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Compound medicament intravascular stent and preparation method thereof

A vascular stent and drug technology, applied in the field of medical devices, can solve the problems of ignoring the specific inhibition of smooth muscle cells and delaying the repair of vascular endothelium, so as to inhibit proliferation and migration, avoid the risk of delayed thrombosis, and increase biocompatibility. Effect

Active Publication Date: 2008-12-24
LEPU MEDICAL TECH (BEIJING) CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The wide application of drug-eluting stents has greatly reduced the occurrence of in-stent restenosis. Although drug-eluting stents can effectively inhibit the proliferation of smooth muscle cells and reduce and prevent intimal hyperplasia, they delay the repair of vascular endothelium; CD34 antibody-engineered stents Although endothelial progenitor cells can be captured in blood vessels based on the antigen-antibody binding theory and rapidly endothelialized on the surface of vascular stents, the specific inhibition of smooth muscle cells is ignored

Method used

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  • Compound medicament intravascular stent and preparation method thereof
  • Compound medicament intravascular stent and preparation method thereof

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preparation example Construction

[0044] A method for preparing a composite drug vascular stent, firstly prepare a large number of holes 101 on the stent body 1 through chemical or physical methods such as corrosion, anodic oxidation, micro-arc oxidation, micro-arc nitriding, etc., or a combination of these methods, or in the stent A layer of coating with holes 101 is formed on the surface, and the stent body is made of medical materials with good biocompatibility. Metal materials such as stainless steel, cobalt-based alloys, titanium alloys, nickel-titanium alloys, and polylactic acid biomaterials can also be used. polymer material; then use a special process to protect the inner surface of the stent, reserve the holes on the inner surface of the stent to fix the antibody that specifically captures endothelial progenitor cells, and at the same time embed, fix and coat a therapeutically effective amount on the outer surface of the stent body 1 One or more anti-smooth muscle cell proliferation drugs 202, the ant...

Embodiment 1

[0060] In this embodiment, the drug 201 for specifically capturing EPC antibodies is fixed on the inner surface of the stent body 1 with holes 101, and the rapamycin anti-smooth muscle cell proliferation drug 202 is directly dissolved in an organic solvent and sprayed directly on the outer surface of the stent body 1. Its process steps:

[0061] ①Pretreatment of the surface of the stent body, ②Preparation of holes, ③Post-treatment process steps of the surface of the stent body are the same as described above;

[0062] ④ Drug preparation: add 0.2g rapamycin to 10ml tetrahydrofuran solution;

[0063] ⑤ Coating on the outer surface: protect the inner surface of the stent body 1 with holes with a balloon, and disperse the above-mentioned prepared drug evenly at room temperature, then spray on the outer surface of the stent body 1, and cure in the air for 60 minutes; repeat ⑤ on the outer surface Coating step until the drug loading reaches 1.4-2.2 μg / mm 2 ; Place the bracket body...

Embodiment 2

[0068] In this embodiment, the drug 201 that specifically captures endothelial progenitor cell antibodies is fixed on the inner surface of the stent body 1 with holes 101, and the anti-smooth muscle cell proliferation drug 202 is coated on the outer surface with the help of biodegradable polymer materials. Spray coating in an organic solvent containing polylactic acid (PLA), the process steps:

[0069] ①Pretreatment of the surface of the stent body, ②Preparation of holes, ③Post-treatment process steps of the surface of the stent body are the same as described above;

[0070] ④ Drug preparation: add 0.1g polylactic acid (PLA) to 10ml tetrahydrofuran solution, then add 0.5g rapamycin to prepare polylactic acid tetrahydrofuran solution containing rapamycin;

[0071] ⑤ Coating on the outer surface: protect the inner surface of the stent body 1 with holes by using a balloon, mix and disperse the above-mentioned drug prepared evenly at room temperature, and then evenly coat the poly...

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Abstract

The invention relates to a composite drug stent and a preparation method thereof. The stent includes a stent body and active drugs; wherein, the stent body is a perforated medical material with good biocompatibility, which can be made by optionally using stainless steel, cobalt-based alloy, titanium alloy, nickel-titanium alloy, or polylactic acid bio-polymer material; the active drugs include special endothelial progenitor cell antibody drug and anti-smooth muscle cell proliferation drug. The internal surface of the perforated stent body is fixedly provided with the special endothelial cell antibody drug, while the external surface of the perforated stent body is coated with the anti-smooth muscle cell proliferation drug. The preparation method includes as follows: (1) pretreating the surface of the stent body; (2) making holes; (3) post-treating the surface of the stent body; (4) dispensing medicines; (5) coating the external surface; (6) fixing the internal surface; (7) drying at low temperature. The preparation method can selectively absorb endothelial progenitor cells and facilitate in repairing endodermis, and can effectively inhibit the proliferation and migration of vascular smooth muscle cells, persistently and effectively reduce the newborn endangium, effectively prevent the stent from narrowing, and avoid the risk of tardive thrombosis.

Description

technical field [0001] The invention belongs to the field of medical devices, and relates to a novel composite medicine vascular stent and a preparation method thereof. Background technique [0002] Since 1987, when Sigwart et al first applied intravascular metal stents to coronary arteries, it has provided a good way to treat vascular occlusive diseases. The main reason for the efficacy of treatment (PCI). The main mechanism of in-stent restenosis is the hyperplasia of vascular intima and the delay of vascular endothelialization. Therefore, the prevention and treatment of in-stent restenosis is mainly to promote the rapid repair of vascular endothelium and inhibit the excessive proliferation of smooth muscle cells. [0003] The wide application of drug-eluting stents has greatly reduced the occurrence of in-stent restenosis. Although drug-eluting stents can effectively inhibit the proliferation of smooth muscle cells and reduce and prevent intimal hyperplasia, they delay t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L31/02A61L31/16A61F2/82
Inventor 余占江蒲忠杰
Owner LEPU MEDICAL TECH (BEIJING) CO LTD
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