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无抗生素磷脂酰甘油/二十二碳六烯酸层状和非层状液晶纳米颗粒的抗菌和抗生物膜活性。

Antibacterial and anti-biofilm activities of antibiotic-free phosphatidylglycerol/docosahexaenoic acid lamellar and non-lamellar liquid crystalline nanoparticles.

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen Ø, Denmark.

Department of Immunology and Microbiology, Costerton Biofilm Center, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen N, Denmark.

出版信息

J Colloid Interface Sci. 2024 Sep;669:537-551. doi: 10.1016/j.jcis.2024.04.186. Epub 2024 Apr 26.

Abstract

Infectious diseases, particularly those associated with biofilms, are challenging to treat due to an increased tolerance to commonly used antibiotics. This underscores the urgent need for innovative antimicrobial strategies. Here, we present an alternative simple-by-design approach focusing on the development of biocompatible and antibiotic-free nanocarriers from docosahexaenoic acid (DHA) that has the potential to combat microbial infections and phosphatidylglycerol (DOPG), which is attractive for use as a biocompatible prominent amphiphilic component of Gram-positive bacterial cell membranes. We assessed the anti-bacterial and anti-biofilm activities of these nanoformulations (hexosomes and vesicles) against S. aureus and S. epidermidis, which are the most common causes of infections on catheters and medical devices by different methods (including resazurin assay, time-kill assay, and confocal laser scanning microscopy on an in vitro catheter biofilm model). In a DHA-concentration-dependent manner, these nano-self-assemblies demonstrated strong anti-bacterial and anti-biofilm activities, particularly against S. aureus. A five-fold reduction of the planktonic and a four-fold reduction of biofilm populations of S. aureus were observed after treatment with hexosomes. The nanoparticles had a bacteriostatic effect against S. epidermidis planktonic cells but no anti-biofilm activity was detected. We discuss the findings in terms of nanoparticle-bacterial cell interactions, plausible alterations in the phospholipid membrane composition, and potential penetration of DHA into these membranes, leading to changes in their structural and biophysical properties. The implications for the future development of biocompatible nanocarriers for the delivery of DHA alone or in combination with other anti-bacterial agents are discussed, as novel treatment strategies of Gram-positive infections, including biofilm-associated infections.

摘要

传染病,特别是与生物膜相关的传染病,由于对常用抗生素的耐受性增加,治疗起来具有挑战性。这凸显了创新抗菌策略的迫切需求。在这里,我们提出了一种替代的简单设计方法,专注于从二十二碳六烯酸(DHA)开发生物相容性且无抗生素的纳米载体,该方法有可能对抗微生物感染和磷脂酰甘油(DOPG),后者作为革兰氏阳性细菌细胞膜的生物相容性突出的两亲性成分很有吸引力。我们评估了这些纳米制剂(hexosomes 和 vesicles)对金黄色葡萄球菌和表皮葡萄球菌的抗细菌和抗生物膜活性,金黄色葡萄球菌和表皮葡萄球菌是导管和医疗器械感染的最常见原因,我们使用不同的方法(包括resazurin 测定法、时间杀伤测定法和体外导管生物膜模型上的共聚焦激光扫描显微镜)进行了评估。这些纳米自组装体以 DHA 浓度依赖的方式表现出强大的抗细菌和抗生物膜活性,特别是对金黄色葡萄球菌。用 hexosomes 处理后,观察到浮游生物的五倍减少和金黄色葡萄球菌生物膜种群的四倍减少。这些纳米粒子对表皮葡萄球菌浮游细胞具有抑菌作用,但未检测到抗生物膜活性。我们根据纳米粒子-细菌细胞相互作用、磷脂膜组成的可能变化以及 DHA 进入这些膜的潜在渗透,讨论了这些发现,导致它们的结构和生物物理性质发生变化。讨论了单独或与其他抗菌剂联合使用 DHA 的生物相容性纳米载体的未来发展的意义,作为革兰氏阳性感染(包括生物膜相关感染)的新治疗策略。

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