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作 者:张薇薇[1] 林明美[1] 王瑛[1] 董皓 郝仙娣
机构地区:[1]北京市临床药学研究所
出 处:《中国药物滥用防治杂志》1998年第2期26-37,共12页Chinese Journal of Drug Abuse Prevention and Treatment
摘 要:本文在第一报〔1〕的基础上,对实验条件,方法的灵敏度和29种有关药物及空白尿对方法的干扰情况等进行了系统考察;同时与GC-MS和试剂盒进行方法比较;对吗啡衍生物(RSO2-M)进行结构分析;临床验证247例。方法灵敏度为10ng(板上);SI展开剂的平均Rf值为0.29,SD为0.024;SⅡ展开剂的平均Rf值为0.38,SD为0.072;酸水解的最佳条件为100℃加热30分钟,衍生化的最佳条件为pH8-9,70℃水浴10分钟;除可待因,蒂巴因外其余26种相关药物和空白尿对方法均无干扰;定性结果与GC-MS完全一致,半定量结果与GC-MS具有一定可比性;临床验证结果满意。On the basis of the first report,the conditions of the experiment,the sensitivity of the method,the interference of the 29 kinds of concerned drugs and the normal urine were described in this report.Our method compared with GC-MS and Surestep TM Drug Screen (morphine).The clinical test were 247 instances.The results showed that the limit of detection is 10ng(on the silica gel plate),the R f of the first solvent is 0.29 and the SD is 0.024,the R f of the second solvent is 0.38 and the SD is 0.072.It is the best conditions of the urine acid hydrolysis that the urine are heated at 100℃ for 30 minutes;It is the best conditions of the derivation that the urine are heated at pH8-9 and 70℃ for 10 minutes in waterbath.All 26 kinds of the drugs and the normal urine did not interfer with the method,except codeine and thebaine.The results of qualitative were same as GC-MS and the results of semiquantitative were proportionate with GC-MS.The results of clinical test were most satisfactory.
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