Lorenzo Moroni

This study develops marrow-mimic scaffolds that enhance cRBC production by supporting macrophage-erythroblast interactions in high-density cultures.

The paper develops a hollow electrospun scaffold (hydrocup) for in vivo cell delivery, showing it retains cells and releases cytokines for 6 weeks in rats.

The paper develops reCardioids, a human heart organoid model, to study doxorubicin and radiotherapy-induced cardiotoxicity, showing improved cellular maturity and response to treatment.

This study investigates how scaffold geometry and material affect vibrational behavior under mechanical stimulation in electrospun bundles for tendon/ligament and enthesis tissue regeneration.

The paper introduces a thyroid-on-chip platform using mouse embryonic stem cell-derived thyroid organoids to dynamically screen endocrine disrupting chemicals (EDCs) and identify molecular signatures of thyroid disruption.

This study develops a hybrid 3D construct that supports both vascular network formation and osteogenic differentiation in vitro using tailored hydrogel chemistry and cell co-culture.

This study develops a 3D thyroid in vitro model using microfluidic bioprinting to test endocrine disruptors and assess their effects.

This paper develops a bioprinting method using hPDC spheroids in HAMA hydrogels to promote endochondral ossification for bone regeneration, showing enhanced hypertrophic cartilage formation and osteogenic differentiation.

This paper develops a decellularized porcine small intestine scaffold for burn wound treatment, showing good mechanical properties, fluid absorption, and cytocompatibility.

This study develops wave-inspired MEW scaffolds that mimic ligament structure and mechanics, supporting cell adhesion, proliferation, and matrix synthesis.

This study develops biomimetic nanofibrous scaffolds with auxetic properties for enthesis regeneration, showing their mechanical behavior matches natural tendon fascicles.

This paper investigates the structure and mechanics of the sheep calcaneal enthesis to inform scaffold design for tissue engineering.

This paper develops hybrid bioinks and an embedding bioprinting technique to create a multilayered artery model that mimics native blood vessel structure and supports cell viability.

This study shows that low-dose DMSO treatment improves hiPSC differentiation into kidney organoids by enhancing SIX2 expression and altering pluripotent gene expression.

This paper introduces CLADDING, a bioprinting method using a self-healing transparent support bath to enable printing of low-viscosity protein-based bioinks with high cell viability.