Rouan M C
Laboratoires Ciba-Geigy, Biopharmaceutical Research Centre, Rueil-Malmaison, France.
J Chromatogr. 1988 Apr 29;426(2):335-44. doi: 10.1016/s0378-4347(00)81960-x.
The application of microbore systems (15 cm X 1 mm I.D. columns filled with Nucleosil C18, 5 microns particle size) to the determination of cephalexin and cadralazine in plasma was investigated. Factors such as mobile phase flow-rate, detector flow-cell volume and injection volume were examined with regard to the needs of routine drug analysis. Mobile phase flow-rates of 50-60 microliters/min were used. A flow cell with an optical path length of 6 mm and an intermediary volume (2.4 microliters) was selected for UV detection in order to obtain sufficient sensitivity. Large volumes of non-eluting solvent containing the drug were injected on the column. The addition of an ion-pairing reagent to samples containing cephalexin and cefroxadin prior to the injection was found to improve the chromatographic performance. The blood sample size required for analysis with microbore columns was smaller than that with conventional columns. The analysis time was similar and the limit of quantitation was also similar, provided that large sample volumes were injected on the microbore column.
研究了微径系统(内径1毫米、长15厘米、填充粒径为5微米的Nucleosil C18的色谱柱)在血浆中头孢氨苄和卡屈嗪测定中的应用。针对常规药物分析的需求,考察了流动相流速、检测器流通池体积和进样量等因素。使用了50 - 60微升/分钟的流动相流速。为获得足够的灵敏度,选择了光程长6毫米、中间体积为2.4微升的流通池用于紫外检测。将大量含药物的非洗脱溶剂进样到色谱柱上。发现在进样前向含头孢氨苄和头孢沙定的样品中添加离子对试剂可改善色谱性能。使用微径柱进行分析所需的血样量比使用常规柱时少。分析时间相似,且只要向微径柱上进样大体积样品,定量限也相似。