2021
DOI: 10.1007/s00289-020-03533-5
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Stimuli-responsive polymersomes of poly [2-(dimethylamino) ethyl methacrylate]-b-polystyrene

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Cited by 9 publications
(3 citation statements)
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“…For instance, the formation of nanosized aggregates appears to take place when poly­(allylamine hydrochloride) (PAH) solutions is mixed with phosphate and polyphosphate anions. , As solution conformations of PAH change and nanoaggregates form even when adding monovalent H 2 PO 4 – , it seems likely that intermolecular forces other than electrostatic ones may play a role in driving the phenomenon. In particular, the formation of charged hydrogen bonds (c-H-bonds) between the ammonium cation and the phosphate anions may help explaining the described behavior as well as the unusually low “slip plane” potential measured for polymersomes with PDMAEMA arms in the presence of a phosphate buffer with pH ∼ 8 . The formation of c-H-bonds between poly­(acrylic acid) and the sulfonate group in sulfobetaine tensides (i.e., surfactants), , or between ω-carboxylic and carboxylate groups in surfactants, was also suggested to be involved in lowering the critical micelle concentration of the mentioned surfactants.…”
Section: Introductionmentioning
confidence: 92%
“…For instance, the formation of nanosized aggregates appears to take place when poly­(allylamine hydrochloride) (PAH) solutions is mixed with phosphate and polyphosphate anions. , As solution conformations of PAH change and nanoaggregates form even when adding monovalent H 2 PO 4 – , it seems likely that intermolecular forces other than electrostatic ones may play a role in driving the phenomenon. In particular, the formation of charged hydrogen bonds (c-H-bonds) between the ammonium cation and the phosphate anions may help explaining the described behavior as well as the unusually low “slip plane” potential measured for polymersomes with PDMAEMA arms in the presence of a phosphate buffer with pH ∼ 8 . The formation of c-H-bonds between poly­(acrylic acid) and the sulfonate group in sulfobetaine tensides (i.e., surfactants), , or between ω-carboxylic and carboxylate groups in surfactants, was also suggested to be involved in lowering the critical micelle concentration of the mentioned surfactants.…”
Section: Introductionmentioning
confidence: 92%
“…Factors that control the morphology of vesicles include size, wall thickness (a function of the molecular weight of the constituent macromolecules), deformation (due to the pressure difference between the internal lumen and external medium of the vesicle during preparation), and surface topology (modification of the vesicle surface by inserting different compounds or combining vesicle-forming macromolecules) . The architecture of the copolymer can influence the morphology of self-assemblies, and the macromolecules that have been employed for vesicle formation have included block and graft copolymers, as well as branched polymers, in particular, miktoarm stars with asymmetric branching containing at least three polymeric arms. …”
Section: Introductionmentioning
confidence: 99%
“…More than two decades ago, PDMAEMA and its copolymers were synthesized and evaluated as gene transfer agents and carrier systems for DNA [ 32 , 33 ]. Often, they are combined with petrochemical based polymers [ 34 ] or biobased polymers [ 35 , 36 ]. Water swelling tests on interpenetrating network (IPN) hydrogels based on nanofibrillated cellulose (NFC) and PDMAEMA prepared via crosslinking free radical polymerization showed that the IPN hydrogels were both pH-sensitive and temperature-sensitive.…”
Section: Introductionmentioning
confidence: 99%