Efficient drug targeting to rat alveolar macrophages by pulmonary administration of ciprofloxacin incorporated into mannosylated liposomes for treatment of respiratory intracellular parasitic infections
Abstract
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.
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Mannose-functionalized liposomes showed a 1.5-fold higher exposure in alveolar macrophages compared with unmodified liposomes.
“Mannose-functionalized liposomes showed a 1.5-fold higher exposure in alveolar macrophages compared with unmodified liposomes.”
From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [54]
In comparison with free drug, targeted liposomes showed a 23-fold higher bioavailability in the alveolar macrophages.
“In comparison with the free drug, the targeted liposomes showed a 23-fold higher bioavailability in the alveolar macrophages.”
From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [54]
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References 72 · Cited by 164
- Authors
- Chono, S., Tanino, T., Seki, T., & Morimoto, K.
- Affiliations
- Hokkaido Pharmaceutical University (JP)
- Corresponding author
- Chono, Sumio
- ORCID
- Chono, Sumio
- Venue
- Journal of Controlled Release
- Publisher
- Elsevier BV
- Published
- 2008-04
- Volume
- 127
- Issue
- 1
- Pages
- 50-58
- ISSN
- 0168-3659 (ISSN-L)
- OpenAlex
- W2058365894
- Cited by
- 164
- References
- 72
- Citations by year
- 2025: 10 · 2024: 9 · 2023: 8 · 2022: 9 · 2021: 14 · 2020: 10 · 2019: 10 · 2018: 14 · 2017: 11 · 2016: 8 · 2015: 10 · 2014: 13 · 2013: 12 · 2012: 8
- FWCI
- 2.87
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of Controlled Release (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Hokkaido University
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Inhalation and Respiratory Drug Delivery
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Keywords
- ciprofloxacin, mannosylated liposomes, pulmonary drug delivery, alveolar macrophages, targeted drug delivery, pharmacokinetics/pharmacodynamics, antibacterial activity, liposomal drug delivery
- MeSH terms
- Animals, Anti-Bacterial Agents, Cell Line, Ciprofloxacin, Liposomes, Lung, Male, Mannosides, Microbial Sensitivity Tests, Particle Size, Pneumonia, Respiratory Tract Infections, Surface Properties, Tissue Distribution, Macrophages, Alveolar, Rats, Sprague-Dawley, Rats
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