Development of eco-friendly sensitive HPLC method for determination of Letrozole and assessment of validation

• Eco-Friendly HPLC: Uses ethanol-water (50:50) mobile phase, replaces toxic solvents, 3-minute analysis. • Rigorous Validation: ICH-compliant, linear range (0.1–40 µg/mL), precise/accurate for Letrozole tablets. • Sustainability Metrics: AGREE, GAPI, ChlorTox, NQS assess alignment with UN SDGs. • Broad Applications: QC, bioequivalence, routine analysis. The greening of analytical methods has gained interest in the field of quantitative analysis to reduce environmental impact and improve analyst's safety and health. For postmenopausal women with hormone-responsive advanced breast cancer, Letrozole (LTZ) has been a standard first-line endocrine therapy A green HPLC method was developed, optimized, validated, and applied for quantification of the LTZ in tablets. Experiments were conducted on the Inertsil ODS- 3® C18 (5 µm, 150 × 4.6 mm). An isocratic elution was applied using a mobile phase consisting of ethanol: water (50:50, v/v). A wavelength of 230.0 nm was chosen for the analysis. An experiment was finished 3.0 mins. Calibration graphs for each drug were rectilinear in the range of 0.1 – 40.0 µg/mL. Validation studies were carried out based on International Conference on Harmonization (ICH) recommendations. The student (t) test for means and the (F) test for standard deviations were used to compare the results. In this study, we utilized the ChlorTox Scale, Greenness Index, AGREE, GAPI, and NQS Indicator to comprehensively evaluate the environmental, safety, and sustainability aspects of analytical methodology, aligning our approach with the United Nations Sustainable Development Goals (SDGs). It can be applied to quality control, bioequivalence studies, and routine analysis.

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Publication Details

Journal
Talanta Open
Published
2025-02-26
DOI
https://doi.org/10.1016/j.talo.2025.100425
Citations
6
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
Field-Weighted Citation Impact
4.51
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article

Development of eco-friendly sensitive HPLC method for determination of Letrozole and assessment of validation

Gizem Tırıs, Reem H. Obaydo, M. Soner Bay, Nevin Erk et al.
6 citations
Talanta Open
Analytical Methods in Pharmaceuticals
4.51
article

Development of eco-friendly sensitive HPLC method for determination of Letrozole and assessment of validation

Gizem Tırıs, Reem H. Obaydo, M. Soner Bay, Nevin Erk, Asena Ayse Genc, Hayam M. Lotfy
article en
6 citations

Abstract

• Eco-Friendly HPLC: Uses ethanol-water (50:50) mobile phase, replaces toxic solvents, 3-minute analysis. • Rigorous Validation: ICH-compliant, linear range (0.1–40 µg/mL), precise/accurate for Letrozole tablets. • Sustainability Metrics: AGREE, GAPI, ChlorTox, NQS assess alignment with UN SDGs. • Broad Applications: QC, bioequivalence, routine analysis. The greening of analytical methods has gained interest in the field of quantitative analysis to reduce environmental impact and improve analyst's safety and health. For postmenopausal women with hormone-responsive advanced breast cancer, Letrozole (LTZ) has been a standard first-line endocrine therapy A green HPLC method was developed, optimized, validated, and applied for quantification of the LTZ in tablets. Experiments were conducted on the Inertsil ODS- 3® C18 (5 µm, 150 × 4.6 mm). An isocratic elution was applied using a mobile phase consisting of ethanol: water (50:50, v/v). A wavelength of 230.0 nm was chosen for the analysis. An experiment was finished 3.0 mins. Calibration graphs for each drug were rectilinear in the range of 0.1 – 40.0 µg/mL. Validation studies were carried out based on International Conference on Harmonization (ICH) recommendations. The student (t) test for means and the (F) test for standard deviations were used to compare the results. In this study, we utilized the ChlorTox Scale, Greenness Index, AGREE, GAPI, and NQS Indicator to comprehensively evaluate the environmental, safety, and sustainability aspects of analytical methodology, aligning our approach with the United Nations Sustainable Development Goals (SDGs). It can be applied to quality control, bioequivalence studies, and routine analysis.

Talanta OpenVol. 11
Responsible consumption and production
Openalex Percentile: Top 6%
Analytical Methods in Pharmaceuticals
4.51
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