| Wiggenhorn, Michael (2007): Scale-Up of Liposome Manufacturing: Combining High Pressure Liposome Extrusion with Drying Technologies. Dissertation, LMU München: Faculty of Chemistry and Pharmacy |
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PDF
Wiggenhorn_Michael.pdf 9Mb |
Abstract
The study provides a comprehensive overview on different stabilization techniques for liposomal formulations. The selection of the appropriate technology for a particular formulation can thereby be based on several considerations. If free flowable particulate bulk material is desired the spraying-technologies are preferred over lyophilization. Another advantage of spraying-based technologies is the possibility to combine the liposome formation step and the drying step within the same process. It is a prerequisite for the selection of the stabilization technique that the integrity of the liposomes is preserved with the incorporated drug after the process. Spray-drying is related to a thermal stress for the formulation but only for a short time. For heat labile drugs processes with low process temperatures, e.g. freeze-drying, spray freeze-drying, inert-spray drying or supercritical drying are most adequate. However, for technologies with a freezing step a sufficient stabilization against freezing induced stress e.g. by the selection of appropriate cryoprotectors is needed.
| Item Type: | Thesis (Dissertation, LMU Munich) | |
|---|---|---|
| Subjects: | 600 Natural sciences and mathematics > 540 Chemistry and allied sciences 600 Natural sciences and mathematics | |
| Faculties: | Faculty of Chemistry and Pharmacy | |
| Language: | English | |
| Date Accepted: | 30. July 2007 | |
| 1. Referee: | Winter, Gerhard | |
| Persistent Identifier (URN): | urn:nbn:de:bvb:19-84870 | |
| MD5 Checksum of the PDF-file: | c8e1266661e4333bb14eeafb005425bf | |
| Signature of the printed copy: | 0001/UMC 16909 | |
| ID Code: | 8487 | |
| Deposited On: | 26. May 2008 12:30 | (UTC) |
| Last Modified: | 16. Oct 2012 08:17 | (UTC) |

