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采用毛细管区带电泳法同时测定片剂中盐酸西替利嗪、对乙酰氨基酚和盐酸去氧肾上腺素的方法开发与验证

Method development and validation for the simultaneous determination of cetirizine dihydrochloride, paracetamol, and phenylpropanolamine hydrochloride in tablets by capillary zone electrophoresis.

作者信息

Azhagvuel S, Sekar R

机构信息

Analytical Chemistry Division, Indian Institute of Chemical Technology, Hyderabad 500007, India.

出版信息

J Pharm Biomed Anal. 2007 Feb 19;43(3):873-8. doi: 10.1016/j.jpba.2006.08.028. Epub 2006 Oct 4.

Abstract

A simple, selective, and cost effective capillary zone electrophoresis (CZE) method has been developed for the simultaneous separation and determination of cetirizine dihydrochloride (CTZ), paracetamol (PARA), and phenylpropanolamine hydrochloride (PPA) in tablets. A 10 mM sodium tetraborate background electrolyte (BGE) solution (pH 9.0) was found to be suitable for separation of all the analytes. An uncoated fused-silica capillary of a total length of 76 cm (effective length 64.5 cm) was used for separation. All the analytes were completely separated within 10 min at the applied voltage of 20 kV (current produced approximately 21 microA), and detection was performed at 195 nm with an UV detector. Ibuprofen was used as internal standard (I.S.) for the quantification of the drugs. Validation of the method was performed in terms of linearity, accuracy, precision, limit of detection (LOD), and quantification (LOQ). The linearity of the calibration curves for CTZ, PARA, and PPA (tested range) were 2-50 microg ml(-1) (r(2)=0.9982), 10-1000 microg ml(-1) (r(2)=0.9978), and 10-100 microg ml(-1) (r(2)=0.9986), respectively. The proposed method has been applied for the determination of active ingredients in tablets, and the recovery was found to be > or =98.60% with the relative standard deviation (R.S.D.) < or =1.56%. The LOQ of the CTZ, PARA, and PPA was found to be 2.0, 2.0, and 4.0 microg ml(-1), respectively. There were no interfering peaks due to the excipients present in the pharmaceutical tablets. Thus, the proposed method is simple and suitable for the simultaneous analysis of active ingredients in tablet dosage forms.

摘要

已开发出一种简单、选择性好且成本效益高的毛细管区带电泳(CZE)方法,用于同时分离和测定片剂中的盐酸西替利嗪(CTZ)、对乙酰氨基酚(PARA)和盐酸苯丙醇胺(PPA)。发现10 mM硼酸钠背景电解质(BGE)溶液(pH 9.0)适用于所有分析物的分离。使用总长76 cm(有效长度64.5 cm)的未涂层熔融石英毛细管进行分离。在20 kV的施加电压下(产生的电流约为21微安),所有分析物在10分钟内完全分离,并用紫外检测器在195 nm处进行检测。布洛芬用作药物定量的内标(I.S.)。该方法通过线性、准确度、精密度、检测限(LOD)和定量限(LOQ)进行验证。CTZ、PARA和PPA校准曲线的线性(测试范围)分别为2 - 50 μg ml⁻¹(r² = 0.9982)、10 - 1000 μg ml⁻¹(r² = 0.9978)和10 - 100 μg ml⁻¹(r² = 0.9986)。所提出的方法已用于测定片剂中的活性成分,回收率≥98.60%,相对标准偏差(R.S.D.)≤1.56%。CTZ、PARA和PPA的LOQ分别为2.0、2.0和4.0 μg ml⁻¹。由于药物片剂中存在的辅料没有干扰峰。因此,所提出的方法简单,适用于同时分析片剂剂型中的活性成分。

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