去唾液酸糖蛋白受体
基因传递
药物输送
单核吞噬细胞系统
甘露糖
化学
遗传增强
药理学
生物化学
生物
肝细胞
免疫学
基因
体外
有机化学
作者
Marya Ahmed,Ravin Narain
出处
期刊:Nanomedicine
[Future Medicine]
日期:2015-07-01
卷期号:10 (14): 2263-2288
被引量:42
摘要
The insult to liver by toxic materials leads to cirrhosis, hepatitis and cancer. Upon administration, drugs accumulate in liver, which is systemically cleared by reticuloendothelial system. However, specific targeting of drugs to liver is a serious challenge. Specific delivery of molecules to hepatocytes is accomplished by targeting cell surface lectins, asialoglycoprotein receptors. Asialofetuin, N-acetyl glucosamine and galactose are high-affinity ligands of asialoglycoprotein receptors. The bioconjugation of drugs, fluorescent molecules and gene delivery vectors with lectin-targeting agents, and their delivery in liver hepatocytes, is discussed. Mannose and N-acetyl glucosamine conjugates are evaluated for their delivery to hepatic stellate and kupffer cells. The glycosylated gene and drug delivery vectors in clinical trials are outlined.
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