'First generation USCA' p2 Searchterm 'First generation USCA' found in 8 articles 1 term [ • ] - 4 definitions [• ] - 3 booleans [• ]Result Pages : •
SonoGen (QW7437) is an anionically charged 2% perfluorocarbon emulsion under development as a transpulmonary myocardial ultrasound contrast agent (UCA). The SonoGen microbubbles have a reduced adherence to the negatively charged vascular endothelium and reduced coalescence. SonoGen, a second generation USCA has the theoretical potential to provide high safety and efficacy and improved tissue grayscale persistence compared to first generation fluorocarbon contrast agents.
Drug Information and Specification
RESEARCH NAME
DEVELOPER
INDICATION -
DEVELOPMENT STAGE Echocardiography - Phase 1
APPLICATION
Intravenous injection
TYPE
Microbubble
Surfactant
CHARGE
Negative
Dodecafluoropentane
MICROBUBBLE SIZE
-
PREPARATION
-
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From Bracco Diagnostics, Inc.
SonoVue® was first launched in October 2001 and is now available in all European countries. SonoVue is a second generation USCA, designed and optimized with regard to the resistance to pressure. SonoVue is an example of an important family of microbubbles whose membrane consists of phospholipids. SonoVue microbubbles are filled with sulfur hexafluoride (SF6), a gas which has a low solubility and diffuses slowly in blood for the gaseous phase of the microbubbles. In particular, the SonoVue microbubbles, thanks to the high flexibility of their shell, are strongly echogenic in a wide range of frequencies and acoustic pressure and therefore can be used with both destructive and conservative contrast bubble specific imaging methods. See also Coherent Contrast Imaging.
Drug Information and Specification
RESEARCH NAME
BR1
DEVELOPER
INDICATION -
DEVELOPMENT STAGE Contrast enhanced ultrasound -
for sale APPLICATION
Intravenous
TYPE
Microbubble
Lipids: Macrogol 4000, DSPC, DPPG, Palmitic acid
CHARGE
Negative
Sulfurhexafluoride
MICROBUBBLE SIZE
99% < 11μm
PRESENTATION
Presentation 01(with integral Bio-Set transfer system) -25 mg of dry, lyophilized powder in an atmosphere of sulphur hexafluoride in a colorless Type I glass vial, with elastomeric closure and integral transfer system.Type I glass pre-filled syringe containing 5 ml sodium chloride 0.9%w/v solution for injection. - Presentation 02 (with separate MiniSpike transfer system)
STORAGE
No special precautions for storage
PREPARATION
Reconstitute with 5 ml saline
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NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT!
Distribution Information
TERRITORY
DISTRIBUTOR
USA, EU
•
From GE Healthcare;; Optison is the first 'second generation USCA' marketed in the US. Ultrasound contrast agents used during an ultrasound imaging procedure, enable more accurate diagnosis of the patient's heart condition. The application of Optison allows to image the endocardial borders of the heart, to see cardiac wall motion abnormalities and to guide the selection and monitoring of treatment. Optison represents a class of microbubbles with a shell formed by sonicating a solution of capsules filled with a perfluoropropane gas. The high molecular weight slows microbubble dissolution and prolongs the enhancement for several minutes. The human albumin-stabilized cavitation bubbles have a surface tension of 0.9 N/m and a surface dilatational viscosity 0.08 msP. 'August 06, 2001 Molecular Biosystems Inc., a subsidiary of Alliance Pharmaceutical Corp, announced the amendment of the Optison Product Rights Agreement (OPRA) dated May 9, 2000 with Mallinckrodt Inc, a unit of Tyco Healthcare. Optison, an intravenous ultrasound contrast agent, was developed by MBI and is being marketed by Mallinckrodt in the U.S. and Europe. Under the amended agreement, MBI will receive an immediate cash payment plus additional unspecified royalties for a two-year period. The amendment of OPRA coincides with an announcement by Nycomed Amersham Imaging that Nycomed and Mallinckrodt will terminate their joint commercialization and development agreement for ultrasound contrast agents, including Optison, effective Dec. 31, 2001. Effective Jan. 1, 2002, all selling and marketing activities will be resumed solely by Nycomed Amersham.'
Drug Information and Specification
RESEARCH NAME
FS069
DEVELOPER
INDICATION -
DEVELOPMENT STAGE LVO -
For sale APPLICATION
intravenous/oral
TYPE
AlbuminN-acetyltryptophan,Caprylic acid
CHARGE
Slight Negative
Octafluoropropane
MICROBUBBLE SIZE
93% < 10μm
PRESENTATION
Five 3ml vials
STORAGE
Refrigerate 2-8 °C
PREPARATION
Hand agitate
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NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT!
Distribution Information
TERRITORY
DISTRIBUTOR
USA, EU
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