Hydroxylapatite ceramic spinal fusion device

A technology of hydroxyapatite and cages, applied in the direction of spinal implants, fixators, internal fixators, etc., can solve problems such as cage loosening or slippage, stress shielding, implant site collapse, etc., and meet mechanical requirements , Improve fracture toughness and enhance mechanical strength

Inactive Publication Date: 2009-01-21
崔福斋
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the elastic modulus of metal spinal fusion is much higher than that of cortical bone, which will cause stress shielding in the body, resulting in complications such as osteoporosis, bone atrophy, collapse of the implantation site, loosening or slippage of the fusion cage, etc.
Moreover, the debris produced by the metal fusion device causes the body to produce macrophages, interleukin-1, interleukin-6, prostaglandin E2, tumor necrosis factor, etc., affecting bone fusion
In addition, metal materials cannot pass through X-rays, which affects the observation of bone fusion sites after surgery
[0004] Spinal fusion cages made of synthetic non-metallic and non-degradable materials (such as polyetheretherketone, PEEK), although the elastic modulus matches the vertebral bone, have good corrosion resistance, and can transmit X-rays, but As it cannot be degraded in the body, it will eventually require a second surgery to remove it
The second operation not only causes high cost, but also causes secondary harm to the patient's physiology and causes great psychological pressure
However, conventional hydroxyapatite ceramics are brittle materials, in which the hydroxyapatite grains are relatively large (generally greater than 2 microns), and its compressive strength is low (less than 0.5GPa), which can only be used for artificial joint coatings. Application of biomaterials in non-load-bearing conditions such as bone

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0017] Hydroxyapatite ceramic spinal fusion device, the material used in the spinal fusion device is a hydroxyapatite ceramic material with a grain size of less than 100 nanometers, in which ZrO 2 The content is less than 0.5% (mass ratio), and the fracture toughness can reach 1.57MPam 1 / 2 .

[0018] The spinal fusion cage is cube-shaped, with a width of 13mm, a depth of 13mm, a height of 6mm, and a wall thickness of 2.5mm. The upper and lower surfaces have anatomical structures, and the height of the occlusal teeth on it is 0.5mm.

[0019] Suitable for patients with L5 / S1 intervertebral disc herniation.

Embodiment 2

[0021] The structure is the same as in Example 1, but the cage has an inclination of 5 degrees higher at the front and lower at the rear. The width is 23mm, the depth is 13mm, the height is 13mm, and the wall thickness is 2.5mm.

[0022] The material of the hydroxyapatite ceramic spinal fusion cage is a hydroxyapatite ceramic material with a grain size less than 100 nanometers.

[0023] Suitable for patients with L4 / L5 intervertebral disc herniation.

Embodiment 3

[0025] The structural size of the spinal fusion device is the same as in Example 1.

[0026] The material used in the spinal fusion cage is hydroxyapatite ceramic material with a grain size of less than 190nm, which is prepared by two-stage sintering method, and the fracture toughness is 1.92MPam 1 / 2 .

[0027] Suitable for patients with L5 / S1 intervertebral disc herniation.

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Abstract

The invention discloses a hydroxyapatite ceramics spinal fusion cage, and the material of the spinal fusion cage is the hydroxyapatite ceramics material, the grain size of which is less than 300 nanometers. The hydroxyapatite ceramics spinal fusion cage of the invention can enhance the mechanical strength and especially improve fracture ductility, thus overcoming the brittleness of ordinary hydroxyapatite ceramics and satisfying the dynamical requirement of the spinal fusion cage. Furthermore, the hydroxyapatite ceramics spinal fusion cage can keep the bioactivity of the hydroxyapatite and achieve synosteosis with bones in the human body.

Description

technical field [0001] The invention belongs to the field of biomedical materials. It particularly relates to a hydroxyapatite ceramic spinal fusion device. Background technique [0002] Spinal fusion is an effective means of treating spinal diseases such as spinal tuberculosis, infection, deformity, degenerative disease and intervertebral disc injury. The intervertebral fusion device can stretch the intervertebral space, make the anterior longitudinal ligament in a state of tension, restore the intervertebral height, and realize the stability of the intervertebral fusion device and promote the intervertebral fusion through the contraction of the lumbar muscles and the compression of the intervertebral fusion device by its own body weight. Bone fusion between bodies. Spinal fusion surgery was first proposed by Hibbs in 1911, and after Mercer proposed the theory of intervertebral fusion in 1936, spinal fusion achieved rapid development and has now become an important means ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L31/02A61B17/70
CPCA61F2/4455A61F2310/00215A61L31/026A61F2310/00293A61F2310/00239A61F2310/00161A61F2/30965
Inventor 崔福斋
Owner 崔福斋
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