Synthesis, Characterization, and Application in HeLa Cells of an NIR Light Responsive Doxorubicin Delivery System Based on NaYF4:Yb,Tm@SiO2-PEG Nanoparticles
Source abstract
Abstract
Herein, we present a phototriggered drug delivery system based on light responsive nanoparticles, which is able to release doxorubicin upon NIR light illumination. The proposed system is based on upconversion fluorescence nanoparticles of β-NaYF4:Yb,Tm@SiO2-PEG with a mean diameter of 52±2.5 nm that absorb the NIR light and emit UV light. The UV radiation causes the degradation of photodegradable ortho-nitrobenzyl alcohol derivates, which are attached on one side to the surface of the nanoparticles and on the other to doxorubicin. This degradation triggers the doxorubicin release. This drug delivery system has been tested "in vitro" with HeLa cells. The results of this study demonstrated that this system caused negligible cytotoxicity when they were not illuminated with NIR light. In contrast, under NIR light illumination, the HeLa cell viability was conspicuously reduced. These results demonstrated the suitability of the proposed system to control the release of doxorubicin via an external NIR light stimulus.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Ga2O3 and related materials · Nanoplatforms for cancer theranostics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physical-Chemistry II, Pharmacy Faculty, Complutense University of Madrid, 28040 Madrid, Spain
Department of Chemical and Physical Biology, Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Ramiro de Maeztu 9, 28040 Madrid, Spain
Funding
European Cooperation in Science and Technology · Ministerio de Educación, Cultura y Deporte · Comunidad de Madrid · Ministerio de Economía y Competitividad
References (37)
Show source-provided references
1. Du J. · J. Am. Chem. Soc. · 2011 · 1756010.1021/ja207150n ↗
2. Dai Y. · ACS Nano · 2012 · 6 · 332710.1021/nn300303q ↗
3. You J. · ACS Nano · 2010 · 4 · 103310.1021/nn901181c ↗
4. Satarkar N. S. · Soft Matter · 2010 · 6 · 236410.1039/b925218p ↗
5. Tang L. · Mol. Pharmaceutics · 2013 · 10 · 88310.1021/mp300684a ↗
6. Wu E. C. · ACS Nano · 2008 · 2 · 240110.1021/nn800592q ↗
7. Gai S. · Adv. Funct. Mater. · 2010 · 20 · 116610.1002/adfm.200902274 ↗
8. Serrano-Ruiz D. · J. Biomed. Mater. Res., Part B · 2013 · 101 · 49810.1002/jbm.b.32792 ↗
9. Ruiz-Hernández E. · ACS Nano · 2011 · 5 · 125910.1021/nn1029229 ↗
10. Weaver C. · ACS Nano · 2014 · 8 · 183410.1021/nn406223e ↗
11. Alvarez-lorenzo C. · Photochem. Photobiol. · 2009 · 85 · 84810.1111/j.1751-1097.2008.00530.x ↗
12. Yuan Q. · ACS Nano · 2012 · 633710.1021/nn3018365 ↗
13. Liu J. · Angew. Chem., Int. Ed. · 2013 · 52 · 437510.1002/anie.201300183 ↗
14. Son S. · Biomacromolecules · 2014 · 15 · 62810.1021/bm401670t ↗
15. Chien Y. · ACS Nano · 2013 · 7 · 851610.1021/nn402399m ↗
16. Griffin D. R. · J. Am. Chem. Soc. · 2012 · 134 · 1310310.1021/ja305280w ↗
17. Luo Y.-L. · ACS Nano · 2011 · 5 · 779610.1021/nn201592s ↗
18. Ju E. · ACS Appl. Mater. Interfaces · 2014 · 6 · 436410.1021/am5000883 ↗
19. Yan B. · J. Am. Chem. Soc. · 2012 · 134 · 1655810.1021/ja308876j ↗
20. Wang F. · Nat. Mater. · 2011 · 10 · 96810.1038/nmat3149 ↗
21. Sedlmeier A. · Nanoscale · 2012 · 4 · 709010.1039/c2nr32314a ↗
22. Cui S. · ACS Nano · 2013 · 7 · 67610.1021/nn304872n ↗
23. Hao S. · Theranostics · 2013 · 3 · 33110.7150/thno.5305 ↗
24. Dai Y. · J. Am. Chem. Soc. · 2013 · 135 · 1892010.1021/ja410028q ↗
25. Zhao H. · Macromolecules · 2012 · 172310.1021/ma201924h ↗
26. Pelliccioli A. P. · Photochem. Photobiol. Sci. · 2002 · 1 · 44110.1039/b200777k ↗
27. Fedoryshin L. L. · ACS Appl. Mater. Interfaces · 2014 · 27 · 1360010.1021/am503039f ↗
28. Li Z. · Nanotechnology · 2008 · 19 · 1
29. Serrano-Ruiz D. · J. Polym. Sci., Part A: Polym. Chem. · 2014 · 52 · 296610.1002/pola.27338 ↗
30. Han Y. · Langmuir · 2008 · 584210.1021/la703440p ↗
31. Vaz A. M. · Colloids Surf., B · 2014 · 114 · 1110.1016/j.colsurfb.2013.09.051 ↗
32. Alonso-Cristobal P. · J. Polym. Sci., Part A: Polym. Chem. · 2012 · 53 · 4569
33. Li G.-Z. · Polym. Chem. · 2010 · 1 · 119610.1039/c0py00100g ↗
34. Greenfield R. S. · Cancer Res. · 1990 · 50 · 6600
35. Carling C. J. · Angew. Chem., Int. Ed. · 2010 · 49 · 378210.1002/anie.201000611 ↗
36. Li W. · J. Am. Chem. Soc. · 2014 · 136 · 224810.1021/ja412364m ↗
37. Dongmei Y. · Chem. Soc. Rev. · 2015 · 44 · 141610.1039/C4CS00155A ↗