| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2083334 | European Journal of Pharmaceutics and Biopharmaceutics | 2015 | 10 Pages |
•We investigated the interaction between an API and FaSSIF using NMR-spectroscopy.•Interaction was understood on a molecular level using DOSY and NOE experiments.•Enhanced solubility by lecithin and taurocholate was explained by mixed micelles.•A phase diagram describing presence of different types of micelles was derived.
The interaction between an ampholytic and amphiphilic Active Pharmaceutical Ingredient (API) showing unusual pH dependent solubility and Fasted State Simulated Intestinal Fluid (FaSSIF) was studied by NMR spectroscopy. Solubility in FaSSIF was drastically increased, about 30 fold, compared to simulated gastrointestinal fluid without bile salts. Our studies aimed at understanding the mechanisms that lead to this drastic enhancement. All species present in solution at various concentrations of API were characterised by Diffusion Ordered Spectroscopy (DOSY) NMR measurements. These indicated the presence of mixed taurocholate–lecithin and pure taurocholate micelles in pure FaSSIF, and formation of mixed taurocholate–API micelles after addition of API. The formation of taurocholate–API micelles was also supported by Nuclear Overhauser Effect/Enhancement (NOE) contacts between taurocholate and the API. Formation of mixed taurocholate–API micelles took place at the expense of pure taurocholate micelles, whereas mixed taurocholate–lecithin micelles remained uninfluenced by the presence of API. Our results showed that the increase in solubility was due to similar amphiphilic properties of the API and taurocholate which enabled formation of mixed taurocholate–API micelles. From results of determination of solubility as well as NMR experiments a phase diagram comprising several micellar species was derived.
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