The aim of this study is to develop a kinetic model for the quantitative evaluation of, and to examine dose dependency in liposome degradation in blood circulation in vivo. Multilamellar liposomes labeled with 3H-inulin were administered intravenously into rats and the time courses of blood concentr
Kinetic modelling of liposome degradation in peritoneal macrophages
β Scribed by Hideyoshi Harashima; Noriko Hirai; Hiroshi Kiwada
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 608 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0142-2782
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The objective of this study was to quantify and model the degradation process of liposomes in peritoneal macrophages (PMs). Iodinated albumin (^125^Iβalb) was chosen to be the marker of liposome degradation. The time course of the degradation of free ^125^Iβalb after pinocytosis by PMs followed firstβorder kinetics with a halfβlife of 23 min. The degradation of liposomally encapsulated ^125^Iβalb was also quantified. Kinetic modelling of liposome degradation indicated the existence of two kinetically different processes, one with a halfβlife of 13 min and the other with a halfβlife of 7.5 h. Comparing the degradation of liposomal and free ^125^Iβalb suggested that ^125^Iβalb was delivered to lysosomes much faster through phagocytosis than pinocytosis. These results indicate that the intracellular degradation kinetics of pinosomes and phagosomes is different. This method can quantify the rate and extent of liposomal degradation in macrophages and provide kinetic information on the intracellular destiny of liposomally encapsulated compounds.
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