Aerosolized nanostructured itraconazole as prophylaxis against invasive pulmonary aspergillosis

被引:32
作者
Alvarez, Carlos A.
Wiederhold, Nathan P.
McConville, Jason T.
Peters, Jay I.
Najvar, Laura K.
Graybill, John R.
Coalson, Jacqueline J.
Talbert, Robert L.
Burgess, David S.
Bocanegra, Rosie
Johnston, Keith P.
Williams, Robert O., III
机构
[1] Univ Texas, Hlth Sci Ctr, PERC, San Antonio, TX 78229 USA
[2] Univ Texas, Coll Pharm, Univ Stn 1, Austin, TX 78712 USA
[3] Univ Texas, Hlth Sci Ctr, Dept Med, Div Pulm Dis Crit Care Med, San Antonio, TX 78229 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Med, Div Infect Dis, San Antonio, TX 78229 USA
[5] Univ Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX 78229 USA
[6] Univ Texas, Coll Engn, Dept Chem Engn, Univ Stn 1, Austin, TX 78712 USA
关键词
invasive aspergillosis; prophylaxis; itraconazole; AMPHOTERICIN-B DEOXYCHOLATE; MURINE MODEL; ANTIFUNGAL PROPHYLAXIS; FUNGAL-INFECTIONS; IN-VITRO; EFFICACY; THERAPY; MULTICENTER; FLUCONAZOLE; TRIAZOLE;
D O I
10.1016/j.jinf.2007.01.014
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objective: Prophylactic strategies against invasive pulmonary aspergillosis are often limited by drug interactions and toxicities. Targeted airway delivery of antifungals to the lungs may avoid these pitfalls. We evaluated the effectiveness of an aerosolized nanostructured formulation of itraconazole produced by spray freezing into liquid (SFL) as prophylaxis against invasive pulmonary aspergillosis caused by A. fumigatus. Methods: Immunocompromised Balb/C mice received either itraconazole by oral gavage (Sporanox Oral Liquid [SOL] 30 mg/kg TID) or by aerosolization (SFL 30 mg/kg via 20 min aerosolizations, or control, BID). Dosing began 2 days prior to pulmonary inoculation with A. fumigatus and continued for 7 days post-inoculation. Changes in lung histopathology were also assessed. In the survival arm, mice were monitored over a 5 day period following discontinuation of therapy and survival was assessed by Kaplan-Meier analysis. Results: SFL survival (35%) was greater compared to control (10%; p = 0.03) and SOL (10%; p = 0.02). Histopathology demonstrated severe invasive disease involving vessels and small airways in control and SOL animals. SFL animals demonstrated colonization with some invasion predominately of large airways. Conclusions: Prophylactic aerosolization of nanostructured SFL significantly improved survival and limited invasive disease of small airways due to A. fumigatus. (c) 2007 The British Infection Society. Published by Elsevier Ltd. All rights reserved.
引用
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页码:68 / 74
页数:7
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