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作 者:Bing Lu Yuying Huang Jiachen Xia Yong Yao
机构地区:[1]College of Chemistry and Chemical Engineering,Nantong University,Nantong 226019,China
出 处:《Frontiers of Chemical Science and Engineering》2024年第11期391-398,共8页化学科学与工程前沿(英文版)
基 金:National Natural Science Foundation of China(Grant No.32301184);Universities Natural Science Research Project of Jiangsu Province(Grant No.23KJB150027).
摘 要:Nowadays,although functionalized pillararenes have been widely designed to be used in drug delivery system,targeted group modified pillararenes have been seldom reported and used in tumor multimodal therapy.Herein,a functionalized pillararene with a polyethylene glycol chain and triphenylphosphonium cation WP5-PEG-TPP was designed and synthesized.Subsequently,an active targeted drug delivery system was constructed based on its host-guest interactions with a newly designed porphyrin derivative,Py-Por.The experimental results demonstrated that this drug delivery system has exhibited excellent targeting ability against tumor cells,but interestingly it could not enter normal cells.After loading the hypoxia-activated prodrug tirapazamine,the prepared nanodrugs displayed high lethality to tumor cells due to their chemo/photodynamic synergistic therapy capability,but negligible toxicity to normal cells.Preliminary therapeutic mechanism study elucidated the synergistic therapy process.
关 键 词:durg delivery system active targeting pillararene chemo photodynamic synergistic therapy
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