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对用于集成到分析和医疗设备中作为纳米平台的二苯丙氨酸肽自组装纳米结构的见解。

Insights into diphenylalanine peptide self-assembled nanostructures for integration as nanoplatforms in analytical and medical devices.

作者信息

Domingos da Silveira Géssica, Izabelle Charlotte, Saubamea Bruno, Varenne Anne, d'Orlyé Fanny

机构信息

Institute of Chemistry for Life & Health Sciences (iCLeHS), UMR 8060 CNRS, Chimie ParisTech, PSL University, 75005, Paris, France.

Plateforme d'Imagerie Cellulaire et Moléculaire (PICMO), US25 Inserm, UAR3612 CNRS, Faculté de Pharmacie, Université Paris Cité, 75006, Paris, France.

出版信息

Int J Pharm. 2023 Oct 27:123559. doi: 10.1016/j.ijpharm.2023.123559.

Abstract

New insights on the self-assembling process of diphenylalanine (FF) into nanostructures in view of its application as an alternative nanomaterial for bioanalytical and biomedical systems are presented in the frame of the present work. Experimental conditions, such as peptide concentration and solubilization medium pH, were explored to understand the hierarchical process involved in the formation of self-assembled nanostructures arising from the simple and short diphenylalanine peptide. Optical microscopic and TEM images supported by DLS data authenticated the hierarchical self-assembly outcoming from the original nature of the first nanostructures, showing individual nanotubes and vesicles stacking to grow well-defined microtubes. Moreover, the influence of metal cations on peptide self-assembly was evaluated for the first time in the presence of Mg and compared with other ions, such as Na, K, and Ca. The results evidenced a tendency of Mg to interact with diphenylalanine peptides to form self-assembled nanostructures showing vesicle- and ellipse-like morphologies. FF solubilization in water prepared under sonication in a bath at 65-68°C followed by dilution into chloride metal cation solutions at 50 mmol.L proved to be optimal conditions to obtain metal-coordinated self-assembled FF structures. Besides, the latter revealed fluorescence features and electron-transfer properties on carbon-based electrode surfaces, that can be further explored in analytical and bioanalytical devices for fully integrated platforms. In this context, self-assembled nanostructures achieved in the presence of Mg and Ca were implemented for the surface modification of carbon screen-printed electrodes and proved to increase the electrochemical response toward a redox probe. This proof of concept is particularly interesting for further use of these peptide-based nanoarchitectures as nanoplatforms for clinical imaging, therapeutic and diagnosis purposes.

摘要

鉴于二苯基丙氨酸(FF)作为生物分析和生物医学系统的替代纳米材料的应用,本文介绍了其自组装成纳米结构过程的新见解。探索了诸如肽浓度和溶解介质pH等实验条件,以了解由简单且短的二苯基丙氨酸肽形成自组装纳米结构所涉及的分级过程。光学显微镜和透射电子显微镜图像以及动态光散射数据证实了最初纳米结构的分级自组装,显示出单个纳米管和囊泡堆叠形成定义明确的微管。此外,首次在镁存在的情况下评估了金属阳离子对肽自组装的影响,并与其他离子(如钠、钾和钙)进行了比较。结果表明,镁有与二苯基丙氨酸肽相互作用形成具有囊泡状和椭圆形形态的自组装纳米结构的趋势。在65 - 68°C的水浴中超声处理后在水中溶解FF,然后稀释到50 mmol.L的氯化物金属阳离子溶液中,被证明是获得金属配位自组装FF结构的最佳条件。此外,后者在碳基电极表面显示出荧光特性和电子转移特性,可在用于完全集成平台的分析和生物分析设备中进一步探索。在此背景下,在镁和钙存在下实现的自组装纳米结构被用于碳丝网印刷电极的表面修饰,并证明可增强对氧化还原探针的电化学响应。这一概念验证对于进一步将这些基于肽的纳米结构用作临床成像、治疗和诊断目的的纳米平台特别有意义。

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