Design method of achromatic extended-depth-of-focus endoscopic optical coherence tomography probe

By dividing the diffractive optical element into rings and utilizing two-photon 3D printing technology, the chromatic aberration and focal depth extension problems of the endoscopic optical coherence tomography probe were solved, achieving high-quality imaging effects.

CN119235260BActive Publication Date: 2025-10-03SHANGHAI JIAOTONG UNIV
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Patent Information

Application Number
CN202411379451.0
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2024-09-29
Publication Date
2025-10-03
Estimated Expiration
2044-09-29

AI Technical Summary

Technical Problem

Existing endoscopic optical coherence tomography probes have chromatic aberration effects when using broadband light sources, resulting in imaging artifacts and blur, and have a limited depth of focus, making it difficult to achieve both achromatic aberration and extended depth of focus at the same time.

Method used

By dividing the diffractive optical element into multiple rings and printing the diffractive optical element on the end face of the optical fiber using two-photon 3D printing technology, the output light field distribution and quality factor function (FOM) are calculated, and the ring height is optimized to achieve achromatism and extended depth of focus.

Benefits of technology

It enables light of different wavelengths to focus on the same position, extends the depth of focus, reduces optical distortion, and improves imaging accuracy and image quality.

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Abstract

The present invention discloses a method for designing an achromatic, extended-depth-of-focus endoscopic optical coherence tomography probe, which relates to the technical field of optical endoscopic probe design. The method comprises the following steps: S100, structure initialization; S200, calculation of the output light field distribution and the figure of merit function (FOM); S300, iterative calculation of a single circular ring; S400, determination of height variation perturbation stagnation; S500, optimization of height variation perturbation stagnation; S600, structure preservation; and S700, probe fabrication. The present invention achieves achromatic aberration and extended depth of focus, reducing the difficulty of assembling a spliced ​​endoscopic probe.
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Description

Technical Field

[0001] The present invention relates to the technical field of optical endoscope probe design, and in particular to a design method of an achromatic focal depth extended endoscope optical coherence tomography probe. Background Art

[0002] When light of different wavelengths passes through the same focusing optical element, the focused light field shifts, meaning it cannot focus to the same position, causing chromatic aberration. In the field of endoscopic optical coherence tomography (OCT), broadband light sources are commonly used to achieve high longitudinal resolution. However, broadband sources can increase chromatic aberration, resulting in imaging artifacts and blurring. Furthermore, during endoscopic procedures, probes must navigate confined tissues. Chromatic aberration can increase optical distortion caused by probe motion and changes in viewing angle, reducing the accuracy of real-time imaging. Therefore, achromatic probes can compensate and correct for chromatic aberration caused by broadband light sources, allowing the broad spectrum of signals to be effectively utilized without compromising imaging accuracy, thereby improving overall image quality. Current achromatic design approaches mostly focus on a single focal plane or near-diffraction-limited achromatic designs. Such designs typically result in a short depth of focus. In OCT, the captured high-resolution image can only be maintained within the focal depth; once out of focus, image resolution drops dramatically. Therefore, achieving both achromatic aberration and extended depth of focus is a pressing challenge for endoscopic OCT probes.

[0003] Therefore, those skilled in the art are committed to developing a design method for an achromatic and extended depth of focus endoscopic optical coherence tomography probe. Summary of the Invention

[0004] In view of the above-mentioned defects of the prior art, the technical problem to be solved by the present invention is how to design an endoscopic optical coherence tomography probe that can achieve both achromatism and extended depth of focus.

[0005] Research has found that by considering achromatism while expanding the axial light field, it is possible to achieve achromatism while also expanding the depth of focus to a certain extent.

