• Aucun résultat trouvé

A micro-mechanical model of the vocal-fold upper layers

N/A
N/A
Protected

Academic year: 2021

Partager "A micro-mechanical model of the vocal-fold upper layers"

Copied!
2
0
0

Texte intégral

(1)

HAL Id: hal-01419743

https://hal.archives-ouvertes.fr/hal-01419743

Submitted on 5 Jan 2017

HAL is a multi-disciplinary open access

archive for the deposit and dissemination of

sci-entific research documents, whether they are

pub-lished or not. The documents may come from

teaching and research institutions in France or

abroad, or from public or private research centers.

L’archive ouverte pluridisciplinaire HAL, est

destinée au dépôt et à la diffusion de documents

scientifiques de niveau recherche, publiés ou non,

émanant des établissements d’enseignement et de

recherche français ou étrangers, des laboratoires

publics ou privés.

A micro-mechanical model of the vocal-fold upper layers

Thibaud Cochereau, Lucie Bailly, Laurent Orgéas, Nathalie Henrich

Bernardoni, Philippe Chaffanjon

To cite this version:

Thibaud Cochereau, Lucie Bailly, Laurent Orgéas, Nathalie Henrich Bernardoni, Philippe Chaffanjon.

A micro-mechanical model of the vocal-fold upper layers. 22nd Congress of the European Society of

Biomechanics, European Society of Biomechanics, Jul 2016, Lyon, France. �hal-01419743�

(2)

22nd Congress of the European Society of Biomechanics, July 10 - 13, 2016, Lyon, France

A MICRO-MECHANICAL MODEL OF THE VOCAL-FOLD UPPER LAYERS

Thibaud Cochereau(1,2,3,4), Lucie Bailly(1,2), Laurent Orgéas(1,2), Nathalie Henrich Bernardoni(3,4), Philippe Chaffanjon(3,4,5)

1. Univ. Grenoble Alpes, 3SR Lab, F-38000, Grenoble, France; 2. CNRS, 3SR Lab, F-38000, Grenoble, France; 3. Univ. Grenoble Alpes, GIPSA-lab, F-38000, Grenoble, France; 4. CNRS, GIPSA-lab, F-38000,

Grenoble, France; 5. Univ.Grenoble Alpes, LADAF, F-38000, Grenoble, France

Introduction

The vocal folds are soft multi-layered laryngeal tissues, owning remarkable vibro-mechanical performances. Composed of collagen and elastin microfibrils’ networks, the upper layers play a major role in the vocal-fold vibrations. However, the impact of these tissues’ histological features on their mechanical behavior is still poorly known. This is mainly ascribed to their challenging experimental characterization: vocal folds together with their fibrous architectures are not easily observable in vivo; ex vivo mechanical tests are rare and complex to interpret [1]. Consequently, most of the vocal-fold mechanical models developed so far rely on phenomenological macroscopic approaches, roughly assuming a homogeneous vocal tissue with linear-elastic properties. Since 2010, a few authors have started to investigate and model the vocal-tissue collagenous fibrous microstructure, opening a new insight into voice biomechanics [2]. Theoretical formulations at the fiber scale still need to be developed. Thereby, this study aims at: (i) proposing an idealized but relevant model of the fibrous architecture of the vocal-fold upper layers; (ii) building a mechanical model able to predict the layers’ multiscale properties from the above idealized architectures; (iii) assessing its relevance by comparison with a reference tensile database.

Methods

Idealization of the layer fibrous architectures – The vocal-fold upper layers can be seen as a 3D composite structure made of a soft isotropic hyperelastic matrix, reinforced by a periodic network of bundles of wavy collagen fibrils displaying preferred orientations. This fibrous architecture is idealized by the Representative Elementary Cell (REC) shown in Fig.1(a). Most of the REC parameters can be extracted from existing histological data [1,2,4]: fibril diameter (𝑑0≈ 0.1 µm)

and length 𝑙𝑓, initial tortuosity (𝜉

0≈ 0.84; 0.92) and

lattice length (𝑙0≈ 𝜉0𝑙𝑓 ≈ 20; 30 µm), collagen fibrils

content (𝜙 ≈ 0.15), initial orientation of fibril bundles (𝜃0≈ 67.5°) with respect to vocal-fold main direction.

