Systems and methods for monitoring time based photo active agent delivery or photo active marker presence
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61B-003/10
A61N-005/06
A61B-003/107
A61B-003/135
A61F-009/007
A61K-049/00
A61F-009/008
A61N-005/067
A61M-037/00
출원번호
US-0488097
(2012-06-04)
등록번호
US-9020580
(2015-04-28)
발명자
/ 주소
Friedman, Marc D.
Kamaev, Pavel
Muller, David
Pertaub, Radha
Scharf, Ronald
Sherr, Evan
Usher, David
출원인 / 주소
Avedro, Inc.
대리인 / 주소
McDonnell Boehnen Hulbert & Berghoff LLP
인용정보
피인용 횟수 :
0인용 특허 :
78
초록▼
Devices and approaches for monitoring time based photo active agent delivery or photo active marker presence in an eye. A monitoring system is provided for measuring the presence of a photo active marker by illuminating the eye so as to excite the photo-active marker and then observing characteristi
Devices and approaches for monitoring time based photo active agent delivery or photo active marker presence in an eye. A monitoring system is provided for measuring the presence of a photo active marker by illuminating the eye so as to excite the photo-active marker and then observing characteristic emission from the photo active marker. Example systems incorporate Scheimpflug optical systems or slit lamp optical systems to observe cross sectional images of an eye to monitor instantaneous distribution, diffusion pattern, and rate of uptake of a photo active agent applied to an eye. Systems and methods further allow for utilizing the monitored distribution of photo active agent in the eye as feedback for a cross-linking system.
대표청구항▼
1. A system to determine a distribution of a photo-active marker applied to a corneal tissue by a treatment system, comprises: an excitation source that directs light to the corneal tissue treated with the photo-active marker, wherein the light causes the photo-active marker to fluoresce;an image ca
1. A system to determine a distribution of a photo-active marker applied to a corneal tissue by a treatment system, comprises: an excitation source that directs light to the corneal tissue treated with the photo-active marker, wherein the light causes the photo-active marker to fluoresce;an image capture system that captures one or more cross-sectional images of the corneal tissue in response to the excitation source that directs the light to the corneal tissue, wherein each cross-sectional image shows fluorescing photo-active marker along a respective cross-section of the corneal tissue; anda controller that receives the one or more cross-sectional images and determines information relating to a distribution of the photo-active marker at varying depths across the corneal tissue,wherein the excitation source directs the light to the corneal tissue along an axis; the image capture system includes a camera and a lens; the camera captures the one or more cross-sectional images of the corneal tissue via the lens; the camera and the lens are offset from the axis defined by the light; the camera defines an image plane; the lens defines a lens plane; the lens plane is separate from the image plane; the one or more cross-sectional images of the corneal tissue are associated with a focal plane defined by the camera and the lens; and the camera and the lens are oriented such that the image plane, the lens plane, and the focal plane all intersect each other at a common intersection. 2. The system of claim 1, wherein the excitation source directs the light to the corneal tissue as one or more slits of light, and the camera captures the one or more cross-sectional images of the corneal tissue according to the one or more slits of light. 3. The system of claim 2, wherein the one or more cross-sectional images of the corneal tissue provides a profile of a volume of the corneal tissue corresponding to one half of a cornea. 4. The system of claim 2, wherein the excitation source includes a multiple line generator using an optical grating or a scanning mirror system to selectively direct the light to the corneal tissue as more than one slits of light. 5. The system of claim 1, wherein the excitation source includes a digital micro-mirror device (DMD) to selectively direct the light to the corneal tissue. 6. The system of claim 1, wherein the focal plane is approximately parallel to a plane that is tangent to an apex of a corneal surface that corresponds to a treated corneal tissue being captured by the camera. 7. The system of claim 6, wherein the common intersection and the excitation source are disposed on opposing sides of the apex of the corneal surface. 8. The system of claim 1, wherein the excitation source and the image capture system rotate about the corneal tissue to capture a plurality of cross-sectional images of the corneal tissue. 9. The system of claim 1, wherein the controller determines a distribution of the photo-active marker at varying depths across the corneal tissue over a period of time to determine a rate of uptake of the photo-active marker by the corneal tissue. 10. The system of claim 1, further comprising the treatment system, wherein the photo-active marker is a cross-linking agent, and the treatment system adjusts the treatment of the eye by applying a pattern of ultraviolet light to the corneal tissue to activate cross-linking activity in the corneal tissue. 11. The system of claim 10, wherein the treatment system applies the pattern of ultraviolet light via a digital micro-mirror device (DMD). 12. The system of claim 10, wherein the treatment system applies the pattern of ultraviolet light via multiphoton excitation. 13. The system of claim 1, further comprising the treatment system, wherein the treatment system adjusts the treatment of the corneal tissue by applying additional photo-active marker to achieve a desired distribution of the photo-active marker. 