Analytical Method Development and Validation of Selexipag by different quantitative Analytical Techniques

Fuente: Zenodo
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: C. Sushma, L Sivasanker Reddy, S Gejalakshmi, R. Nageswara Rao
Format: Recurso digital
Veröffentlicht: Zenodo 2025
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1866901607478722560
author C. Sushma
L Sivasanker Reddy
S Gejalakshmi
R. Nageswara Rao
author_facet C. Sushma
L Sivasanker Reddy
S Gejalakshmi
R. Nageswara Rao
contents <p>Selexipag, a selective prostacyclin IP receptor agonist, is used for the treatment of pulmonary arterial hypertension (PAH). Analytical methods such as reversed-phase high-performance liquid chromatography (RP-HPLC), ultraviolet-visible (UV) spectroscopy, and their combination (RP-HPLCUV) are critical for the accurate quantification and quality control of selexipag in bulk and pharmaceutical formulations. This review comprehensively discusses the development, optimization, and validation of RPHPLC, UV, and RP-HPLC-UV methods for selexipag, focusing on their principles, applications, and compliance with International Conference on Harmonization (ICH) guidelines. Recent advancements, challenges, and future perspectives in these analytical techniques are also highlighted.</p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_18052898
institution Zenodo
language
publishDate 2025
publisher Zenodo
record_format zenodo
spellingShingle Analytical Method Development and Validation of Selexipag by different quantitative Analytical Techniques
C. Sushma
L Sivasanker Reddy
S Gejalakshmi
R. Nageswara Rao
<p>Selexipag, a selective prostacyclin IP receptor agonist, is used for the treatment of pulmonary arterial hypertension (PAH). Analytical methods such as reversed-phase high-performance liquid chromatography (RP-HPLC), ultraviolet-visible (UV) spectroscopy, and their combination (RP-HPLCUV) are critical for the accurate quantification and quality control of selexipag in bulk and pharmaceutical formulations. This review comprehensively discusses the development, optimization, and validation of RPHPLC, UV, and RP-HPLC-UV methods for selexipag, focusing on their principles, applications, and compliance with International Conference on Harmonization (ICH) guidelines. Recent advancements, challenges, and future perspectives in these analytical techniques are also highlighted.</p>
title Analytical Method Development and Validation of Selexipag by different quantitative Analytical Techniques
url https://doi.org/10.5281/zenodo.18052898