Nanoscale Structures of Poly(oligo ethylene glycol methyl ether methacrylate) Hydrogels Revealed by Small-Angle Neutron Scattering
Nanoscale Structures of Poly(oligo ethylene glycol methyl ether methacrylate) Hydrogels Revealed by Small-Angle Neutron Scattering
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DOI:
10.1021/acs.macromol.1c02259
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发表时间:
2022-02
期刊:
影响因子:
5.5
通讯作者:
Takuma Kureha;Masashi Ohira;Yuki Takahashi;Xiang Li;E. Gilbert;M. Shibayama
中科院分区:
文献类型:
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作者:
Takuma Kureha;Masashi Ohira;Yuki Takahashi;Xiang Li;E. Gilbert;M. Shibayama
The nanostructures of temperature-responsive and biocompatible gels were investigated by small-angle neutron scattering (SANS). The gels were copolymerized using two types of monomers with different ethylene glycol side chain lengths: diethylene glycol methacrylate (MeO2MA) (short side chain) and oligo-ethylene glycol methyl ether methacrylate (OEGMA) (long side chain). The temperature-responsive behavior was ascribed to the nanoscale structures and depended on the copolymerization ratio. The SANS profiles of swollen OEGMA-rich gels exhibited a characteristic peak, indicating a strong correlation with the hydrophobic main chain domains in the hydrophilic matrix. The long hydrophilic side chains of OEGMA acted as a cushioning material between the domains. On the other hand, the domains were randomly distributed in the MeO2MA-rich gels. As the temperature increased, the domains grew in the gels due to hydrophobic interactions between the dehydrated polymers. As a result, the peaks, that is, the domain periodicity, disappeared in the SANS profiles. The results of this study should lead to a synthesis strategy to control the physical properties and structures of such hydrogels for advanced applications, for example, biofilms, coatings, and carriers.