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丁香酚和茴脑与盐酸奥替尼啶联合使用对 和 的疗效增强。

Improved efficacy of eugenol and -anethole in combination with octenidine dihydrochloride against and .

机构信息

Department of Allergology and Respiratory Rehabilitation; Medical University, Łódź, Poland.

Department of Diagnostic Immunology; Pomeranian Medical University, Szczecin, Poland.

出版信息

Ann Agric Environ Med. 2023 Mar 31;30(1):204-210. doi: 10.26444/aaem/157995. Epub 2023 Jan 17.

Abstract

INTRODUCTION AND OBJECTIVE

Candidiasis is a fungal infection caused by yeasts from the Ogenus Candida. Considering increasing antifungal resistance rates the activity was analyzed of natural compounds to eradicate spp. The aim of the study was to check the antifungal activity of selected essential oil compounds (EOCs; thymol, menthol, eugenol [E], carvacrol, trans-anethole [TA]) alone, and in combination with octenidine dihydrochloride (OCT) against and reference, and clinical strains.

MATERIAL AND METHODS

Investigated clinical isolates were obtained from skin wounds of patients treated for superficial wounds candidiasis. The following parameters were studied: antifungal susceptibility testing using the VITEK system, antifungal activity of EOCs alone and in combination with OCT using microdilution and checkerboard assays, antifungal efficacy of selected chemicals using time-kill curve assay, and changes in cell permeability in the presence of selected chemicals using crystal violet assay.

RESULTS

Clinical isolates of and were resistant to fluconazole and voriconazole. The highest inhibition activity against Candida isolates was observed for E. The OCT - TA and OCT - E combinations showed synergistic and additive activities against all strains, respectively. These combinations also appeared to affect the rate of yeast cell killing and increasing the permeability of Candida cells.

CONCLUSIONS

The study indicates that E and TA potentially used in formulation with OCT might eradicate pathogenic yeasts; however, microbiological and clinical studies are still required.

摘要

简介与目的

念珠菌病是一种真菌感染,由酵母属的念珠菌引起。鉴于抗真菌药物耐药率不断上升,本研究分析了天然化合物对消灭念珠菌属的活性。本研究的目的是检测选定的精油化合物(EOC;麝香草酚、薄荷醇、丁香酚[E]、香芹酚、反式茴香脑[TA])单独使用以及与奥替尼啶二盐酸盐(OCT)联合使用对 和 参考株以及临床分离株的抗真菌活性。

材料与方法

研究中使用的临床分离株来自接受浅部伤口念珠菌病治疗的患者的皮肤伤口。研究了以下参数:使用 VITEK 系统进行抗真菌药敏试验、使用微稀释和棋盘试验检测 EOC 单独使用和与 OCT 联合使用的抗真菌活性、使用时间杀伤曲线试验检测选定化学品的抗真菌功效、以及使用结晶紫试验检测选定化学品存在时细胞通透性的变化。

结果

和 临床分离株对氟康唑和伏立康唑耐药。E 对念珠菌分离株的抑制活性最高。OCT-TA 和 OCT-E 组合分别对所有菌株表现出协同和相加作用。这些组合似乎还影响酵母细胞的杀伤速度并增加念珠菌细胞的通透性。

结论

本研究表明,E 和 TA 与 OCT 联合使用可能能够消灭致病性酵母;然而,仍需要进行微生物学和临床研究。

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