Gadoteric acid
Clinical data
Trade namesArtirem, Dotarem, Clariscan, others[1]
Other namesDOTA-Gd, Gadoterate meglumine (USAN US)
AHFS/Drugs.comInternational Drug Names
License data
Routes of
administration		Intravenous
ATC code
Legal status
Legal status
Identifiers
  • gadolinium(3+) 2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetate
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H25GdN4O8
Molar mass558.65 g·mol−1
3D model (JSmol)
  • [Gd+3].OC(=O)CN1CCN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC([O-])=O)CC1
  • InChI=1S/C16H28N4O8.Gd/c21-13(22)9-17-1-2-18(10-14(23)24)5-6-20(12-16(27)28)8-7-19(4-3-17)11-15(25)26;/h1-12H2,(H,21,22)(H,23,24)(H,25,26)(H,27,28);/q;+3/p-3
  • Key:GFSTXYOTEVLASN-UHFFFAOYSA-K
 ☒NcheckY (what is this?)  (verify)

Gadoteric acid, sold under the brand name Dotarem among others, is a macrocycle-structured gadolinium-based MRI contrast agent (GBCA). It consists of the organic acid DOTA as a chelating agent, and gadolinium (Gd3+), and is used in form of the meglumine salt (gadoterate meglumine).[3][4] 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 it has magnetic properties, gadoteric acid develops a magnetic moment when put under a magnetic field, which increases the signal intensity (brightness) of tissues during MRI imaging.[6]

Medical uses

It is widely used in the United States for Breast MRI imaging for women who have or are suspected to have breast cancer. It is also used for imaging of blood vessels and inflamed or diseased tissue where the blood vessels become 'leaky'. It is often used when viewing intracranial lesions with abnormal vascularity or abnormalities in the blood–brain barrier. Gadoteric acid is used for MRI imaging of the brain, spine, and associated tissues for adult and pediatric (2 years of age or older) patients. The meglumine salt it takes the form of crosses the blood brain barrier of tissue with abnormal vasculature, highlighting the affected area with MRI. Gadoterate does cross the intact blood-brain barrier, so it might affect or enhance normal brain tissue in imaging.[6] Dotarem is administered through an intravenous bolus injection, either manually or through a power injection. Dotarem can stay in the body for years. [3][4]

Adverse effects

It is retained in the brain at a measurable level after an injection at standard dose (0.1 mmol/kg).[7] In vitro studies found it neurotoxic, less so than linears agents.[8]

Drugs with gadolinium-based contrasting agents can cause nephrogenic systemic fibrosis (NSF, or gadolinium-induced fibrosis) for those with impaired elimination of the drug. Those most at risk for NSF include patients with chronic or severe kidney disease and acute kidney injury.[3][4][9]

The rate of side effects are uncommon (0.1 to 1.0%), including nausea, headache, injection site reactions, hypertension, hypotension, dizziness, feeling hot, and somnolence.[10]

Pharmacology

A 2020 study found Clariscan was retained more in the cerebrum, cerebellum, kidney and liver of rats than those injected with Dotarem.[11]

History

The drug, under the brand name Dotarem, was brought to market by Guerbet.[12] It was launched on French market in 1989 and was FDA-approved in United States in March 2013.[12] As of 2013, gadoteric acid was approved in around 70 countries.[13][14] Dotarem is the seventh FDA-approved GBCA for use in central nervous system MRI.

In 2019, GE Healthcare launched gadoteric acid medication (as gadoterate meglumine) under the brand name Clariscan.[4][15]

References

  1. ↑ "Gadoteric Acid International". Drugs.com. 6 January 2021. Retrieved 21 January 2021.
  2. ↑ "Dotagraf 0.5 mmol/ml solution for injection - Summary of Product Characteristics (SmPC)". (emc). Retrieved 29 August 2021.
  3. 1 2 3 4 "Dotarem- gadoterate meglumine injection". DailyMed. Retrieved 29 August 2021.
  4. 1 2 3 4 5 "Clariscan- gadoterate meglumine injection, solution". DailyMed. Retrieved 29 August 2021.
  5. ↑ "Gadoteric acid intra articular formulation list nationally authorised medicinal products" (PDF). ema.europa.eu. Retrieved 20 May 2023.
  6. 1 2 DrugBank, ed. (22 August 2016). "Gadoteric acid". DrugBank.
  7. ↑ Stanescu AL, Shaw DW, Murata N, Murata K, Rutledge JC, Maloney E, et al. (March 2020). "Brain tissue gadolinium retention in pediatric patients after contrast-enhanced magnetic resonance exams: pathological confirmation". Pediatric Radiology. 50 (3): 388–396. doi:10.1007/s00247-019-04535-w. PMID 31989188. S2CID 210913930.
  8. ↑ Bower DV, Richter JK, von Tengg-Kobligk H, Heverhagen JT, Runge VM (August 2019). "Gadolinium-Based MRI Contrast Agents Induce Mitochondrial Toxicity and Cell Death in Human Neurons, and Toxicity Increases With Reduced Kinetic Stability of the Agent". Investigative Radiology. 54 (8): 453–463. doi:10.1097/RLI.0000000000000567. PMID 31265439. S2CID 164486744.
  9. ↑ Todd DJ, Kay J (2016). "Gadolinium-Induced Fibrosis". Annual Review of Medicine. 67: 273–91. doi:10.1146/annurev-med-063014-124936. PMID 26768242.
  10. ↑ "Summary of product characteristics - Dotarem 279.32 mg/ml Solution for injection in pre-filled syringes" (PDF). Guerbet. Archived from the original (PDF) on 13 December 2022. Retrieved 13 December 2022.
  11. ↑ Bussi S, Coppo A, Celeste R, Fanizzi A, Fringuello Mingo A, Ferraris A, et al. (February 2020). "Macrocyclic MR contrast agents: evaluation of multiple-organ gadolinium retention in healthy rats". Insights into Imaging. 11 (1): 11. doi:10.1186/s13244-019-0824-5. PMC 7000570. PMID 32020385.
  12. 1 2 Hollmer M (6 January 2014). "Dotarem: A safe(r) gadolinium-based contrast imaging agent". FierceBiotech.
  13. ↑ "Gadoteric Acid international brands". Drugs.com. Retrieved 7 March 2017.
  14. ↑ Guerbet LLC (14 February 2013). "Advisory Committee Briefing Document for NDA 204-781". FDA.
  15. ↑ "Clariscan 0.5 mmol/ ml solution for injection" (PDF). Archived from the original (PDF) on 1 March 2017. Retrieved 28 February 2017.

Further reading

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