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Result : Searchterm 'Osmolality' found in 1 term [] and 23 definitions []
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Radiographic low-osmolar nonionic contrast agents have less side effects and fewer nephrotoxicity than ionic, high-osmolar agents. Gadolinium-based MRI contrast agents have a different formulation from iodinated X-ray contrast media, and there is no known cross sensitivity between these two types of contrast agents. Intravenous MRI contrast agents, specifically the gadolinium chelates have a high safety and lack of nephrotoxicity compared with X-ray contrast media.
The used gadolinium chelates differ in following properties: linear (e.g., gadodiamide and gadoversetamide have nonionic linear structures) vs. macrocyclic cores, and ionic vs. nonionic types. The nonionic molecules have lower osmolality and viscosity, which increase digestibility at greater concentrations, and make faster bolus injections conceivable.
The macrocyclic molecules (e.g., gadoteridol has a nonionic macrocyclic ring structure) are more stable and show fewer tendencies to dissociate free Gd.
See also ProHance®, Omniscan®, OptiMARK®, Ionic Intravenous Contrast Agents.
See also the related poll result: ' MRI will have replaced 50% of x-ray exams by' | | | | | | | | | Further Reading: | News & More:
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OptiMARK® is a formulation of a nonionic gadolinium chelate of diethylenetriamine pentaacetic acid bismethoxyethylamide ( gadoversetamide), for use as a paramagnetic MRI contrast agent.
OptiMARK® ( gadoversetamide injection) is to be administered by intravenous injection.
OptiMARK® 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 OptiMARK® for sale | | | | • View the DATABASE results for 'OptiMARK®' (5).
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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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Primovist™ (U.S brand name Eovist®) 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.
Primovistâ„¢ 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 Primovistâ„¢. 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 µmol/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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Drug Information and Specification T1, Predominantly positive enhancement PHARMACOKINETIC Intravascular, extracellular, renal excretion CONCENTRATION 0.5 mol/L, 279.3mg/ml PREPARATION Finished product INDICATION Neuro/whole body DEVELOPMENT STAGE For sale PRESENTATION Vials of 5, 10, 15 and 20 mL
Glass syringes of 5, 10, 15 and 17 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 USA EU ProHance® for sale Australia ProHance® for sale Japan ProHance® for sale | | | | • View the DATABASE results for 'ProHance®' (6).
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