Articular Cartilage (Construct)
Articular cartilage is the smooth white tissue that covers the ends of bones where they come together to form joints.
About this material
Articular cartilage is the smooth white tissue that covers the ends of bones where they come together to form joints. Articular cartilage is an avascular tissue and therefore, has low regenerative capacity. In order to treat cartilage lesions, researchers have developed different strategies including the implantation of a cartilage construct at the defect site. The construct is engineered to mimic native tissue structure and function. During an arthroscopy, a cartilage biopsy is harvested. Cartilage cells (called chondrocytes) are collected and expanded in an incubator. They are then placed in suspension in a 3D support matrix (e.g. a hydrogel). To promote the production of cartilage’s extracellular matrix components, mechanical stimulation (axial and/or sheer) is often applied. At the end of the incubation period, its mechanical properties can be evaluated.
Test configurations (11)
Indentation (Stiffness)
Impact

Temperature Control
Positioning (Manual Tilt)
Mechanical Stimulation (Tension)
Mechanical Stimulation (Compressive)
External Analog Sensors
Camera Feed
Positioning (Manual)
Positioning (X Auto)
Case studies (2)
Related resources (11)
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effects of additional sodium bicarbonate on Extra/intra cellular factors in a continuous flow bioreactor for the production of tissue engineered articular cartilage
Thesis, Queen’s University, 2012.
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Thesis, Queen’s University, 2012.
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Biotechnology and Bioengineering. 2011.
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Tissue Engineering Part C: Methods. 2011;17(9):939-948.
33 citations · 0 in 2025–2026
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Igal Raizman; J.N. Amritha De Croos; Robert Pilliar; Rita A. Kandel
Cell Calcium. 2010;48(4):232–242.
44 citations · 2 in 2025–2026
Tissue engineering cartilage for focal defects
Mississippi State University. M.S. thesis, Biomedical Engineering. 2010-08.
0 citations · 0 in 2025–2026
Harnessing the purinergic receptor pathway to develop functional engineered cartilage constructs
S.D. Waldman; J. Usprech; L.E. Flynn; A.A. Khan
Osteoarthritis and Cartilage. 2010.
25 citations · 0 in 2025–2026
The effect of intermittent static biaxial tensile strains on tissue engineered cartilage
Jackie C. Y. Fan; Stephen D. Waldman
Annals of Biomedical Engineering 38(4), 1672–1682 (2010). Complete original abstract retrieved from PubMed PMID 20087771 through Europe PMC. Exact article methods read in author-deposited text indexed on ResearchGate (Stephen D. Waldman); no local article PDF obtained. The thickness and indentation/relaxation characterization are separate from dead-weight biaxial stimulation. This is not the Fan thesis or the later JoVE protocol. Donor species remains unassigned pending the original sample-preparation section. Month precision comes from publisher citation metadata; no fabricated day.
39 citations · 1 in 2025–2026
Matrix accumulation by articular chondrocytes during mechanical stimulation is influenced by integrin‐mediated cell spreading
Caroline Spiteri; Igal Raizman; Robert M. Pilliar; Rita A. Kandel
Journal of Biomedical Materials Research Part A. 2010.
19 citations · 2 in 2025–2026
Improved bioengineered cartilage tissue formation following cyclic compression is dependent on upregulation of MT1‐MMP
J. N. Amrith De Croos; Peter J. Roughley; Rita A. Kandel
Journal of Orthopaedic Research. 2010;28(7):921-927. DOI:10.1002/jor.21064. First online 2010-01-07. Methods provenance:earlier ORS2009poster1051;distinctive MT1MMPsiRNA/MMP13 result correspondence. Not official reprint;final journal methods not independently read.
7 citations · 1 in 2025–2026
A Therapeutic Dose of Adenosine Triphosphate (ATP) for Cartilage Tissue Engineering
Queen’s University. MASc, Mechanical and Materials Engineering. 2010
0 citations · 0 in 2025–2026
The support of matrix accumulation and the promotion of sheep articular cartilage defects repair in vivo by chitosan hydrogels
T. Hao; N. Wen; J.-K. Cao; H.-B. Wang; S.-H. Lü; T. Liu; Q.-X. Lin; C.-M. Duan; C.-Y. Wang
Osteoarthritis and Cartilage. 2010;18(2):257-265.
