Efficacy of prophylactic aerosol amphotericin B lipid complex in a rat model of pulmonary aspergillosis

被引:53
作者
Cicogna, CE
White, MH
Bernard, EM
Ishimura, T
Sun, M
Tong, WP
Armstrong, D
机构
[1] MEM SLOAN KETTERING CANC CTR,INFECT DIS SERV,NEW YORK,NY 10021
[2] MEM SLOAN KETTERING CANC CTR,DEPT BIOSTAT & EPIDEMIOL,NEW YORK,NY 10021
[3] MEM SLOAN KETTERING CANC CTR,PHARMACOL LAB,NEW YORK,NY 10021
关键词
D O I
10.1128/AAC.41.2.259
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Invasive pulmonary aspergillosis remains an important cause of morbidity and mortality among transplant recipients and patients receiving cancer chemotherapy, The lipid-associated formulation of amphotericin B (AmB), AmB lipid complex (ABLC), was evaluated for its prophylactic efficacy when it was administered as an aerosol in a rat model of pulmonary aspergillosis. Aerosol ABLC (aero-ABLC), in doses from 0.4 to 1.6 mg/kg of body weight given 2 days before infection, significantly delayed mortality compared to the mortality of rats given placebo (P < 0.001), At day 10 postinfection, 50% of rats in the 0.4-mg/kg group and 75% of rats in the 1.6-mg/kg group were alive, while all control animals had died, In a second trial aero-ABLC was more effective than an equivalent dose of aerosol AmB (aero-AmB) in prolonging survival, with 100% survival at day 14 postinfection in the ABLC group, compared to 62.5% survival in the AmB group, Mean concentrations of AmB in lungs were 3.7 times higher at day 1 (P < 0.002) and almost six times higher at day 7 (P < 0.001) after treatment with aero-ABLC than after treatment with a similar dose of aero-AmB. We conclude that aero-ABLC provided higher and more prolonged levels of the parent compound in the lungs than aero-AmB and was more effective in delaying mortality from aspergillosis in this model.
引用
收藏
页码:259 / 261
页数:3
相关论文
共 17 条
[1]   PROPHYLACTIC EFFICACY OF AEROSOLIZED LIPOSOMAL (AMBISOME) AND NON-LIPOSOMAL (FUNGIZONE) AMPHOTERICIN-B IN MURINE PULMONARY ASPERGILLOSIS [J].
ALLEN, SD ;
SORENSEN, KN ;
NEJDL, MJ ;
DURRANT, C ;
PROFFIT, RT .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 34 (06) :1001-1013
[2]  
[Anonymous], 35 INT C ANT AG CHEM
[3]   AEROSOL AMPHOTERICIN-B FOR PREVENTION OF INVASIVE PULMONARY ASPERGILLOSIS [J].
BEYER, J ;
BARZEN, G ;
RISSE, G ;
WEYER, C ;
MIKSITS, K ;
DULLENKOPF, K ;
HUHN, D ;
SIEGERT, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (06) :1367-1369
[4]   DISTRIBUTION AND ACTIVITY OF AMPHOTERICIN-B IN HUMANS [J].
CHRISTIANSEN, KJ ;
BERNARD, EM ;
GOLD, JWM ;
ARMSTRONG, D .
JOURNAL OF INFECTIOUS DISEASES, 1985, 152 (05) :1037-1043
[5]   AMPHOTERICIN-B LIPID COMPLEX THERAPY OF EXPERIMENTAL FUNGAL-INFECTIONS IN MICE [J].
CLARK, JM ;
WHITNEY, RR ;
OLSEN, SJ ;
GEORGE, RJ ;
SWERDEL, MR ;
KUNSELMAN, L ;
BONNER, DP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (04) :615-621
[6]   THERAPEUTIC EVALUATION OF FREE AND LIPOSOME-ENCAPSULATED AMPHOTERICIN-B IN THE TREATMENT OF SYSTEMIC CANDIDIASIS IN MICE [J].
GONDAL, JA ;
SWARTZ, RP ;
RAHMAN, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (09) :1544-1548
[7]   THE TOXICITY OF DAILY INHALED AMPHOTERICIN-B [J].
GRYN, J ;
GOLDBERG, J ;
JOHNSON, E ;
SIEGEL, J ;
INZERILLO, J .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1993, 16 (01) :43-46
[8]  
HEINEMANN V, 1992, ANN HEMATOL S1, V78, pA110
[9]   TREATMENT OF SYSTEMIC FUNGAL-INFECTIONS WITH LIPOSOMAL AMPHOTERICIN-B [J].
LOPEZBERESTEIN, G ;
BODEY, GP ;
FAINSTEIN, V ;
KEATING, M ;
FRANKEL, LS ;
ZELUFF, B ;
GENTRY, L ;
MEHTA, K .
ARCHIVES OF INTERNAL MEDICINE, 1989, 149 (11) :2533-2536
[10]  
MEYER RD, 1973, AM J MED, V56, P6