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Degradable sheath interface screw assembly and manufacturing process thereof

A technology of interface screw and manufacturing process, applied in fastening devices, medical science, internal bone synthesis, etc., can solve the problems of product residue, secondary injury, etc., to prevent tendon cutting, prevent screw breakage, and eliminate product residue hazards. Effect

Active Publication Date: 2022-01-11
花沐医疗科技(上海)有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The technical problem to be solved by the present invention is to solve the problem of product residue or secondary damage caused by the existing titanium alloy interface screw and PEEK interface screw that need to be implanted in the human body for a long time or taken out by a second operation, and provide a degradable tape The sheath interface screw assembly and its manufacturing process can be absorbed by the human body, eliminating the hazards of product residues, eliminating the need for secondary surgery to remove, and avoiding secondary injuries; in addition, through the structural design of the interface nail body, it can Prevents screw breakage and prevents tendon cuts during the procedure

Method used

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  • Degradable sheath interface screw assembly and manufacturing process thereof
  • Degradable sheath interface screw assembly and manufacturing process thereof
  • Degradable sheath interface screw assembly and manufacturing process thereof

Examples

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Effect test

Embodiment 1

[0031] Example 1: Take 60 parts of L-polylactic acid, 30 parts of hydroxyapatite, and 10 parts of β-tricalcium phosphate, put millimeter-sized polylactic acid into a freezing grinder, and freeze and grind it until it is ground into micron-sized small particles. Lactic acid, the freezing temperature is -196±10°C liquid nitrogen, the cooling time is 5-100min, the grinding time is 10min-120min, and then put into a vacuum dryer for high-temperature drying. The vacuum drying temperature is 40°C-80°C. The time is 0.5 to 8 hours; the hydroxyapatite and the β-tricalcium phosphate are dried separately, and then the two are put into a mechanical mixer according to the weight ratio, and stirred until they are evenly mixed; the dried polylactic acid powder is Said parts by weight are put into a mechanical mixer, and stirred again until evenly mixed to obtain mixed raw material powder. The mixed raw material powder obtained by mixing is put into a tablet press, and the mixed raw material p...

Embodiment 2

[0032]Example 2: Take 65 parts of L-polylactic acid, 30 parts of hydroxyapatite, and 5 parts of β-tricalcium phosphate, put millimeter-sized polylactic acid into a freeze grinder, and freeze and grind it until it is ground into micron-sized small particles of polylactic acid. Lactic acid, the freezing temperature is -196±10°C liquid nitrogen, the cooling time is 5-100min, the grinding time is 10min-120min, and then put into a vacuum dryer for high-temperature drying. The vacuum drying temperature is 40°C-80°C. The time is 0.5 to 8 hours; the hydroxyapatite and the β-tricalcium phosphate are dried separately, and then the two are put into a mechanical mixer according to the weight ratio, and stirred until they are evenly mixed; the dried polylactic acid powder is Said parts by weight are put into a mechanical mixer, and stirred again until evenly mixed to obtain mixed raw material powder. The mixed raw material powder obtained by mixing is put into a tablet press, and the mixed...

Embodiment 3

[0033] Embodiment 3: Take 70 parts of L-polylactic acid, 25 parts of hydroxyapatite, and 5 parts of β-tricalcium phosphate, put millimeter-sized polylactic acid into a freezing grinder, and freeze and grind it until it is ground into micron-sized small particles of polylactic acid. Lactic acid, the freezing temperature is -196±10°C liquid nitrogen, the cooling time is 5-100min, the grinding time is 10min-120min, and then put into a vacuum dryer for high-temperature drying. The vacuum drying temperature is 40°C-80°C. The time is 0.5 to 8 hours; the hydroxyapatite and the β-tricalcium phosphate are dried separately, and then the two are put into a mechanical mixer according to the weight ratio, and stirred until they are evenly mixed; the dried polylactic acid powder is Said parts by weight are put into a mechanical mixer, and stirred again until evenly mixed to obtain mixed raw material powder. The mixed raw material powder obtained by mixing is put into a tablet press, and the...

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Abstract

The invention relates to a degradable sheath interface screw assembly and a manufacturing process thereof. In the manufacturing process, the raw materials of the interface screw and the matched screw sheath are polylactic acid, hydroxyapatite and beta-tricalcium phosphate. The invention further relates to a specific manufacturing method of the degradable sheath interface screw assembly, and a screw body and a matched screw sheath structure of the degradable sheath interface screw assembly. According to the degradable sheath interface screw assembly and the manufacturing process thereof, the problem of product residue or secondary injury to a patient due to the fact that an existing titanium alloy interface screw and an existing PEEK interface screw needs to be implanted into a human body for a long time or taken out through secondary operation is solved, the degradable sheath interface screw assembly can be absorbed by the human body, product residue harm is eliminated, secondary-operation taking out is not needed, and secondary damage is also avoided; and the main body and the screw sheath of the interface screw body are designed to form an expansion pressing structure combination, so that the interface screw body has the effects of preventing the screw from being broken and preventing the tendon from being cut in the implantation process.

Description

technical field [0001] The invention relates to the field of medical consumables, in particular to a degradable sheathed interface screw assembly and a manufacturing process thereof. Background technique [0002] The interface screw is a medical consumable for the treatment of anterior and posterior cruciate ligament injuries, and is used by doctors to reconstruct the cruciate ligament under arthroscopy. Specifically, the doctor takes the patient's own tendon for braiding, drills the bone tunnels for fixing the ligaments in the tibia and femur of the knee joint, and then uses interface screws to squeeze the ligaments on the inner wall of the bone tunnels. After the repair of the human body's own tissues, the ligaments finally grow in On the bone tract, the patient's cruciate ligament regained its function. [0003] At present, the interface screws used in China are mainly imported, and the existing domestic interface screws on the market are also mainly made of titanium all...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L31/02A61L31/06A61L31/14A61B17/86B29C45/00B29B9/08
CPCA61L31/028A61L31/06A61L31/148A61L31/14A61B17/8625A61B17/866A61B17/8685B29C45/0001B29B9/08B29K2071/00C08L67/04Y02W90/10
Inventor 韩加双董超杰罗宇星胡叶枫
Owner 花沐医疗科技(上海)有限公司