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1.
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: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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