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Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect

PURPOSE: To develop an UPLC-MS/MS method for the quantitative analysis of pentoxifylline in beagle dog plasma and apply it to a pharmacokinetic study of food effect. METHODS: Sample separation was achieved using a Kinetex Phenyl-Hexyl column (50 × 2.1 mm, 1.7 μm) with a gradient elution program in 5...

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Autores principales: Xu, Yuxiang, Gao, Xiaonan, Zhu, Yunfang, Zhang, Qi, Qie, Hongxin, Zhao, Haopeng, Gao, Jinglin, Wang, Mingxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693274/
https://www.ncbi.nlm.nih.gov/pubmed/38046282
http://dx.doi.org/10.2147/DDDT.S434492
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author Xu, Yuxiang
Gao, Xiaonan
Zhu, Yunfang
Zhang, Qi
Qie, Hongxin
Zhao, Haopeng
Gao, Jinglin
Wang, Mingxia
author_facet Xu, Yuxiang
Gao, Xiaonan
Zhu, Yunfang
Zhang, Qi
Qie, Hongxin
Zhao, Haopeng
Gao, Jinglin
Wang, Mingxia
author_sort Xu, Yuxiang
collection PubMed
description PURPOSE: To develop an UPLC-MS/MS method for the quantitative analysis of pentoxifylline in beagle dog plasma and apply it to a pharmacokinetic study of food effect. METHODS: Sample separation was achieved using a Kinetex Phenyl-Hexyl column (50 × 2.1 mm, 1.7 μm) with a gradient elution program in 5.5 min after a simple protein precipitation with methanol. Using the mobile phase that made up by 0.2% formic acid and 5mM ammonium formate water (A) and methanol (B). Quantitation was carried out using the positive ionization mode with multiple reaction monitoring (MRM). A randomized, single-dose, two-period crossover study was conducted in six fasted or fed beagles that received 400 mg pentoxifylline sustained-release tablets (Brand name: Shuanling™, CSPC Pharmaceutical Group). WinNonlin(®) software was used to calculate pharmacokinetic parameters. RESULTS: The linear calibration range was 2–1000 ng/mL (r(2)> 0.99). Both intra- and inter-batch precision were less than 6.27%, and the accuracy ranged from 88.65% to 97.18%. Pentoxifylline was readily absorbed in fasted and fed dogs administered a dose of 400 mg (t(max):1.54h vs 1.83h). Compared to the fasted group, the AUC(0→t) and C(max) in the fed group increased by 1.71-fold and 1.30-fold, respectively. In the fasted group, the AUC(0→t) and C(max) values were 4684.08 h•ng/mL and 2402.33 ng/mL, respectively. In the fed group, these values were 8027.75 h•ng/mL and 3119.67 ng/mL. The difference in AUC(0-t) between the fed and fasted group was statistically significant. CONCLUSION: The novel optimized UPLC-MS/MS assay is an effective tool for the determination of pentoxifylline and has been successfully applied in pharmacokinetic studies of pentoxifylline in beagle dogs. The administration of pentoxifylline sustained-release tablets with food significantly increased the area under the time curve, and it is recommended that they should be administered during or shortly after feeding.
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spelling pubmed-106932742023-12-03 Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect Xu, Yuxiang Gao, Xiaonan Zhu, Yunfang Zhang, Qi Qie, Hongxin Zhao, Haopeng Gao, Jinglin Wang, Mingxia Drug Des Devel Ther Original Research PURPOSE: To develop an UPLC-MS/MS method for the quantitative analysis of pentoxifylline in beagle dog plasma and apply it to a pharmacokinetic study of food effect. METHODS: Sample separation was achieved using a Kinetex Phenyl-Hexyl column (50 × 2.1 mm, 1.7 μm) with a gradient elution program in 5.5 min after a simple protein precipitation with methanol. Using the mobile phase that made up by 0.2% formic acid and 5mM ammonium formate water (A) and methanol (B). Quantitation was carried out using the positive ionization mode with multiple reaction monitoring (MRM). A randomized, single-dose, two-period crossover study was conducted in six fasted or fed beagles that received 400 mg pentoxifylline sustained-release tablets (Brand name: Shuanling™, CSPC Pharmaceutical Group). WinNonlin(®) software was used to calculate pharmacokinetic parameters. RESULTS: The linear calibration range was 2–1000 ng/mL (r(2)> 0.99). Both intra- and inter-batch precision were less than 6.27%, and the accuracy ranged from 88.65% to 97.18%. Pentoxifylline was readily absorbed in fasted and fed dogs administered a dose of 400 mg (t(max):1.54h vs 1.83h). Compared to the fasted group, the AUC(0→t) and C(max) in the fed group increased by 1.71-fold and 1.30-fold, respectively. In the fasted group, the AUC(0→t) and C(max) values were 4684.08 h•ng/mL and 2402.33 ng/mL, respectively. In the fed group, these values were 8027.75 h•ng/mL and 3119.67 ng/mL. The difference in AUC(0-t) between the fed and fasted group was statistically significant. CONCLUSION: The novel optimized UPLC-MS/MS assay is an effective tool for the determination of pentoxifylline and has been successfully applied in pharmacokinetic studies of pentoxifylline in beagle dogs. The administration of pentoxifylline sustained-release tablets with food significantly increased the area under the time curve, and it is recommended that they should be administered during or shortly after feeding. Dove 2023-11-28 /pmc/articles/PMC10693274/ /pubmed/38046282 http://dx.doi.org/10.2147/DDDT.S434492 Text en © 2023 Xu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Xu, Yuxiang
Gao, Xiaonan
Zhu, Yunfang
Zhang, Qi
Qie, Hongxin
Zhao, Haopeng
Gao, Jinglin
Wang, Mingxia
Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect
title Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect
title_full Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect
title_fullStr Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect
title_full_unstemmed Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect
title_short Development and Validation a UPLC-MS/MS Method for Quantification of Pentoxifylline in Beagle Plasma: Application for Pharmacokinetic Study of Food Effect
title_sort development and validation a uplc-ms/ms method for quantification of pentoxifylline in beagle plasma: application for pharmacokinetic study of food effect
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693274/
https://www.ncbi.nlm.nih.gov/pubmed/38046282
http://dx.doi.org/10.2147/DDDT.S434492
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