Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/5794
Title: Targeting Stealth liposomes in a murine model of human small cell lung cancer
Authors: Moreira, João N. 
Gaspar, Rogério 
Allen, Theresa M. 
Keywords: Pegylated liposome; Doxorubicin; Targeting; Antagonist G; Small cell lung cancer
Issue Date: 2001
Citation: Biochimica et Biophysica Acta (BBA) - Biomembranes. 1515:2 (2001) 167-176
Abstract: Tumor accumulation and therapeutic activity of Stealth liposomes loaded with doxorubicin (DXR) were examined in Balb/c nude mice xenografts inoculated subcutaneously with the human small cell lung cancer (SCLC) cell line, H69. Mice were treated with non-targeted liposomes (SL) or liposomes targeted with antagonist G coupled to the liposome surface (SLG). SLG showed 30-44-fold higher binding to H69 cells harvested from H69 xenografts than SL. At 48 and 72 h post injection, tumor accumulation of [125I]tyraminylinulin-containing liposomes was shown to be dependent on liposome size but independent of the presence of the targeting ligand. Maximum tumor uptake of either SLG or SL ranged from 2 to 4% of injected dose/g of tissue. In therapeutic studies, mice received three weekly injections of 3 or 6 mg free DXR/kg or 3 or 10 mg liposomal DXR/kg at initial tumor volumes of either 7 or 33 mm3. The therapeutic efficacy of DXR-containing SL or SLG was significantly improved over free DXR, but SLG did not improve anti-tumor efficacy relative to SL. Stealth liposomes containing DXR have potential as a therapy against human SCLC tumors.
URI: http://hdl.handle.net/10316/5794
DOI: 10.1016/S0005-2736(01)00411-4
Rights: openAccess
Appears in Collections:FFUC- Artigos em Revistas Internacionais

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