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Open AccessJournal ArticleDOI

Hybrid Ferritin Nanoparticles as Activatable Probes for Tumor Imaging

TLDR
Activatable probes are developed, designed to be fluorescently quenched at a quiescent stage but activatable when encountering a specific trigger, which leads to a structural or conformational change and restores fluorescence activities.
Abstract
Near-infrared fluorescence (NIRF) imaging is emerging as an important tool in preclinical studies.[1–5] As the technology is being established and implemented worldwide, a wave of effort has been spurred to develop novel imaging probes that can accurately recognize and report diseases, such as cancer.[3,6] One common drawback of NIRF imaging, however, is its high background and as a consequence of that, low specificity.[7,8] To address this issue, we and others have developed activatable probes with various approaches. Such probes, constructed by bringing into proximity an energy donor and receptor, are designed to be fluorescently quenched at a quiescent stage but activatable when encountering a specific trigger, which leads to a structural or conformational change and restores fluorescence activities.[7–9] This technique allows the signals to be only amplified at diseased areas upon a designated environment change, a feature which can greatly improve the signal-to-background ratio.

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Magnetoferritin nanoparticles for targeting and visualizing tumour tissues

TL;DR: In this article, magnetoferritin nanoparticles (M-HFn) are used to target and visualize tumour tissues without the use of any targeting ligands or contrast agents, which can distinguish cancerous cells from normal cells with a sensitivity of 98% and specificity of 95%.
Journal ArticleDOI

RGD-modified apoferritin nanoparticles for efficient drug delivery to tumors

TL;DR: It is shown that after being precomplexed with Cu(II), doxorubicin can be loaded onto RGD modified apoferritin nanocages with high efficiency and showed a longer circulation half-life, higher tumor uptake, better tumor growth inhibition, and less cardiotoxicity than free doxorbicin.
Journal ArticleDOI

Graphene-based nanomaterials for bioimaging ☆

TL;DR: This review will summarize the current advances in bioimaging of graphene-based nanomaterials, including graphene, graphene oxide (GO), reduced graphene oxide(rGO), graphene quantum dots (GQDs), and their derivatives, and highlight the molecular imaging modalities.
Journal ArticleDOI

Biodegradable and Renal Clearable Inorganic Nanoparticles.

TL;DR: An overview of emerging biologically safe inorganic nanoplatforms is provided, along with considerations of the challenges that need to be overcome for cancer theranostics with inorganic nanoparticles to become a reality.
Journal ArticleDOI

Dual-stimuli responsive and reversibly activatable theranostic nanoprobe for precision tumor-targeting and fluorescence-guided photothermal therapy

TL;DR: This work fabricates a dual-stimuli-responsive and reversibly activatable nanoprobe from asymmetric cyanine and glycosyl-functionalized gold nanorods with matrix metalloproteinases-specific peptide as a linker to achieve MMPs/pH synergistic and pH reversible activation.
References
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Journal ArticleDOI

Quantum Dots for Live Cells, in Vivo Imaging, and Diagnostics

TL;DR: The new generations of qdots have far-reaching potential for the study of intracellular processes at the single-molecule level, high-resolution cellular imaging, long-term in vivo observation of cell trafficking, tumor targeting, and diagnostics.
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Matrix Metalloproteinases: Regulators of the Tumor Microenvironment

TL;DR: In addition to their role in extracellular matrix turnover and cancer cell migration, MMPs regulate signaling pathways that control cell growth, inflammation, or angiogenesis and may even work in a nonproteolytic manner.
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In vivo near-infrared fluorescence imaging

TL;DR: This review focuses on those parameters that affect image signal and background during in vivo imaging with near-infrared light and exogenous contrast agents.
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Fluorescence imaging with near-infrared light: new technological advances that enable in vivo molecular imaging.

TL;DR: FMT, a technique that can three-dimensionally image gene expression by resolving fluorescence activation in deep tissues by focusing on optical imaging technologies used for non-invasive imaging of the distribution of such probes, is discussed.
Journal ArticleDOI

Near-infrared fluorescence: application to in vivo molecular imaging

TL;DR: Recent advances in understanding of factors that define the effectiveness of imaging agents in vivo as they pertain to the application of optical reporters for in vivo imaging are discussed in this review.
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