Departamento de Biotecnología, Universidad Autónoma Metropolitana-Iztapalapa, Apartado Postal 55-534, CDMX 09340, Mexico.
Departamento de Preparatoria Agrícola, Universidad Autónoma Chapingo, Km. 38.5, Carretera México-Texcoco, Texcoco 56230, Mexico.
Food Res Int. 2019 May;119:829-838. doi: 10.1016/j.foodres.2018.10.066. Epub 2018 Oct 24.
Recently the structuring of liquid oils with low molecular weight organogelators has received much attention. Food products devoid of trans fats, with tailored rheological and textural properties can be designed for desired applications by properly selecting the organogelator and cooling rate used in their formation. Nevertheless, studies regarding these points are still scarce. In this work the effect of two different food-grade gelators (glyceryl monostearate, GM and sorbitan monostearate, SM) and different cooling rates (1, 3 and 9 °C/min) on the microstructural, viscoelastic and texture properties of chia seed oleogels (GMO and SMO, respectively) were evaluated. Gelator and chia seed oil (ChSO) were mixed in 1:10 mass ratio. SMO formed crystalline needle-like structures, with faster cooling rates producing smaller crystals (higher crystallinity index) and a more compact network. GMO showed an opposite crystallinity index dependence with cooling rate than SMO. GMO hardness higher than that of SMO, and increased while that of SMO decreased as cooling rate was faster. Both GMO and SMO showed a thixotropic dependence of the storage (G') and loss (G") moduli with forward-backward temperature ramp (5-80-5 °C). Both moduli values were higher for GMO than for SMO independently of cooling rate used. A thixotropic index was obtained, which reflected that GMO had a more thermo-reversible structure than SMO. The results of this study indicate that the formation mechanism of chia seed oleogels was affected by the cooling rate and the chemical nature of the gelator, and elicited completely different microstructural and mechanical responses.
最近,人们对低分子量有机凝胶剂的液体油结构进行了大量研究。通过适当选择用于形成油凝胶的有机凝胶剂和冷却速率,可以设计出不含反式脂肪且具有定制流变学和质构特性的食品产品,以满足特定应用的需求。然而,关于这些方面的研究仍然很少。在这项工作中,研究了两种不同的食品级凝胶剂(甘油单硬脂酸酯 GM 和山梨醇单硬脂酸酯 SM)和不同的冷却速率(1、3 和 9°C/min)对奇亚籽油凝胶(GMO 和 SMO,分别)微观结构、粘弹性和质构特性的影响。凝胶剂和奇亚籽油(ChSO)以 1:10 的质量比混合。SMO 形成了结晶针状结构,冷却速率越快,晶体越小(结晶度指数越高),网络越紧凑。GMO 的结晶度指数随冷却速率的变化与 SMO 相反。GMO 的硬度高于 SMO,并且随着冷却速率的增加而增加,而 SMO 的硬度随着冷却速率的增加而降低。GMO 和 SMO 的储能模量(G')和损耗模量(G")均随正反向温度斜坡(5-80-5°C)表现出触变性依赖关系。无论使用的冷却速率如何,GMO 的两个模量值均高于 SMO。得到了触变指数,它反映了 GMO 比 SMO 具有更热可逆的结构。这项研究的结果表明,奇亚籽油凝胶的形成机制受到冷却速率和凝胶剂化学性质的影响,产生了完全不同的微观结构和力学响应。