Method for preparing cardiovascular drug eluting stent
A drug coating and cardiovascular technology, which is applied in the direction of drug devices, cardiovascular system diseases, pharmaceutical formulations, etc., can solve the problem that the coating is easy to fall off, so that it is not easy to fall off, improves the infiltration and spreadability, improves the uniformity and The effect of binding firmness
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Embodiment 1
[0027] Take a 316L stainless steel bracket, clean it ultrasonically with acetone and isopropanol, and dry it. Place the cleaned stent in the plasma chamber and use N 2 to process. The processing conditions are: background vacuum 5.0×10 -3 Pa, RF voltage 200v, bias voltage 100v, gas flow rate 0.30mL / min, processing time 20min. After the above-mentioned treated stent was taken out, it was quickly immersed in a solution containing 0.01 g of paclitaxel, 0.19 g of ethylene-vinyl acetate, and 7.8 g of toluene for 100 seconds, taken out, and dried in vacuum at 60° C. for 20 hours. It can be seen under the SEM microscope that the prepared drug coating thickness is smooth and flat, such as figure 1 .
Embodiment 2
[0029] Take a 316L stainless steel bracket, clean it ultrasonically with acetone and isopropanol, and dry it. The cleaned stent is placed in the plasma cavity, and treated with argon and nitrogen mixed gas plasma. The processing conditions are: background vacuum 5.0×10 -3 Pa, RF voltage 250v, bias voltage 300v, nitrogen: argon = 1:1, gas flow rate 0.40mL / min, processing time 10min. After the above stent was taken out, it was quickly immersed in a solution containing 0.008 g of paclitaxel, 0.16 g of ethylene-vinyl acetate, and 7.832 g of toluene for 30 seconds, taken out, and dried under vacuum at 60° C. for 20 hours. It can be seen under the SEM microscope that the prepared drug coating has a smooth and flat surface, and its appearance is similar to the stent prepared in Example 1.
Embodiment 3
[0031] Take a 316L stainless steel bracket, clean it ultrasonically with acetone and isopropanol, and dry it. Place the cleaned stent in the plasma cavity, and treat it sequentially with argon and nitrogen plasma. Argon gas treatment conditions are: background vacuum 5.0×10 -3 Pa, RF voltage 100v, bias voltage 200v, gas flow rate 0.10mL / min, processing time 5min. The nitrogen treatment process is: back vacuum 5.0×10 -3Pa, RF voltage 340v, bias voltage 200v, gas flow rate 0.30mL / min, processing time 2min. After the above-mentioned stent was taken out, it was quickly immersed in a solution containing 0.016 g of paclitaxel, 0.24 g of propylene-vinyl acetate, and 7.744 g of toluene for 30 seconds, taken out, and dried under vacuum at 60° C. for 20 hours. It can be seen under the SEM microscope that the prepared drug coating has a smooth and flat surface, and its appearance is similar to the stent prepared in Example 1.
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