Medical cold compress patch and preparation method
20200206146 ยท 2020-07-02
Inventors
Cpc classification
A61K47/10
HUMAN NECESSITIES
A61K31/164
HUMAN NECESSITIES
A61K9/703
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K47/36
HUMAN NECESSITIES
International classification
A61K9/70
HUMAN NECESSITIES
A61K31/164
HUMAN NECESSITIES
A61K47/10
HUMAN NECESSITIES
A61K47/36
HUMAN NECESSITIES
Abstract
A medical cold compress patch includes a backing layer, a gel layer and a covering layer. The gel layer includes various raw materials, and each raw material is measured as following mass percentage, 2 to 15 mass percent of macromolecule substance, 2 to 10 mass percent of epidermal growth factor, 2 to 8 mass percent of ceramide, 3 to 8 mass percent of humectant, 3 to 10 mass percent of bupleurum sinensis extract, 2 to 8 mass percent of dandelion extract, 3 to 12 mass percent of cortex phellodendri extract, 5 to 10 mass percent of aloe vera extract, 2 to 10 mass percent of honeysuckle flowers extract and the balance being purified water. A method for preparing medical cold compress patch is also disclosed.
Claims
1. A medical cold compress patch comprising a backing layer, a gel layer, and a covering layer, characterized in that the gel layer is consisted of various raw materials and each raw material is measured by mass percentage, 2 to 15 mass percent of macromolecule substance, 2 to 10 mass percent of epidermal growth factor, 2 to 8 mass percent of ceramide, 3 to 8 mass percent of humectant, 3 to 10 mass percent of bupleurum sinensis extract, 2 to 8 mass percent of dandelion extract, 3 to 12 mass percent of cortex phellodendri extract, 5 to 10 mass percent of aloe vera extract, 2 to 10 mass percent of honeysuckle flowers extract and the balance being purified water.
2. The medical cold compress patch in accordance with claim 1, comprising a backing layer, a gel layer, and a covering layer, characterized in that the gel layer is comprised of various raw materials and each raw material is measured as the following mass percentage, 5 to 10 mass percent of macromolecule substance, 5 to 8 mass percent of epidermal growth factor, 4 to 8 mass percent of ceramide, 3 to 8 mass percent of humectant, 5 to 8 mass percent of bupleurum sinensis extract, 4 to 6 mass percent of dandelion extract, 5 to 10 mass percent of cortex phellodendri extract, 7 to 9 mass percent of aloe vera extract, 4 to 7 mass percent of honeysuckle flowers extract and the balance being purified water.
3. The medical cold compress patch in accordance with claim 1, comprising a backing layer, a gel layer, and a covering layer, characterized in that the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 10 mass percent of macromolecule substance, 6 mass percent of epidermal growth factor, 5 mass percent of ceramide, 4 mass percent of humectant, 6 mass percent of bupleurum sinensis extract, 5 mass percent of dandelion extract, 7 mass percent of cortex phellodendri extract, 8 mass percent of aloe vera extract, 6 mass percent of honeysuckle flowers extract and the balance being purified water.
4. The medical cold compress patch in accordance with claim 1, characterized in that the macromolecule substance comprises one or more mixtures selected from the group of polyvinyl alcohol, sodium polyacrylate, carbomer, hydroxyl propyl methyl cellulose sodium, and chitosan.
5. The medical cold compress patch in accordance with claim 1, characterized in that the humectant comprises one or more mixtures selected from the group of glycerin, sodium hyaluronate, aloe vera barbadensis leaf juice, and sorbitol.
6. The medical cold compress patch in accordance with claim 1, characterized in that the ceramide is a light brown liquid with a PH value between 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
7. The medical cold compress patch in accordance with claim 1, characterized in that the total bacterial count in the purified water is less than 100 cfu/ml.
8. The medical cold compress patch in accordance with claim 1, characterized in that the backing layer is made of nonwoven or composite nonwoven fabrics, the covering layer is one of polyethylene film layer, polypropylene film layer and polycarbonate film layer.
9. The medical cold compress patch in accordance with claim 1, characterized in that the medical cold compress patch is configured to be a shape of split-type facial mask, a shape similar to female sanitary pad and a shape of rain drop.
10. A preparation method of the medical cold compress patch, comprising the following steps of: Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer; Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and mixing the solution evenly at a rate of 150-300 r/min for 15-30 min at normal temperature to obtain the constituent 1; Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 50-100 r/min for 10-20 min to obtain the constituent 2, Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 100-200 r/min for 20-40 min to obtain the constituent 3; Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 100-200 r/min for 20-40 min to obtain a clear gel; and Step F: coating the clear gel evenly on a backing layer and pressing a covering layer against the clear gel and cutting, solidifying and packing it to obtain the finished product of the medical cold compress patch
Description
DESCRIPTION OF THE DRAWINGS
[0017]
[0018]
[0019]
[0020]
SPECIFIC EMBODIMENTS
Embodiment 1
[0021] A medical cold compress patch is provided, comprising a backing layer, a gel layer, and a covering layer, the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 4 mass percent of macromolecule substance, 3 mass percent of epidermal growth factor, 2 mass percent of ceramide, 4 mass percent of humectant, 4 mass percent of bupleurum sinensis extract, 2 mass percent of dandelion extract, 4 mass percent of cortex phellodendri extract, 6 mass percent of aloe vera extract, 3 mass percent of honeysuckle flowers extract and the balance being purified water.
