An innovative combination of Box-Behnken design and ecofriendly approaches for the simultaneous determination of aspirin, clopidogrel, atorvastatin and rosuvastatin in their fixed-dose combination tablets

• Published in: BMC chemistry 2023-11, Vol.17 (1), p.164-164, Article 164
• Main Authors: Mostafa, Eman A., El‐Ashrey, Mohamed K., Mahmoud, Sally Tarek
• Format: Article
• Language: English
• Subjects: Acetonitrile; All terrain vehicles; Analysis; Aspirin; Atorvastatin; Box-Behnken design; Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Cholesterol; Chromatography; Clopidogrel; Computer software industry; Computers; Design of experiments; Design optimization; Dosage and administration; Drug therapy, Combination; Drugs; Green design; High performance liquid chromatography; HPLC–DAD; Mathematical analysis; Methods; Packaging; Potassium phosphates; Quality control; Room temperature; Rosuvastatin; Separation; Services
• ISSN: 2661-801X; 2661-801X
• DOI: 10.1186/s13065-023-01079-x

Three-levels Box-Behnken design was used in the experimental design approach for the optimization of chromatographic parameters to achieve the optimum resolution and sharp peak shape within a reasonable run time. A method that is sensitive, reliable, and selective was constructed and validated for the simultaneous measurement of a combination therapy that contains blood-thinning and cholesterol-lowering compounds. The four cited drugs namely, aspirin (ASP), clopidogrel (CLP), atorvastatin (ATV) and rosuvastatin (ROS) were estimated in bulk and in pharmaceutical dosage forms in line with International Council for Harmonization guidelines. The separation was done utilizing Kinetex 2.6 C18 column (100 mm, 4.6 mm, 5 m) and RP-HPLC with diode array detector. The separation of the cited drugs and the degradation product of ASP was achieved with mobile phase composed of acetonitrile: KH 2 PO 4 buffer in a gradient mode with pH 3.2 at room temperature. The four drugs were linear over the concentration range (0.05–50 µg/mL). The technique is feasible to be used in quality control laboratories. To picture the green profile of the developed method, four greenness assessment tools were applied. National environmental methods index (NEMI), analytical eco-scale assessment (ESA), green analytical procedure index (GAPI) and analytical greenness metric (AGREE) are the most widely used metrics. They were employed to evaluate the greenness profile of the proposed method and to perform a detailed greenness comparison between the developed method and some of the reported methods for the determination of the investigated drugs. The developed method was found to be relatively green with 0.54 AGREE score.