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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Assay of total and free propranolol in plasma by liquid chromatography with fluorometric detection.
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Assay of total and free propranolol in plasma by liquid chromatography with fluorometric detection.

机译:液相色谱-荧光检测法测定血浆中总普萘洛尔和游离普萘洛尔的含量。

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摘要

We report a liquid-chromatographic method for assay of total and free propranolol and its metabolite, propranolol glycol, in plasma. An ultrafiltration device is used to separate the free drugs from the protein-bound drugs. The total and free drugs are isolated from plasma or ultrafiltrate by liquid-solid extraction on a Waters C18 SEP-PAK and the drugs are quantified on a C18 mu-Bondpak radial-compression column. The mobile phase consists of equal parts of methanol and a solution of potassium 50 mmol/L phosphate and 2.5 mmol/L 1-pentane-sulfonic acid, pH 5.0. Detection was by fluorescence, with excitation at 296 nm and emission at 338 nm. Time required for sample preparation for total-propranolol assay is 40 min per eight samples. Sample preparation for free-propranolol assay requires an additional 1 h per eight samples. Chromatography requires 15 min per sample. The extraction recovery is approximately 75% and the assay curve is linear from 5 to 400 micrograms/L. The run-to-run CV is 4% for total propranolol, 15% for free propranolol.
机译:我们报告了一种液相色谱法,用于测定血浆中的总和游离普萘洛尔及其代谢产物普萘洛尔乙二醇。超滤装置用于将游离药物与结合蛋白质的药物分离。通过在Waters C18 SEP-PAK上进行液固萃取,从血浆或超滤液中分离出总药物和游离药物,并在C18 mu-Bondpak径向压缩柱上对药物进行定量。流动相由等份的甲醇和50 mmol / L磷酸钾和2.5 mmol / L 1-戊烷磺酸的pH 5.0溶液组成。通过荧光进行检测,在296 nm处激发,在338 nm处发射。用于全心得安测定的样品制备时间为每8个样品40分钟。游离普萘洛尔测定的样品制备需要每8个样品额外1 h。色谱法每个样品需要15分钟。提取回收率约为75%,测定曲线在5至400微克/升之间呈线性关系。每次普萘洛尔的每次运行CV为4%,游离普萘洛尔为15%。

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