[0006] In one embodiment of the present invention, a method for designing an achromatic extended depth of focus endoscopic optical coherence tomography probe is provided, comprising:

[0007] S100, structure initialization, dividing the diffractive optical element with a diameter of 124 μm into T rings, setting the ring width and height of each ring, where T is a positive integer;

[0008] S200, calculating the output light field distribution and the quality factor function FOM, calculating the output light field distribution and the quality factor function FOM corresponding to the diffractive optical element with the structure initialized;

[0009] S300, iterative calculation of a single ring, traversing and selecting each ring and updating the height change Δh, updating the structure of the diffractive optical element, calculating the output light field distribution and the figure of merit function (FOM) corresponding to each ring, and retaining the diffractive optical element structure that increases the figure of merit function (FOM);

[0010] S400, judging whether the height change disturbance is stagnant, comparing the quality factor function FOM of the first ring with the quality factor function FOM of the last ring. If the quality factor function FOM of the last ring is greater than the quality factor function FOM of the first ring, then re-execute step S300; otherwise, the height change Δh disturbance of each ring is stagnant, and execute step S500;

[0011] S500, height change disturbance stagnation optimization, the height change Δh is randomly updated within a specified range, and steps S300 to S400 are re-executed. If the height change Δh disturbance stagnation optimization exceeds a specified number of times, step S600 is executed;

[0012] S600: retain the structure, retain the current diffractive optical element structure;

[0013] S700, probe production, using two-photon 3D printing technology to print diffraction optical elements onto the end face of the optical fiber to complete the production of endoscopic optical coherence tomography probe.

[0014] Optionally, in the endoscopic optical coherence tomography probe design method in the above embodiment, step S100 includes:

[0015] S110, ring width setting, set the width of each ring to

[0016] S120: Height setting: setting the height of each ring to a random value.

[0017] Preferably, in the endoscopic optical coherence tomography probe design method in the above embodiment, T is set to be 124, and the width of each circular ring is 0.5 μm.

[0018] Furthermore, in the endoscopic optical coherence tomography probe design method in the above embodiment, the range of the random value is between 1 μm and 15 μm.

[0019] Optionally, in the endoscopic optical coherence tomography probe design method in any of the above embodiments, step S200 includes:

[0020] S210. Calculate the incident light field distribution of the diffractive optical element. The incident light of the diffractive optical element is Gaussian distributed. That is, the amplitude distribution of the fundamental mode light source emitted from the core of the single-mode optical fiber after passing through the beam expansion cylinder printed by two-photon 3D printing is Gaussian distributed. The formula is as follows:

[0021] A0(u,v,r)=U·exp[-(u 2 +v 2 ) / r 2 ]

[0022] Where U is the amplitude of the incident Gaussian light, r is the Gaussian light 1 / e 2 The radius, (u, v) is the spatial coordinate;

[0023] S220, convert the phase into the corresponding phase distribution according to the geometric structure of the diffractive optical element The formula is as follows:

[0024]

[0025] Among them, n DOE is the refractive index of the photoresist used in two-photon printing, H(u,v) is the geometric height distribution of the diffractive optical element, and λ is the wavelength of the incident light;

[0026] S230, calculate the output light field distribution, calculate the output light field distribution corresponding to the diffractive optical element according to the Fresnel diffraction integral formula, and calculate the output light field distribution at a distance z from the output surface of the diffractive optical element. n The light field distribution at is as follows:

[0027]

[0028] in, is the imaginary unit, is the wave number, λ m is the wavelength of the incident light, (x,y) is the exit surface z n The spatial coordinates at (u, v) are the spatial coordinates of the exit surface of the diffractive optical element, is the light field distribution on the exit surface of the diffractive optical element;

[0029] S240, calculate the quality factor function FOM, calculate the quality factor function FOM according to the light field distribution of the diffractive optical element, expand the focal depth of the focused light field corresponding to different wavelengths, and calculate the quality factor function FOM according to the light field distribution of the diffractive optical element. M ) corresponding to the same axial observation area (z1, z2, ... z N ) are included in the FOM, and the formula is as follows:

[0030]

[0031] Where M is the number of discretized wavelengths within the incident light source bandwidth, N is the number of discretized observation planes within the axial observation area, and E desired (x,y,λ m ,z n)=exp[-(u 2 +v 2 ) / (λ m z n / 4r DOE )] represents different z in the observation area j The light field distribution in the plane is at the diffraction limit, r DOE is the diameter of the designed diffractive optical element.

[0032] Preferably, in the endoscopic optical coherence tomography probe design method in any of the above embodiments, the height change Δh is 100 nm.

[0033] Optionally, in the endoscopic optical coherence tomography probe design method in any of the above embodiments, the iterative calculation traverses each ring from inside to outside or from outside to inside.

