Protein–polymer conjugation — moving beyond PEGylation
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In this review, we summarize-from a materials science perspective-the current state of the field of polymer conjugates of peptide and protein drugs, with a focus on polymers that have been developed as alternatives to the current gold standard, poly(ethylene glycol) (PEG). PEGylation, or the covalent conjugation of PEG to biological therapeutics to improve their therapeutic efficacy by increasing their circulation half-lives and stability, has been the gold standard in the pharmaceutical industry for several decades. After years of research and development, the limitations of PEG, specifically its non-degradability and immunogenicity have become increasingly apparent. While PEG is still currently the best polymer available with the longest clinical track record, extensive research is underway to develop alternative materials in an effort to address these limitations of PEG. Many of these alternative materials have shown promise, though most of them are still in an early stage of development and their in vivo distribution, mechanism of degradation, route of elimination and immunogenicity have not been investigated to a similar extent as for PEG. Thus, further in-depth in vivo testing is essential to validate whether any of the alternative materials discussed in this review qualify as a replacement for PEG.
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High molecular weight PEGylation has the disadvantage of poor biodegradability.
“However, high molecular weight PEGylation has its disadvantage of poor biodegradability.36”
From Catalase-Integrated Hyaluronic Acid as Nanocarriers for Enhanced Photodynamic Therapy in Solid Tumor (2019) · cites this paper as [36]
Polysaccharides such as dextran and hyaluronic acid as biodegradable polymers have been explored for modifications on proteins.
“In light of this, polysaccharides such as dextran and hyaluronic acid (HA) as biodegradable polymers 36,39 have been explored for modifications on proteins.”
From Catalase-Integrated Hyaluronic Acid as Nanocarriers for Enhanced Photodynamic Therapy in Solid Tumor (2019) · cites this paper as [36]
Polymer modification has advantages including improved stability, solubility, and pharmacokinetics.
“Numerous advantages of such polymer modification include the improved stability, solubility and pharmacokinetics.36,37”
From Catalase-Integrated Hyaluronic Acid as Nanocarriers for Enhanced Photodynamic Therapy in Solid Tumor (2019) · cites this paper as [36]
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References 101 · Cited by 176
- Authors
- Qi, Y., & Chilkoti, A.
- Affiliations
- Duke University (US)
- Corresponding author
- Chilkoti, Ashutosh
- ORCID
- Chilkoti, Ashutosh
- Venue
- Current Opinion in Chemical Biology
- Publisher
- Elsevier BV
- Published
- 2015-10
- Volume
- 28
- Pages
- 181-193
- ISSN
- 1367-5931 (ISSN-L)
- PMC
- PMC4624571
- OpenAlex
- W1478059225
- Cited by
- 176
- References
- 101
- Citations by year
- 2026: 5 · 2025: 14 · 2024: 13 · 2023: 19 · 2022: 18 · 2021: 22 · 2020: 16 · 2019: 23 · 2018: 19 · 2017: 12 · 2016: 13 · 2015: 2
- FWCI
- 1.72
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Chemical Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Foundation for the National Institutes of Health (R01-DK091789, R01-DK092665)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
- Keywords
- protein-polymer conjugation, PEGylation, polyethylene glycol, protein and peptide drugs, drug stability, immunogenicity, in vivo biodistribution, polymer degradation, circulation half-life
- MeSH terms
- Animals, Humans, Peptides, Polyethylene Glycols, Polymers, Proteins, Chemistry Techniques, Synthetic
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