Citation Export
DC Field | Value | Language |
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dc.contributor.author | Yoo, Jihye | - |
dc.contributor.author | Choi, Sangkee | - |
dc.contributor.author | Son, Jihwan | - |
dc.contributor.author | Yi, Gawon | - |
dc.contributor.author | Kim, Eunha | - |
dc.contributor.author | Koo, Heebeom | - |
dc.date.issued | 2019-07-12 | - |
dc.identifier.uri | https://dspace.ajou.ac.kr/dev/handle/2018.oak/30725 | - |
dc.description.abstract | For 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.sponsorship | This 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.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.subject.mesh | Animals | - |
dc.subject.mesh | Cell Line, Tumor | - |
dc.subject.mesh | Click Chemistry | - |
dc.subject.mesh | Cyclooctanes | - |
dc.subject.mesh | Drug Delivery Systems | - |
dc.subject.mesh | Irinotecan | - |
dc.subject.mesh | Mice, Inbred BALB C | - |
dc.subject.mesh | Mice, Nude | - |
dc.subject.mesh | Nanoparticles | - |
dc.subject.mesh | Neoplasms, Experimental | - |
dc.subject.mesh | Protein Binding | - |
dc.subject.mesh | Receptor, ErbB-2 | - |
dc.subject.mesh | Tissue Distribution | - |
dc.subject.mesh | Topoisomerase I Inhibitors | - |
dc.subject.mesh | Trastuzumab | - |
dc.title | Click chemistry-mediated tumor-targeting of SN38-loaded nanoparticles using trastuzumab | - |
dc.type | Article | - |
dc.citation.endPage | 213 | - |
dc.citation.startPage | 207 | - |
dc.citation.title | Biochemical and Biophysical Research Communications | - |
dc.citation.volume | 515 | - |
dc.identifier.bibliographicCitation | Biochemical and Biophysical Research Communications, Vol.515, pp.207-213 | - |
dc.identifier.doi | 10.1016/j.bbrc.2019.05.128 | - |
dc.identifier.pmid | 31146921 | - |
dc.identifier.scopusid | 2-s2.0-85066085527 | - |
dc.identifier.url | http://www.sciencedirect.com/science/journal/0006291X | - |
dc.subject.keyword | Click chemistry | - |
dc.subject.keyword | Drug delivery | - |
dc.subject.keyword | In vivo imaging | - |
dc.subject.keyword | Nanoparticle | - |
dc.subject.keyword | SN38 | - |
dc.subject.keyword | Trastuzumab | - |
dc.description.isoa | false | - |
dc.subject.subarea | Biophysics | - |
dc.subject.subarea | Biochemistry | - |
dc.subject.subarea | Molecular Biology | - |
dc.subject.subarea | Cell Biology | - |
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