Insight into glycyrrhetinic acid: The role of the hydroxyl group on liver targeting

PEG比率 乙二醇 化学 纳米颗粒 壳聚糖 核化学 立体化学 生物化学 纳米技术 有机化学 材料科学 财务 经济
作者
Qing Tian,Xiuhua Wang,Wei Wang,Chuangnian Zhang,Yuan Liu,Zhi Yuan
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:400 (1-2): 153-157 被引量:43
标识
DOI:10.1016/j.ijpharm.2010.08.032
摘要

Two kinds of glycyrrhetinic acid-modified chitosan/poly(ethylene glycol) nanoparticles (CTS/PEG-GA NPs) were prepared by an ionic gelation process in which the liver targeting ligand glycyrrhetinic acid (GA) was introduced into the nanoparticles at the C30-carboxyl group (CTS/PEG-GA(c) NPs) or the C3-hydroxyl group (CTS/PEG-GA(h) NPs). Their characteristics, especially their ability to target the liver, were compared. The results showed that both the CTS/PEG-GA(c) NPs and the CTS/PEG-GA(h) NPs are remarkably targeted to the liver. The accumulation in the liver is 51.3% and 56.5% of the injected dose for the CTS/PEG-GA(c)4.60% NPs (the subscript number denotes the GA content as weight percent in nanoparticles) and the CTS/PEG-GA(h)4.57% NPs at 3 h after injection, respectively. This is nearly 2.6–2.8 times higher than that obtained with the CTS/PEG NPs. According to our results, there is no significant difference between the CTS/PEG-GA(c) NPs and the CTS/PEG-GA(h) NPs in their ability to target the liver, when they were formed under identical conditions. This indicated that the C3-hydroxyl group in GA has little influence on the targeting ability.
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