Lectin-mediated mucosal delivery of drugs and microparticles

被引:173
作者
Clark, MA
Hirst, BH
Jepson, MA [1 ]
机构
[1] Univ Newcastle Upon Tyne, Sch Med, Dept Physiol Sci, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
[3] Univ Bristol, Sch Med Sci, Cell Imaging Facil, Bristol BS8 1TD, Avon, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
M cells; microparticles; lectins; mucosal vaccines; Peyer's patches; microbial adhesins; bioadhesins; targeting; fimbriae; invasin;
D O I
10.1016/S0169-409X(00)00070-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Absorption of drugs and vaccines at mucosal surfaces may be enhanced by conjugation to appropriate bioadhesins which bind to mucosal epithelia. Bioadhesins might also permit cell- and site-selective targeting. One approach is to exploit surface carbohydrates on mucosal epithelial cells for lectin-mediated delivery. We review work supporting the use of lectins as mucosal bioadhesins in the gastrointestinal and respiratory tracts, the oral cavity and the eye. The gastrointestinal tract is particularly favoured fur mucosal delivery. Many studies have demonstrated that the antigen sampling intestinal hi cells offer a portal for absorption of colloidal delivery vehicles. Evidence is presented that M cell targeting may be achieved using ill cell-specific lectins, microbial adhesins or immunoglobulins. While many hurdles must be overcome before mucosal bioadhesins can guarantee consistent, safe, effective mucosal delivery, this is an exciting area of research that has important implications fur future drug and vaccine formulation. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:207 / 223
页数:17
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