14. The system of claim 13, wherein, after applying the additional photo-active marker, the image capture system captures additional cross-sectional images of the corneal tissue in response to the excitation source which directs additional light to the corneal tissue, and the controller determines additional information relating to the distribution of the photo-active marker at varying depths across the corneal tissue to determine whether a desired distribution has been achieved. 15. The system of claim 13, wherein the treatment system modifies an uptake of the photo-active marker by the corneal tissue. 16. The system of claim 15, wherein the treatment system includes a permeability regulation system that modifies a permeability of the corneal tissue to increase an uptake of the photo-active marker by the corneal tissue. 17. The system of claim 15, wherein the treatment system applies a diffusion-influencing substance to the corneal tissue. 18. The system of claim 1, wherein the excitation source includes a plurality of slit lamps arranged about the eye tissue, and the image capture system captures the one or more cross-sectional images of the corneal tissue in response to the plurality of slit lamps which directs the light to the corneal tissue. 19. The system of claim 1, wherein the excitation source directs the light to the eye tissue as a slit at an incident angle in a range from approximately 20 degrees to approximately 70 degrees relative to the image capture system. 20. The system of claim 1, wherein the common intersection, the camera, and the lens are disposed on a same side of the axis defined by the light. 21. A system to determine a distribution of a photo-active agent applied to a corneal tissue by a treatment system, comprises: an excitation source that directs light along an axis to the corneal tissue treated with the photo-active marker, wherein the light causes the photo-active marker to fluoresce;a first image capture system that includes a first camera and a first lens, wherein: the first camera and the first lens are offset on a first side of an axis defined by the light;the first camera captures, via the first lens, one or more first cross-sectional images showing fluorescing photo-active marker in a first half of the corneal tissue disposed on the first side of the axis defined by the light;the first camera defines a first image plane;the first lens defines a first lens plane;the first lens plane is separate from the first image plane;the one or more first cross-sectional images are associated with a first focal plane defined by the first camera and the first lens; andthe first camera and the first lens are oriented such that the first image plane, the first lens plane, and the first focal plane all intersect each other at a first common intersection;a second image capture system that includes a second camera and a second lens, wherein: the second camera and the second lens are offset on a second side of the axis defined by the light, opposite from the first side;the second camera captures, via the second lens, one or more second cross-sectional images showing the fluorescing photo-active marker in a second half of the corneal tissue disposed on the second side of the axis defined by the light;the second camera defines a second image plane;the second lens defines a second lens plane;the second lens plane is separate from the second image plane;the one or more second cross-sectional images are associated with a second focal plane defined by the second camera and the second lens; andthe second camera and the second lens are oriented such that the second image plane, the second lens plane, and the second focal plane all intersect each other at a second common intersection;a controller that receives the first cross-sectional images and the second cross-sectional images and determines information relating to a distribution of the photo-active marker at varying depths across the first half and the second half of the corneal tissue. 22. The system of claim 21, wherein the excitation source directs the light to the corneal tissue as one or more slits of light. 23. The system of claim 21, wherein the first cross-sectional images and the second cross-sectional images of the corneal tissue provides a profile of a volume of the corneal tissue corresponding to two halves of a cornea. 24. The system of claim 21, wherein the first focal plane is approximately parallel to a first plane that is tangent to a first apex of a first corneal surface corresponding to the first half of the corneal tissue, and the second focal plane is approximately parallel to a second plane that is tangent to a second apex of a second corneal surface corresponding to the second half of the corneal tissue. 25. The system of claim 24, wherein the first common intersection and the axis defined by the light are disposed on opposing sides of the first apex of the first corneal surface, and the second common intersection and the axis are disposed on opposing sides of the second apex of the second corneal surface. 26. The system of claim 21, wherein the first common intersection is disposed on the first side of the axis and the second common intersection is disposed on the second side of the axis. 27. The system of claim 21, wherein the controller determines a distribution of the photo-active marker at varying depths across the corneal tissue over a period of time, thereby determines a rate of uptake of the photo-active marker by the corneal tissue. 28. The system of claim 21, further comprising the treatment system, wherein the photo-active marker is a cross-linking agent, and the treatment system adjusts the treatment of the eye by applying a pattern of ultraviolet light to the corneal tissue to activate cross-linking activity in the corneal tissue.
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