PEG-modified biopharmaceuticals
Abstract
PEGylation is a process in which one or more units of chemically activated polyethylene glycol reacts with a biomolecule, usually a protein, peptide, small molecule or oligonucleotide, creating a putative new molecular entity possessing physicochemical and physiological characteristics that are distinct from its predecessor molecules. In recent years, PEGylation has been used not only as a drug delivery technology but used also as a drug modification technology to transform existing biopharmaceuticals clinically more efficacious than before their PEGylation. PEGylation bestows several useful properties upon the native molecule, resulting in improved pharmacokinetic and pharmacodynamic properties, which in turn enable the native molecule to achieve maximum clinical potency. In addition, PEGylation results in sustained clinical response with minimal dose and less frequency of dosing, leading to improved quality of life via increased patient compliance and reduced cost. During the course of development of various pegylated protein therapeutics, several new insights have been gained. This review article focuses on the approaches, strategies and the utilization of modern PEGylation concepts in the design and development of well-characterized pegylated protein therapeutics.
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PEG is a versatile and biocompatible synthetic biomaterial for postoperative anti-adhesion barrier films, primarily due to its hydrophilic nature, low protein adsorption, and tunable degradation.
“Polyethylene glycol (PEG) has established itself as a versatile and biocompatible synthetic biomaterial in postoperative anti-adhesion barrier films, primarily due to its hydrophilic nature, low protein adsorption, and tunable degradation properties [207,208].”
From Biomaterials in Postoperative Adhesion Barriers and Uterine Tissue Engineering (2025) · cites this paper as [207]
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PEGylation of therapeutic proteins
Jevševar, S., Kunstelj, M., & Porekar, V. G. (2010) · Biotechnology Journal · doi:10.1002/biot.200900218 · Cited by 681 · see citing works
Poly (2-oxazoline) s as polymer therapeutics
Luxenhofer, R., Han, Y., Schulz, A., Tong, J., He, Z., Kabanov, A. V., & Jordan, R. (2012) · Macromolecular Rapid Communications · doi:10.1002/marc.201200354 · Cited by 470 · see citing works
Biomaterials in Postoperative Adhesion Barriers and Uterine Tissue Engineering
Fazel Anvari-Yazdi, A., Badea, I., & Chen, X. (2025) · Gels · doi:10.3390/gels11060441 · Cited by 20 · see citing works
- Authors
- Bailon, P., & Won, C.-Y.
- Affiliations
- Johnson & Johnson (United States) (US)
- Venue
- Expert Opinion on Drug Delivery
- Publisher
- Informa UK Limited
- Published
- 2009-01
- Volume
- 6
- Issue
- 1
- Pages
- 1-16
- ISSN
- 1742-5247 (ISSN-L)
- 1744-7593
- OpenAlex
- W2094375186
- Cited by
- 366
- References
- 0
- Citations by year
- 2026: 13 · 2025: 13 · 2024: 12 · 2023: 16 · 2022: 6 · 2021: 13 · 2020: 15 · 2019: 26 · 2018: 16 · 2017: 16 · 2016: 27 · 2015: 26 · 2014: 27 · 2013: 32 · 2012: 36
- FWCI
- 3.62
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Expert Opinion on Drug Delivery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Keywords
- PEGylation, polyethylene glycol, PEGylated proteins, biopharmaceuticals, drug delivery, pharmacokinetics, pharmacodynamics, drug modification, therapeutic proteins, dosing frequency, medication adherence
- MeSH terms
- Chemistry, Pharmaceutical, Dose-Response Relationship, Drug, Drug Administration Schedule, Humans, Peptides, Polyethylene Glycols, Proteins, Drug Delivery Systems, Medication Adherence
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