Proceedings of the PSK Conference (대한약학회:학술대회논문집)
- 2003.04a
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- Pages.295.2-295.2
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- 2003
Lipid nanodispersion for parenteral drug delivery: in vitro characterization
- Lee, Jung-Min (College of Pharmacy, Chung-Ang University) ;
- Choi, Sung-Up (College of Pharmacy, Chung-Ang University) ;
- Lee, Byoung-Moo (College of Pharmacy, Chung-Ang University) ;
- Lee, Sung-Jae (College of Pharmacy, Chung-Ang University) ;
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Choi, Young-Wook
(College of Pharmacy, Chung-Ang University)
- Published : 2003.04.01
Abstract
Lipid nanodispersion (LN) composed of biocompatible lipids and surfactants is an alternative parenteral drug delivery system especially for lipophilic drugs. It has been studied for versatile applications such as oral, parenteral, topical, ocular, vaccine, and peptide drug delivery. The purpose of this study was to produce a novel LN system for intravenous injection using the high pressure homogenization. (omitted)
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