Targeted delivery of antigens to the gut-associated lymphoid tissues: 2. Ex vivo evaluation of lectin-labelled albumin microspheres for targeted delivery of antigens to the M-cells of the Peyer's patches

被引:20
作者
Akande, Janet
Yeboah, Kwame G. [2 ]
Addo, Richard T. [3 ]
Siddig, Aladin [4 ]
Oettinger, Carl W. [5 ]
D'Souza, Martin J. [1 ]
机构
[1] Mercer Univ, Coll Pharm & Hlth Sci, Grad Program, Atlanta, GA 30341 USA
[2] Harding Univ, Coll Pharm, Searcy, AR USA
[3] Shenandoah Univ, Sch Pharm, Winchester, VA USA
[4] Univ Charleston, Coll Pharm, Charleston, WV USA
[5] Dialysis Clin Inc, Atlanta, GA USA
关键词
Lectins; zeta potential; Peyer's patches; microspheres; bioactivity of proteins; BIODEGRADABLE MICROSPHERES; POLYSTYRENE MICROSPHERES; GASTROINTESTINAL MUCOSA; INTESTINAL UPTAKE; IMMUNE-RESPONSES; VACCINE DELIVERY; TRANSLOCATION; NANOPARTICLES; TRANSPORT; DRUG;
D O I
10.3109/02652040903191834
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The purpose of this study was to evaluate the possibility of lectin-coupled microspheres to improve the targeted delivery of protein antigens to the lymphoid tissues of mucosal surfaces. Bovine serum albumin containing acid phosphatase model protein and polystyrene microspheres were coupled with mouse M-cell-specific Ulex europaeus lectin. The coupling efficiency, physical characteristics and the binding capabilities of the microspheres to the follicle associated epithelium of the Peyer's patches were evaluated in vitro and ex vivo in mice intestine. The results showed that coupling of lectin to albumin microspheres did not significantly affect the bioactivity of the encapsulated acid phosphatase model protein. It was also shown that there was preferential binding of the lectin-coupled microspheres to the follicle-associated epithelium. It was concluded from the results of the study that coupling of ligands such as lectin specific to cells of the follicle associated epithelium can increase the targeting of encapsulated candidate antigens for delivery to the Peyer's patches of the intestine for improved oral delivery.
引用
收藏
页码:325 / 336
页数:12
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