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• Eco-friendly, stability-indicating HPTLC method developed for carvedilol estimation. • The method reduces solvent use, enhancing sustainability without losing accuracy. • Greenness assessed via NEMI Scale, AGREE, Eco scale assessment, GAPI and White Analytical Chemistry metrics. • Robust under stress conditions, suitable for carvedilol stability analysis. • Promotes green chemistry for sustainable pharmaceutical analytical methods. A robust, sensitive, and ecofriendly stability-indicating HPTLC method was developed for the quantification of carvedilol and validated. The method was optimized to avoid carcinogenic solvents, employing a mobile phase of toluene, isopropanol, ammonia (7.5:2.5:0.1, v/v/v), ensuring sharp and symmetric peaks with minimal tailing. The separation was attained on a silica gel 60F254 TLC plate, using ascending development up to 75 mm at room temperature. The developed method demonstrated excellent linearity in the range of 20–120 ng/band with a R 2 value 0.995. Forced degradation studies revealed the effective separation of carvedilol and degradant, with an Rf value of 0.44 ± 0.02 for the parent compound. Carvedilol was found to be stable under neutral, photolytic, and thermal conditions, while significant degradation was observed under acidic, alkaline, and oxidative stress conditions. The proposed method was useful to the assay of three brands of carvedilol tablets, yielding results between 99% and 101% of the labelled claim. Greenness assessment using NEMI scale, AGREE software, Eco scale assessment, GAPI and white analytical chemistry highlighted the method's environmental benefits, surpassing published chromatographic methods. The simplicity, accuracy, and eco-friendly nature of the developed method make it an ideal choice for tedious quality control and stability studies of carvedilol.
Rabadiya et al. (Sat,) studied this question.