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Materials, devices and methods for implantation of transformable implants

An implant and implantable technology, applied in spinal implants, medical science, surgery, etc., can solve the difficulty of surgical installation of implants, the difficulty of flexible implants, and the inability of flexible devices to damage areas or areas of the body. structure to provide adequate support, etc.

Inactive Publication Date: 2007-12-05
WARSAW ORTHOPEDIC INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0017] However, flexible implants such as spinal fixation devices and intervertebral discs also have some disadvantages
Flexible implants are more easily deformed or deflected by surrounding tissue during implantation, making surgical installation of the implant more difficult
Especially when using minimally invasive surgical techniques such as laparoscopy, flexible implants are difficult to install because flexible materials cannot easily pass through laparoscopic probes and other similar devices
Additionally, flexible devices do not provide adequate support to damaged areas or structures of the body, especially during the initial healing of the area or structure

Method used

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  • Materials, devices and methods for implantation of transformable implants
  • Materials, devices and methods for implantation of transformable implants
  • Materials, devices and methods for implantation of transformable implants

Examples

Experimental program
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Embodiment 1

[0080] A hollow rod consisting of high modulus polyethylene fibers (SPECTRA(R) fibers, commercially available from Honeywell International, Inc., Colonial Heights, VA) was cut in half, and one half was elongated and inserted into the other half to form a two-layer composite rod . The polyethylene fiber composite rod constitutes the primary phase or material and the gelatin constitutes the secondary phase or material. Composite deformable rods are initially relatively flexible. Fill the composite rod with gelatin until full, tie the ends of the hollow rod, wipe off excess gelatin, and allow the clear glue-soaked composite rod to dry under ambient conditions. After drying, the rod hardens. The rigid composite rods were then rehydrated in 37°C water and the rods eventually became flexible. The composite rod remained rigid for a few minutes after rehydration, but slowly became more flexible over a period of about 1 hour over time. The composite rod can be used as a stabilizing...

Embodiment 2

[0082] A gelatin solution was cast into a polyethylene fiber braid to create a deformable front tension band. The polyethylene fiber braid constitutes the primary phase or material and the gelatin solution constitutes the secondary phase or material. The deformable strip is initially relatively flexible. Excess gelatin is removed from the surface of the tape, and the tape is substantially dehydrated by heating or otherwise in a vacuum oven. Once substantially dehydrated, the deformable tape becomes relatively rigid because the movement of the polyethylene fibers is restricted by the dry gelatin particles embedded in the fibres. During insertion into the body, the gelatin absorbs body fluids, thereby lubricating the outer surface of the deformable band and facilitating insertion. Next, the deformable band will be attached to the vertebrae by anchoring means such as shackles or screws. By tensioning the vertebrae, the stress shielding effect is avoided because the vertebrae a...

Embodiment 3

[0084] A gelatin solution was cast into a polyethylene fiber braided tether to create a deformable disc implant. The polyethylene fiber braid constitutes the primary phase or material and the gelatin solution constitutes the secondary phase or material. Excess gelatin is removed from the surface of the tether, and the tether is substantially dehydrated by heating or otherwise in a vacuum oven. Once substantially dehydrated, the deformable tethers become relatively rigid because the movement of the polyethylene fibers is restricted by the xerogel particles embedded in the fibers. The tethers are cut into shorter segments and they are inserted into the disc or nuclear space by, for example, a cannula. The gelatin is rehydrated by body fluids in the disc or nuclear space, and the deformable segment returns to the relatively flexible state of the braided tether.

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Abstract

A transformable implantable device is disclosed comprising primary and secondary phases or materials. The secondary phase or material is relatively rigid compared to the primary phase or material and also renders the transformable implantable device relatively rigid compared to the primary phase or material. The secondary phase or material, upon implantation, becomes more flexible, thereby rendering the transformable implantable device more flexible also.

Description

field of invention [0001] The present invention relates generally to implantable devices, and more particularly to implantable devices that are initially rigid but become flexible after implantation. Background of the invention [0002] Implantable devices are used to correct a variety of medical conditions. For example, implants are often used to treat conditions in the spine. The spine is a biomechanical structure mainly composed of ligaments, muscles, vertebrae, and intervertebral discs. The biomechanical functions of the spine include (i) supporting the body; (ii) regulating motion between the head, trunk, arms, pelvis, and legs; and (iii) protecting the spinal cord and nerve roots. [0003] Injury to one or more spinal components, such as the intervertebral discs, can be the result of disease or trauma that can lead to instability of some or all of the spine. A common treatment for a damaged spine is spinal immobilization or fusion, in which some or all of the interv...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61B17/70A61F2/44
CPCA61F2002/30304A61B17/7059A61F2002/30677A61B17/8085A61B17/7031A61F2/442A61B17/701A61F2002/444A61F2210/0061A61F2230/0063A61F2002/30075A61B2017/00831
Inventor H·H·特里优M·C·舍曼
Owner WARSAW ORTHOPEDIC INC