scholarly journals Terahertz toroidal metasurface biosensor for sensitive distinction of lung cancer cells

Nanophotonics ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Chiben Zhang ◽  
Tingjia Xue ◽  
Jin Zhang ◽  
Longhai Liu ◽  
Jianhua Xie ◽  
...  

Abstract Lung cancer is the most frequently life-threatening disease and the prominent cause of cancer-related mortality among human beings worldwide, where poor early diagnosis and expensive detection costs are considered as significant reasons. Here, we try to tackle this issue by proposing a novel label-free and low-cost strategy for rapid detection and distinction of lung cancer cells relying on plasmonic toroidal metasurfaces at terahertz frequencies. Three disjoint regions are displayed in identifiable intensity-frequency diagram, which could directly help doctors determine the type of lung cancer cells for clinical treatment. The metasurface is generated by two mirrored gold split ring resonators with subwavelength sizes. When placing analytes on the metasurface, apparent shifts of both the resonance frequency and the resonance depth can be observed in the terahertz transmission spectra. The theoretical sensitivity of the biosensor over the reflective index reaches as high as 485.3 GHz/RIU. Moreover, the proposed metasurface shows high angular stability for oblique incident angle from 0 to 30°, where the maximum resonance frequency shift is less than 0.66% and the maximum transmittance variation keeps below 1.33%. To experimentally verify the sensing strategy, three types of non-small cell lung cancer cells (Calu-1, A427, and 95D) are cultured with different concentrations and their terahertz transmission spectra are measured with the proposed metasurface biosensor. The two-dimensional fingerprint diagram considering both the frequency and transmittance variations of the toroidal resonance dip is obtained, where the curves for different cells are completely separated with each other. This implies that we can directly distinguish the type of the analyte cells and its concentration by only single spectral measurement. We envisage that the proposed strategy has potential for clinical diagnosis and significantly expands the capabilities of plasmonic metamaterials in biological detection.

2020 ◽  
Vol 56 (13) ◽  
pp. 2055-2055
Author(s):  
Lin Cui ◽  
Meng Wang ◽  
Bing Sun ◽  
Shiyun Ai ◽  
Shaocong Wang ◽  
...  

Correction for ‘Substrate-free and label-free electrocatalysis-assisted biosensor for sensitive detection of microRNA in lung cancer cells’ by Lin Cui et al., Chem. Commun., 2019, 55, 1172–1175.


2014 ◽  
Vol 37 (6) ◽  
pp. 457-466 ◽  
Author(s):  
Hophil Min ◽  
Dohyun Han ◽  
Yikwon Kim ◽  
Jee Yeon Cho ◽  
Jonghwa Jin ◽  
...  

2019 ◽  
Vol 55 (8) ◽  
pp. 1172-1175 ◽  
Author(s):  
Lin Cui ◽  
Meng Wang ◽  
Bing Sun ◽  
Shiyun Ai ◽  
Shaocong Wang ◽  
...  

We develop a substrate-free and label-free electrocatalysis-assisted biosensor for sensitive detection of microRNA with FeCN as the catalytic element.


2018 ◽  
Vol 40 ◽  
pp. 505-518 ◽  
Author(s):  
Suman Shrestha ◽  
Aditi Deshpande ◽  
Tannaz Farrahi ◽  
Thomas Cambria ◽  
Tri Quang ◽  
...  

2017 ◽  
Vol 5 (1) ◽  
Author(s):  
Lingyan Wang ◽  
Jiayun Hou ◽  
Minghuan Zheng ◽  
Lin Shi

Actinidia Chinensis Planch roots (acRoots) are used to treat many cancers, although the anti-tumor mechanism by which acRoots inhibit cancer cell growth remains unclear. The present study aims at investigating inhibitory effects of acRoots on human lung cancer cells and potential mechanisms. Our data demonstrate that the inhibitory effects of acRoots on lung cancer cells depend on genetic backgrounds and phenotypes of cells. We furthermore found the expression of metabolism-associated gene profiles varied between acRoots-hypersensitive (H460) or hyposensitive lung cancer cells (H1299) after screening lung cancer cells with different genetic backgrounds. We selected retinoic acid receptor beta (RARB) as the core target within metabolism-associated core gene networks and evaluated RARB changes and roles in cells treated with acRoots at different concentrations and timeframes. Hypersensitive cancer cells with the deletion of RARB expression did not response to the treatment with acRoots, while RARB deletion did not change effects of acRoots on hyposensitive cells. Thus, it seems that RARB as the core target within metabolism-associated networks plays important roles in the regulation of lung cancer cell sensitivity to acRoots.


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