Preparation of Angiopep-2 Peptide-Modified Bubble Liposomes for Delivery to the Brain

被引:0
|
作者
Endo-Takahashi, Yoko [1 ]
Ooaku, Kotomi [1 ]
Ishida, Kazuma [1 ]
Suzuki, Ryo [2 ]
Maruyama, Kazuo [2 ]
Negishi, Yoichi [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, Dept Drug Delivery & Mol Biopharmaceut, 1432-1 Horinouchi, Hachioji, Tokyo 1920392, Japan
[2] Teikyo Univ, Fac Pharma Sci, Lab Drug & Gene Delivery Res, Itabashi Ku, 2-11-1 Kaga, Tokyo 1738605, Japan
基金
日本学术振兴会;
关键词
Bubble liposome; ultrasound; Angiopep-2; brain; RECEPTOR-RELATED PROTEIN; DRUG-DELIVERY; LIPOPROTEIN RECEPTOR; GENE DELIVERY; ENDOTHELIAL-CELLS; IN-VIVO; ULTRASOUND; MICROBUBBLES; BARRIER; GLIOMA;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the development of therapeutic approaches for central nervous system diseases, a significant obstacle is efficient drug delivery across the blood-brain barrier owing to its low permeability. Various nanocarriers have been developed for brain-targeted drug delivery by modification with specific ligands. We have previously developed polyethylene glycol-modified liposomes (Bubble liposomes [BLs]) that entrap ultrasound (US) contrast gas and can serve as both plasmid DNA or small interfering RNA carriers and US contrast agents. In this study, we attempted to prepare brain-targeting BLs modified with Angiopep-2 (Ang2) peptide (Ang2-BLs). Ang2 is expected to be a useful ligand for the efficient delivery of nanocarriers to the brain. We showed that Ang2-BLs interacted specifically with brain endothelial cells via low-density lipoprotein receptor-related protein-1. We also confirmed that Ang2-BLs could entrap US contrast gas and had US imaging ability as well as unmodified BLs. Furthermore, we demonstrated that Ang2-BLs accumulated in brain tissue after intravascular injection. These results suggested that Ang2-BLs may be a useful tool for brain-targeted delivery and US imaging via systemic administration.
引用
收藏
页码:977 / 983
页数:7
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