• Laser & Optoelectronics Progress
  • Vol. 62, Issue 2, 0200002 (2025)
Yirui Zhu1、*, Jiulin Shi1, Lingkai Huang1, Lihua Fang1, Tomas E. Gomez Alvarez-Arenas2, and Xingdao He1
Author Affiliations
  • 1Key Laboratory for Optoelectronic Information Perception and Instrumentation of Jiangxi Province, Nanchang Hangkong University, Nanchang 330063, Jiangxi , China
  • 2Information and Physical Technologies Institute, Spanish National Research Council, Madrid 28006, Spain
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    DOI: 10.3788/LOP241618 Cite this Article Set citation alerts
    Yirui Zhu, Jiulin Shi, Lingkai Huang, Lihua Fang, Tomas E. Gomez Alvarez-Arenas, Xingdao He. Advances in Optical Coherence Elastography and Its Applications[J]. Laser & Optoelectronics Progress, 2025, 62(2): 0200002 Copy Citation Text show less
    Three main steps of the classical OCE technique[45]
    Fig. 1. Three main steps of the classical OCE technique[45]
    Elastography of human breast cancer tissues obtained from elastography across different spatial scales[68-71]
    Fig. 2. Elastography of human breast cancer tissues obtained from elastography across different spatial scales[68-71]
    Different excitation methods for OCE technology[72]
    Fig. 3. Different excitation methods for OCE technology[72]
    OCT-based OCE system setup. (a) SD-OCE system; (b) SS-OCE system
    Fig. 4. OCT-based OCE system setup. (a) SD-OCE system; (b) SS-OCE system
    M-scan mode with temporal repetitive scanning at a particular transverse position x0 to obtain vibration information at that position over time
    Fig. 5. M-scan mode with temporal repetitive scanning at a particular transverse position x0 to obtain vibration information at that position over time
    M-B scanning mode. (a) M-B scanning optical path setup with the OCT probe beam completing the B-scan in the x-z plane; (b) M-B scanning timing control program; (c) 3D dataset acquired in the M-B scanning mode (x, z, t)
    Fig. 6. M-B scanning mode. (a) M-B scanning optical path setup with the OCT probe beam completing the B-scan in the x-z plane; (b) M-B scanning timing control program; (c) 3D dataset acquired in the M-B scanning mode (x, z, t)
    Tissue model in the 3D Cartesian coordinate system (x,y,z)
    Fig. 7. Tissue model in the 3D Cartesian coordinate system (x,y,z)
    Types of mechanical waves in biological tissues
    Fig. 8. Types of mechanical waves in biological tissues
    Imaging results of LSW with AC-ARF non-contact excitation in the agar model[63]. (a) M-scan mode results of LSW, while white arrows indicate the different detection moments; (b) vibrational displacement curves of LSW along the depth direction at different detection moments
    Fig. 9. Imaging results of LSW with AC-ARF non-contact excitation in the agar model[63]. (a) M-scan mode results of LSW, while white arrows indicate the different detection moments; (b) vibrational displacement curves of LSW along the depth direction at different detection moments
    OCE results for SAW and SRW in agar[127]. (a) 2D vibrational displacement propagation images of SAW and SRW within agar at different moments, with yellow arrows at the top of the image indicating excitation points; (b) 3D surfaces (x, z, t) reconstructed for SAW and SRW, with white arrows indicating SAW wavefronts and black arrows indicating SRW wavefronts; (c) 2D OCT images of the agar; (d) the displacement profiles of SRW and SAW at 2.7 ms at the depths shown by the blue line in Fig. 10 (a); (e) the spatiotemporal displacement of SRW and SAW at the depths shown by the blue line in Fig. 10(a)
    Fig. 10. OCE results for SAW and SRW in agar[127]. (a) 2D vibrational displacement propagation images of SAW and SRW within agar at different moments, with yellow arrows at the top of the image indicating excitation points; (b) 3D surfaces (x, z, t) reconstructed for SAW and SRW, with white arrows indicating SAW wavefronts and black arrows indicating SRW wavefronts; (c) 2D OCT images of the agar; (d) the displacement profiles of SRW and SAW at 2.7 ms at the depths shown by the blue line in Fig. 10 (a); (e) the spatiotemporal displacement of SRW and SAW at the depths shown by the blue line in Fig. 10(a)
    Lamb wave propagation modes in thin plates. (a) Symmetric mode; (b) antisymmetric mode
    Fig. 11. Lamb wave propagation modes in thin plates. (a) Symmetric mode; (b) antisymmetric mode
    Application areas of optical coherent elastography
    Fig. 12. Application areas of optical coherent elastography
    OCE results after corneal-3D refractive surgery[136]. (a) 2D structural image of the cornea, with red arrows indicating the boundary between the corneal cap and residual stromal bed; (b) corneal depth resolved elastography results, with red arrows indicating the boundary between the Young's modulus of the corneal cap and residual stromal bed after surgery
