AQbD‐Based Development and Optimization of a Stability‐Indicating RP‐HPLC Method for Imeglimin With Integration of Lean Six Sigma Principles

ABSTRACT An accurate and green RP‐HPLC stability indicating method has been developed for estimation of Imeglimin with an AQbD approach. Method optimization was done based on Box–Behnken design by changing factors like mobile phase, pH, and flow rate for optimum resolution and retention time. Lean Six Sigma (DMAIC) and statistical process control techniques ensured the consistency of the method. Water–methanol in the ratio of 65:35 (v/v) adjusted to pH 4.0 was used as the mobile phase at a flow rate of 0.8 mL/min, having an approximate retention time of 3.7 min. Method validation was performed as per the ICH guidelines, and the method exhibited a high correlation coefficient ( R 2 = 0.9994), low %RSD (< 2%), and good accuracy (99.45%–100.35%). LOD and LOQ were found to be 1.04 and 3.15 μg/mL, respectively. The results of forced degradation experiments showed significant degradation in the presence of alkaline, oxidative, and thermal stress conditions, whereas Imeglimin remained stable under photolytic stress conditions. HR‐MS and FTIR studies indicated that N‐dealkylation and N‐demethylation were possible degradation pathways. The greenness assessment of the developed method was carried out using AGREE, GAPI, BAGI, and CLICK indices.

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Publication Details

Journal
Biomedical Chromatography
Published
2026-07-24
DOI
https://doi.org/10.1002/bmc.70563
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

AQbD‐Based Development and Optimization of a Stability‐Indicating RP‐HPLC Method for Imeglimin With Integration of Lean Six Sigma Principles

Vidhya K. Bhusari, Kamini Sethy, Samiksha Ghorpade
Biomedical Chromatography
Analytical Methods in Pharmaceuticals
article

AQbD‐Based Development and Optimization of a Stability‐Indicating RP‐HPLC Method for Imeglimin With Integration of Lean Six Sigma Principles

Vidhya K. Bhusari, Kamini Sethy, Samiksha Ghorpade
article en

Abstract

ABSTRACT An accurate and green RP‐HPLC stability indicating method has been developed for estimation of Imeglimin with an AQbD approach. Method optimization was done based on Box–Behnken design by changing factors like mobile phase, pH, and flow rate for optimum resolution and retention time. Lean Six Sigma (DMAIC) and statistical process control techniques ensured the consistency of the method. Water–methanol in the ratio of 65:35 (v/v) adjusted to pH 4.0 was used as the mobile phase at a flow rate of 0.8 mL/min, having an approximate retention time of 3.7 min. Method validation was performed as per the ICH guidelines, and the method exhibited a high correlation coefficient ( R 2 = 0.9994), low %RSD (< 2%), and good accuracy (99.45%–100.35%). LOD and LOQ were found to be 1.04 and 3.15 μg/mL, respectively. The results of forced degradation experiments showed significant degradation in the presence of alkaline, oxidative, and thermal stress conditions, whereas Imeglimin remained stable under photolytic stress conditions. HR‐MS and FTIR studies indicated that N‐dealkylation and N‐demethylation were possible degradation pathways. The greenness assessment of the developed method was carried out using AGREE, GAPI, BAGI, and CLICK indices.

Biomedical ChromatographyVol. 40(9)
Hindu College of Pharmacy (IN), Smt. Kashibai Navale Medical College and General hospital (IN), Centurion University of Technology and Management (IN), Savitribai Phule Pune University (IN)
Openalex Percentile: Top 12%
Analytical Methods in Pharmaceuticals
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AQbD‐Based Development and Optimization of a Stability‐Indicating RP‐HPLC Method for Imeglimin With Integration of Lean Six Sigma Principles — Vidhya K. Bhusari, Kamini Sethy, et al. · Biomedical Chromatography (2026) | TGRS Research Map | TGRS