154 citations · 8 in 2025–2026
Articular cartilage subpopulations respond differently to cyclic compression in vitro
Igal Raizman; J.N. Amritha De Croos; Jean-Philippe St-Pierre; Robert M. Pilliar; Rita A. Kandel
Tissue Engineering Part A. 2009;15(12):3789–3798.
12 citations · 1 in 2025–2026
Calcium Regulates Cyclic Compression-Induced Early Changes In Chondrocytes During In Vitro Tissue Formation
Master of Science thesis, University of Toronto, 2009.
Effects of Intermittent Static and Dynamic Tension on Articular Chondrocytes in High Density Culture
Thesis, Queen’s University, 2009.
Mechanical Forces Regulate Cartilage Tissue Formation by Chondrocytes Via Integrin-mediated Cell Spreading
Thesis, University of Toronto, 2009.
0 citations · 0 in 2025–2026
Multi-axial mechanical stimulation of tissue engineered cartilage: Review
Department of Mechanical and Materials Engineering, Department of Chemical Engineering, Queen's University, Kingston, Ontario, Canada; SD Waldman; DC Couto; MD Grynpas; RM Pilliar; RA Kandel
European Cells and Materials. 2007.
84 citations · 4 in 2025–2026
Chondrocyte culture in agarose: age dependence and characterization of interfacial growth [English translation]
PhD thesis, École Polytechnique de Montréal, April 2007. English translation of original French title: Culture de chondrocytes en agarose: dépendance avec l'âge et caractérisation de la croissance en interface.
Membrane type-1 matrix metalloproteinase is induced following cyclic compression of in vitro grown bovine chondrocytes
J.N.A. De Croos; B. Jang; S.S. Dhaliwal; M.D. Grynpas; R.M. Pilliar; R.A. Kandel
Osteoarthritis and Cartilage. 2007;15(11):1301-1310.
20 citations · 0 in 2025–2026
Repair of osteochondral defects with biphasic cartilage-calcium polyphosphate constructs in a Sheep model
R.A. Kandel; M. Grynpas; R. Pilliar; J. Lee; J. Wang; S. Waldman; P. Zalzal; M. Hurtig
Biomaterials. 2006.
208 citations · 6 in 2025–2026
A single application of cyclic loading can accelerate matrix deposition and enhance the properties of tissue-engineered cartilage
S.D. Waldman; D.C. Couto; M.D. Grynpas; R.M. Pilliar; R.A. Kandel
Osteoarthritis and Cartilage. 2006;14(4):323–330.
110 citations · 6 in 2025–2026
Long‐term intermittent shear deformation improves the quality of cartilaginous tissue formed in vitro
Stephen D. Waldman; Caroline G. Spiteri; Marc D. Grynpas; Robert M. Pilliar; Rita A. Kandel
Journal of Orthopaedic Research. 2003.
199 citations · 5 in 2025–2026
Aged bovine chondrocytes display a diminished capacity to produce a collagen-rich, mechanically functional cartilage extracellular matrix
N TRANKHANH; C HOEMANN; M MCKEE; J HENDERSON; M BUSCHMANN
Journal of Orthopaedic Research. 2005.
123 citations · 0 in 2025–2026
Tissue engineering of cartilage using an injectable and adhesive chitosan-based cell-delivery vehicle
C.D. Hoemann; J. Sun; A. Légaré; M.D. McKee; M.D. Buschmann
Osteoarthritis and Cartilage. 2005.
358 citations · 3 in 2025–2026
Formation of a cartilage-biomaterial biphasic construct with a calcified cartilage zone
University of Toronto. Master of Applied Science thesis, Materials Science and Engineering. 2005.
0 citations · 0 in 2025–2026
Long-Term Intermittent Compressive Stimulation Improves the Composition and Mechanical Properties of Tissue-Engineered Cartilage
Stephen D. Waldman; Caroline G. Spiteri; Marc D. Grynpas; Robert M. Pilliar; Rita A. Kandel
Tissue Engineering. 2004.
