dc.contributor.author | McAuley, William J. | |
dc.contributor.author | Mader, Kerstin T. | |
dc.contributor.author | Tetteh, John | |
dc.contributor.author | Lane, Majella E. | |
dc.contributor.author | Hadgraft, Jonathan | |
dc.date.accessioned | 2013-01-11T14:29:08Z | |
dc.date.available | 2013-01-11T14:29:08Z | |
dc.date.issued | 2009-11-05 | |
dc.identifier.citation | McAuley , W J , Mader , K T , Tetteh , J , Lane , M E & Hadgraft , J 2009 , ' Simultaneous monitoring of drug and solvent diffusion across a model membrane using ATR-FTIR spectroscopy ' , European Journal of Pharmaceutical Sciences , vol. 38 , no. 4 , pp. 378-383 . https://doi.org/10.1016/j.ejps.2009.09.002 | |
dc.identifier.issn | 0928-0987 | |
dc.identifier.uri | http://hdl.handle.net/2299/9586 | |
dc.description.abstract | Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy has been used to simultaneously follow the diffusion of model drugs and solvent across polydimethylsiloxane (silicone) membrane. Three model drugs, cyanophenol (CNP), methyl nicotinate (MN) and butyl paraben (BP) were selected to cover a range of lipophilicities. Isostearyl isostearate (ISIS) was chosen as the solvent because its large molecular weight should facilitate observation of whether the drug molecules are able to diffuse through the membrane independently of the solvent. The diffusion of the three drugs and the solvent was successfully described by a Fickian model. The effects of parameters such as the absorption wavelength used to follow diffusion on the calculated diffusion coefficient were investigated. Absorption wavelength which affects the depth of penetration of the infrared radiation into the membrane did not significantly affect the calculated diffusion coefficient over the wavelength range tested. Each of the model drugs was observed to diffuse independently of the solvent across the membrane. The diffusion of a CNP-ISIS hydrogen bonded complex across the membrane was also monitored. The relative diffusion rates of the solute and solvent across the membrane can largely be accounted for by the molecular size of the permeant. (C) 2009 Elsevier B.V. All rights reserved. | en |
dc.format.extent | 6 | |
dc.format.extent | 267465 | |
dc.language.iso | eng | |
dc.relation.ispartof | European Journal of Pharmaceutical Sciences | |
dc.subject | Diffusion | |
dc.subject | Solvation | |
dc.subject | Polydimethylsiloxane | |
dc.subject | Penetration enhancement | |
dc.subject | ATR-FTIR spectroscopy | |
dc.subject | INTERNAL-REFLECTION SPECTROSCOPY | |
dc.subject | IN-VITRO | |
dc.subject | TRANSDERMAL DELIVERY | |
dc.subject | SYNTHETIC MEMBRANES | |
dc.subject | SOLUTE INTERACTIONS | |
dc.subject | SILICONE MEMBRANES | |
dc.subject | PERMEABILITY DATA | |
dc.subject | PROPYLENE-GLYCOL | |
dc.subject | SKIN PERMEATION | |
dc.subject | BENZOIC-ACID | |
dc.title | Simultaneous monitoring of drug and solvent diffusion across a model membrane using ATR-FTIR spectroscopy | en |
dc.contributor.institution | School of Life and Medical Sciences | |
dc.contributor.institution | Centre for Research into Topical Drug Delivery and Toxicology | |
dc.contributor.institution | Pharmaceutics | |
dc.contributor.institution | Skin and Nail Group | |
dc.contributor.institution | Pharmaceutical Analysis and Product Characterisation | |
dc.contributor.institution | Department of Clinical, Pharmaceutical and Biological Science | |
dc.description.status | Peer reviewed | |
rioxxterms.versionofrecord | 10.1016/j.ejps.2009.09.002 | |
rioxxterms.type | Journal Article/Review | |
herts.preservation.rarelyaccessed | true | |