Please use this identifier to cite or link to this item:
Title: Intracellular drug delivery by sulfatide-mediated liposomes to gliomas
Authors: Shao, K.
Hou, Q.
Duan, W. 
Wong, K.P.
Li, Q.-T. 
Go, M.L. 
Keywords: Doxorubicin
Intracellular drug delivery
Issue Date: 2006
Citation: Shao, K., Hou, Q., Duan, W., Wong, K.P., Li, Q.-T., Go, M.L. (2006). Intracellular drug delivery by sulfatide-mediated liposomes to gliomas. Journal of Controlled Release 115 (2) : 150-157. ScholarBank@NUS Repository.
Abstract: We described here a liposomal carrier system in which the targeting ligand was sulfatide, a glycosphingolipid known to bind several extracellular matrix (ECM) glycoproteins whose expression was highly up-regulated in many tumors. In vitro experiments with human glioma cell lines demonstrated that robust intracellular uptake of the liposomes depended specifically on the presence of sulfatide as the key liposomal component. Significant amount of the liposomes remained largely intact in the cytoplasm for hours following their internalization. When anticancer drug doxorubicin (DOX) was encapsulated in such liposomes, most of the drug was preferably delivered into the cell nuclei to exert its cytotoxicity. Use of this drug delivery system to deliver DOX for treatment of tumor-bearing nude mice displayed much improved therapeutic effects over the free drug or the drug carried by polyethylene glycol (PEG)-grafted liposomes. Our results demonstrate a close link between effective intracellular uptake of the drug delivery system and its therapeutic outcome. Moreover, the sulfatide-containing liposomes (SCL) may represent an interesting ligand-targeted drug carrier for a wide spectrum of cancers in which sulfatide-binding ECM glycoproteins are expressed. © 2006 Elsevier B.V. All rights reserved.
Source Title: Journal of Controlled Release
ISSN: 01683659
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.


checked on Feb 28, 2018


checked on Dec 31, 2018

Page view(s)

checked on Apr 19, 2019

Google ScholarTM


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.