Literature DB >> 24094750

Optimized superficially porous particles for protein separations.

Stephanie A Schuster1, Brian M Wagner, Barry E Boyes, Joseph J Kirkland.   

Abstract

Continuing interest in larger therapeutic molecules by pharmaceutical and biotech companies provides the need for improved tools for examining these molecules both during the discovery phase and later during quality control. To meet this need, larger pore superficially porous particles with appropriate surface properties (Fused-Core(®) particles) have been developed with a pore size of 400 Å, allowing large molecules (<500 kDa) unrestricted access to the bonded phase. In addition, a particle size (3.4 μm) is employed that allows high-efficiency, low-pressure separations suitable for potentially pressure-sensitive proteins. A study of the shell thickness of the new fused-core particles suggests a compromise between a short diffusion path and high efficiency versus adequate retention and mass load tolerance. In addition, superior performance for the reversed-phase separation of proteins requires that specific design properties for the bonded-phase should be incorporated. As a result, columns of the new particles with unique bonded phases show excellent stability and high compatibility with mass spectrometry-suitable mobile phases. This report includes fast separations of intact protein mixtures, as well as examples of very high-resolution separations of larger monoclonal antibody materials and associated variants. Investigations of protein recovery, sample loading and dynamic range for analysis are shown. The advantages of these new 400 Å fused-core particles, specifically designed for protein analysis, over traditional particles for protein separations are demonstrated.
Copyright © 2013 Elsevier B.V. All rights reserved.

Keywords:  Core–shell particles; Fused-core particles; Monoclonal antibodies; Pore size; Protein separations; Superficially porous particles

Mesh:

Substances:

Year:  2013        PMID: 24094750      PMCID: PMC8214819          DOI: 10.1016/j.chroma.2013.09.054

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  16 in total

1.  Evaluation of a new wide pore core-shell material (Aeris WIDEPORE) and comparison with other existing stationary phases for the analysis of intact proteins.

Authors:  Szabolcs Fekete; Róbert Berky; Jenő Fekete; Jean-Luc Veuthey; Davy Guillarme
Journal:  J Chromatogr A       Date:  2012-03-10       Impact factor: 4.759

2.  Gradient elution separation and peak capacity of columns packed with porous shell particles.

Authors:  Nicola Marchetti; Alberto Cavazzini; Fabrice Gritti; Georges Guiochon
Journal:  J Chromatogr A       Date:  2007-06-28       Impact factor: 4.759

3.  Characteristics of superficially-porous silica particles for fast HPLC: some performance comparisons with sub-2-microm particles.

Authors:  J J Destefano; T J Langlois; J J Kirkland
Journal:  J Chromatogr Sci       Date:  2008-03       Impact factor: 1.618

4.  A universal algorithm for fast and automated charge state deconvolution of electrospray mass-to-charge ratio spectra.

Authors:  Z Zhang; A G Marshall
Journal:  J Am Soc Mass Spectrom       Date:  1998-03       Impact factor: 3.109

Review 5.  Shell particles, trials, tribulations and triumphs.

Authors:  Georges Guiochon; Fabrice Gritti
Journal:  J Chromatogr A       Date:  2011-02-23       Impact factor: 4.759

6.  The effect of pressure and mobile phase velocity on the retention properties of small analytes and large biomolecules in ultra-high pressure liquid chromatography.

Authors:  Szabolcs Fekete; Jean-Luc Veuthey; David V McCalley; Davy Guillarme
Journal:  J Chromatogr A       Date:  2012-11-03       Impact factor: 4.759

7.  Fast high performance liquid chromatography separations for proteomic applications using Fused-Core® silica particles.

Authors:  Stephanie A Schuster; Barry E Boyes; Brian M Wagner; Joseph J Kirkland
Journal:  J Chromatogr A       Date:  2011-07-30       Impact factor: 4.759

8.  Superficially porous silica particles with wide pores for biomacromolecular separations.

Authors:  Brian M Wagner; Stephanie A Schuster; Barry E Boyes; Joseph J Kirkland
Journal:  J Chromatogr A       Date:  2012-09-25       Impact factor: 4.759

9.  Rapid, high-resolution HPLC separation of peptides using small particles at elevated temperatures.

Authors:  B E Boyes; J J Kirkland
Journal:  Pept Res       Date:  1993 Sep-Oct

10.  Comparison of fused-core and conventional particle size columns by LC-MS/MS and UV: application to pharmacokinetic study.

Authors:  Wei Song; Deepthi Pabbisetty; Elizabeth A Groeber; Rick C Steenwyk; Douglas M Fast
Journal:  J Pharm Biomed Anal       Date:  2009-05-22       Impact factor: 3.935

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  6 in total

1.  Superficially porous particles with 1000Å pores for large biomolecule high performance liquid chromatography and polymer size exclusion chromatography.

Authors:  Brian M Wagner; Stephanie A Schuster; Barry E Boyes; Taylor J Shields; William L Miles; Mark J Haynes; Robert E Moran; Joseph J Kirkland; Mark R Schure
Journal:  J Chromatogr A       Date:  2017-01-31       Impact factor: 4.759

2.  Size exclusion chromatography with superficially porous particles.

Authors:  Mark R Schure; Robert E Moran
Journal:  J Chromatogr A       Date:  2016-12-09       Impact factor: 4.759

3.  Continuous Elution Proteoform Identification of Myelin Basic Protein by Superficially Porous Reversed-Phase Liquid Chromatography and Fourier Transform Mass Spectrometry.

Authors:  Daniel A Plymire; Casey E Wing; Dana E Robinson; Steven M Patrie
Journal:  Anal Chem       Date:  2017-10-31       Impact factor: 6.986

4.  Reversed-phase chromatography with large pore superficially porous particles for high throughput immunoglobulin G2 disulfide isoform separation.

Authors:  Bingchuan Wei; Bing Zhang; Barry Boyes; Yonghua Taylor Zhang
Journal:  J Chromatogr A       Date:  2017-10-18       Impact factor: 4.601

Review 5.  Different Stationary Phase Selectivities and Morphologies for Intact Protein Separations.

Authors:  A Astefanei; I Dapic; M Camenzuli
Journal:  Chromatographia       Date:  2016-09-23       Impact factor: 2.044

6.  A simple microfluidic chip design for fundamental bioseparation.

Authors:  Alan S Chan; Michael K Danquah; Dominic Agyei; Patrick G Hartley; Yonggang Zhu
Journal:  J Anal Methods Chem       Date:  2014-01-08       Impact factor: 2.193

  6 in total

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