Acousto-optical characterization of the viscoelastic nature of a nuchal elastin tissue scaffold.

A nondestructive, acousto-optical method for characterizing the mechanical loss factor of biological tissues and tissue scaffolds is presented and applied to the characterization of an elastin tissue scaffold derived from bovine nuchal ligament. The method relies on launching guided surface acoustic waves into the tissue scaffold with a small speaker and simultaneously illuminating a small region of the scaffold distant from the speaker with a low-power HeNe laser. The phase lag between the driving acoustic wave and the shift in the backscattered laser speckle pattern is determined as a measure of the mechanical loss factor of the scaffold, tan delta. Measurements of tan delta and elastic modulus were also made by traditional dynamic mechanical loading techniques. Through the central portion of the loading cycle, the elastic modulus of the elastin scaffold was 1.2 x 10(6) +/- 1 x 10(5) N x m(-2) (parallel to fiber orientation). The estimated value of tan delta in the direction parallel to the elastin fibers was 0.03 +/- 0.017 by traditional methods and 0.029 +/- 0.03 when using the acousto-optical method. In the direction perpendicular to fiber orientation, tan delta was measured as 0.14 +/- 0.056 by the acousto-optical method. Because of a lack of mechanical integrity, it was not possible to measure tan delta in the direction perpendicular to fiber orientation by traditional methods. The acousto-optical method may prove to be useful in the mechanical characterization of developing engineered tissues.

[1]  J. Yee,et al.  Mechanical strain- and high glucose-induced alterations in mesangial cell collagen metabolism: role of TGF-beta. , 1998, Journal of the American Society of Nephrology : JASN.

[2]  J M Anderson,et al.  Cyclic strain effects on human monocyte interactions with endothelial cells and extracellular matrix proteins. , 1999, Tissue engineering.

[3]  M Bottlang,et al.  Gap junctions regulate responses of tendon cells ex vivo to mechanical loading. , 1999, Clinical orthopaedics and related research.

[4]  Sean J. Kirkpatrick,et al.  Surface mechanics of biological tissues using low-frequency rayleigh waves detected by laser speckle , 2002, Saratov Fall Meeting.

[5]  S J Kirkpatrick,et al.  Transform method of processing for speckle strain-rate measurements. , 1994, Applied optics.

[6]  M Eastwood,et al.  Effect of precise mechanical loading on fibroblast populated collagen lattices: morphological changes. , 1998, Cell motility and the cytoskeleton.

[7]  L. Wilson,et al.  Spectral tissue strain: a new technique for imaging tissue strain using intravascular ultrasound. , 1994, Ultrasound in medicine & biology.

[8]  S J Kirkpatrick,et al.  High resolution imaged laser speckle strain gauge for vascular applications. , 2000, Journal of biomedical optics.

[9]  T. Kulik,et al.  Effect of stretch on growth and collagen synthesis in cultured rat and lamb pulmonary arterial smooth muscle cells , 1993, Journal of cellular physiology.

[10]  B. Sumpio,et al.  Effect of strain on human keratinocytes in vitro , 1997, Journal of cellular physiology.

[11]  V. Tuchin Handbook of Optical Biomedical Diagnostics , 2002 .

[12]  F. M. Schultz,et al.  Dynamic pressure transmission through agarose gels. , 2000, Tissue engineering.

[13]  Keith Worden,et al.  Rayleigh and Lamb Waves ‐ Basic Principles , 2001 .

[14]  S J Kirkpatrick,et al.  Processing algorithms for tracking speckle shifts in optical elastography of biological tissues. , 2001, Journal of biomedical optics.

[15]  Raja Muthupillai,et al.  Magnetic resonance imaging of transverse acoustic strain waves , 1996, Magnetic resonance in medicine.

[16]  L V Wang,et al.  Theoretical and experimental studies of ultrasound-modulated optical tomography in biological tissue. , 2000, Applied optics.

[17]  J. Rose Ultrasonic Waves in Solid Media , 1999 .

