ENHANCEMENT OF CHEMOTHERAPEUTIC EFFECT BY ENTRAPPING 1‐β‐D‐ARABINOFURANOSYLCYTOSINE IN LIPID VESICLES AND ITS MODE OF ACTION *
- 1 June 1978
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 308 (1) , 387-394
- https://doi.org/10.1111/j.1749-6632.1978.tb22036.x
Abstract
A-beta-D-arabinofuranosylcytosine (ara-C) trapped in multilamellar liposomes exerted enhanced chemotherapeutic effect against L1210 murine leukemia. Among four types of liposomes, the one composed of sphingomyelin, stearylamine and cholesterol was most potent in enhancing chemotherapeutic effect of ara-C. And the findings that ara-C was released gradually from liposome in vitro and that ara-C in liposome was chemotherapeutically effective against subsequently inoculated L1210 cells suggested that slow but long-lasting release of ara-C from liposome was partially responsible for enhanced chemotherapeutic effect.Keywords
This publication has 4 references indexed in Scilit:
- Targeting of drugsNature, 1977
- Complement-dependent damage to liposomes prepared from pure lipids and Forssman haptenBiochemistry, 1969
- Phospholipid spherules (liposomes) as a model for biological membranesJournal of Lipid Research, 1968
- Studies on the Production of Wassermann ReaginThe Journal of Immunology, 1962