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毛细管气相色谱法测定药物制剂中的苯丙醇胺。

Capillary gas chromatographic determination of phenylpropanolamine in pharmaceutical preparation.

作者信息

Abbasi K, Bhanger M I, Khuhawar M Y

机构信息

National Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro, Pakistan.

出版信息

J Pharm Biomed Anal. 2006 Jun 7;41(3):998-1001. doi: 10.1016/j.jpba.2006.01.004. Epub 2006 Apr 24.

Abstract

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%.

摘要

已开发出一种分析方法,用于气相色谱法测定苯丙醇胺(PPA),该方法使用三氟乙酰丙酮(FAA)作为衍生试剂。洗脱在HP-5柱(30 m×0.32 mm内径)上进行,膜厚0.25微米,初始柱温70℃保持5分钟,然后以10℃/分钟的升温速率升至120℃。进样口温度保持在270℃。氮气流速为2毫升/分钟,检测采用FID。PPA浓度在30 - 150微克/毫升范围内获得线性校准曲线,检测限为6.0微克/毫升。该方法用于测定辛那特(Sinutab)和特韦吉-D(Tavegyl-D)片剂中的PPA。药物制剂分析的相对标准偏差(R.S.D.)在0.4 - 0.9%范围内。

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