JOURNAL ARTICLE

Preparation of PEGylated Paclitaxel Liposomes and Tissue Distribution Study in Mice

Abstract

A long circulation paclitaxel liposome was prepared by dispersion of film method. The size of liposomes was around 207 nm and drug encapsulation efficiency was 96.5%. The PEGylated paclitaxel liposomes were very stable when stored in PBS, pH 6.5 at 4degC. After 22 days, leakage of drug from liposomes was only 6%. In vivo biodistribution of paclitaxel liposomes and free paclitaxel were compared in prostate tumor-bearing mice by intravenous injection. Drug concentration of paclitaxel liposomes in tumor was remarkably higher than that of free paclitaxel. These results suggest that this stable, long circulation paclitaxel- containing liposome may be a feasible targeting delivery system for paclitaxel and other hydrophobic or toxic compounds.

Keywords:
Liposome Paclitaxel Biodistribution Drug delivery Pharmacology In vivo Chemistry Drug Pharmacokinetics Chemotherapy In vitro Medicine Biochemistry Surgery Biology Organic chemistry

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