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Capillary gas chromatographic determination of phenylpropanolamine in pharmaceutical preparation.

机译:毛细管气相色谱法测定药物制剂中的苯丙醇胺

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摘要

Analytical procedure has been developed for the gas chromatographic determination of phenylpropanolamine (PPA) using trifluoroacetylacetone (FAA) as derivatizing reagent. Elution is carried out from the column HP-5 (30 mx0.32 mm i.d.) with film thickness 0.25 microm at initial column temperature 70 degrees C for 5 min, followed by heating rate 10 degrees C/min up to 120 degrees C. Injection port temperature was maintained at 270 degrees C. Nitrogen flow rate was 2 ml/min and detection was by FID. The linear calibration curve was obtained with 30-150 microg/ml PPA with detection limit of 6.0 microg/ml. The method was used for the determination of PPA from Sinutab and Tavegyl-D tablets. The relative standard deviation (R.S.D.) for the analysis of pharmaceutical preparation was obtained within 0.4-0.9%.
机译:已经开发了使用三氟乙酰丙酮(FAA)作为衍生试剂的气相色谱法测定苯丙醇胺(PPA)的分析程序。从膜厚0.25微米的HP-5色谱柱(30 mx0.32 mm内径)在70°C的初始柱温下洗脱5分钟,然后以10°C / min的速度加热到120°C。入口温度保持在270℃。氮气流速为2ml / min,并通过FID检测。用30-150 microg / ml PPA获得线性校准曲线,检测极限为6.0 microg / ml。该方法用于测定Sinutab和Tavegyl-D片剂中的PPA。分析药物制剂的相对标准偏差(R.S.D.)在0.4-0.9%之内。

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