Leveraging the use of in vitro and computational methods to support the development of enabling oral drug products: An InPharma commentary

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Date
2023-07-13
Authors
Reppas, Christos
Kuentz, Martin
Bauer-Brandl, Annette
Carlert, Sara
Dallmann, André
Dietrich, Shirin
Dressman, Jennifer
Ejskjaer, Lotte
Frechen, Sebastian
Guidetti, Matteo
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Elsevier B.V.
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Abstract
Due to the strong tendency towards poorly soluble drugs in modern development pipelines, enabling drug formulations such as amorphous solid dispersions, cyclodextrins, co-crystals and lipid-based formulations are frequently applied to solubilize or generate supersaturation in gastrointestinal fluids, thus enhancing oral drug absorption. Although many innovative in vitro and in silico tools have been introduced in recent years to aid development of enabling formulations, significant knowledge gaps still exist with respect to how best to implement them. As a result, the development strategy for enabling formulations varies considerably within the industry and many elements of empiricism remain. The InPharma network aims to advance a mechanistic, animal-free approach to the assessment of drug developability. This commentary focuses current status and next steps that will be taken in InPharma to identify and fully utilize 'best practice' in vitro and in silico tools for use in physiologically based biopharmaceutic models.
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Keywords
Enabling formulations In vitroIn silico , PBBMrDCS , Computational , Amorphous solid dispersions , Lipid-based formulations , Cyclodextrins , Co-crystals , Salts
Citation
Reppas, C., Kuentz, M., Bauer-Brandl, A., Carlert, S., Dallmann, A., Dietrich, S., Dressman, J., Ejskjaer, L., Frechen, S., Guidetti, M., Holm, R., Holzem, F. L., Karlsson, E., Kostewicz, E., Panbachi, S., Paulus, F., Senniksen, M. B., Stillhart, C., Turner, D. B., Vertzoni, M., Vrenken, P., Zöller, L., Griffin, B. T. and O'Dwyer, P. J. (2023) 'Leveraging the use of in vitro and computational methods to support the development of enabling oral drug products: An InPharma commentary', European Journal of Pharmaceutical Sciences, 188, 106505 (22pp). doi: 10.1016/j.ejps.2023.106505
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