Aerosol delivery of liposome-encapsulated ciprofloxacin: Aerosol characterization and efficacy against Francisella tularensis infection in mice

被引:57
作者
Conley, J
Yang, HM
Wilson, T
Blasetti, K
DiNinno, V
Schnell, G
Wong, JP
机构
[1] DEF RES ESTAB SUFFIELD, MED COUNTERMEASURES SECT, RALSTON, AB, CANADA
[2] SCILAB CONSULTING INC, RALSTON, AB, CANADA
关键词
D O I
10.1128/AAC.41.6.1288
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aerosol delivery of liposome-encapsulated ciprofloxacin by using 12 commercially available jet nebulizers was evaluated in this study. Aerosol particles containing liposome-encapsulated ciprofloxacin generated by the nebulizers were analyzed with a laser aerodynamic particle sizer. Mean mass aerodynamic diameters (MMADs) and geometric standard deviations (GSDs) were determined, and the drug contents of the sampling filters from each run onto which aerosolized liposome-encapsulated ciprofloxacin had been deposited were analyzed spectrophotometrically. The aerosol particles of liposome-encapsulated ciprofloxacin generated by these nebulizers ranged from 1.94 to 3.5 mu m, with GSDs ranging from 1.51 to 1.84 mu m. The drug contents of the sampling filters exposed for 1 min to aerosolized liposome-encapsulated ciprofloxacin range from 12.7 to 40.5 mu g/ml (0.06 to 0.2 mg/filter). By using the nebulizer selected on the basis of most desirable MMADs, particle counts, and drug deposition, aerosolized liposome-encapsulated ciprofloxacin was used for the treatment of mice infected with 10 times the 50% lethal dose of Francisella tularensis. All mice treated with aerosolized liposome-encapsulated ciprofloxacin survived the infection, while all ciprofloxacin-treated or untreated control mice succumbed to the infection (P < 0.001). These results suggest that aerosol delivery of liposome-encapsulated ciprofloxacin to the lower respiratory tract is Feasible and that ii: may provide an effective therapy for the treatment of respiratory tract infections.
引用
收藏
页码:1288 / 1292
页数:5
相关论文
共 30 条
[1]   SAFETY AND PHARMACOKINETICS OF RIMANTADINE SMALL-PARTICLE AEROSOL [J].
ATMAR, RL ;
GREENBERG, SB ;
QUARLES, JM ;
WILSON, SZ ;
TYLER, B ;
FELDMAN, S ;
COUCH, RB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (11) :2228-2233
[2]  
Bergogne-Berezin E., 1993, QUINOLONES B, V10, P1
[3]   CIPROFLOXACIN, A QUINOLONE CARBOXYLIC-ACID COMPOUND ACTIVE AGAINST AEROBIC AND ANAEROBIC-BACTERIA [J].
CHIN, NX ;
NEU, HC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 25 (03) :319-326
[4]   THERAPEUTIC AEROSOLS .2. DRUGS AVAILABLE BY THE INHALED ROUTE [J].
CLARKE, SW ;
NEWMAN, SP .
THORAX, 1984, 39 (01) :1-7
[5]  
DEBS RJ, 1987, AM REV RESPIR DIS, V135, P731
[6]  
DININNO VL, 1993, J INFECT DIS, V168, P793
[7]   TECHNETIUM-99M AS A MARKER OF LIPOSOMAL DEPOSITION AND CLEARANCE IN THE HUMAN-LUNG [J].
FARR, SJ ;
KELLAWAY, IW ;
PARRYJONES, DR ;
WOOLFREY, SG .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1985, 26 (03) :303-316
[8]   COMPARATIVE INVITRO ACTIVITIES OF CIPROFLOXACIN AND OTHER 4-QUINOLONES AGAINST MYCOBACTERIUM-TUBERCULOSIS AND MYCOBACTERIUM-INTRACELLULARE [J].
FENLON, CH ;
CYNAMON, MH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (03) :386-388
[9]   LIVE VACCINE STRAIN OF FRANCISELLA-TULARENSIS - INFECTION AND IMMUNITY IN MICE [J].
FORTIER, AH ;
SLAYTER, MV ;
ZIEMBA, R ;
MELTZER, MS ;
NACY, CA .
INFECTION AND IMMUNITY, 1991, 59 (09) :2922-2928
[10]   INVITRO ACTIVITIES OF NORFLOXACIN AND CIPROFLOXACIN AGAINST MYCOBACTERIUM-TUBERCULOSIS, MYCOBACTERIUM-AVIUM COMPLEX, M-CHELONEI, MYCOBACTERIUM-FORTUITUM, AND MYCOBACTERIUM-KANSASII [J].
GAY, JD ;
DEYOUNG, DR ;
ROBERTS, GD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 26 (01) :94-96