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Research Article | Open Access

A Multi-Layer Finite Element Model Based on Anisotropic Hyperelastic Fiber Reinforcements within Intestinal Walls

Dasheng Liu1,2,3( )Guozheng Yan1,3
Department of Instrument Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai JiaoTong University, Shanghai, 200240, China
National Center for Translational Medicine, Collaborative Innovational Center for System Biology, Shanghai Jiao Tong University, Shanghai 200240, China
Shanghai Engineering Research Center for Intelligent diagnosis and treatment instrument, Shanghai 200240, China
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Abstract

The intestinal wall is considered as a highly composite heterogeneous tissue characterized by a strong nonlinear stress-strain passive response with an exponential stiffening effect at higher deformations. The conventional theory of fiber-reinforced elastic solids allows one to describe the anisotropic strain energy as a function of the pseudo-invariants arising from the coupling of the elastic deformation and the direction of fiber reinforcement. In this paper, a multi-layer finite element model of the intestine walls is developed, based on an anisotropic hyperelastic theory of the layered structure, in which each layer may be considered as a composite reinforced by two families of fibers that are arranged in symmetrical spirals. A potential is proposed to model the intestine walls as a fiber-reinforced composite consisting of two directions of muscle-fiber reinforcement and a cross-ply collagen arrangement. Moreover, finite element simulations of a specimen cut from the intestinal walls were carried out by using the same form of strain-energy function, described by a well-known Gasser-Ogden-Holzapfel (GOH) model, for each layer. The model parameters were optimized by fitting the model to the experimental stress-stretch responses in both longitudinal and circumferential directions. In order to verify the proposed model, finite element analyses were carried out to investigate the distributions of equivalent stress in the intestine after the complete deployment of capsule robot legs.

References

[1]

C. Zhang, H. Liu, and H. Li, Experimental investigation of intestinal frictional resistance in the starting process of the capsule robot. Tribology International, 2014, 70: 11-17.

[2]

H.M. Kim, S. Yang, J. Kim, et al., Active locomotion of a paddling-based capsule endoscope in an in vitro and in vivo experiment (with videos). Gastrointestinal Endoscopy, 2010, 72(2): 381-387.

[3]

H. Zhou, A locomotion driving of the capsule robot in intestinal tract. International conference on intelligent robotics and applications. Springer International Publishing, 2014: 438-445.

[4]

J. Gao, G. Yan, Z. Wang, et al., A capsule robot powered by wireless power transmission: Design of its receiving coil. Sensors and Actuators A: Physical, 2015, 234(Supplement C): 133-142.

[5]

S.S. Mapara, V.B. Patravale, Medical capsule robots: A renaissance for diagnostics, drug delivery and surgical treatment. Journal of Controlled Release, 2017, 261 (Supplement C): 337-351.

[6]

W. El-Matary, Wireless capsule endoscopy: indications, limitations, and future challenges. Journal of Pediatric Gastroenterology & Nutrition, 2008, 46(1): 4-12.

[7]

G.A. Holzapfel, T.C. Gasser, and R.W. Ogden, A new constitutive framework for arterial wall mechanics and a comparative study of material models. Journal of Elasticity and the Physical Science of Solids, 2000, 61(1): 1-48.

[8]

G.A. Holzapfel, Determination of material models for arterial walls from uniaxial extension tests and histological structure. Journal of Theoretical Biology, 2006, 238(2): 290-302.

[9]

S. Federico, A. Grillo, G. Giaquinta, et al., Convex Fung-type potentials for biological tissues. Meccanica, 2008, 43(3): 279-288.

[10]

D.R. Nolan, A.L. Gower, M. Destrade, et al., A robust anisotropic hyperelastic formulation for the modelling of soft tissue. Journal of the Mechanical Behavior of Biomedical Materials, 2014, 39: 48-60.

[11]

Y. Zhu, G. Kang, and Q. Kan, et al., A finite viscoelastic–plastic model for describing the uniaxial ratchetting of soft biological tissues. Journal of Biomechanics, 2014, 47(5): 996-1003.

[12]

H. Khayyeri, A. Gustafsson, A. Heuijerjans, et al., A fibre-reinforced poroviscoelastic model accurately describes the biomechanical behaviour of the rat achilles tendon. PLOS ONE, 2015, 10(6): e0126869.

[13]

J.A. Peña, M.A. Martínez, and E. Peña, Layer-specific residual deformations and uniaxial and biaxial mechanical properties of thoracic porcine aorta. Journal of the Mechanical Behavior of Biomedical Materials, 2015, 50: 55-69.

[14]

Y. Zhu, G. Kang, C. Yu, et al., Logarithmic rate based elasto-viscoplastic cyclic constitutive model for soft biological tissues. Journal of the Mechanical Behavior of Biomedical Materials, 2016, 61: 397-409.

[15]

L.J. Sliker, G. Ciuti, M.E. Rentschler, et al., Frictional resistance model for tissue-capsule endoscope sliding contact in the gastrointestinal tract. Tribology International, 2016, 102: 472-484.

[16]

D.M. Pierce, T.E. Fastl, B. Rodriguezvila, et al., A method for incorporating three-dimensional residual stretches/stresses into patient-specific finite element simulations of arteries. Journal of the Mechanical Behavior of Biomedical Materials, 2015, 47: 147.

[17]

B. Fereidoonnezhad, R. Naghdabadi, S. Sohrabpour, et al., A mechanobiological model for damage-induced growth in arterial tissue with application to in-stent restenosis. Journal of the Mechanics and Physics of Solids, 2017, 101: 311-327.

[18]

P. Ciarletta, P. Dario, F. Tendick, et al., Hyperelastic model of anisotropic fiber reinforcements within intestinal walls for applications in medical robotics. The International Journal of Robotics Research, 2009, 28(10): 1279-1288.

[19]

D. Sokolis, I.K. Orfanidis, M. Peroulis, Biomechanical testing and material characterization for the rat large intestine: regional dependence of material parameters. Physiological Measurement, 2011, 32(12): 1969-1982.

[20]

D. Sokolis, S. Sassani, E. Kritharis, et al., Differential histomechanical response of carotid artery in relation to species and region: mathematical description accounting for elastin and collagen anisotropy. Medical & Biological Engineering & Computing, 2011, 49(8): 867-79.

[21]

D. Sokolis, S.G. Sassani, Microstructure-based constitutive modeling for the large intestine validated by histological observations. Journal of the Mechanical Behavior of Biomedical Materials, 2013, 21(3): 149-166.

[22]

Y. Zeng, A. Qiao, J. Yu, et al., Collagen fiber angle in the submucosa of small intestine and its application in gastroenterology. World Journal of Gastroenterology, 2003, 9(4): 804-807.

[23]

T.C. Gasser, R.W. Ogden, and G.A. Holzapfel, Hyperelastic modelling of arterial layers with distributed collagen fibre orientations. Journal of The Royal Society Interface, 2006, 3(6): 15-35.

Nano Biomedicine and Engineering
Pages 291-297
Cite this article:
Liu D, Yan G. A Multi-Layer Finite Element Model Based on Anisotropic Hyperelastic Fiber Reinforcements within Intestinal Walls. Nano Biomedicine and Engineering, 2017, 9(4): 291-297. https://doi.org/10.5101/nbe.v9i4.p291-297

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Received: 18 October 2017
Accepted: 28 November 2017
Published: 08 December 2017
© Dasheng Liu, and Guozheng Yan,

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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