Research output: Contribution to journal › Article › peer-review
Modulating Photodissociation and Photobleaching via Plasmon Resonance to Enhance Light-Induced Nitric Oxide Release. / Shershnev, Danil V.; Virts, Natalia A.; Gladskikh, Igor A. et al.
In: Applied Nano, Vol. 6, No. 3, 17, 01.09.2025.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Modulating Photodissociation and Photobleaching via Plasmon Resonance to Enhance Light-Induced Nitric Oxide Release
AU - Shershnev, Danil V.
AU - Virts, Natalia A.
AU - Gladskikh, Igor A.
AU - Geydt, Pavel V.
AU - Panfilov, Mikhail A.
AU - Vorob’ev, Alexey Yu
AU - Moskalensky, Alexander E.
N1 - The study was supported by the Ministry of Science and Higher Education of the Russian Federation (project FSUS-2025-0011).
PY - 2025/9/1
Y1 - 2025/9/1
N2 - Localized therapeutic action and targeted drug release offer compelling advantages over traditional systemic drug administration. This is particularly important for nitric oxide (NO), whose biological effects vary greatly depending on concentration and cellular environment. Light-sensitive NO donors are promising for achieving precise, on-demand NO release. However, their efficiency and photostability are limited by competing photophysical processes and the generation of reactive oxygen species (ROS). In this study, we investigate hybrid systems composed of photosensitive nitric oxide (NO) donors and silver island films (SIFs). The influence of localized surface plasmon on non-radiative relaxation pathways and ROS generation is the main focus of the paper. Upon excitation at 500 nm, we observed several-fold increase in NO release, attributed to resonant interactions between the plasmonic field and the dye molecules. By tuning the thickness of a SiO2 buffer layer, we identified key parameters affecting process efficiency: the spectral overlap between the plasmon resonance and the sensitizer’s absorption band, and the distance between the nanoparticle and the molecule. Additionally, singlet oxygen generation increase was observed. These findings demonstrate the potential of plasmonic enhancement to controllably boost photochemical activity in organic systems, paving the way for advanced applications in phototherapy and biomedical diagnostics.
AB - Localized therapeutic action and targeted drug release offer compelling advantages over traditional systemic drug administration. This is particularly important for nitric oxide (NO), whose biological effects vary greatly depending on concentration and cellular environment. Light-sensitive NO donors are promising for achieving precise, on-demand NO release. However, their efficiency and photostability are limited by competing photophysical processes and the generation of reactive oxygen species (ROS). In this study, we investigate hybrid systems composed of photosensitive nitric oxide (NO) donors and silver island films (SIFs). The influence of localized surface plasmon on non-radiative relaxation pathways and ROS generation is the main focus of the paper. Upon excitation at 500 nm, we observed several-fold increase in NO release, attributed to resonant interactions between the plasmonic field and the dye molecules. By tuning the thickness of a SiO2 buffer layer, we identified key parameters affecting process efficiency: the spectral overlap between the plasmon resonance and the sensitizer’s absorption band, and the distance between the nanoparticle and the molecule. Additionally, singlet oxygen generation increase was observed. These findings demonstrate the potential of plasmonic enhancement to controllably boost photochemical activity in organic systems, paving the way for advanced applications in phototherapy and biomedical diagnostics.
KW - localized plasmon resonance
KW - nitric oxide donor
KW - photodissociation
KW - singlet oxygen
UR - https://www.mendeley.com/catalogue/9a7ec57a-b5f6-3203-a09d-8a2fcb850e44/
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105017480082&origin=inward
U2 - 10.3390/applnano6030017
DO - 10.3390/applnano6030017
M3 - Article
VL - 6
JO - Applied Nano
JF - Applied Nano
SN - 2673-3501
IS - 3
M1 - 17
ER -
ID: 70396255