Turley C P, Kearns G L, Jacobs R F
Department of Pathology, University of Arkansas for Medical Sciences, Little Rock 72205.
Antimicrob Agents Chemother. 1988 Oct;32(10):1481-3. doi: 10.1128/AAC.32.10.1481.
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.
我们报告了一种用于定量血清中头孢匹罗(HR 810)的微量分析高效液相色谱法。该药物用含内标物β-羟丙基茶碱的0.2 ml异丙醇从0.05 ml血清中萃取。在室温下于C18柱上进行分离,检测波长为240 nm。流动相由含氢氧化四丁铵的醋酸盐缓冲液(0.05 M醋酸钠)和甲醇组成(pH 5.1;70:30,体积/体积)。该方法在每毫升500微克头孢匹罗范围内呈线性,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%。记录了其在4至8℃下1周以及在-20℃下30天的稳定性。未发现与常用抗生素、镇痛药、甲基黄嘌呤和抗惊厥药有干扰。小样本量和易于制备使该方法适用于头孢匹罗的儿科药代动力学研究。