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公开(公告)号:US20240245838A1
公开(公告)日:2024-07-25
申请号:US18424827
申请日:2024-01-28
Applicant: SINO MEDICAL SCIENCES TECHNOLOGY INC.
Inventor: Jianhua SUN , Christophe BUREAU , Wenbin CAI , Tianzhu LI , Xiaoran KANG
IPC: A61L31/16 , A61F2/82 , A61K31/337 , A61K31/436 , A61L31/10 , A61L33/18 , B05D1/00 , B05D1/02 , B05D3/04
CPC classification number: A61L31/16 , A61F2/82 , A61K31/337 , A61K31/436 , A61L31/10 , A61L33/18 , B05D1/002 , B05D1/02 , B05D3/0486 , A61L2300/256 , A61L2300/258 , A61L2300/412 , A61L2300/416 , A61L2300/604 , A61L2420/08
Abstract: Drug eluting stents, methods of making, using, and verifying long-term stability of the drug eluting stents, and methods for predicting long term stent efficacy and patient safety after implantation of a drug eluting stent are disclosured. In one embodiment, a drug eluting stent may include a stent framework; a drug-containing layer; a drug embedded in the drug-containing layer; and a biocompatible base layer disposed over the stent framework and supporting the drug-containing layer. The drug-containing layer may have an uneven coating thickness. In addition or in alternative, the drug-containing layer may be configured to significantly dissolve/dissipate, disappear between 45 days and 60 days after stent implantation. Stents may reduce, minimize, or eliminate patient risks associated with the implantation of a stent, including, for example, restenosis, thrombosis, and or MACE.
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2.
公开(公告)号:US20180042738A1
公开(公告)日:2018-02-15
申请号:US15797862
申请日:2017-10-30
Applicant: SINO MEDICAL SCIENCES TECHNOLOGY INC.
Inventor: Jianhua SUN , Christophe BUREAU , Wenbin CAI , Tianzhu LI , Xiaoran KANG
CPC classification number: A61F2/82 , A61F2250/0067 , A61L31/022 , A61L31/06 , A61L31/10 , A61L31/148 , A61L31/16 , A61L2300/416 , A61L2300/608 , A61L2420/02 , A61L2420/06 , C08L67/04
Abstract: The present disclosure relates to drug eluting stents, methods of making, using, and verifying long-term stability of the drug eluting stents, and methods for predicting long term stent efficacy and patient safety after implantation of a drug eluting stent. In one embodiment, a drug eluting stent may include a stent framework; a drug-containing layer; a drug embedded in the drug-containing layer; and a biocompatible base layer disposed over the stent framework and supporting the drug-containing layer. The drug-containing layer may have an uneven coating thickness. In addition or in alternative, the drug-containing layer may be configured to significantly dissolve/dissipate/disappear between 45 days and 60 days after stent implantation. Stents of the present disclosure may reduce, minimize, or eliminate patient risks associated with the implantation of a stent, including, for example, restenosis, thrombosis, and/or MACE.
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公开(公告)号:US20200030083A1
公开(公告)日:2020-01-30
申请号:US16337555
申请日:2017-12-04
Applicant: SINO MEDICAL SCIENCES TECHNOLOGY INC.
Inventor: Tianzhu LI , Jianxiang MA , Lei MENG
IPC: A61F2/24
Abstract: Medical devices and methods for endovascularly or transcatheterly replacing a patient's heart valve, including: a delivery system (9) having an entry profile of 30 Fr or less; a self-expandable annulus ring (10) disposed in the delivery system (9) including a self-expandable anchoring and clipping structure and multiple bridges (4) connected to the anchoring and clipping structure; and a replacement heart valve (11) disposed in the delivery system (9) and connected to the bridges (4). The bridges (4) are formed of a shape memory material; during deployment, the bridges (4) fold upwardly inside the self-expandable anchoring and clipping structure to lift the replacement heart valve (11) into position.
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公开(公告)号:US20210361449A1
公开(公告)日:2021-11-25
申请号:US17322829
申请日:2021-05-17
Applicant: SINO MEDICAL SCIENCES TECHNOLOGY INC.
Inventor: Jianhua SUN , Christophe BUREAU , Wenbin CAI , Tianzhu LI , Xiaoran KANG
Abstract: The present disclosure relates to drug eluting stents, methods of making, using, and verifying long-term stability of the drug eluting stents, and methods for predicting long term stent efficacy and patient safety after implantation of a drug eluting stent. In one embodiment, a drug eluting stent may include a stent framework; a drug-containing layer; a drug embedded in the drug-containing layer; and a biocompatible base layer disposed over the stent framework and supporting the drug-containing layer. The drug-containing layer may have an uneven coating thickness. In addition or in alternative, the drug-containing layer may be configured to significantly dissolve/dissipateldisappear between 45 days and 60 days after stent implantation. Stents of the present disclosure may reduce, minimize, or eliminate patient risks associated with the implantation of a stent, including, for example, restenosis, thrombosis, and/or MACE.
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公开(公告)号:US20210361418A1
公开(公告)日:2021-11-25
申请号:US17049636
申请日:2018-12-06
Applicant: SINO MEDICAL SCIENCES TECHNOLOGY INC.
Inventor: Zhonghua LI , Tianzhu LI , Jianxiang MA , Jinhong ZHAO , Lei MENG
Abstract: The present invention provides a transapical implantable mitral valve device, which includes an outer valve stent comprising an outer valve stent body that is composed of a plurality of first structure units arranged in the circumferential direction and an anchoring unit that is disposed on the outer valve stent body for anchoring the mitral valve device in a human body, at least one of an inner surface and an outer surface of the outer valve stent body being covered with an outer skirt; an inner valve stent disposed inside the outer valve stent and interconnected with the outer valve stent, a cavity being formed between the outer valve stent and the inner valve stent; and a valve leaflet structure disposed in the inner valve stent to form a prosthetic valve.
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