Novel polymeric nanoparticles targeting the lipopolysaccharides of Pseudomonas aeruginosa

Considering outburst of various infectious diseases globally, nanoparticle assisted targeted drug delivery has emerged as a promising strategy that can enhance the therapeutic efficacy and minimize the undesirable side effects of an antimicrobial agents. Molecular imprinting is a newly developed strategy that can synthesize a drug carrier with highly stable ligand-like ‘cavity’, may serve as a new platform of ligand-free targeted drug delivery systems. In this study, we use the amphiphilic lipopolysaccharides, derived from Pseudomonas aeruginosa as imprinting template and obtained an evenly distributed sub-40 nm polymeric nanoparticles by using inverse emulsion method. These molecularly imprinted nanoparticles (MIPNPs) showed specific binding to the lipopolysaccharide as determined by fluorescence polarization and microscale thermophoresis. MIPNPs showed selective recognition of target bacteria as detected by flow cytometry. Additionally, MIPNPs exhibited the in vivo targeting capabilities in both the keratitis model and meningitis model. Moreover, the photosensitizer methylene blue-loaded MIPNPs presented significantly strong inhibition of bacterial Growth, compared to non-imprinted controls for in vitro model of the photodynamic therapy. Our study shows an attempt to design a magic bullet by molecular imprinting that may provide a novel approach to generate synthetic carrier for targeting pathogen and treatment for a variety of infectious human diseases.

We used serotype specific LPS as a natural template and a process of inverse microemulsion polymerization to prepare surface molecularly imprinted NPs that exhibited highly specific targeting to P. aeruginosa strains and infection sites, both in vivo and in vitro. In combination with drug delivery, these “magic plastic bullets” could serve as a promising alternative to the ligand-modified nanocarriers currently used for targeted diagnosis and therapy.Figure optionsDownload high-quality image (177 K)Download as PowerPoint slide