Heptad green metrics and quality by design tool evaluated chromatography method for content determination of Bexagliflozin in formulation product

• UPLC method developed for analysing the content in Bexagliflozin formulation with 2.5 mins run time. • The method robustness was evaluated by using Quality by Design software and validated as per the current regulatory guidelines. • The method Greenness was assessed by 7 advanced metrics (NEMI, Modified NEMI, GAPI, Complex GAPI, AGREE, AGREEprep and Analytical Eco-scale). The study created an eco-friendly, rapid, sensitive, cost-efficient, stability-assessing method for analyzing Bexagliflozin in pharmaceuticals using a RP-UPLC approach. The method's specificity was achieved using an XBridge analytical column (100 mm x 2.1 mm, 3.5 µm) with a mobile phase consisting of 10 mM Ammonium acetate and Methanol in a ratio of 55:45 (v/v). The flow rate is 0.2 mL/min, the injection volume is 1 µL, and the UV detection wavelength is 220 nm. The total run time is 2.5 minutes. The technique was meticulously validated, strictly adhering to the ICH criteria, and demonstrated specificity, linearity, ruggedness, robustness, and accuracy. The technique robustness analysis was carried out by using the QbD tool to build DoE's and assess their robustness. The methodology exhibited a linear trend as the concentration level increased from 5µg/mL to 30ug/mL. The recovery process ranged from 50% to 150%, with the average recovery considered adequate. Method stability indicating nature proved by forced degradation study. Analytical Eco-scale value found 81. NEMI showing the three quadrants showing the green, Modified NEMI has only one red quadrant. GAPI have five green, 5 yellow and 5 red parts. Complex GAPI have 12 green, 7 yellow and 6 red parts in the whole pictogram. AGREE shown the quantitative value 0.64 and pictogram shown 7 green parts, three yellow parts and 2 red parts. Green metric tools NEMI, modified NEMI, GAPI, complex GAPI Eco-scale, AGREE, and AGREEprep are used to express the method's greenness.

Authors

Institutions

Publication Details

Journal
Green Analytical Chemistry
Published
2025-05-20
DOI
https://doi.org/10.1016/j.greeac.2025.100280
Citations
2
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
Field-Weighted Citation Impact
1.50
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Heptad green metrics and quality by design tool evaluated chromatography method for content determination of Bexagliflozin in formulation product

Sreekantha Babu Jonnalagadda, Naresh Kumar Katari, Phani Raja Kanuparthy, Leela Prasad Kowtharapu et al.
2 citations
Green Analytical Chemistry
Analytical Methods in Pharmaceuticals
1.50
article

Heptad green metrics and quality by design tool evaluated chromatography method for content determination of Bexagliflozin in formulation product

Sreekantha Babu Jonnalagadda, Naresh Kumar Katari, Phani Raja Kanuparthy, Leela Prasad Kowtharapu, Satyajit Raj Nethekar, Vishnuvardhana Kishore Polisetti, Pankaj Kumar Lahoti
article en
2 citations

Abstract

• UPLC method developed for analysing the content in Bexagliflozin formulation with 2.5 mins run time. • The method robustness was evaluated by using Quality by Design software and validated as per the current regulatory guidelines. • The method Greenness was assessed by 7 advanced metrics (NEMI, Modified NEMI, GAPI, Complex GAPI, AGREE, AGREEprep and Analytical Eco-scale). The study created an eco-friendly, rapid, sensitive, cost-efficient, stability-assessing method for analyzing Bexagliflozin in pharmaceuticals using a RP-UPLC approach. The method's specificity was achieved using an XBridge analytical column (100 mm x 2.1 mm, 3.5 µm) with a mobile phase consisting of 10 mM Ammonium acetate and Methanol in a ratio of 55:45 (v/v). The flow rate is 0.2 mL/min, the injection volume is 1 µL, and the UV detection wavelength is 220 nm. The total run time is 2.5 minutes. The technique was meticulously validated, strictly adhering to the ICH criteria, and demonstrated specificity, linearity, ruggedness, robustness, and accuracy. The technique robustness analysis was carried out by using the QbD tool to build DoE's and assess their robustness. The methodology exhibited a linear trend as the concentration level increased from 5µg/mL to 30ug/mL. The recovery process ranged from 50% to 150%, with the average recovery considered adequate. Method stability indicating nature proved by forced degradation study. Analytical Eco-scale value found 81. NEMI showing the three quadrants showing the green, Modified NEMI has only one red quadrant. GAPI have five green, 5 yellow and 5 red parts. Complex GAPI have 12 green, 7 yellow and 6 red parts in the whole pictogram. AGREE shown the quantitative value 0.64 and pictogram shown 7 green parts, three yellow parts and 2 red parts. Green metric tools NEMI, modified NEMI, GAPI, complex GAPI Eco-scale, AGREE, and AGREEprep are used to express the method's greenness.

Green Analytical ChemistryVol. 13
Rutgers, The State University of New Jersey (US), Deloitte (United States) (US), Lamar State College–Port Arthur (US), GITAM University (IN), University of KwaZulu-Natal (ZA)
Openalex Percentile: Top 19%
Analytical Methods in Pharmaceuticals
1.50
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.