Polypeptide-based multilayer nanoarchitectures: Controlled assembly on planar and colloidal substrates for biomedical applications

IF 15.9 1区 化学 Q1 CHEMISTRY, PHYSICAL
Maria Angela Motta , Lucinda Mulko , Edurne Marin , Aitor Larrañaga , Marcelo Calderón
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引用次数: 0

Abstract

Polypeptides have shown an excellent potential in nanomedicine thanks to their biocompatibility, biodegradability, high functionality, and responsiveness to several stimuli. Polypeptides exhibit high propensity to organize at the supramolecular level; hence, they have been extensively considered as building blocks in the layer-by-layer (LbL) assembly. The LbL technique is a highly versatile methodology, which involves the sequential assembly of building blocks, mainly driven by electrostatic interactions, onto planar or colloidal templates to fabricate sophisticated multilayer nanoarchitectures. The simplicity and the mild conditions required in the LbL approach have led to the inclusion of biopolymers and bioactive molecules for the fabrication of a wide spectrum of biodegradable, biocompatible, and precisely engineered multilayer films for biomedical applications. This review focuses on those examples in which polypeptides have been used as building blocks of multilayer nanoarchitectures for tissue engineering and drug delivery applications, highlighting the characteristics of the polypeptides and the strategies adopted to increase the stability of the multilayer film. Cross-linking is presented as a powerful strategy to enhance the stability and stiffness of the multilayer network, which is a fundamental requirement for biomedical applications. For example, in tissue engineering, a stiff multilayer coating, the presence of adhesion promoters, and/or bioactive molecules boost the adhesion, growth, and differentiation of cells. On the contrary, antimicrobial coatings should repel and inhibit the growth of bacteria. In drug delivery applications, mainly focused on particles and capsules at the micro- and nano-meter scale, the stability of the multilayer film is crucial in terms of retention and controlled release of the payload. Recent advances have shown the key role of the polypeptides in the adsorption of genetic material with high loading efficiency, and in addressing different pathways of the particles/capsules during the intracellular uptake, paving the way for applications in personalized medicine. Although there are a few studies, the responsiveness of the polypeptides to the pH changes, together with the inclusion of stimuli-responsive entities into the multilayer network, represents a further key factor for the development of smart drug delivery systems to promote a sustained release of therapeutics. The degradability of polypeptides may be an obstacle in certain scenarios for the controlled intracellular release of a drug once an external stimulus is applied. Nowadays, the highly engineered design of biodegradable LbL particles/capsules is oriented on the development of theranostics that, limited to use of polypeptides, are still in their infancy.

Abstract Image

基于多肽的多层纳米结构:平面和胶体基底上的可控装配,用于生物医学应用
多肽具有生物相容性、生物可降解性、高功能性和对多种刺激的响应性,因此在纳米医学中显示出巨大的潜力。多肽在超分子水平上表现出很强的组织倾向,因此被广泛认为是逐层组装(LbL)的构件。逐层组装技术是一种通用性很强的方法,主要通过静电相互作用将构件依次组装到平面或胶体模板上,从而制造出复杂的多层纳米结构。由于 LbL 方法简单且所需条件温和,因此可将生物聚合物和生物活性分子纳入其中,从而制造出各种可生物降解、生物相容和精确设计的多层薄膜,用于生物医学应用。本综述重点介绍多肽作为多层纳米结构的构件用于组织工程和给药应用的实例,突出多肽的特性以及为提高多层膜的稳定性而采用的策略。交联是增强多层网络稳定性和刚度的有力策略,这是生物医学应用的基本要求。例如,在组织工程中,坚硬的多层涂层、粘附促进剂和/或生物活性分子的存在可促进细胞的粘附、生长和分化。相反,抗菌涂层则应能排斥和抑制细菌的生长。在以微米和纳米级颗粒和胶囊为主的药物输送应用中,多层薄膜的稳定性对有效载荷的保持和控制释放至关重要。最近的研究进展表明,多肽在以高负载效率吸附遗传物质、解决颗粒/胶囊在细胞内吸收过程中的不同途径方面起着关键作用,为个性化医疗的应用铺平了道路。虽然研究不多,但多肽对 pH 值变化的反应能力,以及多层网络中的刺激响应实体,是开发智能给药系统以促进治疗药物持续释放的另一个关键因素。在某些情况下,一旦施加外部刺激,多肽的降解性可能会阻碍药物在细胞内的可控释放。如今,生物可降解 LbL 颗粒/胶囊的高度工程化设计正着眼于治疗学的发展,但仅限于多肽的使用,仍处于起步阶段。
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来源期刊
CiteScore
28.50
自引率
2.60%
发文量
175
审稿时长
31 days
期刊介绍: "Advances in Colloid and Interface Science" is an international journal that focuses on experimental and theoretical developments in interfacial and colloidal phenomena. The journal covers a wide range of disciplines including biology, chemistry, physics, and technology. The journal accepts review articles on any topic within the scope of colloid and interface science. These articles should provide an in-depth analysis of the subject matter, offering a critical review of the current state of the field. The author's informed opinion on the topic should also be included. The manuscript should compare and contrast ideas found in the reviewed literature and address the limitations of these ideas. Typically, the articles published in this journal are written by recognized experts in the field.
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