Bhoopendra Singh Kushwah

Employment

• Syngene International (India) Research Investigator
  2022 - Present
• Aurigene Discovery Technologies (India)
  2016 - 2017

Education

• National Institute of Pharmaceutical Education and Research Ph.D
  2017 - 2022
• National Institute of Pharmaceutical Education and Research M.S. (Pharm.)
  2014 - 2016

Projects & Funding

Projects & funding information is unavailable.

Publications (20)

• First Method for Trace-Level Quantification of the Potential Genotoxic Impurity Bis(neopentyl glycolato)diboron Using GC–MS
  Organic Process Research & Development 2026 DOI: 10.1021/acs.oprd.5c00507
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• Multi-method coamorphous systems of lumefantrine with alpha ketoglutaric acid: Comprehensive characterization, biological evaluation and stability analysis
  International Journal of Pharmaceutics 2025 DOI: 10.1016/j.ijpharm.2024.125056
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• Analytical Artifact Due to Residual HCN in Acetonitrile: Identification and Control Strategies
  Organic Process Research & Development 2024 DOI: 10.1021/acs.oprd.4c00336
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• Analytical Strategy for Low-Level Estimation of Unstable Genotoxic Boronate Ester Impurities
  Organic Process Research & Development 2024 DOI: 10.1021/acs.oprd.4c00065
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• In vivo and in vitro metabolite profiling of nirmatrelvir using LC–Q‐ToF–MS/MS along with the in silico approaches for prediction of metabolites and their toxicity
  Biomedical Chromatography 2024 DOI: 10.1002/bmc.5849
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• Chromatographic separation of tiropramide hydrochloride and its degradation products along with their structural characterization using liquid chromatography quadrupole time‐of‐flight tandem mass spectrometry and nuclear magnetic resonance
  Biomedical Chromatography 2023 DOI: 10.1002/bmc.5636
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• LC-HRMS and NMR studies for characterization of forced degradation impurities of ponatinib, a tyrosine kinase inhibitor, insights into in-silico degradation and toxicity profiles
  Journal of Pharmaceutical and Biomedical Analysis 2023 DOI: 10.1016/j.jpba.2023.115280
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• Characterization of potential degradation products of brexpiprazole by liquid chromatography/quadrupole–time‐of‐flight mass spectrometry and nuclear magnetic resonance, and prediction of their physicochemical properties by ADMET Predictor™
  Rapid Communications in Mass Spectrometry 2023 DOI: 10.1002/rcm.9415
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• Development of stability‐indicating method for separation and characterization of benidipine forced degradation products using LC–MS/MS
  Biomedical Chromatography 2023 DOI: 10.1002/bmc.5517
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• Structural characterization of novel hydrolytic and oxidative degradation products of acalabrutinib by LC-Q-TOF-MS, H/D exchange and NMR
  Journal of Pharmaceutical and Biomedical Analysis 2022 DOI: 10.1016/j.jpba.2022.115077
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