The debranched starch was obtained from normal corn starch by enzymatic modification according to the method (Sun, Li, Dai, Ji, & Xiong, 2014). Briefly, the gelatinized starch slurry (20% wt) was cooled to 58 °C, debranched with pullulanase (4, 8, and 12 h), and then heated in boiling water for pullulanase deactivation. Finally, DBS powders were obtained by freeze-dried (-80℃ for 72 h) and the corresponding samples were coded as DBS4, DBS8, and DBS12, respectively.
The fabrication of Gels was according to our previous method (Qin et al., 2020). Firstly, PVA powder (4% wt) was dispersed in deionized water at 90 °C and stirred for 1 h until PVA was dissolved completely. Subsequently, the DBS and PVA homogeneous solution was prepared by the addition of DBS powders (10% wt) into cooled PVA solution (25 °C) and stirred at 135 °C for 30 min in an oil-bath. To avoid the evaporation of water, the heating and stirring process was performed in a hermetically sealed flask. Furthermore, the solution was sonicated for 5 min to remove residual bubbles. The resultant solution was quickly poured into the cylindrical molds (Φ = 25 and 4 mm), and then retrograded (4 °C for 24 h) to form a starch network. After that, the specimen was treated with a frozen and thawed cycle (-40 °C for 8 h and 25 °C for 4 h) to further obtain PVA network. Note that the freeze–thaw cycle was applied two times. Finally, the as-prepared hydrogels were coded as Gel4, Gel8, and Gel12, respectively.
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