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DC Field | Value | Language |
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dc.contributor.author | Parawee Rattanakit | en_US |
dc.contributor.author | Simon E. Moulton | en_US |
dc.contributor.author | Karen S. Santiago | en_US |
dc.contributor.author | Saisunee Liawruangrath | en_US |
dc.contributor.author | Gordon G. Wallace | en_US |
dc.date.accessioned | 2018-09-04T06:13:29Z | - |
dc.date.available | 2018-09-04T06:13:29Z | - |
dc.date.issued | 2012-01-17 | en_US |
dc.identifier.issn | 18733476 | en_US |
dc.identifier.issn | 03785173 | en_US |
dc.identifier.other | 2-s2.0-84655162789 | en_US |
dc.identifier.other | 10.1016/j.ijpharm.2011.11.007 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84655162789&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/51983 | - |
dc.description.abstract | A novel extrusion printing system was used to create drug delivery structures wherein dexamethasone-21-phosphate disodium salt (Dex21P) was encapsulated within a biodegradable polymer (PLGA) and water soluble poly(vinyl alcohol) (PVA) configurations. The ability to control the drug release profile through the spatial distribution of drug within the printed 3-dimensional structures is demonstrated. The fabricated configurations were characterised by optical microscopy and SEM to evaluate surface morphology. The results clearly demonstrate the successful encapsulation of dexamethasone within a laminated PLGA:PVA structure. The resulting drug release profiles from the structures show a two stage release profile with distinctly different release rates and minimal initial burst release observed. Dexamethasone release was monitored over a 4-month period. This approach clearly demonstrates that the extrusion printing technique provides a facile and versatile approach to fabrication of novel drug delivery platforms. © 2011 Elsevier B.V. | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Extrusion printed polymer structures: A facile and versatile approach to tailored drug delivery platforms | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | International Journal of Pharmaceutics | en_US |
article.volume | 422 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | University of Wollongong | en_US |
article.stream.affiliations | University of Santo Tomas, Manila | en_US |
Appears in Collections: | CMUL: Journal Articles |
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