6533b855fe1ef96bd12b0ab7

RESEARCH PRODUCT

High-performance liquid chromatographic determination of sumatriptan after in vitro transdermal diffusion studies.

Vicente RodillaA. Femenía-fontVirginia MerinoAlicia López-castellano

subject

Detection limitChromatographyChemistrySumatriptanSwineDiffusionSkin AbsorptionClinical BiochemistryAnalytical chemistryPharmaceutical ScienceAbsorption (skin)Reversed-phase chromatographyIn Vitro TechniquesAdministration CutaneousHigh-performance liquid chromatographyAnalytical ChemistrySumatriptan SuccinateDrug DiscoveryAnimalsDiffusion Chambers CultureQuantitative analysis (chemistry)SpectroscopyChromatography High Pressure LiquidTransdermalSkin

description

A simple, accurate, precise and rapid HPLC method with UV detection has been validated in order to determine the in vitro transdermal absorption of sumatriptan succinate. The HPLC method is a modification of that described by Nozal et al. [M.J. Nozal, J.L. Bernal, L. Toribio, M.T. Martin, F.J. Diez, J. Pharm. Biomed. Anal. 30 (2002) 285-291]. Separation was carried out on a 250 mm Kromasil C18 column at room temperature. The detector response, at 282.7 nm, was found to be linear in a concentration range between 0.145 and 145 microM. The limit of detection (LOD) was 0.019 microM and the limit of quantification (LOQ) was 0.145 microM.

10.1016/j.jpba.2004.11.029https://pubmed.ncbi.nlm.nih.gov/15740926