Please use this identifier to cite or link to this item: https://doi.org/10.1002/jps.21207
DC FieldValue
dc.titleBiodegradable films developed by electrospray deposition for sustained drug delivery
dc.contributor.authorXie, J.
dc.contributor.authorTan, J.C.
dc.contributor.authorWang, C.-H.
dc.date.accessioned2014-06-17T07:36:38Z
dc.date.available2014-06-17T07:36:38Z
dc.date.issued2008-08
dc.identifier.citationXie, J., Tan, J.C., Wang, C.-H. (2008-08). Biodegradable films developed by electrospray deposition for sustained drug delivery. Journal of Pharmaceutical Sciences 97 (8) : 3109-3122. ScholarBank@NUS Repository. https://doi.org/10.1002/jps.21207
dc.identifier.issn00223549
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/63538
dc.description.abstractThe objective of present study is to develop biodegradable films with controllable thickness for sustained release applications using a combination of electrospray deposition techniques. The model anticancer drug-paclitaxel is encapsulated inside PLGA films. The morphology observed by atomic force microscopy and scanning electron microscopy reveals that the film has a flat surface together with a dense structure. X-ray photo-electron spectroscopy results show that some amount of paclitaxel is found on the surface layer of films. X-ray diffractometry (XRD) analysis suggests that paclitaxel is in an amorphous form in the polymer matrix even for up to 30% drug loading. Differential scanning calorimetry (DSC) study further proved that paclitaxel is in a solid solution state in polymer films. In vitro release profile indicates that sustained release of paclitaxel from the films is for more than 85 days, without the tri-phasic release profile typically for PLGA films. The phase contrast images clearly suggests a slight decrease in the number of C6 glioma cells as the paclitaxel loading within the polymeric films is increased. The results of MTT assay employed to quantify the cell viability correlates well with the observation from phase contrast microscopy. © 2007 Wiley-Liss, Inc. and the American Pharmacists Association.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/jps.21207
dc.sourceScopus
dc.subjectControlled delivery
dc.subjectEncapsulation
dc.subjectPaclitaxel
dc.subjectPolymeric drug carrier
dc.subjectPolymeric drug delivery systems
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1002/jps.21207
dc.description.sourcetitleJournal of Pharmaceutical Sciences
dc.description.volume97
dc.description.issue8
dc.description.page3109-3122
dc.description.codenJPMSA
dc.identifier.isiut000258081100017
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