Mannose-displaying fluorescent framboidal nanoparticles containing phenylboronic acid groups as a potential drug carrier for macrophage targeting.

Colloids Surf B Biointerfaces

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan; Frontier Research Center, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

Published: December 2015

AI Article Synopsis

  • Functional polymeric nanoparticles (PBA NPs) with framboidal morphology were created using a unique one-step polymerization method involving specific monomers and crosslinkers.
  • Fluorescent and mannosylated PBA NPs were developed for applications like drug delivery and bioimaging, incorporating Nile Blue for fluorescence and mannosamine for targeted function.
  • Cellular uptake studies indicated that mannosylated PBA NPs are selectively absorbed by macrophages, suggesting their potential for targeted drug delivery to immune cells.

Article Abstract

Functional polymeric nanoparticles have been used for various applications in the biomaterials field. Recently, we reported phenylboronic acid-containing nanoparticles (PBA NPs) having an unique framboidal morphology, prepared in a single-step by the aqueous dispersion polymerization of N-acryloyl-3-aminophenylboronic acid (PBAAM) in the presence of poly(ethylene glycol) acrylamide (PEGAM) as a polymerizable dispersant and N,N'-methylenebisacrylamide (MBAM) as a crosslinker. In this study, we prepared mannosylated and fluorescent PBA NPs that could be used for different applications such as drug delivery and bioimaging. Fluorescent PBA NPs were synthesized by including the fluorescent Nile Blue acrylamide monomer in the reaction mixture during the dispersion polymerization of PBAAM. By using a carboxyl group-bearing PEGAM dispersant, carboxyl group-bearing PBA NPs were prepared that were modified with mannosamine to yield mannosylated PBA NPs. Cellular uptake studies showed that the mannosylated PBA NPs were selectively taken up by murine RAW264.7 macrophages. These results show that PBA NPs allow for flexible modification with various functionalities and could therefore be a potential platform for targeted delivery of drugs to macrophages.

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Source
http://dx.doi.org/10.1016/j.colsurfb.2015.11.011DOI Listing

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