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反相高效液相色谱法测定人血浆中替米沙坦的浓度 被引量:10

Determination of telmisartan in human plasma by RP-HPLC
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摘要 目的 建立RP -HPLC法测定人血浆中替米沙坦浓度。方法 用AgilentZORBAX×ODS柱 (4 .6× 1 5 0mm ,5 μm) ,流动相为水 -乙腈 -三乙胺 (6 0∶4 0∶0 .1 ) ,荧光检测激发波长为 30 0nm ,发射波长为 380nm ,采用萘乙酸为内标。结果 替米沙坦保留时间为 9min左右 ,浓度线性范围 1 0~ 35 0 0 μg·L-1 。结论 该法准确、快速、简便 。 Aim To establish a high performance liquid chromatography(RP-HPLC)method to determine the concentration of telmisartan in human plasma.Methods Separation was achieved on the Agilent ZORBAX×ODS column(4.6×150mm,5μm).The mobile phase consisted of water-Acetonitrile-Triethylamine(60∶40∶0.1,v/v/v) and was used at the flow rate of 1.0ml/min.The fluorimetric excitation and emission wavelengths were set at 300nm and 380nm,respectively.Naphtalene-1-acetic acid was used as internal standard.Results The retention time of telmisartan was about 9min.The calibration curves were linear in the range of 10~3 500μg·L -1 .Conclusion The HPLC method can be used to determine the concentration of telmisartan in human plasma.
出处 《解放军药学学报》 CAS 2004年第2期138-140,共3页 Pharmaceutical Journal of Chinese People's Liberation Army
关键词 反相高效液相色谱法 测定 替米沙坦 血药浓度 Telmisartan HPLC TDM Plasma levels
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  • 1朱珠.抗高血压新药——替米沙坦[J].中国药学杂志,1999,34(12):855-856. 被引量:23
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  • 3Robert E,Dinnebier,PS,Herbert N,et al.Structural Characterization of Three Crystalline Modifications of Telmisartan by Single Crystal and High-Resolution X-ray Powder Diffraction[J].Journal of Pharmaceutical Sciences,2000,89(11):1465
  • 4Joachim Stangier,PhD,Chung-An P.F.Su,MD.Pharmacokinetics and safety of intravenous and oral telmisartan 20mg and 120mg in subjects with hepatic impairment compared with healthy volunteers[J].J Clin Pharmacol,2000,40:1355
  • 5Joachim Stangier,PhD,Jochen Schmid,PhD .Absorption,Metabolism,and Excretion of Intravenously and orally administered[C14]Telmisartan in healthy volunteers[J].J Clin Pharmacol,2000,40:1312
  • 6Joachim Stangier,PhD,Chung-An P.F.Su,MD. Pharmacological of Repeated Oral Doses of Amlodipine and Amlodipine Plus Telmisartan in Healthy Volunteers[J].Clin Pharmacol,2000.40:1347

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