Liposome Encapsulation of Ciprofloxacin Improves Protection against Highly Virulent Francisella tularensis Strain Schu S4

被引:24
作者
Hamblin, Karleigh A. [1 ]
Armstrong, Stuart J. [1 ]
Barnes, Kay B. [1 ]
Davies, Carwyn [1 ]
Wong, Jonathan P. [2 ]
Blanchard, James D. [3 ]
Harding, Sarah V. [1 ]
Simpson, Andrew J. H. [1 ]
Atkins, Helen S. [1 ]
机构
[1] Def Sci & Technol Lab, Dept Biomed Sci, Salisbury, Wilts, England
[2] Def Res & Dev Canada, Suffield Res Ctr, Ralston, AB, Canada
[3] Aradigm Corp, Hayward, CA USA
关键词
BIOLOGICAL WEAPON; TULAREMIA; INFECTION; EFFICACY; ANTIBIOTICS; MACROPHAGES; DELIVERY; VACCINE; ANTHRAX; MOUSE;
D O I
10.1128/AAC.02555-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Liposome-encapsulated ciprofloxacin for inhalation (CFI) was investigated as a putative postexposure therapeutic for two strains of Francisella tularensis. The efficacies of oral ciprofloxacin and intranasally instilled CFI could not be distinguished in a mouse model of infection with the F. tularensis live vaccine strain (LVS), where a single dose of either formulation offered full protection against a lethal challenge. However, mouse studies with the more virulent Schu S4 strain of F. tularensis demonstrated that a higher level of protection against a lethal aerosol infection is provided by CFI than by oral ciprofloxacin. In addition, using this infection model, it was possible to discriminate the efficacy of intranasally instilled CFI from that of aerosolized CFI, with aerosolized CFI providing full protection after just a single dose. The improved efficacy of CFI compared to oral ciprofloxacin is likely due to the high sustained concentrations of ciprofloxacin in the lung. In summary, CFI may be a promising therapy, perhaps enabling the prophylactic regimen to be shortened, for use in the event of a deliberate release of F. tularensis. The prophylactic efficacy of CFI against other biological warfare (BW) threat agents also warrants investigation.
引用
收藏
页码:3053 / 3059
页数:7
相关论文
共 31 条
[21]  
Oyeka ICA, 2012, INT J ENG SCI TECHNO, V4, P811
[22]   Tularaemia:: Bioterrorism defence renews interest in Francisella tularensis [J].
Oyston, PCF ;
Sjostedt, A ;
Titball, RW .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (12) :967-978
[23]   Tularemia epidemic in northwestern Spain:: Clinical description and therapeutic response [J].
Pérez-Castrillón, JL ;
Bachiller-Luque, P ;
Martín-Luquero, M ;
Mena-Martín, FJ ;
Herreros, V .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (04) :573-576
[24]   In vivo efficacy of fluoroquinolones against systemic tularaemia infection in mice [J].
Piercy, T ;
Steward, J ;
Lever, MS ;
Brooks, TJG .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (06) :1069-1073
[25]  
Rowland M, 2010, CLIN PHARMACOKINET, P159
[26]   Liposome-encapsulated aminoglycosides in pre-clinical and clinical studies [J].
Schiffelers, R ;
Storm, G ;
Bakker-Woudenberg, I .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 (03) :333-344
[27]   INHALED ANTIBIOTICS FOR LOWER RESPIRATORY TRACT INFECTIONS: FOCUS ON CIPROFLOXACIN [J].
Serisier, D. J. .
DRUGS OF TODAY, 2012, 48 (05) :339-351
[28]   Inhaled, dual release liposomal ciprofloxacin in non-cystic fibrosis bronchiectasis (ORBIT-2): a randomised, double-blind, placebo-controlled trial [J].
Serisier, David J. ;
Bilton, Diana ;
De Soyza, Anthony ;
Thompson, Philip J. ;
Kolbe, John ;
Greville, Hugh W. ;
Cipolla, David ;
Bruinenberg, Paul ;
Gonda, Igor .
THORAX, 2013, 68 (09) :812-817
[29]   Treatment of murine pneumonic Francisella tularensis infection with gatifloxacin, moxifloxacin or ciprofloxacin [J].
Steward, J. ;
Piercy, T. ;
Lever, M. S. ;
Simpson, A. J. H. ;
Brooks, T. J. G. .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2006, 27 (05) :439-443
[30]   Liposome delivery of ciprofloxacin against intracellular Francisella tularensis infection [J].
Wong, JP ;
Yang, HM ;
Blasetti, KL ;
Schnell, G ;
Conley, J ;
Schofield, LN .
JOURNAL OF CONTROLLED RELEASE, 2003, 92 (03) :265-273