Interaction of polymers with bile salts - Impact on solubilisation and absorption of poorly water-soluble drugs

Pigliacelli, Claudia, Belton, Peter, Wilde, Peter, Baldelli Bombelli, Francesca, Kroon, Paul A., Winterbone, Mark S. and Qi, Sheng ORCID: https://orcid.org/0000-0003-1872-9572 (2023) Interaction of polymers with bile salts - Impact on solubilisation and absorption of poorly water-soluble drugs. Colloids and Surfaces B: Biointerfaces, 222. ISSN 0927-7765

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Abstract

Formulating poorly soluble drugs with polymers in the form of solid dispersions has been widely used for improving drug dissolution. Endogenous surface-active species present in the gut, such as bile salts, lecithin and other phospholipids, have been shown to play a key role in facilitating lipids and poorly soluble drugs solubilisation in the gut. In this study, we examined the possible occurrence of interactions between a model bile salt, sodium taurocholate (NaTC), and model spray dried solid dispersions comprising piroxicam and Hydroxypropyl Methylcellulose (HPMC), a commonly used hydrophilic polymer for solid dispersion preparation. Solubility measurements revealed the good solubilisation effect of NaTC on the crystalline drug, which was enhanced by the addition of HPMC, and further boosted by the drug formulation into solid dispersion. The colloidal behaviour of the solid dispersions upon dissolution in biorelevant media, with and without NaTC, revealed the formation of NaTC-HPMC complexes and other mixed colloidal species. Cellular level drug absorption studies obtained using Caco-2 monolayers confirmed that the combination of drug being delivered by solid dispersion and the presence of bile salt and lecithin significantly contributed to the improved drug absorption. Together with the role of NaTC-HPMC complexes in assisting the drug solubilisation, our results also highlight the complex interplay between bile salts, excipients and drug absorption.

Item Type:	Article
Additional Information:	Acknowledgments: The authors would like to thank the University of East Anglia for the PhD studentship funding and the Biotechnology and Biological Sciences Research Council (BBSRC) for supporting this research through an Institute Strategic Programme Grant (Food Innovation and Health, BB/R012512/1) and its constituent project(s) BBS/E/F/000PR10343 (Theme 1, Food Innovation) and BBS/E/F/000PR10345 (Theme 2, Digestion in the Upper GI Tract).
Faculty \ School:	Faculty of Science > School of Pharmacy (former - to 2024) Faculty of Science > School of Chemistry (former - to 2024)
UEA Research Groups:	Faculty of Science > Research Groups > Pharmaceutical Materials and Soft Matter
Depositing User:	LivePure Connector
Date Deposited:	22 Nov 2022 11:31
Last Modified:	13 Dec 2024 01:35
URI:	https://ueaeprints.uea.ac.uk/id/eprint/89945
DOI:	10.1016/j.colsurfb.2022.113044

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