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本文引用的文献

1
Development of interpretive breakpoints for antifungal susceptibility testing: conceptual framework and analysis of in vitro-in vivo correlation data for fluconazole, itraconazole, and candida infections. Subcommittee on Antifungal Susceptibility Testing of the National Committee for Clinical Laboratory Standards.抗真菌药敏试验解释性断点的制定：氟康唑、伊曲康唑和念珠菌感染的体外-体内相关性数据的概念框架与分析。美国国家临床实验室标准委员会抗真菌药敏试验小组委员会
Clin Infect Dis. 1997 Feb;24(2):235-47. doi: 10.1093/clinids/24.2.235.
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In vitro studies of activity of voriconazole (UK-109,496), a new triazole antifungal agent, against emerging and less-common mold pathogens.新型三唑类抗真菌药物伏立康唑（UK-109,496）对新出现的及较少见霉菌病原体活性的体外研究。
Antimicrob Agents Chemother. 1997 Apr;41(4):841-3. doi: 10.1128/AAC.41.4.841.
3
Activity of voriconazole (UK-109,496) against clinical isolates of Aspergillus species and its effectiveness in an experimental model of invasive pulmonary aspergillosis.伏立康唑（UK-109,496）对曲霉属临床分离株的活性及其在侵袭性肺曲霉病实验模型中的有效性。
Antimicrob Agents Chemother. 1997 Mar;41(3):696-8. doi: 10.1128/AAC.41.3.696.
4
Comparison of voriconazole (UK-109,496) and itraconazole in prevention and treatment of Aspergillus fumigatus endocarditis in guinea pigs.伏立康唑（UK-109,496）与伊曲康唑预防和治疗豚鼠烟曲霉性心内膜炎的比较。
Antimicrob Agents Chemother. 1997 Jan;41(1):13-6. doi: 10.1128/AAC.41.1.13.
5
In vitro studies of two triazole antifungal agents (voriconazole [UK-109,496] and fluconazole) against Candida species.两种三唑类抗真菌剂（伏立康唑[UK-109,496]和氟康唑）对念珠菌属的体外研究。
Antimicrob Agents Chemother. 1996 Aug;40(8):1948-9. doi: 10.1128/AAC.40.8.1948.
6
Efficacy of UK-109496, a new azole antifungal agent, in an experimental model of invasive aspergillosis.新型唑类抗真菌药UK-109496在侵袭性曲霉病实验模型中的疗效
Antimicrob Agents Chemother. 1996 Jan;40(1):86-91. doi: 10.1128/AAC.40.1.86.

伏立康唑对某些临床重要真菌的体外评价。

In vitro evaluation of voriconazole against some clinically important fungi.

作者信息

McGinnis M R, Pasarell L, Sutton D A, Fothergill A W, Cooper C R, Rinaldi M G

机构信息

Department of Pathology and WHO Collaborating Center for Tropical Diseases, University of Texas Medical Branch, Galveston 77555-0609, USA.

出版信息

Antimicrob Agents Chemother. 1997 Aug;41(8):1832-4. doi: 10.1128/AAC.41.8.1832.

DOI:10.1128/AAC.41.8.1832
PMID:9257773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC164017/
Abstract

Voriconazole was compared to amphotericin B, fluconazole, and itraconazole by using an in vitro macrobroth dilution test based upon current National Committee for Clinical Laboratory Standards tentative standards against the dimorphic fungi and several opportunistic molds and yeasts. In all instances, the voriconazole MICs were lower than those of fluconazole. In most instances, the MICs were lower than the recorded MICs of amphotericin B and itraconazole.

摘要

通过使用基于美国国家临床实验室标准委员会针对双相真菌以及几种机会性霉菌和酵母菌的现行暂行标准的体外常量肉汤稀释试验，将伏立康唑与两性霉素B、氟康唑和伊曲康唑进行了比较。在所有情况下，伏立康唑的最低抑菌浓度（MIC）均低于氟康唑。在大多数情况下，其MIC低于两性霉素B和伊曲康唑所记录的MIC。