<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li A</submitter><funding>Science and Technology Commission of Shanghai Municipality</funding><funding>Cooperation Program of the Xuhui District Medical College with Enterprises</funding><funding>Program of National Key Research and Development</funding><funding>Young Scientists Fund of the National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China</funding><pagination>e2414307</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11884613</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(9)</volume><pubmed_abstract>Pulmonary metastasis represents one of the most prevalent forms of metastasis in advanced melanoma, with mortality rates reaching 70%. Current treatments including chemotherapy, targeted therapy, and immunotherapy frequently exhibit limited efficacy or present high costs. To address these clinical needs, this study presents a biomimetic drug delivery system (Ce6-pTP-CsA) utilizing cryoshocked adipocytes (CsA) encapsulating the prodrug triptolide palmitate (pTP) and the photosensitizer Ce6, exploiting the characteristic of tumor cells to recruit and lipolyze adipocytes for energy. CsA substantially enhances the drug-loading capacity of adipocytes, with its particle size characteristics enabling targeted delivery of pTP to the lungs. The combination of photodynamic therapy (PDT) and pTP acti</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Cryoshocked Adipocytes Mediated Dual-Modal Strategy Combining Photodynamic Therapy and Triptolide Palmitate for Pulmonary Metastatic Melanoma Treatment.</pubmed_title><pmcid>PMC11884613</pmcid><funding_grant_id>2023YFC3404103</funding_grant_id><funding_grant_id>23XHYD-24</funding_grant_id><funding_grant_id>82274103</funding_grant_id><funding_grant_id>82305039</funding_grant_id><funding_grant_id>82074272</funding_grant_id><funding_grant_id>24S11901500</funding_grant_id><funding_grant_id>23S21900200</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Qi F</pubmed_authors><pubmed_authors>He M</pubmed_authors><pubmed_authors>Li A</pubmed_authors><pubmed_authors>Liu R</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Cai H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cryoshocked Adipocytes Mediated Dual-Modal Strategy Combining Photodynamic Therapy and Triptolide Palmitate for Pulmonary Metastatic Melanoma Treatment.</name><description>Pulmonary metastasis represents one of the most prevalent forms of metastasis in advanced melanoma, with mortality rates reaching 70%. Current treatments including chemotherapy, targeted therapy, and immunotherapy frequently exhibit limited efficacy or present high costs. To address these clinical needs, this study presents a biomimetic drug delivery system (Ce6-pTP-CsA) utilizing cryoshocked adipocytes (CsA) encapsulating the prodrug triptolide palmitate (pTP) and the photosensitizer Ce6, exploiting the characteristic of tumor cells to recruit and lipolyze adipocytes for energy. CsA substantially enhances the drug-loading capacity of adipocytes, with its particle size characteristics enabling targeted delivery of pTP to the lungs. The combination of photodynamic therapy (PDT) and pTP acti</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-20T01:50:55.263Z</modification><creation>2025-04-20T01:50:55.263Z</creation></dates><accession>S-EPMC11884613</accession><cross_references><pubmed>39804941</pubmed><doi>10.1002/advs.202414307</doi></cross_references></HashMap>