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PET is a molecular imaging that is able to create images from physiological and metabolic processes.
Another method of molecular imaging that can assess the molecular and cellular tumor matrix is PET.
It was the promise of molecular imaging that drove General Electric 's $9.5 billion acquisition of Amersham in October 2003.
For instance, this is the case of optical molecular imaging that uses near-infrared fluorescent probes [ 14, 17].
Positron emission tomography (PET) is a form of molecular imaging that relies on derangement of physiological and biochemical processes for the detection of many diseases.
On the other hand, laser ablation electrospray ionization or infrared MALDI are other useful methods of molecular imaging that are applicable to water-rich specimens to ionize the analytes [ 12, 13].
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Techniques for molecular level imaging that have been adapted from the cell culture setting and applied in vivo include fluorescence recovery after photobleaching (FRAP).
Positron emission tomography/magnetic resonance imaging (PET/MRI) offers the potential for a powerful "one-stop shop" combination of structural, functional, and molecular imaging technology that may be superior to that of MRI imaging alone.
Imaging mass spectrometry (IMS) is a molecular imaging technology that can deliver such spatial information with high chemical specificity for various classes of biomolecules, including metabolites, lipids, peptides, and proteins.
We present a new class of ultrasound molecular imaging agents that extend upon the design of micromotors that are designed to move through fluids by catalyzing hydrogen peroxide (H2O2) and propelling forward by escaping oxygen microbubbles.
In vivo molecular imaging approaches that 'track' Aβ peptides non-invasively are dynamic methods that can be used for assessing Aβ levels in response to treatments.
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