Development of chitosan sponges for buccal administration of insulin

被引:81
作者
Portero, Ana [1 ]
Teijeiro-Osorio, Desiree [1 ]
Alonso, Maria J. [1 ]
Remunan-Lopez, Carmen [1 ]
机构
[1] Univ Santiago de Compostela, Dept Pharm & Pharmaceut Technol, Fac Pharm, Santiago De Compostela 15782, Spain
关键词
bilayered drug delivery device; buccal peptide administration; chitosan; insulin; mucoadhesive sponge;
D O I
10.1016/j.carbpol.2006.07.028
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This paper describes the development of a new highly porous, flexible device for buccal peptide administration by a very simple and mild casting/freeze-drying procedure. It consists of a mucoadhesive chitosan layer containing the peptide drug and an impermeable protective layer made of ethylcellulose. This structure was expected to provide unidirectional drug release to the mucosa and avoid loss of drug due to washout with saliva. Insulin release was modulated by varying some formulation variables (chitosan salt type and M-w, chitosan solution pH, insulin dose). The main factor affecting insulin release was its diffusion across the matrix, this being related to the water uptake/swelling and dissolution properties of chitosan and the viscosity of the gel formed upon hydration. In addition, an electrostatic interaction could occur between chitosan amino groups and the insulin carboxylic groups. Preliminary mucoadhesion studies showed that the affinity of chitosan sponges to mucin surfaces was related to the swelling and solubility properties of the different salts of chitosan. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:617 / 625
页数:9
相关论文
共 33 条
[31]   In vitro and in vivo degradation of films of chitin and its deacetylated derivatives [J].
Tomihata, K ;
Ikada, Y .
BIOMATERIALS, 1997, 18 (07) :567-575
[32]   In vitro degradation rates of partially N-acetylated chitosans in human serum [J].
Varum, KM ;
Myhr, MM ;
Hjerde, RJN ;
Smidsrod, O .
CARBOHYDRATE RESEARCH, 1997, 299 (1-2) :99-101
[33]   Factors and strategies for improving buccal absorption of peptides [J].
Veuillez, F ;
Kalia, YN ;
Jacques, Y ;
Deshusses, J ;
Buri, P .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2001, 51 (02) :93-109