Drug intelligence / Profile preview

inhaled liposomal ciprofloxacin

Development stage
Unknown
Lead developer
Aradigm
Modality
Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Inhalation
01

Overview

Inhaled liposomal ciprofloxacin is a formulation of the broad-spectrum fluoroquinolone antibiotic **ciprofloxacin** designed for pulmonary delivery via inhalation. In this formulation, ciprofloxacin is encapsulated in liposomes to allow **sustained release in the lungs**, increase drug residence time, and minimize systemic exposure. This improves tolerability, reduces dosing frequency, and allows for high local concentrations, targeting respiratory pathogens (notably *Pseudomonas aeruginosa*) in diseases such as **cystic fibrosis** and **non-cystic fibrosis bronchiectasis**. The liposomal encapsulation also facilitates ciprofloxacin uptake by phagocytic cells, potentially enhancing treatment of intracellular infections, including nontuberculous mycobacteria. Two main products have been developed: Lipoquin (liposomal ciprofloxacin) and Pulmaquin (dual release, combining free and liposomal ciprofloxacin). The mechanism of action is **inhibition of bacterial topoisomerase II (DNA gyrase) and IV**, thus blocking bacterial DNA replication and transcription[1][3][4].

Brand names
LipoquinPulmaquin
Other names
liposomal ciprofloxacin for inhalationciprofloxacin for inhalationinhaled liposomal ciprofloxacindual release ciprofloxacin for inhalation
02

Targets

DNA gyraseTopo IV (Bacterial Topoisomerase IV)

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