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SCH51048在肺曲霉病实验模型中的评估。

Evaluation of SCH51048 in an experimental model of pulmonary aspergillosis.

作者信息

Allendoerfer R, Loebenberg D, Rinaldi M G, Graybill J R

机构信息

Department of Medicine, University of Texas Health Science Center at San Antonio, USA.

出版信息

Antimicrob Agents Chemother. 1995 Jun;39(6):1345-8. doi: 10.1128/AAC.39.6.1345.

Abstract

The efficacy of a novel triazole, SCH51048, was assessed with a murine model of pulmonary aspergillosis and was compared with those of SCH39304 and itraconazole. A wide range of doses of SCH51048 (5 to 50 mg/kg of body weight) was evaluated. Mortality was significantly delayed in mice treated with doses of 5 mg of SCH51048 per kg or greater in comparison with mortality in controls (P < 0.05). Both SCH51048 and SCH39304 at higher doses (30 and 50 mg/kg) reduced the number of viable Aspergillus fumigatus organisms in lung tissue (P < 0.05). In the present model, itraconazole neither delayed mortality nor significantly reduced the counts in tissue at the doses used. We conclude that SCH51048 is an effective therapy for murine pulmonary aspergillosis.

摘要

利用小鼠肺曲霉病模型评估了新型三唑类药物SCH51048的疗效,并将其与SCH39304和伊曲康唑的疗效进行了比较。评估了SCH51048的多种剂量(5至50毫克/千克体重)。与对照组相比,每千克给予5毫克或更高剂量SCH51048治疗的小鼠死亡率显著延迟(P<0.05)。较高剂量(30和50毫克/千克)的SCH51048和SCH39304均减少了肺组织中烟曲霉活菌数量(P<0.05)。在本模型中,伊曲康唑既未延迟死亡率,在所使用的剂量下也未显著减少组织中的菌数。我们得出结论,SCH51048是治疗小鼠肺曲霉病的有效疗法。

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本文引用的文献

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