Peng G W, Gadalla M A, Peng A, Smith V, Chiou W L
Clin Chem. 1977 Oct;23(10):1838-44.
A rapid, specific method for measuring gentamicin in plasma by high-pressure liquid chromatography was developed. After deproteinization, gentamicin in the supernate was dansylated and extracted into ethyl acetate. The organic extract was chromatographed on a microparticulate reversed-phase column, which was eluted with aqueous acetonitrile. Use of the dansyl derivative enables fluorometry, for more sensitive quantitation. Various factors that could affect the assay sensitivity were investigated. With 0.2-ml plasma samples, the method can accurately measure as little as 1 mg of gentamicin per liter. We encountered no interferences from plasma supplemented with various drugs or plasma of patients who were on therapy with other drugs. This method can also separate gentamicin C1 from C1a and C2, all of which are present in various ratios in commercial dosage forms. This method is also applicable to gentamicin determination in urine.
开发了一种通过高压液相色谱法快速、特异性地测定血浆中庆大霉素的方法。去蛋白后,将上清液中的庆大霉素进行丹磺酰化并萃取到乙酸乙酯中。有机萃取物在微粒反相柱上进行色谱分析,用乙腈水溶液洗脱。使用丹磺酰衍生物可进行荧光测定,以实现更灵敏的定量。研究了各种可能影响测定灵敏度的因素。对于0.2毫升血浆样本,该方法能够准确测定低至每升1毫克的庆大霉素。我们未遇到来自添加各种药物的血浆或正在接受其他药物治疗患者的血浆的干扰。该方法还可以将庆大霉素C1与C1a和C2分离,所有这些在商业剂型中都以不同比例存在。该方法也适用于尿液中庆大霉素的测定。