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Result : Searchterm 'Relaxivity' found in 1 term [] and 50 definitions []
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OptiMARKĀ® is a formulation of a nonionic gadolinium chelate of diethylenetriamine pentaacetic acid bismethoxyethylamide ( gadoversetamide), for use as a paramagnetic MRI contrast agent.
OptiMARKĀ® ( gadoversetamide injection) is to be administered by intravenous injection.
OptiMARKĀ® is indicated for MRI diagnostic procedures to provide increased enhancement and visualization of lesions of the brain, spine and liver, including tumors. WARNING: NEPHROGENIC SYSTEMIC FIBROSIS
Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with acute or chronic severe renal insufficiency (glomerular filtration rate less than 30 mL/min/1.73m 2), or acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.
Drug Information and Specification T1, Predominantly positive enhancement PHARMACOKINETIC Intravascular, extracellular DOSAGE 0.1 mmol/kg / 0.2 mL/kg PREPARATION Finished product INDICATION Neuro/whole body PRESENTATION Vials of 5, 10, 15, 20, 50 mL and
Pre-filled syringes of 10, 15, 20 and 30 mL DO NOT RELY ON THE INFORMATION PROVIDED HERE, THEY ARE NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT!
Distribution Information TERRITORY TRADE NAME DEVELOPMENT STAGE DISTRIBUTOR Australia OptiMARKĀ® for sale | | | | | Further Reading: | | Basics:
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Drug Information and Specification NAME OF COMPOUND Barium suspensions, clay mineral particles, iron oxide crystals CENTRAL MOIETY Ba3+, Al3+, Si2+, Fe T2, Predominantly negative enhancement CONCENTRATION Various mixtures DOSAGE Depending on the mixture PREPARATION Depending on the product INDICATION Gastrointestinal bowel marking DEVELOPMENT STAGE No clinical development DO NOT RELY ON THE INFORMATION PROVIDED HERE, THEY ARE NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT! | | | | • View the DATABASE results for 'Oral Magnetic Particles' (4).
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Short name: P760, chemical compound: tetraazacyclododecanetetraacetic acid (DOTA), central moity: Gd
P760 ( Guerbet SA) is a low-diffusion gadolinium complex with a macrocyclic core based on a tetraazacyclododecanetetraacetic acid (DOTA)
structure, which is substituted with bulky hydrophilic
groups.
The relaxivity of P760 at 0.47 T is very high compared to Gd-DOTA. | | | | • View the DATABASE results for 'P760' (2).
| | | • View the NEWS results for 'P760' (1).
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Short name: PION, generic name: Polycrystalline iron oxide nanoparticles, central moiety: Fe2+/Fe3+, relaxivity: T2*enhanced, r2//r1=4.4, r2//r1=7
A substance under development (preclin.) as an RES-directed MRI contrast agent (larger particles = DDM 128, PION-ASF) for MR lymphography and the detection of liver lesions. | | | | • View the DATABASE results for 'Polycrystalline Iron Oxide Nanoparticles' (2).
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Primovistā¢ (U.S brand name EovistĀ®) is a highly specific MRI contrast agent for the imaging, detection and characterization of liver conditions, including liver tumors, cysts, as well as other malignant and benign lesions. It is a water-soluble ethoxybenzyl derivative of Gd-DTPA. This compound is taken up by the hepatocytes (approximately 30% of the dose goes to the hepatocytes) and is equally excreted renal and biliary in humans.
Primovistā¢ brightens the signal of T1 weighted MR images immediately after contrast administration.
Dynamic scanning and imaging of the accumulation phase (best after 20 min.) can also be performed after bolus injection of PrimovistĆ¢āĀ¢. The hepatocytes uptake will increase the signal intensity of normal liver parenchyma. This results in improved lesion-to-liver contrast because malignant tumors (metastases, the majority of hepatocellular carcinomas) do not contain either hepatocytes or their functioning is hampered.
WARNING:
Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with acute or chronic severe renal insufficiency (glomerular filtration rate less than 30 mL/min/1.73m 2), or acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.
Drug Information and Specification T1, Predominantly positive enhancement PHARMACOKINETIC 50% hepatobiliary, 50% renal excretion DOSAGE 12,5 - 25 ĆĀµmol/kg PREPARATION Finished product DEVELOPMENT STAGE for sale DO NOT RELY ON THE INFORMATION PROVIDED HERE, THEY ARE NOT A SUBSTITUTE FOR THE ACCOMPANYING PACKAGE INSERT!
Distribution Information TERRITORY TRADE NAME DEVELOPMENT STAGE DISTRIBUTOR | | | | • View the DATABASE results for 'Primovist™' (7).
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