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VINCENZO LA CARRUBBA

Double flow bioreactor for in vitro test of drug delivery

  • Autori: La Carrubba, V.; Ghersi, G.; Greco, S.; CARFI' PAVIA, F.; Brucato, V.
  • Anno di pubblicazione: 2017
  • Tipologia: Articolo in rivista (Articolo in rivista)
  • Parole Chiave: Bioreactor; Fluid dynamic; Phase separation; Poly-L-lactic acid; Shear stress; Vascular tissue engineering; Drug Evaluation, Preclinical; Equipment Design; Humans; Particle Size; Pharmaceutical Preparations; Polymers; Surface Properties; Bioreactors; Drug Delivery Systems; Medicine (all); 3003
  • OA Link: http://hdl.handle.net/10447/260302

Abstract

In this work, double-structured polymeric scaffolds were produced, and a double flow bioreactor was designed and set up in order to create a novel system to carry out advanced in vitro drug delivery tests. The scaffolds, consisting of a cylindrical porous matrix, are able to host cells, thus mimicking a three-dimensional tumor mass: moreover, a “pseudo-vascular” structure was embedded into the matrix, with the aim of allowing a flow circulation. The structure that emulates a blood vessel is a porous tubular-shaped scaffold prepared by Diffusion Induced Phase Separation (DIPS), with an internal lumen of 2 mm and a wall thickness of 200 micrometers. The as-prepared vessel was incorporated into a three-dimensional matrix, prepared by Thermally Induced Phase Separation (TIPS), characterized by a high porosity (about 95%) and pore size adequate to accommodate tumor cells and/or mesenchymal cells. The morphology of the multifunctional scaffolds is easy-tunable in terms of pore size, porosity and thickness and therefore adaptable to various cell or tissue types. At the same time, a double flow bioreactor was designed and built up, in order to be able to carry out biological tests on the scaffold under dynamic conditions. The device allows a separate control of the two flows (one for the tubular scaffold, one for the porous matrix) through the scaffolds. Preliminary characterizations and tests carried out suggest the presented system as a candidate to suitably “in vitro” assess the effects of different drugs on various cell populations.