Asian Journal of Pharmaceutical Analysis

Table of Contents

• RESEARCH ARTICLE

  Integrated In-Silico Toxicological Risk Assessment of Vonoprazan Degradation Products using Complementary QSAR Approaches

  • Author: Bhairavi Vijayanand Saraf, Preeti Rajeev Mehta, Rahul Subhash Somani
  • DOI: 10.52711/2231-5675.2026.00011

• Reverse Phase High Performance Liquid Chromatography Method for Simultaneous Estimation of Budesonide and Formoterol in Pure and Tablet

  • Author: M. Venkata Ramana, Podishetty Akhila, Salla Pujitha, Akula Ganesh, Yerolla Soundarya
  • DOI: 10.52711/2231-5675.2026.00012

• Isolation, Characterization and Purity Assessment of Caffeine from Commercial Tea Products

  • Author: Jorige Archana, Mudigiri Ravali, M. Vijaya Bhargavi
  • DOI: 10.52711/2231-5675.2026.00013

• Development and Validation of Analytical Method for Estimation of Zinc and Manganese by Atomic Absorption Spectrophotometer in Multivitamin and Multimineral Syrup

  • Author: Sachin Khopade, Vikram Gharge, Balasaheb Jadhav, Geetanjali Kadam, Shraddha Patil
  • DOI: 10.52711/2231-5675.2026.00014

• Development and Validation of the NP-HPTLC Method for the Estimation of Dimenhydrinate in Bulk and Tablet Formulation

  • Author: Yashodeep Shinde, Harun Patel
  • DOI: 10.52711/2231-5675.2026.00015

• Eco-Friendly QbD-Driven RP-HPLC Method for Stability Analysis of Lamotrigine

  • Author: S. S. Hindole, V.B. Panchabhai, Moein S. Attar, Ram S Sakhare, Nandini Hotkar, Ankita Yadav
  • DOI: 10.52711/2231-5675.2026.00016

• Central Composite Design Aided Method Development and Validation of a Reverse Phase HPLC Method for Escitalopram in Synthetic Mixture

  • Author: Kajal Vable Deshmukh, Priti Kale, Madhuri Deshmukh, Minal Ghante
  • DOI: 10.52711/2231-5675.2026.00017

• Analytical Method Development and Validation of Vadadustat in Bulk and Pharmaceutical Dosage Forms by Using RP-HPLC

  • Author: Shaleena Munwar, Appala Anjali, PSS Prasanna Kumar, B Prem Kumar
  • DOI: 10.52711/2231-5675.2026.00018

• A Novel RP-HPLC Method Development and Validation for Determination of Palbociclib drug in tablet Formulation

  • Author: Omkar D. Garje, Sunil S. Hindole
  • DOI: 10.52711/2231-5675.2026.00019

• REVIEW ARTICLE

  Emerging and Established Methods for Cefepime Quantification: A Detailed Review

  • Author: Diptimayee Jena, Apurba Poria, Adityanarayan Das, Debashis Mishra, Kirtimaya Mishra
  • DOI: 10.52711/2231-5675.2026.00020

• Contemporary Trends in Analytical Method Development for Dapagliflozin and Pioglitazone: A Critical Review of Spectroscopic and Chromatographic Approaches

  • Author: Prushti P. Bhakhar, Hiral S. Popaniya, Khushi V. Rathod, Payal N. Vaja
  • DOI: 10.52711/2231-5675.2026.00021

• Role of Forced Degradation in Stability Indicating Method Development: A Comprehensive Review

  • Author: Vidya R. Mhatre, Ashish S. Jain, Mukesh S. Patil, Shrikant V Joshi, Vilas Surana, Sanika M. Kawade, Anushka D. Patil, Siddh A. Chaudhari, Om S. Lohar, Sakshi S. Sangle
  • DOI: 10.52711/2231-5675.2026.00022

• Simultaneous Estimation of Multicomponent Drugs by HPLC: A Comprehensive Review on Method Development and Validation

  • Author: Sanika M. Kawade, Bhushan R. Rane, Mukesh S. Patil, Ashish S. Jain, Vidya R. Mhatre, Anushka D. Patil, Siddh A. Chaudhary, Om S. Lohar, Sakshi S. Sangle
  • DOI: 10.52711/2231-5675.2026.00023

• RESEARCH ARTICLE

  Development of Ion- pair Extractive Spectrophotometry Method for the determination of Ranolazine in Pharmaceutical Dosage Forms

  • Author: Jitendra Yadav, Prashant Kumar Sahu, Jayesh Verma, Ashutosh Kumar Singh, Aakanksha Sinha, Sanjay J. Daharwal
  • DOI: 10.52711/2231-5675.2026.00024