'Contrast Agent' p14 Searchterm 'Contrast Agent' found in 101 articles 8 terms [ • ] - 93 definitions [• ] Result Pages : •
Founded in 1991, ImaRx Pharmaceutical Corp. designs, develops and markets pharmaceuticals for medical imaging (MRI, ultrasound and computed tomography) for the radiological imaging industry.
ImaRx Pharmaceutical Corp., announced 1999 that it has been acquired by E.I DuPont de Nemours & Co., Inc. The terms of the acquisition provide a royalty-free licensing arrangement with a newly-formed company, ImaRx LLC ('LLC'), to pursue and develop new products and technologies for drug and gene delivery independent from DuPont. Yamanouchi Pharmaceutical Co. Ltd., ImaRx' licensee for Asian territories for this product, will continue to develop the product in Asia as DuPont's licensee. ImaRx LLC will have ownership of all other targeted and therapeutic products previously owned by ImaRx, including imaging products outside of diagnostic ultrasound imaging and two other imaging products, SonoRx® and LumenHance®, which are both FDA approved and licensed to BRACCO Diagnostics. See also Lantheus Medical Imaging and Definity®. Ultrasound Contrast Agents: •
The perfect image quality is dependent on some assumptions of the propagation of ultrasound waves in tissues after generating in an imaging system. These assumptions are important for the developing of optimal ultrasound imaging systems.
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The propagation of ultrasound is straight ahead.
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The amplitudes of the echoes are proportional to the difference of the acoustical impedance caused by different tissue layers.
See also Coded Excitation, Validation and Refraction Artifact, Q-Value, Ultrasound Phantom, Dead Zone, Narrow Bandwidth. Further Reading: News & More: •
Imagent® is an injectable suspension for intravenous administration during a sonogram. This diagnostic contrast agent for enhancement of ultrasound images contains perflexane lipid microspheres. Imagent® US is indicated in the assessment of heart function and perfusion, as well as the detection of tumors and blood flow abnormalities by using gray scale, color Doppler, and harmonic ultrasound imaging techniques. During the course of its development, the brand name for this product has changed from Imagent to Imavist (between August 2000 and March 2002) back to Imagent. The manufacturer's 06/03/02 press release announcing FDA approval refers to the product as 'Imagent (formerly Imavist),' and the approval notice and monograph posted at the FDA site refers to the product as Imagent. Jointly developed by Alliance Pharmaceutical Corp and Bayer Schering Pharma AG (Germany). Source: PR Newswire - 10/10/96, 03/31/98, 10/13/99, 03/13/01, 10/08/01; FDA approvals - 05/31/02; Alliance Pharmaceutical press release - 06/03/02. Currently the production of Imagent® is discontinued.
Drug Information and Specification
RESEARCH NAME
AF0150
DEVELOPER
IMCOR Pharmaceuticals, Inc.
INDICATION
APPLICATION
Intravenous
TYPE
Lipid: DMPC
CHARGE
Neutral
Perfluorohexane/Nitrogen
MICROBUBBLE SIZE
99.8% < 10μm
PRESENTATION
-
STORAGE
Room Temp 15−30 °C
PREPARATION
Reconstitute with 10 ml water
DO NOT RELY ON THE INFORMATION PROVIDED HERE, THEY ARE
NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT! •
(AE) Induced acoustic emission is an effect of ultrasound contrast agents, presenting the interaction between the agent and the incident ultrasound wave. Microbubbles break down in high-amplitude diagnostic ultrasound energy. The bubble rupture produces a transient pressure wave, which results in a characteristic mosaic pattern from tissues containing the agent. It is important to note that the color patterns of induced acoustic emission do not represent flow signals. •
Ultrasound contrast agents (USCAs) improve the sensitivity of various ultrasound applications. They usually stay within the vascular space and can be injected several times. Nevertheless the contrast enhancement is limited caused by physiologic clearance and bubble destruction. Different injection techniques to improve the imaging:
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Bolus injection generally results in a more or less prolonged blooming phase and a relatively short enhancing period of approximately 2- to 3 minutes.
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Slow injection provides markedly prolonged enhancement by minimizing over-contrast artifacts.
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Continuous perfusion achieves stable and uniform enhancement, lasting until the infusion is stopped.
Continuous infusion yield a steady-state concentration of the USCAs, greater examination time with optimal enhancement, avoid bloom and possibly other artifacts. Continuous infusion also allows the sonographer to optimize the effective dose individually during the examination. See also Power Modulation. Further Reading: News & More: Result Pages : |