4.5 Article

When Interactions Between Bile Salts and Cyclodextrin Cause a Negative Food Effect: Dynamic Dissolution/Permeation Studies with Itraconazole (Sporanox®) and Biomimetic Media

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 112, Issue 5, Pages 1372-1378

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.xphs.2022.12.010

Keywords

Bioavailability; Cyclodextrin(s); Food effect(s); In vitro model(s); Oral absorption; Poorly water-soluble drug(s); Precipitation; Solubility; Solubilization; Supersaturation

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This study investigated the influence of bile salts and phospholipids on the absorption of itraconazole from Sporanox(R) oral solution. It was found that both bile salts and phospholipids increased the solubility of itraconazole, but higher concentrations of bile salts resulted in a faster decrease in solubility and reduced in vitro permeation.
The marketed oral solution of itraconazole (Sporanox (R)) contains 40% (259.2 mM) of 2-hydroxypropyl-b-cyclodextrin (HP -b-CD). The obvious role of HP -b-CD is to solubilize itraconazole and to overcome its poor aqueous solubility that restricts its absorption. In this study, we investigated the biorelevance of in vitro experiments by the influence of biomimetic media (containing bile salts and phospholipids) on the predicted itraconazole absorption from the commercial HP -b-CD-based Sporanox (R) solution. We performed phase-solubility studies of itraconazole and dynamic 2-step-dissolution/permeation studies using a biomimetic artificial barrier, Sporanox (R) solution, and fasted state simulated intestinal fluid (FaSSIF_V1). Both FaSSIF_V1 and HP -b-CD increased the apparent solubility of itraconazole when used individually. In combination, their solubility-enhancing effects were not additive probably due to the competition of bile salts with itraconazole for the hydrophobic cavity of HP -b-CD. Our combined dissolution/permeation experi-ments indicated the occurrence of a transient supersaturation from Sporanox (R) upon two-step dissolution. Through systematic variation of bile salt concentrations in the biomimetic media, it was observed that the extent and the duration of supersaturation depend on the concentrations of bile salts: supersaturation was rather stable in the absence of bile salts and phospholipids. The higher the bile salt concentration, the faster the collapse of the transient supersaturation occurred, an effect which is nicely mirrored by reduced in vitro permeation across the barrier. This is an indication of a negative food effect, which in fact correlates well with what earlier had been observed in clinical studies for Sporanox (R) solution. In essence, we could demonstrate that in vitro two-stage dissolution/permeation experiments using an artificial barrier and selected biomimetic media may predict the negative effects of the latter on cyclodextrin-based drug formulations like Sporanox (R) Oral Solution and, at the same time, provide a deeper mechanistic insight.(c) 2022 The Authors. Published by Elsevier Inc. on behalf of American Pharmacists Association. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)

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