of gold nanoparticles within a cell used to assess DNA damage under proton irradiation.


Author(s):  
Ting-Hsiang Wu ◽  
Fan Xiao ◽  
Sheraz Kalim ◽  
Tara Teslaa ◽  
Michael A. Teitell ◽  
...  

A massively-parallel molecular delivery system for mammalian cells is demonstrated by pulsed-laser irradiation of a gold nanoparticle array situated below a cell monolayer. This system is capable of high throughput and spatially-targeted delivery into desired areas of a cell culture by designing the laser irradiation pattern. Rapid fabrication of gold nanoparticle arrays over large areas (>1 mm2) is achieved by polymer mold guided near-field photothermal annealing.


2019 ◽  
Vol 20 (17) ◽  
pp. 4280 ◽  
Author(s):  
Peukert ◽  
Kempson ◽  
Douglass ◽  
Bezak

Gold nanoparticles (GNPs) are promising radiosensitizers with the potential to enhance radiotherapy. Experiments have shown GNP enhancement of proton therapy and indicated that chemical damage by reactive species plays a major role. Simulations of the distribution and yield of reactive species from 10 ps to 1 µs produced by a single GNP, two GNPs in proximity and a GNP cluster irradiated with a proton beam were performed using the Geant4 Monte Carlo toolkit. It was found that the reactive species distribution at 1 µs extended a few hundred nm from a GNP and that the largest enhancement occurred over 50 nm from the nanoparticle. Additionally, the yield for two GNPs in proximity and a GNP cluster was reduced by up to 17% and 60% respectively from increased absorption. The extended range of action from the diffusion of the reactive species may enable simulations to model GNP enhanced proton therapy. The high levels of absorption for a large GNP cluster suggest that smaller clusters and diffuse GNP distributions maximize the total radiolysis yield within a cell. However, this must be balanced against the high local yields near a cluster particularly if the cluster is located adjacent to a biological target.


Cancers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 2245
Author(s):  
Hideo Takakura ◽  
Honoka Sato ◽  
Kohei Nakajima ◽  
Motofumi Suzuki ◽  
Mikako Ogawa

In molecular imaging, a targeting strategy with ligands is widely used because specificity can be significantly improved. In fluorescence imaging based on a targeting strategy, the fluorescent dyes conjugated with ligands may affect the targeting efficiency depending on the chemical properties. Herein, we used a cell-penetrating peptide (CPP) as a ligand with a variety of fluorescent cyanine dye. We investigated in vitro and in vivo cell uptake of the dye-CPP conjugates when cyanine dyes with differing charge and hydrophilicity/lipophilicity were used. The results showed that the conjugates with positively charged and lipophilic cyanine dyes accumulated in cancer cells in vitro, but there was almost no accumulation in tumors in vivo. On the other hand, the conjugates with negatively charged and hydrophilic cyanine dyes did not accumulate in cancer cells in vitro, but fluorescence was observed in tumors in vivo. These results show that there are some cases in which the cell uptake of the dye-peptide conjugates may differ significantly between in vitro and in vivo experiments due to the chemical properties of the fluorescent dyes. This suggests that attention should be paid to the chemical properties of fluorescent dyes in fluorescence imaging based on a targeting strategy.


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