[0022] The macromolecule substance comprises a mixture of polyvinyl alcohol and carbomer.
[0023] The humectant is glycerin.
[0024] The ceramide is a light brown liquid with a PH value of 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
[0025] The total bacterial count in the purified water is less than 100 cfu/ml.
[0026] The backing layer is made of nonwoven fabrics and the covering layer is polyethylene film layer.
[0027] The medical cold compress patch is in shape of rain drop.
[0028] The preparation method of medical cold compress patch comprises the following steps of:
Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer;
Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and at normal temperature stirring the solution evenly at a rate of 180 r/min for 20 min to obtain the constituent 1;
Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 60 r/min for 13 min to obtain the constituent 2;
Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 120 r/min for 28 min to obtain the constituent 3;
Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 180 r/min for 40 min to obtain a clear gel; and
Step F: coating the clear gel evenly on a backing layer and pressing a covering layer on the clear gel for tailoring, solidifying and packaging prior to obtain the finished product of the medical cold compress patch
Embodiment 2
[0029] A medical cold compress patch is provided, comprising a backing layer, a gel layer, and a covering layer, the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 4 mass percent of macromolecule substance, 3 mass percent of epidermal growth factor, 2 mass percent of ceramide, 4 mass percent of humectant, 4 mass percent of bupleurum sinensis extract, 2 mass percent of dandelion extract, 4 mass percent of cortex phellodendri extract, 6 mass percent of aloe vera extract, 3 mass percent of honeysuckle flowers extract and the balance being purified water.
[0030] The macromolecule substance is a mixture of polyvinyl alcohol and carbomer.
[0031] The humectant is glycerin.
[0032] The ceramide is a light brown liquid with a PH value of 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
[0033] The total bacterial count in the purified water is less than 100 cfu/ml.
[0034] The backing layer is made of nonwoven fabrics and the covering layer is polyethylene film layer.
[0035] The medical cold compress patch is in a shape of rain drop.
[0036] The preparation method of medical cold compress patch comprises the following steps of:
Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer;
Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and at normal temperature stirring the solution evenly at a rate of 260 r/min for 20 min to obtain the constituent 1;
Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 80 r/min for 14 min to obtain the constituent 2;
Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 180 r/min for 30 min to obtain the constituent 3;
Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 220 r/min for 45 min to obtain a clear gel; and
Step F: coating the clear gel evenly on a backing layer and pressing a covering layer on the clear gel for tailoring, solidifying and packaging prior to obtain the finished product of the medical cold compress patch
Embodiment 3
[0037] A medical cold compress patch is provided, comprising a backing layer, a gel layer, and a covering layer, the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 10 mass percent of macromolecule substance, 8 mass percent of epidermal growth factor, 8 mass percent of ceramide, 8 mass percent of humectant, 8 mass percent of bupleurum sinensis extract, 6 mass percent of dandelion extract, 10 mass percent of cortex phellodendri extract, 9 mass percent of aloe vera extract, 7 mass percent of honeysuckle flowers extract and the balance being purified water.
[0038] The macromolecule substance is a mixture of sodium polyacrylate and chitosan.
[0039] The humectant comprises a mixture of sodium hyaluronate and aloe vera barbadensis leaf juice.
[0040] The ceramide is a light brown liquid with a PH value of 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
[0041] The total bacterial count in the purified water is less than 100 cfu/ml.
[0042] The backing layer is made of nonwoven fabrics and, the covering layer is polycarbonate film layer.
[0043] The medical cold compress patch is in a shape similar to female sanitary pad.
[0044] The preparation method of medical cold compress patch comprises the following steps of:
Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer;
Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and at normal temperature stirring the solution evenly at a rate of 260 r/min for 30 min to obtain the constituent 1;
Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 80 r/min for 20 min to obtain the constituent 2;
Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 160-200 r/min for 36 min to obtain the constituent 3;
Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 290 r/min for 40 min to obtain a clear gel; and
Step F: coating the clear gel evenly on a backing layer and pressing a covering layer on the clear gel for tailoring, solidifying and packaging prior to obtain the finished product of the medical cold compress patch
Embodiment 4
[0045] A medical cold compress patch is provided, comprising a backing layer, a gel layer, and a covering layer, the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 10 mass percent of macromolecule substance, 8 mass percent of epidermal growth factor, 8 mass percent of ceramide, 8 mass percent of humectant, 8 mass percent of bupleurum sinensis extract, 6 mass percent of dandelion extract, 10 mass percent of cortex phellodendri extract, 9 mass percent of aloe vera extract, 7 mass percent of honeysuckle flowers extract and the balance being purified water.
[0046] The macromolecule substance comprises a mixture of sodium polyacrylate and chitosan.
[0047] The humectant comprises a mixture of sodium hyaluronate and aloe vera barbadensis leaf juice.
