Behnke C E, Reddy M N
Department of Pathology, Children's Hospital of Wisconsin, Milwaukee, USA.
Ther Drug Monit. 1997 Jun;19(3):301-6. doi: 10.1097/00007691-199706000-00010.
A simple and rapid procedure to determine felbamate (2-phenyl-1,3-propanediol dicarbamate) concentrations in human plasma/serum by high-performance liquid chromatography is described. The method employs a high-performance liquid chromatography unit equipped with a C18 reverse-phase cartridge (3-microliters particle diameter, 3.2 x 40 mm), an acetonitrile/water gradient, and detection at 210 nm. The sample is deproteinized with acetonitrile containing internal standard (2-methyl-2-phenyl-1,3-propanediol dicarbamate), and the resulting supernatant, after diluting 1:1 with water, is injected onto the column. The felbamate and internal standard are eluted with a linear gradient of 0% to 22% acetonitrile for 11 minutes at a flow rate of 0.8 ml/minute. Under these conditions, felbamate and the internal standard are eluted at 9.2 +/- 0.03 and 10.8 +/- 0.03 minutes, respectively. The assay is linear from 10 to 400 microgram/ml. It is highly reproducible; at 100 micrograms/ml felbamate, within-day and between-day coefficients of variation are less than 0.5% and 4.3%, respectively. Recovery is > or = 95%. No interferences from other common antiepileptic drugs and analgesics are observed. Advantages of this method include simple and fast sample preparation; use of a gradient to eliminate interferences; and use of a cartridge column, which is economical, provides good resolution, allows rapid equilibration and elution, and operates at low back pressures. The method requires samples of only 100 microliters and is ideal for pediatric samples.
描述了一种通过高效液相色谱法测定人血浆/血清中非氨酯(2-苯基-1,3-丙二醇二氨基甲酸酯)浓度的简单快速方法。该方法采用配备C18反相柱(粒径3微米,3.2×40毫米)的高效液相色谱仪,乙腈/水梯度洗脱,并在210纳米处进行检测。样品用含内标(2-甲基-2-苯基-1,3-丙二醇二氨基甲酸酯)的乙腈进行脱蛋白处理,所得上清液用水1:1稀释后注入色谱柱。非氨酯和内标以0%至22%乙腈的线性梯度在11分钟内以0.8毫升/分钟的流速洗脱。在这些条件下,非氨酯和内标分别在9.2±0.03分钟和10.8±0.03分钟洗脱。该测定法在10至400微克/毫升范围内呈线性。它具有高度的重现性;在100微克/毫升非氨酯浓度下,日内和日间变异系数分别小于0.5%和4.3%。回收率≥95%。未观察到其他常见抗癫痫药物和镇痛药的干扰。该方法的优点包括样品制备简单快速;使用梯度洗脱以消除干扰;使用柱管柱,经济实惠,分离效果好,平衡和洗脱速度快,且背压低。该方法仅需100微升样品,非常适合儿科样本。