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Engineered therapeutic proteins for sustained-release drug delivery systemsopen access

Authors
Nguyen, Thoa Thi KimPham, Khang-YenYook, Simmyung
Issue Date
Nov-2023
Publisher
Acta Materialia Inc
Keywords
Long-term delivery systems; Nanoparticles; Protein therapeutics; Structural modification; Sustained release
Citation
Acta Biomaterialia, v.171, pp 131 - 154
Pages
24
Indexed
SCIE
SCOPUS
Journal Title
Acta Biomaterialia
Volume
171
Start Page
131
End Page
154
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/108832
DOI
10.1016/j.actbio.2023.09.018
ISSN
1742-7061
1878-7568
Abstract
Proteins play a vital role in diverse biological processes in the human body, and protein therapeutics have been applied to treat different diseases such as cancers, genetic disorders, autoimmunity, and inflammation. Protein therapeutics have demonstrated their advantages, such as specific pharmaceutical effects, low toxicity, and strong solubility. However, several disadvantages arise in clinical applications, including short half-life, immunogenicity, and low permeation, leading to reduced drug effectiveness. The structure of protein therapeutics can be modified to increase molecular size, leading to prolonged stability and increased plasma half-life. Notably, the controlled-release delivery systems for the sustained release of protein drugs and preserving the stability of cargo proteins are envisioned as a potential approach to overcome these challenges. In this review, we summarize recent research progress related to structural modifications (PEGylation, glycosylation, poly amino acid modification, and molecular biology-based strategies) and promising long-term delivery systems, such as polymer-based systems (injectable gel/implants, microparticles, nanoparticles, micro/nanogels, functional polymers), lipid-based systems (liposomes, solid lipid nanoparticles, nanostructured lipid carriers), and inorganic nanoparticles exploited for protein therapeutics. Statement of significance: In this review, we highlight recent advances concerning modifying proteins directly to enhance their stability and functionality and discuss state-of-the-art methods for the delivery and controlled long-term release of active protein therapeutics to their target site. In terms of drug modifications, four widely used strategies, including PEGylation, poly amino acid modification, glycosylation, and genetic, are discussed. As for drug delivery systems, we emphasize recent progress relating to polymer-based systems, lipid-based systems developed, and inorganic nanoparticles for protein sustained-release delivery. This review points out the areas requiring focused research attention before the full potential of protein therapeutics for human health and disease can be realized. © 2023 Acta Materialia Inc.
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