Magnevist (Gadopentetic Acid)
Magnevist (Gadopentetic Acid) Uses, Dosage, Side Effects, Food Interaction and all others data.
A complex of gadolinium with a chelating agent, diethylenetriamine penta-acetic acid (DTPA see pentetic acid), that is given to enhance the image in cranial and spinal MRIs. (From Martindale, The Extra Pharmacopoeia, 30th ed, p706)
| Trade Name | Magnevist (Gadopentetic Acid) |
| Generic | Gadopentetic acid |
| Gadopentetic acid Other Names | Acide gadopentetique, ácido gadopentético, Acidum gadopenteticum, Gadolinium diethylenetriamine pentaacetic acid, Gadolinium DTPA, Gadopentetate, Gadopentetic acid |
| Type | |
| Formula | C14H20GdN3O10 |
| Weight | Average: 547.58 Monoisotopic: 548.03898 |
| Groups | Approved |
| Therapeutic Class | |
| Manufacturer | |
| Available Country | Austria, Belgium, Bosnia & Herzegowina, Bulgaria, Canada, China, Colombia, Croatia (Hrvatska), Denmark, Ecuador, Egypt, Estonia, France, Georgia, Germany, Greece, Hungary, Iceland, India, Ireland, Italy, Japan, Latvia, Lithuania, Malta, Myanmar, New Zealand, Norway, Oman, Poland, Portugal, Romania, Serbia, Slovakia, Spain, Sweden, Tunisia, Turkey, United Kingdom, Vietnam |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
Magnevist (Gadopentetic Acid) is a gadolinium compound used as a contrast agent in MRIs.
For use with magnetic resonance imaging (MRI) in adults, and pediatric patients (2 years of age and older) to visualize lesions with abnormal vascularity in the brain (intracranial lesions), spine and associated tissues as well as lesions with abnormal vascularity in the head and neck. Also used to facilitate the visualization of lesions with abnormal vascularity in the body (excluding the heart).
How Magnevist (Gadopentetic Acid) works
Based on the behavior of protons when placed in a strong magnetic field, which is interpreted and transformed into images by magnetic resonance (MR) instruments. MR images are based primarily on proton density and proton relaxation dynamics. MR instruments are sensitive to two different relaxation processes, the T1 (spin-lattice or longitudinal relaxation time) and T2 (spin-spin or transverse relaxation time). Paramagnetic agents contain one or more unpaired electrons that enhance the T1 and T2 relaxation rates of protons in their molecular environment. The proton relaxation effect (PRE) of an unpaired electron is 700 times stronger than that of a proton itself. In MRI, visualization of normal and pathological brain tissue depends in part on variations in the radio frequency signal intensity that occur with changes in proton density, alteration of the T1, and variation in T2. When placed in a magnetic field, gadopentetate dimeglumine shortens the T1 and T2 relaxation times in tissues where it accumulates. In the central nervous system (CNS), gadopentetate dimeglumine enhances visualization of normal tissues that lack a blood-brain barrier, such as the pituitary gland and the meninges. Gadopentetate dimeglumine does not cross the intact blood-brain barrier; therefore, it does not accumulate in normal brain tissue or in CNS lesions that have not caused an abnormal blood-brain barrier (e.g., cysts, mature post-operative scars). Abnormal vascularity or disruption of the blood-brain barrier allows accumulation of gadopentetate dimeglumine in lesions such as neoplasms, abscesses, and subacute infarcts. Outside the CNS, gadopentetate dimeglumine rapidly reaches equilibrium in the interstitial compartment and enhances signal in all tissues as a function of delivery and size of the interstitial compartment. This compound has also been found to inhibit human erythrocyte 6-phosphogluconate dehydrogenase.
Food Interaction
No interactions found.Volume of Distribution
- 266 ± 43 mL/kg
Half Life
Distribution half life 12 minutes, elimination half 100 minutes
Clearance
- 1.94 +/- 0.28 mL/min/kg [Normal subjects]
Elimination Route
Gadopentetate is exclusively eliminated in the urine with 83 ± 14% (mean ± SD) of the dose excreted within 6 hours and 91 ± 13% (mean ± SD) by 24 hours, post-injection.
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