Pharmaceutical Analysis

Separation Science in collaboration with Agilent

Recent Posts

Separation of Amphetamine Enantiomers by SFC

Agilent Technologies has produced an application note demonstrating the separation of enantiomers of amphetamines and their positional isomers on chiral phase columns using SFC with mass spectrometry.

Extractables and Leachables Analysis Using an Accurate Mass GC/Q-TOF

Agilent Technologies has produced an application note presenting a novel tool to study E&L compounds using a high-resolution accurate mass GC/Q-TOF equipped with a low-energy EI capable ion source.

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High-Resolution Sampling 2D-LC for Pharmaceutical Impurity Analysis

Agilent Technologies has produced an application note demonstrating the use of high-resolution (HiRes) sampling 2D-LC for the separation and detection of impurities, exemplified for different isomers of chlorodifluorobenzoic acid at relative...

Chiral Multicolumn Method Development on the Agilent 1260 Infinity II Analytical SFC System

Agilent Technologies has produced an application note demonstrating the use of the Agilent ChemStation Method Scouting Wizard for the development of a chiral separation method on the Agilent 1260 Infinity II Analytical SFC system. The SFC system was...

Extractables and Leachables from Single Use Bioprocess Systems

Extractables and leachables (E&Ls) are small molecules present in a polymer system including antioxidants, surfactants, slip agents, plasticizers, acid scavengers, cross linking agents, residual monomers and oligomers, polymerization side products...

Discover Single-Digit ppm Host Cell Proteins in Purified Antibody Samples

Recombinant biopharmaceutical proteins are expressed in host cell systems that contain numerous host cell proteins (HCPs). Even after a series of purifications, low levels of HCPs can remain in the purified biotherapeutics, which could reduce drug...

Peptide Mapping- A Comprehensive Workflow Solution from Sample to Answer

Peptide mapping is vital to understanding the structure of proteins and monitoring critical quality attributes. To create effective, high-quality biotherapeutics, you have to get this right. Renowned for accuracy and reliability, Agilent offers a...

2D-LC Solutions for the Analysis of Biopharmaceuticals

The presentation summarizes the latest updates for the analysis of biopharmaceuticals using the Agilent 1290 Infinity II 2D-LC Solution. After a short introduction to the principle mode of operation, I will explain the latest 2D-LC modes; multiple...

Analysis of mAb N-glycans by HILIC

Routine analysis of therapeutic protein N-glycosylation has become important in biopharma discovery, development and QC labs. This presentation will briefly review recent advances in automated sample preparation and ultra-high performance HILIC...

Developing Workflow Solutions for Charge Variants and Aggregation Quantification

Biotherapeutics – recombinant proteins, such as monoclonal antibodies – are highly complex molecules produced by fermentation. Unlike small molecule drugs they can contain numerous sites of heterogeneity as well as other impurities (which can arise...

Trends and Applications in the Analysis of Biotherapeutics

Want to know more about new methods for biotherapeutics analysis? Looking to streamline your bioprocess workflows? Need help with your data quality? If so, then this on-demand event is for you...

Proof of Equivalency for the Analysis of Beta-Blockers

Agilent Technologies has produced an application note that shows the seamless transfer of a method for the analysis of beta-blockers from an Agilent 1260 Infinity LC to an Agilent 1260 Infinity II LC. It proves that equivalent results in terms of...

Proof of Equivalency for the Analysis of Local Anesthetics

Agilent Technologies has produced an application note proving equivalency of the Agilent 1200 Series Binary LC and the Agilent 1260 Infinity II LC for the analysis of local anesthetics.

Method Equivalency for The Analysis of Paracetamol

Agilent Technologies has produced an application note describing a method to achieve seamless method transfer for the analysis of paracetamol and its impurities and signficantly decrease analysis time.

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