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Click chemistry-mediated tumor-targeting of SN38-loaded nanoparticles using trastuzumab
  • Yoo, Jihye ;
  • Choi, Sangkee ;
  • Son, Jihwan ;
  • Yi, Gawon ;
  • Kim, Eunha ;
  • Koo, Heebeom
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dc.contributor.authorYoo, Jihye-
dc.contributor.authorChoi, Sangkee-
dc.contributor.authorSon, Jihwan-
dc.contributor.authorYi, Gawon-
dc.contributor.authorKim, Eunha-
dc.contributor.authorKoo, Heebeom-
dc.date.issued2019-07-12-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/30725-
dc.description.abstractFor efficient drug delivery, we introduce a click-chemistry-mediated two-step tumor-targeting strategy for nanoparticles (NPs). We modified HER2-binding trastuzumab with trans-cyclooctene (TCO-Trb), and fabricated tetrazine-modified NPs containing the anticancer drug, SN38 (SN38-Tz-NPs). To target tumor cells with the Tz-NPs, the tumor cells are first treated with TCO-Trb. The TCO-Trb binds HER2s and presents multiple TCO groups on the cell surface. Subsequently, the cells are treated with SN38-Tz-NPs that can bind the cell surface via click chemistry between Tz and TCO. This click chemistry-mediated binding resulted in enhanced tumor-targeting of Tz-NPs to the target tumor cells. In our study, this strategy was performed and analyzed in vitro and in vivo, and the results show that this is a promising strategy for tumor-targeted drug delivery by NPs.-
dc.description.sponsorshipThis work was supported by Basic Research Program ( 2016R1C1B3013951 ) through the National Research Foundation of Korea funded by the Korean Government ( Ministry of Science, ICT, & Future Planning ).-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.subject.meshAnimals-
dc.subject.meshCell Line, Tumor-
dc.subject.meshClick Chemistry-
dc.subject.meshCyclooctanes-
dc.subject.meshDrug Delivery Systems-
dc.subject.meshIrinotecan-
dc.subject.meshMice, Inbred BALB C-
dc.subject.meshMice, Nude-
dc.subject.meshNanoparticles-
dc.subject.meshNeoplasms, Experimental-
dc.subject.meshProtein Binding-
dc.subject.meshReceptor, ErbB-2-
dc.subject.meshTissue Distribution-
dc.subject.meshTopoisomerase I Inhibitors-
dc.subject.meshTrastuzumab-
dc.titleClick chemistry-mediated tumor-targeting of SN38-loaded nanoparticles using trastuzumab-
dc.typeArticle-
dc.citation.endPage213-
dc.citation.startPage207-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.volume515-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, Vol.515, pp.207-213-
dc.identifier.doi10.1016/j.bbrc.2019.05.128-
dc.identifier.pmid31146921-
dc.identifier.scopusid2-s2.0-85066085527-
dc.identifier.urlhttp://www.sciencedirect.com/science/journal/0006291X-
dc.subject.keywordClick chemistry-
dc.subject.keywordDrug delivery-
dc.subject.keywordIn vivo imaging-
dc.subject.keywordNanoparticle-
dc.subject.keywordSN38-
dc.subject.keywordTrastuzumab-
dc.description.isoafalse-
dc.subject.subareaBiophysics-
dc.subject.subareaBiochemistry-
dc.subject.subareaMolecular Biology-
dc.subject.subareaCell Biology-
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College of Bio-convergence Engineering
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