IMTAKT NON-POROUS ODS COLUMN Presto FF-C18

World’s First High-Resolution 2 μm Non-Porous ODS Column

IMTAKT NON-POROUS ODS COLUMN Presto FF-C18

FEATURES

Reversed-phase separation of biomolecules and synthetic polymers up to several tens of millions Da

Exceptional separation performance for peptides and proteins

Ultra-high theoretical plate column with 2 μm particle size and 250 mm length

Separation characteristics different from porous ODS columns

Shows high separation performance at low flow rates even with standard HPLC

Demonstrates outstanding performance in reversed-phase separation of proteins such as antibodies

Demonstrates outstanding performance in reversed-phase separation of proteins such as antibodies

Using the non-porous ODS column Presto FF-C18, many peaks previously unseen with traditional wide-pore reversed-phase columns are detected for proteins and monoclonal antibodies (mAb). Peaks that appeared broad with conventional columns are actually multiple components. This is likely due to Presto FF-C18 recognizing conformational differences related to S-S bond positions in protein folding, rather than denaturation. Variations in amino acid sequences, impurities, or glycosylation may also contribute, highlighting the column's ability to detect higher-order protein structures.
The detection of many peaks previously unseen with traditional columns using Presto FF-C18 is expected to advance structural analysis for antibody drugs and other protein therapeutics.

The non-porous ODS column Presto FF-C18 excels in reversed-phase separation not only for proteins but also for biomolecules such as polysaccharides and DNA. It is also applicable to synthetic polymers. Sharp, quantifiable peaks that were difficult to achieve with traditional SEC mode can be obtained. The use of detectors suitable for high polymers, such as ELSD, is expected to introduce a new reversed-phase separation method for polymer analysis.

Low Carryover

Presto FF-C18 exhibits excellent low carryover performance in pharmaceutical LC-MS analysis. This is likely due to its nonporous silica, which avoids non-specific adsorption occurring inside pores.

Reference:
Universal LC-MS Method for Minimized Carryover in a Discovery Bioanalytical Setting
John S. Williams, Stephanie H. Donahue, Hong Gao, Christopher L. Brummel
Bioanalysis (2012) 4(9), 1025-1037
https://www.researchgate.net/publication/225051947_Universal_LC-MS_method_for_minimized_carryover_in_a_discovery_bioanalytical_setting

Key Application

Technical Information

Applications NEW

Peptides and Proteins

Others

User Reports

User Articles

Growth phase diets diminish histone acetyltransferase Gcn5 function and shorten lifespan of Drosophila males


Development of a HPLC system using a phase-separation multiphase flow as an eluent: an influence of column pressure on phase separation and chromatogram at room temperature


Tocilizumab degradation via photo-catalytic ozonation process from aqueous


Extremely Simple and Rapid HPLC Analysis of Tocilizumab in Human Serum with Selective Precipitation Using Alkylamine


>Combining offline high performance liquid chromatography fractionation of peptides and intact proteins to enhance proteome coverage in bottom-up proteomics.


Comparing Offline Hplc Fractionation of Peptides Versus Intact Proteins to Enhance Detection of Low Abundance Proteins in Liquid Chromatography-Tandem Mass Spectrometry


Analysis of the interaction of cyclosporine congeners with cell membrane models


Recycling gradient-elution liquid chromatography for the analysis of chemical-composition distributions of polymers


Peptide nucleic acid-dependent artifact can lead to false-positive triplex gene editing signals


The elution behavior of cyclosporine congeners in a developed HPLC system reflects the lipophilicity


Simple and rapid analysis of tocilizumab using HPLC-fluorescence detection method


RNAi of the sesquiterpene cyclase gene for phytoalexin production impairs pre- and post-invasive resistance to potato blight pathogens


Rapid Analysis of Cyclic Peptide Cyclosporine A by HPLC Using a Column Packed with Nonporous Particles


Glycosyltransferase MDR1 assembles a dividing ring for mitochondrial proliferation comprising polyglucan nanofilaments


An Efficient and Rapid Method to Monitor the Oxidative Degradation of Protein Pharmaceuticals: Probing Tyrosine Oxidation with Fluorogenic Derivatization


Photo-oxidation of IgG1 and Model Peptides: Detection and Analysis of Triply Oxidized His and Trp Side Chain Cleavage Products


Critical conditions of polymer adsorption and chromatography on non-porous substrates


Development of a quantitative method for active epidermal growth factor extracted from dissolving microneedle by solid phase extraction and liquid chromatography electrospray ionization mass spectrometry


High throughput sequencing of cyclic peptide immobilized on a gel-type single bead


発蛍光標識化タンパク質の網羅定量解析法の開発と応用


A trial proteomics fingerprint analysis of HepaRG cells by FD-LC-MS/MS


Do Not Drop: Mechanical Shock in Vials Causes Cavitation, Protein Aggregation, and Particle Formation


Structure-based comprehensive identification of erythropoiesis-stimulating agents and their biosimilars


Improved separation of fluorogenic derivatized intact proteins with high resolution and efficiency using a reversed-phase liquid chromatographic system


Comprehensive and temporal analysis of secreted proteins in the medium from IL-6 exposed human hepatocyte


Efficient chromatographic separation of intact proteins derivatized with a fluorogenic reagent for proteomics analysis


High-performance liquid chromatography separation of monoclonal IgG2 isoforms on a column packed with nonporous particles


Fluorogenic Tagging Methodology Applied to Characterize Oxidized Tyrosine and Phenylalanine in an Immunoglobulin Monoclonal Antibody


Universal LC-MS method for minimized carryover in a discovery bioanalytical setting


Development of iodoacetic acid-based cysteine mass tags: detection enhancement for cysteine-containing peptide by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry


Alteration of intracellular secretory acute phase response proteins expressed in human hepatocyte induced by exposure with interleukin-6


Liquid chromatographic separation of proteins derivatized with a fluorogenic reagent at cysteinyl residues on a non-porous column for differential proteomics analysis


Peak parking-moment analysis: A strategy for the measurement of molecular diffusivity in liquid phase

Related Info