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authors |
Monteiro, AR; Ramos, CIV; Fateixa, S; Moura, NMM; Neves, MGPMS; Trindade, T |
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nationality |
International |
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journal |
ACS OMEGA |
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keywords |
CATIONIC PORPHYRIN; PHOTOTHERMAL THERAPY; BRAIN CANCER; LIGANDS; FUNCTIONALIZATION; RECOGNITION; DERIVATIVES; TELOMERASE; SURFACE; RAMAN |
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abstract |
Telomerase inhibition has been an important strategy in cancer therapies, but for which effective drugs are still required. Here, noncovalent hybrid nanoplatforms containing the tetracationic 5,10,15,20-tetrakis(1-methyl-pyridinium-4-yl) porphyrin (TMPyP) and graphene oxide (GO) were prepared for promoting telomerase inhibition through the selective detection and stabilization of DNA guanine-quadruplex (G-Q) structures. Upon binding TMPyP to the GO sheets, the typical absorption bands of porphyrin have been red-shifted and the fluorescence emission was quenched. Raman mapping was used for the first time to provide new insights into the role of the electrostatic and pi-pi stacking interactions in the formation of such hybrids. The selective recovery of fluorescence observed during the titration of TMPyP@GO with G-Q, resembles a selective "turn-off-on" fluorescence sensor for the detection of G-Q, paving the way for a new class of antitumor drugs. |
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publisher |
AMER CHEMICAL SOC |
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issn |
2470-1343 |
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year published |
2018 |
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volume |
3 |
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issue |
9 |
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beginning page |
11184 |
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ending page |
11191 |
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digital object identifier (doi) |
10.1021/acsomega.8b01366 |
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web of science category |
Chemistry, Multidisciplinary |
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subject category |
Chemistry |
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unique article identifier |
WOS:000446186000082
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ciceco authors
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