Asian Journal of Pharmaceutical Analysis

ISSN

2231-5675 (Online)
2231-5667 (Print)


Submit Article

Search Results:

Analytical Method Validation and Quantitative Analysis for Active Pharmaceutical Ingredient and Marketed Formulation of Teneligliptin Hydrobromide by UV Spectroscopy

Author(s): Kalyani Farkade, Mukund Tawar

DOI: 10.52711/2231-5675.2021.00034

Views: 104 (pdf),       4153 (html)

Access: Open Access

Cite: Kalyani Farkade, Mukund Tawar. Analytical Method Validation and Quantitative Analysis for Active Pharmaceutical Ingredient and Marketed Formulation of Teneligliptin Hydrobromide by UV Spectroscopy. Asian Journal of Pharmaceutical Analysis. 2021; 11(3):195-8. doi: 10.52711/2231-5675.2021.00034


Read More

Development and Validation of RP-HPLC Method for the Estimation of Linezolid from Bulk and Formulations

Author(s): Kalyani Farkade, Vikrant Salode, Tejashri Kadu

DOI: 10.52711/2231-5675.2023.00045

Views: 57 (pdf),       3804 (html)

Access: Open Access

Cite: Kalyani Farkade, Vikrant Salode, Tejashri Kadu. Development and Validation of RP-HPLC Method for the Estimation of Linezolid from Bulk and Formulations. Asian Journal of Pharmaceutical Analysis. 2023; 13(4):273-7. doi: 10.52711/2231-5675.2023.00045


Read More

Asian Journal of Pharmaceutical Analysis (AJPA) is an international, peer-reviewed journal, devoted to pharmaceutical analysis...... Read more >>>

RNI: Not Available                     
DOI: 10.5958/2231–5675 

Journal Policies & Information



Quick Links


Latest Issues

Popular Articles


Recent Articles



Integrated In-Silico Toxicological Risk Assessment of Vonoprazan Degradation Products using Complementary QSAR Approaches
Emerging and Established Methods for Cefepime Quantification: A Detailed Review
Contemporary Trends in Analytical Method Development for Dapagliflozin and Pioglitazone: A Critical Review of Spectroscopic and Chromatographic Approaches
Role of Forced Degradation in Stability Indicating Method Development: A Comprehensive Review
Simultaneous Estimation of Multicomponent Drugs by HPLC: A Comprehensive Review on Method Development and Validation
Development of Ion- pair Extractive Spectrophotometric Method for the determination of Ranolazine in Pharmaceutical Dosage Forms
Reverse Phase High Performance Liquid Chromatography Method for Simultaneous Estimation of Budesonide and Formoterol in Pure and Tablet
Isolation, Characterization and Purity Assessment of Caffeine from Commercial Tea Products
Development and Validation of Analytical Method for Estimation of Zinc and Manganese by Atomic Absorption Spectrophotometer in Multivitamin and Multimineral Syrup
Development and Validation of the NP-HPTLC Method for the Estimation of Dimenhydrinate in Bulk and Tablet Formulation
Eco-Friendly QbD-Driven RP-HPLC Method for Stability Analysis of Lamotrigine
Central Composite Design Aided Method Development and Validation of a Reverse Phase HPLC Method for Escitalopram in Synthetic Mixture
Analytical Method Development and Validation of Vadadustat in Bulk and Pharmaceutical Dosage Forms by Using RP-HPLC
A Novel RP-HPLC Method Development and Validation for Determination of Palbociclib drug in tablet Formulation
Analytical Quality by Design-Based RP-HPLC Method for Simultaneous Estimation of Lobeglitazone sulfate and Glimeperide in Pharmaceutical Formulations
Beyond Chromatograms: Green Analytical Frontiers in the Nutraceutical Era
Method Development and Validation for the Assay of the Anticoagulant dosage form by HPLC
Validation of the UV Spectrophotometric Method for the Quantitative measurement of Clopidogrel bisulphate in Pharmaceutical Dosage Form and Bulk
Analytical method development and validation for Simultaneous Estimation of Rifampicin and Levofloxacin in Bulk and Synthetic Mixtures Using Validated RP- HPLC Technique
A High-Precision RP–HPLC Method for Ondansetron Hydrochloride: Development, Optimization and Validation

Tags