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[1]
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Structural Elucidation of Novel Degradation Impurities of Ibrutinib in Ibrutinib Tablets Using Preparative Chromatography, LCMS, HRMS and 2D NMR Techniques
Journal of Chromatographic Science,
2025
DOI:10.1093/chromsci/bmae002
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[2]
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Structural Elucidation of Novel Degradation Impurities of Ibrutinib in Ibrutinib Tablets Using Preparative Chromatography, LCMS, HRMS and 2D NMR Techniques
Journal of Chromatographic Science,
2024
DOI:10.1093/chromsci/bmae002
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[3]
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Box-Behnken design in optimization of the green liquid chromatographic method for the quantification of Afatinib in drug product: AQbD approach
Journal of Liquid Chromatography & Related Technologies,
2024
DOI:10.1080/10826076.2024.2384039
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[4]
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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
Biomedical Chromatography,
2024
DOI:10.1002/bmc.6001
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[5]
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Box-Behnken design in optimization of the green liquid chromatographic method for the quantification of Afatinib in drug product: AQbD approach
Journal of Liquid Chromatography & Related Technologies,
2024
DOI:10.1080/10826076.2024.2384039
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[6]
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Using the AQbD Approach, Development and Validation of a Simple, Rapid Stability Indicating Chromatographic Method for Quantification of Related Impurities of Apixaban
Journal of Chromatographic Science,
2024
DOI:10.1093/chromsci/bmad065
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[7]
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A QBD WITH THE FRACTIONAL FACTORIAL DESIGN WAS USED TO MATCH THE SIMILARITY BETWEEN RANOLAZINE EXTENDED-RELEASE TABLETS 500 MG AND 1000 MG
International Journal of Applied Pharmaceutics,
2023
DOI:10.22159/ijap.2023v15i2.47241
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[8]
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A comprehensive review on QbD driven analytical procedures developed for the analysis of various drugs
Journal of Liquid Chromatography & Related Technologies,
2023
DOI:10.1080/10826076.2023.2204238
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[9]
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Generic approach in a gradient elution HPLC method development that enables troubleshooting free method transfer
Journal of Pharmaceutical and Biomedical Analysis,
2022
DOI:10.1016/j.jpba.2021.114367
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[10]
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Optimization and Validation in Liquid Chromatography Using Design of Experiments
Chemistry Africa,
2022
DOI:10.1007/s42250-022-00344-1
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[11]
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Generic approach in a gradient elution HPLC method development that enables troubleshooting free method transfer
Journal of Pharmaceutical and Biomedical Analysis,
2022
DOI:10.1016/j.jpba.2021.114367
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[12]
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Statistically Designed, Targeted Profile UPLC Method Development for Assay and Purity of Haloperidol in Haloperidol Drug Substance and Haloperidol 1 mg Tablets
Chromatographia,
2020
DOI:10.1007/s10337-020-03889-w
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[13]
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QbD-driven development and validation of HPLC method for determination of Bisphenol A and Bis-sulphone in environmental samples
International Journal of Environmental Analytical Chemistry,
2019
DOI:10.1080/03067319.2019.1629585
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[14]
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Ultra-high performance liquid chromatography-MS/MS (UHPLC-MS/MS) in practice: analysis of drugs and pharmaceutical formulations
Future Journal of Pharmaceutical Sciences,
2019
DOI:10.1186/s43094-019-0007-8
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[15]
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Development and validation of chromatographic methods for the quantification of dabigatran etexilate mesylate in the presence of its risky degradation products
JPC - Journal of Planar Chromatography - Modern TLC,
2018
DOI:10.1556/1006.2018.31.6.6
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[16]
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An overview of experimental designs in HPLC method development and validation
Journal of Pharmaceutical and Biomedical Analysis,
2017
DOI:10.1016/j.jpba.2017.05.006
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