Innovative green stability-indicating HPLC method coupled with fluorescence detection for determination of antidiabetic agent canagliflozin

• Stability indicating HPLC-FD technique for the determination of CANA in the presence of its OXD in laboratory-prepared mixtures and the dosage form based on their native fluorescence. • The analytical eco-scale, green analytical procedure index and AGREE evaluation method ensure the greenness of HPLC method with the aid of whiteness, and blueness assessment to ensure sustainability of HPLC method. • The HPLC approach utilizing a fluorescence detector exhibited greater sensitivity and specificity compared to other published methods employing UV detection. This study exhibits a sustainable, easy, and reliable stability indicating HPLC approach utilizing fluorometric detection for quantification of canagliflozin (CANA) in the presence of its hepatotoxic oxidative degradation product (OXD). The chromatographic separation was accomplished using Symmetry® C18 column (3.5 μm, 4.6 × 100 mm). The mobile phase consists of 0.1 M phosphate buffer pH 2 and ethanol (40:60 v/v) pumped at a flow rate of 1.0 mL/min throughout the run. The eluted peaks were monitored by the fluorescence detector, and the chromatogram was extracted at emission wavelength of 410 nm for CANA and OXD after excitation at 290 nm which was suitable for both CANA and OXD. Performance of the suggested approach was assessed in accordance with ICH guidelines for linearity, accuracy, precision, robustness, detection, and quantitation limits. Linear relationship was achieved in the range of 0.50–10.00 μg/mL and 0.10–2.00 μg/mL for CANA and OXD, respectively with correlation coefficient 0.9999 for both components. The validated method was effectively utilized for the analysis of CANA in its pure form and drug tablets. The environmental sustainability of the suggested approach was evaluated and validated using various tools, including the analytical eco-scale, the Green Analytical Procedure Index (GAPI), and AGREE. Additional applications were employed to evaluate the ideas of 'blueness' and 'whiteness' through the newly developed Blue Applicability Grade Index (BAGI) and Red-Green-Blue 12 (RGB 12) algorithms. The elevated BAGI score (85) signified exceptional applicability, while the RGB12 score (92.2) verified the cost-effectiveness and sustainability of the used approach.

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Publication Details

Journal
Talanta Open
Published
2025-03-18
DOI
https://doi.org/10.1016/j.talo.2025.100436
Citations
7
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
Field-Weighted Citation Impact
5.27
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article

Innovative green stability-indicating HPLC method coupled with fluorescence detection for determination of antidiabetic agent canagliflozin

Hala E. Zaazaa, Sally S. El‐Mosallamy, Nada Nabil, Ghada A. Sedik
7 citations
Talanta Open
Analytical Methods in Pharmaceuticals
5.27
article

Innovative green stability-indicating HPLC method coupled with fluorescence detection for determination of antidiabetic agent canagliflozin

Hala E. Zaazaa, Sally S. El‐Mosallamy, Nada Nabil, Ghada A. Sedik
article en
7 citations

Abstract

• Stability indicating HPLC-FD technique for the determination of CANA in the presence of its OXD in laboratory-prepared mixtures and the dosage form based on their native fluorescence. • The analytical eco-scale, green analytical procedure index and AGREE evaluation method ensure the greenness of HPLC method with the aid of whiteness, and blueness assessment to ensure sustainability of HPLC method. • The HPLC approach utilizing a fluorescence detector exhibited greater sensitivity and specificity compared to other published methods employing UV detection. This study exhibits a sustainable, easy, and reliable stability indicating HPLC approach utilizing fluorometric detection for quantification of canagliflozin (CANA) in the presence of its hepatotoxic oxidative degradation product (OXD). The chromatographic separation was accomplished using Symmetry® C18 column (3.5 μm, 4.6 × 100 mm). The mobile phase consists of 0.1 M phosphate buffer pH 2 and ethanol (40:60 v/v) pumped at a flow rate of 1.0 mL/min throughout the run. The eluted peaks were monitored by the fluorescence detector, and the chromatogram was extracted at emission wavelength of 410 nm for CANA and OXD after excitation at 290 nm which was suitable for both CANA and OXD. Performance of the suggested approach was assessed in accordance with ICH guidelines for linearity, accuracy, precision, robustness, detection, and quantitation limits. Linear relationship was achieved in the range of 0.50–10.00 μg/mL and 0.10–2.00 μg/mL for CANA and OXD, respectively with correlation coefficient 0.9999 for both components. The validated method was effectively utilized for the analysis of CANA in its pure form and drug tablets. The environmental sustainability of the suggested approach was evaluated and validated using various tools, including the analytical eco-scale, the Green Analytical Procedure Index (GAPI), and AGREE. Additional applications were employed to evaluate the ideas of 'blueness' and 'whiteness' through the newly developed Blue Applicability Grade Index (BAGI) and Red-Green-Blue 12 (RGB 12) algorithms. The elevated BAGI score (85) signified exceptional applicability, while the RGB12 score (92.2) verified the cost-effectiveness and sustainability of the used approach.

Talanta OpenVol. 11
Cairo University (EG), Badr University in Cairo (EG)
Openalex Percentile: Top 4%
Analytical Methods in Pharmaceuticals
5.27
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