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The Column
JULY 20, 2017
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Top Story

The Heightened Role of HILIC in Biopharmaceutical Analysis

Valentina D’Atri from the University of Geneva spoke to The Column about the evolving role of HILIC in biopharmaceutical analysis. read more


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Fast, Reproducible Cannabis Potency Analysis

One of the newest and most exciting fields in analytical testing is medical and retail marijuana. With new legislation passing for the distribution of marijuana and marijuana related products, an urgent need for fast, reliable and economical testing protocols exists. Both the product purity and potency are of major concern from a quality control and patient consumer safety standpoint. Learn more

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Features


Meeting Analytical Demands for Biopharmaceuticals with Mass Spectrometry in Late Development, Manufacturing, and Quality Control

The rapid growth of biologics in development, the increasing demand for more robust analytical technologies to directly monitor the critical quality attributes (CQAs) of these new drugs, and longer term industry initiatives aimed at improving quality and productivity, such as quality by design (QbD) regulatory submissions and continuous manufacturing, are all fueling a greater need for mass monitoring with MS. read more


Improving Biopharmaceutical Purification Using LFMC

Biopharmaceutical purification techniques can be slow and cumbersome with poor scalability. A new device using laterally-fed membrane chromatography (LMFC) was developed to address these issues. Raja Ghosh from McMaster University in Hamilton, Ontario, Canada, spoke to The Column about this new device and its potential applications. read more

Application Notes

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Proof of Equivalency for the Analysis of Local Anesthetics

This application note proves equivalency of the Agilent 1200 Series Binary LC and the Agilent 1260 Infinity II LC for the analysis of local anesthetics. Learn more


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Transfer the USP Method for Ceftizoxime within Chapter 621 Guidelines

A traditional method of USP assay of ceftizoxime using a 5-µm column can be successfully transferred to a superficial porous column. Learn more


More FEATURES

Addressing the Challenges of Drug-to-Antibody Measurement

The chromatographic methods used to determine drug-to-antibody ratio (DAR), including hydrophobic interaction chromatography (HIC), reversed phase, and liquid chromatography–mass spectrometry (LC–MS) are discussed. read more


NEWS

New Vaccine Quality Assessment Assay Developed Using Conformation-Dependent Antibodies Coupled to SE-HPLC

Researchers have developed and validated a stability- and potency-indicating assay protocol for high-throughput quality assessment of vaccines consisting of recombinant virus- "like" particles (VLPs) using conformation-dependent antibodies coupled to size-exclusion high performance liquid chromatography (SE-HPLC). read more


FEATURED PRODUCT

DryLab®4 – method development software

DryLab®4 is the (U) HPLC method development and optimization software that predicts chromatograms under a much wider range of experimental conditions than would ever be possible in the laboratory. / Learn more /

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