I-GLAD:制造抗菌表面的新策略。

0 MATERIALS SCIENCE, MULTIDISCIPLINARY
Chuang Qu, Jesse Rozsa, Mark Running, Shamus McNamara, Kevin Walsh
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引用次数: 0

摘要

论文利用倒置闪烁角沉积(I-GLAD)技术制造抗菌表面。抗菌表面存在于自然界中,如昆虫的翅膀、眼睛和植物叶子上。由于这些表面的杀菌机制纯粹是物理性的,因此可以克服细菌对传统化学抗生素的抗药性。由于天然抗菌表面大多由三维分层微纳结构组成,如何模仿、合成和放大这些抗菌表面并将其用于实际应用是一个技术难题。本文提出使用 I-GLAD 作为一种自下而上的新型纳米制造技术,来放大受生物启发的纳米结构抗菌表面。我们创新的 I-GLAD 纳米制造技术包括传统的 GLAD 沉积工艺和关键的倒转工艺。制造完成后,我们使用两种细菌探索了 I-GLAD 表面的抗菌功效:大肠杆菌(一种革兰氏阴性细菌)和金黄色葡萄球菌(一种革兰氏阳性细菌)。扫描电子显微镜(SEM)显示,I-GLAD 纳米针的针尖很小,D/P(特征尺寸大于周期)比很灵活,这是实现理想的杀菌机制所必需的。通过实现大肠杆菌和金黄色葡萄球菌的平坦生长曲线以及在扫描电镜下的直接观察,验证了 I-GLAD 样品的抗菌特性。论文填补了 GLAD 种子技术和 I-GLAD 工艺控制/优化方面的知识空白,从而调整了纳米突起的形态。I-GLAD 表面对革兰氏阴性菌和革兰氏阳性菌均有效,在医院环境和日常生活表面具有巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

I-GLAD: a new strategy for fabricating antibacterial surfaces.

I-GLAD: a new strategy for fabricating antibacterial surfaces.

The paper uses inverted glancing angle deposition (I-GLAD) for creating antibacterial surfaces. Antibacterial surfaces are found in nature, such as on insect wings, eyes, and plant leaves. Since the bactericidal mechanism is purely physical for these surfaces, the antimicrobial resistance of bacteria to traditional chemical antibiotics can be overcome. The technical problem is how to mimic, synthesize, and scale up the naturally occurring antibacterial surfaces for practical applications, given the fact that most of those surfaces are composed of three-dimensional hierarchical micro-nano structures. This paper proposes to use I-GLAD as a novel bottom-up nanofabrication technique to scale up bio-inspired nano-structured antibacterial surfaces. Our innovative I-GLAD nanofabrication technique includes traditional GLAD deposition processes alongside the crucial inverting process. Following fabrication, we explore the antibacterial efficacy of I-GLAD surfaces using two types of bacteria: Escherichia coli (E. coli), a gram-negative bacterium, and Staphylococcus aureus (S. aureus), a gram-positive bacterium. Scanning electron microscopy (SEM) shows the small tips and flexible D/P (feature size over period) ratio of I-GLAD nanoneedles, which is required to achieve the desired bactericidal mechanism. Antibacterial properties of the I-GLAD samples are validated by achieving flat growth curves of E. coli and S. aureus, and direct observation under SEM. The paper bridges the knowledge gaps of seeding techniques for GLAD, and the control/optimization of the I-GLAD process to tune the morphologies of the nano-protrusions. I-GLAD surfaces are effective against both gram-negative and gram-positive bacteria, and they have tremendous potentials in hospital settings and daily surfaces.

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