Joern W A
Clin Chem. 1978 Sep;24(9):1458-9.
In this 10-min gas-chromatographic assay for theophylline, a 25-microliter portion of serum or saliva sample, 100 microliter of extraction reagent, and 1.0 ml of solvent were mixed, the solvent separated and evaporated, and an aliquot of the reconstituted extract injected into the gas chromatograph. At a concentration of 11 mg/liter, within-run precision (CV) was 3.6% and run-to-run 2.9%. At 22 mg/liter, within-run precision was 2.8%. Concentration and instrument response are linearly related between 2 and 40 mg/liter. The limit of detection was 0.4 mg/liter. Results correlated well (r = 0.98) with those by another micro-scale gas-chromatographic procedure. Analytical recovery was estimated to exceed 90%, and no interferences from other xanthines or related drugs were observed.
在这项针对茶碱的10分钟气相色谱测定法中,将25微升血清或唾液样品、100微升萃取试剂和1.0毫升溶剂混合,分离并蒸发溶剂,然后将一份复溶提取物注入气相色谱仪。在浓度为11毫克/升时,批内精密度(CV)为3.6%,批间精密度为2.9%。在22毫克/升时,批内精密度为2.8%。浓度与仪器响应在2至40毫克/升之间呈线性相关。检测限为0.4毫克/升。结果与另一种微量气相色谱法的结果相关性良好(r = 0.98)。分析回收率估计超过90%,未观察到其他黄嘌呤或相关药物的干扰。