Literature DB >> 19560301

Characterization of new types of stationary phases for fast liquid chromatographic applications.

Szabolcs Fekete1, Jeno Fekete, Katalin Ganzler.   

Abstract

The performance of a narrow bore silica based monolith column (5 cm x 2 mm) was compared to 5 cm long narrow bore (internal diameter < or = 2.1 mm) columns, packed with shell particles (2.7 microm) and totally porous sub-2 microm particles (1.5 microm, 1.7 microm and 1.9 microm) in gradient and isocratic elution separations of steroids. The highest peak capacity could be achieved with the column packed with 1.5 microm totally porous particles. The columns packed with porous 1.7 microm and shell 2.7 microm particles showed very similar capacity. The monolith column provided the lowest capacity during gradient elution. The plate height (HETP) of the 2.7 microm Ascentis Express column was very similar to the HETP obtained with 1.5 microm and 1.7 microm totally porous particles. The Chromolith monolithic column displayed an efficiency that is comparable to that of columns packed with spherical particles having their diameter between 3 microm and 4 microm. A kinetic plot analysis is presented to compare the theoretical analysis speed of different separation media. At 200 bar, the monolith column provided the highest performance when the required plate number was higher than 5000 (N>5000), however the efficiency drifted off faster in the range of N<5000 than in the case of packed columns. If the possibility of maximum performance was utilized (1000 bar for sub-2 microm particles, 600 bar for shell particles and 200 bar for monolith column) the monolith column would provide the poorest efficiency, while the column, packed with 1.5 microm particles offered the shortest impedance time.

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Year:  2009        PMID: 19560301     DOI: 10.1016/j.jpba.2009.05.039

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  8 in total

1.  Optimization of data-dependent acquisition parameters for coupling high-speed separations with LC-MS/MS for protein identifications.

Authors:  Darryl Johnson; Barry Boyes; Taylor Fields; Rachel Kopkin; Ron Orlando
Journal:  J Biomol Tech       Date:  2013-07

2.  Optimized superficially porous particles for protein separations.

Authors:  Stephanie A Schuster; Brian M Wagner; Barry E Boyes; Joseph J Kirkland
Journal:  J Chromatogr A       Date:  2013-09-19       Impact factor: 4.759

3.  Performance characteristics of new superficially porous particles.

Authors:  Joseph J Destefano; Stephanie A Schuster; Jason M Lawhorn; Joseph J Kirkland
Journal:  J Chromatogr A       Date:  2012-08-17       Impact factor: 4.759

4.  Are sub-2 μm particles best for separating small molecules? An alternative.

Authors:  Joseph J DeStefano; Barry E Boyes; Stephanie A Schuster; William L Miles; Joseph J Kirkland
Journal:  J Chromatogr A       Date:  2014-10-06       Impact factor: 4.759

5.  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

6.  The use of ammonium formate as a mobile-phase modifier for LC-MS/MS analysis of tryptic digests.

Authors:  Darryl Johnson; Barry Boyes; Ron Orlando
Journal:  J Biomol Tech       Date:  2013-12

7.  Strategies for Developing Sensitive and Automated LC-MS/MS Assays of a Pharmaceutical Compound and Its Metabolite from Whole Blood Matrix.

Authors:  Raymond N Xu; Jill Polzin; Michelle Kranz; Phillip Vaca; Maria Metchkarova; Matthew J Rieser; Tawakol A El-Shourbagy
Journal:  Pharmaceutics       Date:  2010-04-30       Impact factor: 6.321

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

Authors:  Szabolcs Horváth; Fabrice Gritti; Róbert Kormány; Krisztián Horváth
Journal:  Molecules       Date:  2019-08-06       Impact factor: 4.411

  8 in total

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