Drug diffusion in biomimetic hydrogels: importance for drug transport and delivery in non-vascular tumor tissue

•Establishment and validation of a tumor ECM relevant in vitro diffusion method.•Biomimetic hydrogels reduce diffusion coefficients by 60-70% in vitro.•Spatio-temporal tissue concentration modelling translated in vitro diffusion to liver tumor penetration. Hydrogels of varying complexity are routine...

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Veröffentlicht in:European journal of pharmaceutical sciences 2022-05, Vol.172, p.106150-106150, Article 106150
Hauptverfasser: Degerstedt, Oliver, Gråsjö, Johan, Norberg, Anton, Sjögren, Erik, Hansson, Per, Lennernäs, Hans
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Sprache:eng
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Zusammenfassung:•Establishment and validation of a tumor ECM relevant in vitro diffusion method.•Biomimetic hydrogels reduce diffusion coefficients by 60-70% in vitro.•Spatio-temporal tissue concentration modelling translated in vitro diffusion to liver tumor penetration. Hydrogels of varying complexity are routinely used as scaffolds and 3D structures for in vitro tumor models to increase physiological relevance within pre-clinical cancer research. Relatively simple hydrogels such as agarose are well characterised, meanwhile biomimetic gels containing collagen and fibrin(ogen) have been studied to a much lesser extent. In this study, hydrogels mimicking the biophysical characteristics of liver cancer progression were investigated in terms of their UV-properties and influence on diffusion coefficients of different substances. UV-imaging technology was used to both visualize and quantify the diffusion process in a simple and rapid way. In general, agarose gel diffusion agreed well with predictions using the Stokes-Einstein equation meanwhile the biomimetic gels reduced diffusion coefficients by up to 70%. For doxorubicin, spatio-temporal tissue concentration modelling was used to translate in vitro diffusion to the more clinical context of tumor penetration in a solid liver tumor supplied by arterial blood. [Display omitted]
ISSN:0928-0987
1879-0720
1879-0720
DOI:10.1016/j.ejps.2022.106150