Novel mucoadhesion tests for polymers and polymer-coated particles to design optimal mucoadhesive drug delivery systems

被引:277
作者
Takeuchi, H [1 ]
Thongborisute, J [1 ]
Matsui, Y [1 ]
Sugihara, H [1 ]
Yamamoto, H [1 ]
Kawashima, Y [1 ]
机构
[1] Gifu Pharmaceut Univ, Lab Pharmaceut Engn, Gifu 5028585, Japan
基金
日本学术振兴会;
关键词
mucoadhesion; mucin particle; BIACORE; confocal laser scanning microscopy; peptide drug; oral administration;
D O I
10.1016/j.addr.2005.07.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To design an effective particulate drug delivery system having mucoadhesive function, several mucoadhesion tests for polymers and the resultant particulate systems were developed. Mucin particle method is a simple mucoadhesion test for polymers, in which the commercial mucin particles are used. By measuring the change in particle size or zeta potential of the mucin particle in a certain concentration of polymer solution, we could estimate the extent of their mucoadhesive property. BIACORE method is also a novel mucoadhesion test for polymers. On passing through the mucin suspension on the polymer-immobilized chip of BIACORE instrument, the interaction was quantitatively evaluated with the change in its response diagram. By using these mucoadhesion tests, we detected a strong mucoadhesive property of several types of chitosan and Carbopol. Evaluation of mucoadhesive property of polymer-coated particulate systems was demonstrated with the particle counting method developed by us. To detect the mucoadhesive phenomena in the intestinal tract, we observed the rat intestine with the confocal laser scanning microscope (CLSM) after oral administration of the particulate systems. The resultant photographs clearly showed a longer retention of submicron-sized chitosan-coated liposomes (ssCS-Lip) in the intestinal tract than other liposomal particles tested such as non-coated liposomes and chitosan-coated multilamellar one. These observations explained well the superiority of the ssCS-Lip as drug carrier in oral administration of calcitonin in rats than other liposomal particles. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1583 / 1594
页数:12
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