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    • 6. 发明授权
    • Method for making a light energized tissue adhesive
    • 制造光通电组织粘合剂的方法
    • US06780840B1
    • 2004-08-24
    • US09973263
    • 2001-10-09
    • Dale P. DeVoreBraden P. DeVoreBarbara A. SoltzRobert SoltzMichael A. Soltz
    • Dale P. DeVoreBraden P. DeVoreBarbara A. SoltzRobert SoltzMichael A. Soltz
    • A61K3800
    • A61B18/22A61B17/00491A61B2017/0007A61B2017/00084A61B2017/005A61B2017/00508A61B2017/00517A61L24/102
    • Consistent with the present invention, tissue adhesive compositions and an associated laser exposure system are provided for bonding or sealing biological tissues. The compositions are comprised of chemically derivatized soluble collagen which is formulated to concentrations ranging from 300 mg/ml (30%) to 800 mg/ml (80%) collagen protein. In particular, Type I collagen, for example, is first prepared by extraction from bovine or porcine hide and purified. The collagen preparations are then chemically derivatized with sulfhydryl reagents to improve cohesive strength and with secondary derivatizing agents, such as carboxyl groups, to improve the adhesive strength of the solder to the tissue. The compositions are then formed into viscous solutions, gels or solid films, which when exposed to energy generated from an infrared laser, for example, undergo thermally induced phase transitions. Solid or semi-solid protein compositions become less viscous enabling the high concentration protein to penetrate the interstices of treated biological tissue or to fill voids in tissue. As thermal energy is released into the surrounding environment, the protein compositions again become solid or semi-solid, adhering to the treated tissue or tissue space.
    • 根据本发明,提供组织粘合剂组合物和相关联的激光曝光系统用于粘合或密封生物组织。 组合物由化学衍生的可溶性胶原组成,其被配制成浓度范围为300mg / ml(30%)至800mg / ml(80%))的胶原蛋白。 特别地,例如,首先通过从牛或猪皮提取而制备I型胶原并纯化。 然后将胶原蛋白制剂用巯基试剂进行化学衍生,以提高内聚强度,并与二级衍生剂(如羧基)一起提高焊料对组织的粘合强度。 然后将组合物形成粘稠溶液,凝胶或固体膜,当暴露于由红外激光产生的能量时,例如经历热诱导相变。 固体或半固体蛋白质组合物变得粘稠,使得高浓度蛋白质能够渗透经处理的生物组织的间隙或填充组织中的空隙。 随着热能释放到周围环境中,蛋白质组合物再次变得固体或半固体,粘附到处理过的组织或组织空间。
    • 8. 发明授权
    • Surgical instrument debris collection system
    • 手术器械碎片收集系统
    • US08734730B2
    • 2014-05-27
    • US11731409
    • 2007-03-30
    • Michael A. SoltzJoshua StopekWojciech KisielJennifer Broom
    • Michael A. SoltzJoshua StopekWojciech KisielJennifer Broom
    • A61L2/00A61L9/00B65D83/10A61B17/06A61B19/02A61L15/00
    • A61B90/70A61B17/3462
    • The presently disclosed debris collection system includes an elongate body having a first end, a second end, and a bore extending therethrough. The first end of the elongate body is hermetically closed while the second end has an opening. The elongated body is made of an impermeable material. A cap fixed to the elongated body and has a bore extending therethrough. A port, which is attached to the cap, is designed for introducing fluid into the elongated body. A watertight seal, such as a gasket, is attached to the cap. The seal is also made of an impermeable material. In operation, a liquid is introduced into the debris collection system. A surgical tool must then be introduced into the system. Thereafter, a vortex is created within the system to debride debris from the surgical tool.
    • 目前公开的碎片收集系统包括细长体,其具有第一端,第二端和延伸穿过其中的孔。 细长体的第一端密封,而第二端具有开口。 细长体由不渗透材料制成。 固定在细长主体上并具有延伸穿过其中的孔的盖。 连接到盖子上的端口被设计成将流体引入细长体中。 一个防水密封件,如一个垫圈,连接到盖子上。 密封也由不渗透材料制成。 在操作中,将液体引入碎片收集系统中。 然后必须将外科手术工具引入系统。 此后,在系统内产生涡流以清除手术工具中的碎屑。