2011
DOI: 10.1016/j.ijpharm.2011.03.051
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Higuchi equation: Derivation, applications, use and misuse

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Cited by 766 publications
(477 citation statements)
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“…Drug release will be proceeded by the dissolution of the existing drug on the surface of the system and follow by swelling matrix polymer. The drug in the deeper parts will come out of the system when the drug on the surface had separated, so the concentration increases [35]. The release profile of NA from NA-CS, NA-CMC-D1, and NA-CMC-D3 with respect to time can be shown in Table 2 and Fig.…”
Section: Encapsulation Efficiency and Nicotinamide Releasementioning
confidence: 99%
See 1 more Smart Citation
“…Drug release will be proceeded by the dissolution of the existing drug on the surface of the system and follow by swelling matrix polymer. The drug in the deeper parts will come out of the system when the drug on the surface had separated, so the concentration increases [35]. The release profile of NA from NA-CS, NA-CMC-D1, and NA-CMC-D3 with respect to time can be shown in Table 2 and Fig.…”
Section: Encapsulation Efficiency and Nicotinamide Releasementioning
confidence: 99%
“…It indicates that drug release mechanism is not only influenced by the drug diffusion process, but also degradation of the polymeric matrix. Based on these models can be estimated that the release process through 2 steps, (i) drug release fully caused by drug diffusion and (ii) the degradation of polymer matrix [35]. Determination of drug release of all samples was done in a longer time that is 12 hours to know the stability of the system as depicted in Table 3 and Fig.…”
Section: Encapsulation Efficiency and Nicotinamide Releasementioning
confidence: 99%
“…The outcome of fitting (Table 2) showed that only the s-C-15h provided an excellent goodness of fit (R 2 > 0.95) and the n parameter indicated an anomalous (non-Fickian) transport (0.45 < n < 1.00) [51,52]. In contrast, s-C-1h gave a good goodness of fit (0.90 < R 2 < 0.95) but did not allow for drawing any conclusion on the limiting mechanism of release as the parameter (n) did not correspond to any known range according to the KP assumptions.…”
Section: Drug Releasementioning
confidence: 99%
“…However, it is unlikely that there will be one mathematical model that will be able to describe any type of release of ions or molecules from biomaterials. It is much more likely that there will be different mathematical models, applicable to specific types of systems that differ in geometry and composition (Arifin et al 2006;Brazel and Peppas 2000;Dash et al 2010;Fredenberg et al 2011;Frenning 2003;Frenning et al 2005;Frenning and Strømme 2003;Polakovič et al 1999;Siepmann and Peppas 2011;Siepmann and Siepmann 2008). Over the past few years, a few lattice-based three-dimensional (3D) mathematical models have been proposed to study the in vivo bone formation process in porous biodegradable CaP scaffolds (Adachi et al 2006;Byrne et al 2007;Sun et al 2013).…”
Section: Introductionmentioning
confidence: 99%