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奥昔康唑,一种独特的糖脂肽抗真菌药物的非临床毒理学评价。

Nonclinical toxicological evaluation of occidiofungin, a unique glycolipopeptide antifungal.

机构信息

Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.

出版信息

Int J Toxicol. 2012 Jul-Aug;31(4):326-36. doi: 10.1177/1091581812445185. Epub 2012 Jun 11.

Abstract

Occidiofungin, a glycolipopeptide obtained from the liquid culture of Burkholderia contaminans MS14, has been identified as a novel fungicide. The present study was designed to initially assess the in vitro toxicity in a rat hepatoma (H4IIE) cell line and acute toxicological effects of occidiofungin using a mouse model. In vitro toxicity was observed in all variables at 5 μmol/L. B6C3F1 mice were given single and repeat doses of occidiofungin up to 20 mg/kg. Key effects were a reduction in body and organ weights. However, no significant decrease in body weight was noted at a dose of 1 mg/kg, which is comparable to the dose level of other cyclic glycopeptide antifungal agents currently approved for human use. Microscopic examination of treated mice did not identify any signs of organ-specific toxicity at the dose levels tested.

摘要

由被玷污的伯克霍尔德菌 MS14 的液体培养物中获得的一种糖脂肽——occidiofungin,已被鉴定为一种新型杀真菌剂。本研究旨在初步评估其在大鼠肝癌(H4IIE)细胞系中的体外毒性和在小鼠模型中的急性毒理学效应。在 5μmol/L 时,所有变量均观察到体外毒性。B6C3F1 小鼠单次和重复给予 occidiofungin 剂量高达 20mg/kg。主要作用是体重和器官重量减轻。然而,在 1mg/kg 剂量时,体重没有明显下降,这与目前批准用于人类使用的其他环肽类抗真菌药物的剂量水平相当。在测试的剂量水平下,对处理过的小鼠进行显微镜检查未发现任何特定器官毒性的迹象。

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