Analytical Method Development and Validation for Estimation of Vanoprazan in Pharmaceutical Dosage Forms Including Bioanalysis: A Comprehensive Literature Review

Fuente: Zenodo
Enregistré dans:
Détails bibliographiques
Auteurs principaux: N. Spandana, P. Pooja, Jutta Swathi, P.Vivek Sagar*
Format: Recurso digital
Langue:anglais
Publié: Zenodo 2025
Sujets:
Accès en ligne:
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
_version_ 1866902011897708544
author N. Spandana
P. Pooja
Jutta Swathi
P.Vivek Sagar*
author_facet N. Spandana
P. Pooja
Jutta Swathi
P.Vivek Sagar*
contents <p><span>Vanoprazan fumarate, a potassium-competitive acid blocker (PCAB), is a novel therapeutic agent for acid-related diseases. Accurate analytical methods for its quantification in pharmaceutical dosage forms and biological matrices are essential for quality control, formulation development, and pharmacokinetic studies. This review consolidates advances in analytical method development and validation for vanoprazan using UV-visible spectroscopy, high-performance liquid chromatography (HPLC), liquid chromatography-tandem mass spectrometry (LC-MS/MS), and other bioanalytical techniques. Validation according to ICH guidelines, method parameters, sample preparation, and applications are emphasized, providing a thorough overview of modern and classical methods.</span></p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_17789553
institution Zenodo
language eng
publishDate 2025
publisher Zenodo
record_format zenodo
spellingShingle Analytical Method Development and Validation for Estimation of Vanoprazan in Pharmaceutical Dosage Forms Including Bioanalysis: A Comprehensive Literature Review
N. Spandana
P. Pooja
Jutta Swathi
P.Vivek Sagar*
Vanoprazan fumarate
HPLC
UV-visible spectrophotometry
LC-MS/MS.
<p><span>Vanoprazan fumarate, a potassium-competitive acid blocker (PCAB), is a novel therapeutic agent for acid-related diseases. Accurate analytical methods for its quantification in pharmaceutical dosage forms and biological matrices are essential for quality control, formulation development, and pharmacokinetic studies. This review consolidates advances in analytical method development and validation for vanoprazan using UV-visible spectroscopy, high-performance liquid chromatography (HPLC), liquid chromatography-tandem mass spectrometry (LC-MS/MS), and other bioanalytical techniques. Validation according to ICH guidelines, method parameters, sample preparation, and applications are emphasized, providing a thorough overview of modern and classical methods.</span></p>
title Analytical Method Development and Validation for Estimation of Vanoprazan in Pharmaceutical Dosage Forms Including Bioanalysis: A Comprehensive Literature Review
topic Vanoprazan fumarate
HPLC
UV-visible spectrophotometry
LC-MS/MS.
url https://doi.org/10.5281/zenodo.17789553