Poly(N-isopropylacrylamide) (PNIPAM) is a widely-studied polymers due to its excellent temperature sensitivity. PNIPAM-MAPOSS hybrid hydrogel, based on the introduction of acrylolsobutyl polyhedral oligomeric silsesquioxane (MAPOSS) into the PNIPAM matrix in the presence of polyethylene glycol, was prepared via radical polymerization. The modified hydrogels exhibited a thick, heterogeneous porous structure. PEG was used as a pore-forming agent to adjust the pore size. MAPOSS reduced the swelling ratios of gels, and decreased the LCST, causing the hydrogels to shrink at lower temperatures. However, its hydrophobicity helped to improve the temperature response rate. The incorporation of rigid MAPOSS into the polymer network greatly increased the compressive modulus of the hydrogel. It is worth noting that, by adjusting the amount of MAPOSS and PEG, the hydrogel could have both ideal mechanical properties and swelling behavior. In addition, hydrogel containing 8.33 wt % MAPOSS could achieve stable and sustained drug release. Thus, the prepared PNIPAM-MAPOSS hybrid hydrogel can serve as drug carrier for 5-fluorouracil and may have potential application in other biomedical fields.

An effective method was described here to improve the thermal insulation and stability of polysiloxane foam (SIF) by controlling the chain length of hydroxyl-terminated polydimethylsiloxane (OH-PDMS). A series of SIFs were prepared through foaming and cross-linking processes with different cross-linking densities. The morphology of SIF was investigated by environmental scanning electron microscopy. The results demonstrated that increasing the chain length of OH-PDMS reduced the average cell size from 932 μm to 220 μm. Cell density ranged from 4.92 × 10⁶ cells per cm³ to 1.64 × 10⁸ cells per cm³. The thermal insulation capability was significantly enhanced, and the SIF derived from the long-chain OH-PDMSs yielded a minimum thermal conductivity of 0.077 W mK⁻¹. Cell size reduction and an increase in cell density were considered to be the main factors to reduce thermal conductivity. Thermal stability, which was also improved, mainly depended on the free motion rate of the polysiloxane chains and cross-linking density of the polysiloxane networks.