Brendel E, Zschunke M, Meineke I
J Chromatogr. 1985 May 3;339(2):359-65. doi: 10.1016/s0378-4347(00)84663-0.
A high-performance liquid chromatographic assay for determination of cefonicid concentrations in human plasma and urine samples has been developed using cefazolin as an internal standard. For the analysis of plasma samples two calibration curves were utilized covering the cefonicid concentration ranges of 0.05-1.0 microgram/ml and 1.0-50.0 micrograms/ml, respectively. Coefficients of variation of 7.4% or less were obtained for cefonicid concentrations of 0.05-50.0 micrograms/ml. Mean bias was +6.0% at 0.05 micrograms/ml cefonicid and between -2.1% and +1.6% for 1.0-50.0 micrograms/ml cefonicid. Plasma samples containing 30 ng/ml cefonicid could be well distinguished from blank plasma samples. Urine samples were analysed by using a calibration curve for cefonicid concentrations between 1.0 and 50.0 micrograms/ml. ranged from 8.6% at a cefonicid concentration of 1.0 microgram/ml to 0.5% at 50.0 micrograms/ml with a mean bias between -3.0% and +0.3%.
已开发出一种高效液相色谱法,以头孢唑林作为内标物,用于测定人血浆和尿液样本中的头孢尼西浓度。对于血浆样本分析,使用了两条校准曲线,分别覆盖头孢尼西浓度范围为0.05 - 1.0微克/毫升和1.0 - 50.0微克/毫升。对于浓度为0.05 - 50.0微克/毫升的头孢尼西,变异系数在7.4%或更低。在头孢尼西浓度为0.05微克/毫升时,平均偏差为 +6.0%,而在1.0 - 50.0微克/毫升时,平均偏差在 -2.1%至 +1.6%之间。含有30纳克/毫升头孢尼西的血浆样本能够与空白血浆样本很好地区分开。尿液样本通过使用头孢尼西浓度在1.0至50.0微克/毫升之间的校准曲线进行分析。变异系数范围从头孢尼西浓度为1.0微克/毫升时的8.6%到50.0微克/毫升时的0.5%,平均偏差在 -3.0%至 +0.3%之间。