179 citations · 4 in 2025–2026
Improved cartilage integration and interfacial strength after enzymatic treatment in a cartilage transplantation model
Jarno van de Breevaart Bravenboer; Caroline D In der Maur; P Koen Bos; Louw Feenstra; Jan AN Verhaar; Harrie Weinans; Gerjo JVM van Osch
Arthritis Res Ther. 2004;6(5):R469-76. Epub 2004 Aug 6
127 citations · 1 in 2025–2026
Towards a Complete Intervertebral Disc: Modulation of the Biochemical and Mechanical Properties of in vitro formed Nucleus Pulposus Tissue
MASc thesis, University of Toronto, 2004.
0 citations · 0 in 2025–2026
The use of specific chondrocyte populations to modulate the properties of tissue-engineered cartilage
Stephen D. Waldman; Marc D. Grynpas; Robert M. Pilliar; Rita A. Kandel
Journal of Orthopaedic Research. 2003;21(1):132–138. Wiley archive migration date excluded from bibliographic date.
97 citations · 0 in 2025–2026
A fibril-network-reinforced biphasic model of cartilage in unconfined compression
J. Soulhat; M. D. Buschmann; A. Shirazi-Adl
Journal of Biomechanical Engineering, Jun, 121(3), 340-347. (1999)
250 citations · 9 in 2025–2026
FAQ
What is Poroelasticity?+
Mach-1 Analysis – Poroelastic Model in Unconfined Compression – Parameters
Mach-1 Analysis – Poroelastic Model in Confined Compression – Parameters
Mach-1 Analysis – Poroelastic Model in Confined Compression – Example
Mach-1 Analysis – Poroelastic Model in Unconfined Compression – Cartilage
Mach-1 Analysis – Poroelastic Model in Unconfined Compression – Example
LAB MODULE – Torsion of Disk-Shaped Samples – Student Version
How does the "Poroelastic Model in Confined Compression" feature works?+
This model is well adapted for the mechanical characterization of samples containing a liquid fraction and a solid matrix, for example: cartilage or gel samples. A user license is required in order to obtain the results of the poroelastic model in confined compression (Software Add-On, contact Biomomentum to obtain your license).
Mechanical properties can be obtained from the stress relaxation curves obtained under confined compression such as the aggregate modulus (HA) and the hydraulic permeability (k). The aggregate modulus is a measure of stiffness of the sample at equilibrium while the hydraulic permeability is the ability of the fluid to flow through the cartilage matrix.
For example, (Figure 2) shows parameters used for the “Stress Relaxation” function in a confined compression testing protocol on human cartilage disks. Corresponding results are shown in (Figure 1).
Mach-1 Analysis – Poroelastic Model in Confined Compression – Parameters
Mach-1 Analysis – Poroelastic Model in Confined Compression – Example
How does the "Poroelastic Model in Unconfined Compression" feature works?+
The nonhomogeneous composite model (i.e. linear fibril-network-reinforced biphasic model) is an extension of the previously developed isotropic homogeneous biphasic model, and was achieved by reinforcing the latter with a network of nonlinear fibrils distributed homogeneously in the r, θ, z directions and which resist extension only (Figure 2). The isotropic matrix is described by the drained elastic constants Em (Young’s modulus), vm (Poisson’s ratio) and a hydraulic permeability k. The fibril network is described by the Young’s modulus of individual fibrils ef which, combined with a fibril volume fraction χ (fibrils volume/ total-volume), results in an equivalent tensile modulus of the fibril network, Ef = 1/3 χ ef (since 1/3 of the fibrils are oriented in each of three mutually orthogonal directions).
For example, (Figure 3) shows parameters used for the “Stress Relaxation” function in an unconfined compression testing protocol on ovine cartilage disks. Corresponding results are shown in (Figure 1).
Mach-1 Analysis – Poroelastic Model in Unconfined Compression – Parameters
Mach-1 Analysis – Poroelastic Model in Unconfined Compression – Cartilage
Mach-1 Analysis – Poroelastic Model in Unconfined Compression – Example


