PEGylation of therapeutic proteins
Autor: | Simona Jevsevar, Menci Kunstelj, Vladka Gaberc Porekar |
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Rok vydání: | 2010 |
Předmět: |
Drug
Drug Carriers Chemistry Drug Compounding media_common.quotation_subject Proteins 02 engineering and technology General Medicine Computational biology Pharmacology 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences Applied Microbiology and Biotechnology Polyethylene Glycols 3. Good health 0104 chemical sciences Food and drug administration Coated Materials Biocompatible Molecular size PEG ratio PEGylation Molecular Medicine 0210 nano-technology media_common |
Zdroj: | Biotechnology Journal. 5:113-128 |
ISSN: | 1860-7314 1860-6768 |
DOI: | 10.1002/biot.200900218 |
Popis: | Since the first PEGylated product was approved by the Food and Drug Administration in 1990, PEGylation has been widely used as a post-production modification methodology for improving biomedical efficacy and physicochemical properties of therapeutic proteins. Applicability and safety of this technology have been proven by use of various PEGylated pharmaceuticals for many years. It is expected that PEGylation, as the most established technology for extension of drug residence in the body, will play an important role in the next generation therapeutics, such as peptides, protein nanobodies and scaffolds, which due to their diminished molecular size need half-life extension. This review focuses on several factors important in the production of PEGylated biopharmaceuticals enabling efficient preparation of highly purified PEG-protein conjugates that have to meet stringent regulatory criteria for their use in human therapy. Areas addressed are PEG properties, the specificity of PEGylation reactions, separation and large-scale purification, the availability and analysis of PEG reagents, analysis of PEG-protein conjugates, the consistency of products and processes and approaches used for rapid screening of pharmacokinetic properties of PEG-protein conjugates. |
Databáze: | OpenAIRE |
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