Related Experiment Video
Updated: Jan 20, 2026

Dendrimer-based Uneven Nanopatterns to Locally Control Surface Adhesiveness: A Method to Direct Chondrogenic Differentiation
Published on: January 20, 2018
Orthopedic implant surface modification with nanoengineered [YSZ/HAp-Ag]n multilayer coatings to promote osteoblast
E Lorena Medina1,2,3, J J Vaca-González4,5, Diego Quexada-Rodríguez2,6
1BEST/CB3S, UMR CNRS 7244, Institut Galilée, Université Sorbonne Paris Nord, Villetaneuse, 93430, France.
Background:
Metallic implants frequently face three critical challenges that compromise long-term clinical performance: (i) limited biofunctionality that delays osteointegration, (ii) corrosion processes that deteriorate the implant surface and release harmful ions, and (iii) bacterial biofilm formation, which increases the risk of persistent infection. This study explores multilayer [YSZ/HAp-Ag]n coatings engineered to overcome these issues by enhancing osteoblastic response, improving surface stability, and providing antimicrobial potential.
Materials And Methods:
Multilayer coatings with different bilayer numbers (n = 1, 10, 30, 50, 70) were deposited on titanium substrates using magnetron sputtering. Structural and surface characterization included morphology, roughness, wettability, and stiffness. MC3T3-E1 osteoblastic cells were cultured on the coatings to evaluate adhesion, viability (MTT), and differentiation through alkaline phosphatase (ALP) activity at 7 and 14 days.
Results:
Crater-like surface textures, roughness above 220 nm, and higher hydrophilicity promoted enhanced cell spreading, greater confluence, and decreased circularity, indicative of strong anchorage. All coatings exhibited >70 % cell viability, confirming non-cytotoxic behavior. Rougher and more hydrophilic surfaces outperformed uncoated titanium. Stiffer coatings produced a significant increase in ALP activity at day 7, suggesting accelerated early osteogenic differentiation, followed by a decrease at day 14 consistent with cellular maturation. Among all configurations, the 30-bilayer coating (n30) offered the most balanced structural and mechanical properties, resulting in the highest biological performance.
Conclusions:
Multilayer [YSZ/HAp-Ag]n coatings effectively stimulate osteoblastic adhesion, viability, and early differentiation while addressing key limitations of metallic implants. Their tunable architecture-especially the n30 configuration-represents a promising strategy to enhance implant integration and long-term functional performance.
Related Concept Videos
14:46Dendrimer-based Uneven Nanopatterns to Locally Control Surface Adhesiveness: A Method to Direct Chondrogenic Differentiation
13:21Graphene Coatings for Biomedical Implants
12:19Multi-Scale Modification of Metallic Implants With Pore Gradients, Polyelectrolytes and Their Indirect Monitoring In vivo
09:11Using Cell-substrate Impedance and Live Cell Imaging to Measure Real-time Changes in Cellular Adhesion and De-adhesion Induced by Matrix Modification
06:54Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
12:31Chemoselective Modification of Viral Surfaces via Bioorthogonal Click Chemistry

