Lin Junzhang, Yu Weiting, Liu Xiudong, Xie Hongguo, Wang Wei, Ma Xiaojun
Laboratory of Biomedical Material Engineering, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, PR China.
J Biosci Bioeng. 2008 Jun;105(6):660-5. doi: 10.1263/jbb.105.660.
Oral administration of artificial cell microcapsules entrapping live bacterial cells is a promising approach in disease therapy. However, the current technology of microcapsules limits this approach. In this study, alginate-chitosan-alginate (ACA) microcapsules entrapping live bacterial cells were prepared with the purpose of oral delivery for therapy, and their in vitro and in vivo properties were investigated. Genetically engineered Escherichia coli DH5 were used as the model bacterial strain. ACA microcapsules remained intact and stable in simulated gastrointestinal fluid and the entrapped bacteria cells survived and grew normally. Moreover, ACA microcapsules were more stable than alginate-polylysine-alginate microcapsules in the rat gastrointestinal tract, which was attributed to the enhanced resistance of the ACA microcapsules to enzymatic digestion. Therefore, these results reinforce the potential of ACA microcapsules for the therapeutic oral delivery of live bacterial cells.
口服包载活细菌细胞的人工细胞微胶囊是一种很有前景的疾病治疗方法。然而,目前的微胶囊技术限制了这种方法。在本研究中,制备了包载活细菌细胞的海藻酸盐-壳聚糖-海藻酸盐(ACA)微胶囊用于口服治疗,并对其体外和体内特性进行了研究。使用基因工程大肠杆菌DH5作为模型菌株。ACA微胶囊在模拟胃肠液中保持完整和稳定,包载的细菌细胞存活并正常生长。此外,ACA微胶囊在大鼠胃肠道中比海藻酸盐-聚赖氨酸-海藻酸盐微胶囊更稳定,这归因于ACA微胶囊对酶消化的抗性增强。因此,这些结果增强了ACA微胶囊用于活细菌细胞治疗性口服递送的潜力。