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    • 1. 发明授权
    • Corneal vitrification, methods and devices to produce corneal vitrification and methods of use thereof
    • 角膜玻璃化,产生角膜玻璃化的方法和装置及其使用方法
    • US09532904B2
    • 2017-01-03
    • US14674890
    • 2015-03-31
    • Olivia SerdarevicMichael BerryDonald F. Heller
    • Olivia SerdarevicMichael BerryDonald F. Heller
    • A61B19/00A61F9/008A61F9/007A61N7/00
    • A61F9/008A61F2/142A61F9/0079A61F9/00814A61F2009/00872A61N7/00A61N2007/0004
    • The invention includes: a new composition of matter (a composite comprising a naturally occurring in vivo cornea in an in situ eye together with at least one volume of vitrified non-naturally occurring corneal stromal tissue formed within the naturally occurring corneal stromal tissue) wherein the vitrified tissue is modified in structure and properties from its naturally occurring condition into a non-naturally occurring glass-like condition with modifications including but not limited to increased elastic modulus; methods for producing and using the new composition of matter for modifying corneal structure and properties, including but not limited to corneal optical aberrations; wound closure adhesion and transplant adhesion; and a photovitrification system for producing the new composition of matter comprising at least one photon source with controllable treatment parameters. A reverse template can be added to corneal vitrification systems to increase vitrification and modifications of structure and properties.
    • 本发明包括:一种新的物质组合物(包括在原位眼中的天然存在的体内角膜以及在天然存在的角膜基质组织内形成的至少一个玻璃化非天然存在的角膜基质组织体积的复合物),其中 玻璃化组织的结构和性质从其天然存在的状态改变成非天然存在的玻璃状状态,其中包括但不限于增加的弹性模量; 用于生产和使用用于修饰角膜结构和性质的新组合物的方法,包括但不限于角膜光学像差; 伤口闭合粘连和移植附着力; 以及用于产生包含至少一个具有可控处理参数的光子源的新组合物的光生产系统。 可以向角膜玻璃化系统添加反向模板,以增加玻璃化和结构和性质的修改。
    • 2. 发明授权
    • Corneal vitrification, methods and devices to produce corneal vitrification and methods of use thereof
    • 角膜玻璃化,产生角膜玻璃化的方法和装置及其使用方法
    • US09526656B2
    • 2016-12-27
    • US14674992
    • 2015-03-31
    • Olivia SerdarevicMichael BerryDonald F. Heller
    • Olivia SerdarevicMichael BerryDonald F. Heller
    • A61B18/18A61F9/008A61F9/007
    • A61F9/008A61F2/142A61F9/0079A61F9/00814A61F2009/00872A61N7/00A61N2007/0004
    • The invention includes: a new composition of matter (a composite comprising a naturally occurring in vivo cornea in an in situ eye together with at least one volume of vitrified non-naturally occurring corneal stromal tissue formed within the naturally occurring corneal stromal tissue) wherein the vitrified tissue is modified in structure and properties from its naturally occurring condition into a non-naturally occurring glass-like condition with modifications including but not limited to increased elastic modulus; methods for producing and using the new composition of matter for modifying corneal structure and properties, including but not limited to corneal optical aberrations; wound closure adhesion and transplant adhesion; and a photo vitrification system for producing the new composition of matter comprising at least one photon source with controllable treatment parameters. A reverse template can be added to corneal vitrification systems to increase vitrification and modifications of structure and properties.
    • 本发明包括:一种新的物质组合物(包括在原位眼中的天然存在的体内角膜以及在天然存在的角膜基质组织内形成的至少一个玻璃化非天然存在的角膜基质组织体积的复合物),其中 玻璃化组织的结构和性质从其天然存在的状态改变成非天然存在的玻璃状状态,其中包括但不限于增加的弹性模量; 用于生产和使用用于修饰角膜结构和性质的新组合物的方法,包括但不限于角膜光学像差; 伤口闭合粘连和移植附着力; 以及用于产生包含至少一个具有可控处理参数的光子源的新组合物的照相玻璃化系统。 可以向角膜玻璃化系统添加反向模板,以增加玻璃化和结构和性质的修改。
    • 5. 发明授权
    • Electronically induced multiphoton absorption
    • 电子诱导多光子吸收
    • US4350577A
    • 1982-09-21
    • US93659
    • 1979-11-13
    • Donald F. Heller
    • Donald F. Heller
    • B01D59/34B01D59/00
    • B01D59/34
    • Electronic excitation of polyatomic molecules followed by nonradiative decay provides states from which efficient multiphoton infrared excitation can be achieved. Initial (electronic) excitation can be molecule-specific or isotope-selective. Subsequent multiphoton excitation has a threshold which can be an order of magnitude or more lower than for multiphoton excitation from the ground state. By this method, laser-induced chemical reactions or isotope separation can be achieved with lower infrared laser fluence and/or higher concentration of polyatomic molecules than with prior art methods.
