HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma

Background: The selective occurrence of hepatotoxicity observed with use of pazopanib may be attributed to its high level of plasma protein binding and low hepatic extraction ratio. The primary objective was to investigate changes in free drug concentration amongst patients with varying albumin conc...

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Main Authors: Toh, Yi Long, Pang, Yi Yun, Shwe, Maung, Kanesvaran, Ravindran, Toh, Chee Keong, Chan, Alexandre, Ho, Han Kiat
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/145356
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1453562023-02-28T19:24:49Z HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma Toh, Yi Long Pang, Yi Yun Shwe, Maung Kanesvaran, Ravindran Toh, Chee Keong Chan, Alexandre Ho, Han Kiat School of Physical and Mathematical Sciences Science::Medicine Pazopanib Plasma Free Drug Concentration Background: The selective occurrence of hepatotoxicity observed with use of pazopanib may be attributed to its high level of plasma protein binding and low hepatic extraction ratio. The primary objective was to investigate changes in free drug concentration amongst patients with varying albumin concentrations. Methods: A HPLC-MS/MS method using C18 column (4.6 × 150 mm, 5 μm) with ESI source in positive mode had been developed and validated for the quantitative determination of free pazaopanib concentration in human plasma. Prior to sample preparation, patient samples were subjected to 6-hour equilibrium dialysis with molecular weight cut-off set at 8000 Da. Results: The calibration curves were linear over the range of 5–1000 ng/mL, with a lower limit of quantification of 5 ng/mL. The intra-day and inter-day precisions and accuracies were all within ± 15 %, at 3 different quality controls. Higher median fraction unbound of pazopanib were observed in patients (n = 17) with lower than normal albumin concentrations. Conclusion: With the developed assay, monitoring of plasma free concentrations may be evaluated as an indicator of pazopanib exposure in patients. Published version 2020-12-18T03:09:31Z 2020-12-18T03:09:31Z 2020 Journal Article Toh, Y. L., Pang, Y. Y., Shwe, M., Kanesvaran, R., Toh, C. K., Chan, A., & Ho, H. K. (2020). HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma. Heliyon, 6(4), e03813-. doi:10.1016/j.heliyon.2020.e03813 2405-8440 https://hdl.handle.net/10356/145356 10.1016/j.heliyon.2020.e03813 32373731 4 6 en Heliyon © 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Pazopanib
Plasma Free Drug Concentration
spellingShingle Science::Medicine
Pazopanib
Plasma Free Drug Concentration
Toh, Yi Long
Pang, Yi Yun
Shwe, Maung
Kanesvaran, Ravindran
Toh, Chee Keong
Chan, Alexandre
Ho, Han Kiat
HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
description Background: The selective occurrence of hepatotoxicity observed with use of pazopanib may be attributed to its high level of plasma protein binding and low hepatic extraction ratio. The primary objective was to investigate changes in free drug concentration amongst patients with varying albumin concentrations. Methods: A HPLC-MS/MS method using C18 column (4.6 × 150 mm, 5 μm) with ESI source in positive mode had been developed and validated for the quantitative determination of free pazaopanib concentration in human plasma. Prior to sample preparation, patient samples were subjected to 6-hour equilibrium dialysis with molecular weight cut-off set at 8000 Da. Results: The calibration curves were linear over the range of 5–1000 ng/mL, with a lower limit of quantification of 5 ng/mL. The intra-day and inter-day precisions and accuracies were all within ± 15 %, at 3 different quality controls. Higher median fraction unbound of pazopanib were observed in patients (n = 17) with lower than normal albumin concentrations. Conclusion: With the developed assay, monitoring of plasma free concentrations may be evaluated as an indicator of pazopanib exposure in patients.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Toh, Yi Long
Pang, Yi Yun
Shwe, Maung
Kanesvaran, Ravindran
Toh, Chee Keong
Chan, Alexandre
Ho, Han Kiat
format Article
author Toh, Yi Long
Pang, Yi Yun
Shwe, Maung
Kanesvaran, Ravindran
Toh, Chee Keong
Chan, Alexandre
Ho, Han Kiat
author_sort Toh, Yi Long
title HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
title_short HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
title_full HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
title_fullStr HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
title_full_unstemmed HPLC-MS/MS coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
title_sort hplc-ms/ms coupled with equilibrium dialysis method for quantification of free drug concentration of pazopanib in plasma
publishDate 2020
url https://hdl.handle.net/10356/145356
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