[0034] Optionally, in the endoscopic optical coherence tomography probe design method in any of the above embodiments, step S300 includes:

[0035] S310, calculating the output light field distribution and quality factor function (FOM) of the first circular ring, initially assigning i=1, selecting the i-th ring, increasing its height change by Δh, and keeping the heights of the remaining rings unchanged. The structure of the diffractive optical element is updated, and the output light field distribution and quality factor function (FOM) are calculated.

[0036] S320, determining the quality factor function; if the current quality factor function FOM increases compared to the FOM before the diffractive optical element structure is updated, retaining the current diffractive optical element structure, and updating the quality factor function FOM to the current quality factor function FOM, where i=i+1; otherwise, not retaining the current diffractive optical element structure, and not updating the quality factor function FOM;

[0037] S330, reducing the height change, reducing the height of the i-th ring by the same Δh, keeping the heights of the remaining rings unchanged, and calculating the output light field distribution and the quality factor function FOM;

[0038] S340, determining the quality factor function; if the current quality factor function FOM increases compared to the quality factor function FOM before the diffractive optical element structure is updated, retaining the current diffractive optical element structure, and updating the quality factor function FOM to the current quality factor function FOM, i=i+1; otherwise, not retaining the current diffractive optical element structure, and not updating the quality factor function FOM, i=i+1;

[0039] S350 , traverse all the rings, loop through steps S320 to S340 , and traverse all the rings of the diffractive optical element.

[0040] Optionally, in the endoscopic optical coherence tomography probe design method in any of the above embodiments, the specified range is greater than or equal to 1 nm and less than or equal to 100 nm.

[0041] Preferably, in the endoscopic optical coherence tomography probe design method in the above embodiment, the specified number of times is 5 times.

[0042] The present invention focuses light of different wavelengths to the same position and extends the focal depth of the focused light field corresponding to different wavelengths. The establishment of the quality factor function FOM takes into account the control of light field distribution at different axial positions at different wavelengths. Through two-photon printing technology, it directly prints on the end face of the optical fiber, simultaneously achieving achromatism and extended depth of focus, reducing the difficulty of assembling the spliced ​​endoscopic probe.

[0043] The concept, specific structure and technical effects of the present invention will be further described below in conjunction with the accompanying drawings to fully understand the purpose, characteristics and effects of the present invention. BRIEF DESCRIPTION OF THE DRAWINGS

[0044] Figure 1 is a flow chart illustrating a method for designing an endoscopic optical coherence tomography probe according to an exemplary embodiment;

[0045] Figure 2 is a rendering illustrating an endoscopic optical coherence tomography probe according to an exemplary embodiment;

[0046] Figure 3 is a schematic diagram illustrating an end-face image of an endoscopic optical coherence tomography probe according to an exemplary embodiment;

[0047] Figure 4 is a phase distribution diagram illustrating an end face image of an endoscopic optical coherence tomography probe according to an exemplary embodiment. DETAILED DESCRIPTION

[0048] The following describes several preferred embodiments of the present invention with reference to the accompanying drawings to make its technical content clearer and easier to understand. The present invention can be embodied in many different forms of embodiments, and the scope of protection of the present invention is not limited to the embodiments mentioned herein.

[0049] In the drawings, components with identical structures are denoted by the same reference numerals, and components with similar structures or functions are denoted by similar reference numerals. The size and thickness of each component shown in the drawings are arbitrary and are not limited by the present invention. To enhance clarity, the thickness of components in some places in the drawings is schematically exaggerated.

[0050] The inventors have designed a method for designing an achromatic extended depth of focus endoscopic optical coherence tomography probe, such as Figure 1As shown, the following steps are included:

[0051] In one embodiment of the present invention, a method for designing an achromatic extended depth of focus endoscopic optical coherence tomography probe is provided, comprising:

[0052] S100, structure initialization, dividing the diffractive optical element with a diameter of 124 μm into T rings, setting the ring width and height of each ring, where T is a positive integer; including:

[0053] S110, ring width setting, set the width of each ring to Set T to 124 and the width of each ring to 0.5 μm;

[0054] S120 , height setting: setting the height of each ring to a random value, with the range of the random value being between 1 μm and 15 μm.

