Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method

Introduction. "Eltrombopag" is a thrombopoietin receptor agonist (TPO-RA) that is approved for the treatment of immune thrombocytopenic purpura (ITP). According to the literature, very few analytical methods for determining eltrombopag in biological samples have been reported. To study the...

Full description

Bibliographic Details
Main Authors: А. М. AL-Dhuraibi, A. L. Kulikov, M. V. Pokrovskiy
Format: Article
Language:Russian
Published: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2022-11-01
Series:Разработка и регистрация лекарственных средств
Subjects:
Online Access:https://www.pharmjournal.ru/jour/article/view/1381
_version_ 1797874899429097472
author А. М. AL-Dhuraibi
A. L. Kulikov
M. V. Pokrovskiy
author_facet А. М. AL-Dhuraibi
A. L. Kulikov
M. V. Pokrovskiy
author_sort А. М. AL-Dhuraibi
collection DOAJ
description Introduction. "Eltrombopag" is a thrombopoietin receptor agonist (TPO-RA) that is approved for the treatment of immune thrombocytopenic purpura (ITP). According to the literature, very few analytical methods for determining eltrombopag in biological samples have been reported. To study the pharmacokinetics of new formulations of eltrombopag, a sensitive and specific method is required that allows one to accurately determine the concentration of eltrombopag in human blood plasma. Normally, HPLC methods should provide time, accuracy, and sensitivity as a result, it is necessary to develop fast or ultra-fast methods such as LC-MS/MS without any loss in sensitivity or separation efficiency.Aim. We aimed to develop and validate a method for the quantitative determination of eltrombopag levels in human plasma by using HPLC with mass spectrometric detection for performing the analytical part of pharmacokinetic studies.Materials and methods. Eltrombopag levels were determined in human plasma by HPLC with mass spectrometric detection. The samples were prepared using protein deposition.Results and discussion. The method was validated for selectivity, matrix effect, calibration curve, accuracy, precision, the limit of quantification, carry-over effect, and sample stability.Conclusion. The method for the determination of eltrombopag levels in human plasma has been developed and validated by HPLC-MS. The analytical range of eltrombopag levels in human plasma was 10–6750 ng/ml. This method could be used to determine eltrombopag levels in plasma for PK and BE studies.
first_indexed 2024-04-10T01:39:24Z
format Article
id doaj.art-9a65a0ef26be4b3d9247b623668185f5
institution Directory Open Access Journal
issn 2305-2066
2658-5049
language Russian
last_indexed 2024-04-10T01:39:24Z
publishDate 2022-11-01
publisher LLC Center of Pharmaceutical Analytics (LLC «CPHA»)
record_format Article
series Разработка и регистрация лекарственных средств
spelling doaj.art-9a65a0ef26be4b3d9247b623668185f52023-03-13T09:14:04ZrusLLC Center of Pharmaceutical Analytics (LLC «CPHA»)Разработка и регистрация лекарственных средств2305-20662658-50492022-11-0111422623910.33380/2305-2066-2022-11-4-226-2391040Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS MethodА. М. AL-Dhuraibi0A. L. Kulikov1M. V. Pokrovskiy2Аденский университет; ФГАОУ ВО «Белгородский государственный национальный исследовательский университет» (НИУ «БелГУ)ФГАОУ ВО «Белгородский государственный национальный исследовательский университет» (НИУ «БелГУ)ФГАОУ ВО «Белгородский государственный национальный исследовательский университет» (НИУ «БелГУ)Introduction. "Eltrombopag" is a thrombopoietin receptor agonist (TPO-RA) that is approved for the treatment of immune thrombocytopenic purpura (ITP). According to the literature, very few analytical methods for determining eltrombopag in biological samples have been reported. To study the pharmacokinetics of new formulations of eltrombopag, a sensitive and specific method is required that allows one to accurately determine the concentration of eltrombopag in human blood plasma. Normally, HPLC methods should provide time, accuracy, and sensitivity as a result, it is necessary to develop fast or ultra-fast methods such as LC-MS/MS without any loss in sensitivity or separation efficiency.Aim. We aimed to develop and validate a method for the quantitative determination of eltrombopag levels in human plasma by using HPLC with mass spectrometric detection for performing the analytical part of pharmacokinetic studies.Materials and methods. Eltrombopag levels were determined in human plasma by HPLC with mass spectrometric detection. The samples were prepared using protein deposition.Results and discussion. The method was validated for selectivity, matrix effect, calibration curve, accuracy, precision, the limit of quantification, carry-over effect, and sample stability.Conclusion. The method for the determination of eltrombopag levels in human plasma has been developed and validated by HPLC-MS. The analytical range of eltrombopag levels in human plasma was 10–6750 ng/ml. This method could be used to determine eltrombopag levels in plasma for PK and BE studies.https://www.pharmjournal.ru/jour/article/view/1381«элтромбопаг»плазмавэжх-мс/мсвалидациябиоэквивалентность
spellingShingle А. М. AL-Dhuraibi
A. L. Kulikov
M. V. Pokrovskiy
Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method
Разработка и регистрация лекарственных средств
«элтромбопаг»
плазма
вэжх-мс/мс
валидация
биоэквивалентность
title Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method
title_full Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method
title_fullStr Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method
title_full_unstemmed Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method
title_short Development and Validation of Eltrombopag Determination in Human Plasma Blood by HPLC-MS Method
title_sort development and validation of eltrombopag determination in human plasma blood by hplc ms method
topic «элтромбопаг»
плазма
вэжх-мс/мс
валидация
биоэквивалентность
url https://www.pharmjournal.ru/jour/article/view/1381
work_keys_str_mv AT amaldhuraibi developmentandvalidationofeltrombopagdeterminationinhumanplasmabloodbyhplcmsmethod
AT alkulikov developmentandvalidationofeltrombopagdeterminationinhumanplasmabloodbyhplcmsmethod
AT mvpokrovskiy developmentandvalidationofeltrombopagdeterminationinhumanplasmabloodbyhplcmsmethod