    Fig. 13. OCE results after corneal-3D refractive surgery[136]. (a) 2D structural image of the cornea, with red arrows indicating the boundary between the corneal cap and residual stromal bed; (b) corneal depth resolved elastography results, with red arrows indicating the boundary between the Young's modulus of the corneal cap and residual stromal bed after surgery
    Results of OCE experiments after keratoconus cross-linking surgery[78]. (a) 2D structural image of the keratoconus after 15J-CXL treatment; (b) propagation process of the vibrational displacements at different times after the 15J-CXL treatment; (c) 2D structural image of the keratoconus in vivo after 30J-CXL treatment; (d) propagation process of the vibrational displacements at different times after the 30J-CXL treatment; (e) 15J-CXL depth-resolved image of the internal phase velocity of the keratoconus after treatment; (f) depth-resolved image of the internal phase velocity of the conical cornea after 30J-CXL treatment; (g) comparison of the average velocity values
    Fig. 14. Results of OCE experiments after keratoconus cross-linking surgery[78]. (a) 2D structural image of the keratoconus after 15J-CXL treatment; (b) propagation process of the vibrational displacements at different times after the 15J-CXL treatment; (c) 2D structural image of the keratoconus in vivo after 30J-CXL treatment; (d) propagation process of the vibrational displacements at different times after the 30J-CXL treatment; (e) 15J-CXL depth-resolved image of the internal phase velocity of the keratoconus after treatment; (f) depth-resolved image of the internal phase velocity of the conical cornea after 30J-CXL treatment; (g) comparison of the average velocity values
    Mechanical stiffness of breast cancer tissue based on QEM. (a) Histopathological section of breast cancer; (b) enface diagram of OCT; (c) mechanical stiffness results of breast cancer tissue obtained by QEM technology to the OCT structure diagram
    Fig. 15. Mechanical stiffness of breast cancer tissue based on QEM. (a) Histopathological section of breast cancer; (b) enface diagram of OCT; (c) mechanical stiffness results of breast cancer tissue obtained by QEM technology to the OCT structure diagram
    OCE experimental results of non-contact LSW in isolated porcine brain tissue. (a) In vitro pig brain tissue experimental samples; (b) two-dimensional OCT structural images of cerebral vascular regions; (c) three-dimensional OCT structural images of cerebral vascular regions; (d) M-scan mode image of the LSW propagation process in the left cerebral vascular region; (e) vibration displacement curves of LSW at different times; (f) M-scan mode image of the LSW propagation process in the right cerebral vascular region; (g) vibration displacement curves of LSW at different times
    Fig. 16. OCE experimental results of non-contact LSW in isolated porcine brain tissue. (a) In vitro pig brain tissue experimental samples; (b) two-dimensional OCT structural images of cerebral vascular regions; (c) three-dimensional OCT structural images of cerebral vascular regions; (d) M-scan mode image of the LSW propagation process in the left cerebral vascular region; (e) vibration displacement curves of LSW at different times; (f) M-scan mode image of the LSW propagation process in the right cerebral vascular region; (g) vibration displacement curves of LSW at different times
    Results of OCE experiments based on SRW and SAW models for isolated porcine brain tissue. (a) The three regions of isolated porcine brain tissue selected in the experiments; (b) the propagation process of SRW and SAW at different moments in the FL region; (c) the results of the 3D reconstruction of the wave front surface of the propagation process at different moments of SRW and SAW; (d) the spatio-temporal displacement map of SRW and SAW
    Fig. 17. Results of OCE experiments based on SRW and SAW models for isolated porcine brain tissue. (a) The three regions of isolated porcine brain tissue selected in the experiments; (b) the propagation process of SRW and SAW at different moments in the FL region; (c) the results of the 3D reconstruction of the wave front surface of the propagation process at different moments of SRW and SAW; (d) the spatio-temporal displacement map of SRW and SAW
    Characterization of the scar tissue in vivo with four different OCT modalities[196]. (a) Photograph of the scar area in a 28-year-old male volunteer; (b) its enlarged area with the direction of the mechanical wave propagation in the scar and adjacent skin site; (c) group velocity of the Rayleigh wave in the scar and in the normal skin tissue in two orthogonal directions; (d)‒(e) Structural OCT and OCT angiography images; (f) optic axis orientation map obtained with the PS-OCT system; (g) image of Rayleigh wave group velocity measured in the direction perpendicular to the scar within the area covered by a white dashed rectangle
