Polymer bionic coating and preparation method thereof
A polymer and coating technology, applied in the medical field, can solve problems such as poor blood compatibility, no change in the design of the coating, and a single design of the drug coating, so as to inhibit the occurrence of inflammation and thrombus, high BCI index, The effect of excellent anticoagulant ability
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[0048] The present invention also provides a kind of preparation method of polymer biomimetic coating, comprises the following steps:
[0049] A) Using electrospinning technology or electrostatic spraying technology, the inner layer mixed solution is evenly attached to the surface of the substrate, and the inner layer is obtained after vacuum drying; the inner layer mixed solution includes biocompatible polymers, anti-inflammatory drugs and the first a solvent;
[0050] B) Using electrospinning technology or electrostatic spraying technology, the outer layer mixed solution is evenly attached to the surface of the inner layer, and after vacuum drying, a polymer biomimetic coating is obtained; the outer layer mixed solution includes an inflammation-responsive polymer and second solvent.
[0051] In the preparation method of the polymer biomimetic coating provided by the present invention, the raw materials and components used are the same as above, and will not be repeated here...
Embodiment 1
[0075] Example 1: Metal Substrate
[0076]Using titanium metal alloy (TA1ELI, Tongxiang Metal Materials Co., Ltd.) as the substrate, the titanium metal alloy is fixed on the spinning or spraying receiver for surface coating. 0.3g indomethacin and 1.7g heparin sodium (50000Da) were dissolved in 15g acetic acid and water (2:1, mass ratio) mixed solvent, the mass concentration of indomethacin and heparin sodium was 12%. The mixed solution is then transferred to the injection needle, and is spun or sprayed at an injection speed of 1 mL / h under a potential difference of 22 kv. Receive at 15cm for 2h, dry at 37°C for 48h, and the thickness of the inner layer is 1500μm. Then prepare the outer layer solution. Dissolve 5 g of 0.15 g of 4-methyl-1-(pinacol p-phenylboronic acid)methoxy-2,6-dimethanol (the degree of polymerization is 2000) in dichloromethane solution (mass concentration is 3%) Inject at a rate of 1mL / h under a potential difference of 10kv, receive at a distance of 15cm...
Embodiment 2
[0078] Platelet adhesion assay:
[0079] Fresh blood was drawn from the ear artery of healthy adult New Zealand rabbits (2.5±0.5kg, provided by the Animal Experiment Center of Jilin University), and the blood was collected in blood collection tubes filled with 2mL of 3.5% sodium citrate to prevent coagulation. Blood was centrifuged at two different rotational speeds in order to obtain two different types of plasma. The first type (platelet rich plasma (PRP)) was obtained by centrifugation at 1000 rpm and the second type (platelet poor plasma (PPP)) by centrifugation at 1500 rpm. Plasma was diluted in PBS (Phosphate Buffered Saline) in order to carry out experiments in sufficient quantities. The adsorption of platelets was visually observed by scanning electron microscope.
[0080] The polymer biomimetic coating (2 * 2cm) that prepares described in embodiment 1 2 ) and polycaprolactone spinning coating (2 × 2cm 2 ) were respectively immersed in PRP at 37°C and under continu...
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