http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2016270302-B2

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filingDate 2016-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5bc943b522809214ab7aa02989757e04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_623c8d36f3fc2f6a5c41d2dea0a688c4
publicationDate 2020-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2016270302-B2
titleOfInvention Amine pegylation methods for the preparation of site-specific protein conjugates
abstract Examples include a method of making a protein-PEG conjugate. The method may include providing an aqueous protein solution. The aqueous protein solution may include a protein, a pH buffer, and a chelating agent. The chelating agent may be chosen from the group consisting of an aminopolycarboxylic acid, a hydroxyaminocarboxylic acid, an N-substituted glycine, 2-(2-amino-2-oxocthyl) aminoethane sulfonic acid (BES), and deferoxamine (DEF). The method may also include introducing sodium cyanoborohydride and a methoxy polyethylene glycol aldehyde to the aqueous protein solution. The sodium cyanoborohydride in the methoxy polyethylene glycol aldehyde may have a molar ratio ranging from about 5:1 to about 1.5:1. The method may further include reacting the methoxy polyethylene glycol aldehyde with the protein to form the protein-PEG conjugate. The pH buffer may maintain a pH of the aqueous protein solution ranging from 4.0 to 4.4 during the reaction.
priorityDate 2015-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP01339
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP29971
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP07453
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9DEV3
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ27IM2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP04089

Total number of triples: 318.