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Characterization of Nanoparticles Using DSPE-PEG2000 and Soluplus

R. Takayama, Yutaka Inoue, Isamu Murata, Ikuo Kanamoto

2020Colloids and Interfaces22 citationsDOIOpen Access PDF

Abstract

The aim of this study was to evaluate the characterized hydration method to prepare nanoparticles using Soluplus, a block copolymer with amphipathic properties, and distearoyl phosphatidyl ethanolamine (DSPE)-PEG2000 owing to particle size distribution, zeta potential, particle stability, and transmission electron microscopy (TEM) observed and 31P-NMR spectra. The results showed that, in a suspension of DSPE-PEG2000 and Soluplus at a ratio of 1/1, the prepared microparticles were stable for five days in the dark and at 25 °C. It was also confirmed that the 1/1 suspension of DSPE-PEG2000/Soluplus was stable for five days under the same conditions with the magnesium chloride solution. TEM measurements confirmed the presence of micelle-like particles of 50 to 150 nm in the 1/1 ratio mix of DSPE-PEG2000/Soluplus. 31P-NMR spectral data confirmed that DPSE-PEG2000/Soluplus at mixing ratio of 1/1 has a strong intermolecular with the phosphate group, indicated by the fact that the peak shift and the full width at half maximum were the largest compared with DSPE-PEG2000 with the intermolecular interaction. On the basis of the findings of this study, we conclude that microparticles can be formed using DSPE-PEG2000 and Soluplus via the hydration method, and that the optimum weight ratio of DSPE-PEG2000 to Soluplus is 1/1.

Topics & Concepts

MicelleZeta potentialChemistrySuspension (topology)Particle (ecology)Intermolecular forceDynamic light scatteringParticle sizeCopolymerMaterials scienceNanoparticleChemical engineeringAqueous solutionNanotechnologyPhysical chemistryOrganic chemistryMoleculeGeologyMathematicsPure mathematicsPolymerOceanographyEngineeringHomotopyNanoparticle-Based Drug DeliveryAdvanced Drug Delivery SystemsSurfactants and Colloidal Systems