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 method for preparing the above-mentioned functional composite dressing with sustained drug release and self-antibacterial effects includes the following steps:
[0047] Step 1: Prepare the wound contact layer 1 by the immersion phase precipitation transformation method;
[0048] Add 100 parts by weight of polylactic acid particles, 10-30 parts by weight of polyethylene glycol, and 2-12 parts by weight of sustained-release drugs into the container containing N-methylpyrrolidone, mix and stir to dissolve completely, and prepare A uniform solution with a solid content of 20% to 60%, after deaeration, is evenly coated on the release paper by a coating machine, and then the release paper coated with the mixture layer is soaked in the ethanol solution for 5 to 30 minutes, and then placed Dry the solvent in an oven at 70~100℃, take it out and peel off the release paper to obtain a thickness of 10~150μm, the surface contains evenly distributed through micropores with a diameter ...
Example Embodiment
[0055] Example 1
[0056] Step 1: Preparation of wound contact layer by immersion phase precipitation transformation method
[0057] Will 800g 80g of polyethylene glycol 200, 8g of anesthetic and 8g of coagulant were added to the container containing 5L of N-methylpyrrolidone one by one, mixed and stirred to dissolve completely, after defoaming, it was evenly coated on the release paper by a coating machine After soaking the release paper coated with the mixture layer in ethanol solution for 10 minutes, put it in an 80℃ oven to dry the solvent, take it out and peel off the release paper to obtain a thickness of 40μm, a surface diameter of 30μm, and a hole density 600 pcs / cm 2 Wound contact layer;
[0058] Step 2: Preparation of the outer protective layer
[0059] Put 700g of Add it to a container containing 2L of acetone, stir to dissolve it evenly, after deaeration, coat it evenly on the release paper by a coating machine, put it in a 40℃ oven to dry the solvent, take it out and p...
Example Embodiment
[0064] Example 2
[0065] Step 1: Preparation of wound contact layer by immersion phase precipitation transformation method
[0066] Put 1000g of 100g of polyethylene glycol 200, 10g of analgesic and 10g of anti-inflammatory drugs were added to the container containing 5L of N-methylpyrrolidone one by one, mixed and stirred to dissolve completely, after defoaming, it was evenly applied to the release by the coating machine On the paper, the release paper coated with the mixture layer is soaked in ethanol solution for 10 minutes, and then placed in an oven at 80°C to dry the solvent. After taking it out, peel off the release paper to obtain a thickness of 56μm and a surface pore size of 40μm. The hole density is 800 / cm 2 Wound contact layer;
[0067] Step 2: Preparation of the outer protective layer
[0068] Put 1000g of Add it to a container containing 2L of acetone, stir to dissolve it evenly, after deaeration, coat it evenly on the release paper by a coating machine, put it in a ...
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