IP Library Granted Patent US 10,581,217
Granted Patent B2
US 10,581,217 · App. 16/363,597 · Granted Mar 3, 2020

Picosecond laser apparatus and methods for treating target tissues with same

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Quick Facts
Patent No.
US 10,581,217
App. No.
16/363,597
Granted
Mar 3, 2020
Kind
B2
Abstract

Apparatuses and methods are disclosed for applying laser energy having desired pulse characteristics, including a sufficiently short duration and/or a sufficiently high energy for the photomechanical treatment of skin pigmentations and pigmented lesions, both naturally-occurring (e.g., birthmarks), as well as artificial (e.g., tattoos). The laser energy may be generated with an apparatus having a resonator with the capability of switching between a modelocked pulse operating mode and an amplification operating mode. The operating modes are carried out through the application of a time-dependent bias voltage, having waveforms as described herein, to an electro-optical device positioned along the optical axis of the resonator.

Claims (35)

1. A method of treating a target tissue comprising:

generating, using a laser source, an output beam having a subnanosecond pulse duration;

modifying the output beam, using an optical system, to provide a photomechanically disruptive treatment beam;

directing the photomechanically disruptive treatment beam to one or more regions of the target tissue;

photomechanically disrupting the one or more regions of the target tissue; and

inducing collagen restoration within the target tissue in response to photomechanically disrupting the one or more regions of target tissue.

2. The method of claim 1 further comprising rejuvenating the target tissue.

3. The method of claim 2 wherein rejuvenating the target tissue comprises inducing epithelial cell restoration within the target tissue in response to photomechanically disrupting the one or more regions of the target tissue.

4. The method of claim 2 wherein rejuvenating the target tissue comprises increasing amount of collagen disposed therein relative to untreated tissue.

5. The method of claim 1 wherein the photomechanically disruptive treatment beam has a non-uniform beam profile, the non-uniform beam profile comprising a plurality of regions of relatively high energy per unit area dispersed within a substantially uniform background region of relatively low energy per unit area.

6. The method of claim 5 further comprising increasing temperature of a first region of target tissue to a first temperature T1 and increasing or maintaining temperature of a second region of target tissue to a second temperature T2 in response to distribution of regions of relatively high energy and regions of relatively low energy.

7. The method of claim 6 wherein T1 ranges from about 45 degrees Celsius to about 50 degrees Celsius.

8. The method of claim 6 wherein T1 is approximately 70 degrees Celsius or greater.

9. The method of claim 1 , wherein the photomechanically disruptive treatment beam has an energy spot diameter of about 5 mm.

10. The method of claim 1 , wherein the photomechanically disruptive treatment beam has an energy spot diameter which can be changed according to area of the target tissue.

11. A method of treating a target tissue comprising one or more pigments, the method comprising:

generating, using a laser source, an output beam having a subnanosecond pulse duration;

modifying the output beam, using an optical system, to provide a photomechanically disruptive treatment beam;

directing the photomechanically disruptive treatment beam to one or more pigments of the target tissue, wherein the one or more pigments are visible prior to treatment; and

decreasing visible appearance of one or more pigments within the target tissue in response to the photomechanically disruptive treatment beam.

12. The method of claim 11 , wherein the one or more pigments comprise one or more tattoo pigments.

13. The method of claim 11 , wherein the target tissue is a pigmented lesion.

14. The method of claim 11 wherein the one or more pigments is melanin.

15. The method of claim 11 wherein decreasing visible appearance of one or more pigments comprises decreasing visible appearance of a pigmented lesion within the target tissue.

16. The method of claim 11 , wherein the photomechanically disruptive treatment beam has a non-uniform beam profile, the non-uniform beam profile comprising a plurality of regions of relatively high energy per unit area dispersed within a substantially uniform background region of relatively low energy per unit area.

17. The method of claim 16 further comprising increasing temperature of a first region of target tissue to a first temperature T1 and increasing or maintaining temperature of a second region of target tissue to a second temperature T2 in response to distribution of regions of relatively high energy and regions of relatively low energy.

18. A method of treating tissue comprising oxyhemoglobin, the method comprising:

generating, using a laser source, an output beam having a subnanosecond pulse duration;

modifying the output beam, using an optical system, to provide a photomechanically disruptive treatment beam;

directing the photomechanically disruptive treatment beam to one or more regions of the target tissue comprising oxyhemoglobin, wherein the target tissue comprises a vascular lesion that is visible prior to treatment; and

decreasing visible appearance of the vascular lesion in response to the photomechanically disruptive treatment beam.

19. The method of claim 18 , wherein the photomechanically disruptive treatment beam has a non-uniform beam profile, the non-uniform beam profile comprising a plurality of regions of relatively high energy per unit area dispersed within a substantially uniform background region of relatively low energy per unit area.

20. The method of claim 19 further comprising increasing temperature of a first region of target tissue to a first temperature T1 and increasing or maintaining temperature of a second region of target tissue to a second temperature T2 in response to distribution of regions of relatively high energy and regions of relatively low energy.

21. The method of claim 18 , wherein the photomechanically disruptive treatment beam has an energy spot diameter of about 5 mm.

22. The method of claim 18 , wherein the photomechanically disruptive treatment beam has an energy spot diameter which can be changed according to area of the target tissue.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Mar 1, 2024
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION
To: CYNOSURE, LLC; PALOMAR MEDICAL TECHNOLOGIES, LLC
Reel/Frame 066723/0227 →
TERMINATION AND RELEASE OF PATENTS Recorded Feb 29, 2024
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: CYNOSURE, LLC; PALOMAR MEDICAL TECHNOLOGIES, LLC
Reel/Frame 066707/0957 →
ABL NOTICE AND CONFIRMATION OF GRANT OFSECURITY INTEREST IN PATENTS Recorded Jan 12, 2024
From: CYNOSURE, LLC; PALOMAR MEDICAL TECHNOLOGIES, LLC
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 066222/0937 →
NOTICE AND CONFIRMATION OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Jan 7, 2020
From: CYNOSURE, LLC; PALOMAR MEDICAL TECHNOLOGIES, LLC
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 051496/0579 →
RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Dec 30, 2019
From: BANK OF AMERICA, N.A.
To: CYNOSURE, LLC
Reel/Frame 051447/0536 →
CHANGE OF NAME Recorded Oct 30, 2019
From: CYNOSURE, INC.
To: CYNOSURE, LLC
Reel/Frame 050872/0760 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2019
From: SIERRA, RAFAEL ARMANDO; MIRKOV, MIRKO GEORGIEV
To: CYNOSURE, INC.
Reel/Frame 050839/0470 →
SECURITY INTEREST Recorded Oct 14, 2019
From: HOLOGIC, INC.; CYNOSURE, LLC; CYTYC CORPORATION; FAXITRON BIOPTICS, LLC; FOCAL THERAPEUTICS, INC.; GEN-PROBE INCORPORATED
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 050719/0701 →