首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >High-performance liquid chromatographic determination of sumatriptan after in vitro transdermal diffusion studies.
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High-performance liquid chromatographic determination of sumatriptan after in vitro transdermal diffusion studies.

机译:体外透皮扩散研究后的高效液相色谱法测定舒马普坦。

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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 250mm Kromasil C18 column at room temperature. The detector response, at 282.7nm, was found to be linear in a concentration range between 0.145 and 145muM. The limit of detection (LOD) was 0.019muM and the limit of quantification (LOQ) was 0.145muM.
机译:为了确定舒马普坦琥珀酸酯的体外经皮吸收,已经验证了一种具有紫外线检测功能的简单,准确,精确和快速的HPLC方法。 HPLC方法是Nozal等人(1991年)描述的方法的改进。 [M.J. Nozal,J.L. Bernal,L.Toribio,M.T.马丁(F.J. Diez),J。生物医学。肛门30(2002)285-291]。在室温下在250mm Kromasil C18色谱柱上进行分离。发现在282.7nm处的检测器响应在0.145至145μM的浓度范围内呈线性。检测限(LOD)为0.019μM,定量限(LOQ)为0.145μM。

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