Efficient drug targeting to rat alveolar macrophages by pulmonary administration of ciprofloxacin incorporated into mannosylated liposomes for treatment of respiratory intracellular parasitic infections
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Chono, Sumio
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Hokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, JapanHokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, Japan
Chono, Sumio
[1
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Tanino, Tomoharu
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Hokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, JapanHokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, Japan
Tanino, Tomoharu
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Seki, Toshinobu
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Hokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, JapanHokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, Japan
Seki, Toshinobu
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Morimoto, Kazuhiro
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Hokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, JapanHokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, Japan
Morimoto, Kazuhiro
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[1] Hokkaido Pharmaceut Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Otaru, Hokkaido 0470264, Japan
The efficacy of pulmonary administration of ciprofloxacin (CPFX) incorporated into mannosylated liposomes (mannosylated CPFX-liposomes) for the treatment of respiratory intracellular parasitic infections was evaluated. In brief, mannosylated CPFX-liposomes with 4-aminophenyl-a-D-mannopyranoside (particle size: 1000 nm) were prepared, and the drug targeting to alveolar macrophages (AMs) following pulmonary administration was examined in rats. Furthermore, the antibacterial and mutant prevention effects of mannosylated CPFX-liposomes in AMs were evaluated by pharmacokinetic/pharmacodynamic (PK/PD) analysis. The targeting efficiency of CPFX to rat AMs following pulmonary administration of mannosylated CPFX-liposomes was significantly greater than that of CPFX incorporated into unmodified liposomes (unmodified CPFX-liposomes; particle size: 1000 nm). According to PK/PD analysis, the mannosylated CPFX-liposomes exhibited potent antibacterial effects against many bacteria although unmodified CPFX-liposomes were ineffective against several types of bacteria, and the probability of microbial mutation by mannosylated CPFX-liposomes was extremely low. The present study indicates that mannosylated CPFX-liposomes as pulmonary administration system could be useful for the treatment of respiratory intracellular parasitic infections. (C) 2007 Elsevier B.V. All rights reserved.