Box-Behnken Assisted Validation and Optimization of an RP-HPLC Method for Simultaneous Determination of Domperidone and Lansoprazole

被引:9
作者
Afzal, Mohd [1 ]
Muddassir, Mohd. [1 ]
Alarifi, Abdullah [1 ]
Ansari, Mohammed Tahir [2 ,3 ]
机构
[1] King Saud Univ, Coll Sci, Dept Chem, Riyadh 11451, Saudi Arabia
[2] Univ Kuala Lumpur, Royal Coll Med Perak, Fac Pharm & Hlth Sci, Dept Pharmaceut Technol, Ipoh 31400, Malaysia
[3] Univ Nottingham Malaysia, Sch Pharm, Jalan Broga, Kajang 43500, Selangor, Malaysia
关键词
lansoprazole; domperidone; method validation; Box– Behnken; chromatography;
D O I
10.3390/separations8010005
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A highly specific, accurate, and simple RP-HPLC technique was developed for the real-time quantification of domperidone (DOMP) and lansoprazole (LANS) in commercial formulations. Chromatographic studies were performed using a Luna C8(2), 5 mu m, 100 angstrom, column (250 x 4.6 mm, Phenomenex) with a mobile phase composed of acetonitrile/2 mM ammonium acetate (51:49 v/v), pH 6.7. The flow rate was 1 mL center dot min(-1) with UV detection at 289 nm. Linearity was observed within the range of 4-36 mu g center dot mL(-1) for domperidone and 2-18 mu g center dot mL(-1) for lansoprazole. Method optimization was achieved using Box-Behnken design software, in which three key variables were examined, namely, the flow rate (A), the composition of the mobile phase (B), and the pH (C). The retention time (Y-1 and Y-3) and the peak area (Y-2 and Y-4) were taken as the response parameters. We observed that slight alterations in the mobile phase and the flow rate influenced the outcome, whereas the pH exerted no effect. Method validation featured various ICH parameters including linearity, limit of detection (LOD), accuracy, precision, ruggedness, robustness, stability, and system suitability. This method is potentially useful for the analysis of commercial formulations and laboratory preparations.
引用
收藏
页码:1 / 14
页数:14
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