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高效液相色谱法测定人血浆中莫西沙星浓度
引用本文:王启平,李东,徐王红,阳宇,王大果,郑学庆.高效液相色谱法测定人血浆中莫西沙星浓度[J].中国药师,2009,12(11):1537-1539.
作者姓名:王启平  李东  徐王红  阳宇  王大果  郑学庆
作者单位:1. 深圳市手外科治疗康复中心,深圳市沙井人民医院,广东深圳,518104
2. 暨南大学第二临床医学院
3. 广东医学院附属福田医院
4. 深圳市大鹏人民医院
基金项目:深圳市科技计划(医疗卫生类)项目 
摘    要:目的:建立以高效液相色谱法测定人血浆中莫西沙星浓度的方法。方法:以Kromasil C8柱为固定相,0.05mol·L^-1磷酸二氢钾缓冲液:甲醇:乙腈(65:15:20)为流动相,调节pH至3.0,流速1ml·min^-1,柱温30℃,紫外检测波长296nm,进样量20ul。沉淀剂选用8%高氯酸溶液,以峰面积外标法定量。结果:莫西沙星保留时间为6.2min,线性范围0.08—4.80mg·L^-1,最低定量限为0.08mg·L^-1;方法平均回收率为95.20%~100.85%,绝对回收率为79.98%~91.83%;高、中、低系列浓度日内RSD为4.69%-5.23%,日间RSD为6.08%~7.36%;样品在低温冷冻条件下至少可稳定保存28d。结论:本法简便、快速,灵敏度高,重复性好,适用于临床血药浓度测定及药动学研究。

关 键 词:莫西沙星  高效液相色谱法  血药浓度

Determination of Moxifloxaxin Concentration in Plasma by HPLC
Wang Qiping,Li Dong,Xu Yuhong,Yang Yu,Wang Daguo,Zheng Xueqing.Determination of Moxifloxaxin Concentration in Plasma by HPLC[J].China Pharmacist,2009,12(11):1537-1539.
Authors:Wang Qiping  Li Dong  Xu Yuhong  Yang Yu  Wang Daguo  Zheng Xueqing
Institution:Wang Qiping, Li Dong, Xu Yuhong, Yang Yu, Wang Daguo, Zheng Xueqing ( 1. Hand Surgery Center of Treatment and Recovery in Shenzhen,Shenzhen 518104,China;2. Second Medical College of Ji'nan University, Shenzhen People's Hospital; 3. Affiliated Futian Hospital of Guangdong Medical College ;4. Dapeng People' s Hospital)
Abstract:Objective: To establish an HPLC method for determination of moxifloxacin concentration in human plasma and to study its pharmacokinetics. Method: The separation was performed on a Kromasil C8 column with mobile phase consisted of 65% 0.05mol. L^-1 potassiun dihydrogen phosphorate buffer solution (containing 1% triethylamine, pH adjusted to 3.0), 15% methanol and 20% acetonitrile. The flow rate was 1.0 ml.min^-1 and the detection wavelength was at 296 nm. The column temperature was 30℃ and injection volume was 20ul. 8% perchloric acid was chosen as precipitator. External standard method was used. Result: The retention time of moxifloxacin was about 6.2 min. The calibration curve was linear within the concentration range of 0.08 - 4.80 mg·L^-1. The limit of quantitation (LOQ) was 0.08 mg·L^-1. The recovery of methodology was 95.20% - 100.85% ; and the absolute recovery was 79.98% - 91.83%. RSD for within day precision and between day precision were 4.69% - 5.23% and 6.08% - 7.36% %, respectively. The sample under frozen condition was stable at least within 28 days. Conclusion: The established HPLC method is simple, sensitive and accurate. It could be used for the determination of moxiflocacin concentration in plasma and its pharmacokinetics study.
Keywords:Moxicifloxacin  Plasma concentration  HPLC
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