Yasmeen E. Mostafa, Fawzi Elsebaei, Mohammed El-Sayed Metwally
Abstract Design of experiments has emerged as an influential and proactive approach that demonstrated favored applicability in optimizing chromatographic procedures. Quality-by-design guarantees the long-standing efficiency of the developed HPLC method reducing the need for costly and resource-intensive univariate approach. A low environmental footprint, sensitive, fast, and simple HPLC method was developed for concurrent estimation of cefixime (CFX) and ornidazole (ORN) in their raw materials, laboratory-prepared tablets, and pharmaceutical formulations using 2 3 full factorial design. The separation was performed on a cyano column through UV detection at 300 nm in less than 4 min. The elution was achieved using a mobile phase (pH = 6.0) composed of methanol and 0.3% triethylamine in ratio of (85%: 15%, v/v), respectively with a flow rate of 1 mL/min. The method’s validity was established with ICH $$\:{\text{Q}}_{2}{\text{R}}_{1}$$ regulations. Excellent linear correlation ( r = 0.9999) was established within concentration ranges lies between 1 and 50 µg/mL and 0.5–50 µg/mL with high percent found of 100.04 ± 0.82 and 99.99 ± 1.01 for CFX and ORN, respectively. The approach exhibited high precision (% RDS < 2) and sensitivity with detection limits of 0.07 and 0.09 µg/mL and quantification limits of 0.21 and 0.28 µg/mL for CFX and ORN, respectively. Several metrics evidenced the method’s greenness and sustainability profile.