Yamaguchi M, Monji H, Yamashita K, Aoki I, Yashiki T
Takeda Analytical Research Laboratories, Osaka, Japan.
J Chromatogr B Biomed Appl. 1994 Nov 4;661(1):168-72. doi: 10.1016/0378-4347(94)00331-9.
A sensitive method for the determination of chlorpheniramine in human serum was developed using column-switching high-performance liquid chromatography (HPLC) with ultraviolet detection at 210 nm. The analyte was extracted with diethyl ether from alkalinized serum. After evaporation of the organic layer, the reconstituted residue was analyzed by HPLC using a heart-cut technique. Good recoveries of the analyte from spiked human serum samples were obtained with a coefficient of variation below 7%. A good linear response was obtained for the concentration range 0.5-50 ng/ml, with a correlation coefficient higher than 0.999. The lower limit of quantitation for chlorpheniramine in human serum was 0.5 ng/ml. The method was satisfactorily applied to the determination of chlorpheniramine in human serum after oral administration of chlorpheniramine maleate.
建立了一种采用柱切换高效液相色谱法(HPLC)在210nm处进行紫外检测测定人血清中氯苯那敏的灵敏方法。用乙醚从碱化血清中萃取分析物。有机层蒸发后,采用中心切割技术通过HPLC对重构的残渣进行分析。加标人血清样品中分析物的回收率良好,变异系数低于7%。在0.5 - 50 ng/ml浓度范围内获得了良好的线性响应,相关系数高于0.999。人血清中氯苯那敏的定量下限为0.5 ng/ml。该方法成功应用于口服马来酸氯苯那敏后人血清中氯苯那敏的测定。