Liposome-Based Engineering of Cells To Package Hydrophobic Compounds in Membrane Vesicles for Tumor Penetration

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dc.contributor.authorLee, Jun Sungko
dc.contributor.authorKim, Ji-Youngko
dc.contributor.authorJeong, Moonkyoungko
dc.contributor.authorLee, Hyoungjinko
dc.contributor.authorGoh, Unbyeolko
dc.contributor.authorKim, Hyaeyeongko
dc.contributor.authorKim, Byungjiko
dc.contributor.authorPark, Ji-Hoko
dc.date.accessioned2015-06-29T04:46:06Z-
dc.date.available2015-06-29T04:46:06Z-
dc.date.created2015-06-23-
dc.date.created2015-06-23-
dc.date.created2015-06-23-
dc.date.issued2015-05-
dc.identifier.citationNANO LETTERS, v.15, no.5, pp.2938 - 2944-
dc.identifier.issn1530-6984-
dc.identifier.urihttp://hdl.handle.net/10203/199477-
dc.description.abstractNatural membrane vesicles (MVs) derived from various types of cells play an essential role in transporting biological materials between cells. Here, we show that exogenous compounds are packaged in the MVs by engineering the parental cells via liposomes, and the MVs mediate autonomous intercellular migration of the compounds through multiple cancer cell layers. Hydrophobic compounds delivered selectively to the plasma membrane of cancer cells using synthetic membrane fusogenic liposomes were efficiently incorporated into the membrane of MVs secreted from the cells and then transferred to neighboring cells via the MVs. This liposome-mediated MV engineering strategy allowed hydrophobic photosensitizers to significantly penetrate both spheroids and in vivo tumors, thereby enhancing the therapeutic efficacy. These results suggest that innate biological transport systems can be in situ engineered via synthetic liposomes to guide the penetration of chemotherapeutics across challenging tissue barriers in solid tumors.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleLiposome-Based Engineering of Cells To Package Hydrophobic Compounds in Membrane Vesicles for Tumor Penetration-
dc.typeArticle-
dc.identifier.wosid000354906000026-
dc.identifier.scopusid2-s2.0-84929166867-
dc.type.rimsART-
dc.citation.volume15-
dc.citation.issue5-
dc.citation.beginningpage2938-
dc.citation.endingpage2944-
dc.citation.publicationnameNANO LETTERS-
dc.identifier.doi10.1021/nl5047494-
dc.contributor.localauthorPark, Ji-Ho-
dc.contributor.nonIdAuthorJeong, Moonkyoung-
dc.contributor.nonIdAuthorLee, Hyoungjin-
dc.contributor.nonIdAuthorGoh, Unbyeol-
dc.contributor.nonIdAuthorKim, Hyaeyeong-
dc.contributor.nonIdAuthorKim, Byungji-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorLiposome-
dc.subject.keywordAuthorMembrane vesicle-
dc.subject.keywordAuthornanomedicine-
dc.subject.keywordAuthorphotosensitizer-
dc.subject.keywordAuthorspheroid-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusSOLID TUMORS-
dc.subject.keywordPlusEXOSOMES-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusMICRORNA-
dc.subject.keywordPlusEXCHANGE-
dc.subject.keywordPlusDRUGS-
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