journal article·2023

Photochemical synthesis of fluorescent Au 16 (RGDC) 14 and excited state reactivity with molecular oxygen

Parimah Aminfar, Goonay Yousefalizadeh, Emily Steele, Juan Chen, Gang Zheng, Kevin G. Stamplecoskie

Nanoscale· Volume 15· Issue 33
Publisher page

Abstract

Aqueous metal nanoclusters have emerged as effective materials for biomedical imaging and therapy. Among them, gold nanoclusters (AuNCs) have been widely studied due to their unique electronic structures. These nanoclusters are often optically impure, comprising a mixture of fluorescent clusters with different metal/ligand compositions. The polydispersity of nanoclusters makes it challenging to isolate the most stable structure, and poses further risks for eventual clinical applications. Herein, Au16L14 clusters are reported which are optically pure as assessed by fluorescence excitation-emission matrix (EEM) spectroscopy and parallel factor (PARAFAC) analysis. The reactivity of their excited state with molecular oxygen was also probed, demonstrating that the Au16L14 clusters generate type I reactive oxygen species (ROS), which can make them effective sensitizers for photodynamic therapy.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Advanced Nanomaterials in Catalysis · Neurological Complications and Syndromes

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Queen's University, Kingston, Ontario K7L 3N6, Canada

Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, M5G 1L7, Canada

Institute of Biomaterials and Biomedical Engineering and Department of Medical Biophysics, University of Toronto, Toronto, Ontario, M5S 3G9, Canada

Funding

Natural Sciences and Engineering Research Council of Canada · Canada Foundation for Innovation

References (33)

Show source-provided references
1. Sych · J. Phys. Chem. C · 2018 · 122 · 2954910.1021/acs.jpcc.8b08306 ↗
2. Tang · Chem. Res. Chin. Univ. · 2021 · 37 · 93410.1007/s40242-021-1117-3 ↗
3. Zhang · Talanta · 2019 · 200 · 43210.1016/j.talanta.2019.03.068 ↗
4. Ramsay · Nanoscale · 2019 · 11 · 2052210.1039/C9NR07626C ↗
5. Stamplecoskie · J. Phys. Chem. C · 2014 · 118 · 137010.1021/jp410856h ↗
6. Yousefalizadeh · J. Photochem. Photobiol., A · 2018 · 353 · 25110.1016/j.jphotochem.2017.11.033 ↗
7. Kamat · J. Phys. Chem. C · 2018 · 122 · 1321410.1021/acs.jpcc.8b03349 ↗
8. Cantelli · Dyes Pigm. · 2016 · 135 · 6410.1016/j.dyepig.2016.06.019 ↗
9. Yousefalizadeh · J. Phys. Chem. A · 2018 · 122 · 701410.1021/acs.jpca.8b07072 ↗
10. Poderys · J Photochem Photobiol B · 2020 · 204 · 11180210.1016/j.jphotobiol.2020.111802 ↗
11. McLean · ACS Appl. Nano Mater. · 2020 · 3 · 142010.1021/acsanm.9b02272 ↗
12. Fan · RSC Adv. · 2021 · 11 · 2138410.1039/D1RA03469C ↗
13. Kawasaki · Chem. Mater. · 2014 · 26 · 277710.1021/cm500260z ↗
14. Ding · J. Controlled Release · 2011 · 156 · 27610.1016/j.jconrel.2011.08.019 ↗
15. Roxin · J. Med. Chem. · 2014 · 57 · 22310.1021/jm401538h ↗
16. Ashur · J. Phys. Chem. A · 2009 · 113 · 802710.1021/jp900580e ↗
17. Ho-Wu · J. Phys. Chem. B · 2017 · 121 · 1007310.1021/acs.jpcb.7b09442 ↗
18. Liu · J. Mater. Chem. B · 2019 · 7 · 692410.1039/C9TB01573F ↗
19. Aikens · J. Phys. Chem. Lett. · 2011 · 2 · 9910.1021/jz101499g ↗
20. Nimmala · J. Am. Chem. Soc. · 2014 · 136 · 1701610.1021/ja5103025 ↗
21. Ramsay · RSC Adv. · 2018 · 8 · 4208010.1039/C8RA08751B ↗
22. Conway · Photochem. Photobiol. Sci. · 2008 · 7 · 29010.1039/b715141a ↗
23. Yin · J. Phys. Chem. B · 2013 · 117 · 12510.1021/jp3092804 ↗
24. He · J. Mater. Chem. B · 2017 · 5 · 822810.1039/C7TB02163A ↗
25. Wan · Theranostics · 2020 · 10 · 1183710.7150/thno.49784 ↗
26. Li · Signal Transduction Targeted Ther. · 2022 · 7 · 6410.1038/s41392-022-00906-2 ↗
27. Desgrosellier · Nat. Rev. Cancer · 2010 · 10 · 910.1038/nrc2748 ↗
28. Jockusch · Macromolecules · 2001 · 161910.1021/ma001836p ↗
29. Entradas · J. Photochem. Photobiol., B · 2020 · 204 · 11178710.1016/j.jphotobiol.2020.111787 ↗
30. Lutkus · J. Photochem. Photobiol., A · 2019 · 378 · 13110.1016/j.jphotochem.2019.04.029 ↗
31. Hui · Bioconjugate Chem. · 2020 · 31 · 243910.1021/acs.bioconjchem.0c00485 ↗
32. Gomes · J. Biochem. Biophys. Methods · 2005 · 65 · 4510.1016/j.jbbm.2005.10.003 ↗
33. Chen · Small · 2021 · 17 · 200674210.1002/smll.202006742 ↗