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Upconverting Nanoparticles Coated with Light-Breakable Mesoporous Silica for NIR-Triggered Release of Hydrophobic Molecules.

Authors :
Tam V
Picchetti P
Liu Y
Skripka A
Carofiglio M
Tamboia G
Bresci A
Manetti F
Cerullo G
Polli D
De Cola L
Vetrone F
Cerruti M
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 Jun 05; Vol. 16 (22), pp. 29029-29041. Date of Electronic Publication: 2024 May 21.
Publication Year :
2024

Abstract

Upconverting nanoparticles (UCNPs) doped with Yb <superscript>3+</superscript> and Tm <superscript>3+</superscript> are near-infrared (NIR) to ultraviolet (UV) transducers that can be used for NIR-controlled drug delivery. However, due to the low quantum yield of upconversion, high laser powers and long irradiation times are required to trigger this drug release. In this work, we report the one-step synthesis of a nanocomposite consisting of a LiYbF <subscript>4</subscript> :Tm <superscript>3+</superscript> @LiYF <subscript>4</subscript> UCNP coated with mesoporous UV-breakable organosilica shells of various thicknesses. We demonstrate that a thin shell accelerates the breakage of the shell at 1 W/cm <superscript>2</superscript> NIR light exposure, a laser power up to 9 times lower than that of conventional systems. When the mesopores are loaded with hydrophobic vitamin D <subscript>3</subscript> precursor 7-dehydrocholesterol (7-DH), shell breakage results in subsequent cargo release. Its minimal toxicity in HeLa cells and successful internalization into the cell cytoplasm demonstrate its biocompatibility and potential application in biological systems. The tunability of this system due to its simple, one-step synthesis process and its ability to operate at low laser powers opens up avenues in UCNP-powered NIR-triggered drug delivery toward a more scalable, flexible, and ultimately translational option.

Details

Language :
English
ISSN :
1944-8252
Volume :
16
Issue :
22
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
38771192
Full Text :
https://doi.org/10.1021/acsami.4c03444