“…Additionally, zwitterionic homopolymers show intra-as well as interchain interaction, depending on conditions such as the ionic strength of the solution. [39] All block copolymers prepared were analysed using dynamic light scattering after dissolving the polymers in methanol and diluting the solution with deionised water. Since the particle size can be influenced by the concentration, [36,40] all samples were measured at a constant concentration of 1 mg of polymer in 1 mL solution at 25 8C.…”
Section: Self-organisation Of Block Copolymersmentioning
Amphiphilic block copolymers composed of poly(butyl acrylate) and poly(2-acryloyloxyethyl phosphorylcholine) have been prepared using reversible addition fragmentation transfer (RAFT) polymerisation. The conversion of the polymerisation was determined using online FT NIR spectroscopy. NMR spectroscopy was used not only to support the results obtained from FT NIR spectroscopy but also prove the formation of micelles. Due to the strong aggregation tendency of these block copolymers and the resulting difficulties concerning the molecular weight analysis test experiments were carried out replacing poly(2-acryloyloxyethyl phosphorylcholine) with poly(2-hydroxyethyl acrylate). Micelle size and the aggregation behaviour were investigated using dynamic light scattering. The sizes of the nanocontainers obtained were found to be influenced by the block length as well as the solvent leading to micelles in the range between 40 and 160 nm. The toxicity of the RAFT agent used was then analysed by cell growth inhibition tests.
“…Additionally, zwitterionic homopolymers show intra-as well as interchain interaction, depending on conditions such as the ionic strength of the solution. [39] All block copolymers prepared were analysed using dynamic light scattering after dissolving the polymers in methanol and diluting the solution with deionised water. Since the particle size can be influenced by the concentration, [36,40] all samples were measured at a constant concentration of 1 mg of polymer in 1 mL solution at 25 8C.…”
Section: Self-organisation Of Block Copolymersmentioning
Amphiphilic block copolymers composed of poly(butyl acrylate) and poly(2-acryloyloxyethyl phosphorylcholine) have been prepared using reversible addition fragmentation transfer (RAFT) polymerisation. The conversion of the polymerisation was determined using online FT NIR spectroscopy. NMR spectroscopy was used not only to support the results obtained from FT NIR spectroscopy but also prove the formation of micelles. Due to the strong aggregation tendency of these block copolymers and the resulting difficulties concerning the molecular weight analysis test experiments were carried out replacing poly(2-acryloyloxyethyl phosphorylcholine) with poly(2-hydroxyethyl acrylate). Micelle size and the aggregation behaviour were investigated using dynamic light scattering. The sizes of the nanocontainers obtained were found to be influenced by the block length as well as the solvent leading to micelles in the range between 40 and 160 nm. The toxicity of the RAFT agent used was then analysed by cell growth inhibition tests.
“…[24] Previous reports also have thoroughly examined the difference in dilute aqueous solution properties such as viscosity, hydrodynamic diameter, cloud point, and the degree of binding. [25][26][27][28][29][30][31] These properties provide a reasonable assessment of the macroscopic behavior, however, a detailed analysis using a more sensitive characterization method is required. When naphthalene labels were incorporated into the water-soluble polymer, photophysical properties and the behavior of polymers in aqueous solution could be clearly defined.…”
“…Before UV irradiation, the <R g >/<R h > values of the micelles gradually decreased from 2.1 to 1.4 with raising temperature below LCST, while both the <R g > and <R h > decreased a little as shown in Figure 7 (B), because of intrachain contraction of thermo-responsive PNIPAM chains. 75 The lower value of <R g >/<R h > further confirmed that the collapsed PNIPAM chain became the denser shell in the core-shell micelle. After rather broad size distribution, which is close to the R h of particles in solution obtained by DLS analysis.…”
Section: A C C E P T E D Accepted Manuscriptmentioning
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