Sanjeev Shandilya

Identification, characterization and quantification of new impurities by LC–ESI/MS/MS and LC–UV methods in rivastigmine tartrate active pharmaceutical ingredient

Saji Thomas, Sanjeev Shandilya, Amber Bharati et al. · Journal of Pharmaceutical and Biomedical Analysis · 2011 · 25 citations

Pharmacy, Pharmaceutical Analysis, Pharmacology +14

A stability indicating simultaneous dual wavelength UV–HPLC method for the determination of potential impurities in fampridine active pharmaceutical ingredient

Saji Thomas, Sanjeev Shandilya, Amber Bharti et al. · Journal of Pharmaceutical and Biomedical Analysis · 2011 · 22 citations

Pharmacy, Pharmaceutical Analysis, Pharmaceutics +14

Highly efficient, selective, sensitive and stability indicating RP-HPLC–UV method for the quantitative determination of potential impurities and characterization of four novel impurities in eslicarbazepine acetate active pharmaceutical ingredient by LC/ESI-IT/MS/MS

Saji Thomas, Amber Bharti, Pawan Kumar Maddhesia et al. · Journal of Pharmaceutical and Biomedical Analysis · 2011 · 19 citations

Pharmacy, Pharmaceutical Analysis, Pharmacology +16

A Critical N-Nitrosamine Impurity of Anticoagulant Drug, Rivaroxaban: Synthesis, Characterization, Development of LC–MS/MS Method for Nanogram Level Quantification

Vijaya Kumar Baksam, Saritha Nimmakayala, Subba Rao Devineni et al. · Chromatographia · 2022 · 16 citations

Pharmacy, Pharmaceutical Analysis, Pharmacology +12

Identification and characterization of Prothionamide degradation impurities by mass spectrometry, NMR spectroscopy, and ultra high performance liquid chromatography method development

Vijaya Kumar Baksam, Saritha Nimmakayala, S Mohan et al. · Journal of Separation Science · 2021 · 12 citations

Pharmacy, Chemistry, Pharmaceutical Analysis +17