High-Performance Liquid Chromatography Method for Simultaneous Determination of Guaifenesin, Salbutamol Sulfate and Guaifenesin Impurity (Guaiacol)

被引:9
|
作者
Naguib, Ibrahim A. [1 ]
Farag, Shimaa A. [2 ]
Zaazaa, Hala E. [3 ]
Abdelaleem, Eglal A. [4 ]
机构
[1] Taif Univ, Coll Pharm, Dept Pharmaceut Chem, POB 11099, At Taif 21944, Saudi Arabia
[2] Nahda Univ, Fac Pharm, Analyt Chem Dept, Bani Suwayf 62111, Egypt
[3] Cairo Univ, Fac Pharm, Pharmaceut Analyt Chem Dept, Kasr El Aini St, Cairo 11562, Egypt
[4] Beni Suef Univ, Fac Pharm, Pharmaceut Analyt Chem Dept, Bani Suwayf 62111, Egypt
关键词
VALIDATION;
D O I
10.1093/chromsci/bmaa128
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and reliable HPLC method is developed for isocratic separation of a ternary mixture of Salbutamol Sulfate (SAL), Guaifenesin (GUI) and its impurity Guaiacol (GUA) either in pure powder or in pharmaceutical formulation. Chromatographic separation was applied on a Hypersil GOLD CN column with a mobile phase consisting of 0.05 M KH2PO4 (containing 0.1% triethylamine, pH adjusted to 3.7 by phosphoric acid): methanol (60: 40 by volume) using 0.6 mL min(-1) flow rate and detection of peaks at 275 nm at 25 degrees C with run time around 6 min. The calibration plots were linear over the concentration ranges of 0.5-20, 0.5-30 and 0.1-10 mu g mL(-1) for SAL, GUI and GUA, respectively. ICH guidelines were used for the validation of presented method. The obtained results were compared with the results obtained from the reported HPLC method and no significant difference was found regarding accuracy and precision.
引用
收藏
页码:419 / 424
页数:6
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