Ainhoa Herrero
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Ainhoa Herrero has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Daniel F. de Castro Hernández
Bio2, Biomateriales y Bioimpresión, ICTP-CSIC, 28006 Madrid, Spain
1 shared publication - Fiona Ye Rojo Acero
Bio2, Biomateriales y Bioimpresión, ICTP-CSIC, 28006 Madrid, Spain
1 shared publication - Juan Jose Uriarte
ARIES Research Group, Escuela Politécnica Superior, Universidad Nebrija, 28015 Madrid, Spain
1 shared publication - Luis Maria Rodriguez-Lorenzo
Bio2, Biomateriales y Bioimpresión, ICTP-CSIC, 28006 Madrid, Spain
1 shared publication - María Lisseth Flores-Cedillo
División de Ingeniería Industrial, Tecnológico Nacional de México/Instituto Tecnológico Superior de San Luis Potosí Capital, San Luis Potosí, México, Mexico
1 shared publication - Raquel Villa
Bio2, Biomateriales y Bioimpresión, ICTP-CSIC, 28006 Madrid, Spain
1 shared publication
Latest Publications
- Open Access
Optimization of Bioink Formulations and Bioprinting Conditions for Enhanced Cell Viability in Particle-Containing Constructs
Extrusion-based bioprinting imposes stringent mechanical constraints on bioink formulations, yet the rheological parameters governing cell survival during the printing process are rarely reported in a standardized way, limiting cross-study comparison. In this work, we systematically characterized the viscoelastic properties of alginate/methylcellulose bioinks incorporating strontium-enriched hydroxyapatite (Sr-OHAp) particles and Poloxamer 188, and assessed their effect on PANC-1 cell viability in bioprinted constructs. The power law consistency index K and pseudoplasticity index n were used as quantitative descriptors of bioink behavior. Addition of Poloxamer 188 reduced K by 52.1% in particle-free inks and by 64.6% in particle-containing inks, while n remained largely unchanged (≤2% variation), indicating that particles selectively modulate consistency without compromising shear-thinning behavior. On day 1, bioprinted constructs showed lower cell viability than cell-seeded scaffolds (53.9–58.9% vs. 96.7%); however, constructs containing Sr-OHAp (B3) displayed progressive recovery, reaching 84.0% viability by day 7, compared to 72.9% for particle-free bioinks (B1). These results demonstrate that Sr-OHAp particles act as rheological sensitizers that reduce extrusion-induced shear stress while simultaneously promoting long-term cell recovery, likely through their bioactive surface chemistry. We propose that systematic reporting of K and n indices should become standard practice in bioprinting studies to enable rational bioink design and consistent knowledge accumulation across the field.
Open AccessOptimization of Bioink Formulations and Bioprinting Conditions for Enhanced Cell Viability in Particle-Containing Constructs
Extrusion-based bioprinting imposes stringent mechanical constraints on bioink formulations, yet the rheological parameters governing cell survival during the printing process are rarely reported in a standardized way, limiting cross-study comparison. In this work, we systematically characterized the viscoelastic properties of alginate/methylcellulose bioinks incorporating strontium-enriched hydroxyapatite (Sr-OHAp) particles and Poloxamer 188, and assessed their effect on PANC-1 cell viability in bioprinted constructs. The power law consistency index K and pseudoplasticity index n were used as quantitative descriptors of bioink behavior. Addition of Poloxamer 188 reduced K by 52.1% in particle-free inks and by 64.6% in particle-containing inks, while n remained largely unchanged (≤2% variation), indicating that particles selectively modulate consistency without compromising shear-thinning behavior. On day 1, bioprinted constructs showed lower cell viability than cell-seeded scaffolds (53.9–58.9% vs. 96.7%); however, constructs containing Sr-OHAp (B3) displayed progressive recovery, reaching 84.0% viability by day 7, compared to 72.9% for particle-free bioinks (B1). These results demonstrate that Sr-OHAp particles act as rheological sensitizers that reduce extrusion-induced shear stress while simultaneously promoting long-term cell recovery, likely through their bioactive surface chemistry. We propose that systematic reporting of K and n indices should become standard practice in bioprinting studies to enable rational bioink design and consistent knowledge accumulation across the field.