期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
大分子载体促进多肽和蛋白质的吸收
1
作者 wei-chiang shen 徐志利 《药学进展》 CAS 北大核心 1992年第4期220-224,共5页
一般认为大分子对细胞膜是非渗透性的,因而不能通过生物系统中的运输屏障,利用这种不通透性,许多大分子被用作药物载体,以免药物很快从循环中被清除掉,或者当药物植入组织时取得恒释的效果。
关键词 多肽 蛋白 载体 药物 大分子 吸收
下载PDF
Cationic and amphipathic cell-penetrating peptides (CPPs): Their structures and in vivo studies in drug delivery 被引量:2
2
作者 Jennica L. Zaro wei-chiang shen 《Frontiers of Chemical Science and Engineering》 SCIE EI CAS CSCD 2015年第4期407-427,共21页
Over the past few decades, cell penetrating peptides (CPPs) have become an important class of drug carders for small molecules, proteins, genes and nanoparticle systems. CPPs represent a very diverse set of short pe... Over the past few decades, cell penetrating peptides (CPPs) have become an important class of drug carders for small molecules, proteins, genes and nanoparticle systems. CPPs represent a very diverse set of short peptide sequences (10-30 amino acids), generally classified as cationic or amphipathic, with various mechanisms in cellular internalization. In this review, a more comprehensive assessment of the chemical structural characteristics, including net cationic charge, hydrophobicity and helicity was assembled for a large set of commonly used CPPs, and compared to results from numerous in vivo drug delivery studies. This detailed information can aid in the design and selection of effective CPPs for use as transport carriers in the delivery of different types of drug for therapeutic applications. 展开更多
关键词 cell penetrating peptides amphipathic pep-tides drug delivery
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部