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Original Research Article | OPEN ACCESS

Microbial Metabolism and Inhibition Studies of Phenobarbital

Kummarigunta Kavitha, Maravajhala Vidyavathi , Sepuri Asha, Hima TVL Bindu

Institute of Pharmaceutical Technology, Sri Padmavathi Mahila Viswa Vidyalayam, Tirupathi – 517 502, A.P., India;

For correspondence:-  Maravajhala Vidyavathi   Email: vidyasur@rediffmail.com

Received: 1 February 2011        Accepted: 2 December 2011        Published: 21 February 2012

Citation: Kavitha K, Vidyavathi M, Asha S, Bindu HT. Microbial Metabolism and Inhibition Studies of Phenobarbital. Trop J Pharm Res 2012; 11(1):62-68 doi: 10.4314/tjpr.v11i1.8

© 2012 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: Screening scale studies were performed with eight cultures for their ability to metabolize  phenobarbital, an antiepileptic, sedative, hypnotic and substrate for CYP 2C9 and 2C19. 
Methods: The transformation of phenobarbital was confirmed and characterized by fermentation techniques, high performance liquid chromatography (HPLC), mass spectrometry (MS) and metabolism inhibition studies.
Results: Among the different cultures screened, a fungus, Rhizopus stolonifer NCIM 880, transformed phenobarbital to its metabolite, the N-glucuronide of p- hydroxy phenobarbital. HPLC data show a solvent peak at 2.4 min, culture components peaks at 4.0 and 5.4 min, respectively, and phenobarbital peak at 10.3 min, for both controls and test samples, but only the sample of  Rhizopus stolonifer showed an additional peak at 3.1 min, indicating formation of a metabolite. 
Conclusion: Microbial metabolism of phenobarbital was similar to the metabolism of the drug in mammals. Therefore, Rhizopus stolonifer can be used as a suitable in vitro model to mimic CYP 2C9 metabolism and to synthesize metabolites required for further pharmacological and toxicological studies.

Keywords: Microbial metabolism, Phenobarbital, Inhibition studies, Rhizopus stolonifer, CYP 2C9, Fenofibrate

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Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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