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The World Journal of Biological Psychiatry Volume 7, 2006 - Issue 3
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CASE REPORT

Sulbutiamine, an ‘innocent’ over the counter drug, interferes with therapeutic outcome of bipolar disorder

Athanasios Douzenis Department of General Hospital Psychiatry, Athens University Medical School, ‘Attikon’ Hospital, Athens, Greece
,
Ioannis Michopoulos Department of General Hospital Psychiatry, Athens University Medical School, ‘Attikon’ Hospital, Athens, Greece
&
Lefteris Lykouras Department of General Hospital Psychiatry, Athens University Medical School, ‘Attikon’ Hospital, Athens, GreeceCorrespondence[email protected]
, FICPM , MD , PhD
Pages 183-185 | Received 14 Jul 2005, Published online: 12 Jul 2009

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Hayam M. Lotfy, Mohamed A. Abdallah & Medhat A. Al-Ghobashy. (2016) Development and Validation of Stability Indicating Spectrophotometric Methods for Determination of Sulbutiamine in Tablet Dosage Form. Analytical Chemistry Letters 6:2, pages 159-173.
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Articles from other publishers (5)

Jaeah Kim, Christopher P. Hopper, Kelsey H. Connell, Parisa Darkhal, Jason A. Zastre & Michael G. Bartlett. (2016) Development of a novel method for the bioanalysis of benfotiamine and sulbutiamine in cancer cells. Analytical Methods 8:28, pages 5596-5603.
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Jessica Harder, Samata Sharma & David Gitlin. (2014) Secondary Mania as a Possible Neuropsychiatric Complication of Dengue Fever. Psychosomatics 55:5, pages 512-516.
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Kui Dong Kang, Aman Shah Abdul Majid, Kyung-A Kim, Kyungsu Kang, Hong Ryul Ahn, Chu Won Nho & Sang Hoon Jung. (2010) Sulbutiamine Counteracts Trophic Factor Deprivation Induced Apoptotic Cell Death in Transformed Retinal Ganglion Cells. Neurochemical Research 35:11, pages 1828-1839.
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Tim Sobolevsky & Grigory Rodchenkov. (2010) Sulbutiamine in sports. Drug Testing and Analysis 2:11-12, pages 643-646.
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Marie-Laure Volvert, Sandrine Seyen, Marie Piette, Brigitte Evrard, Marjorie Gangolf, Jean-Christophe Plumier & Lucien Bettendorff. (2008) Benfotiamine, a synthetic S-acyl thiamine derivative, has different mechanisms of action and a different pharmacological profile than lipid-soluble thiamine disulfide derivatives. BMC Pharmacology 8:1.
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