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.
Original language | English |
---|---|
Pages (from-to) | 207-213 |
Number of pages | 7 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 515 |
Issue number | 1 |
DOIs | |
State | Published - 12 Jul 2019 |
Bibliographical note
Funding Information: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 ).
Publisher Copyright:
© 2019 Elsevier Inc.
Keywords
- Click chemistry
- Drug delivery
- In vivo imaging
- Nanoparticle
- SN38
- Trastuzumab