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Microencapsulation of Enteric Bacteriophages in a pH-Responsive Solid Oral Dosage Formulation Using a Scalable Membrane Emulsification Process

机译:使用可扩展膜乳化工艺在pH响应性固体口服制剂中对肠道噬菌体进行微囊化。

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摘要

A scalable low-shear membrane emulsification process was used to produce microencapsulated Escherichia coli-phages in a solid oral dosage form. Uniform pH-responsive composite microparticles (mean size ~100 µm) composed of Eudragit® S100 and alginate were produced. The internal microstructure of the gelled microcapsules was studied using ion-milling and imaging, which showed that the microparticles had a solid internal core. The microencapsulation process significantly protected phages upon prolonged exposure to a simulated gastric acidic environment. Encapsulated phages that had been pre-exposed to simulated gastric acid were added to actively growing bacterial cells using in vitro cell cultures and were found to be effective in killing E. coli. Encapsulated phages were also shown to be effective in killing actively growing E. coli in the presence of human epithelial cells. Confocal microscopy images showed that the morphology of encapsulated phage-treated epithelial cells was considerably better than controls without phage treatment. The encapsulated phages were stable during refrigerated storage over a four-week period. The process of membrane emulsification is highly scalable and is a promising route to produce industrial quantities of pH-responsive oral solid dosage forms suitable for delivering high titres of viable phages to the gastrointestinal tract.
机译:可扩展的低剪切膜乳化工艺用于生产固体口服剂型的微囊化大肠杆菌噬菌体。制备了由Eudragit ® S100和藻酸盐组成的均匀的pH响应复合微粒(平均粒径约100 µm)。使用离子磨和成像研究了凝胶微胶囊的内部微结构,这表明该微粒具有固体内芯。长时间暴露于模拟的胃酸性环境中,微囊化过程可显着保护噬菌体。使用体外细胞培养将预先暴露于模拟胃酸的封装噬菌体添加到活跃生长的细菌细胞中,发现它们可有效杀死大肠杆菌。封装的噬菌体还被证明在存在人类上皮细胞的情况下可有效杀死活跃生长的大肠杆菌。共聚焦显微镜图像显示,经包被的噬菌体处理的上皮细胞的形态明显优于未经噬菌体处理的对照。封装的噬菌体在冷藏存储过程中稳定了四个星期。膜乳化的过程具有高度可扩展性,并且是生产工业量的pH响应性口服固体剂型的有前途的途径,该剂型适合于将高滴度的活噬菌体递送至胃肠道。

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