Feasibility of a bioadhesive drug delivery system targeted to oesophageal tissue

被引:19
作者
Batchelor, HK
Tang, A
Dettmar, PW
Hampson, FC
Jolliffe, IG
Craig, DQM
机构
[1] Aston Univ, Med Res Unit, Inst Pharmaceut Sci, Birmingham B4 7ET, W Midlands, England
[2] Reckitt Benckiser, Kingston Upon Hull, N Humberside, England
[3] Queens Univ Belfast, Sch Pharm, Belfast, Antrim, North Ireland
基金
英国生物技术与生命科学研究理事会;
关键词
bioadhesion; model drug particle; oesophagus; alginate; drug delivery;
D O I
10.1016/j.ejpb.2003.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This contribution examines the feasibility of utilising an oesophageal-adhesive alginate layer to support model drug particles. Such a bioadhesive system offers the prospect of local drug delivery to the oesophagus, which in turn has applications in the treatment of conditions including gastro-oesophageal reflux disease and oesophageal cancer. Surface-modified (amine, carboxylate and sulfate) as well as neutral fluorescent beads were investigated as model drug particles. A fluorescence assay technique was utilised to quantify the extent and duration of adhesion of a fixed dose of these particles to excised porcine oesophageal tissue. Retention of the particles was investigated both from aqueous systems and within an adhesive alginate solution. After 30 min significantly higher adhesion of neutral beads was recorded from the alginate solution as compared to the aqueous suspension (n = 6, P < 0.05). The beads that possessed a negative charge showed significantly greater retention within the alginate carrier (n = 6, P < 0.05). However, the amine-modified beads showed retention profiles that were similar both within the alginate carrier and within the aqueous suspension (n = 6, P > 0.05). (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:295 / 298
页数:4
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