Chromatographia

, Volume 70, Issue 3–4, pp 569–573 | Cite as

N-(1-Naphthyl)ethylenediamine, a New UV Labeling Reagent Used for LC Determination of Valproic Acid in Human Plasma

  • Golnaz Kamalinia
  • Mohammad-Reza Rouini
  • Padideh Ghaeli
  • Mohsen Amini
Full Short Communication

Abstract

A high performance liquid chromatography method is presented for the determination of valproic acid levels in human plasma. The method was based on pre-column derivatization using N-(1-naphthyl)ethylenediamine as a new labeling agent. The calibration curve was linear in the investigated concentration range between 0.1 and 100 μg mL−1 and showed good accuracy and reproducibility. The assay provided a limit of quantification of 0.1 μg mL−1 for valproic acid and a limit of detection of 10 ng mL−1, respectively. The presented method was successfully applied to the determination of valproic acid levels in plasma after oral administration of 600 or 800 mg of sodium valproate.

Keywords

Column liquid chromatography Derivatization N-(1-Naphthyl)ethylenediamine Valproic acid 

Notes

Acknowledgments

This work was supported by a grant from Deputy of Research, Tehran University of Medical Sciences, Tehran, Iran.

References

  1. 1.
    Martindale (1996) 31st edn. Royal Pharmaceutical Society, London, p 390Google Scholar
  2. 2.
    Amini H, Javan M, Ahmadiani A (2006) J Chromatogr B 830:368–371. doi: 10.1016/j.jchromb.2005.11.028 CrossRefGoogle Scholar
  3. 3.
    Lin MC, Kou HS, Chen CC, Wu SM, Wu HL (2004) J Chromatogr B 810:169–172Google Scholar
  4. 4.
    Lucarelli C, Villa P, Lomabaradi E, Prandini P, Berga A (1992) Chromatographia 33:37–40. doi: 10.1007/BF02276848 CrossRefGoogle Scholar
  5. 5.
    Cheng H, Liu Z, Blum W, Byrd J, Klisovic R, Grever MR, Marcucci G, Chan KK (2007) J Chromatogr B 850:206–212. doi: 10.1016/j.jchromb.2006.11.027 CrossRefGoogle Scholar
  6. 6.
    Leis HJ, Windischhofer W, Rechberger GN, Fauler G (2003) J Chromatogr B 784:69–75. doi: 10.1016/S1570-0232(02)00755-9 CrossRefGoogle Scholar
  7. 7.
    Kushida K, Ishizaki T (1985) J Chromatogr 338:131–139. doi: 10.1016/0378-4347(85)80077-3 CrossRefGoogle Scholar
  8. 8.
    Lovett LJ, Nygard GA, Erdmenn GR, Burley CZ, Khalil SKW (1987) J Liq Chromatogr 10:687–699. doi: 10.1080/01483918708069019 CrossRefGoogle Scholar
  9. 9.
    Menyawi IEI, Looareesuwan S, Knapp S, Thalhammer F, Stoiser B, Burgmman H (1998) J Chromatogr B 706:347–351. doi: 10.1016/S0378-4347(97)00570-7 CrossRefGoogle Scholar
  10. 10.
    FDA Guidance for industry, Bioanalytical Method Validation, US Department of Health and Human Services, Food and Drug Administration center for Drug Evaluation and Research (CDER), 2001. http://www.fda.gov/cder/guidance/4252fnl.pdf

Copyright information

© Vieweg+Teubner | GWV Fachverlage GmbH 2009

Authors and Affiliations

  • Golnaz Kamalinia
    • 1
    • 2
  • Mohammad-Reza Rouini
    • 1
  • Padideh Ghaeli
    • 2
  • Mohsen Amini
    • 3
    • 4
  1. 1.Biopharmaceutics and Pharmacokinetics Division, Department of Pharmaceutics, Faculty of PharmacyTehran University of Medical SciencesTehranIran
  2. 2.Department of Pharmacotherapy, Faculty of PharmacyTehran University of Medical SciencesTehranIran
  3. 3.Department of Medicinal Chemistry, Faculty of PharmacyTehran University of Medical SciencesTehranIran
  4. 4.Drug Design & Development Research CenterTehran University of Medical SciencesTehranIran

Personalised recommendations