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A validated UHPLC-MS method for tryptophan metabolites: Application in the diagnosis of multiple sclerosis

Journal of pharmaceutical and biomedical analysis, 2020-06, Vol.185, p.113246-113246, Article 113246

2020

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Robust UHPLC Separation Method Development for Multi-API Product Containing Amlodipine and Bisoprolol: The Impact of Column Selection

Chromatographia, 2014-09, Vol.77 (17-18), p.1119-1127

2014

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A novel tool for structure assignment of hydroxylated metabolites of (arylpiperazinylbutyl)oxindole derivatives based on relative HPLC retention times

Journal of pharmaceutical and biomedical analysis, 2019-06, Vol.170, p.102-111

2019

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Total Synthesis of Bacterial 5-(3-Indolyl)oxazole Alkaloids: Pimprinols A–C

SynOpen (2017), 2019-10, Vol.3 (4), p.148-156

2019

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Utilization of Matrix Effect for Enhancing Resolution in Cation Exchange Chromatography

Molecules (Basel, Switzerland), 2024-07, Vol.29 (15), p.3637

2024

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Az ionkromatográfia alkalmazhatóságának lehetőségei a gyógyszeranalitikában

Scientia et securitas, 2023-04, Vol.3 (3), p.227-233

2023

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Improved sample introduction approach in hydrophilic interaction liquid chromatography to avoid breakthrough of proteins

Journal of Chromatography A, 2024-01, Vol.1713, p.464498, Article 464498

2024

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Revisiting column selectivity choices in ultra-high performance liquid chromatography–Using multidimensional analytical Design Spaces to identify column equivalency

Journal of Chromatography A, 2024-03, Vol.1719, p.464738, Article 464738

2024

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Retention Modeling in an Extended Knowledge Space

Chromatographia, 2018-04, Vol.81 (4), p.585-594

2018

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Development of a Fast and Robust UHPLC Method for Apixaban In-Process Control Analysis

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3505

2021

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Linear solvent strength model on porous graphitic carbon stationary phase using high temperature liquid chromatographic method for allopurinol related substances analysis

Journal of pharmaceutical and biomedical analysis, 2024-08, Vol.245, p.116200-116200, Article 116200

2024

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Updating the European Pharmacopoeia impurity profiling method for cetirizine and suggesting alternative column, using design space comparison

Journal of pharmaceutical and biomedical analysis, 2024-01, Vol.237, p.115776-115776, Article 115776

2024

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Tuning selectivity in cation-exchange chromatography applied for monoclonal antibody separations, part 1: Alternative mobile phases and fine tuning of the separation

Journal of pharmaceutical and biomedical analysis, 2019-05, Vol.168, p.138-147

2019

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Theoretical Analysis of Efficiency of Multi-Layer Core-Shell Stationary Phases in the High Performance Liquid Chromatography of Large Biomolecules

Molecules (Basel, Switzerland), 2019-08, Vol.24 (15), p.2849

2019

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Updating the European Pharmacopoeia impurity profiling method for terazosin and suggesting alternative columns

Journal of pharmaceutical and biomedical analysis, 2020-08, Vol.187, p.113371-113371, Article 113371

2020

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A workflow for column interchangeability in liquid chromatography using modeling software and quality-by-design principles

Journal of pharmaceutical and biomedical analysis, 2017-11, Vol.146, p.220-225

2017

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Development of Analytical Methods for the Determination of N-Bromosuccinimide in Different Active Pharmaceutical Ingredients by High-Performance Ion Chromatography with Suppressed Conductivity Detection

Separations, 2023-01, Vol.10 (1), p.15

2023

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Renewal of an old European Pharmacopoeia method for Terazosin using modeling with mass spectrometric peak tracking

Journal of pharmaceutical and biomedical analysis, 2017-02, Vol.135, p.8-15

2017

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Determination of Genotoxic Azide Impurity in Cilostazol API by Ion Chromatography with Matrix Elimination

