2015
DOI: 10.1016/j.ejpb.2015.07.011
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Solid-state properties and dissolution behaviour of tablets containing co-amorphous indomethacin–arginine

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Cited by 83 publications
(68 citation statements)
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“…After the dissolution experiment, it was evident that PHE and TRP were unable to affect the dissolution of IND. ARG, however, caused a and an ARG dependent in situ amorphization of IND [32,[40][41][42]. In this study, the pH increasing effect of ARG was excluded by adjusting the pH prior to every sample, evidence that at least in FaSSIF blank and FaSSIF, ARG might have acted as a counter ion and caused IND dissociation as described by ElShaer et al [32].…”
Section: Discussionmentioning
confidence: 73%
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“…After the dissolution experiment, it was evident that PHE and TRP were unable to affect the dissolution of IND. ARG, however, caused a and an ARG dependent in situ amorphization of IND [32,[40][41][42]. In this study, the pH increasing effect of ARG was excluded by adjusting the pH prior to every sample, evidence that at least in FaSSIF blank and FaSSIF, ARG might have acted as a counter ion and caused IND dissociation as described by ElShaer et al [32].…”
Section: Discussionmentioning
confidence: 73%
“…The in situ amorphization and the subsequent formation of an amorphous ARG-IND salt are also a possible solubilisation mechanism since the clear supersaturation occurred before reaching the plateau. It may, however, only apply in FeSSIF, since Lenz et al reported that in situ amorphization was observed at pH 4.5 but not at pH 6.8 [40].…”
Section: Discussionmentioning
confidence: 99%
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“…One advantage of ball milling is that it is inflicting only very limited chemical degradation (17), specifically for some indomethacin systems degradation levels of less than 1.5% were found (13). Recently, spray-drying has been demonstrated to be another suitable production method for the preparation of co-amorphous systems (18,19). Co-amorphous formulations, in which a given drug is stabilized by another drug molecule, were introduced in order to reduce the amount of excipient needed and eventually to allow the simultaneous administration of several drugs in a single dosage form.…”
Section: Introductionmentioning
confidence: 98%
“…Coformers that have been successfully applied to stabilize an amorphous drug include saccharin (Gao et al, 2013), nicotinamide (Shayanfar, 2013), carboxylic acids (Lu and Zografi, 1998;Masuda et al, 2012;Hoppu et al, 2007Hoppu et al, & 2009Ali et al, 2015;Han et al, 2016;Hu et al, 2014) and sugars (Descamps et al, 2007). In particular, amino acids capable of forming charge-assisted hydrogen bonds have been widely studied (Löbmann et al, 2013;Jensen et al, 2014Jensen et al, , 2015Jensen et al, & 2016Laitinen et al, 2014;Lenz et al, 2015;Huang et al, 2016;Craye et al, 2015). On the other hand, an increase in the physical stability was observed for coamorphous simvastatin-glipizide, even though there was no evidence for intermolecular interactions, suggesting that molecular level mixing may be sufficient to stabilize the amorphous phase (Löbmann et al, 2012).…”
Section: Introductionmentioning
confidence: 99%