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Pharmacokinetics of Intravenously and Intraperitoneally Administered Mafedine Sodium in Mice

  • MOLECULAR-BIOLOGICAL PROBLEMS OF DRUG DESIGN AND MECHANISM OF DRUG ACTION
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Pharmaceutical Chemistry Journal Aims and scope

Peculiarities of the pharmacokinetics of mafedine sodium salt upon intraperitoneal (i.p.) and intravenous (i.v.) administration to laboratory mice were studied. A high-performance liquid chromatography (HPLC) method for its quantitative determination was proposed. Mafedine sodium salt was found to have a short biological elimination half-life after both i.p. and i.v. administration (15.73 and 6.98 min, respectively) and high i.p. bioavailability (~94%). Features of the alpha-2-adrenomimetic activity of mafedine sodium salt could be elucidated by further searches for and investigations of its metabolites and their pharmacokinetics.

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Correspondence to V. A. Prikhodko.

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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 54, No. 12, pp. 3 – 7, December, 2020.

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Sysoev, Y.I., Whaley, A.K., Prikhodko, V.A. et al. Pharmacokinetics of Intravenously and Intraperitoneally Administered Mafedine Sodium in Mice. Pharm Chem J 54, 1193–1197 (2021). https://doi.org/10.1007/s11094-021-02342-y

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  • DOI: https://doi.org/10.1007/s11094-021-02342-y

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