Cover image of the article: Determination of Isosorbide Dinitrate in Serum by GasChromatography with New Generation of Electron CaptureDetector and its Application in Pharmacokinetic Study

Image Credit:Iran J Pharm Res

Determination of Isosorbide Dinitrate in Serum by GasChromatography with New Generation of Electron CaptureDetector and its Application in Pharmacokinetic Study

Authors

Massoud Mahmoudian1,*, Hamidreza Falahatpishe2, Babak Gholamine3, Ladan Tayebi2
1Department of Pharmacology, Iran University of Medical Sciences, Tehran, Iran
2Pars Biopharmacy Research Laboratory, Tehran, Iran
3Department of Pharmacology and Toxicology, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran
*Corresponding Author: Department of Pharmacology, Iran University of Medical Sciences, Tehran, Iran. Email:masmah99@iums.ac.ir

Iranian Journal of Pharmaceutical Research:Vol. 8, issue 4; 251-255
Published online:Nov 20, 2010
Article type:Research Article
Received:Aug 01, 2008
Accepted:Feb 01, 2009
How to Cite:Mahmoudian M, Falahatpishe H, Gholamine B, Tayebi L. Determination of Isosorbide Dinitrate in Serum by GasChromatography with New Generation of Electron CaptureDetector and its Application in Pharmacokinetic Study. Iran J Pharm Res. 2022;8(4):e128645. doi: https://doi.org/10.22037/ijpr.2010.818

Abstract

Isosorbide dinitrate (ISDN) is an effective drug in treatment of angina pectoris. In this study a new generation of electron capture detector (non-radioactive) with a short, non-polar and wide-bore column was used for analysis of ISDN in human serum. ISDN was extracted from serum by a mixture of ether and ethyl acetate and concentrated at room temperature. The method was linear between 5-50 ng/mL. Recovery and accuracy were 99-108% and greater than 90%, respectively, and inter-day precision was lower than 13%. Pharmacokinetic parameters were analyzed after oral administrations of Isocor 40 mg sustained release tablet in comparison with Isoket Retard 40. The statistical results obtained from comparison of Cmax, Tmax and AUC parameters showed no significant difference between these two productsand therefor they were reported to be bioequivalent. Further more, the method used was found to be sensitive and accurate in pharmacokinetic studies.

Highlights

Copyright

© 2022, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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