Search results
Results from the WOW.Com Content Network
It consists of the organic acid DOTA as a chelating agent, and gadolinium (Gd 3+), and is used in form of the meglumine salt (gadoterate meglumine). [4] [5] The paramagnetic property of gadoteric acid reduces the T1 relaxation time (and to some extent the T2 and T2* relaxation times) in MRI, which is the source of its clinical utility. Because ...
8. 365 by Whole Foods Market, No Salt Albacore Tuna in Water. Whole Foods. Packed in water, this canned tuna has 120 mg of sodium and 5 grams of fat per serving. “The moderate fat content, much ...
Gadopentetic acid, sold under the brand name Magnevist, is a gadolinium-based MRI contrast agent. [2]It is usually administered as a salt of a complex of gadolinium with DTPA (diethylenetriaminepentacetate) with the chemical formula A 2 [Gd(DTPA)(H 2 O)]; when cation A is the protonated form of the amino sugar meglumine the salt goes under the name "gadopentetate dimeglumine".
Meglumine is a sugar alcohol derived from glucose that contains an amino group modification. It is often used as an excipient in pharmaceuticals [ 1 ] and in conjunction with iodinated compounds in contrast media such as diatrizoate meglumine , iothalamate meglumine , and iodipamide meglumine .
Therefore, if you’re a recreational exerciser that doesn’t break too much of a sweat, or if you plan to work out for less than an hour, you can likely get by just drinking water, she says.
The World Health Organization issued a restriction on use of several gadolinium contrast agents in November 2009 stating that "High-risk gadolinium-containing contrast agents (Optimark, Omniscan, Magnevist, Magnegita, and Gado-MRT ratiopharm) are contraindicated in patients with severe kidney problems, in patients who are scheduled for or have ...
In the form of the methylglucamine salt meglumine gadobenate or gadobenate dimeglumine , it is used as a gadolinium-based MRI contrast medium. [4] BOPTA is a derivative of DTPA in which one terminal carboxyl group, –C(O)OH is replaced by -C–O–CH 2 C 6 H 5. Thus gadobenic acid is closely related to gadopentetic acid.
The decahydrate of gadolinium oxalate thermally decomposes to obtain the anhydrous form, which can then be heated to produce gadolinium oxide. [2] Gadolinium oxalate reacts with hydrochloric acid to produce Gd(C 2 O 4)Cl. [3] It also reacts with sodium hydroxide under hydrothermal conditions to produce gadolinium hydroxide. [1]