Interventional medical device and manufacturing method thereof

Abstract

An interventional medical device and manufacturing method thereof. The interventional medical device comprises: a stent body ( 1 ); a surface of the stent body ( 1 ) being provided with a drug releasing structure ( 3 ), and drug in the drug releasing structure ( 3 ) being drug for suppressing proliferation of adventitial fibroblasts and a drug for suppressing proliferation of intimal and/or smooth muscle cells. In use, after interventional medical device is implanted into a human body, the drug for suppressing proliferation of adventitial fibroblasts carried thereon can promote the compensatory expansion of the vessel, and the drug for suppressing proliferation of intimal cells and/or smooth muscle cells carried thereon can suppress intimal proliferation of the vessel. The combination of the two kinds of drugs greatly reduces the occurrence rate of in-stent restenosis.

What is claimed is: 
     
         1 . An interventional medical device, comprising a stent body with a drug releasing structure on its surface, wherein the drugs in the drug releasing structure are drugs for suppressing proliferation of adventitial fibroblasts and for suppressing proliferation of intimal cells and/or smooth muscle cells. 
     
     
         2 . The interventional medical device according to  claim 1 , wherein said drug releasing structure is a dense mixed layer formed by a polymer and the drug for suppressing adventitial fibroblast proliferation and the drug for suppressing proliferation of intimal cells and/or smooth muscle cells. 
     
     
         3 . The interventional medical device according to  claim 2 , wherein said polymer includes polylactic acid, polyethylene glycol, styrene-butene copolymer, polycaprolactone, poly(butyl methacrylate), poly (ethyl methacrylate), polyvinyl ethyl acetate, polyurethane, polyvinyl pyrrolidone, polyphosphorylcholine, silk protein, gelatin, chitin and/or hyaluronic acid. 
     
     
         4 . The interventional medical device according to  claim 1 , wherein, said drug releasing structure is a microporous structure prepared on the surface of said stent body or a microporous coating structure formed on the surface of said stent body, and the drug is loaded into said microporous structure or microporous coating structure. 
     
     
         5 . The interventional medical device according to  claim 1 , wherein, said drug for suppressing adventitial fibroblast proliferation includes at least one drug selected from the group consisting of tanshinone, asiaticoside, madecassoside, ligustrazine, dracorhodin, Rosuvastatin, and angiotensin. 
     
     
         6 . The interventional medical device according to  claim 1 , wherein said drug for suppressing proliferation of intimal cells and/or smooth muscle cells includes at least one drug selected from the group consisting of rapamycin and derivative thereof and paclitaxel and derivative thereof. 
     
     
         7 . The interventional medical device according to  claim 1 , wherein, said stent body comprises coronary artery stent, intracranial vascular stent, peripheral vascular stent, intraoperative stent, heart valve stent, biliary tract stent, esophageal stent, intestinal tract stent, pancreatic duct stent, urethral stent or tracheal stent. 
     
     
         8 . A method for preparing an interventional medical device, wherein said method comprises:
 preparing a microporous structure on the surface of the stent body;   formulating a solution containing a drug for suppressing proliferation of adventitial fibroblasts and a drug for suppressing proliferation of intimal cells and/or smooth muscle cells;   loading the drugs within the formulated solution into said microporous structure;   drying the stent body to obtain said interventional medical device.   
     
     
         9 . The method according to  claim 8 , wherein, preparing a microporous structure on the surface of the stent body comprises forming micropores on the surface of the stent body by anodic oxidation, micro-arc oxidation and/or chemical corrosion. 
     
     
         10 . The method according to  claim 8 , wherein preparing a microporous structure on the surface of the stent body comprises preparing a coating having micropores on the surface of said stent body. 
     
     
         11 . The method according to  claim 8 , wherein loading the drugs within the formulated solution into said microporous structure comprises loading the drugs within said solution into said microporous structure by ultrasonic spraying, air spraying and/or dipping. 
     
     
         12 . A method for preparing an interventional medical device, wherein said method comprises:
 formulating a mixed solution of a drug for suppressing adventitial fibroblast proliferation and a polymer, as well as a mixed solution of a drug for suppressing proliferation of intimal cells and/or smooth muscle cells and a polymer, respectively, or formulating a mixed solution of a drug for suppressing adventitial fibroblast proliferation, a drug for suppressing proliferation of intimal cells and/or smooth muscle cells and a polymer;   successively coating the surface of the stent body with the mixed solution of the drug for suppressing adventitial fibroblast proliferation and the polymer, as well as the mixed solution of the drug for suppressing proliferation of intimal cells and/or smooth muscle cells and the polymer, or coating the surface of the stent body with the mixed solution of the drug for suppressing adventitial fibroblast proliferation, the drug for suppressing proliferation of intimal cells and/or smooth muscle cells and the polymer;   drying the stent body to obtain the interventional medical device.   
     
     
         13 . The method according to  claim 12 , wherein, said coating comprises ultrasonic spraying, air spraying and/or dipping.