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Microanalytical high-performance liquid chromatography assay for cefpirome (HR 810) in serum.

机译:微量分析高效液相色谱法测定血清中的头孢哌酮(HR 810)。

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摘要

We report a microanalytical high-performance liquid chromatography method for quantitation of cefpirome (HR 810) from serum. The drug was extracted from 0.05 ml of serum with 0.2 ml of isopropanol containing beta-hydroxypropyltheophylline, the internal standard. Separations were performed on a C18 column at ambient temperature with detection at 240 nm. The mobile phase consisted of acetate buffer (0.05 M sodium acetate) containing tetrabutylammonium hydroxide and methanol (pH 5.1; 70:30, vol/vol). The method was linear to 500 micrograms of cefpirome per ml and had a sensitivity of 0.6 micrograms/ml. Analytical recovery was greater than 86%, and the between-day coefficient of variation was less than 4.2%. The stability for 1 week at 4 to 8 degrees C and for 30 days at -20 degrees C was documented. Interference with commonly used antibiotics, analgesics, methylxanthines, and anticonvulsants was not found. The small sample volume and ease of preparation make this method suitable for use in pediatric pharmacokinetic investigations of cefpirome.
机译:我们报告了一种微量分析高效液相色谱法,用于从血清中定量测定头孢哌酮(HR 810)。用0.2 ml含内标β-羟丙基茶碱的异丙醇从0.05 ml血清中提取药物。在环境温度下于C18色谱柱上进行分离,检测波长为240 nm。流动相由含有四丁基氢氧化铵和甲醇(pH 5.1; 70:30,体积/体积)的乙酸盐缓冲液(0.05 M乙酸钠)组成。该方法与每毫升500微克头孢吡酮呈线性关系,灵敏度为0.6微克/毫升。分析回收率大于86%,日间变异系数小于4.2%。记录了在4至8摄氏度下1周和在-20摄氏度下30天的稳定性。没有发现干扰常用的抗生素,止痛药,甲基黄嘌呤和抗惊厥药。样品量小且易于制备,使得该方法适用于头孢哌酮的儿科药代动力学研究。

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