Cutting‐edge HPLC and MCR techniques for synchronically quantifying anticholinergic drugs in the presence of C12 and C14 homologs: Robust application to green and white chemistry

Author:

Al‐Wasidi Asma S.1,Ahmed Hoda A.2,Alshammari Manal Falag Abtan3,Nafee Sherif S.4,Mohamed Mahmoud A.5ORCID

Affiliation:

1. Department of Chemistry, College of Science Princess Nourah bint Abdulrahman University Riyadh Saudi Arabia

2. Department of Chemistry, Faculty of Science Cairo University Cairo Egypt

3. Physics Department, Faculty of Science University of Hail Hail Saudi Arabia

4. Physics Department, Faculty of Science King Abdulaziz University Jeddah K.S.A.

5. Hikma Pharmaceutical Company Beni‐Suef Egypt

Abstract

AbstractGreen and white chemistry are vital to revolutionizing the chemical industry through their unparalleled potential to enhance sustainability and efficiency. In this study, nine sustainability tools of both green and white metrics, including green analytical procedure index (GAPI), ComplexGAPI, analytical greenness, analytical greenness metric for sample preparation, Analytical Eco‐Scale (ESA), analytical method greenness score, high‐performance liquid chromatography‐ environmental assessment tool (HPLC‐EAT), analytical method volume intensity, and blue applicability grade index (BAGI), have been developed for appraising environmental friendliness for both innovative and straightforward mean centering of ratio spectra (MCR) and reversed‐phase high‐performance liquid chromatography (RP‐HPLC) strategies utilized for concurrent analysis and separation of cyclopentolate (CYC) and C12 and C14 homologs of benzalkonium chloride (BNZ) in pure and ophthalmic solution. The mobile phase, formed of buffer phosphate and acetonitrile (35:65, v/v), was adjusted to pH 6.3, and 215‐nm UV detection was used. The experimental flow rate was 2.0 mL min−1, and the analytical column was L11 Inertsil Ph‐3 (150 mm × 4.6 mm, 5 µm). All sequences were run at 25°C in the column oven. The MCR approach effectively resolved the drug's spectral overlapping. CYC and BNZ employed this approach at 227.5 and 220.4 nm, respectively. As part of the HPLC analysis, an isocratic method was employed with phosphate buffer and acetonitrile in the mobile phase at 35:65. A correlation coefficient greater than 0.999 was observed between the calibration curves for the HPLC and MCR methods in the ranges of 20–320 µg mL−1 and 5–30 µg mL−1 for all drugs. The technique yields excellent primary recovery rates, ranging from 97.2% to 100.5%. The recommended approach has been validated according to International Council for Harmonization guidelines.

Publisher

Wiley

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