TY - JOUR
T1 - The Route to Artery Mimetics
T2 - Hybrid Bioinks for Embedded Bioprinting of Multimaterial Cylindrical Models
AU - Aizarna-Lopetegui, Uxue
AU - Herrero-Ruiz, Ada
AU - Decarli, Monize C.
AU - Urigoitia-Asua, Ane
AU - Chavarri-Urraca, Karla
AU - Moroni, Lorenzo
AU - Henriksen-Lacey, Malou
AU - de Aberasturi, Dorleta Jimenez
PY - 2025/9/1
Y1 - 2025/9/1
N2 - The integration of biomaterials with living cells and stimuli-responsive materials can be employed to create bioinks capable of generating 3D in vitro models that better recapitulate native tissues. A cellularized, multilayered cylindrical model is introduced that combines such hybrid multifunctional materials to mimic the tunica adventitia arterial wall, and an extracellular matrix (ECM)-based bioink for the tunica media artery layer. The stimuli-responsive hybrid ink integrates inorganic (plasmonic nanoparticles) and organic (polymers) components, providing structural support and introducing diverse functionalities to the system. The cell-laden bioink consists of human vascular smooth muscle cells within a hydrogel based on porcine artery-derived decellularized ECM that fosters optimal cell growth and proliferation. An embedding bioprinting technique is employed for the fabrication of the multimaterial model consisting of functional concentric cylinders. The dimensions of the 3D model and the bioprinting parameters are fine-tuned to ensure effective crosslinking of the multiple concentric layers resulting in the creation of self-supporting constructs. The effectiveness of the hybrid bioink composition and bioprinting parameters in supporting cell viability and proliferation within the multilayered construct is demonstrated, expanding the possibilities of employing novel multi-component materials for the fabrication of 3D vasculature models resembling the structure of native blood vessels.
AB - The integration of biomaterials with living cells and stimuli-responsive materials can be employed to create bioinks capable of generating 3D in vitro models that better recapitulate native tissues. A cellularized, multilayered cylindrical model is introduced that combines such hybrid multifunctional materials to mimic the tunica adventitia arterial wall, and an extracellular matrix (ECM)-based bioink for the tunica media artery layer. The stimuli-responsive hybrid ink integrates inorganic (plasmonic nanoparticles) and organic (polymers) components, providing structural support and introducing diverse functionalities to the system. The cell-laden bioink consists of human vascular smooth muscle cells within a hydrogel based on porcine artery-derived decellularized ECM that fosters optimal cell growth and proliferation. An embedding bioprinting technique is employed for the fabrication of the multimaterial model consisting of functional concentric cylinders. The dimensions of the 3D model and the bioprinting parameters are fine-tuned to ensure effective crosslinking of the multiple concentric layers resulting in the creation of self-supporting constructs. The effectiveness of the hybrid bioink composition and bioprinting parameters in supporting cell viability and proliferation within the multilayered construct is demonstrated, expanding the possibilities of employing novel multi-component materials for the fabrication of 3D vasculature models resembling the structure of native blood vessels.
KW - arteries
KW - dECM-based bioinks
KW - embedded multilayered 3D bioprinting
KW - hybrid materials
KW - stimuli-responsive inks
KW - COLLAGEN FIBRILLOGENESIS
KW - MECHANICAL-PROPERTIES
KW - TISSUE
KW - SCAFFOLDS
U2 - 10.1002/adfm.202419072
DO - 10.1002/adfm.202419072
M3 - Article
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 49
M1 - e19072
ER -