STARCH MICROSPHERES INDUCE PULSATILE DELIVERY OF DRUGS AND PEPTIDES ACROSS THE EPITHELIAL BARRIER BY REVERSIBLE SEPARATION OF THE TIGHT JUNCTIONS

被引:59
作者
BJORK, E
ISAKSSON, U
EDMAN, P
ARTURSSON, P
机构
[1] UPPSALA UNIV,DEPT PHARMACEUT,S-75123 UPPSALA,SWEDEN
[2] KABI PHARM THERAPEUT AB,S-75182 UPPSALA,SWEDEN
关键词
DRUG TRANSPORT; CACO-2; MICROSPHERES; ABSORPTION ENHANCEMENT; TIGHT JUNCTION; INTESTINAL EPITHELIUM;
D O I
10.3109/10611869509015920
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Non-parenteral administration of peptide drugs is prevented by the limited permeability of the epithelia lining the mucosal tissues. As a new approach to non-parenteral delivery, degradable starch microspheres (dsm) were coated with insulin and administered to the mucosal side of monolayers of human intestinal epithelial (Caco-2) cells in vitro. The microspheres induced a pulsed delivery of insulin across the epithelium that lasted for 1-2 h. The pulsed delivery correlated with a reversible appearance of focal dilatations in the tight junctions between the epithelial cells, indicating that dsm enhance the delivery of insulin by the paracellular route. These results provide an explanation for the previously observed absorption enhancing properties of dsm.
引用
收藏
页码:501 / 507
页数:7
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