<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(7)</volume><submitter>Han X</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Currently, the prognosis and survival rate for patients bearing non-small cell lung cancer (NSCLC) is still quite poor, mainly due to lack of efficient theranostic paradigms to exert in time diagnostics and therapeutics. &lt;b>Methods:&lt;/b> Herein, for NSCLC treatment, we offer a customized theranostic paradigm, termed NIR-IIb fluorescence diagnosis and synergistic surgery/starvation/chemodynamic therapeutics, with a newly designed theranostic nanoplatform PEG/MnCuDCNPs@GOx. The nanoplatform is composed of brightly NIR-II emissive downconversion nanoparticles (DCNPs)-core and Mn/Cu-silica shell loaded with glucose oxidase (GOx) to achieve synergistic starvation and chemodynamic therapy (CDT). &lt;b>Results:&lt;/b> It is found that 10% Ce&lt;sup>3+&lt;/sup> doped in the core and 100% Yb&lt;sup>3+&lt;/sup> doped in the middle shell greatly improves the NIR-IIb emission up to even 20.3 times as compared to the core-shell DCNPs without Ce&lt;sup>3+&lt;/sup> doping and middle shell. The bright NIR-IIb emission of the nanoplatform contributes to sensitive margin delineation of early-stage NSCLC (diameter &lt; 1 mm) with a signal-to-background ratio (SBR) of 2.18, and further assists in visualizing drug distribution and guiding surgery/starvation/chemodynamic therapy. Notably, the starvation therapy mediated by GOx-driven oxidation reaction efficiently depletes intratumoral glucose, and supplies H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> to boost the CDT mediated by the Mn&lt;sup>2+&lt;/sup> and Cu&lt;sup>2+&lt;/sup>, which consequently realized a highly effective synergistic treatment for NSCLC. &lt;b>Conclusion:&lt;/b> This research demonstrates an efficient treatment paradigm for NSCLC with NIR-IIb fluorescence diganosis and image-guided synergistic surgery/starvation/chemodynamic therapeutics.</pubmed_abstract><journal>Theranostics</journal><pagination>2176-2191</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10157733</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>NIR-IIb fluorescence-image guided synergistic surgery/starvation/chemodynamic therapy: an innovative treatment paradigm for malignant non-small cell lung cancers.</pubmed_title><pmcid>PMC10157733</pmcid><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Meng Q</pubmed_authors><pubmed_authors>Han X</pubmed_authors><pubmed_authors>Zhong Y</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Feng C</pubmed_authors><pubmed_authors>Dai X</pubmed_authors><pubmed_authors>Lan Z</pubmed_authors><pubmed_authors>Ma C</pubmed_authors><pubmed_authors>He Z</pubmed_authors><pubmed_authors>Gu J</pubmed_authors><pubmed_authors>Mi C</pubmed_authors><pubmed_authors>Guo B</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>NIR-IIb fluorescence-image guided synergistic surgery/starvation/chemodynamic therapy: an innovative treatment paradigm for malignant non-small cell lung cancers.</name><description>&lt;b>Background:&lt;/b> Currently, the prognosis and survival rate for patients bearing non-small cell lung cancer (NSCLC) is still quite poor, mainly due to lack of efficient theranostic paradigms to exert in time diagnostics and therapeutics. &lt;b>Methods:&lt;/b> Herein, for NSCLC treatment, we offer a customized theranostic paradigm, termed NIR-IIb fluorescence diagnosis and synergistic surgery/starvation/chemodynamic therapeutics, with a newly designed theranostic nanoplatform PEG/MnCuDCNPs@GOx. The nanoplatform is composed of brightly NIR-II emissive downconversion nanoparticles (DCNPs)-core and Mn/Cu-silica shell loaded with glucose oxidase (GOx) to achieve synergistic starvation and chemodynamic therapy (CDT). &lt;b>Results:&lt;/b> It is found that 10% Ce&lt;sup>3+&lt;/sup> doped in the core and 100% Yb&lt;sup>3+&lt;/sup> doped in the middle shell greatly improves the NIR-IIb emission up to even 20.3 times as compared to the core-shell DCNPs without Ce&lt;sup>3+&lt;/sup> doping and middle shell. The bright NIR-IIb emission of the nanoplatform contributes to sensitive margin delineation of early-stage NSCLC (diameter &lt; 1 mm) with a signal-to-background ratio (SBR) of 2.18, and further assists in visualizing drug distribution and guiding surgery/starvation/chemodynamic therapy. Notably, the starvation therapy mediated by GOx-driven oxidation reaction efficiently depletes intratumoral glucose, and supplies H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> to boost the CDT mediated by the Mn&lt;sup>2+&lt;/sup> and Cu&lt;sup>2+&lt;/sup>, which consequently realized a highly effective synergistic treatment for NSCLC. &lt;b>Conclusion:&lt;/b> This research demonstrates an efficient treatment paradigm for NSCLC with NIR-IIb fluorescence diganosis and image-guided synergistic surgery/starvation/chemodynamic therapeutics.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-26T14:25:32.518Z</modification><creation>2025-04-06T14:37:07.855Z</creation></dates><accession>S-EPMC10157733</accession><cross_references><pubmed>37153731</pubmed><doi>10.7150/thno.83753</doi></cross_references></HashMap>