Levodopa is a prodrug of dopamine that is administered to patients with Parkinson's due to its ability to cross the blood-brain barrier. Levodopa can be metabolised to dopamine on either side of the blood-brain barrier and so it is generally administered with a dopa decarboxylase inhibitor like carbidopa to prevent metabolism until after it has crossed the blood-brain barrier. Once past the blood-brain barrier, levodopa is metabolized to dopamine and supplements the low endogenous levels of dopamine to treat symptoms of Parkinson's. The first developed drug product that was approved by the FDA was a levodopa and carbidopa combined product called Sinemet that was approved on May 2, 1975.
Levodopa on its own is formulated as an oral inhalation powder indicated for intermittent treatment of off episodes in Parkinson's patients who are already being treated with carbidopa and levodopa. Levodopa is most commonly formulated as an oral tablet with a peripheral dopa decarboxylase inhibitor indicated for treatment of Parkinson's disease, post-encephalitic parkinsonism, and symptomatic parkinsonism following carbon monoxide intoxication or manganese intoxication.
Norfolk&Norwich University Hospitals, Norwich, Norfolk, United Kingdom
Beijing Normal University, Beijing, Beijing, China
Acorda Site #1005, Hallandale Beach, Florida, United States
Acorda Site #1004, Atlanta, Georgia, United States
Acorda Site #1002, Orlando, Florida, United States
New York State Psychiatric Institute, New York, New York, United States
Centre for Neuroimaging Sciences, London, United Kingdom
University of California, Los Angeles, Los Angeles, California, United States
Washington University School of Medicine, Movement Disorders Center, Saint Louis, Missouri, United States
The first affiliated hospital of Zhengzhou university, Zhengzhou, Henan, China
Nuvisan Pharma Services, Neu-Ulm, Germany
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