A mathematical model for the determination of forming tissue moduli in needled-nonwoven scaffolds
Source abstract
Abstract
Formation of engineering tissues (ET) remains an important scientific area of investigation for both clinical translational and mechanobiological studies. Needled-nonwoven (NNW) scaffolds represent one of the most ubiquitous biomaterials based on their well-documented capacity to sustain tissue formation and the unique property of substantial construct stiffness amplification, the latter allowing for very sensitive determination of forming tissue modulus. Yet, their use in more fundamental studies is hampered by the lack of: (1) substantial understanding of the mechanics of the NNW scaffold itself under finite deformations and means to model the complex mechanical interactions between scaffold fibers, cells, and de novo tissue; and (2) rational models with reliable predictive capabilities describing their evolving mechanical properties and their response to mechanical stimulation. Our objective is to quantify the mechanical properties of the forming ET phase in constructs that utilize NNW scaffolds. We present herein a novel mathematical model to quantify their stiffness based on explicit considerations of the modulation of NNW scaffold fiber-fiber interactions and effective fiber stiffness by surrounding de novo ECM. Specifically, fibers in NNW scaffolds are effectively stiffer than if acting alone due to extensive fiber-fiber cross-over points that impart changes in fiber geometry, particularly crimp wavelength and amplitude. Fiber-fiber interactions in NNW scaffolds also play significant role in the bulk anisotropy of the material, mainly due to fiber buckling and large translational out-of-plane displacements occurring to fibers undergoing contraction. To calibrate the model parameters, we mechanically tested impregnated NNW scaffolds with polyacrylamide (PAM) gels with a wide range of moduli with values chosen to mimic the effects of surrounding tissues on the scaffold fiber network. Results indicated a high degree of model fidelity over a wide range of planar strains. Lastly, we illustrated the impact of our modeling approach quantifying the stiffness of engineered ECM after in vitro incubation and early stages of in vivo implantation obtained in a concurrent study of engineered tissue pulmonary valves in an ovine model. Statement of significance Regenerative medicine has the potential to fully restore diseased tissues or entire organs with engineered tissues. Needled-nonwoven scaffolds can be employed to serve as the support for their growth. However, there is a lack of understanding of the mechanics of these materials and their interactions with the forming tissues. We developed a mathematical model for these scaffold-tissue composites to quantify the mechanical properties of the forming tissues. Firstly, these measurements are pivotal to achieve functional requirements for tissue engineering implants; however, the theoretical development yielded critical insight into particular mechanisms and behaviors of these scaffolds that were not possible to conjecture without the insight given by modeling, let alone describe or foresee a priori.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Electrospun Nanofibers in Biomedical Applications · 3D Printing in Biomedical Research · Cellular Mechanics and Interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (55)
Show source-provided references
1. Regenerative medicine: Current therapies and future directions10.1073/pnas.1508520112 ↗
2. Development of a drug screening platform based on engineered heart tissue10.1161/CIRCRESAHA.109.211458 ↗
3. A microfabricated platform to measure and manipulate the mechanics of engineered cardiac microtissues10.1089/ten.tea.2011.0341 ↗
4. Tissue engineering of a collagen-based vascular media: Demonstration of functionality10.4161/org.6.4.12651 ↗
5. Neonatal mouse-derived engineered cardiac tissue: a novel model system for studying genetic heart disease10.1161/CIRCRESAHA.111.242354 ↗
6. Development of biocompatible synthetic extracellular matrices for tissue engineering10.1016/S0167-7799(98)01191-3 ↗
7. Of extracellular matrix, scaffolds, and signaling: tissue architecture regulates development, homeostasis, and cancer10.1146/annurev.cellbio.22.010305.104315 ↗
8. Whole-organ tissue engineering: decellularization and recellularization of three-dimensional matrix scaffolds10.1146/annurev-bioeng-071910-124743 ↗
9. The extracellular matrix as a biologic scaffold material10.1016/j.biomaterials.2007.04.043 ↗
10. Altered structural and mechanical properties in decellularized rabbit carotid arteries10.1016/j.actbio.2008.11.028 ↗
11. Early failure of the tissue engineered porcine heart valve SYNERGRAFT in pediatric patients10.1016/S1010-7940(03)00094-0 ↗
12. Biodegradable polymer scaffolds for tissue engineering
13. A structural model for the flexural mechanics of nonwoven tissue engineering scaffolds10.1115/1.2205371 ↗
