Design, synthesis and biological evaluation of multivalent glucosides with high affinity as ligands for brain targeting liposomes

被引:50
|
作者
Qu, Boyi [1 ]
Li, Xiaocen [1 ]
Guan, Mei [2 ]
Li, Xun [1 ]
Hai, Li [1 ]
Wu, Yong [1 ]
机构
[1] Sichuan Univ, West China Sch Pharm, Educ Minist, Key Lab Drug Targeting, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Cholesterylated glucosides; Brain targeting; GLUT1; transporter; Synthesis; Liposome; DRUG-DELIVERY; ANTICONVULSANT ACTIVITY; 7-CHLOROKYNURENIC ACID; IN-VITRO; DERIVATIVES; BARRIER; IMMUNOLIPOSOMES; TRANSPORTER; PRODRUGS; DOPAMINE;
D O I
10.1016/j.ejmech.2013.10.007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The new bifunctional cluster glucosides were designed and synthesized as liposome ligands for preparing novel liposome to achieve the effective delivery of drug formulations to brain by GLUT1. Docetaxel-loaded five liposomes were prepared successfully and tested in the animals. Results from the in vivo distribution study after i.v. administration of these five liposomes and blank-docetaxel indicated that the coupled liposomes Lip-1, Lip-2, Lip-3, Lip-5 exhibited excellent transport ability across the BBB. In particular, they significantly increased the level of docetaxel in brain compared to blank-docetaxel and Lip. Among them, Lip-5 showed higher brain concentration. Both pharmacokinetics and distribution study in mice confirmed that this novel brain targeting drug delivery system was a promising carrier to enhance brain delivery capacity for CNS drugs. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:110 / 118
页数:9
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