Université Clermont 1, UFR Pharmacie, Centre de Recherche en Nutrition Humaine (CRNH), Equipe de Recherche Technologique 'Conception, Ingénierie et Développement de l'Aliment et duM'dicament' (ERT CIDAM), Clermont-Ferrand, France.
J Microencapsul. 2010;27(4):292-302. doi: 10.3109/02652040903134529.
Viable Saccharomyces boulardii, used as a biotherapeutic agent, was encapsulated in food-grade whey protein isolate (WP) and alginate (ALG) microparticles, in order to protect and vehicle them in gastrointestinal environment. Yeast-loaded microparticles with a WP/ALG ratio of 62/38 were produced with high encapsulation efficiency (95%) using an extrusion/cold gelation method and coated with ALG or WP by a simple immersion method. Swelling, yeast survival, WP loss and yeast release in simulated gastric and intestinal fluids (SGF and SIF, pH 1.2 and 7.5) with and without their respective digestive enzymes (pepsin and pancreatin) were investigated. In SGF, ALG network shrinkage limited enzyme diffusion into the WP/ALG matrix. Coated and uncoated WP/ALG microparticles were resistant in SGF even with pepsin. Survival of yeast cells in microparticles was 40% compared to 10% for free yeast cells and was improved to 60% by coating. In SIF, yeast cell release followed coated microparticle swelling with a desirable delay. Coated WP/ALG microparticles appear to have potential as oral delivery systems for Saccharomyces boulardii or as encapsulation means for probiotic cells in pharmaceutical or food processing applications.
活的布拉氏酵母,用作生物治疗剂,被封装在食品级乳清蛋白分离物(WP)和海藻酸钠(ALG)微球中,以保护它们并将其输送到胃肠道环境中。使用挤出/冷凝胶法,以 WP/ALG 比例为 62/38 生产载有酵母的微球,具有高包封效率(95%),并用简单的浸泡法用 ALG 或 WP 进行涂层。在具有和不具有各自的消化酶(胃蛋白酶和胰蛋白酶)的模拟胃液(SGF 和 SIF,pH 1.2 和 7.5)中研究了膨胀、酵母存活、WP 损失和酵母释放。在 SGF 中,ALG 网络收缩限制了酶扩散到 WP/ALG 基质中。包衣和未包衣的 WP/ALG 微球即使有胃蛋白酶也能在 SGF 中抵抗。与游离酵母细胞的 10%相比,微球中酵母细胞的存活率为 40%,通过涂层提高到 60%。在 SIF 中,酵母细胞释放遵循包衣微球的膨胀,具有理想的延迟。包衣 WP/ALG 微球似乎具有作为布拉氏酵母口服递送系统的潜力,或者作为药物或食品加工应用中益生菌细胞的封装手段。