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Bibliographic Details
Main Authors:	Karad, Jain, Deore
Format:	Recurso digital
Language:
Published:	Zenodo 2026
Online Access:	https://doi.org/10.5281/zenodo.18720440
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Estimation for Azelnipidine & Telmisartan in Bulk & Pharmaceutical Dosage Form by RP–HPLC
by: CH. Bhavani*, Dr. M. Sunitha Reddy
Published: (2025)

Development of RP‐HPLC Method for Simultaneous Determination of Triclabendazole and Ivermectin in Pharmaceutical Suspension Dosage Form
by: Taj Ur Rahman, et al.
Published: (2025)

Stability‐Indicating RP‐HPLC Method Development and Validation for Determination of Impurities in Loperamide Hydrochloride Capsules Dosage Form
by: Sreenivas Pippalla, et al.
Published: (2025)

Development And Validation Method for Estimation for Liraglutide By RP-HPLC From Its Injectable Dosage Form
by: Akhil Bhakhar*, Khyati Bhupta, Dhirendra Kumar Tarai, Dr. Santosh Kirtane
Published: (2025)

RP HPLC Method Development and Validation for The Simultaneous Estimation of Lansoprazole and Domperidone in Bulk and Capsule Dosage Form
by: Kiran Vyavhare*, Aijaz Sheikh, K. Biyani
Published: (2026)

RP-HPLC Method Development and Validation for Simultaneous Estimation of Norfloxacin and Tinidazole in Combined Tablet Dosage Form
by: Mule Munjaji*, Panchbhai Vivek, Thaware Pratibha
Published: (2025)

Stability‐Indicating RP‐HPLC Method Development and Validation for Quantification of Butylated Hydroxyanisole Content in Loperamide Oral Solid Dosage Form
by: Prasanna Kumar Lankalapalli, et al.
Published: (2025)

To Development and Validation RP-HPLC Method for Tinidazole in Bulk and Pharmaceutical Formulation.
by: Asha Chopde*, Babu Anmulwad, Vanita Mehetre, Pooja Sakharkar
Published: (2025)

Stability‐Indicating RP‐HPLC Method Development and Validation for the Quantification of Ketorolac Tromethamine‐Related Impurities in Tablets Solid Oral Dosage Forms
by: Prasanna Kumar Lankalapalli, et al.
Published: (2025)

Analytical Method Development and Validation for Estimation of Vanoprazan in Pharmaceutical Dosage Forms Including Bioanalysis: A Comprehensive Literature Review
by: N. Spandana, et al.
Published: (2025)

Development and Validation of RP‐HPLC Method for the Detection of N‐Nitroso Meglumine in Pharmaceutical Products
by: Naga Chandrarao Jayavarapu, et al.
Published: (2025)

Sustainable RP‐HPLC Method Development Using AQbD Approach for Simultaneous Estimation of Valganciclovir Hydrochloride and Piperine‐Loaded Lipid Nanoparticles
by: Anjali Mahalkari, et al.
Published: (2026)

A Validated HPLC‐PDA Method for Simultaneous Determination of Metronidazole, Miconazole Nitrate, Fluconazole, and Tinidazole: Application in Bulk and in Different Pharmaceutical Dosage Forms
by: Mrunalini Kulkarni, et al.
Published: (2025)

Development and Validation of a Novel and Cost‐Effective RP‐HPLC Method for the Separation of an Isomeric Impurity in Cariprazine Hydrochloride, an Antipsychotic Agent
by: Rajendra S. Shinde, et al.
Published: (2026)

Development and Application of RP‐HPLC Method for Determination of Fluticasone Propionate and Formoterol Fumarate in a Pharmaceutical Inhaler
by: Chirag Chilka, et al.
Published: (2025)

Validation and Application of Screen-Printed Microchip for Potentiometric Determination of Metformin Hydrochloride in Tablet Dosage Form
by: Mohammed Alqarni, et al.
Published: (2024)

Concepts for a New Rapid and Simple HPLC Method for Simultaneous Determination of Rosuvastatin and Perindopril in Dosage Forms
by: Marjan Piponski, et al.
Published: (2024)

Analytical Quality by Design‐Based Stability‐Indicating Ultra‐High Performance Liquid Chromatography Method for Estimation of Acoramidis Hydrochloride in Bulk and Tablet Dosage Forms
by: Ashwinkumar Matta, et al.
Published: (2025)

Development Of a Novel by RP – HPLC Method for The Estimation of Glatiramer Acetate
by: Dr. Namratha Sunkara, Pasupulati Haritha, P. Twila Pushpa, Rudra Sandhya, Dr. Swathi Boddupally*
Published: (2025)

Quality by Design‐Assisted RP‐HPLC Method for Determination of Ritonavir and Darunavir in Pharmaceutical Formulation Using Central Composite Design
by: Bhagavan Rajesh Babu Koppisetty, et al.
Published: (2024)

