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高效毛细管电泳法测定磺胺类药物的离解常数及其制剂的含量 被引量:8

HPCE determination of dissociation constants of sulfonamides and their contents
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摘要 目的:采用毛细管电泳法测定磺胺甲唑(sMZ)、磺胺嘧啶(SD)和甲氧苄啶(TMP)的离解常数及其在制剂中的含量。方法:采用未涂层的弹性石英毛细管柱(60.2 cm×75 μm,有效长度50 cm),柱温25 ℃,正极压力进样,检测波长214 nm。将3种化合物的有效电泳淌度与 pH 进行非线性拟合,测定其离解常数;最佳的分离条件为:50 mmol·L^(-1)磷酸二氢钠(pH 6.0)缓冲液,分离电压27.5 kV,在此条件下测定其在制剂中的含量。结果:SMZ、SD、TMP 的离解常数分别为5.69,6.36,6.68;在0.1~1000μg·mL^(-1)的浓度范围内线性关系良好(相关系数:0.9992~0.9999),回收率为95.6%~105.0%。结论:该方法简便、快速、准确,可用于测定3种磺胺类药物的解离常数及其在制剂中的含量。 Objective:To develop a simultaneous determination the dissociation constant values of sulfamethoxazole (SMZ) ,sulfadiazine(SD) and trimethoprim( TMP), and the contents in their preparations by HPCE. Method: A fused silica capillary column (60.2 cm× 75 μm, effective length 50 cm) was used, the cartridge temperature was 25 ℃, sample was introduced from the anode with pressure injection ,the UV detection wavelength was 214 nm. The dependence of effective mobility of the three compound on pH was investigated, and their apparent dissociation constant values determined by nonlinear simulation;the best separation was achieved with a running buffer of 50 mmol · L^-1 NaH2PO4(pH 6.0) and at the applied voltage of 27.5 kV for determination the contents of the three compounds. Result: The dissociation constant values ( pKa ) of SMZ, SD and TMP were 5.69,6.36 and 6.68, respectively. The linear concentration range of the three compounds was 0. 1 - 1000 μg · mL^-1 with a correlation coefficient of 0. 9992 -0. 9999. The recoveries of the three analytes were 95.6% - 105.0%. Conclusion:The proposed method is simple, fast and accurate for determination the dissociation constant values of sulfonamides and their contents.
出处 《药物分析杂志》 CAS CSCD 北大核心 2008年第2期243-246,共4页 Chinese Journal of Pharmaceutical Analysis
基金 泰山医学院博士启动基金(2006-742)
关键词 高效毛细管电泳 磺胺甲噁唑(SMZ) 磺胺嘧啶(SD) 甲氧苄啶(TMP) pK HPCE sulfamethoxazole ( SMZ ) sulfadiazine ( SD ) trimethoprim (TMP) pKa
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  • 1Takacs - Novak K, Noszal B, Hermecz I, et al. Protonation equilibria of quinolone antibacterials. J Pharm Sci, 1990,79 ( 11 ) : 1023
  • 2Li Qianfeng, Zhang Xiaoyun, Zhang Hongyi, et al. A new method to measure electroosmotic flow mobility of capillary electrophoresis by abrupt change of current de - noising via wavelet transform. Chin J Chem,2001,19 (6) :581
  • 3Li Guanbing, Zhang Ziping, Chen Xingguo, et al. Analysis of ephedrine in ephedra callus by acetonitrile modified capillary zone electrophoresis. Talanta, 1999,48 ( 5 ) : 1023
  • 4SHEN Jian-rain(沈建民),WU Zhen-qing(武振卿).Structure and Preparation of Medicament(药物结构与制剂).Beijing(北京):China Medico-Pharmaceutical Science and Technology Publishing House(中国医药科技出版社),1989.416
  • 5XU Wen-fang(徐文芳).Theories and Methods of New Drug Design(新药设计原理与方法).Beijing(北京):China Medico-Pharmaceutical Science and Technology Publishing House(中国医药科技出版社),2000.40
  • 6ChP(中国药典).2005.Vol Ⅱ(二部):730
  • 7Terabe ST, Yashima N. Tanaka,et al. Separation of oxygen isotopic benzoic acids by capillary zone electrophoresis based on isotope effects on the dissociation of the carboxyl group. Anal Chem, 1988,60 (17) :1673

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