段更利, 陆明廉, 吴柏林. 测定泰必利血药及尿药浓度的反相高效液相色谱法研究J. 药学学报, 1986, 21(12): 917-921.
引用本文: 段更利, 陆明廉, 吴柏林. 测定泰必利血药及尿药浓度的反相高效液相色谱法研究J. 药学学报, 1986, 21(12): 917-921.
DUAN Geng-Li, LU Ming-Lian , Wu Bo-Lin, . REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC DETER MiNATION OF TIAPRIDE IN PLASMA AND URINEJ. Acta Pharmaceutica Sinica, 1986, 21(12): 917-921.
Citation: DUAN Geng-Li, LU Ming-Lian , Wu Bo-Lin, . REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC DETER MiNATION OF TIAPRIDE IN PLASMA AND URINEJ. Acta Pharmaceutica Sinica, 1986, 21(12): 917-921.

测定泰必利血药及尿药浓度的反相高效液相色谱法研究

REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC DETER MiNATION OF TIAPRIDE IN PLASMA AND URINE

  • 摘要: 用国产高效液相色谱仪、反相填料YWG-C18H37及甲醇—三乙胺(10000:0.40)为流动相,研究并建立了测定泰必利血药及尿药浓度的高效液相色谱法。该法具有灵敏、准确、可靠及快速等优点。血样或尿样用7 ml二氯甲烷一次提取,浓缩后进样。泰必利及内标胃复安的保留时间分别为4.50及8.25 min。泰必利标准溶液的检测限为5ng;从标准血样或尿样提取的最低检测浓度分别为0.05μg/ml血清及0.08μg/ml尿液(S/N≥2)。经提取的标准曲线相关系数大干0.99,方法回收率大于98%,日内日间测定的CV小于2.5%。

     

    Abstract: Plasma or urine samples, containing metoclopramide as an IS were extracted at pH 10.58 With dichloromethane The concentrated extract was analysed by HPLC (YSB-Ⅰ Model, China) on a column (150 × 5 mm)oF YWG-C18H37 (10 μm, Tianjin) with methanol-triethylamine solution (10000:0.40) as mobile phase (1.0 ml/min) and detected at 254 nm The retention time of tiapride and internal standard were 4.5 and 8.25 min respectively. The correlation coefficients of the extracted tiapride calibration curves were over 0.99. The minimal detectable concentration of tiapride in serum was 0.05 μg/ml. The recoveries of tiapride in serum and urine were over 98%. The CV of Within-day and day-to-day were less than 2.5%. The results of this method were correlated with that of the ILC method. The HPLC method for detection of tiapride in plasma or urine is highly sensitive, accurate, reproducible and rapid, so it could be applicable for extensive clinical and pharmacological investigations.

     

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