2007
DOI: 10.1002/jps.20915
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Percolative drug diffusion from cylindrical matrix systems with unsealed boundaries

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Cited by 6 publications
(6 citation statements)
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“…This is consistent with the fact that the pore sizes also decreased with increasing Al/Si ratio (see Fig. 4); it is logical that drug diffusion through the geopolymer, and therefore also drug release, is slower in a system of smaller pores [30]. Increasing aluminum content resulted in a more linear release profile, and this linear release should also be attributed to the shift towards smaller pores in the aluminum rich compositions, since it has been shown that polymeric systems with pore diameters in a range comparable with the size of the drug molecules enables zero order release [31].…”
Section: Resultssupporting
confidence: 87%
“…This is consistent with the fact that the pore sizes also decreased with increasing Al/Si ratio (see Fig. 4); it is logical that drug diffusion through the geopolymer, and therefore also drug release, is slower in a system of smaller pores [30]. Increasing aluminum content resulted in a more linear release profile, and this linear release should also be attributed to the shift towards smaller pores in the aluminum rich compositions, since it has been shown that polymeric systems with pore diameters in a range comparable with the size of the drug molecules enables zero order release [31].…”
Section: Resultssupporting
confidence: 87%
“…In addition, an upper threshold was observed, above which the matrix no longer remained intact after drug release. Subsequent work in this field has focused on aspects such as the fractal dimensions of pore networks (Bonny and Leuenberger, 1993), particle size and drug/excipient particle size ratio (Caraballo et al, 1996;Millán et al, 1998) and three-dimensional release (Brohede et al, 2007).…”
Section: Percolation Effectsmentioning
confidence: 99%
“…It is therefore important to analyze and understand these interactions also with respect to identifying possible ways to alter the nanostructure of cellulose in order to achieve better control over the drug release process. Recently, a series of experimental studies investigated the mechanisms at work in the drug release process. In these studies, NaCl was commonly used as a stand-in model for the polar drug components.…”
Section: Introductionmentioning
confidence: 99%