<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Wang H</submitter><pubmed_abstract>Nanoprobes for combined optical and magnetic resonance imaging have tremendous potential in early cancer diagnosis. Gold nanoparticles (AuNPs) co-doped with Gd&lt;sub>2&lt;/sub>O&lt;sub>3&lt;/sub> mesoporous silica nanocomposite (Au/Gd@MCM-41) can produce pronounced contrast enhancement for T1 weighted image in magnetic resonance imaging (MRI). Here, we show the remarkably high sensitivity of Au/Gd@MCM-41 to the human poorly differentiated nasopharyngeal carcinoma (NPC) cell line (CNE-2) using fluorescence lifetime imaging (FLIM). The upconversion luminescences from CNE-2 and the normal nasopharyngeal (NP) cells (NP69) after uptake of Au/Gd@MCM-41 show the characteristic of two-photon-induced-radiative recombination of the AuNPs. The presence of the Gd&lt;sup>3+&lt;/sup> ion induces a much shorter luminescence lifetime in CNE-2 cells. The interaction between AuNPs and Gd&lt;sup>3+&lt;/sup> ion clearly enhances the optical sensitivity of Au/Gd@MCM-41 to CNE-2. Furthermore, the difference in the autofluorescence between CNE-2 and NP69 cells can be efficiently demonstrated by the emission lifetimes of Au/Gd@MCM-41 through the Forster energy transfers from the endogenous fluorophores to AuNPs. The results suggest that Au/Gd@MCM-41 may impart high optical resolution for the FLIM imaging that differentiates normal and high-grade precancers.</pubmed_abstract><journal>Scientific reports</journal><pagination>34367</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5046069</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High sensitivity of gold nanoparticles co-doped with Gd&lt;sub>2&lt;/sub>O&lt;sub>3&lt;/sub> mesoporous silica nanocomposite to nasopharyngeal carcinoma cells.</pubmed_title><pmcid>PMC5046069</pmcid><pubmed_authors>Shao Y</pubmed_authors><pubmed_authors>Tian X</pubmed_authors><pubmed_authors>Hu W</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Li L</pubmed_authors></additional><is_claimable>false</is_claimable><name>High sensitivity of gold nanoparticles co-doped with Gd&lt;sub>2&lt;/sub>O&lt;sub>3&lt;/sub> mesoporous silica nanocomposite to nasopharyngeal carcinoma cells.</name><description>Nanoprobes for combined optical and magnetic resonance imaging have tremendous potential in early cancer diagnosis. Gold nanoparticles (AuNPs) co-doped with Gd&lt;sub>2&lt;/sub>O&lt;sub>3&lt;/sub> mesoporous silica nanocomposite (Au/Gd@MCM-41) can produce pronounced contrast enhancement for T1 weighted image in magnetic resonance imaging (MRI). Here, we show the remarkably high sensitivity of Au/Gd@MCM-41 to the human poorly differentiated nasopharyngeal carcinoma (NPC) cell line (CNE-2) using fluorescence lifetime imaging (FLIM). The upconversion luminescences from CNE-2 and the normal nasopharyngeal (NP) cells (NP69) after uptake of Au/Gd@MCM-41 show the characteristic of two-photon-induced-radiative recombination of the AuNPs. The presence of the Gd&lt;sup>3+&lt;/sup> ion induces a much shorter luminescence lifetime in CNE-2 cells. The interaction between AuNPs and Gd&lt;sup>3+&lt;/sup> ion clearly enhances the optical sensitivity of Au/Gd@MCM-41 to CNE-2. Furthermore, the difference in the autofluorescence between CNE-2 and NP69 cells can be efficiently demonstrated by the emission lifetimes of Au/Gd@MCM-41 through the Forster energy transfers from the endogenous fluorophores to AuNPs. The results suggest that Au/Gd@MCM-41 may impart high optical resolution for the FLIM imaging that differentiates normal and high-grade precancers.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2025-04-18T18:37:39.09Z</modification><creation>2019-03-27T02:25:40Z</creation></dates><accession>S-EPMC5046069</accession><cross_references><pubmed>27694966</pubmed><doi>10.1038/srep34367</doi></cross_references></HashMap>