Author(s): Laxman A. Kawale, Mayuri V. Gophane, Surabhi H. Patil, Vandana S. Nade

Email(s): kawalela@rediffmail.com , mayurigophane5@gmail.com , shpatil@mvpcpn.edu.in , vsnade@mvpcpn.edu.in

DOI: 10.52711/2231-5675.2026.00001   

Address: Laxman A. Kawale1, Mayuri V. Gophane2, Surabhi H. Patil3, Vandana S. Nade4
1Assistant Professor (Pharmaceutical Chemistry), MVP Samaj’s College of Pharmacy, Nashik.
2M. Pharm Student (Pharmaceutical Quality Assurance), MVP Samaj’s College of Pharmacy, Nashik.
3Assistant Professor (Pharmaceutics), MVP Samaj’s College of Pharmacy, Nashik.
4Assistant Professor (Pharmacology), MVP Samaj’s College of Pharmacy, Nashik.
*Corresponding Author

Published In:   Volume - 16,      Issue - 1,     Year - 2026


ABSTRACT:
A simple, precise, accurate, and robust High-Performance Liquid Chromatographic (HPLC) method has been developed for simultaneous estimation of Lobeglitazone sulfate and Glimeperide both in bulk and tablet dosage form. Fishbone diagram was used to identify variables that can affect quality of analytical method. Analytical quality by design (AQbD) approach was implemented for method development process. Box-Behnken Design (BBD) was used to optimise chromatographic conditions. Three factors were selected to design the matrix- percent organic ratio, mobile phase pH and flow rate. Analysis of variance (ANOVA) was applied to confirm if selected factors were significant. The analysis was done on Phenomenex C18(250mm, 4.6mm, 5µm) column, using mobile phase as Acetonitrile: Water [% Orthophosphoric acid (OPA)] (80:20% v/v), (pH: 2.5), flow rate of 1ml/min with 243nm detecting wavelength. ICHQ2 (R2) guidelines were followed for method validation. The method was found to be linear in the range of 5-25µg/ml for Lobeglitazone sulfate and 10-50µg/ml for Glimeperide with correlation coefficients of 0.999. Percent recovery for both drugs was found to be in the range of 98-102%. To estimate precision and repeatability Percent Relative Standard Deviation (%RSD) was calculated. It was found to be below 2% confirming that the proposed method showed good accuracy, robustness.


Cite this article:
Laxman A. Kawale, Mayuri V. Gophane, Surabhi H. Patil, Vandana S. Nade. Analytical Quality by Design-Based RP-HPLC Method for Simultaneous Estimation of Lobeglitazone sulfate and Glimeperide in Pharmaceutical Formulations. Asian Journal of Pharmaceutical Analysis. 2026; 16(1):1-8. doi: 10.52711/2231-5675.2026.00001

Cite(Electronic):
Laxman A. Kawale, Mayuri V. Gophane, Surabhi H. Patil, Vandana S. Nade. Analytical Quality by Design-Based RP-HPLC Method for Simultaneous Estimation of Lobeglitazone sulfate and Glimeperide in Pharmaceutical Formulations. Asian Journal of Pharmaceutical Analysis. 2026; 16(1):1-8. doi: 10.52711/2231-5675.2026.00001   Available on: https://ajpaonline.com/AbstractView.aspx?PID=2026-16-1-1


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DOI: 10.5958/2231–5675 


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