RP HPLC Enabled Novel Analytical Method for the Development and Quantification of Cefuroxime Axetil in its Bulk Drug and Pharmaceutical Formulations
by: Haragouri Mishra, et al.
Published: (2024)

Simultaneous Estimation of Empagliflozin and Linagliptin in Bulk and Pharmaceutical Dosage Form by Reverse Phase-High Performance Liquid Chromatography
by: Divya Jyothi*, Dr. S. Shobha Rani
Published: (2025)

A Simple and Rapid HPLC Method Development for Quantification of Sodium Benzoate Content in Chlorzoxazone Oral Solid Dosage Forms
by: Prasanna Kumar Lankalapalli, et al.
Published: (2024)

Validated RP‐HPLC‐UV Method for Simultaneous Quantification of Aminophenazone, Dipyrine, and Chlorpheniramine Maleate in Pharmaceutical Formulations Considering Dipyrine Decomposition
by: Md. Abid Hasan, et al.
Published: (2026)

Micro‐Determination of the Macro‐Drugs (Pseudoephedrine Hydrochloride‐Ibuprofen) in their Pure Form and Pharmaceutical Preparations
by: Asmaa Saeed Jabouri, et al.
Published: (2025)

A Novel Derivatization‐Free Approach for Analysis of (+)2‐Aminobutanol and Ethambutol Hydrochloride in Tablets Preparation Using RP‐HPLC‐NQAD
by: Hao Ruan, et al.
Published: (2025)

Corrigendum to “Green and High Throughput Assay Using 96‐Microwell Base to Determine Metformin Hydrochloride in the Tablet Dosage Form”
Published: (2025)

RP‐HPLC Based Concurrent Analysis of Empagliflozin and Metoprolol Succinate in a Novel Pharmaceutical Combination Tablet
by: Heena Ninama, et al.
Published: (2025)

Analytical Quality‐by‐Design‐Oriented High‐Performance Liquid Chromatographic Method for Quantification of Metformin Hydrochloride, Teneligliptin Hydrobromide Hydrate and Dapagliflozin in Tablet Dosage Form
by: Kalpana Patel, et al.
Published: (2026)

Analytical Quality by Design Enabled Green RP‐HPLC Method Development and Validation for the Simultaneous Quantitation of the Cleaning Residues of Osimertinib, Binimetinib, and Erdafitinib: An Approach to Prevent the Cross‐Contamination in Shared Facilities of Pharmaceutical Manufacturing
by: Jainendra Kumar Jain, et al.
Published: (2025)

Development of a Stability‐Indicating RP‐HPLC Method for the Quantification of Tolperisone Hydrochloride and Diclofenac Sodium Impurities in Drug Substances and in Combination: Implementation of Analytical Quality by Design and Degradation Kinetics
by: Vikas L. Mohite, et al.
Published: (2025)

Quality by Design–Based RP‐HPLC Method for Simultaneous Estimation of 4‐Hydroxytamoxifen and Thymoquinone in Liposomal Formulation
by: Pavithra Pradeep Prabhu, et al.
Published: (2026)

Rapid, Reliable, and Green: A Novel RP‐HPLC Method for Quercetin Estimation in Green‐Synthesized Nanoparticles
by: Rachana Bhimanwar, et al.
Published: (2025)

Simple and Novel Fluorimetric Protocol for Sitagliptin Estimation Through Sensitivity Enhancement Using Acetic Acid: Application to Pharmaceutical Dosage Form With Green Assessment
by: Tamer Z. Attia, et al.
Published: (2026)

New Stability Indicating RP‐HPLC Methods for the Impurity Profiling of Amifampridine Phosphate
by: A. Karunakar, et al.
Published: (2026)

Investigating the Presence of Falsified and Poor-Quality Fixed-Dose Combination Artemether-Lumefantrine Pharmaceutical Dosage Forms in Kumasi, Ghana
by: Simon Nyarko, et al.
Published: (2024)

A sustainable RP‐HPLC method for concurrent estimation of capecitabine and celecoxib in liposomal formulation: Greenness and whiteness appraisal
by: Rushikesh Sanjay Shewale, et al.
Published: (2024)

RP‐HPLC–Validated Method for Hesperidin Estimation in Rat Skin Following Transdermal Delivery via Dissolving Microneedle Patch
by: Gopika Gopan, et al.
Published: (2025)

Determination of 5‐Hydroxymethylfurfural Content in Marketed Honey: A Modified RP‐HPLC Method
by: Barbara Adu-Brimpong, et al.
Published: (2026)

A Stability Indicating RP‐HPLC Method for Determination of Foslevodopa and Foscarbidopa in Bulk and Formulation
by: Ravisankar Panchumarthy, et al.
Published: (2025)

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