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反相高效液相色谱荧光检测法测定新型咀嚼胶片剂中右美沙芬的血浆浓度
引用本文:刘娟,谭群友,熊华蓉,徐美玲,赵春景,张景勍.反相高效液相色谱荧光检测法测定新型咀嚼胶片剂中右美沙芬的血浆浓度[J].光谱实验室,2011,28(3):1007-1011.
作者姓名:刘娟  谭群友  熊华蓉  徐美玲  赵春景  张景勍
作者单位:1. 重庆医科大学药物高校工程研究中心和生物化学与分子药理学重点实验室,重庆市渝中区医学院路1号,400016
2. 第三军医大学大坪医院野战外科研究所胸外科,重庆市渝中区长江文路10号,400042
3. 重庆医科大学附属第二医院,重庆市渝中区临江路74号,400010
基金项目:教育部博士点基金资助项目(20095503120008); 重庆市教育委员会资助项目(首批高等学校优秀人才资助,KJ090308)
摘    要:建立反相高效液相色谱荧光检测法测定口服新型咀嚼胶片剂后血浆中右美沙芬浓度的方法。采用Hanbon C18(4.6mm×250mm,5μm)色谱柱,以乙腈-水-磷酸-三乙胺(35∶65∶0.14∶0.10,V/V/V/V)为流动相,在流速0.6mL.min-1,进样量50μL,柱温30℃,荧光激发波长(Ex)和发射波长(Em)分别为280nm和320nm条件下,测定咀嚼胶片剂中右美沙芬的兔血药浓度。药物与杂质分离效果良好、线性范围为1—1000ng.mL-1,相关系数为0.9996。方法回收率和提取回收率分别为110.0%和83.9%。当S/N=3时,右美沙芬最低检出浓度可达1ng.mL-1。本方法准确、灵敏,可满足血药浓度检测和研究药代动力学行为的需要。

关 键 词:右美沙芬  反相高效液相色谱  荧光检测法  新型咀嚼胶片剂

Determination of Serous Dextromethorphan from New Chewing Gum Tablet by RP-HPLC with Fluorescence Detection
LIU Juan TAN Qun-Youa XIONG Hua-RongXU Mei-Ling ZHAO Chun-Jingb ZHANG Jing-Qingab.Determination of Serous Dextromethorphan from New Chewing Gum Tablet by RP-HPLC with Fluorescence Detection[J].Chinese Journal of Spectroscopy Laboratory,2011,28(3):1007-1011.
Authors:LIU Juan TAN Qun-Youa XIONG Hua-RongXU Mei-Ling ZHAO Chun-Jingb ZHANG Jing-Qingab
Institution:LIU Juan TAN Qun-Youa XIONG Hua-RongXU Mei-Ling ZHAO Chun-Jingb ZHANG Jing-Qing(Medicine Engineering Research Center in University,Chongqing Key Laboratory of Biochemical & Molecular Pharmacology,Chongqing Medical University,Chongqing 400016,P.R.China)a(Thoracic Surgery Center,Daping Hospital & Research Institute of Surgery,Third Military Medical University,Chongqing 400042,P.R.China)b(Second Affiliated Hospital,Chongqing 400010,P.R.China)
Abstract:An method for the determination of dextromethorphan(DH) concentration after taking new chewing gum tablet in plasma was developed by reversed phase high performance liquid chromatography.Hanbon C18(4.6mm×250mm,5μm) chromatographic column was used with acetonitrile-water-phosphatic acid-triethylamine(35∶65∶0.14∶0.10,V/V/V/V) as the mobile phase at a flow rate of 0.6mL·min1 and injection volumn of 50μL.The concentration of rabbit plasma dextromethorphan from chewing gum tablet was detected under fluorescence exciting wavelength(Ex) and emission wavelength(Em) at 280nm and 320nm,respectively.The column temperature was 30℃.The drug separated well with impurities,and the linear range of DH was 1—1000ng·mL-1 with correlation coefficient of 0.9996.The lower limit of quantification(S/N=3) was 1ng·mL-1.The method recovery and extraction recovery were 109.9%,83.7%,respectively.The method is accurate,sensitive,and meets the need for detection DH concentration in rabbet plasma and for estimation of pharmacokinetic parameters.
Keywords:Dextromethorphan  Reversed Phase High Performance Liquid Chromatography  Fluorescence Detection  New Chewing Gum Table  
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