[0055] S200, calculating the output light field distribution and the quality factor function FOM, calculating the output light field distribution and the quality factor function FOM corresponding to the diffractive optical element with the structure initialized; including:

[0056] S210, calculate the incident light field distribution of the diffractive optical element, the incident light of the diffractive optical element is Gaussian distribution, that is, the fundamental mode light source emitted from the core of the single-mode optical fiber is subjected to two-photon 3D

[0057] The amplitude distribution after the printed beam expansion cylinder is Gaussian distribution, the formula is as follows:

[0058] A0(u,v,r)=U·exp[-(u 2 +v 2 ) / r 2 ]

[0059] Where U is the amplitude of the incident Gaussian light, r is the Gaussian light 1 / e 2 The radius of (u,v) is

[0060] spatial coordinates;

[0061] S220, convert the phase into

[0062] The corresponding phase distribution The formula is as follows:

[0063]

[0064] Among them, n DOE is the refractive index of the photoresist used in two-photon printing, H(u,v) is the derivative

[0065] The geometric height distribution of the incident optical element, λ is the wavelength of the incident light;

[0066] S230, calculate the output light field distribution, calculate the output light field distribution corresponding to the diffractive optical element according to the Fresnel diffraction integral formula, and calculate the output light field distribution at a distance z from the output surface of the diffractive optical element. n The light field distribution at is as follows:

[0067]

[0068] in, is the imaginary unit, is the wave number, λ m is the wavelength of incident light, (x,y)

[0069] is the exit surface z n The spatial coordinates at (u, v) are the spatial coordinates of the exit surface of the diffractive optical element,

[0070] is the light field distribution on the exit surface of the diffractive optical element;

[0071] S240, calculate the quality factor function FOM, calculate the quality factor function FOM according to the light field distribution of the diffractive optical element, expand the focal depth of the focused light field corresponding to different wavelengths, and calculate the quality factor function FOM according to the light field distribution of the diffractive optical element. M ) corresponding to the same axial observation area (z1, z2, ... z N ) are included

[0072] In FOM, the formula is as follows:

[0073]

[0074] Where M is the number of discretized wavelengths within the incident light source bandwidth, N is the number of discretized observation planes within the axial observation area, and E desired (x,y,λ m ,z n )=exp[-(u 2 +v 2 ) / (λ m z n / 4r DOE )]

[0075] Indicates different z in the observation area j The light field distribution in the plane is at the diffraction limit, r DOE is the diameter of the designed diffractive optical element.

[0076] S300, iterative calculation of a single ring, traversing and selecting each ring and updating the height change Δh. In this embodiment, the height change Δh is 100 nm. The structure of the diffractive optical element is updated, and the output light field distribution and the figure of merit function (FOM) corresponding to each ring are calculated. The diffractive optical element structure that increases the figure of merit function (FOM) is retained. The iterative calculation traverses each ring from the inside out or from the outside in. In this embodiment, the method from the inside out is selected. The method includes:

[0077] S310, calculating the output light field distribution and quality factor function (FOM) of the first circular ring, initially assigning i=1, selecting the i-th ring, increasing its height change by Δh, and keeping the heights of the remaining rings unchanged. The structure of the diffractive optical element is updated, and the output light field distribution and quality factor function (FOM) are calculated.

[0078] S320, determining the quality factor function; if the current quality factor function FOM increases compared to the FOM before the diffractive optical element structure is updated, retaining the current diffractive optical element structure, and updating the quality factor function FOM to the current quality factor function FOM, where i=i+1; otherwise, not retaining the current diffractive optical element structure, and not updating the quality factor function FOM;

[0079] S330, reducing the height change, reducing the height of the i-th ring by the same Δh, keeping the heights of the remaining rings unchanged, and calculating the output light field distribution and the quality factor function FOM;

[0080] S340, judging the quality factor function, if the current quality factor function FOM is increased compared to the quality factor function FOM before the diffractive optical element structure is updated, then the current diffractive optical element structure is retained, and the quality factor function FOM is updated to the current quality factor function FOM, i=i+1; otherwise, the current diffractive optical element structure is not retained, and the quality factor function FOM is updated to the current quality factor function FOM, i=i+1;

[0081] The prime factor function FOM is not updated, i=i+1;

[0082] S350 , traverse all the rings, loop through steps S320 to S340 , and traverse all the rings of the diffractive optical element.

