3D‐Printed Lipid Mesophases for the Treatment of Chronic Liver Disease

Author:

Carone Marianna1,Gazzi Rafaela1,Eugster Remo1,Gelli Rita2,Manten Niklaas1,Ganguin Aymar A.1,Valerio Silvia Di3,Yadav Garima1,Castaldo Pasqualina4,Mezzenga Raffaele5,Luciani Paola1,Aleandri Simone1ORCID

Affiliation:

1. Department of Chemistry, Biochemistry and Pharmaceutical Sciences University of Bern Bern 3012 Switzerland

2. Department of Chemistry “Ugo Schiff” and CSGI University of Florence Sesto Fiorentino Florence 50019 Italy

3. Department of Clinical and Molecular Sciences DISCLIMO University “’Politecnica delle Marche”’ Ancona 60126 Italy

4. Department of Biomedical Sciences and Public Health University “’Politecnica delle Marche”’ Ancona 60126 Italy

5. Laboratory of Food & Soft Materials Institute of Food Nutrition and Health Department for Health Sciences and Technology ETH Zurich 8092 Switzerland

Abstract

AbstractAlthough lipid‐based formulations are an attractive approach for enhancing the oral bioavailability of lipophilic drugs, their addition into solid oral dosage forms has been proven challenging due to their high viscosity and heat sensitivity. Therefore, unlike the traditional tableting process, this study employed semi‐solid extrusion 3D‐printing to produce–at room temperature–gastro‐resistant printlets containing a high percentage of bioactive lipids for the effective delivery of lipophilic drugs through self‐emulsification. The bio‐compatible lipidic mesophase ink, owing to a tunable 3D nanostructure, is employed as a starting material to produce printlets via additive manufacturing. An active lipid mixture – with antifibrotic properties – is blended with the antioxidant vitamin E and water, and the ink printability is optimized by carefully tailoring its composition, and thus its phase identity. The obtained printlets disintegrated upon contact with intestinal fluids forming colloidal structures that enhanced the solubility of a poorly water‐soluble drug. The printlets exhibited antifibrotic activity on human hepatic stellate cells, LX‐2, suggesting that the generated self‐emulsified colloidal structures made both the fibrosis‐resolving bioactive excipients and the drug promptly available, enhancing their cell uptake and, in turn, their therapeutic activity.

Publisher

Wiley

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