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Pre-clinical whole-body fluorescence imaging: Review of instruments, methods and applications

TLDR
This paper reviews in vivo in vivo fluorescence imaging with a particular emphasis on its potential uses and limitations, the required instrumentation, and the possible imaging geometries and applications.
Abstract
Fluorescence sampling of cellular function is widely used in all aspects of biology, allowing the visualization of cellular and sub-cellular biological processes with spatial resolutions in the range from nanometers up to centimeters. Imaging of fluorescence in vivo has become the most commonly used radiological tool in all pre-clinical work. In the last decade, full-body pre-clinical imaging systems have emerged with a wide range of utilities and niche application areas. The range of fluorescent probes that can be excited in the visible to near-infrared part of the electromagnetic spectrum continues to expand, with the most value for in vivo use being beyond the 630 nm wavelength, because the absorption of light sharply decreases. Whole-body in vivo fluorescence imaging has not yet reached a state of maturity that allows its routine use in the scope of large-scale pre-clinical studies. This is in part due to an incomplete understanding of what the actual fundamental capabilities and limitations of this imaging modality are. However, progress is continuously being made in research laboratories pushing the limits of the approach to consistently improve its performance in terms of spatial resolution, sensitivity and quantification. This paper reviews this imaging technology with a particular emphasis on its potential uses and limitations, the required instrumentation, and the possible imaging geometries and applications. A detailed account of the main commercially available systems is provided as well as some perspective relating to the future of the technology development. Although the vast majority of applications of in vivo small animal imaging are based on epi-illumination planar imaging, the future success of the method relies heavily on the design of novel imaging systems based on state-of-the-art optical technology used in conjunction with high spatial resolution structural modalities such as MRI, CT or ultrasound.

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Polymer-encapsulated organic nanoparticles for fluorescence and photoacoustic imaging

TL;DR: The latest advances in the development of polymer encapsulated CP and AIE fluorogen nanoparticles are summarized, including preparation methods, material design and matrix selection, nanoparticle fabrication and surface functionalization for fluorescence and photoacoustic imaging.
Journal ArticleDOI

A review of progress in single particle tracking: from methods to biophysical insights.

TL;DR: The foundations of SPT are described together with novel optical implementations that nowadays allow the investigation of single molecule dynamic events with increasingly high spatiotemporal resolution using molecular densities closer to physiological expression levels.
Journal ArticleDOI

Translation of Near-Infrared Fluorescence Imaging Technologies: Emerging Clinical Applications

TL;DR: Emerging NIRF imaging is described within the context of nuclear imaging technologies that remain the "gold standard" of molecular imaging.
Journal ArticleDOI

Using lanthanide ions in molecular bioimaging

TL;DR: Trivalent lanthanide ions offer remarkable opportunities in the design of bioimaging agents: this review presents an accessible discussion of their application in both optical and magnetic resonance imaging.
Journal ArticleDOI

In vivo time-gated fluorescence imaging with biodegradable luminescent porous silicon nanoparticles

TL;DR: Time-gated imaging of porous silicon nanoparticles accumulated in a human ovarian cancer xenograft following intravenous injection is demonstrated in a live mouse and the potential for multiplexing of images in the time domain by using separate porous Silicon nanoparticles engineered with different excited state lifetimes is discussed.
References
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Journal ArticleDOI

In vivo cancer targeting and imaging with semiconductor quantum dots

TL;DR: Sensitive and multicolor fluorescence imaging of cancer cells under in vivo conditions are achieved and a whole-body macro-illumination system with wavelength-resolved spectral imaging is integrated for efficient background removal and precise delineation of weak spectral signatures.
Journal ArticleDOI

Fourier transform profilometry for the automatic measurement of 3-D object shapes

Mitsuo Takeda, +1 more
- 15 Dec 1983 - 
TL;DR: A new computer-based technique for automatic 3-D shape measurement is proposed and verified by experiments that has a much higher sensitivity than the conventional moire technique and is capable of fully automatic distinction between a depression and an elevation on the object surface.
Journal ArticleDOI

Quantitative optical spectroscopy for tissue diagnosis

TL;DR: This review describes optical interactions pursued for biomedical applications (fluorescence, fluorescence lifetime, phosphorescence, and Raman from cells, cultures, and tissues) and provides a descriptive framework for light interaction based upon tissue absorption and scattering properties.
Journal ArticleDOI

In Vivo Fluorescence Spectroscopy and Imaging for Oncological Applications

TL;DR: This poster presents a probabilistic procedure to characterize the response of the immune cells of the central nervous system to laser-spot assisted chemoreception and excites the immune system.
Journal ArticleDOI

Peptide-Labeled Near-Infrared Quantum Dots for Imaging Tumor Vasculature in Living Subjects

TL;DR: The in vivo targeting and imaging of tumor vasculature using arginine-glycine-aspartic acid (RGD) peptide-labeled quantum dots (QDs) opens up new perspectives for integrin-targeted near-infrared optical imaging and may aid in cancer detection and management including imaging-guided surgery.
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