Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.ijpharm.2013.05.006
DC FieldValue
dc.titleNovel alternatives to reduce powder retention in the dry powder inhaler during aerosolization
dc.contributor.authorHeng, D.
dc.contributor.authorLee, S.H.
dc.contributor.authorNg, W.K.
dc.contributor.authorChan, H.-K.
dc.contributor.authorKwek, J.W.
dc.contributor.authorTan, R.B.H.
dc.date.accessioned2014-10-09T06:55:38Z
dc.date.available2014-10-09T06:55:38Z
dc.date.issued2013
dc.identifier.citationHeng, D., Lee, S.H., Ng, W.K., Chan, H.-K., Kwek, J.W., Tan, R.B.H. (2013). Novel alternatives to reduce powder retention in the dry powder inhaler during aerosolization. International Journal of Pharmaceutics 452 (1-2) : 194-200. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ijpharm.2013.05.006
dc.identifier.issn03785173
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89597
dc.description.abstractDry powder inhalers (DPIs) are used predominantly for the treatment of pulmonary diseases by delivering drugs directly into the lungs. The drug delivery efficiency is typically low and there is significant drug retention inside the DPI. An innovative 'green' initiative aimed at minimizing drug wastage via channeling the residual drug into the useful inhaled therapeutic fraction was pioneered. Drug retention could be minimized via coating the drug capsule and delivery device with pharmaceutically acceptable forcecontrol agents. This coating reduces the adhesion between the drug particles and the internal surfaces of the DPI, which in turn increases the fine particle dose by as much as 300%. © 2013 Elsevier B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.ijpharm.2013.05.006
dc.sourceScopus
dc.subjectBiomimicry
dc.subjectCapsule
dc.subjectDevice
dc.subjectDry powder inhaler
dc.subjectForce control agents
dc.subjectPowder retention
dc.subjectSurface coating
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1016/j.ijpharm.2013.05.006
dc.description.sourcetitleInternational Journal of Pharmaceutics
dc.description.volume452
dc.description.issue1-2
dc.description.page194-200
dc.description.codenIJPHD
dc.identifier.isiut000321496200023
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