Biomimetic peptide conjugates as emerging strategies for controlled release from protein-based materials.

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Delivery Pub Date : 2025-12-01 Epub Date: 2025-01-09 DOI:10.1080/10717544.2025.2449703
Juthatip Manissorn, Jaturong Promsuk, Kittikhun Wangkanont, Peerapat Thongnuek
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Abstract

Biopolymers, such as collagens, elastin, silk fibroin, spider silk, fibrin, keratin, and resilin have gained significant interest for their potential biomedical applications due to their biocompatibility, biodegradability, and mechanical properties. This review focuses on the design and integration of biomimetic peptides into these biopolymer platforms to control the release of bioactive molecules, thereby enhancing their functionality for drug delivery, tissue engineering, and regenerative medicine. Elastin-like polypeptides (ELPs) and silk fibroin repeats, for example, demonstrate how engineered peptides can mimic natural protein domains to modulate material properties and drug release profiles. Recombinant spider silk proteins, fibrin-binding peptides, collagen-mimetic peptides, and keratin-derived structures similarly illustrate the ability to engineer precise interactions and to design controlled release systems. Additionally, the use of resilin-like peptides showcases the potential for creating highly elastic and resilient biomaterials. This review highlights current achievements and future perspectives in the field, emphasizing the potential of biomimetic peptides to transform biopolymer-based biomedical applications.

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仿生肽偶联物作为蛋白质基材料控释的新兴策略。
生物聚合物,如胶原蛋白、弹性蛋白、丝素蛋白、蜘蛛丝、纤维蛋白、角蛋白和弹性蛋白,由于其生物相容性、生物可降解性和机械性能,已因其潜在的生物医学应用而获得了极大的兴趣。本文将重点介绍仿生肽的设计和整合到这些生物聚合物平台中,以控制生物活性分子的释放,从而增强其在药物传递、组织工程和再生医学方面的功能。例如,弹性蛋白样多肽(ELPs)和丝素蛋白重复序列证明了工程肽如何模拟天然蛋白质结构域来调节材料特性和药物释放谱。重组蛛丝蛋白、纤维蛋白结合肽、模拟胶原肽和角蛋白衍生结构同样说明了设计精确相互作用和设计控制释放系统的能力。此外,类树脂肽的使用展示了创造高弹性和弹性生物材料的潜力。本文综述了该领域目前的成就和未来的展望,强调了仿生肽在改变生物聚合物生物医学应用方面的潜力。
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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
期刊最新文献
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