Lofentanil

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lofentanil.svg

Lofentanil is a highly potent synthetic opioid analgesic drug, which is an analog of fentanyl. It is primarily used in veterinary medicine for the sedation and anesthesia of large animals. Lofentanil is known for its high potency and long duration of action.

Chemical Structure and Properties[edit | edit source]

Lofentanil belongs to the 4-anilidopiperidine class of synthetic opioids. Its chemical structure is similar to that of fentanyl, with modifications that increase its potency. The molecular formula of lofentanil is C22H28N2O2, and its IUPAC name is N-[1-[2-(4-[[methoxymethyl]phenyl]ethyl]-4-piperidyl]-N-phenylpropanamide.

Pharmacology[edit | edit source]

Lofentanil acts primarily as an agonist at the μ-opioid receptor, which is responsible for its analgesic and sedative effects. It has a high affinity for these receptors, leading to its potent effects. The drug's high potency means that only small doses are required to achieve the desired effects, which can be beneficial in a controlled medical setting but also increases the risk of overdose and side effects.

Medical Uses[edit | edit source]

Lofentanil is used in veterinary medicine, particularly for the sedation and anesthesia of large animals such as elephants and bears. Its long duration of action makes it suitable for procedures that require extended periods of sedation.

Side Effects and Risks[edit | edit source]

As with other opioids, lofentanil can cause a range of side effects, including respiratory depression, bradycardia, and hypotension. Due to its high potency, there is a significant risk of overdose, which can be fatal. Proper dosing and monitoring are essential when using this drug.

Regulation and Legal Status[edit | edit source]

Lofentanil is classified as a Schedule I controlled substance in many countries, meaning it is considered to have a high potential for abuse and no accepted medical use in humans. Its use is strictly regulated, and it is primarily available for veterinary use under controlled conditions.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD