Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats

Nimodipine is a calcium channel blocker used for the prevention of cerebral vasospasm after subarachnoid hemorrhage, a type of strokes. Its unique ability to selectively dilate blood vessels in the brain makes it a crucial medication in neurology. Pharmaceutical analysis of nimodipine is important...

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Main Authors: Samir Hasson Aziz Ramadhan, Khalid Kadhem Al-Kinani
Format: Article
Language:English
Published: College of Pharmacy University of Baghdad 2025-03-01
Series:Iraqi Journal of Pharmaceutical Sciences
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Online Access:https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/3055
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author Samir Hasson Aziz Ramadhan
Khalid Kadhem Al-Kinani
author_facet Samir Hasson Aziz Ramadhan
Khalid Kadhem Al-Kinani
author_sort Samir Hasson Aziz Ramadhan
collection DOAJ
description Nimodipine is a calcium channel blocker used for the prevention of cerebral vasospasm after subarachnoid hemorrhage, a type of strokes. Its unique ability to selectively dilate blood vessels in the brain makes it a crucial medication in neurology. Pharmaceutical analysis of nimodipine is important to ensure its safety, efficacy, and quality, and to establish optimal dosage regimens for patients. Hence, a bioanalytical method based on high performance liquid chromatography (HPLC) was developed and validated to determine the concentration of nimodipine in rat’s plasma that has been spiked with the drug. The current method development included the processing of plasma followed by injection into HPLC system with ultraviolet detector. Sample preparation involved utilizing 1-pentanol as an extraction solvent. Chromatographic separation was performed on octadecylsilane (ODS) column using water/methanol as mobile phase. Nifedipine was used as an internal standard (IS). The validation results indicated that the proposed method is specific and linear for nimodipine within the concentration range of 10.0 to 150.0 ng/mL. The accuracy and precision of the method were assessed for both inter-day and intra-day measurements. The results revealed accuracies ranging from 97.00% to 99.66% and 95.12% to 101.28%, respectively. In terms of precision, the values ranged from 1.17% to 3.10% for inter-day measurement and 1.00% to 2.23%, for intra-day measurements. The recovery rates for nimodipine and nifedipine were 95.91% and 86.61%, respectively. Furthermore, the method demonstrated good stability at short-term room temperature (99.44%), long-term freeze temperature (97.80%), and freeze/thaw (97.04%) conditions. Overall, these findings suggest that the method is suitable for use in pre-clinical pharmacokinetic studies involving involving nimodipine-containing drug delivery system.
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spelling doaj-art-535cd7db90cc46debd370e62d21635ee2025-08-20T02:48:19ZengCollege of Pharmacy University of BaghdadIraqi Journal of Pharmaceutical Sciences1683-35972521-35122025-03-0134110.31351/vol34iss1pp133-142Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of RatsSamir Hasson Aziz Ramadhan0Khalid Kadhem Al-Kinani1Ministry of Health ,National Center for Drugs Research and Control, Directorate of Technical Affairs ,Baghdad, Iraq.Department of Pharmaceutics, College of Pharmacy, University of Baghdad, Baghdad, Iraq. Nimodipine is a calcium channel blocker used for the prevention of cerebral vasospasm after subarachnoid hemorrhage, a type of strokes. Its unique ability to selectively dilate blood vessels in the brain makes it a crucial medication in neurology. Pharmaceutical analysis of nimodipine is important to ensure its safety, efficacy, and quality, and to establish optimal dosage regimens for patients. Hence, a bioanalytical method based on high performance liquid chromatography (HPLC) was developed and validated to determine the concentration of nimodipine in rat’s plasma that has been spiked with the drug. The current method development included the processing of plasma followed by injection into HPLC system with ultraviolet detector. Sample preparation involved utilizing 1-pentanol as an extraction solvent. Chromatographic separation was performed on octadecylsilane (ODS) column using water/methanol as mobile phase. Nifedipine was used as an internal standard (IS). The validation results indicated that the proposed method is specific and linear for nimodipine within the concentration range of 10.0 to 150.0 ng/mL. The accuracy and precision of the method were assessed for both inter-day and intra-day measurements. The results revealed accuracies ranging from 97.00% to 99.66% and 95.12% to 101.28%, respectively. In terms of precision, the values ranged from 1.17% to 3.10% for inter-day measurement and 1.00% to 2.23%, for intra-day measurements. The recovery rates for nimodipine and nifedipine were 95.91% and 86.61%, respectively. Furthermore, the method demonstrated good stability at short-term room temperature (99.44%), long-term freeze temperature (97.80%), and freeze/thaw (97.04%) conditions. Overall, these findings suggest that the method is suitable for use in pre-clinical pharmacokinetic studies involving involving nimodipine-containing drug delivery system. https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/3055bioanalytical methodHPLCnimodipinepre-clinical pharmacokineticsvalidation
spellingShingle Samir Hasson Aziz Ramadhan
Khalid Kadhem Al-Kinani
Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats
Iraqi Journal of Pharmaceutical Sciences
bioanalytical method
HPLC
nimodipine
pre-clinical pharmacokinetics
validation
title Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats
title_full Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats
title_fullStr Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats
title_full_unstemmed Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats
title_short Development and Validation of a Bioanalytical Method for the Determination of Nimodipine Concentration in Plasma of Rats
title_sort development and validation of a bioanalytical method for the determination of nimodipine concentration in plasma of rats
topic bioanalytical method
HPLC
nimodipine
pre-clinical pharmacokinetics
validation
url https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/3055
work_keys_str_mv AT samirhassonazizramadhan developmentandvalidationofabioanalyticalmethodforthedeterminationofnimodipineconcentrationinplasmaofrats
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