Development and validation of the methods for determination of tenophovir in the blood plasma of rabbits

Scribes development and validation of HPLC method with UV detection at 260 nm for determination of tenofovir in rabbit plasma. Plasma samples were treated by protein precipitation using methanol. HPLC analysis was performed on Waters Atlantis T3 column (5 μm, 4,6 x 150 mm), with precolumn Waters Atl...

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Published inSechenovskiĭ vestnik no. 3-4; pp. 24 - 30
Main Authors Yu. V. Medvedev, G. V. Ramenskaya, I. E. Shokhin, T. A. Yarushok, M. A. Sheveleva
Format Journal Article
LanguageRussian
Published Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University) 01.12.2022
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Abstract Scribes development and validation of HPLC method with UV detection at 260 nm for determination of tenofovir in rabbit plasma. Plasma samples were treated by protein precipitation using methanol. HPLC analysis was performed on Waters Atlantis T3 column (5 μm, 4,6 x 150 mm), with precolumn Waters Atlantis T3 (5 μm, 4,6 x 20 mm). Acetonitrile –phosphate buffer pH 5.70 (16:84) at 1.0 mL/min was used as mobile phase. The standard curve was linear over the range 0.23 μg/ml to 112,98 μg/ml of tenofovir in plasma. Method precision (RSD, %) was 6.08 % to 12.36 % determined on spiked samples. The accuracy of the method (ε, %) was – 2.96 % to 14.55 %. The lower limit of quantification was 0.23 μg/ml. The method was applied to preclinical pharmacokinetics study of tenofovir drug products in rabbits.
AbstractList Scribes development and validation of HPLC method with UV detection at 260 nm for determination of tenofovir in rabbit plasma. Plasma samples were treated by protein precipitation using methanol. HPLC analysis was performed on Waters Atlantis T3 column (5 μm, 4,6 x 150 mm), with precolumn Waters Atlantis T3 (5 μm, 4,6 x 20 mm). Acetonitrile –phosphate buffer pH 5.70 (16:84) at 1.0 mL/min was used as mobile phase. The standard curve was linear over the range 0.23 μg/ml to 112,98 μg/ml of tenofovir in plasma. Method precision (RSD, %) was 6.08 % to 12.36 % determined on spiked samples. The accuracy of the method (ε, %) was – 2.96 % to 14.55 %. The lower limit of quantification was 0.23 μg/ml. The method was applied to preclinical pharmacokinetics study of tenofovir drug products in rabbits.
Author T. A. Yarushok
I. E. Shokhin
M. A. Sheveleva
Yu. V. Medvedev
G. V. Ramenskaya
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  fullname: M. A. Sheveleva
  organization: First MSMU named after I. M. Sechenov
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Snippet Scribes development and validation of HPLC method with UV detection at 260 nm for determination of tenofovir in rabbit plasma. Plasma samples were treated by...
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SubjectTerms derivatization
hplc
plasma
rabbits
tenofovir
Title Development and validation of the methods for determination of tenophovir in the blood plasma of rabbits
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