Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh

A simple, specific and sensitive reversed-phase high performance liquid chromatography method was developed to determine insulin in rat plasma. The method involves direct injection of rat plasma sample after deproteinization using acetonitrile - propanol (1:1). The mobile phase comprises a mixture o...

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Main Author: Salleh, Eda Frida
Format: Thesis
Language:English
Published: 2012
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Online Access:https://ir.uitm.edu.my/id/eprint/65561/1/65561.pdf
https://ir.uitm.edu.my/id/eprint/65561/
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Institution: Universiti Teknologi Mara
Language: English
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spelling my.uitm.ir.655612022-11-07T07:10:58Z https://ir.uitm.edu.my/id/eprint/65561/ Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh Salleh, Eda Frida Drugs and their actions A simple, specific and sensitive reversed-phase high performance liquid chromatography method was developed to determine insulin in rat plasma. The method involves direct injection of rat plasma sample after deproteinization using acetonitrile - propanol (1:1). The mobile phase comprises a mixture of water and acetonitrile containing 0.1% v/v trifloroacetic acid (TFA) with gradient analysis by increasing the proportion of mobile phase of water from 25% v/v to 40% v/v within 20 minutes. A Phenomenon C18 column (5μm 4.6 x 150 mm) was used for the chromatographic separation which was delivered at a flow rate of 0.6 mL/min at 210 nm wavelength. Under these conditions, the method was validated with respect to linearity, recovery, specificity, accuracy, precision, and stability. The method was proven to be linear over the concentration range of 0.39 - 50.00 μg/ml with mean correlation coefficient of 0.9994. The mean extraction recovery was 97.4%, while the precision of within-day and between-day measurements was a <9%. The limit of detection (LOD) and limit of quantitation (LOQ) of the method were 0.13 μg/ml and 0.39 μg/ml, respectively. The short run time, specificity, sensitivity and reproducibility of this method were found to be satisfactory and thus suitable for routine determination of insulin in rat. 2012 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/65561/1/65561.pdf Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh. (2012) Degree thesis, thesis, Universiti Teknologi MARA (UiTM). <http://terminalib.uitm.edu.my/65561.pdf>
institution Universiti Teknologi Mara
building Tun Abdul Razak Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
url_provider http://ir.uitm.edu.my/
language English
topic Drugs and their actions
spellingShingle Drugs and their actions
Salleh, Eda Frida
Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh
description A simple, specific and sensitive reversed-phase high performance liquid chromatography method was developed to determine insulin in rat plasma. The method involves direct injection of rat plasma sample after deproteinization using acetonitrile - propanol (1:1). The mobile phase comprises a mixture of water and acetonitrile containing 0.1% v/v trifloroacetic acid (TFA) with gradient analysis by increasing the proportion of mobile phase of water from 25% v/v to 40% v/v within 20 minutes. A Phenomenon C18 column (5μm 4.6 x 150 mm) was used for the chromatographic separation which was delivered at a flow rate of 0.6 mL/min at 210 nm wavelength. Under these conditions, the method was validated with respect to linearity, recovery, specificity, accuracy, precision, and stability. The method was proven to be linear over the concentration range of 0.39 - 50.00 μg/ml with mean correlation coefficient of 0.9994. The mean extraction recovery was 97.4%, while the precision of within-day and between-day measurements was a <9%. The limit of detection (LOD) and limit of quantitation (LOQ) of the method were 0.13 μg/ml and 0.39 μg/ml, respectively. The short run time, specificity, sensitivity and reproducibility of this method were found to be satisfactory and thus suitable for routine determination of insulin in rat.
format Thesis
author Salleh, Eda Frida
author_facet Salleh, Eda Frida
author_sort Salleh, Eda Frida
title Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh
title_short Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh
title_full Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh
title_fullStr Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh
title_full_unstemmed Development and validation of a gradient HPLC method for the determination of insulin in rat plasma: application to pharmacokinetic study / Eda Frida Salleh
title_sort development and validation of a gradient hplc method for the determination of insulin in rat plasma: application to pharmacokinetic study / eda frida salleh
publishDate 2012
url https://ir.uitm.edu.my/id/eprint/65561/1/65561.pdf
https://ir.uitm.edu.my/id/eprint/65561/
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