Core-shell type multiarm star poly(ε-caprolactone) with high molecular weight hyperbranched polyethylenimine as core: Synthesis, characterization and encapsulation properties

Abstract

Core-shell type multiarm star copolymers with poly(ε-caprolactone) (PCL) as shells and hyperbranched polyethylenimine (PEI) as core have been successfully prepared by the Sn(Oct) 2 catalyzed ring-opening polymerization of ε-caprolactone (CL) using high molecular weigh PEIs directly as macroinitiators. The initiation efficiency is in the range of 91–95% for PEI with M n = 10 4 (PEI10K) and only around 60% for PEI with M n = 2.5 × 10 4 (PEI25K), leading to star polymers with an average arm number in the range of 155–276. The thermal property of the obtained multiarm star polymers were also investigated by DSC. The melting and crystallization temperatures of the star polymers increase as the PCL arm length increases when the PEI core is fixed. The fusion enthalpy, crystalline enthalpy and degree of crystallinity values of the star polymers with PEI10K core are less than those with PEI1.8K core. Due to the polarity difference between PCL arm and PEI core, the resulting multiarm star polymers can act as inverted micellar nanocapsules capable of extracting and encapsulating water soluble guests. Increasing the size and polarity of the hydrophilic PEI core of the star nanocapsules are two effective ways to enhance their hydrophilic guest encapsulation capacity. Increasing the hydrophobic PCL arm length can increase the molar ratio, whereas reduce the weight ratio of the encapsulated hydrophilic guests to the star nanocapsules. Unexpectedly, the obtained nanocapsules can entrap the bigger size hydrophilic congo red guests more than the smaller size methyl orange.