Kovacs-Nolan Jennifer, Mine Yoshinori
Department of Food Science, University of Guelph, Guelph, Ontario, Canada N1G 2W1.
J Immunol Methods. 2005 Jan;296(1-2):199-209. doi: 10.1016/j.jim.2004.11.017. Epub 2004 Dec 16.
Avian immunoglobulin (Ig) Y is a promising alternative for the treatment and prevention of enteric infections, and has shown to be effective against a number of gastrointestinal pathogens, including Escherichia coli, Salmonella, and rotavirus. However, its application is limited by its sensitivity to human gastrointestinal conditions. Here, we report on the enteric coating of IgY-containing granules with a pH-sensitive methacrylic acid copolymer. A 35% (w/w) polymer coating was found to protect IgY from gastric inactivation in vitro, maintaining greater than 95% activity after 6 h in simulated gastric fluid. The IgY was slowly released from the microencapsulated granules upon exposure to simulated intestinal fluid, and retained 80% activity after 8 h exposure to pancreatic enzymes. In vivo, using pigs as a model of human digestion, the encapsulated IgY retained significantly more activity than non-encapsulated IgY, indicating that microencapsulation with a methacrylic acid copolymer may be an effective method of protecting IgY from gastrointestinal inactivation, enabling its use for oral passive immunotherapy.
禽免疫球蛋白(Ig)Y是治疗和预防肠道感染的一种有前景的替代物,并且已显示对多种胃肠道病原体有效,包括大肠杆菌、沙门氏菌和轮状病毒。然而,其应用受到对人类胃肠道条件敏感性的限制。在此,我们报道了用pH敏感的甲基丙烯酸共聚物对含IgY颗粒进行肠溶包衣。发现35%(w/w)的聚合物包衣可在体外保护IgY不被胃灭活,在模拟胃液中6小时后活性维持在95%以上。当暴露于模拟肠液时,IgY从微囊化颗粒中缓慢释放,在暴露于胰酶8小时后仍保留80%的活性。在体内,以猪作为人类消化的模型,包封的IgY比未包封的IgY保留了显著更多的活性,表明用甲基丙烯酸共聚物进行微囊化可能是保护IgY不被胃肠道灭活的有效方法,使其能够用于口服被动免疫疗法。