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Current Trends in the Analysis of Biologics,
Biosimilars & Biobetters
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08
What’s Happening
Webinar
Development and production of biopharmaceuticals is a growing segment of pharmaceutical industry. A thorough
characterization of therapeutic biomolecules is A key for the successful submission of research and production
data for regulatory approval of new drugs. The introduction of the first so-called biosimilars has further in-
creased the demand for highly efficient analytical methods. Tosoh Bioscience will host a webinar on this topic on
November 12, 2015.
Over the last decade, ultrahigh-performance liquid chromatography
(UHPLC) has made its way into routine labs for the analysis of small
molecules and active pharmaceutical ingredients (APIs). It has trigge-
red a leap in efficiency and throughput of LC and LC-MS methods and
there is an increased interest in applying UHPLC also to biopharma-
ceutical analysis.
The analysis of the aggregate content and charge heterogeneity are ty-
pical applications applied to characterize therapeutic proteins, such as
monoclonals. Smaller peptides or the oligosaccharides of the glycan
structure of a protein are typically analysed after enzymatic cleavage.
Recently, the analysis of antibody drug conjugates (ADCs), bispecific
antibodies, and therapeutic oligonucleotides by chromatographic me-
thods gained attention to characterise these new drug formats.
The webinar will summarize current trends in UHPLC applications
for biomolecules. Case studies will illustrate the potential of using
UHPLC for applications, which are frequently used in development
and production of biologics, biosimilars, and biobetters. New bio-
column developments supporting these techniques will be presented.
Hyphenation of these LC Methods with sophisticated techniques such
as mass spectrometric, light scattering, or Raman detection will also
be covered.
Register for the webinar at
