Silva Marluci P, Tulini Fabricio L, Ribas Marcela M, Penning Manfred, Fávaro-Trindade Carmen S, Poncelet Denis
Departamento de Engenharia de Alimentos (ZEA), Faculdade de Zootecnia e Engenharia de Alimentos (FZEA), Universidade de São Paulo (USP), Pirassununga, São Paulo, Brazil; Ecole Nationale Vétérinaire, Agroalimentaire et de l'alimentation de Nantes-Atlantique (ONIRIS), Nantes, France.
Departamento de Engenharia de Alimentos (ZEA), Faculdade de Zootecnia e Engenharia de Alimentos (FZEA), Universidade de São Paulo (USP), Pirassununga, São Paulo, Brazil.
Food Res Int. 2016 Nov;89(Pt 1):582-590. doi: 10.1016/j.foodres.2016.09.008. Epub 2016 Sep 7.
Microcapsules containing Lactobacillus paracasei BGP-1 were produced by co-extrusion technology using alginate and alginate-shellac blend as wall materials. Sunflower oil and coconut fat were used as vehicles to incorporate BGP-1 into the microcapsules. The microcapsules were evaluated with regard the particle size, morphology, water activity and survival of probiotics after 60days of storage at room temperature. Fluidized bed and lyophilization were used to dry the microcapsules and the effect of these processes on probiotic viability was also evaluated. Next, dried microcapsules were exposed to simulated gastrointestinal fluids to verify the survival of BGP-1. Microcapsules dried by fluidized bed had spherical shape and robust structures, whereas lyophilized microcapsules had porous and fragile structures. Dried microcapsules presented a medium size of 0.71-0.86mm and a ranging from 0.14 to 0.36, depending on the drying process. When comparing the effects of drying processes on BGP-1 viability, the fluidized bed was less aggressive than lyophilization. The alginate-shellac blend combined with coconut fat as core effectively protected the encapsulated probiotic under simulated gastrointestinal conditions. Thus, the production of microcapsules by co-extrusion followed by drying using the fluidized bed is a promising strategy for protection of probiotic cells.
采用海藻酸钠和海藻酸钠-虫胶混合物作为壁材,通过共挤出技术制备了含有副干酪乳杆菌BGP-1的微胶囊。使用向日葵油和椰子油作为载体将BGP-1包封到微胶囊中。对微胶囊的粒径、形态、水分活度以及在室温下储存60天后益生菌的存活率进行了评估。使用流化床干燥和冻干法对微胶囊进行干燥,并评估了这些过程对益生菌活力的影响。接下来,将干燥后的微胶囊置于模拟胃肠液中,以验证BGP-1的存活率。流化床干燥的微胶囊呈球形且结构坚固,而冻干的微胶囊具有多孔且易碎的结构。干燥后的微胶囊中等尺寸为0.71 - 0.86mm,水分活度在0.14至0.36之间,具体取决于干燥过程。比较干燥过程对BGP-1活力的影响时,流化床干燥比冻干的损伤性小。海藻酸钠-虫胶混合物与椰子油作为核心有效地保护了微胶囊中的益生菌在模拟胃肠条件下的活性。因此,通过共挤出制备微胶囊然后使用流化床干燥是一种保护益生菌细胞的有前景的策略。