A 3D Biohybrid Real-Scale Model of the Brain Cancer Microenvironment for Advanced In Vitro Testing.

Adv Mater Technol

Smart Bio-Interfaces, Istituto Italiano di Tecnologia, Viale Rinaldo Piaggio 34, Pontedera 56025, Italy.

Published: October 2020

AI Article Synopsis

  • The study presents a 3D-printed biohybrid model of the brain tumor microenvironment aimed at improving drug screening for CNS conditions.
  • It features a microfluidic device that supports the co-culture of cells mimicking the blood-brain barrier and glioblastoma cells, enabling a realistic representation of drug interactions.
  • The model successfully demonstrates selective barrier properties and the ability to test chemotherapy-loaded nanocarriers, showcasing its potential for high-throughput applications in CNS disease treatment.

Article Abstract

The modeling of the pathological microenvironment of the central nervous system (CNS) represents a disrupting approach for drug screening for advanced therapies against tumors and neuronal disorders. The in vitro investigations of the crossing and diffusion of drugs through the blood-brain barrier (BBB) are still not completely reliable, due to technological limits in the replication of 3D microstructures that can faithfully mimic the in vivo scenario. Here, an innovative 1:1 scale 3D-printed realistic biohybrid model of the brain tumor microenvironment, with both luminal and parenchyma compartments, is presented. The dynamically controllable microfluidic device, fabricated through two-photon lithography, enables the triple co-culture of hCMEC/D3 cells, forming the internal biohybrid endothelium of the capillaries, of astrocytes, and of magnetically-driven spheroids of U87 glioblastoma cells. Tumor spheroids are obtained from culturing glioblas-toma cells inside 3D microcages loaded with superparamagnetic iron oxide nanoparticles (SPIONs). The system proves to be capable in hindering dextran diffusion through the bioinspired BBB, while allowing chemotherapy-loaded nanocarriers to cross it. The proper formation of the selective barrier and the good performance of the anti-tumor treatment demonstrate that the proposed device can be successfully exploited as a realistic in vitro model for high-throughput drug screening in CNS diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116223PMC
http://dx.doi.org/10.1002/admt.202000540DOI Listing

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