[0083] S400, height change disturbance stagnation judgment, compare the quality factor function FOM of the first ring with the quality factor function FOM of the last ring, if the quality factor function FOM of the last ring is greater than the quality factor function FOM of the first ring, then re-execute step S300; otherwise, the height change Δh disturbance of each ring becomes stagnant, and execute step S500.

[0084] S500, height change disturbance stagnation optimization, the height change Δh is randomly updated within the specified range, and steps S300-S400 are re-executed. If the height change Δh disturbance stagnation optimization exceeds the specified number of times, step S600 is executed, the specified range is greater than or equal to 1nm and less than or equal to 100nm, and the specified number of times is 5 times.

[0085] S600: retain the structure, retain the current diffractive optical element structure.

[0086] S700, probe production, using two-photon 3D printing technology to print diffraction optical elements onto the end face of the optical fiber to complete the production of endoscopic optical coherence tomography probe.

[0087] In order to verify whether the method proposed in this patent can achieve dispersion correction while achieving extended depth of focus, a numerical simulation was carried out. The parameter settings are: M = 5, the expected achromatic bandwidth is 200nm, that is, λ1 = 750nm, λ2 = 800nm, λ3 = 850nm, λ4 = 900nm, λ5 = 950nm, N = 200, z1 = 1mm, z 200 =3mm, that is, the observation area is 1mm to 3mm in the axial direction and is divided into 200 observation planes at equal intervals. The diameter of the diffractive optical element is 124μm and is divided into 124 circular rings, and the width of each circular ring is 500nm. The control group uses the same aperture, central wavelength λ3 = 850nm, and focal length of 1.5mm for simulation. Similarly, the observation area is 1mm to 3mm in the axial direction and is divided into 200 observation planes at equal intervals. The results are shown in the figure. Figure 2 As shown in the figure, (a) is the light field distribution corresponding to the designed endoscopic optical coherence tomography probe at 5 discrete wavelengths. It can be seen that the position of the focused light field distribution does not change with the change of wavelength, and the dispersion is well corrected. In the control group (b), the focused light field obviously moves with the change of wavelength, and the dispersion effect is obvious. At the same time, the numerical simulation results show that the resolution of the focused light field in (a) and (b) is about 14μm, but the average focal depth at each wavelength in (a) is about 800μm, while the average focal depth in (b) is about 500μm, indicating that the designed endoscopic optical coherence tomography probe can not only achieve good dispersion correction, but also extend the focal depth. Figure 3 To optimize the acquisition of endoscopic optical coherence tomography probe end-face images. Figure 4 is the corresponding phase distribution diagram.

[0088] The above describes in detail the preferred embodiments of the present invention. It should be understood that those skilled in the art can make numerous modifications and variations based on the concepts of the present invention without inventive effort. Therefore, any technical solutions that can be derived by those skilled in the art through logical analysis, reasoning, or limited experimentation based on the concepts of the present invention and the prior art should be within the scope of protection defined by the claims.

Claims

1. A method for designing an achromatic extended depth of focus endoscopic optical coherence tomography probe, characterized in that: include: S100, structure initialization, the diffractive optical element with a diameter of 124μm is divided into Rings, set the width and height of each ring, T is a positive integer; S200, calculating the output light field distribution and the quality factor function FOM, calculating the output light field distribution and the quality factor function FOM corresponding to the diffractive optical element with the structure initialized; S300, iterative calculation of a single ring, traversing each ring and updating the height change Δh , updating the structure of the diffractive optical element, calculating the output light field distribution and the quality factor function FOM corresponding to each ring, and retaining the diffractive optical element structure that increases the quality factor function FOM; S400, height change disturbance stagnation judgment, compare the quality factor function FOM of the first ring with the quality factor function FOM of the last ring, if the quality factor function FOM of the last ring is greater than the FOM of the first ring, then re-execute step S300; otherwise, the height change of each ring Δh If the disturbance becomes stagnant, step S500 is executed; S500, height change disturbance stagnation optimization, the height change Δh Randomly update within the specified range and re-execute steps S300-S400. Δh If the disturbance stagnation optimization exceeds the specified number of times, step S600 is executed; S600: retain the structure, retain the current diffractive optical element structure; S700, probe production: using two-photon 3D printing technology, the diffraction optical element is printed onto the end face of the optical fiber to complete the production of the endoscopic optical coherence tomography probe.

2. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The step S100 includes: S110, ring width setting, set the width of each ring to μm ; S120: Height setting: setting the height of each ring to a random value.

3. The method for designing an endoscopic optical coherence tomography probe according to claim 2, wherein: Set T to 124 and the width of each ring to 0.5 μm .

4. The method for designing an endoscopic optical coherence tomography probe according to claim 3, wherein: The random value range is 1 μm to 15 μm between.

5. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The step S200 includes: S210, calculating the incident light field distribution of the diffractive optical element. The incident light of the diffractive optical element is Gaussian distributed, that is, the amplitude distribution of the fundamental mode light source emitted from the core of the single-mode optical fiber after passing through the two-photon 3D printed beam expansion cylinder is Gaussian distributed. The formula is as follows: ; in, is the amplitude of the incident Gaussian light, It is Gaussian light The radius, is the spatial coordinate; S220, converting the phase into a corresponding phase distribution according to the geometric structure of the diffractive optical element , the formula is as follows: ; in, is the refractive index of the photoresist used in two-photon printing, is the geometric height distribution of the diffractive optical element, is the wavelength of incident light; S230, calculate the output light field distribution, calculate the output light field distribution corresponding to the diffractive optical element according to the Fresnel diffraction integral formula, and calculate the output light field distribution at a distance from the output surface of the diffractive optical element. The light field distribution at is as follows: ; in, is the imaginary unit, is the wave number, is the wavelength of incident light, For the exit surface The spatial coordinates of is the spatial coordinate of the exit surface of the diffractive optical element, is the light field distribution on the exit surface of the diffractive optical element; S240, calculating the quality factor function FOM, calculating the quality factor function FOM according to the light field distribution of the diffractive optical element, and extending the focal depth of the focused light field corresponding to different wavelengths, and ( ) corresponding to the same axial observation area ( ) are included in the FOM, and the formula is as follows: ; in, is the number of discretized wavelengths within the bandwidth of the incident light source, is the number of discretized observation planes in the axial observation area, Indicates that different The light field distribution in the plane is at the diffraction limit, is the diameter of the designed diffractive optical element.

6. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The height change Δh is 100 nm .

7. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The iterative calculation traverses each ring from the inside to the outside or from the outside to the inside.

8. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The step S300 includes: S310, calculate the output light field distribution and quality factor function FOM of the first ring, initially assign i=1, select the i-th ring, and increase its height change Δh , the heights of the remaining rings remain unchanged, the structure of the diffractive optical element is updated, and the output light field distribution and the quality factor function FOM are calculated; S320, determining a figure of merit function; if the current figure of merit function FOM increases compared to the FOM before the diffractive optical element structure is updated, retaining the current diffractive optical element structure, and updating the figure of merit function FOM to the current figure of merit function FOM, where i=i+1; otherwise, not retaining the current diffractive optical element structure, and not updating the figure of merit function FOM; S330, reducing the height change, reducing the height of the i-th ring by the same Δh, keeping the heights of the remaining rings unchanged, and calculating the output light field distribution and the quality factor function FOM; S340, determining the quality factor function; if the current quality factor function FOM increases compared to the quality factor function FOM before the diffractive optical element structure is updated, retaining the current diffractive optical element structure, and updating the quality factor function FOM to the current quality factor function FOM, i=i+1; otherwise, not retaining the current diffractive optical element structure, and not updating the quality factor function FOM, i=i+1; S350 , traverse all the rings, loop through steps S320 to S340 , and traverse all the rings of the diffractive optical element.

9. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The specified range is greater than or equal to 1 nm , less than or equal to 100 nm .

10. The method for designing an endoscopic optical coherence tomography probe according to claim 1, wherein: The specified number of times is 5 times.

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