PolySciTech (
www.polyscitech.com)
provides a wide variety of block copolymers as well as reactive
intermediates. A variety of new
intermediates are now available from PolySciTech based on the PLGA-PEG diblock
configuration and possessing a variety of reactive endcaps including
iodoacetamide (PolyVivo AI83), bromoacetamide (PolyVivo AI84), and azide
(PolyVivo AI85). Read more about the conjugation chemistry which can be used to
couple these to ligands here: Roberts, M. J., M. D. Bentley, and J. M. Harris.
"Chemistry for peptide and protein PEGylation." Advanced drug
delivery reviews 54, no. 4 (2002): 459-476. Full-Text:
http://www.creativepegworks.com/chemistry_for_peptide_and_protein_pegylation.pdf
“Abstract: Poly(ethylene glycol) (PEG) is a
highly investigated polymer for the covalent modification of biological
macromolecules and surfaces for many pharmaceutical and biotechnical
applications. In the modification of biological macromolecules, peptides and
proteins are of extreme importance. Reasons for PEGylation (i.e. the covalent
attachment of PEG) of peptides and proteins are numerous and include shielding
of antigenic and immunogenic epitopes, shielding receptor-mediated uptake by
the reticuloendothelial system (RES), and preventing recognition and degradation
by proteolytic enzymes. PEG conjugation also increases the apparent size of the
polypeptide, thus reducing the renal filtration and altering biodistribution.
An important aspect of PEGylation is the incorporation of various PEG
functional groups that are used to attach the PEG to the peptide or protein. In
this paper, we review PEG chemistry and methods of preparation with a
particular focus on new (second-generation) PEG derivatives, reversible
conjugation and PEG structures. Keywords PEGylation; PEG-protein; PEG
conjugation; PEG chemistry”

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