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However, their synergistic anticancer efficacy is often limited by tumor hypoxia, and thermotolerance induced by high expression of heat shock proteins (HSP). Fortunately, hydrogen sulfide (H\n                    <jats:sub>2<\/jats:sub>\n                    S), known for its direct cytotoxic effect on tumor cells, has been recognized for its ability to enhance PTT and PDT. The effectiveness of H\n                    <jats:sub>2<\/jats:sub>\n                    S in these therapies is challenged by its low loading efficiency, poor stability, and short diffusion distance. To address these issues, a nanoscale emulsion drop template created through the salting\u2010out effect is employed to construct a robust H\n                    <jats:sub>2<\/jats:sub>\n                    S delivery system. Polydopamine (PDA), chosen for its interfacial polymerization tendency and excellent photothermal conversion rate, is utilized as a carrier for the H\n                    <jats:sub>2<\/jats:sub>\n                    S donor (ADT) and Zinc phthalocyanine (ZnPc) to fabricate a novel nanomedicine termed APZ NPs. The temperature\u2010responsive APZ NPs are designed to release H\n                    <jats:sub>2<\/jats:sub>\n                    S during the PTT process. Elevated H\n                    <jats:sub>2<\/jats:sub>\n                    S levels promoted vasodilation, thereby enhancing the enhanced permeability and retention effect (EPR) of APZ NPs within solid tumors. This strategy effectively alleviated tumor hypoxia by disrupting the mitochondrial respiratory chain and mitigated tumor cell heat tolerance by inhibiting HSP expression.\n                  <\/jats:p>","DOI":"10.1002\/adhm.202400803","type":"journal-article","created":{"date-parts":[[2024,7,22]],"date-time":"2024-07-22T05:08:18Z","timestamp":1721624898000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["Hydrogen Sulfide Delivery System Based on Salting\u2010Out Effect for Enhancing Synergistic Photothermal and Photodynamic Cancer Therapies"],"prefix":"10.1002","volume":"13","author":[{"given":"Aimei","family":"Zhang","sequence":"first","affiliation":[{"name":"Animal\u2010Derived Chinese Medicine and Functional Peptides International Collaboration Joint Laboratory School of Pharmacy Nanjing University of Chinese Medicine  Nanjing Jiangsu 210023 P. R. 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