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dc.contributor.authorZeng, Xin
dc.contributor.authorSun, Jie
dc.contributor.authorLi, Suping
dc.contributor.authorShi, Jiyun
dc.contributor.authorGao, Han
dc.contributor.authorSun Leong, Wei
dc.contributor.authorWu, Yiqi
dc.contributor.authorLi, Minghui
dc.contributor.authorLiu, Chengxin
dc.contributor.authorLi, Ping
dc.contributor.authorKong, Jing
dc.contributor.authorWu, Yi-Zhou
dc.contributor.authorNie, Guangjun
dc.contributor.authorFu, Yuming
dc.contributor.authorZhang, Gen
dc.date.accessioned2022-02-10T20:20:34Z
dc.date.available2021-09-20T18:21:34Z
dc.date.available2022-02-10T20:20:34Z
dc.date.issued2020-01
dc.date.submitted2019-06
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/1721.1/132267.2
dc.description.abstract© 2020, The Author(s). Since the discovery of metal nanoparticles (NPs) in the 1960s, unknown toxicity, cost and the ethical hurdles of research in humans have hindered the translation of these NPs to clinical use. In this work, we demonstrate that Pt NPs with protein coronas are generated in vivo in human blood when a patient is treated with cisplatin. These self-assembled Pt NPs form rapidly, accumulate in tumors, and remain in the body for an extended period of time. Additionally, the Pt NPs are safe for use in humans and can act as anti-cancer agents to inhibit chemotherapy-resistant tumor growth by consuming intracellular glutathione and activating apoptosis. The tumor inhibitory activity is greatly amplified when the Pt NPs are loaded in vitro with the chemotherapeutic drug, daunorubicin, and the formulation is effective even in daunorubicin-resistant models. These in vivo-generated metal NPs represent a biocompatible drug delivery platform for chemotherapy resistant tumor treatment.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41467-019-14131-zen_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleBlood-triggered generation of platinum nanoparticle functions as an anti-cancer agenten_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-01-08T17:03:15Z
dspace.orderedauthorsZeng, X; Sun, J; Li, S; Shi, J; Gao, H; Sun Leong, W; Wu, Y; Li, M; Liu, C; Li, P; Kong, J; Wu, Y-Z; Nie, G; Fu, Y; Zhang, Gen_US
dspace.date.submission2021-01-08T17:03:23Z
mit.journal.volume11en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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