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本文引用的文献

1
Correlation of in vitro activity, serum levels, and in vivo efficacy of posaconazole against Rhizopus microsporus in a murine disseminated infection.泊沙康唑对小孢根霉致小鼠播散性感染的体外活性、血清水平与体内疗效的相关性研究。
Antimicrob Agents Chemother. 2009 Dec;53(12):5022-5. doi: 10.1128/AAC.01026-09. Epub 2009 Sep 28.
2
Recent advances in the management of mucormycosis: from bench to bedside.毛霉菌病治疗的最新进展:从实验室到临床
Clin Infect Dis. 2009 Jun 15;48(12):1743-51. doi: 10.1086/599105.
3
Spectrum of zygomycete species identified in clinically significant specimens in the United States.在美国具有临床意义的标本中鉴定出的接合菌物种谱。
J Clin Microbiol. 2009 Jun;47(6):1650-6. doi: 10.1128/JCM.00036-09. Epub 2009 Apr 22.
4
Posaconazole mono- or combination therapy for treatment of murine zygomycosis.泊沙康唑单药或联合治疗小鼠接合菌病。
Antimicrob Agents Chemother. 2009 Feb;53(2):772-5. doi: 10.1128/AAC.01124-08. Epub 2008 Oct 20.
5
Posaconazole combined with amphotericin B, an effective therapy for a murine disseminated infection caused by Rhizopus oryzae.泊沙康唑联合两性霉素B是治疗由米根霉引起的小鼠播散性感染的有效疗法。
Antimicrob Agents Chemother. 2008 Oct;52(10):3786-8. doi: 10.1128/AAC.00628-08. Epub 2008 Aug 11.
6
Activities of antifungal agents against yeasts and filamentous fungi: assessment according to the methodology of the European Committee on Antimicrobial Susceptibility Testing.抗真菌剂对酵母和丝状真菌的活性:根据欧洲抗菌药物敏感性测试委员会的方法进行评估。
Antimicrob Agents Chemother. 2008 Oct;52(10):3637-41. doi: 10.1128/AAC.00662-08. Epub 2008 Aug 11.
7
Comparison of Neo-Sensitabs tablet diffusion assay with CLSI broth microdilution M38-A and disk diffusion methods for testing susceptibility of filamentous fungi with amphotericin B, caspofungin, itraconazole, posaconazole, and voriconazole.采用两性霉素B、卡泊芬净、伊曲康唑、泊沙康唑和伏立康唑,比较Neo-Sensitabs片剂扩散法与CLSI肉汤微量稀释法M38-A及纸片扩散法检测丝状真菌药敏性的效果。
J Clin Microbiol. 2008 May;46(5):1793-803. doi: 10.1128/JCM.01883-07. Epub 2008 Mar 12.
8
Treatment of zygomycosis: current and new options.毛霉病的治疗:当前及新的选择
J Antimicrob Chemother. 2008 Jan;61 Suppl 1:i35-40. doi: 10.1093/jac/dkm429.
9
Pharmacokinetics of oral posaconazole in allogeneic hematopoietic stem cell transplant recipients with graft-versus-host disease.口服泊沙康唑在患有移植物抗宿主病的异基因造血干细胞移植受者中的药代动力学。
Pharmacotherapy. 2007 Dec;27(12):1627-36. doi: 10.1592/phco.27.12.1627.
10
In vitro susceptibilities of 217 clinical isolates of zygomycetes to conventional and new antifungal agents.217株接合菌临床分离株对传统和新型抗真菌药物的体外敏感性
Antimicrob Agents Chemother. 2007 Jul;51(7):2587-90. doi: 10.1128/AAC.00452-07. Epub 2007 Apr 23.

泊沙康唑对体外活性与体内抗米根霉感染疗效的相关性研究。

Correlation between in vitro activity of posaconazole and in vivo efficacy against Rhizopus oryzae infection in mice.

机构信息

Unitat de Microbiologia, Facultat de Medicina, Universitat Rovira i Virgili, Reus, Spain.

出版信息

Antimicrob Agents Chemother. 2010 May;54(5):1665-9. doi: 10.1128/AAC.01463-09. Epub 2010 Feb 9.

DOI:10.1128/AAC.01463-09
PMID:20145077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2863673/
Abstract

We have evaluated the in vitro activity of posaconazole (PSC) against 50 clinical strains of Rhizopus oryzae using a broth microdilution method, the Neo-Sensitabs tablet diffusion method, and minimal fungicidal concentration (MFC) determination. In general, PSC showed low MICs against this fungus, and the MICs correlated with the inhibition zone diameters. Most of the MFCs, however, were from 1 to 4 dilutions higher than their corresponding MICs. We then investigated the efficacies of several different doses of PSC in a murine model. All treatments began 24 h after challenge and lasted for 7 days. The drug was administered twice a day to mice infected with three strains that showed intermediate PSC susceptibility (MIC = 2 microg/ml) and three PSC-susceptible strains (MIC = 0.25 microg/ml). A dose of 10 mg/kg of body weight was ineffective, while doses of 20 and 30 mg/kg prolonged the survival of the mice. The 50 strains tested were segregated into two groups on the basis of the in vitro data. For the group with the most strains (85%), the strains had low PSC MICs, mice infected with the strains showed higher rates of survival (30 to 40%), and PSC was able to reduce the fungal load in the kidney and less regularly in the brain. For the second group (15% of the strains), the strains had intermediate PSC MICs, mice infected with the strains had lower survival rates (10 to 20%), and PSC treatment resulted in variable and no reductions in the fungal loads in the kidneys and brains, respectively.

摘要

我们采用肉汤微量稀释法、Neo-Sensitabs 药敏纸片扩散法和最小杀菌浓度(MFC)测定法,评估了泊沙康唑(PSC)对 50 株临床米根霉的体外活性。一般来说,PSC 对该真菌的 MIC 较低,MIC 与抑菌圈直径相关。然而,大多数 MFC 比相应 MIC 高 1-4 个稀释度。然后,我们在一种小鼠模型中研究了几种不同剂量 PSC 的疗效。所有治疗均在感染后 24 小时开始,持续 7 天。药物每天两次给药,感染三种显示中间 PSC 敏感性(MIC = 2μg/ml)和三种 PSC 敏感菌株(MIC = 0.25μg/ml)的小鼠。10mg/kg 体重的剂量无效,而 20mg/kg 和 30mg/kg 的剂量可延长小鼠的存活时间。根据体外数据,将 50 株受试菌株分为两组。对于大多数菌株(85%)的组,菌株具有低 PSC MIC,感染菌株的小鼠具有更高的存活率(30-40%),PSC 能够降低肾脏中的真菌负荷,且更不规则地降低大脑中的真菌负荷。对于第二组(15%的菌株),菌株具有中间 PSC MIC,感染菌株的小鼠存活率较低(10-20%),PSC 治疗分别导致肾脏和大脑中的真菌负荷发生变化且无减少。