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

[1]  I. Molnár,et al.  Automated UHPLC separation of 10 pharmaceutical compounds using software‐modeling , 2018, Journal of pharmaceutical and biomedical analysis.

[2]  Róbert Kormány,et al.  Retention Modeling in an Extended Knowledge Space , 2018, Chromatographia.

[3]  Maria Kristina Parr,et al.  Life cycle management of analytical methods , 2018, Journal of pharmaceutical and biomedical analysis.

[4]  D. Guillarme,et al.  A workflow for column interchangeability in liquid chromatography using modeling software and quality‐by‐design principles , 2017, Journal of pharmaceutical and biomedical analysis.

[5]  D. Guillarme,et al.  Analysis of recombinant monoclonal antibodies in hydrophilic interaction chromatography: A generic method development approach , 2017, Journal of pharmaceutical and biomedical analysis.

[6]  J. Veuthey,et al.  Achievable separation performance and analysis time in current liquid chromatographic practice for monoclonal antibody separations , 2017, Journal of pharmaceutical and biomedical analysis.

[7]  Róbert Kormány,et al.  Renewal of an old European Pharmacopoeia method for Terazosin using modeling with mass spectrometric peak tracking , 2017, Journal of pharmaceutical and biomedical analysis.

[8]  Serge Rudaz,et al.  Optimization of non-linear gradient in hydrophobic interaction chromatography for the analytical characterization of antibody-drug conjugates. , 2017, Journal of chromatography. A.

[9]  Yimin Hua,et al.  A platform analytical quality by design (AQbD) approach for multiple UHPLC-UV and UHPLC-MS methods development for protein analysis. , 2016, Journal of pharmaceutical and biomedical analysis.

[10]  medicines.org.uk katrinaann.dedace Atorvastatin calcium trihydrate , 2015 .

[11]  J. Fekete,et al.  Establishing column batch repeatability according to Quality by Design (QbD) principles using modeling software. , 2015, Journal of pharmaceutical and biomedical analysis.

[12]  Davy Guillarme,et al.  Reliability of simulated robustness testing in fast liquid chromatography, using state-of-the-art column technology, instrumentation and modelling software. , 2014, Journal of pharmaceutical and biomedical analysis.

[13]  D. Guillarme,et al.  Robust UHPLC Separation Method Development for Multi-API Product Containing Amlodipine and Bisoprolol: The Impact of Column Selection , 2014, Chromatographia.

[14]  Róbert Kormány,et al.  Exploring better column selectivity choices in ultra-high performance liquid chromatography using quality by design principles. , 2013, Journal of pharmaceutical and biomedical analysis.

[15]  I. Molnár,et al.  Using an innovative Quality-by-Design approach for development of a stability indicating UHPLC method for ebastine in the API and pharmaceutical formulations. , 2013, Journal of pharmaceutical and biomedical analysis.

[16]  I. Molnár,et al.  Quality by Design: Multidimensional exploration of the design space in high performance liquid chromatography method development for better robustness before validation. , 2012, Journal of chromatography. A.

[17]  E. Elkady,et al.  Liquid chromatographic determination of sitagliptin either alone or in ternary mixture with metformin and sitagliptin degradation product. , 2011, Talanta.

[18]  I. Molnár,et al.  Aspects of the "Design Space" in high pressure liquid chromatography method development. , 2010, Journal of chromatography. A.

[19]  L. Snyder,et al.  Two-dimensional optimization using different pairs of variables for the reversed-phase high-performance liquid chromatographic separation of a mixture of acidic compounds. , 2002, Journal of chromatography. A.

[20]  H. Reinhard,et al.  Reversed-phase liquid chromatographic behavior of the mycotoxins citrinin and ochratoxin A. , 1999, Journal of chromatography. A.

[21]  L. Snyder,et al.  Computer simulation for the prediction of separation as a function of pH for reversed-phase high-performance liquid chromatography. I. Accuracy of a theory-based model. , 1992, Journal of chromatography.

[22]  L. Snyder,et al.  High-performance liquid chromatographic computer simulation based on a restricted multi-parameter approach : I. Theory and verification , 1990 .

[23]  J. Dolan,et al.  DryLab computer simulation for high-performance liquid chromatographic method development. II. Gradient elution. , 1989, Journal of chromatography.

[24]  James M. Minor,et al.  Optimization of solvent strength and selectivity for reversed-phase liquid chromatography using an interactive mixture-design statistical technique , 1980 .

[25]  D. Guillarme,et al.  Method development for the separation of monoclonal antibody charge variants in cation exchange chromatography, Part II: pH gradient approach. , 2015, Journal of pharmaceutical and biomedical analysis.

[26]  Gesa Schada,et al.  3-Dimensional Retention Modelling of Gradient Time , Ternary Solvent-Strength and Temperature of the Reversed-phase Gradient Liquid Chromatography of a Complex Mixture of 22 Basic and Neutral Analytes using DryLab ® 2010 , 2010 .