用抗菌肽装饰的聚鞣酸包覆聚乳酸(PLGA)纳米粒子,用于协同治疗细菌和促进感染性伤口愈合

IF 5.4 2区 医学 Q1 BIOPHYSICS
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引用次数: 0

摘要

细菌感染对人类健康构成巨大威胁。因此,开发新的抗菌剂或方法迫在眉睫。在这项研究中,我们制备了表面装饰有抗菌肽(AMP)Dermaseptin-PP(Der)的聚对苯二甲酸(pTA)涂层聚乳酸(PLGA)纳米颗粒,得到 PLGA-pTA-Der。这种纳米平台可将 AMP 与 pTA 介导的光热处理(PTT)结合起来,实现协同杀菌。体外实验结果表明,PLGA-pTA-Der 纳米粒子在近红外激光(2.0 W-cm-2,5 分钟)照射下,可消灭近 99% 的大肠杆菌和金黄色葡萄球菌,表现出优异的抗菌性能。此外,原子力显微镜(AFM)结果表明,PLGA-pTA-Der 在激光照射下能极大地破坏细菌外膜的机械完整性。而Der的存在可以加剧PLGA-pTA NPs对细菌的热损伤,有利于降低PTT杀死细菌所需的临界温度。体内实验表明,PLGA-pTA-Der 纳米粒子在激光照射下能明显加速伤口愈合,抑制细菌生长。此外,它还能在温和的温度(45℃)下实现较强的光热抗菌效果,且不会对周围正常皮肤组织造成明显的热损伤。免疫荧光染色结果表明,PLGA-pTA-Der + 激光组的 CD31(新生血管形成的标志物)表达量明显高于其他组,而促炎分子 TNF-α 的表达量则明显低于其他组,这表明 PLGA-pTA-Der 纳米颗粒通过增强血管生成和减轻炎症反应加速了伤口愈合。总之,PLGA-pTA-Der 纳米粒子是一种治疗细菌感染和促进伤口愈合的抗菌纳米平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Poly-tannic acid coated PLGA nanoparticle decorated with antimicrobial peptide for synergistic bacteria treatment and infectious wound healing promotion

Bacterial infections pose a great threat to human health. Therefore, the development of new antibacterial agents or methods is in urgent need. In this study, we prepared polytannic acid (pTA)-coated PLGA nanoparticles decorated with Dermaseptin-PP (Der), an antimicrobial peptide (AMP), on the surface to obtain PLGA-pTA-Der. This nanoplatform could combine AMPs with photothermal treatment (PTT) mediated by pTA to achieve synergistic bacterial killing. The results of in vitro experiments showed that the PLGA-pTA-Der nanoparticles could eliminate nearly 99 % of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) upon near-infrared (NIR) laser irradiation (2.0 W·cm−2, 5 min), demonstrating excellent antibacterial properties. In addition, the results of atomic force microscopy (AFM) revealed that PLGA-pTA-Der with laser irradiation can greatly destroy the mechanical integrity of the bacterial outer membrane. And the presence of Der could exacerbate the heat damage caused by the PLGA-pTA NPs to the bacteria, which is helpful to reduce the critical temperature required for bacteria killing by PTT. In vivo experiments showed that PLGA-pTA-Der nanoparticles with laser irradiation significantly accelerated the wound healing process and inhibited the growth of bacterial. Moreover, it can achieve a strong photothermal antibacterial effect at a mild temperature (<45℃) and does not cause any obvious thermal damage to the surrounding normal skin tissues. Results of immunofluorescence staining showed that the expression of CD31 (a marker of new blood vessel formation) was significantly higher in the PLGA-pTA-Der + laser group than other groups, while the pro-inflammatory molecule TNF-α was significantly lower, indicating that PLGA-pTA-Der nanoparticles accelerated wound healing by enhancing angiogenesis and reducing the inflammatory response. In conclusion, PLGA-pTA-Der nanoparticles was a promising antimicrobial nanoplatform for treating bacterial infections and promoting wound healing.

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来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
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