Carboxymethyl high amylose starch for F4 fimbriae gastro-resistant oral formulation

被引:39
作者
Calinescu, Carmen
Nadeau, Eric
Mulhbacher, Jerome
Fairbrother, John Morris
Mateescu, Mircea-Alexandru
机构
[1] Univ Quebec, Dept Chem & Ctr BioMed, Montreal, PQ H3C 3P8, Canada
[2] Univ Montreal, Fac Med Vet, St Hyacinthe, PQ J2S 7C6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
carboxymethyl high amylose starch; F4; fimbriae; vaccine; oral administration; tablet; gastro-resistance;
D O I
10.1016/j.ijpharm.2007.04.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The carboxymethyl high amylose starch (CM-HAS) was proposed as excipient able to protect F4 fimbriae oral vaccine against gastric acidity and pepsin, allowing its subsequent liberation in the intestinal fluid. Thus, F4 fimbriae formulated with CM-HAS as tablets displayed a markedly higher stability after 2 h of incubation in simulated gastric fluid (containing pepsin) than the free, non-protected F4 fimbriae, which, in these conditions, were almost completely digested after 120 min. In the presence of pancreatin (with alpha-amylase, lipase and proteolytic activities) in simulated intestinal conditions, the F4 fimbriae were liberated from CM-HAS tablets over a period of up to 5 h. The presence of pancreatin in intestinal medium did not affect the structural stability of the F4 fimbriae major subunits. Thus, F4 fimbriae formulated with CM-HAS would retain their receptor binding activity essential for the induction of an intestinal mucosal immune response. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 25
页数:8
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