A drug-coated balloon and its preparation method and application
A drug coating and balloon technology, which is applied in the field of biomedicine, can solve the problems of single drug loading, no coating technology, inability to achieve anticoagulation and antiproliferative endothelial growth at the same time, and achieve broad application prospects, Improves blood flushing and prolongs residence time
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Embodiment 1
[0031] A method for preparing a drug-coated balloon, comprising the steps of:
[0032] 1) Preparation of mesoporous-macroporous micro-nano tubular motors
[0033] Such as figure 1 Shown: take 10g tetraethyl orthosilicate and 74.8μL concentrated H 2 SO 4 Dissolved in 5.5g H 2 The first solution was obtained in O and 9 g ethanol; 2.83 g P123 was dissolved in 27 g ethanol and 5.55 g H 2 0 obtains the second solution; the first solution and the second solution are mixed uniformly and suction filtered into the polycarbonate template; the polycarbonate template after the suction filtration is soaked in the above-mentioned solution subsequently, keeps 8 days; The magnesium powder solution of 50nm-10μm is suction filtered to the polycarbonate template, dissolves the polycarbonate template, and releases to obtain the mesoporous-macroporous micro-nano tubular motor; the transmission electron microscope image of the mesoporous-macroporous micro-nano tubular motor is as figure 2 As ...
Embodiment 2
[0038] A method for preparing a drug-coated balloon, comprising the steps of:
[0039] 1) Preparation of mesoporous-macroporous micro-nano spherical motors
[0040] Take 1×1cm -2The size of the polymer film, the magnesium powder is evenly dispersed on the surface of the polymer film and placed in 10ml50mg·ml -1 In the dopamine Tris-HCl buffer solution, let it stand for 24 hours in the dark. After the reaction, wash and dry to obtain polydopamine-magnesium powder-polymer film; disperse 0.15ml hydrazine hydrate and 9.6μl tetraethyl orthosilicate in 30ml of water and stirred for 10 minutes to obtain a dispersion, polydopamine-magnesium powder-polymer film was placed in the dispersion and allowed to stand at 37°C for 5 hours; 2.4ml of 25% cetyltrimethyl Ammonium bromide, 0.18g triethylamine, 1.6ml cyclohexane, and 0.4ml tetraethylorthosilicate were mixed and stirred for 10 minutes, and left to stand at 37°C for 5 hours; the polymer film was removed with an organic solvent to rel...
Embodiment 3
[0045] Step 1) and step 2) are the same as step 1) and step 2) in Example 2 to prepare a mesoporous-macroporous micro-nano spherical motor loaded with growth factors, anti-tissue hyperplasia drugs and anticoagulant drugs. The mesoporous-macroporous micro-nano spherical motors of factors, anti-tissue hyperplasia drugs and anticoagulant drugs were evenly spin-coated on the bare balloon, then dried, and the balloon was taken out and washed three times with water and ethanol respectively to obtain the mesoporous-macroporous micro-nano spherical motor. Nanospherical motor drug-coated balloons, such as Figure 7 Shown: A is a bare balloon, B is a mesoporous-macroporous micro-nano spherical motor drug-coated balloon, and the surface of the mesoporous-macroporous micro-nano spherical motor drug-coated balloon is evenly coated with a layer of growth Mesoporous-macroporous micro-nano spherical motors for anti-proliferative and anticoagulant drugs.
[0046] The thickness of the drug coa...
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