    Fig. 18. Characterization of the scar tissue in vivo with four different OCT modalities[196]. (a) Photograph of the scar area in a 28-year-old male volunteer; (b) its enlarged area with the direction of the mechanical wave propagation in the scar and adjacent skin site; (c) group velocity of the Rayleigh wave in the scar and in the normal skin tissue in two orthogonal directions; (d)‒(e) Structural OCT and OCT angiography images; (f) optic axis orientation map obtained with the PS-OCT system; (g) image of Rayleigh wave group velocity measured in the direction perpendicular to the scar within the area covered by a white dashed rectangle
    ModePalpationUSEMRELSEPAECBMOCE
    MethodTouchSound waveMagnetic waveLaserUltrasonicsLaserLaser
    Spatial resolutionSubjective~500 µm~500 µm~µm~50 µm~3 µm~10 µm
    Imaging depthSubjectivecmcm~1 mmcm~100 µm~ mm
    Proposed time~1991~1995~2012~2011~2008~1998
    Non-destructive, noninvasiveYesYesYesYesYesYesYes
    Table 1. Comparison of different elastography technical parameters
    SampleConditionMethodShear modulus /PaYoung’s modulus /Pa
    In vivo rabbit corneaNormalARF-OCE27.4×103‒88.7×103136142
    cold cataract lens30.4×103[142
    NormalAir pulse-OCE93.7×103‒131.1×103[148
    Corneal collagen cross-linking (CXL)142.9×103‒203.2×103[148
    NormalSpace-coupled ultrasound OCE246.4×103[149
    Corneal collagen cross-linking (CXL)1.627×106[149
    Ex vivo rabbit corneaCorneal flap after FLExARF-OCE(71.7±24.6)×103[133
    Residual stromal bed after the FLEx surgery(305.8±48.5)×103[133
    Corneal cap after SMILE surgery(219.5±54.9)×103[133
    Residual stromal bed after SMILE surgery(221.5±43.2)×103[133
    Normal(91.7±28.1)×103[133
    Normal44.9×103‒58.5×103[150
    NormalARF-OCE53.1×103[151
    Space-coupled ultrasound OCE34×103‒261×103[15220×106‒44×106[152
    SS-OCE35×103‒80×103[153
    Ex vivo porcine corneaNormalARF-OCE12.45×103‒32.35×103[154-155
    Air pulse- OCE(5.70±2.26)×103[156(17.0±7.93)×103[156
    LF-OCE(198.25±5.97)×103[157
    Mechanical probe OCE20.5×103[102
    Ex vivohuman corneaKeratoconusARF-OCE49.1×103‒60.3×103[150
    Scarring corneaARF-OCE219.2×103‒294.9×103[151
    In vivohuman corneaNormalUltrasound elastography(696±113)×103[158
    Corneal indentation(755±159)×103[159
    Central corneaAir pulse- OCE(692±64)×103[139
    Limb(852±82)×103[139
    Normal(733 ± 164)×103[139
    Age(25‒67)Mechanical probe OCE(72±14)×103[137
    Table 2. Elastic modulus results of the corneal tissue obtained from different OCE experiments
    SampleConditionMethodShear modulus /PaYoung’s modulus/Pa
    Ex vivo rabbit eye lensNormal (juvenile)ARF-OCE(7.74±1.56)×103[160
    Normal (mature)(15.15±4.52)×103[160
    Ex vivo porcine eye lensNormalAir pulse-OCE2.7×103‒3.8×103[161
    NormalAir pulse-OCE(8.8±1.5)×103[162
    Oxidative cataract (added hydrogen peroxide)(123.6±20.8)×103[162
    Oxidative cataract with α-lipoic acid added(45.1±24.1)×103[162
    NormalAir pulse-OCE(11.3±3.4)×103[163
    Cold cataracts(21.8±7.8)×103[163
    Anterior part of the lensBrillouin Microscopy and OCE(1.98±0.74)×103[164
    The posterior part of the lens(2.93±1.13)×103[164
    Nucleus of the lens(11.90±2.94)×103[164
    Table 3. Elastic modulus results of the crystalline lens obtained from different OCE experiments
    SampleConditionMethodShear modulus /MPaYoung’s modulus /Pa
    In vivo rabbit eye scleraNormalARF-OCE
    Ex vivo rabbit eye scleraMechanical probe OCE248×103[165
    Ex vivo porcine eye sclerascleraMechanical vibration OCE0.56‒0.67166
    Limbal scleraARF-OCE48.43×103‒489.92×103[167
    Perioptic disc sclera29.87×103‒175.16×103[167
    NormalPZT probe OCE0.71±0.12168
    UV-riboflavin is crosslinking1.50±0.39168
    The sclera of the human eyeNormalMechanical probe OCE0.31±0.15137
    Table 4. Elastic modulus results of sclera tissue obtained from different OCE experiments
    SampleConditionMethodShear modulus /PaYoung’s modulus /Pa
    In vivo rabbit eye retinaNormalARF-OCE3.09×103‒140×103[143169
    Mechanical probe OCE50.4×103‒134.6×103[165
    Ex vivo porcine retina of the eyeARF-OCE141.21×103±5.24×103[155
    ARF-OCE6.2×103[170
    Table 5. Elastic modulus results of retinal tissue obtained from different OCE experiments
    Yirui Zhu, Jiulin Shi, Lingkai Huang, Lihua Fang, Tomas E. Gomez Alvarez-Arenas, Xingdao He. Advances in Optical Coherence Elastography and Its Applications[J]. Laser & Optoelectronics Progress, 2025, 62(2): 0200002
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