Development and Comparison of Stability-Indicating HPLC and UPLC Methods for the Determination and Validation of
Aysen Kurt Cucu1, Engin Ozturk2
1Marmara University, Department of Analytical Chemistry, Faculty of Pharmacy, Istanbul 34854, Turkey.
Background:
Pantoprazole is a selective proton pump inhibitor used in its sodium form in pharmaceuticals. Determining its impurities is crucial for drug purity and safety.
Objective:
This study aims to develop a faster impurity analysis method than the European Pharmacopoeia (EP) method.
Methods:
An Agilent Zorbax SB Phenyl (250 × 4.6 mm, 5.0 µm) column was used for HPLC, and a Restek Ultra Biphenyl (100 × 2.1 mm, 3.0 µm) column for Ultra Performance Liquid Chromatography (UPLC). A potassium dihydrogen/dipotassium hydrogen phosphate buffer (pH 7.40)-acetonitrile (65 + 35, v/v) mixture was the mobile phase. Analyses were performed at 290 nm with flow rates of 1.0 mL/min (HPLC) and 0.25 mL/min (UPLC). Injection volumes were 20 µL (HPLC) and 3.5 µL (UPLC).
Results:
The analysis times of the impurity determination methods developed are 15 min shorter for the HPLC method and 30 min shorter for the UPLC method compared to the EP method. The developed methods were validated according to International Conference on Harmonisation (ICH) guidelines, demonstrating high linearity (R2 >0.99 over the concentration range of 0.03-2.27 µg/mL), accuracy with mean recoveries ranging from 95.0 to 105.0%, and precision with intra- and inter-day RSD values below 2%. Forced degradation studies under acidic, alkaline, oxidative, thermal, and photolytic conditions confirmed that the methods are stability-indicating, with the ability to separate all major degradation products of pantoprazole sodium.
Conclusion:
The method was validated according to ICH guidelines, and forced degradation studies were also performed. This study presents optimized HPLC and UPLC methods that allow faster impurity analysis and detection of an additional non-compendial impurity, pantoprazole-N-oxide.
Highlights:
As a result of shorter analysis times, a significant cost reduction has also been proven with numerical data. In addition, a performance-cost comparison of two different analytical technologies was made.
More Related Videos
07:29HPLC Coupled with Chemical Fingerprinting for Multi-Pattern Recognition for Identifying the Authenticity of Clematidis Armandii Caulis
Published on: November 11, 2022
11:00Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry UPLC-HRMS
Published on: May 20, 2013
Related Concept Videos
High-Performance Liquid Chromatography: Elution Process
High-Performance Liquid Chromatography: Introduction
In HPLC, two phases play a critical role in the separation process:
Drug Dissolution: Requirements and Profile Comparison
High-Performance Liquid Chromatography: Instrumentation
Data Validation
Key parameters for method validation include:
High-Performance Liquid Chromatography: Types of Detectors
