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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
Citations

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Publication Year
2019-07-12
Publisher
Elsevier B.V.
Citation
Biochemical and Biophysical Research Communications, Vol.515, pp.207-213
Keyword
Click chemistryDrug deliveryIn vivo imagingNanoparticleSN38Trastuzumab
Mesh Keyword
AnimalsCell Line, TumorClick ChemistryCyclooctanesDrug Delivery SystemsIrinotecanMice, Inbred BALB CMice, NudeNanoparticlesNeoplasms, ExperimentalProtein BindingReceptor, ErbB-2Tissue DistributionTopoisomerase I InhibitorsTrastuzumab
All Science Classification Codes (ASJC)
BiophysicsBiochemistryMolecular BiologyCell Biology
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.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30725
DOI
https://doi.org/10.1016/j.bbrc.2019.05.128
Fulltext

Type
Article
Funding
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 ).
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Kim, Eun ha김은하
College of Bio-convergence Engineering
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