凝聚
手性(物理)
形态学(生物学)
离子强度
盐(化学)
化学
相(物质)
化学工程
离子键合
离子液体
纳米技术
混合(物理)
药物输送
生物物理学
钠盐
化学物理
降级(电信)
两亲性
组合化学
聚电解质
合理设计
材料科学
作者
Kimiasadat Mirlohi,Anuja Thapa,Donghui Zhang,Whitney C. Blocher McTigue
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2025-10-08
卷期号:26 (11): 7646-7655
标识
DOI:10.1021/acs.biomac.5c01165
摘要
Liquid-liquid phase separation (LLPS), particularly through coacervation, offers a groundbreaking approach to drug delivery by encapsulating therapeutic agents within phase-separated droplets, enhancing their stability, solubility, and controlled release. Polypeptides and polypeptoids, with their structural diversity and tunability, emerge as promising candidates for exploring these systems, with polypeptoids offering unique advantages, such as resistance to enzymatic degradation and increased control over interactions. This study examines the impact of chirality, mixing charge fraction, and salt concentration on the phase behavior and morphology of homochiral, mixed-chiral, and achiral polymers. By exploring the role of chirality and ionic strength in determining the presence and morphology of complexation, this research provides critical insights for designing tunable coacervate systems. Our results show that polypeptides and polypeptoids demonstrate chirality-dependent complexation. Additionally, we show that the presence and morphology of phase separation within these systems are influenced by the concentration of charged species in each sample, enabling the control and tunability of complex formation. These findings have the potential to advance the development of biomaterials for applications ranging from gene therapy to vaccine stabilization, offering innovative solutions to pressing biomedical challenges.
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