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机构地区:[1]厦门市药品检验所,厦门361012
出 处:《药物分析杂志》2015年第1期129-132,共4页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立GC法同时测定复方牙痛酊中樟脑和乙酸龙脑酯的含量。方法:采用DB-WAX毛细管柱(30 m×0.25 mm×0.25μm),氢火焰离子检测器(FID);以萘为内标;进样口温度230℃,检测器温度250℃,程序升温(初始温度105℃,保持3min,以3℃·min^-1的速率升至140℃,再以100℃·min^-1的速率升至210℃,保持5 min),分流进样,分流比2.0∶1,进样量1μL。结果:樟脑、乙酸龙脑酯浓度分别在1.81-27.18μg·m L^-1和5.53-82.95μg·m L^-1范围内呈良好的线性关系(r=0.999 9),平均回收率(n=9)分别为103.9%和105.2%。结论:本方法可用于测定复方牙痛酊中樟脑和乙酸龙脑酯的含量。Objective: To establish a GC method for simultaneous determination of contents of camphor and borneol acetate in compound Yatong tincture. Methods: A DB-WAX capillary column( 30 m × 0. 250 mm × 0. 25 μm)and a FID were adopted. Naphthalene was used as an internal standard substance. The injector temperature was230 ℃ and the detector temperature was 250 ℃. The initial temperature was 105 ℃,maintained for 3 min,rose to140 ℃ with a rate of 3 ℃ ·min^-1,then rose to 210 ℃ with a rate of 100 ℃·min^-1,maintained for 5 minutes.The split ratio for split stream sampling was 2. 0 ∶ 1. The injection volume was 1 μL. Results: The linear ranges of camphor and borneol acetate were 1. 81-27. 18 μg·m L^-1( r =0. 999 9) and 5. 53-82. 95 μg·m L^-1( r =0. 999 9),respectively. Their average recovery rates( n = 9) were 103. 9 % and 105. 2 %,respectively. Conclusion:The developed method is suitable for the determination of camphor and borneol acetate in compound Yatong tincture.
关 键 词:复方牙痛酊 樟脑 乙酸龙脑酯 樟木 宽叶缬草 苗药 气相色谱法 含量测定
分 类 号:R917[医药卫生—药物分析学]
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