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HPLC法同时测定阿咖酚胶囊中三种成分的含量 被引量:1

Determination of Three Constituents in Paracetamol Caffeine and Aspirin Capsules by HPLC
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摘要 目的:建立同时测定阿咖酚胶囊中三种成分(对乙酰氨基酚、咖啡因、阿司匹林)的HPLC法。方法:色谱柱为Phenomenex C8柱(4.6mm×250mm,5μm),流动相为磷酸盐缓冲液(取0.01mol·L^-1磷酸二氢钾溶液,用磷酸调节pH至2.6±0.1)-甲醇(65:35),流速为1.0mL·min^-1,检测波长为229nm,柱温为30℃。结果:对乙酰氨基酚、咖啡因和阿司匹林的进样量分别在0.4084~4.084,0.0938~0.938和0.7476~7.476μg范围内与峰面积呈良好线性关系,r分别为1.0000,1.0000,0.9999(n=6),平均加样回收率分别为100.6%,100.5%和100.3%,RSD分别为0.8%,1.6%和1.2%(n=9)。结论:本方法快速简便,准确可靠,可用于阿咖酚胶囊的质量控制。 Objective:To establish a method for determination of three constituents( paraeetamol, caffeine and aspirin)in Paraeetamol Caffeine and Aspirin Capsules by HPLC. Method:The analytical column was Phenomenex C18 (4.6mm×250mm,5μm) set at 30 ℃ ;The mobile phase was phosphate buffer (0. 01 mol · L^-1 potassium phosphate monobasic adjust to pH 2. 6± 0. 1 by phosphoric acid)-methanol (65: 35) with flow rate 1.0 mL · min^-1. Detection wavelength was set at 229 nm. Results: The linear ranges of Paracetamol, Caffeine, and Aspirin were 0. 408 4 -4. 084,0. 093 8 -0. 938 and 0. 747 6 -7. 476 mg · L^-1 with relative coefficient r = 1. 000 0,r = 1. 000 0, and r = 0. 999 9 ( n = 6 ) , respectively. The average recoveries of Paracetamol , Caffeine and Aspirin were 100. 6 % (RSD =0. 8% ), 100. 5% (RSD = 1.6% )and 100. 3% (RSD =0. 8% ), respectively. Conclusion:The method is simple , accurate ,and suitable for determination of the three constituents in the Paracetamol,Caffeine and Aspirin Capsules.
作者 杨学军
出处 《中国药品标准》 CAS 2009年第5期369-372,共4页 Drug Standards of China
关键词 对乙酰氨基酚 咖啡因 阿司匹林 HPLC Paracetamol Caffeine Aspirin HPLC
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参考文献3

  • 1国家药品标准.化学药品地标升国标.第6册[S].WS-1001-(HD-0533)-2002.
  • 2国家药品标准.化学药品地标升国标.第10册[s].WS-1001.(HD-0941)-2002.
  • 3陈新谦,金有豫,汤光.新编药物学[M]第5版.北京:人民卫生出版社,2004.180.

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  • 1WS-10001-(HD-1021)-2002,国家药品标准·化学药品地标升国标(第16册)[S].

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