Abstract
Important recent technological developments in liposome research for parenteral drug delivery are discussed. The chapter is divided into two major sections. The first section provides an overview of liposome physicochemical properties and the mechanism of vesicle formation. Various liposome preparation methods are reviewed, including film hydration method, organic solvent injection method, and reverse phase evaporation. Then several drug encapsulation/loading techniques are discussed. In the second part, the use of liposomes for parenteral drug delivery is discussed with specific examples of marketed products as well as those that are currently under investigation. In particular, the in vivo fate of drug containing liposomes and several successful examples of formulation approaches to alter the drug/liposome in vivo disposition are discussed.
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Abbreviations
- DMPC:
-
Dimyristoyl-phosphatidylcholine
- DMPG:
-
Dqqqimyristoyl-phosphatidylglycerol
- DOPE:
-
Dioleoyl-phosphatidylethanolamine
- DPPC:
-
Dipalmitoyl-phosphatidylcholine
- DSPC:
-
Distearoyl-phosphatidylcholine
- DSPG:
-
Distearyl phosphatidylglycerol
- GV:
-
Giant vesicles
- LUV:
-
Large unilamellar vesicles
- MLV:
-
Multilamellar vesicles
- MPS:
-
Mononuclear phagocyte system
- MVV:
-
Multivesicular vesicles
- RES:
-
Reticuloendothelial system
- REV:
-
Reverse-phase evaporation vesicles
- SUV:
-
Small unilamellar vesicles
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Xu, X., Burgess, D.J. (2012). Liposomes as Carriers for Controlled Drug Delivery. In: Wright, J., Burgess, D. (eds) Long Acting Injections and Implants. Advances in Delivery Science and Technology. Springer, Boston, MA. https://doi.org/10.1007/978-1-4614-0554-2_11
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