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However, a key problem is the recovery difficulty of the copolymers forming aqueous two-phase systems.
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The methyl-substitution increased the solubility of the copolymers in organic solvents by disrupting copolymer aggregation.
Knowing the copolymer microstructure is useful to predict the properties of the copolymers.
Because the introduction of IBoA into the copolymer increased the T g values of the copolymers, we carefully controlled the copolymer compositions in order to exhibit similar T g values for the copolymers with and without the IBoA unit.
Crystallisation of the copolymers is complicated.
Scheme 1 describes the synthetic route of the copolymers.
The phase transition temperature of the copolymers could be tuned by variation of the monomers ratios.
After PEI conjugation to the side chain, the solubility of the copolymers significantly changed.
The biodistribution of the copolymers was evaluated by means of MRI, γ-scintigraphy and HPLC.
The structures of the copolymers were characterized by H NMR spectroscopy in CDCl3.
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