The proposed intelligent nanoprobe is composed of a rationally designed UV light-responsive triangular DNA nano sucker (TDS) and upconversion nanoparticles (UCNPs), named UCNPs@TDS (UTDS).
First-pass extracted concept
UCNPs@TDS
Aliases
near-infrared (NIR) light-activated multicomponent detection intelligent nanoprobe, UTDS
Evidence Snippets
Supporting Sources
Linked Claims
UCNPs@TDS can enter cells autonomously through endocytosis.
which can enter cells autonomously through endocytosis
The near-infrared light-activated UTDS can distinguish different kinds of cell lines with different miRNA expression levels.
distinguishing different kinds of cell lines with different miRNA expressions levels can be also achieved through this NIR light-activated intelligent UTDS
UCNPs@TDS is composed of a UV light-responsive triangular DNA nano sucker and upconversion nanoparticles.
The proposed intelligent nanoprobe is composed of a rationally designed UV light-responsive triangular DNA nano sucker (TDS) and upconversion nanoparticles (UCNPs), named UCNPs@TDS (UTDS)
UCNPs@TDS enables remote regulation of on-demand accurate imaging for multiple intracellular miRNAs using near-infrared light illumination at a chosen time and place.
enable remote regulation of on-demand accurate imaging for multiple intracellular miRNAs using NIR light illumination at a chosen time and place
The authors developed a near-infrared light-activated multicomponent detection intelligent nanoprobe for spatially and temporally controlled on-demand accurate imaging of multiple intracellular miRNAs.
in this work, we developed a near-infrared (NIR) light-activated multicomponent detection intelligent nanoprobe for spatially and temporally controlled on-demand accurate imaging of multiple intracellular miRNAs
UCNPs@TDS resists nonspecific activation, avoids false-positive signals, and improves the accuracy of imaging of multiple intracellular miRNAs.
it can resist nonspecific activation as well as effectively avoid false-positive signals and improve the accuracy of imaging of multiple intracellular miRNAs