SE
SANTHOSH KUMAR ETTABOINA
Aurex Laboratories LLC, Jawaharlal Nehru Technological University Hyderabad, Kakatiya University of Pharmaceutical Sciences
0000-0002-7094-9161
Employment
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Aurex Laboratories LLC Associate-QC2020 - Present
Education
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Jawaharlal Nehru Technological University Hyderabad Master of pharmacy2016 - 2018
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Kakatiya University of Pharmaceutical Sciences Bachelor of Pharmacy2012 - 2016
Projects & Funding
Projects & funding information is unavailable.
Publications (21)
- Ultra‐Sensitive and Green LC–MS/MS Method for Trace‐Level Determination of Nitrosamine Drug Substance‐Related Impurities in the Anti‐Diuretic Drug Furosemide Save
- Microwave‐Assisted Synthesis and Structural Characterization of N‐Nitroso Tofacitinib: Janus Kinase Inhibitor Save
- 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 Save
- 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 Save
- 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 Save
- 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 Save
- 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 Save
- Implementation of Analytical Quality by Design and Green Chemistry Principles to Develop a Novel UPLC Method for the Determination of Fluocinolone Acetonide Impurities from its Drug Substance and Topical Oil Formulations Save
- Implementation of Analytical Quality by Design and Green Chemistry Principles to Develop a Novel UPLC Method for the Determination of Fluocinolone Acetonide Impurities from its Drug Substance and Topical Oil Formulations Save
- Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Erythromycin Related Impurities in Topical Dosage Form Save