Preparation and characterization of cationic Pluronic for surface modification and functionalization of polymeric drug delivery nanoparticles

• DOI: 10.3144/expresspolymlett.2016.20
• Publication Date: 2016-01-05T15:49:58Z
• Authors: G. Gyulai; A. Magyar; J. Rohonczy; J. Orosz; M. Yamasaki; Sz. Bosze; E. Kiss
• Keywords: QD01 Analytical chemistry / analitikai kémia; Chemical technology; TP1-1185; 02 engineering and technology; Pluronic derivatization; Biodegradable polymers; 3. Good health; PLGA nanoparticles; QD04 Organic chemistry / szerves kémia; Peptide conjugation; TA401-492; 0210 nano-technology; Materials of engineering and construction. Mechanics of materials; Polymeric drug delivery

Biodegradable poly(lactic-co-glycolic acid) copolymer, PLGA nanoparticles (NPs) with a surface layer of poly (ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymers, Pluronics, are promising drug carrier systems. With the aim to increase the potential of targeted drug delivery the end group derivative of Pluronics was synthesized in a straightforward way to obtain Pluronic-amines. The formation of functional amine groups was confirmed by fluorescamine method and NMR analysis of their N-(tert-Butoxycarbonyl)-L-phenylalanine (Boc-Phe-OH) and N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine (Fmoc-Phe-OH) conjugates. Pluronic and Pluronic-amine stabilized PLGA NPs prepared by nanoprecipitation were characterized by dynamic light scattering and zeta potential measurements. All of the systems showed high colloidal stability checked by electrolyte induced aggregation, although the presence of Pluronicamine on the surface decreased the zeta potential in some extent. The introduction of reactive primary amine groups into the surface layer of PLGA NPs while preserving the aggregation stability, provides a possibility for coupling of various ligands allowing targeted delivery and also contributes to the improved membrane affinity of NPs.