Amidotrizoate

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Amidotrizoate is a contrast agent used in radiology to enhance the visibility of internal structures in X-ray-based imaging techniques such as angiography, urography, and computed tomography (CT). It is an iodinated contrast medium, meaning it contains iodine, which is highly effective at absorbing X-rays. This property allows it to outline blood vessels, organs, and other structures, making them more visible on an X-ray image.

Chemistry[edit | edit source]

Amidotrizoate, chemically known as 3,5-Bis(acetylamino)-2,4,6-triiodobenzoic acid, belongs to the class of organic compounds known as benzoic acids. The presence of three iodine atoms in its structure is critical for its function as a contrast agent. Amidotrizoate is water-soluble, which is essential for its application in medical imaging.

Pharmacology[edit | edit source]

When administered, amidotrizoate rapidly distributes into the extracellular space and selectively opacifies the vascular and urinary systems. Its high iodine content allows it to absorb X-rays efficiently, thereby delineating the structures it fills or surrounds. The compound is eventually excreted unchanged primarily through the kidneys, making renal function an important consideration in its use.

Clinical Uses[edit | edit source]

Amidotrizoate is used in various diagnostic procedures, including:

Side Effects[edit | edit source]

As with all contrast media, amidotrizoate can cause side effects, ranging from mild (such as nausea and vomiting) to severe (including allergic reactions and contrast-induced nephropathy). The risk of adverse effects necessitates careful patient selection and monitoring during its use.

Contraindications[edit | edit source]

Patients with a history of hypersensitivity to iodinated contrast media, severe hyperthyroidism, or poor kidney function may be contraindicated for amidotrizoate administration due to the increased risk of adverse reactions or complications.

Regulation and Approval[edit | edit source]

Amidotrizoate, like other contrast agents, is subject to regulation and approval by health authorities such as the Food and Drug Administration (FDA) in the United States. Its use must comply with guidelines that ensure patient safety and efficacy of the product.

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Contributors: Prab R. Tumpati, MD