Engineered therapeutic proteins for sustained-release drug delivery systems

被引:5
|
作者
Nguyen, Thoa Thi Kim [1 ]
Pham, Khang-Yen [1 ,4 ,5 ]
Yook, Simmyung [1 ,2 ,3 ,4 ,5 ]
机构
[1] Keimyung Univ, Coll Pharm, 1095 Dalgubeol Daero, Daegu 42601, South Korea
[2] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
[3] Sungkyunkwan Univ, Dept Biopharmaceut Convergence, Suwon 16419, South Korea
[4] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
[5] Sungkyunkwan Univ, Dept Biopharmaceut Convergence, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
Protein therapeutics; Sustained release; Structural modification; Long-term delivery systems; Nanoparticles; SOLID LIPID NANOPARTICLES; SITE-SPECIFIC PEGYLATION; MESOPOROUS SILICA NANOPARTICLES; PHASE INVERSION DYNAMICS; ORGANIC FRAMEWORK NANOPARTICLES; HALF-LIFE EXTENSION; ORAL DELIVERY; PHYSICOCHEMICAL PROPERTIES; POLYETHYLENE-GLYCOL; CHEMICAL-SYNTHESIS;
D O I
10.1016/j.actbio.2023.09.018
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 in-flammation. 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 sta-bility 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 ap-proach 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 (li-posomes, 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 sta-bility 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. (c) 2023 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:131 / 154
页数:24
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