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一锅法微流控技术利用“光点击”化学制备壳聚糖纳米颗粒偶联抗菌肽:以胃细菌为例的验证

One-Pot Microfluidics to Engineer Chitosan Nanoparticles Conjugated with Antimicrobial Peptides Using "Photoclick" Chemistry: Validation Using the Gastric Bacterium .

机构信息

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135 Porto, Portugal.

Instituto Nacional de Engenharia Biomédica, Universidade do Porto, R. Alfredo Allen 208, 4200-135 Porto, Portugal.

出版信息

ACS Appl Mater Interfaces. 2024 Mar 27;16(12):14533-14547. doi: 10.1021/acsami.3c18772. Epub 2024 Mar 14.

Abstract

Surface bioconjugation of antimicrobial peptides (AMP) onto nanoparticles (AMP-NP) is a complex, multistep, and time-consuming task. Herein, a microfluidic system for the one-pot production of AMP-NP was developed. Norbornene-modified chitosan was used for NP production (NorChit-NP), and thiolated-AMP was grafted on their surface via thiol-norbornene "photoclick" chemistry over exposure of two parallel UV LEDs. The MSI-78A was the AMP selected due to its high activity against a high priority (level 2) antibiotic-resistant gastric pathogen: . AMP-NP (113 ± 43 nm; zeta potential 14.3 ± 7 mV) were stable in gastric settings without a cross-linker (up to 5 days in pH 1.2) and bactericidal against two highly pathogenic strains (10 NP/mL with 96 μg/mL MSI-78A). Eradication was faster for 26695 (30 min) than for J99 (24 h), which was explained by the lower minimum bactericidal concentration of soluble MSI-78A for 26695 (32 μg/mL) than for J99 (128 μg/mL). AMP-NP was bactericidal by inducing cell membrane alterations, intracellular reorganization, generation of extracellular vesicles, and leakage of cytoplasmic contents (transmission electron microscopy). Moreover, NP were not cytotoxic against two gastric cell lines (AGS and MKN74, ATCC) at bactericidal concentrations. Overall, the designed microfluidic setup is a greener, simpler, and faster approach than the conventional methods to obtain AMP-NP. This technology can be further explored for the bioconjugation of other thiolated-compounds.

摘要

抗菌肽(AMP)的表面生物缀合到纳米颗粒(AMP-NP)上是一项复杂、多步骤且耗时的任务。在此,开发了一种用于一锅法生产 AMP-NP 的微流控系统。用降冰片烯修饰壳聚糖进行 NP 生产(NorChit-NP),并通过硫醇-降冰片烯“光点击”化学在两个平行的 UV LED 暴露下将巯基化的 AMP 接枝到其表面。选择 MSI-78A 作为 AMP,因为它对高优先级(级别 2)抗药性胃病原体具有高活性:。在没有交联剂的情况下,AMP-NP(113 ± 43nm;ζ电位 14.3 ± 7mV)在胃环境中稳定(在 pH 1.2 下长达 5 天),并且对两种高致病性 菌株具有杀菌作用(10 NP/mL 用 96μg/mL MSI-78A)。 26695(30 分钟)的消除速度快于 J99(24 小时),这可以解释可溶性 MSI-78A 的最低杀菌浓度较低,对 26695(32μg/mL)的作用比对 J99(128μg/mL)的作用快。AMP-NP 通过诱导细胞膜改变、细胞内重组、产生细胞外囊泡和细胞质内容物泄漏来杀菌(透射电子显微镜)。此外,在杀菌浓度下,NP 对两种胃细胞系(AGS 和 MKN74,ATCC)没有细胞毒性。总体而言,与传统方法相比,设计的微流控装置是一种更环保、更简单、更快的获得 AMP-NP 的方法。这项技术可以进一步探索用于其他巯基化合物的生物缀合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19e/10982938/03911eac48cd/am3c18772_0001.jpg

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