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Result : Searchterm 'R2' found in 1 term [] and 26 definitions []
| previous 21 - 25 (of 27) nextResult Pages : [1] [2 3 4 5 6] | | | | Searchterm 'R2' was also found in the following services: | | | | |
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Drug Information and Specification T1, Predominantly positive enhancement PHARMACOKINETIC Intravascular, extracellular, renal excretion CONCENTRATION 287 mg/mL,0.5 mol/L DOSAGE 0.1-0.2 mmol/kg / 0.2-0.4 ml/kg PREPARATION Finished product INDICATION Neuro/whole body DEVELOPMENT STAGE For sale PRESENTATION Vials of 10 mL, 15 mL and 20 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 Omniscan® for sale | | | | | Further Reading: | | Basics:
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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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Reciprocals of the relaxation times, T1 and T2 ( R1 = 1/T1 and R2 = 1/T2). There is often a linear relation between the concentration of MR contrast agents and the resulting change in relaxation rate.
The rate of relaxation is influenced by molecules with protons that are tumbling. A slower tumble rate will result in faster relaxation rate (shorter relaxation time). Due to the molecular structure of fat with its larger size than water, fat will tumble slower than water molecules. The slower tumble rate of fat enables a faster relaxation rate.
| | | | • View the DATABASE results for 'Relaxation Rates' (5).
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The ability of magnetic compounds to increase the relaxation
rates of the surrounding water proton spins.
Relaxivity is used to improve the contrast of the image, and
to study tissue specific areas where the contrast agent
better diffuses or to perform functional magnetic resonance imaging.
The relaxivity of MRI contrast agents depends on the
molecular structure and kinetic of the complex.
To increase the number of water molecules that are in the inner sphere
of the complex, or to slow down the molecular rotational
correlation time, are possibilities to improve the water relaxivity.
Relaxivity units ( r1, r2) are mM -1 * sec -1 (at varying temperatures). | | | | • View the DATABASE results for 'Relaxivity' (51).
| | | • View the NEWS results for 'Relaxivity' (2).
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Resovist® is an organ-specific MRI contrast agent, used for the detection and characterization of especially small focal liver lesions.
Resovist® consists of superparamagnetic iron oxide ( SPIO) nanoparticles coated with carboxydextran, which are accumulated by phagocytosis in cells of the reticuloendothelial system (RES) of the liver. The uptake of Resovist® Injection in the reticuloendothelial cells results in a decrease of the signal intensity of normal liver parenchyma on both T2- and T1 weighted images.
Most malignant liver tumors do not contain RES cells and therefore do not uptake the iron particles. The resulting imaging effect is an improved contrast between the tumor (bright) and the surrounding tissue (dark).
Resovist® can be injected as an intravenous bolus, which allows immediate imaging of the liver and reduces the overall examination time. A dynamic imaging strategy after bolus injection supports to characterize lesions.
In comprehensive clinical trials, it demonstrated an excellent safety profile.
In 2001, Resovist® was approved for the European market.
See also Superparamagnetic Iron Oxide.
Resovist® competed with Primovist™, the other liver imaging agent of Bayer Schering Pharma AG. Due to this reason, the production of Resovist® has been abandoned in 2009.
Drug Information and Specification T2/T1, Predominantly negative enhancement PHARMACOKINETIC RES-directed CONCENTRATION 0.5 mol Fe/L DOSAGE Less than 60 kg = 0.9 ml, greater than 60 kg = 1.4 ml PREPARATION Finished product PRESENTATION
Pre-filled syringes of 0.9 and 1.4 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 Japan Resovist® approved - Australia Resovist® Approved - | | | | • View the DATABASE results for 'Resovist®' (6).
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