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.
Original language | English |
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Pages (from-to) | 378-383 |
Number of pages | 6 |
Journal | European Journal of Pharmaceutical Sciences |
Volume | 38 |
Issue number | 4 |
DOIs | |
Publication status | Published - 5 Nov 2009 |
Keywords
- Diffusion
- Solvation
- Polydimethylsiloxane
- Penetration enhancement
- ATR-FTIR spectroscopy
- INTERNAL-REFLECTION SPECTROSCOPY
- IN-VITRO
- TRANSDERMAL DELIVERY
- SYNTHETIC MEMBRANES
- SOLUTE INTERACTIONS
- SILICONE MEMBRANES
- PERMEABILITY DATA
- PROPYLENE-GLYCOL
- SKIN PERMEATION
- BENZOIC-ACID