Pranitis P A, Stolman A
J Forensic Sci. 1975 Oct;20(4):726-300.
Biological fluids and tissue extracts prepared according to a previously published method were passed through a column of Amberlite XAD-2 resin for removal of drugs. The differential elution of the adsorbed drugs from the resin was performed by sequential elution of the drugs in four steps. The column was first washed with 30 ml of 0.05M sodium acetate buffer, pH 4.55. Drugs exhibiting acidic or neutral characteristics were then eluted from the column with 100 ml of chloroform in 20-ml aliquots. The column was then washed with 30 ml of 0.1M potassium carbonate, which was discarded. Drugs exhibiting basic characteristics were then eluted from the column with 100 ml of chloroform:isopropanol (3:1) in 20-ml aliquots. Sensitivity of drug detection with this method by thin-layer chromatography was 0.5 mug/ml in a 10-ml sample for nearly all drugs tested.
按照先前发表的方法制备的生物体液和组织提取物通过Amberlite XAD - 2树脂柱以去除药物。通过分四步依次洗脱树脂上吸附的药物来进行差异洗脱。首先用30毫升pH 4.55的0.05M醋酸钠缓冲液冲洗柱子。然后用100毫升氯仿以20毫升等份洗脱柱子,洗脱呈现酸性或中性特征的药物。接着用30毫升0.1M碳酸钾冲洗柱子,冲洗液弃去。随后用100毫升氯仿:异丙醇(3:1)以20毫升等份洗脱柱子,洗脱呈现碱性特征的药物。对于几乎所有测试药物,该方法通过薄层色谱在10毫升样品中的药物检测灵敏度为0.5微克/毫升。