氯胺酮的薄层层析和气相色谱质谱分析  被引量:14

Determination of ketamin by use of TLC and GC-MS

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作  者:王玉瑾[1] 刘玲[1] 贾娟[1] 廖林川[2] 王英元[1] 

机构地区:[1]山西医科大学法医学院,山西太原030001 [2]四川大学华西基础医学与法医学院,四川成都610041

出  处:《中国医院药学杂志》2005年第6期497-499,共3页Chinese Journal of Hospital Pharmacy

基  金:国家自然科学基金资助项目(编号:30371577);山西医科大学学生创新项目基金资助项目(编号2004037)

摘  要:目的:建立氯胺酮的薄层层析法(TLC)和气相色谱质谱(GC-MS)测定方法。方法:样品在pH13条件下用醋酸乙酯萃取,SKF525A为内标,以DB5MS石英毛细管柱、EI源、不分流进样GCMS法测定氯胺酮药物;斑点颜色结合比移值和光密度扫描图TLC法定性分析吗啡、海洛因和氯胺酮。结果:TLC法中氯胺酮与吗啡、海洛因分离良好。GCMS分析中,氯胺酮药物血药浓度在0.5~20.0mg·L$C1范围内呈线性关系,r=0.9987,最低检出限为0.2mg·L$C1(S/N=3)。结论:建立的TLC和GCMS法可用于毒品中氯胺酮的检验和氯胺酮中毒的法医学鉴定。OBJECTIVETo establish two methods for determining the ketamin by TLC and GC-MS. METHODSThe specimens were alkalized and extracted with ethyl acetate. In GC-MS analysis the DB-5MS quartz capillary column with Electron Impact source(EI) were used for ketamin determination using SKF(525A )as a internal standard. Qualitative analysis can be condncted for morphine, Heroin and ketamin by the combined R(f) of drugs spots and the TLC spectrum scaning chart. RESULTSBy TLC method,ketamin, morphine and heroin had a good separation. In the GC-MS analysis, the linear range was (0.5)-(20.0) mg·L^( 1) (r=(0.998 7)). The detective limit was (0.2) mg·L^( 1) (S/N=3). CONCLUSIONThe TLC and GC-MS methods can be used to detect ketamin from drugs and for the forensic medical identification of ketamin abuse.

关 键 词:氯胺酮 薄层层析 气相色谱-质谱 血浆药物浓度 

分 类 号:R927[医药卫生—药学]

 

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