Development of a sensitive bioanalytical method for the quantification of lacosamide in rat plasmaapplication to preclinical pharmacokinetics studies in rats

S. Shah, S. G. Vasantharaju, K. Arumugam, B. S. Muddukrishna, N. Desai

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

A sensitive and selective high performance liquid chromatographic (HPLC) method was developed and validated for quantification of lacosamide in rat plasma. A liquid-liquid extraction procedure was optimized to extract lacosamide from rat plasma. Chromatographic separation was accomplished using a reversed phase C 18 Hichrom (250×4.6 mm, 5 m) column with the mobile phase consisting of acetonitrile-phosphate buffer (pH 3.2±0.1; 20 mM) (21:79, v/v) at a flow rate of 1 mL/min. Both intra- and inter day assay precision and accuracy were lower than 15% CV. The lower limit of quantitation was 25 ng/mL for lacosamide and the response was linear in a concentration range from 25 to 10 000 ng/mL. The developed method was successfully used for the preclinical pharmacokinetic study of lacosamide in rats.

Original languageEnglish
Pages (from-to)243-246
Number of pages4
JournalArzneimittel-Forschung/Drug Research
Volume62
Issue number5
DOIs
Publication statusPublished - 05-2012

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Pharmacokinetics
Liquid-Liquid Extraction
Buffers
Phosphates
lacosamide

All Science Journal Classification (ASJC) codes

  • Drug Discovery

Cite this

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abstract = "A sensitive and selective high performance liquid chromatographic (HPLC) method was developed and validated for quantification of lacosamide in rat plasma. A liquid-liquid extraction procedure was optimized to extract lacosamide from rat plasma. Chromatographic separation was accomplished using a reversed phase C 18 Hichrom (250×4.6 mm, 5 m) column with the mobile phase consisting of acetonitrile-phosphate buffer (pH 3.2±0.1; 20 mM) (21:79, v/v) at a flow rate of 1 mL/min. Both intra- and inter day assay precision and accuracy were lower than 15{\%} CV. The lower limit of quantitation was 25 ng/mL for lacosamide and the response was linear in a concentration range from 25 to 10 000 ng/mL. The developed method was successfully used for the preclinical pharmacokinetic study of lacosamide in rats.",
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AU - Shah, S.

AU - Vasantharaju, S. G.

AU - Arumugam, K.

AU - Muddukrishna, B. S.

AU - Desai, N.

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N2 - A sensitive and selective high performance liquid chromatographic (HPLC) method was developed and validated for quantification of lacosamide in rat plasma. A liquid-liquid extraction procedure was optimized to extract lacosamide from rat plasma. Chromatographic separation was accomplished using a reversed phase C 18 Hichrom (250×4.6 mm, 5 m) column with the mobile phase consisting of acetonitrile-phosphate buffer (pH 3.2±0.1; 20 mM) (21:79, v/v) at a flow rate of 1 mL/min. Both intra- and inter day assay precision and accuracy were lower than 15% CV. The lower limit of quantitation was 25 ng/mL for lacosamide and the response was linear in a concentration range from 25 to 10 000 ng/mL. The developed method was successfully used for the preclinical pharmacokinetic study of lacosamide in rats.

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