期刊
CHEMICAL SCIENCE
卷 13, 期 1, 页码 39-43出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1sc05398a
关键词
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资金
- National Natural Science Foundation of China [21972057]
- Fundamental Research Funds for the Central Universities [JUSRP21937]
- MOE [B13025]
- Hong Kong Special Administration Region (HKSAR) General Research Fund [CUHK14304619, 2130642]
- Central Laboratory, School of Chemical and Material Engineering, Jiangnan University
- SAFEA [B13025]
This paper successfully fabricated a hybrid poly(N-isopropylacrylamide)-based microgel with tunable wettability from hydrophilicity to hydrophobicity through temperature regulation. By synthesizing engineered microgels in inverse emulsions stabilized with hydrophobic silica nanoparticles and utilizing swelling-induced feature, the microgel can undergo phase inversion with temperature change, stabilizing Pickering emulsions and achieving stability of water-in-oil emulsions with encapsulated enzymes.
Thermo-responsive microgels are unique stabilizers for stimuli-sensitive Pickering emulsions that can be switched between the state of emulsification and demulsification by changing the temperature. However, directly temperature-triggering the phase inversion of microgel-stabilized emulsions remains a great challenge. Here, a hybrid poly(N-isopropylacrylamide)-based microgel has now been successfully fabricated with tunable wettability from hydrophilicity to hydrophobicity in a controlled manner. Engineered microgels are synthesized from an inverse emulsion stabilized with hydrophobic silica nanoparticles, and the swelling-induced feature can make the resultant microgel behave like either hydrophilic or hydrophobic colloids. Remarkably, the phase inversion of such microgel-stabilized Pickering emulsions can be in situ regulated by temperature change. Moreover, the engineered microgels were capable of stabilizing water-in-oil Pickering emulsions and encapsulation of enzymes for interfacial bio-catalysis, as well as rapid cargo release triggered by phase inversion.
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