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Publications (13)
- A Green and Ultra‐Sensitive Liquid Chromatography–Tandem Mass Spectrometry Method for Simultaneous Trace‐Level Quantification of Nitrosamine Drug Substance Related Impurities in Clozapine: Method Development, Validation, and Greenness Evaluation Save
- A Rapid and Sensitive Liquid Chromatography–Tandem Mass Spectrometry Method for the Quantification of Nitrosamine Impurities in an Anticoagulant Drug: Application to Drug Substance and Pharmaceutical Dosage Forms Save
- Strategic approaches to elevate quality and sustainability of NDSRIs method development: Synthesis and a simultaneous quantification study of multiple tamsulosin NDSRIs Save
- A facile and eco-friendly simultaneous quantification LC-TQ-MS/MS approach for N-Nitroso Moxifloxacin and di-nitroso pyrrolopiperidine in Moxifloxacin tablets and eye drops Save
- A novel LC-TQ-MS/MS method for quantifying mefenamic acid-NDSRI (N-nitroso drug substance-related impurity) in mefenamic acid tablet and pediatric suspension dosage forms: a comparative study with a cost-effective white, green, and blue UPLC method Save
- A sustainable and novel LC-TQ-MS/MS method for quantifying mutagenic Ketoconazole-NDSRIs aligned with green and white analytical chemistry principles Save
- A novel and eco-friendly UPLC-ESI-MS method for the quantification of Aceclofenac-NDSRI (Nitroso Drug Substance Related Impurity) from Aceclofenac drug substance and combination formulations Save
- Synthesis and Trace-Level Quantification of Mutagenic and Cohort-of-Concern Ciprofloxacin Nitroso Drug Substance-Related Impurities (NDSRIs) and Other Nitroso Impurities Using UPLC-ESI-MS/MS─Method Optimization Using I-Optimal Mixture Design Save
- A sensitive ultra‐performance liquid chromatography‐tandem mass spectrometry method for the simultaneous quantification of assay and trace‐level genotoxic tosylate analogs (methyl and ethyl) in empagliflozin and its tablet dosage forms Save
- A sensitive UPLC-MS/MS method for the simultaneous assay and trace level genotoxic impurities quantification of SARS-CoV-2 inhibitor-Molnupiravir in its pure and formulation dosage forms using fractional factorial design Save