[0048] The ceramide is a light brown liquid with a PH value of 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
[0049] The total bacterial count in the purified water is less than 100 cfu/ml.
[0050] The backing layer is made of nonwoven fabrics and, the covering layer is polycarbonate film layer.
[0051] The medical cold compress patch is similar to a shape similar to female sanitary pad.
[0052] The preparation method of medical cold compress patch comprises the following steps of:
Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer;
Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and at normal temperature stirring the solution evenly at a rate of 260 r/min for 20 min to obtain the constituent 1;
Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 80 r/min for 14 min to obtain the constituent 2;
Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 180 r/min for 30 min to obtain the constituent 3;
Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 220 r/min for 45 min to obtain a clear gel; and
Step F: coating the clear gel evenly on a backing layer, then pressing a covering layer on the clear gel and obtaining the finished product of a medical cold compress patch after tailoring, solidifying and packaging the layers.
Embodiment 5
[0053] A medical cold compress patch is provided, comprising a backing layer, a gel layer, and a covering layer, the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 10 mass percent of macromolecule substance, 6 mass percent of epidermal growth factor, 5 mass percent of ceramide, 4 mass percent of humectant, 6 mass percent of bupleurum sinensis extract, 5 mass percent of dandelion extract, 7 mass percent of cortex phellodendri extract, 8 mass percent of aloe vera extract, 6 mass percent of honeysuckle flowers extract and the balance being purified water.
[0054] The macromolecule substance comprises a mixture of carbomer, hydroxyl propyl methyl cellulose sodium and chitosan.
[0055] The humectant comprises a mixture of glycerin, sodium hyaluronate and aloe vera barbadensis leaf juice.
[0056] The ceramide is a light brown liquid with a PH value of 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
[0057] The total bacterial count in the purified water is less than 100 cfu/ml.
[0058] The backing layer is made of composite nonwoven fabrics and the covering layer is polycarbonate film layer.
[0059] The medical cold compress patch is in a shape of split facial mask.
[0060] The preparation method of medical cold compress patch comprises the following steps of:
Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer;
Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and at normal temperature stirring the solution evenly at a rate of 260 r/min for 20 min to obtain the constituent 1;
Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 80 r/min for 14 min to obtain the constituent 2;
Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 180 r/min for 30 min to obtain the constituent 3;
Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 220 r/min for 45 min to obtain a clear gel; and
Step F: coating the clear gel evenly on a backing layer and pressing a covering layer on the clear gel for tailoring, solidifying and packaging prior to obtain the finished product of the medical cold compress patch.
Embodiment 6
[0061] A medical cold compress patch is provided, comprising a backing layer, a gel layer, and a covering layer, the gel layer is comprised of various raw materials and each raw material is measured as following mass percentage, 10 mass percent of macromolecule substance, 6 mass percent of epidermal growth factor, 5 mass percent of ceramide, 4 mass percent of humectant, 6 mass percent of bupleurum sinensis extract, 5 mass percent of dandelion extract, 7 mass percent of cortex phellodendri extract, 8 mass percent of aloe vera extract, 6 mass percent of honeysuckle flowers extract and the balance being purified water.
[0062] The macromolecule substance comprises a mixture of sodium carbomer, hydroxyl propyl methyl cellulose sodium and chitosan.
[0063] The humectant is a mixture of glycerin, sodium hyaluronate and aloe vera barbadensis leaf juice.
[0064] The ceramide is a light brown liquid with a PH value of 5.0 to 6.0 and a total bacterial count of less than 100 cfu/g.
[0065] The total bacterial count in the purified water is less than 100 cfu/ml.
[0066] The backing layer is made of composite nonwoven fabrics and, the covering layer comprises polycarbonate film layer.
[0067] The medical cold compress patch is in a shape of split facial mask.
[0068] The preparation method of medical cold compress patch comprises the following steps of:
Step A: accurately weighing and preparing each raw material for use according to the ratios of each raw material in the gel layer;
Step B: dissolving the prepared epidermal growth factor, ceramide, humectant and aloe vera extract in water and at normal temperature stirring the solution evenly at a rate of 180 r/min for 20 min to obtain the constituent 1;
Step C: dissolving the prepared macromolecule substance in water to swell the macromolecule substance at normal temperature for 20 min and stirring the solution evenly at a rate of 60 r/min for 13 min to obtain the constituent 2;
Step D: dissolving prepared the bupleurum sinensis extract, dandelion extract, cortex phellodendri extract, aloe vera extract, and honeysuckle flowers extract in water and at normal temperature stirring the solution evenly at a rate of 120 r/min for 28 min to obtain the constituent 3;
Step E: mixing above-mentioned three constituents and at normal temperature stirring the mixture evenly at a rate of 180 r/min for 40 min to obtain a clear gel; and
Step F: coating the clear gel evenly on a backing layer and pressing a covering layer on the clear gel for tailoring, solidifying and packaging prior to obtain the finished product of the medical cold compress patch
[0069] The specific embodiments of the present invention are only a part of the embodiments of the present invention, and are not intended to limit the invention. All other embodiments obtained by those skilled in the art based on the embodiments of the present invention without creative efforts are within the scope of the present invention.