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增强茶树油的功能特性:体外抗菌活性及微胶囊化策略

Enhancing the Functional Properties of Tea Tree Oil: In Vitro Antimicrobial Activity and Microencapsulation Strategy.

作者信息

Manzanelli Franco Antonio, Ravetti Soledad, Brignone Sofia Gisella, Garro Ariel Gustavo, Martínez Sol Romina, Vallejo Mariana Guadalupe, Palma Santiago Daniel

机构信息

Centro de Investigaciones y Transferencia de Villa María (CIT VM), Villa María 5900, Argentina.

Instituto Académico Pedagógico de Ciencias Humanas, Universidad Nacional de Villa María, Villa María 5900, Argentina.

出版信息

Pharmaceutics. 2023 Oct 19;15(10):2489. doi: 10.3390/pharmaceutics15102489.

DOI:10.3390/pharmaceutics15102489
PMID:37896249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10610334/
Abstract

In the context of addressing antimicrobial drug resistance in periocular infections, Tea Tree Oil (TTO) has emerged as a promising therapeutic option. This study aimed to assess the efficacy of TTO against bacterial strains isolated from ocular infections, with a particular focus on its ability to inhibit biofilm formation. Additionally, we designed and analyzed microcapsules containing TTO to overcome certain unfavorable physicochemical properties and enhance its inherent biological attributes. The quality of TTO was confirmed through rigorous analysis using GC-MS and UV-Vis techniques. Our agar diffusion assay demonstrated the effectiveness of Tea Tree Oil (TTO) against ocular bacterial strains, including spp., coagulase-negative Staphylococcus spp., and , as well as a reference strain of (ATCC 25923). Notably, the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) for all tested microorganisms were found to be 0.2% and 0.4%, respectively, with the exception of spp., which exhibited resistance to TTO. Furthermore, TTO exhibited a substantial reduction in biofilm biomass, ranging from 30% to 70%, as determined by the MTT method. Through the spray-drying technique, we successfully prepared two TTO-containing formulations with high encapsulation yields (80-85%), microencapsulation efficiency (90-95%), and embedding rates (approximately 40%). These formulations yielded microcapsules with diameters of 6-12 μm, as determined by laser scattering particle size distribution analysis, and exhibited regular, spherical morphologies under scanning electron microscopy. Importantly, UV-Vis analysis post-encapsulation confirmed the presence of TTO within the capsules, with preserved antioxidant and antimicrobial activities. In summary, our findings underscore the substantial therapeutic potential of TTO and its microcapsules for treating ocular infections.

摘要

在解决眼周感染中的抗菌药物耐药性问题的背景下,茶树油(TTO)已成为一种有前景的治疗选择。本研究旨在评估茶树油对从眼部感染分离出的细菌菌株的疗效,特别关注其抑制生物膜形成的能力。此外,我们设计并分析了含有茶树油的微胶囊,以克服某些不利的物理化学性质并增强其固有的生物学特性。通过使用气相色谱 - 质谱联用(GC - MS)和紫外 - 可见光谱(UV - Vis)技术进行严格分析,确认了茶树油的质量。我们的琼脂扩散试验证明了茶树油(TTO)对眼部细菌菌株的有效性,包括 属菌株、凝固酶阴性葡萄球菌属菌株以及 ,还有 (ATCC 25923)的参考菌株。值得注意的是,除了 属菌株对茶树油表现出耐药性外,所有测试微生物的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)分别为0.2%和0.4%。此外,通过MTT法测定,茶树油使生物膜生物量大幅减少,减少幅度在30%至70%之间。通过喷雾干燥技术,我们成功制备了两种含茶树油的制剂,其包封率高(80 - 85%)、微囊化效率高(90 - 95%)且嵌入率约为40%。通过激光散射粒度分布分析确定,这些制剂产生的微胶囊直径为6 - 12μm,并且在扫描电子显微镜下呈现规则的球形形态。重要的是,包封后的紫外 - 可见光谱分析证实了微胶囊内存在茶树油,其抗氧化和抗菌活性得以保留。总之,我们的研究结果强调了茶树油及其微胶囊在治疗眼部感染方面的巨大治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/907db202effa/pharmaceutics-15-02489-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/b11731c87185/pharmaceutics-15-02489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/6340a9795b71/pharmaceutics-15-02489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/1cb9df21b9d4/pharmaceutics-15-02489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/aa54468ead67/pharmaceutics-15-02489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/dcaa3e04d575/pharmaceutics-15-02489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/e98ef1dc6631/pharmaceutics-15-02489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/907db202effa/pharmaceutics-15-02489-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/b11731c87185/pharmaceutics-15-02489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/6340a9795b71/pharmaceutics-15-02489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/1cb9df21b9d4/pharmaceutics-15-02489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/aa54468ead67/pharmaceutics-15-02489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/dcaa3e04d575/pharmaceutics-15-02489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/e98ef1dc6631/pharmaceutics-15-02489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f433/10610334/907db202effa/pharmaceutics-15-02489-g007.jpg

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