14. The structure of needle punched fabric10.1016/0015-0568(71)90014-5 ↗
15. On the nature of deformation of needled fabrics10.1016/0015-0568(72)90003-6 ↗
16. Scaffolds for engineering smooth muscle under cyclic mechanical strain conditions10.1115/1.429651 ↗
17. The relevance of large strains in functional tissue engineering of heart valves10.1055/s-2003-38993 ↗
18. From stem cells to viable autologous semilunar heart valve10.1161/CIRCULATIONAHA.104.498378 ↗
19. Functional living trileaflet heart valves grown in vitro
20. De novo reconstitution of a functional mammalian urinary bladder by tissue engineering10.1038/6146 ↗
21. Functional arteries grown in vitro10.1126/science.284.5413.489 ↗
22. Bone morphogenetic proteins-2, -12, and -13 modulate in vitro development of engineered cartilage10.1089/107632702760240517 ↗
23. Mechanics of elastic performance of textile materials. 16. Bending rigidity of nonwoven fabrics10.1177/004051756503500106 ↗
24. Prediction of extracellular matrix stiffness in engineered heart valve tissues based on nonwoven scaffolds10.1007/s10237-007-0102-1 ↗
25. The independent role of cyclic flexure in the early in vitro development of an engineered heart valve tissue10.1016/j.biomaterials.2004.02.035 ↗
26. A triphasic constrained mixture model of engineered tissue formation under in vitro dynamic mechanical conditioning10.1007/s10237-015-0687-8 ↗
27. Large strain stimulation promotes extracellular matrix production and stiffness in an elastomeric scaffold model10.1016/j.jmbbm.2016.05.005 ↗
28. In vivo monitoring of function of autologous engineered pulmonary valve10.1016/j.jtcvs.2009.11.006 ↗
29. Three-dimensional quantitative micromorphology of pre- and post-implanted engineered heart valve tissues10.1007/s10439-010-0162-8 ↗
30. Elastica-based strain energy functions for soft biological tissue10.1016/j.jmps.2007.07.005 ↗
31. Elastic model for crimped collagen fibrils10.1115/1.1934145 ↗
32. Biaxial mechanical properties of the natural and glutaraldehyde treated aortic valve cusp–Part I: Experimental results10.1115/1.429624 ↗
33. A fibril-network-reinforced biphasic model of cartilage in unconfined compression10.1115/1.2798330 ↗
34. A conewise linear elasticity mixture model for the analysis of tension-compression nonlinearity in articular cartilage10.1115/1.1324669 ↗
35. Incorporation of experimentally-derived fiber orientation into a structural constitutive model for planar-collagenous tissues10.1115/1.1544508 ↗
36. Comparison of a multi-layer structural model for arterial walls with a fung-type model, and issues of material stability10.1115/1.1695572 ↗
37. A novel fibre-ensemble level constitutive model for exogenous cross-linked collagenous tissues10.1098/rsfs.2015.0090 ↗
38. A novel constitutive model for passive right ventricular myocardium: evidence for myofiber-collagen fiber mechanical coupling
39. Holzapfel · 2000
40. The influence of the invariant I-8 on the stress-deformation and ellipticity characteristics of doubly fiber-reinforced non-linearly elastic solids10.1016/j.ijnonlinmec.2006.02.001 ↗
41. Myotubes differentiate optimally on substrates with tissue-like stiffness: pathological implications for soft or stiff microenvironments10.1083/jcb.200405004 ↗
42. Guidance of engineered tissue collagen orientation by large-scale scaffold microstructures10.1016/j.jbiomech.2005.05.020 ↗
43. A small angle light scattering device for planar connective tissue microstructural analysis10.1007/BF02684845 ↗
44. A generalized method for the analysis of planar biaxial mechanical data using tethered testing configurations10.1115/1.4029266 ↗
45. Biaxial mechanical evaluation of planar biological materials10.1023/A:1010917028671 ↗
46. A structural theory for the homogeneous biaxial stress-strain relationships in flat collagenous tissues10.1016/0021-9290(79)90027-7 ↗
47. Insights Into Regional Adaptations in the Growing Pulmonary Artery Using a Meso-Scale Structural Model: Effects of Ascending Aorta Impingement10.1115/1.4026457 ↗
48. Surface geometric analysis of anatomic structures using biquintic finite element interpolation10.1114/1.1306342 ↗
49. Constitutive equations for fibrous connective tissues10.1016/0021-9290(83)90041-6 ↗
50. A meso-scale layer-specific structural constitutive model of the mitral heart valve leaflets10.1016/j.actbio.2015.12.001 ↗
51. Engineering smooth muscle tissue with a predefined structure10.1002/(SICI)1097-4636(199808)41:2<322::AID-JBM18>3.0.CO;2-M ↗
52. A study of needled fabrics. 2. Effects of needling process
53. Determination of a constitutive relation for passive myocardium: I. A new functional form10.1115/1.2891193 ↗
54. Biomechanical experiments on excised myocardium: theoretical considerations10.1016/0021-9290(89)90052-3 ↗
55. An in vitro model system to quantify stress generation, compaction, and retraction in engineered heart valve tissue10.1089/ten.tec.2011.0070 ↗