Li Ran, Zhang Yufeng, Polk D Brent, Tomasula Peggy M, Yan Fang, Liu LinShu
State Key Laboratory of Hollow Fiber Membrane Materials and Processes, Tianjin Polytechnic University, No. 399 Binshuixi Road, Xiqing District, Tianjin 300387, PR China; Dairy and Functional Foods Research Unit, Eastern Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, 600 E. Mermaid Lane, Wyndmoor, PA 19038, USA.
State Key Laboratory of Hollow Fiber Membrane Materials and Processes, Tianjin Polytechnic University, No. 399 Binshuixi Road, Xiqing District, Tianjin 300387, PR China.
J Control Release. 2016 May 28;230:79-87. doi: 10.1016/j.jconrel.2016.04.009. Epub 2016 Apr 7.
Probiotics have shown beneficial effects on health and prevention of diseases in humans. However, a concern for application of probiotics is the loss of viability during storage and gastrointestinal transit. The aim of this study was to develop an encapsulation system to preserve viability of probiotics when they are administrated orally and apply Lactobacillus rhamnosus GG (LGG) as a probiotic model to evaluate the effectiveness of this approach using in vitro and in vivo experiments. LGG was encapsulated in hydrogel beads prepared using pectin, a food grade polysaccharide, glucose, and calcium chloride, and lyophilized by freeze-drying. Encapsulated LGG was cultured in vitro under the condition that mimicked the physiological environment of the human gastrointestinal tract. Compared to non-encapsulated LGG, encapsulation increased tolerance of LGG in the acid condition, protected LGG from protease digestion, and improved shelf time when stored at the ambient condition, in regard of survivability and production of p40, a known LGG-derived protein involved in LGG's beneficial effects on intestinal homeostasis. To evaluate the effects of encapsulation on p40 production in vivo and prevention of intestinal inflammation by LGG, mice were gavaged with LGG containing beads and treated with dextran sulphate sodium (DSS) to induce intestinal injury and colitis. Compared to non-encapsulated LGG, encapsulated LGG enhanced more p40 production in mice, and exerted higher levels of effects on prevention of DSS-induced colonic injury and colitis and suppression of pro-inflammatory cytokine production. These data indicated that the encapsulation system developed in this study preserves viability of LGG in vitro and in vivo, leading to longer shelf time and enhancing the functions of LGG in the gastrointestinal tract. Thus, this encapsulation approach may have the potential application for improving efficacy of probiotics.
益生菌已显示出对人类健康和疾病预防的有益作用。然而,益生菌应用中的一个问题是在储存和胃肠道转运过程中活力丧失。本研究的目的是开发一种封装系统,以在口服益生菌时保持其活力,并应用鼠李糖乳杆菌GG(LGG)作为益生菌模型,通过体外和体内实验评估该方法的有效性。LGG被封装在用果胶(一种食品级多糖)、葡萄糖和氯化钙制备的水凝胶珠中,并通过冷冻干燥进行冻干。将封装的LGG在模拟人类胃肠道生理环境的条件下进行体外培养。与未封装的LGG相比,封装提高了LGG在酸性条件下的耐受性,保护LGG免受蛋白酶消化,并在室温条件下储存时提高了保质期,在存活率和p40(一种已知的源自LGG且参与LGG对肠道稳态有益作用的蛋白质)的产生方面均如此。为了评估封装对体内p40产生以及LGG预防肠道炎症的影响,给小鼠灌胃含LGG的珠子并用葡聚糖硫酸钠(DSS)处理以诱导肠道损伤和结肠炎。与未封装的LGG相比,封装的LGG在小鼠中增强了更多的p40产生,并对预防DSS诱导的结肠损伤和结肠炎以及抑制促炎细胞因子产生发挥了更高水平的作用。这些数据表明,本研究开发的封装系统在体外和体内均能保持LGG的活力,从而延长保质期并增强LGG在胃肠道中的功能。因此,这种封装方法可能具有提高益生菌功效的潜在应用价值。