Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.chemmater.9b01518
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dc.titlePhotosensitizer-Bacteria Biohybrids Promote Photodynamic Cancer Cell Ablation and Intracellular Protein Delivery
dc.contributor.authorWu, Min
dc.contributor.authorWu, Wenbo
dc.contributor.authorDuan, Yukun
dc.contributor.authorLi, Xueqi
dc.contributor.authorQi, Guobin
dc.contributor.authorLIU BIN
dc.date.accessioned2020-06-15T02:06:55Z
dc.date.available2020-06-15T02:06:55Z
dc.date.issued2019-09-24
dc.identifier.citationWu, Min, Wu, Wenbo, Duan, Yukun, Li, Xueqi, Qi, Guobin, LIU BIN (2019-09-24). Photosensitizer-Bacteria Biohybrids Promote Photodynamic Cancer Cell Ablation and Intracellular Protein Delivery. CHEMISTRY OF MATERIALS 31 (18) : 7212-7220. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.chemmater.9b01518
dc.identifier.issn08974756
dc.identifier.issn15205002
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/169747
dc.description.abstract© 2019 American Chemical Society. Live bacteria have drawn widespread interest as carriers to deliver genes and proteins into eukaryotic cells for the treatment of various cancer types owing to their good biocompatibility and active targeting ability. However, how to realize effective gene and protein release remains an issue and whether the bacteria could efficiently deliver therapeutic agents has not been successfully realized. Herein, we report a new biohybrid system composed of aggregation-induced emission photosensitizer (PS) nanoparticles TDNPP-coated Escherichia coli (E. coli), which serve as a PS delivery vector for effective imaging and ablation of tumor cells. The TDNPP coating layer on the surface of E. coli could facilitate bacteria to invade cancer cells and efficiently release protein through the production of reactive oxygen species (ROS) upon light irradiation. Furthermore, multifunctional TDNPPs delivered by bacteria have also achieved enhanced cancer cell imaging and effective light-mediated cancer killing in vitro as compared to the same PS NPs without the bacteria carrier. Our study thus presents an alternative strategy to optimize bacteria-mediated cancer therapy and intracellular protein delivery.
dc.language.isoen
dc.publisherAMERICAN CHEMICAL SOCIETY
dc.sourceElements
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectTechnology
dc.subjectChemistry, Physical
dc.subjectMaterials Science, Multidisciplinary
dc.subjectChemistry
dc.subjectMaterials Science
dc.subjectAGGREGATION-INDUCED-EMISSION
dc.subjectLIGHT-UP PROBE
dc.subjectCOATED BACTERIA
dc.subjectNANOPARTICLES
dc.subjectSALMONELLA
dc.subjectAIE
dc.subjectPERMEABILITY
dc.subjectTHERAPY
dc.typeArticle
dc.date.updated2020-06-09T02:18:37Z
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/acs.chemmater.9b01518
dc.description.sourcetitleCHEMISTRY OF MATERIALS
dc.description.volume31
dc.description.issue18
dc.description.page7212-7220
dc.published.statePublished
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