Department of Biological and Agricultural Engineering, University of California, Davis, CA 95616, USA.
J Microencapsul. 2012;29(3):286-95. doi: 10.3109/02652048.2011.651494. Epub 2012 Jan 18.
Microencapsulation of biomolecules, cells and chemicals is widely used in the food and pharmaceutical industries to improve stability, delivery and to control the release of encapsulated moieties. Among encapsulation matrices, alginate is preferred due to its low cost, biodegradability and biocompatibility. Current methods for producing stable alginate gels involve dropping alginate suspensions into divalent cation solutions. This procedure is difficult to scale-up and produces undesirably large alginate beads. In our novel encapsulation method, alginate gelation occurs during spray drying upon volatilisation of a base and rapid release of otherwise unavailable calcium ions. The resulting particles, with median particle sizes in the range 15-120 µm, are insoluble in solution. Cellulase and hemicellulase activities encapsulated by this method were not compromised during spray drying and remained stable over prolonged storage. The procedure described here offers a one-step alternative to other encapsulation methods that are costly and difficult to scale-up.
生物分子、细胞和化学物质的微胶囊化广泛应用于食品和制药行业,以提高封装部分的稳定性、传递效率和控制释放。在封装基质中,由于成本低、可生物降解性和生物相容性,海藻酸盐是首选。目前生产稳定海藻酸盐凝胶的方法涉及将海藻酸盐悬浮液滴入二价阳离子溶液中。该方法难以放大,并且会产生不理想的大海藻酸盐珠。在我们的新型封装方法中,海藻酸盐在喷雾干燥过程中发生胶凝作用,当基础物质挥发时,否则无法获得的钙离子迅速释放。所得颗粒的中值粒径在 15-120μm 范围内,在溶液中不溶解。用这种方法包封的纤维素酶和半纤维素酶活性在喷雾干燥过程中没有受到影响,并且在长时间储存过程中保持稳定。这里描述的方法提供了一种替代其他昂贵且难以放大的封装方法的一步法。