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HPLC法测定丁丙诺啡纳洛酮舌下片中两种主药的量

Determination of content of buprenorphine hydrochloride and naloxone hydrochloride sublingual tablets by gradient HPLC

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【作者】 臧可昕马克苏慕君刘亚梅杨昕

【Author】 ZANG Ke-xin1,MA Ke2,SU Mu-jun1,LIU Ya-mei2,YANG Xin2 1 Tianjin Institute of Pharmaceutical Research,Tianjin 300193,China;2 TIPR Pharmaceutical Responsible Co.,Tianjin 300193,China

【机构】 天津药物研究院天津药物研究院药业有限责任公司

【摘要】 目的:建立梯度洗脱HPLC法同时测定丁丙诺啡纳洛酮舌下片中两种主药的量。方法:采用梯度洗脱,用DiamonsilC18(250mm×4.6mm,5μm)色谱柱;以甲醇-乙腈-0.02mol/L磷酸二氢钾溶液(48:32:20)(用磷酸调pH4.0)为流动相A,甲醇-乙腈-0.02mol/L磷酸二氢钾溶液(6:4:90)(用磷酸调pH4.0)为流动相B;体积流量1.0mL/min;检测波长为230nm。结果:纳洛酮在5.0~30.0μg/mL线性关系良好(r=0.9998),回收率为99.68%(RSD=0.92%);丁丙诺啡在20.0~120.0μg/mL线性关系良好(r=0.9999),回收率为99.74%(RSD=0.53%)。结论:采用梯度洗脱HPLC法同时测定丁丙诺啡纳洛酮舌下片中两主药的量,方法简便、灵敏、专属,重现性好,该方法可以监控药品质量。

【Abstract】 Objective:To establish agradient elution HPLC method for determination of the contents of buprenorphine hydrochloride and naloxone hydrochloride sublingual tablets at the same time.Methods:The column was Diamonsil C18(250 mm×4.6 mm,5 μm).Mobile phase A was methanol:acetonitrile:0.02mol/L potassium dihydrogen phosphate buffer(48:32:20)(pH 4.0);Mobile phase B was methanol:acetonitrile:0.02 mol/L potassium dihydrogen phosphate buffer(6:4:90)(pH 4.0).Flow rate was 1.0 mL/min.Detection wavelength was 314 nm.Results:The calibration curve was linear in the range of buprenorphine 5.0-30.0 μg/mL(r = 0.999 8),coefficient of recovery was 99.68%(RSD = 0.92%).The calibration curve was linear in the range of naloxone 20.0-120.0 μg/mL(r = 0.999 9),coefficient of recovery was 99.74%(RSD = 0.53%).Conclusion:The method is simple,sensitive,specific,reproducible,accurate and suitable for examination of the contents of buprenorphine hydrochloride and naloxone hydrochloride sublingual tablets at the same time.The Methods could be used to monitor drug quality.

  • 【文献出处】 药物评价研究 ,Drug Evaluation Research , 编辑部邮箱 ,2010年06期
  • 【分类号】R927.2
  • 【被引频次】1
  • 【下载频次】71
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