Trimaille Thomas, Verrier Bernard
Ingénierie des Matériaux Polymères, Univ Lyon, CNRS, Université Claude Bernard Lyon 1, INSA Lyon, Université Jean Monnet, UMR 5223, CEDEX, 69622 Villeurbanne, France.
Laboratoire de Biologie Tissulaire et d'Ingénierie Thérapeutique, Univ Lyon, CNRS, Université Claude Bernard Lyon 1, UMR 5305, 7 Passage du Vercors, CEDEX 07, 69367 Lyon, France.
Pharmaceutics. 2023 Oct 17;15(10):2481. doi: 10.3390/pharmaceutics15102481.
Historically used for the delivery of hydrophobic drugs through core encapsulation, amphiphilic copolymer micelles have also more recently appeared as potent nano-systems to deliver protein and peptide therapeutics. In addition to ease and reproducibility of preparation, micelles are chemically versatile as hydrophobic/hydrophilic segments can be tuned to afford protein immobilization through different approaches, including non-covalent interactions (e.g., electrostatic, hydrophobic) and covalent conjugation, while generally maintaining protein biological activity. Similar to many other drugs, protein/peptide delivery is increasingly focused on stimuli-responsive nano-systems able to afford triggered and controlled release in time and space, thereby improving therapeutic efficacy and limiting side effects. This short review discusses advances in the design of such micelles over the past decade, with an emphasis on stimuli-responsive properties for optimized protein/peptide delivery.
两亲性共聚物胶束在历史上曾用于通过核心包封递送疏水性药物,最近也作为递送蛋白质和肽类治疗药物的有效纳米系统出现。除了制备简便和可重复性外,胶束在化学性质上具有多样性,因为疏水/亲水链段可以进行调整,以通过不同方法实现蛋白质固定,包括非共价相互作用(如静电、疏水作用)和共价结合,同时通常保持蛋白质的生物活性。与许多其他药物类似,蛋白质/肽递送越来越关注能够在时间和空间上实现触发和控释的刺激响应性纳米系统,从而提高治疗效果并限制副作用。这篇简短的综述讨论了过去十年中此类胶束设计的进展,重点是用于优化蛋白质/肽递送的刺激响应特性。