<HashMap><database>biostudies-literature</database><scores/><additional><submitter>He S</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>National Natural Science Foundation of China</funding><pagination>8817-8827</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8163376</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(33)</volume><pubmed_abstract>Carrying out the &lt;i>in vivo&lt;/i> syntheses of drugs toxic to tumors based on the specific features of the tumor microenvironment is critical for ensuring specific antitumor efficacy. However, achieving &lt;i>in situ&lt;/i> high-yield synthetic toxic drugs from non-toxic agents and reducing their drug resistance in hypoxic tumors remain challenges. Herein we created a tumor-microenvironment-responsive porous Pt/Pt(iv) methylene blue coordination polymer nanoshuttle (Pt/PtMBCPNS) photosensitizer with spatiotemporally controlled O&lt;sub>2&lt;/sub> and singlet oxygen (&lt;sup>1&lt;/sup>O&lt;sub>2&lt;/sub>) self-sufficient for the &lt;i>in vivo&lt;/i> high-yield synthesis of drugs and efficient hypoxic tumor therapy. After being endocytosed, the nanophotosensitizer as a cascade catalyst was observed to effectively catalyze </pubmed_abstract><journal>Chemical science</journal><pubmed_title>Spatiotemporally controlled O&lt;sub>2&lt;/sub> and singlet oxygen self-sufficient nanophotosensitizers enable the &lt;i>in vivo&lt;/i> high-yield synthesis of drugs and efficient hypoxic tumor therapy.</pubmed_title><pmcid>PMC8163376</pmcid><funding_grant_id>lzujbky-2018-it03</funding_grant_id><funding_grant_id>21671088</funding_grant_id><funding_grant_id>21904052</funding_grant_id><funding_grant_id>21977041</funding_grant_id><funding_grant_id>21431002</funding_grant_id><funding_grant_id>lzujbky-2019-kb12</funding_grant_id><funding_grant_id>21876072</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Chen F</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>He S</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Sun S</pubmed_authors><pubmed_authors>Lu S</pubmed_authors><pubmed_authors>Liang K</pubmed_authors><pubmed_authors>Hai J</pubmed_authors><pubmed_authors>Meng G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spatiotemporally controlled O&lt;sub>2&lt;/sub> and singlet oxygen self-sufficient nanophotosensitizers enable the &lt;i>in vivo&lt;/i> high-yield synthesis of drugs and efficient hypoxic tumor therapy.</name><description>Carrying out the &lt;i>in vivo&lt;/i> syntheses of drugs toxic to tumors based on the specific features of the tumor microenvironment is critical for ensuring specific antitumor efficacy. However, achieving &lt;i>in situ&lt;/i> high-yield synthetic toxic drugs from non-toxic agents and reducing their drug resistance in hypoxic tumors remain challenges. Herein we created a tumor-microenvironment-responsive porous Pt/Pt(iv) methylene blue coordination polymer nanoshuttle (Pt/PtMBCPNS) photosensitizer with spatiotemporally controlled O&lt;sub>2&lt;/sub> and singlet oxygen (&lt;sup>1&lt;/sup>O&lt;sub>2&lt;/sub>) self-sufficient for the &lt;i>in vivo&lt;/i> high-yield synthesis of drugs and efficient hypoxic tumor therapy. After being endocytosed, the nanophotosensitizer as a cascade catalyst was observed to effectively catalyze </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-05T10:31:07.099Z</modification><creation>2022-02-10T14:43:29.398Z</creation></dates><accession>S-EPMC8163376</accession><cross_references><pubmed>34123135</pubmed><doi>10.1039/d0sc02387f</doi></cross_references></HashMap>