Pharmaceutical Analysis

Trace element analysis of pharmaceutical products

This useful compendium from Thermo Fisher provides detailed methods for the analysis of trace elements in pharmaceutical products using AAS, ICP-OES and ICP-MS covered by the NEW USP chapters 232 and 233.

Essential applications for (U)HPLC analysis of biomolecules

Tosoh Bioscience has produced Volume 1 of its 'Biopharmaceutical Application Notebook' for the (U)HPLC analysis of biomolecules. This essential application notebook will keep you informed of all the latest developments in the biopharmaceutical...

Enabling single-software multiple attribute methodology for assessment of biopharmaceutical product quality attributes

This technical note from SCIEX will highlight how to implement a complete and easy-to-use Multiple Attribute Methodology (MAM) workflow for biotherapeutic PQA monitoring using accurate mass LC–MS. It will demonstrate how this new streamlined MAM...

Doubling chromatographic throughput using dual LC for pharmaceutical analysis

Thermo Fisher Scientific has produced an application note describing a novel Dual LC workflow, which provides a unique concept by using two separated flow paths in one system. It shows how the Thermo Scientific Vanquish Duo system for Dual LC...

How to analyse small pharmaceuticals and peptide mixtures using chemically stable merged inorganic/organic silica material

Kromasil has produced an application note demonstrating how, by using merged inorganic/organic silica materials with newly developed C8, C18 or phenyl hexyl phases, it is possible to use a stationary phase with a wider pH range. 

Monitoring Antibody Oxidation at The Subunit Level

SCIEX has produced an application note demonstrating how to monitor biotherapeutic oxidation levels in a simple and automated way using the X500B QTOF system and powerful BioPharmaView™ Software.

Routine Workflow for Comparability Assessment of Protein Biopharmaceuticals using High-resolution LC-MS

SCIEX has produced an application note demonstrating using a reproducible and robust method for analysing intact biotherapeutic proteins on the X500B QTOF System with automated batch processing using BioPharmaView™ software.

Comparative Peptide Mapping Between Two Manufacturers of Trastuzumab 

SCIEX has produced an application note describing a simple and rapid methodology to characterize and quantify differences between biotherapeutic batches, using high-resolution peptide mapping by LC-MS.

Biopharmaceutical Application Notebook for (U)HPLC Analysis of Biomolecules

Tosoh Bioscience has produced Volume 1 of its 'Biopharmaceutical Application Notebook' for the (U)HPLC analysis of biomolecules. This essential application notebook will keep you informed of all the latest developments in the biopharmaceutical...

HPAE-PAD - A very useful tool for glycan analysis

Looking for analytical advantage with your glycan and glycosylation analysis? If so, then high-performance anion-exchange chromatography with pulsed amperometric detection may well be worth a look...

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...

Achieve Fast Glycan Labelling and Analysis

SCIEX has produced an application note describing the N-glycosylation profiling of carbohydrates associated with therapeutic antibodies for faster, more cost-effective development of biologics.

Phospholipid Analysis for Four Types of Mouse Tissues using Triple Quadrupole LC-MS/MS with SimLipid

Shimadzu has produced an application note describing phospholipid analysis for four types of mouse tissues performed by precursor ion scan (PIS) or neutral loss scan (NLS) with a triple quadrupole mass spectrometer.

How can light scattering can improve your GPC/SEC

Learn about the advantages and benefits of light scatttering techniques and how they can help your analysis of polymeric excipients.

High-Sensitivity Analysis of Residual Solvents in Drug Products - USP <467> Residual Solvents Procedure A

Shimadzu has produced an application note presenting data obtained from Class 1 and Class 2 standard solutions, in accordance with Water-Soluble Articles, Procedure A, in USP <467> Residual Solvents.

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