23 February 2017:
Our researchers and collaborators have made a breakthrough in the development of practical super-resolution optical microscopy that will pave the way for the detailed study of live cells and organisms, on a scale 10 times smaller than can currently be achieved with conventional microscopy.
Reported in Nature, it was demonstrated that bright luminescent nanoparticles can be switched on and off using a low-power infrared laser beam, and used to achieve images with a super resolution of 28nm (about 1/36 the wavelength of light).
Find out more by accessing the paper online.
Title: Amplified stimulated emission in upconversion nanoparticles for super-resolution nanoscopy.
Authors: Yujia Liu, Yiqing Lu, Xusan Yang, Xianlin Zheng, Shihui Wen, Fan Wang, Xavier Vidal, Jiangbo Zhao, Deming Liu, Zhiguang Zhou, Chenshuo Ma, Jiajia Zhou, James A. Piper, Peng Xi & Dayong Jin.
10 February 2017:
A new publication from CNBP researchers Aziz Ul Rehman (pictured), Ayad Anwer, Martin Gosnell, Saabah Mahbub, Guozhen Liu and Ewa Goldys demonstrates the validation of an innovative hyperspectral unmixing methodology, that can derive chemical information from cell colour.
The work has just been reported in the journal ‘Biomedical Optics Express’ and is accessible online.
Journal: Biomedical Optics Express.
Title: Fluorescence quenching of free and bound NADH in HeLa cells determined by hyperspectral imaging and unmixing of cell autofluorescence.
Authors: Aziz Ul Rehman, Ayad G. Anwer, Martin E. Gosnell, Saabah B. Mahbub, Guozhen Liu, and Ewa M. Goldys.
Abstract: Carbonyl cyanide-p-trifluoro methoxyphenylhydrazone (FCCP) is a well-known mitochondrial uncoupling agent. We examined FCCP-induced fluorescence quenching of reduced nicotinamide adenine dinucleotide / nicotinamide adenine dinucleotide phosphate (NAD(P)H) in solution and in cultured HeLa cells in a wide range of FCCP concentrations from 50 to 1000µM. A non-invasive label-free method of hyperspectral imaging of cell autofluorescence combined with unsupervised unmixing was used to separately isolate the emissions of free and bound NAD(P)H from cell autofluorescence. Hyperspectral image analysis of FCCP-treated HeLa cells confirms that this agent selectively quenches fluorescence of free and bound NAD(P)H in a broad range of concentrations. This is confirmed by the measurements of average NAD/NADH and NADP/NADPH content in cells. FCCP quenching of free NAD(P)H in cells and in solution is found to be similar, but quenching of bound NAD(P)H in cells is attenuated compared to solution quenching possibly due to a contribution from the metabolic and/or antioxidant response in cells. Chemical quenching of NAD(P)H fluorescence by FCCP validates the results of unsupervised unmixing of cell autofluorescence.
2 February 2017:
A new publication from CNBP researchers Wei Deng (pictured), Sandhya Clement and Ewa Goldys indicates that gold-loaded liposomes incorporating photosensitizers may serve as improved agents in photodynamic therapy and chemotherapy. The work has just been reported in the International Journal of Nanomedicine and is accessible online.
Journal: International Journal of Nanomedicine.
Title: Light-triggered liposomal cargo delivery platform incorporating photosensitizers and gold nanoparticles for enhanced singlet oxygen generation and increased cytotoxicity
Authors: Zofia Kautzka, Sandhya Clement, Ewa M Goldys and Wei Deng.
Abstract: We developed light-triggered liposomes incorporating 3–5 nm hydrophobic gold
nanoparticles and Rose Bengal (RB), a well-known photosensitizer used for photodynamic
therapy. Singlet oxygen generated by these liposomes with 532 nm light illumination was
characterized for varying the molar ratio of lipids and gold nanoparticles while keeping
the amount of RB constant. Gold nanoparticles were found to enhance the singlet oxygen
generation rate, with a maximum enhancement factor of 1.75 obtained for the molar ratio of hydrogenated soy l-α-phosphatidylcholine:1,2-dioleoyl-sn-glycero-3-hosphoethanolamineN-(hexanoylamine): gold of 57:5:17 compared with liposomes loaded with RB alone. The experimental results could be explained by the local electric field enhancement caused by gold nanoparticles. We further assessed cellular cytotoxicity of gold-loaded liposomes by encapsulating an antitumor drug, doxorubicin (Dox); such Dox-loaded liposomes were applied to human colorectal cancer cells (HCT116) and exposed to light. Gold-loaded liposomes containing RB and Dox where Dox release was triggered by light were found to exhibit higher cytotoxicity compared with the liposomes loaded with RB and Dox alone. Our results indicate that goldloaded liposomes incorporating photosensitizers may serve as improved agents in photodynamic therapy and chemotherapy.