Santhosh Kumar Ettaboina
6PUBLICATIONS
7CO-AUTHORS
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Publications (6)
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|Jun 24, 2025
Development and Validation of an RP-HPLC Method for Organic Impurity Profiling in Baclofen Utilizing Robustness Through a Quality-by-Design (QbD) Approach: A Comprehensive Forced Degradation Assessment.Santhosh Kumar Ettaboina, Satyasree Nannapaneni, Naresh Kumar Katari
|Sep 05, 2024
Development, evaluation of critical method variables and stability assessment using a Box-Behnken design for the determination of organic impurities in a pharmaceutical dosage form of a centrally acting muscle relaxant drug chlorzoxazone.Santhosh Kumar Ettaboina, Satyasree Nannapaneni, Nagalakshmi Jeedimalla
|Jul 01, 2023
Quality by design tool-evaluated stability-indicating ultra-performance liquid chromatography method for the determination of drugs (ritonavir and darunavir) used to treat the human immunodeficiency virus/acquired immunodeficiency syndrome.Jyothsna Menda, Phani Raja Kanuparthy, Naresh Kumar Katari
|Jan 24, 2023
An effective and stability-indicating method development and optimization utilizing the Box-Behnken design for the simultaneous determination of acetaminophen, caffeine, and aspirin in tablet formulation.Parvateesam Yenda, Naresh Kumar Katari, Santhosh Kumar Ettaboina
|Oct 25, 2021
A simple isocratic LC method for quantification of trace-level inorganic degradation impurities (ferricyanide, ferrocyanide, nitrite, and nitrate) in sodium nitroprusside injection and robustness by quality using design approach.Parvateesam Yenda, Naresh Kumar Katari, Thirupathi Dongala
|Feb 19, 2021
Development and validation of LC-MS method for the determination of heptaethylene glycol monomethyl ether in benzonatate bulk drugs.Lakshmi Narasimha Rao Katakam, Santhosh Kumar Ettaboina, Vishnu Murthy Marisetti
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