Whole 3D shape reconstruction of vascular segments under pressure via fringe projection techniques

被引:27
作者
Genovese, Katia
Pappalettere, Carmine
机构
[1] Univ Basilicata, Dipartimento Ingn & Fis Ambiente, I-85100 Potenza, Italy
[2] Politecn Bari, Dipartimento Ingn Meccan & Gest, I-70126 Bari, Italy
关键词
blood vessel wall deformation; fringe projection technique; 360 degrees 3D shape reconstruction;
D O I
10.1016/j.optlaseng.2005.12.005
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Understanding and modelling vascular wall mechanics is a primary issue in the study of circulatory diseases. Although theoretical and numerical studies on arteries compliance are continuously increasing, relatively little work has been documented on the use of non-invasive imaging techniques for monitoring 3D vascular wall deformations. Usually, 2D video dimension analyzer (VDA) systems recover diameter and length variations during inflation/extension tests by tracking position changes of few markers put on the blood vessel surface. Then, strain determination relies on the assumption of axisymmetric deformations. However, more rigorous evaluations of whole wall deformation map are required for properly modelling the highly anisotropic and inhomogeneous vascular tissue mechanical response. This paper describes the development and application of a fringe projection (FP)-based procedure for the 360 degrees 3D shape reconstruction of tubular samples subjected to internal pressure. A specially designed fixture for mounting and inflating the tubular segment allows specimen rotation about its axis. Movement is controlled by a high-precision rotational stage. This yields accurate positioning of the surface to be investigated with respect to the viewing direction. Data point clouds obtained from multiple recorded images are then processed and merged in a CAD environment, thus providing the whole shape of the sample with very high spatial resolution. The entire procedure has successfully been applied to latex specimens and porcine vascular segments. Further improvements will make the present procedure suitable for in vitro tests under more closely reproduced physiological conditions. (C) 2006 Elsevier.Ltd. All rights reserved.
引用
收藏
页码:1311 / 1323
页数:13
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