Assessment and Computational Estimation of Omeprazole and Levosulpiride Impurities in Fixed Dose Combination by AQbD Approach

This study focuses on novel high-performance liquid chromatography (HPLC) method to simultaneously identify and quantify degradation products of esomeprazole and levosulpiride in capsule dosage form, enhancing analytical precision and reliability. The gradient was thoroughly optimized for proper separation of all the peaks in the chromatogram. Chromatographic separation was obtained on Octadecylsilane 250 x 4.6 mm, 5 µm column. Mobile phase A consisting of buffer (Ammonium acetate 50 mM) pH 5.0: Acetonitrile: Water, in ratio 10:10:80 (v/v), whereas mobile phase B consisting of Acetonitrile and Water in ratio 80:20 (v/v). Gradient programme was set as follow: time in min/% of mobile phase A 0/100, 10/80, 15/80, 30/20, 35/100, 45/100. The flow rate was 1.0 mL/min-1 with UV detection at 302 nm. The method development incorporated an analytical quality by design (AQbD) approach, offering a systematic optimization strategy employing Box-Behnken design. The developed method was aligned and validated according to the ICH guidelines. Received: 23 July 2024 | Revised: 21 October 2024 | Accepted: 15 November 2024 Conflicts of Interest The authors declare that they have no conflicts of interest to this work. Data Availability Statement Data available on request from the corresponding author upon reasonable request. Author Contribution Statement Vikram Gharge: Conceptualization, Supervision, Project administration; Satish Jadhao: Conceptualization, Methodology, Supervision, Project administration; Balasaheb Jadhav: Methodology; Pranav Bang: Software, Formal analysis, Investigation, Data curation, Writing - original draft, Writing - review & editing, Visualization; Gurudatt Hendge: Validation, Formal analysis, Data curation, Writing - original draft, Writing - review & editing, Visualization; Nayan Jadhav: Formal analysis, Investigation, Data curation, Writing - original draft, Writing - review & editing, Visualization; Rutuja Mulik: Formal analysis, Resources, Data curation, Writing - original draft, Writing - review & editing, Visualization; Shubham Bhange: Formal analysis, Investigation, Data curation, Writing - original draft, Writing - review & editing, Visualization; Laxman Ingole: Formal analysis, Resources, Data curation, Writing - original draft, Writing - review & editing, Visualization.

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Publication Details

Journal
Archives of Advanced Engineering Science
Published
2024-11-25
DOI
https://doi.org/10.47852/bonviewaaes42023874
Citations
1
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
Field-Weighted Citation Impact
0.24
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article

Assessment and Computational Estimation of Omeprazole and Levosulpiride Impurities in Fixed Dose Combination by AQbD Approach

Sanjivani Jadhao, Balasaheb S. Jadhav, Vikram Gharge, Rahul S. Mulik et al.
1 citations
Archives of Advanced Engineering Science
Analytical Methods in Pharmaceuticals
0.24
article

Assessment and Computational Estimation of Omeprazole and Levosulpiride Impurities in Fixed Dose Combination by AQbD Approach

Sanjivani Jadhao, Balasaheb S. Jadhav, Vikram Gharge, Rahul S. Mulik, N. H. Jadhav, Shubham Bhange, Pranav Bang, Gurudatt Hendge, Laxman Ingole
article en
1 citations

Abstract

This study focuses on novel high-performance liquid chromatography (HPLC) method to simultaneously identify and quantify degradation products of esomeprazole and levosulpiride in capsule dosage form, enhancing analytical precision and reliability. The gradient was thoroughly optimized for proper separation of all the peaks in the chromatogram. Chromatographic separation was obtained on Octadecylsilane 250 x 4.6 mm, 5 µm column. Mobile phase A consisting of buffer (Ammonium acetate 50 mM) pH 5.0: Acetonitrile: Water, in ratio 10:10:80 (v/v), whereas mobile phase B consisting of Acetonitrile and Water in ratio 80:20 (v/v). Gradient programme was set as follow: time in min/% of mobile phase A 0/100, 10/80, 15/80, 30/20, 35/100, 45/100. The flow rate was 1.0 mL/min-1 with UV detection at 302 nm. The method development incorporated an analytical quality by design (AQbD) approach, offering a systematic optimization strategy employing Box-Behnken design. The developed method was aligned and validated according to the ICH guidelines. Received: 23 July 2024 | Revised: 21 October 2024 | Accepted: 15 November 2024 Conflicts of Interest The authors declare that they have no conflicts of interest to this work. Data Availability Statement Data available on request from the corresponding author upon reasonable request. Author Contribution Statement Vikram Gharge: Conceptualization, Supervision, Project administration; Satish Jadhao: Conceptualization, Methodology, Supervision, Project administration; Balasaheb Jadhav: Methodology; Pranav Bang: Software, Formal analysis, Investigation, Data curation, Writing - original draft, Writing - review & editing, Visualization; Gurudatt Hendge: Validation, Formal analysis, Data curation, Writing - original draft, Writing - review & editing, Visualization; Nayan Jadhav: Formal analysis, Investigation, Data curation, Writing - original draft, Writing - review & editing, Visualization; Rutuja Mulik: Formal analysis, Resources, Data curation, Writing - original draft, Writing - review & editing, Visualization; Shubham Bhange: Formal analysis, Investigation, Data curation, Writing - original draft, Writing - review & editing, Visualization; Laxman Ingole: Formal analysis, Resources, Data curation, Writing - original draft, Writing - review & editing, Visualization.

Archives of Advanced Engineering Science
Zydus Lifesciences Limited (India) (IN)
Clean water and sanitation
Openalex Percentile: Top 49%
Analytical Methods in Pharmaceuticals
0.24
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