Multiscale model – To determine the macroscale mechanical response of the as-idealized upper layers under simple uniaxial tensile loading, a non-linear and anisotropic multiscale model is proposed. This theoretical model is written using the homogenization method for periodic discrete structures, as already applied to the context of vascular biomechanics [3]. For that purpose, attention is paid to build a relevant micromechanical model describing the unfolding and

the tensile deformation of wavy collagen fibrils, accounting for their elastic properties [4, 5].

Results and discussion

The prediction of collagen fibrils’ tensile behavior (𝜎𝑓, 𝜆𝑓) is plotted in Fig.1(a) for two typical fibril

tortuosities: 𝜉0≈ 0.84; 0.92 [2]. Unfolding the fibrils

conducts to typical J-shaped stress-elongation curves depending on 𝜉0. Once the fibril unfolded, curves show

a linear evolution with a tangent modulus of 1 GPa [4].

Figure 1: Stress-elongation curves for tensile tests

along ey: (a) model predictions for the fibril (b) model

predictions and experimental data for the tissue.

The macroscale predictions of the multiscale model are given by the stress-elongation curves plotted in Fig.1(b) for the same 𝜉0 values. The mechanical

behavior of the vocal ligament under tension is also illustrated in Fig.1(b), as an experimental reference recently reported using DIC measurements [1]. As observed at the microscale in Fig.1(a), both macroscale curves exhibit a J-shaped non-linear mechanical behavior, characteristic of collagenous soft tissues. Fig.1(b) also demonstrates a fairly good quantitative agreement with the reference mechanical data, keeping in mind that all model parameters derived from histological evidences. Further used to simulate in vivo loadings, this model will help to understand the role of the fibrous networks in vocal-fold vibratory properties. It will also provide proper guidelines to design new composites mimicking vocal-fold biomechanics.

References

1. Kelleher et al, J. Acoust. Soc. Am., 133:1625-1636, 2013. 2. Miri et al, Laryngoscope, 122:356–363, 2012.

3. Bailly et al, JMBBM, 10:151-165, 2012. 4. Yang, PhD Thesis, 2008.

5. Kabla and Mahadevan, JRSI, 4:99-109, 2007.

Acknowledgements

This work is supported by the Labex Tec21 (Investissements d’Avenir - grant agreement ANR-11-LABX-0030).

1 1.05 1.1 1.15 1.2 0 0.05 0.1 0.15 6f <f (M P a ) 1 1.05 1.1 1.15 1.2 1.25 0 0.01 0.02 0.03 0.04 0.05 6yy <y y (M P a ) 90=0.92 90=0.84 Kelleher et al. a) b)

Figure

Figure  1:  Stress-elongation  curves  for  tensile  tests  along  e y : (a) model predictions for the fibril (b) model  predictions and experimental data for the tissue

Références

Documents relatifs

The model was later coupled with a profile analysis method to calculate tire/road friction from actual profiles of surface texture. Friction calculation require only characteristics

Instead, the proposed model employs a single oscillator to describe only the motion of the lower portion of the vocal fold, while phase difference effects are simulated through

In order to better understand the role of mechanical inter- actions between cells during the first developmental stage of the mammal embryo, we developed a 3-dimensional

If p sub were instead kept constant, we would observe an increasing OQ and decreasing amplitudes of glottal flow and vocal fold oscillations throughout the glide but the

The influence of both the folding angle and the fold length are extracted automat- ically from a set of experimental values exhibiting a deterministic behavior and a variability due

We have proposed a method inspired by the NTFA (Nonlinear Transformation Field Analysis), which allows the model reduction of a complete elastic viscoplastic

In this paper, we first present our kinetic model and the phenomena taken into account, then we give a numerical solver of the kinetic equation by a particle method, and we

S chest : V diaphragm the rib cage volume under the diaphragm (which corresponds approximately to the volume of the portion of the abdominal cavity encompassed by the zone of