Separations, 2021-10, Vol.8 (10), p.162

2021

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Simultaneous optimization of mobile phase composition and pH using retention modeling and experimental design

Journal of pharmaceutical and biomedical analysis, 2018-10, Vol.160, p.336-343

2018

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Reliability of simulated robustness testing in fast liquid chromatography, using state-of-the-art column technology, instrumentation and modelling software

Journal of pharmaceutical and biomedical analysis, 2014-02, Vol.89, p.67-75

2014

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Hydrazine determination in allopurinol using derivatization and SPE for sample preparation

Journal of pharmaceutical and biomedical analysis, 2018-04, Vol.152, p.25-30

2018

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Establishing column batch repeatability according to Quality by Design (QbD) principles using modeling software

Journal of pharmaceutical and biomedical analysis, 2015-04, Vol.108, p.1-10

2015

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Exploring better column selectivity choices in ultra-high performance liquid chromatography using Quality by Design principles

Journal of pharmaceutical and biomedical analysis, 2013-06, Vol.80, p.79-88

2013

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Reliability of computer-assisted method transfer between several column dimensions packed with 1.3–5μm core–shell particles and between various instruments

Journal of pharmaceutical and biomedical analysis, 2014-06, Vol.94, p.188-195

2014

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A validated UHPLC-MS method for tryptophan metabolites: Application in the diagnosis of multiple sclerosis

Robust UHPLC Separation Method Development for Multi-API Product Containing Amlodipine and Bisoprolol: The Impact of Column Selection

A novel tool for structure assignment of hydroxylated metabolites of (arylpiperazinylbutyl)oxindole derivatives based on relative HPLC retention times

Total Synthesis of Bacterial 5-(3-Indolyl)oxazole Alkaloids: Pimprinols A–C

Utilization of Matrix Effect for Enhancing Resolution in Cation Exchange Chromatography

Az ionkromatográfia alkalmazhatóságának lehetőségei a gyógyszeranalitikában

Improved sample introduction approach in hydrophilic interaction liquid chromatography to avoid breakthrough of proteins

Revisiting column selectivity choices in ultra-high performance liquid chromatography–Using multidimensional analytical Design Spaces to identify column equivalency

Retention Modeling in an Extended Knowledge Space

Development of a Fast and Robust UHPLC Method for Apixaban In-Process Control Analysis

Linear solvent strength model on porous graphitic carbon stationary phase using high temperature liquid chromatographic method for allopurinol related substances analysis

Updating the European Pharmacopoeia impurity profiling method for cetirizine and suggesting alternative column, using design space comparison

Tuning selectivity in cation-exchange chromatography applied for monoclonal antibody separations, part 1: Alternative mobile phases and fine tuning of the separation

Theoretical Analysis of Efficiency of Multi-Layer Core-Shell Stationary Phases in the High Performance Liquid Chromatography of Large Biomolecules

Updating the European Pharmacopoeia impurity profiling method for terazosin and suggesting alternative columns

A workflow for column interchangeability in liquid chromatography using modeling software and quality-by-design principles

Development of Analytical Methods for the Determination of N-Bromosuccinimide in Different Active Pharmaceutical Ingredients by High-Performance Ion Chromatography with Suppressed Conductivity Detection

Renewal of an old European Pharmacopoeia method for Terazosin using modeling with mass spectrometric peak tracking

Determination of Genotoxic Azide Impurity in Cilostazol API by Ion Chromatography with Matrix Elimination

Simultaneous optimization of mobile phase composition and pH using retention modeling and experimental design

Reliability of simulated robustness testing in fast liquid chromatography, using state-of-the-art column technology, instrumentation and modelling software

Hydrazine determination in allopurinol using derivatization and SPE for sample preparation

Establishing column batch repeatability according to Quality by Design (QbD) principles using modeling software

Exploring better column selectivity choices in ultra-high performance liquid chromatography using Quality by Design principles

Reliability of computer-assisted method transfer between several column dimensions packed with 1.3–5μm core–shell particles and between various instruments

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