Shanghai Institute of Materia Medica, Chinese Academy of Sciences , 501 Haike Road, Shanghai, 201203 , China +86 21 20231000 1424 ; +86 21 20231000 1425 ;
Expert Opin Drug Deliv. 2014 Sep;11(9):1435-47. doi: 10.1517/17425247.2014.924500. Epub 2014 Jun 25.
In the past decade, extensive efforts have been devoted to designing 'active targeted' drug delivery systems (ATDDS) to improve oral absorption of proteins and peptides. Such ATDDS enhance cellular internalization and permeability of proteins and peptides via molecular recognition processes such as ligand-receptor or antigen-antibody interaction, and thus enhance drug absorption.
This review focuses on recent advances with orally ATDDS, including ligand-protein conjugates, recombinant ligand-protein fusion proteins and ligand-modified carriers. In addition to traditional intestinal active transport systems of substrates and their corresponding receptors, transporters and carriers, new targets such as intercellular adhesion molecule-1 and β-integrin are also discussed.
ATDDS can improve oral absorption of proteins and peptides. However, currently, no clinical studies on ATDDS for proteins and peptides are underway, perhaps due to the complexity and limited knowledge of transport mechanisms. Therefore, more research is warranted to optimize ATDDS efficiency.
在过去的十年中,人们致力于设计“主动靶向”药物传递系统(ATDDS)以提高蛋白质和肽类的口服吸收。这些 ATDDS 通过分子识别过程(如配体-受体或抗原-抗体相互作用)增强蛋白质和肽类的细胞内化和通透性,从而增强药物吸收。
本综述重点介绍了口服 ATDDS 的最新进展,包括配体-蛋白质缀合物、重组配体-蛋白质融合蛋白和配体修饰的载体。除了底物及其相应受体的传统肠道主动转运系统外,还讨论了新的靶标,如细胞间黏附分子-1 和β-整合素。
ATDDS 可以提高蛋白质和肽类的口服吸收。然而,目前,尚无针对蛋白质和肽类的 ATDDS 的临床研究正在进行中,这可能是由于转运机制的复杂性和有限的知识。因此,需要进行更多的研究来优化 ATDDS 的效率。