Clark M A, Hirst B H, Jepson M A
Department of Physiological Sciences, Medical School, University of Newcastle upon Tyne, NE2 4HH, Newcastle upon Tyne, UK.
Adv Drug Deliv Rev. 2000 Sep 30;43(2-3):207-23. doi: 10.1016/s0169-409x(00)00070-3.
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 for mucosal delivery. Many studies have demonstrated that the antigen sampling intestinal M cells offer a portal for absorption of colloidal delivery vehicles. Evidence is presented that M cell targeting may be achieved using M 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 for future drug and vaccine formulation.
通过与结合到粘膜上皮的合适生物粘附素结合,可增强药物和疫苗在粘膜表面的吸收。生物粘附素还可能实现细胞和部位选择性靶向。一种方法是利用粘膜上皮细胞上的表面碳水化合物进行凝集素介导的递送。我们综述了支持将凝集素用作胃肠道、呼吸道、口腔和眼部粘膜生物粘附素的研究工作。胃肠道特别适合粘膜给药。许多研究表明,抗原采样肠M细胞为胶体递送载体的吸收提供了一个入口。有证据表明,使用M细胞特异性凝集素、微生物粘附素或免疫球蛋白可实现对M细胞的靶向。虽然在粘膜生物粘附素能够保证持续、安全、有效的粘膜给药之前,必须克服许多障碍,但这是一个令人兴奋的研究领域,对未来的药物和疫苗制剂具有重要意义。