[18]  C. Enwemeka,et al.  Combined ultrasound, electrical stimulation, and laser promote collagen synthesis with moderate changes in tendon biomechanics. , 1997, American journal of physical medicine & rehabilitation.

[19]  L. Robert,et al.  Interaction between cells and elastin, the elastin-receptor. , 1999, Connective tissue research.

[20]  K. Parker,et al.  "Sonoelasticity" images derived from ultrasound signals in mechanically vibrated tissues. , 1990, Ultrasound in medicine & biology.

[21]  K J Parker,et al.  Imaging of the elastic properties of tissue--a review. , 1996, Ultrasound in medicine & biology.

[22]  Joan E. Sanders,et al.  A device to apply user-specified strains to biomaterials in culture , 2001, IEEE Transactions on Biomedical Engineering.

[23]  Geng Ku,et al.  Ultrasound-modulated optical tomography of biological tissue by use of contrast of laser speckles. , 2002, Applied optics.

[24]  M. Raspanti,et al.  Ultrastructure of the bovine nuchal ligament. , 1991, Journal of anatomy.

[25]  J. Ophir,et al.  Elastography: A Quantitative Method for Imaging the Elasticity of Biological Tissues , 1991, Ultrasonic imaging.

[26]  J. Cooke,et al.  Management of the patient with intermittent claudication , 1991 .

[27]  Yasuteru Muragaki,et al.  Stretch-Induced Collagen Synthesis in Cultured Smooth Muscle Cells from Rabbit Aortic Media and a Possible Involvement of Angiotensin II and Transforming Growth Factor-β , 1998, Journal of Vascular Research.

[28]  Lihong V Wang,et al.  Methods for parallel-detection-based ultrasound-modulated optical tomography. , 2002, Applied optics.

[29]  T. Matsuda,et al.  Behavior of Arterial Wall Cells Cultured on Periodically Stretched Substrates , 1993, Cell transplantation.

[30]  P. Gounon,et al.  Interaction between cells and elastin fibers: An ultrastructural and immunocytochemical study , 1994, Journal of cellular physiology.

[31]  S. Gorfien,et al.  Cyclic biaxial strain of pulmonary artery endothelial cells causes an increase in cell layer-associated fibronectin. , 1990, American journal of respiratory cell and molecular biology.

[32]  H. Ives,et al.  Estrogen inhibits mechanical strain-induced mitogenesis in human vascular smooth muscle cells via down-regulation of Sp-1. , 2001, Cardiovascular research.

[33]  R. Duncan,et al.  Human osteoblast-like cells respond to mechanical strain with increased bone matrix protein production independent of hormonal regulation. , 1995, Endocrinology.

[34]  J. Rosenbloom [9] Elastin: An overview , 1987 .

[35]  C Neidlinger-Wilke,et al.  Cyclic stretching of human osteoblasts affects proliferation and metabolism: A new experimental method and its application , 1994, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[36]  P. Howard,et al.  Effect of mechanical forces on extracellular matrix synthesis by bovine urethral fibroblasts in vitro. , 1993, The Journal of urology.

[37]  S. Glagov,et al.  A new in vitro system for studying cell response to mechanical stimulation. Different effects of cyclic stretching and agitation on smooth muscle cell biosynthesis. , 1977, Experimental cell research.

[38]  Qingbo Xu,et al.  Cyclic Strain Stress-induced Mitogen-activated Protein Kinase (MAPK) Phosphatase 1 Expression in Vascular Smooth Muscle Cells Is Regulated by Ras/Rac-MAPK Pathways* , 1999, The Journal of Biological Chemistry.

[39]  R. Weiss,et al.  Mechanical strain induces growth of vascular smooth muscle cells via autocrine action of PDGF , 1993, The Journal of cell biology.

[40]  S J Kirkpatrick,et al.  Micromechanical behavior of cortical bone as inferred from laser speckle data. , 1998, Journal of biomedical materials research.

[41]  D J Mooney,et al.  Scaffolds for engineering smooth muscle under cyclic mechanical strain conditions. , 2000, Journal of biomechanical engineering.