Bardonnet P L, Faivre V, Pugh W J, Piffaretti J C, Falson F
Laboratoire de Pharmacie Galénique Industrielle, EA 3741, ISPB, Université Claude Bernard, Lyon I, 8 av. Rockefeller, 69373 Lyon, France.
J Control Release. 2006 Mar 10;111(1-2):1-18. doi: 10.1016/j.jconrel.2005.10.031. Epub 2006 Jan 5.
The challenge to develop efficient gastroretentive dosage forms began about 20 years ago, following the discovery of Helicobacter pylori by Warren and Marshall. In order to understand the real difficulty of increasing the gastric residence time of a dosage form, we have first summarized the important physiologic parameters, which act upon the gastric residence time. Afterwards, we have reviewed the different drug delivery systems designed until now, i.e. high-density, intragastric floating, expandable, superporous hydrogel, mucoadhesive and magnetic systems. Finally, we have focused on gastroretentive dosage forms especially designed against H. pylori, including specific targeting systems against this bacterium.
大约20年前,随着沃伦和马歇尔发现幽门螺杆菌,开发高效胃滞留剂型的挑战随之而来。为了理解增加剂型胃内滞留时间的真正困难,我们首先总结了影响胃内滞留时间的重要生理参数。之后,我们回顾了迄今为止设计的不同药物递送系统,即高密度、胃内漂浮、可膨胀、高吸水性水凝胶、粘膜粘附和磁性系统。最后,我们重点关注了专门针对幽门螺杆菌设计的胃滞留剂型,包括针对这种细菌的特异性靶向系统。