凝聚
羧甲基纤维素
明胶
化学
表征(材料科学)
纤维素
机制(生物学)
化学工程
钠
色谱法
材料科学
生物化学
纳米技术
有机化学
哲学
工程类
认识论
作者
Emmanuel Duhoranimana,Eric Karangwa,Lingfeng Lai,Xing Xu,Jin Yu,Shuqin Xia,Xiaoming Zhang,Bertrand Muhoza,Ildephonse Habinshuti
标识
DOI:10.1016/j.foodhyd.2017.01.035
摘要
The complexation mechanism of gelatin (G) and carboxymethyl cellulose (CMC) and their coacervates formation process were studied as a function of pH and protein (Pr) to polysaccharide (Ps) mixing ratio (Pr:Ps). Three different CMCs were chosen (FL9, FH9 and FVH6) and five mixing ratio of 1:1, 6:1, 7:1, 8:1 and 9:1 (w/w), were studied to disclose their individual coacervates transition pattern for zeta potential, turbidity, morphology, size distribution and coacervates yield. The coacervates formation mechanism and stability of formed coacervates were examined using Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR), Circular Dichroism (CD), Thermogravimetric Analysis (TGA) and Differential Scanning Calorimetry (DSC). Coacervates with better morphology, good size distribution and highest yield were observed with G-FL9 at mixing ratio of 7:1 and pH 4.40. The evaluation of coacervates formation mechanism showed that G molecules experienced a conformational change in its secondary structure from a flexible pattern to an ordered poly-proline II (PPII) helix. The vibrations of OH and NH bonds spectra at 3437 and 3449 cm−1, respectively for G/CMC coacervates, shifted to lower wave numbers due to the conformational changes of gelatin and CMC, during the coacervates formation. G/CMC complex coacervates were more thermally stable than individual gelatin. Therefore, these complex coacervates will be able to protect and deliver heat sensitive bioactives and food ingredients.
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