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Anti-neovascular therapy by use of tumor neovasculature-targeted long-circulating liposome.
Effect of Polyethyleneglycol (PEG) Chain on Cell Uptake of PEG-Modified Liposomes
TLDR
It was suggested that the increase in liposome uptake into the tumor cell was induced by modification of PEG-lipids with apparent stability, and PEG 2,000-DPG, which had a high rate of residual P EG-Lipid on liposomal membrane depending on the re-uptake to lipOSomal membrane, met to this requirement.
Determination of the thickness of the fixed aqueous layer around polyethyleneglycol-coated liposomes.
TLDR
A correlation was indicated to exist between the circulation time of liposomes and the thickness of the aqueous layer around the liposome and the electrical potential distributions near the membrane surfaces were shown to be different between adriamycin-encapsulatingliposomes with and without PEG coating.
Liposomalization of SN-38 as active metabolite of CPT-11.
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