卢立康唑:一种抗耳霉病的新型强效咪唑活性药物

IF 0.2 Q4 OTORHINOLARYNGOLOGY Indian Journal of Otology Pub Date : 2023-01-01 DOI:10.4103/indianjotol.indianjotol_197_22
Bavadharani Sukumar, Thayanidhi Premamalini, Nivetha Shree Sasikumar, Somu Lakhmanan, Anupma Jyoti Kindo
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引用次数: 0

摘要

背景:黑曲霉和黄曲霉是耳霉菌病最常见的病原体,分布在世界各地。对于难治性耳真菌病,需要广泛的手术清创和全身抗真菌治疗。露立康唑目前被证实用于皮肤癣的局部治疗。此外,还发现露立康唑对一些霉菌和酵母菌具有体外活性。目的:本研究的目的是评估露立康唑与常规使用的三唑类抗真菌药物对从耳真菌病病例中提取的曲霉分离物的疗效。材料与方法:本研究于2020年3月至2022年2月在微生物学系进行。从耳霉菌病病例中分离得到55株曲霉,经宏观和微观鉴定均得到证实。采用微量肉汤稀释法测定伊曲康唑、伏立康唑、泊沙康唑和露立康唑的抗真菌药敏型,方法参照美国临床实验室标准学会M38-A2指南。结果:在所检测的唑类药物中,最低抑菌浓度(MIC)几何平均值(0.00309 μg/ml)、MIC50 (0.00098 μg/ml)和MIC90 (0.00781 μg/ml)均为luliconazole;曲霉病首选药物伏立康唑MIC50和MIC90值略高,分别为1 μg/ml和2 μg/ml。即使是对pan azole耐药的分离株(n = 3),也发现在MIC值较低的情况下luliconazole更有效。结论:本研究结果表明,露立康唑具有较好的体外活性,其MIC值低于三唑类药物。因此,这种新型咪唑抗真菌药物可以被认为是治疗由黑曲霉和黄曲霉引起的耳真菌病的合适候选药物。此外,luliconazole对pan azole耐药菌株的疗效较好,MIC值较低,提示luliconazole可能是治疗pan azole耐药菌株引起的曲霉病的潜在抗真菌药物。
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Luliconazole: A Novel Potent Imidazole Activity against Aspergillus niger and Aspergillus flavus Causing Otomycosis
Background: Aspergillus niger and Aspergillus flavus are the most common causative agents of otomycosis with worldwide distribution. Extensive surgical debridement and systemic antifungal therapy are needed in cases of refractory otomycosis. Luliconazole is currently confirmed for the topical therapy of dermatophytosis. Moreover, it is found that luliconazole has in vitro activity against some molds and yeast species. Objectives: The aim of the present study was to evaluate the efficacy of luliconazole in comparison to routinely used triazole antifungals on Aspergillus isolates, obtained from otomycosis cases using microbroth dilution method. Materials and Methods: This study was carried out in the department of microbiology, from March 2020 to February 2022. A total of 55 strains of Aspergillus isolates obtained from otomycosis cases were confirmed based on macroscopic and microscopic identification. Antifungal susceptibility patterns of itraconazole, voriconazole, posaconazole and luliconazole were determined by broth microdilution method as per the Clinical Laboratory Standards Institute M38-A2 guidelines. Results: Among the azoles tested, the lowest minimum inhibitory concentration (MIC) geometric mean (0.00309 μg/ml), MIC50 (0.00098 μg/ml), and MIC90 (0.00781 μg/ml) values were attributed to luliconazole. Being the drug of choice for aspergillosis, voriconazole had a slightly higher MIC50 and MIC90 value of 1 μg/ml and 2 μg/ml, respectively. Even for the pan azole resistant isolates ( n = 3), luliconazole was found to be more effective with lower MIC values. Conclusion: The results of this study showed that luliconazole had an excellent in vitro activity with a lower MIC values than the triazoles tested. Hence, this novel imidazole antifungal agent can be considered an appropriate candidate for the treatment of otomycosis caused by A. niger and A. flavus strains. Furthermore, luliconazole showed better efficacy with lower MIC values for pan azole resistant isolates, suggesting that it could be a potential antifungal for treating aspergillosis caused by pan azole resistant isolates.
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来源期刊
Indian Journal of Otology
Indian Journal of Otology OTORHINOLARYNGOLOGY-
CiteScore
0.40
自引率
0.00%
发文量
21
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