In vivo study of the pharmacokinetic effect of amlodipine and gliclazide

It was found that there is kind of pharmacodynamic interaction between calcium channels blockers and sulfonylurea. The addition of amlodipine (AMLO) to gliclazide (GLZ) course caused significant decrease in glucose lowering effect of GLZ. The mechanism of AMLO-GLZ interaction is not well understood....

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Main Authors: Helaluddin, Abul Bashar Mohammed, Alaama, Mohammed, Awang, Mohamed, Abbas, Syed Atif
Format: Conference or Workshop Item
Language:English
Published: Centre of Lipids Engineering and Applied Research (CLEAR), Universiti Teknologi Malaysia (UTM) 2017
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Online Access:http://irep.iium.edu.my/60342/
http://irep.iium.edu.my/60342/
http://irep.iium.edu.my/60342/1/ICOST%202017.pdf
id iium-60342
recordtype eprints
spelling iium-603422017-12-27T02:31:42Z http://irep.iium.edu.my/60342/ In vivo study of the pharmacokinetic effect of amlodipine and gliclazide Helaluddin, Abul Bashar Mohammed Alaama, Mohammed Awang, Mohamed Abbas, Syed Atif QD Chemistry RS Pharmacy and materia medica RS403 Materia Medica-Pharmaceutical Chemistry It was found that there is kind of pharmacodynamic interaction between calcium channels blockers and sulfonylurea. The addition of amlodipine (AMLO) to gliclazide (GLZ) course caused significant decrease in glucose lowering effect of GLZ. The mechanism of AMLO-GLZ interaction is not well understood. There is a possibility that this interaction can be a result of pharmacokinetic interaction of both drugs; therefore, this study was designed to investigate the pharmacokinetic interaction between AMLO and GLZ in animal model. The pharmacokinetic interaction was evaluated using Sprauge Dawly rates as they were divided into three groups. The controle group received saline and the gliclazide groupe received gliclazide orally in the dose of 1.44 mg/kg, while the Amlo-Gliclazide groupe has received amlodipine and gliclazide orally with a dose of 0.09 mg/kg and 1.44 mg/kg respectively. After dosing, animals were anesthetized and the blood was collected using retro orbital blood collection method after 1, 2, 4, 6, 8, 12, 24 hours of the dose. A new and novel LC-MS/MS method was developed and validated for the determination of GLZ in and rat plasma. The results showed that the pharmacokinetic parameters such as Cmax (ng/ml), Tmax (hr) were not altered significantly by AMLO administration. However, the administration of AMLO lead to significant increase (p = 0.000672) in AUC. In conclusion the plasma GLZ concentration increased when it was co administered with AMLO, while Cmax and Tmax remain unchanged. This study suggests that AMLO might reduce GLZ elimination. Centre of Lipids Engineering and Applied Research (CLEAR), Universiti Teknologi Malaysia (UTM) 2017-04 Conference or Workshop Item PeerReviewed application/pdf en http://irep.iium.edu.my/60342/1/ICOST%202017.pdf Helaluddin, Abul Bashar Mohammed and Alaama, Mohammed and Awang, Mohamed and Abbas, Syed Atif (2017) In vivo study of the pharmacokinetic effect of amlodipine and gliclazide. In: 2nd International Conferenec on Separation Technology (ICoST) 2017, 15th-16th April 2017, Johor Bharu, Johor. https://clear.utm.my/icost2017/
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
topic QD Chemistry
RS Pharmacy and materia medica
RS403 Materia Medica-Pharmaceutical Chemistry
spellingShingle QD Chemistry
RS Pharmacy and materia medica
RS403 Materia Medica-Pharmaceutical Chemistry
Helaluddin, Abul Bashar Mohammed
Alaama, Mohammed
Awang, Mohamed
Abbas, Syed Atif
In vivo study of the pharmacokinetic effect of amlodipine and gliclazide
description It was found that there is kind of pharmacodynamic interaction between calcium channels blockers and sulfonylurea. The addition of amlodipine (AMLO) to gliclazide (GLZ) course caused significant decrease in glucose lowering effect of GLZ. The mechanism of AMLO-GLZ interaction is not well understood. There is a possibility that this interaction can be a result of pharmacokinetic interaction of both drugs; therefore, this study was designed to investigate the pharmacokinetic interaction between AMLO and GLZ in animal model. The pharmacokinetic interaction was evaluated using Sprauge Dawly rates as they were divided into three groups. The controle group received saline and the gliclazide groupe received gliclazide orally in the dose of 1.44 mg/kg, while the Amlo-Gliclazide groupe has received amlodipine and gliclazide orally with a dose of 0.09 mg/kg and 1.44 mg/kg respectively. After dosing, animals were anesthetized and the blood was collected using retro orbital blood collection method after 1, 2, 4, 6, 8, 12, 24 hours of the dose. A new and novel LC-MS/MS method was developed and validated for the determination of GLZ in and rat plasma. The results showed that the pharmacokinetic parameters such as Cmax (ng/ml), Tmax (hr) were not altered significantly by AMLO administration. However, the administration of AMLO lead to significant increase (p = 0.000672) in AUC. In conclusion the plasma GLZ concentration increased when it was co administered with AMLO, while Cmax and Tmax remain unchanged. This study suggests that AMLO might reduce GLZ elimination.
format Conference or Workshop Item
author Helaluddin, Abul Bashar Mohammed
Alaama, Mohammed
Awang, Mohamed
Abbas, Syed Atif
author_facet Helaluddin, Abul Bashar Mohammed
Alaama, Mohammed
Awang, Mohamed
Abbas, Syed Atif
author_sort Helaluddin, Abul Bashar Mohammed
title In vivo study of the pharmacokinetic effect of amlodipine and gliclazide
title_short In vivo study of the pharmacokinetic effect of amlodipine and gliclazide
title_full In vivo study of the pharmacokinetic effect of amlodipine and gliclazide
title_fullStr In vivo study of the pharmacokinetic effect of amlodipine and gliclazide
title_full_unstemmed In vivo study of the pharmacokinetic effect of amlodipine and gliclazide
title_sort in vivo study of the pharmacokinetic effect of amlodipine and gliclazide
publisher Centre of Lipids Engineering and Applied Research (CLEAR), Universiti Teknologi Malaysia (UTM)
publishDate 2017
url http://irep.iium.edu.my/60342/
http://irep.iium.edu.my/60342/
http://irep.iium.edu.my/60342/1/ICOST%202017.pdf
first_indexed 2023-09-18T21:25:32Z
last_indexed 2023-09-18T21:25:32Z
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