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Biocatalytic Conversion and Detoxification of Imipramine by the Laccase-Mediated System Publisher



Tahmasbi H1, 2 ; Khoshayand MR3 ; Bozorgikoushalshahi M1 ; Heidary M1 ; Ghazikhansari M2 ; Faramarzi MA1
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Authors Affiliations
  1. 1. Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, P.O. Box 14155-6451, Tehran, 1417614411, Iran
  2. 2. Department of Pharmacology, Faculty of Medicine, Tehran University of Medical Science, P.O. Box 13145-784, Tehran, 1417614411, Iran
  3. 3. Department of Drug and Food Control, Faculty of Pharmacy and Pharmaceuticals Quality Assurance Research Center, Tehran University of Medical Sciences, Tehran, 1417614411, Iran

Source: International Biodeterioration and Biodegradation Published:2016


Abstract

This study describes the enzymatic elimination of imipramine and four other tricyclic antidepressants (TCAs) by laccase-mediated catalysis in aqueous solution. The results showed that TCAs demonstrated dissimilar enzymatic elimination behavior: up to 67% of clomipramine and 82% of imipramine were significantly removed during the first 6 h. The elimination percentages of amitriptyline, doxepin, and nortriptyline were 11%, 6%, and 23%, respectively, after 72 h laccase-based treatment. Due to the rapid and high percentage of removal, imipramine was selected for detailed toxicity evaluation. Optimal levels for the main factors in the enzymatic removal process of imipramine were obtained as pH (4.9), incubation time (5.7 h), imipramine concentration (0.12 μg mL-1), and enzyme activity (1.63 U mL-1). Laccase-catalyzed transformation of imipramine led to the formation of an unknown metabolite which was subsequently purified and spectroscopically characterized as 3-(2,7-dihydroxy-10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-1-hydroxy-N,N-dimethyl-3-oxopropan-1-amine oxide. The toxicity reduction of the bio-product was assessed by MTT cell and Caco-2 cell line. © 2015 Elsevier Ltd.
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