共 50 条
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.
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页码:110 / 118
页数:9
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