    • 多原子分子的电子激发随后是非辐射衰减,提供可以实现有效的多光子红外激发的状态。 初始(电子)激发可以是分子特异性或同位素选择性的。 随后的多光子激发具有的阈值可以比来自基态的多光子激发低一个数量级或更多。 通过这种方法,与现有技术方法相比,激光诱导的化学反应或同位素分离可以用较低的红外激光注量和/或更高浓度的多原子分子来实现。
    • 6. 发明授权
    • Corneal vitrification, methods and devices to produce corneal vitrification and methods of use thereof
    • 角膜玻璃化,产生角膜玻璃化的方法和装置及其使用方法
    • US09545339B2
    • 2017-01-17
    • US14512952
    • 2014-10-13
    • Olivia SerdarevicMichael BerryDonald F. Heller
    • Olivia SerdarevicMichael BerryDonald F. Heller
    • A61F9/008A61F9/007A61N7/00
    • A61F9/008A61F2/142A61F9/0079A61F9/00814A61F2009/00872A61N7/00A61N2007/0004
    • The invention includes: a new composition of matter (a composite comprising a naturally occurring in vivo cornea in an in situ eye together with at least one volume of vitrified non-naturally occurring corneal stromal tissue formed within the naturally occurring corneal stromal tissue) wherein the vitrified tissue is modified in structure and properties from its naturally occurring condition into a non-naturally occurring glass-like condition with modifications including but not limited to increased eletastic modulus; methods for producing and using the new composition of matter for modifying cortical structure and properties, including but not limited to corneal optical aberrations; wound closure adhesion and transplant adhesion; and a photovitrification system for producing the new composition of matter comprising at least one photon source with controllable treatment parameters. A reverse template can be added to corneal vitrification systems to increase vitrification and modifications of structure and properties.
    • 本发明包括:一种新的物质组合物(包括在原位眼中的天然存在的体内角膜以及在天然存在的角膜基质组织内形成的至少一个玻璃化非天然存在的角膜基质组织体积的复合物),其中 玻璃化组织在结构和性质上从其天然存在的状态改变成非天然存在的玻璃样状态,其中包括但不限于增加的电化学模量; 用于生产和使用新的组合物用于改变皮层结构和性质的方法,包括但不限于角膜光学像差; 伤口闭合粘连和移植附着力; 以及用于产生包含至少一个具有可控处理参数的光子源的新组合物的光生产系统。 可以向角膜玻璃化系统添加反向模板,以增加玻璃化和结构和性质的修改。
    • 10. 发明申请
    • SYSTEMS AND DEVICES FOR SHAPING HUMAN CORNEA AND METHODS OF USE THEREOF
    • 用于形成人造脊椎的系统和装置及其使用方法
    • US20140276678A1
    • 2014-09-18
    • US14215772
    • 2014-03-17
    • Michael BerryOlivia SerdarevicDonald F. Heller
    • Michael BerryOlivia SerdarevicDonald F. Heller
    • A61F9/008
    • A61F9/009A61F2009/00872
    • In some embodiments, the instant invention provides for a system for shaping a human cornea of an eye that includes at least the following components: a sapphire applanation window/suction ring (SAWSR) system, where the SAWSR system includes a sapphire applanation window/suction ring (SAWSR), a conical holder, an illuminator, and a temperature control, where the SAWSR system is configured to: (i) be positioned on the eye, (ii) applanate the human cornea of the eye, (iii) generate and position a centration aid, and (iv) maintain temperature control; an optical delivery system, where the optical delivery system includes: (i) a laser, (ii) a fiber delivery holder, and (iii) a laser control subsystem, where the laser control subsystem is configured to display a user interface to: 1) control a power and a temporal waveform of each of the beamlets of light, and 2) irradiate the human cornea of the eye.
    • 在一些实施例中,本发明提供了一种用于整形眼睛的人类角膜的系统,该系统至少包括以下部件:蓝宝石压平窗/吸力环(SAWSR)系统,其中SAWSR系统包括蓝宝石压平窗/抽吸 (SAWSR),锥形保持器,照明器和温度控制器,其中SAWSR系统被配置为:(i)定位在眼睛上,(ii)压制眼睛的人类角膜,(iii)产生和 定位助剂,(iv)保持温度控制; 光学传送系统,其中所述光学传送系统包括:(i)激光器,(ii)光纤传送保持器,以及(iii)激光控制子系统,其中所述激光控制子系统被配置为显示用户界面以:1 )控制每个子束光的功率和时间波形,以及2)照射眼睛的人角膜。