Functional composite dressing with drug sustained release and self-antibacterial effects and preparation method thereof
A slow-release, drug-based technology, applied in dressings, viscous dressings, non-adhesive dressings, etc., can solve problems such as not being able to be used for a long time, easy to breed bacteria, and easy to stick to granulation, so as to reduce the frequency, reduce the chance of re-injury, reduce The effect of wound scars
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[0046] The preparation method of the above-mentioned functional composite dressing with drug sustained release and self-antibacterial effect, the steps are as follows:
[0047] Step 1, preparing the wound contact layer 1 by the immersion phase precipitation transformation method;
[0048] Add 100 parts by weight of polylactic acid granules, 10-30 parts by weight of polyethylene glycol, and 2-12 parts by weight of sustained-release drugs into a container containing N-methylpyrrolidone, mix and stir to dissolve completely, and prepare A uniform solution with a solid content of 20% to 60%, after defoaming, is evenly coated on the release paper by a coating machine, and then the release paper coated with the mixture layer is soaked in ethanol solution for 5 to 30 minutes, and then put Dry the solvent in an oven at 70-100°C, take it out and peel off the release paper to obtain transparent micropores with a thickness of 10-150 μm and a uniform distribution of pore diameters of 5-50 ...
Embodiment 1
[0056] Step 1. Preparation of wound contact layer by immersion phase precipitation transformation method
[0057] 800g of Add 80g of polyethylene glycol 200, 8g of anesthetic and 8g of blood coagulant into the container containing 5LN-methylpyrrolidone one by one, mix and stir to dissolve completely, and after defoaming, apply it evenly on the release paper by a coating machine , and then soak the release paper coated with the mixture layer in ethanol solution for 10 minutes, put it in an oven at 80°C to dry the solvent, take it out and peel off the release paper to obtain a thickness of 40 μm, a surface pore size of 30 μm, and a pore density of 600 pieces / cm 2 wound contact layer;
[0058] Step 2. Preparation of the external protective layer
[0059] 700g of Add it into a container containing 2L of acetone, stir and dissolve evenly, after defoaming, apply it evenly on the release paper with a coating machine, put it in a 40°C oven to dry the solvent, take it out and pee...
Embodiment 2
[0065] Step 1. Preparation of wound contact layer by immersion phase precipitation transformation method
[0066] 1000g of Add 100g of polyethylene glycol 200, 10g of analgesic and 10g of anti-inflammatory drug into the container containing 5LN-methylpyrrolidone one by one, mix and stir to dissolve completely, and after defoaming, apply it evenly on the release form with a coating machine On the paper, soak the release paper coated with the mixture layer in ethanol solution for 10 minutes, put it in an oven at 80°C to dry the solvent, take it out and peel off the release paper to obtain a thickness of 56 μm and a surface pore size of 40 μm. Hole density is 800 / cm 2 wound contact layer;
[0067] Step 2. Preparation of the external protective layer
[0068] 1000g of Add it into a container containing 2L of acetone, stir and dissolve evenly, after defoaming, apply it evenly on the release paper with a coating machine, put it in a 40°C oven to dry the solvent, take it out an...
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Abstract
Description
Claims
Application Information
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