Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid

Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid Научная публикация

Журнал

Journal of Pharmaceutical and Biomedical Analysis
ISSN: 0731-7085 , E-ISSN: 1873-264X

Вых. Данные

Год: 2021, Том: 199, Номер статьи : 114062, Страниц : DOI: 10.1016/j.jpba.2021.114062

Ключевые слова

Liquid chromatography; Pharmacokinetics; Sample preparation; Sample stability; Tandem mass spectrometry; Validation

Авторы

Rogachev A.D. ^1,2 , Putilova V.P. ^1,2 , Zaykovskaya A.V. ³ , Yarovaya O.I. ^1,2 , Sokolova A.S. ¹ , Fomenko V.V. ¹ , Pyankov O.V. ³ , Maksyutov R.A. ³ , Pokrovsky A.G. ² , Salakhutdinov N.F. ^1,2

Организации

1	N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, acad. Lavrentiev ave., 9, Novosibirsk, 630090, Russian Federation
2	Novosibirsk State University, Pirogov str., 2, Novosibirsk, 630090, Russian Federation
3	State Research Center of Virology and Biotechnology VECTOR, Novosibirsk region, Koltsovo, 630559, Russian Federation

The stability of the new antifiloviral agent AS-358, which is a derivative of borneol and 3-(piperidin-1-yl)propanoic acid, was studied in the blood and blood plasma of rats in vitro. It was found that both in the blood and in the plasma stabilized by EDTA or heparin, the compound is rapidly hydrolyzed at the ester bond. When sodium fluoride was added to the whole blood, the decomposition of the compound was significantly slowed down, which made it possible to develop and validate a method for the quantitative determination of the agent in this matrix. The method was validated in terms of selectivity, calibration dependence, LLOQ, accuracy and precision, stability in an autosampler, recovery, and carry-over. A 8:2 v/v mixture of methanol containing 2-adamantylamine hydrochloride (internal standard, IS) with 0.2 M aqueous zinc sulfate was used for blood sample treatment and protein precipitation. Analysis was performed by HPLC-MS/MS using reversed phase chromatography. MS/MS detection was performed on a triple quadrupole mass spectrometer 6500 QTRAP (SCIEX) in multiple reaction monitoring (MRM) mode. The transitions 294.5→158.2/98.1 and 152.2→107.2/93.1 were monitored for AS-358 and the IS, respectively. The calibration curve was built in the concentration range of 1−500 ng/mL, the intra-day and inter-day accuracy and precision, carry-over and recovery were within the acceptable limits. The developed method was used for a preliminary study of the pharmacokinetics of the agent AS-358 after its oral administration to rats. It was shown that when the substance was administered at a dose of 200 mg/kg, its concentration in the blood of animals reached 550 ng/mL after 1 h, despite its instability in blood. © 2021 Elsevier B.V.

Rogachev A.D. , Putilova V.P. , Zaykovskaya A.V. , Yarovaya O.I. , Sokolova A.S. , Fomenko V.V. , Pyankov O.V. , Maksyutov R.A. , Pokrovsky A.G. , Salakhutdinov N.F.
Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
Journal of Pharmaceutical and Biomedical Analysis. 2021. V.199. 114062 . DOI: 10.1016/j.jpba.2021.114062 WOS Scopus РИНЦ

Опубликована в печати:

1 мая 2021 г.

Web of science	WOS:000644480600003
Scopus	2-s2.0-85103973953
РИНЦ	46796906
OpenAlex	W3147883041