Publications by authors named "S Omarsdottir"

Glycan profile comparisons are one of the most tedious analytical exercises for establishing compliance with recombinant therapeutic protein batches. Based on its intensive research, the FDA has confirmed that lectin array binding with fluorescent monitoring is the fastest and most reliable method for profile comparisons. Using a database of over 150 biological products expressed in nine diverse mammalian cell systems, the FDA immobilized 74 lectins to study their binding using fluorescently labeled glycoproteins.

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Article Synopsis
  • The development of biosimilars like AVT02, a version of Humira, involves extensive comparisons to the original product, ensuring no significant clinical differences exist regarding structure and function.
  • AVT02 showed high structural similarity to Humira through various scientific methods, with minimal differences that didn’t affect its biological activity or safety.
  • Clinical studies confirmed that AVT02 matched Humira in pharmacokinetics and safety profiles, supporting its approval for all global indications where Humira is used.
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For over a century, researchers have cultured microorganisms together on solid support─typically agar─in order to observe growth inhibition via antibiotic production. These simple bioassays have been critical to both academic researchers that study antibiotic production in microorganisms and to the pharmaceutical industry's global effort to discover drugs. Despite the utility of agar assays to researchers around the globe, several limitations have prevented their widespread adoption in advanced high-throughput compound discovery and dereplication campaigns.

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Geobarrettin D (), a new bromoindole alkaloid, was isolated from the marine sponge collected from Icelandic waters. Its structure was elucidated by 1D, and 2D NMR (including H-N HSQC, H-N HMBC spectra), as well as HRESIMS data. Geobarrettin D () is a new 6-bromoindole featuring an unusual purinium herbipoline moiety.

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Usnic acid is an antibiotic metabolite produced by a wide variety of lichenized fungal lineages. The enantiomers of usnic acid have been shown to display contrasting bioactivities, and hence it is important to determine their spatial distribution, amounts and enantiomeric ratios in lichens to understand their roles in nature and grasp their pharmaceutical potential. The overall aim of the study was to characterise the spatial distribution of the predominant usnic acid enantiomer in lichens by combining spatial imaging and chiral chromatography.

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