Orally-taken preparation for treating urticaria and preparation method thereof

A technology for urticaria and preparations, which is applied in the field of urticaria medication, can solve problems such as not being able to be used for a long time, finding out the cause of the disease, treating the symptoms but not the root cause, etc., to achieve the effects of eliminating allergic symptoms, improving human immunity, and reducing drug side effects

Inactive Publication Date: 2016-05-11
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The treatment of urticaria is mainly to find out the cause to eliminate the cause, and it is combined with adjuvant treatment of other symptoms. However, since it is difficult for most patients to find out the cause, they can only try to avoid contact with things that may cause allergies in diet and daily life. In order to reduce the number of induction, and once the outbreak is generally treated with conventional drugs, there are external medicine and internal medicine. External medicine can ge

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0014] An oral preparation for treating urticaria is composed of the following components by weight: 10 parts of paeonol, 8 parts of lentinan, 7.4 parts of betulinic acid, 6 parts of tannins, 5.5 parts of volatile oil, 4 parts of beta-sitosterol, 3 parts of camelliaside, 3 parts of cyproheptadine, 2 parts of flavonoid glycosides, 0.7 part of purple taro extract, 0.6 part of wild sesame extract, 0.4 part of lycopodium chinensis extract, 0.03 part of vitamin C, 0.01 part of vitamin P .

[0015] The preparation method of the oral preparation for treating the urticaria is as follows: extracting the weight components of paeonol, lentinan, betulinic acid, tannin, beta-sitosterol, camellin, cyproheptadine, flavonoid glycosides and purple taro The extract, the extract of wild sesame, the extract of lycopodium, vitamin C, and vitamin P were stirred with a mixer at a speed of 300 r / min for 15 minutes, and the obtained mixture was pulverized into a fine powder with an ultra-fine pulveriz...

Embodiment 2

[0018] An oral preparation for treating urticaria is composed of the following components by weight: 20 parts of paeonol, 17 parts of lentinan, 16.2 parts of betulinic acid, 13 parts of tannin, 12 parts of volatile oil, 10 parts of beta-sitosterol, 9 parts of camelliaside, 8.5 parts of cyproheptadine, 6 parts of flavone glycosides, 3 parts of purple taro extract, 2.4 parts of wild sesame extract, 2.0 parts of lycopodium chinensis extract, 0.095 parts of vitamin C, 0.06 parts of vitamin P .

[0019] The preparation method of the oral preparation for treating the urticaria is as follows: extracting the weight components of paeonol, lentinan, betulinic acid, tannin, beta-sitosterol, camellin, cyproheptadine, flavonoid glycosides and purple taro 15min of 300r / min rotation speed with a mixer, the obtained mixture was pulverized into fine powder with an ultrafine pulverizer, passed through a 200-mesh sieve, and then the volatile oil Spray directly on the fine powder, then add 9 par...

Embodiment 3

[0022] An oral preparation for treating urticaria is composed of the following components by weight: 30 parts of paeonol, 26 parts of lentinan, 25 parts of betulinic acid, 20 parts of tannin, 18.5 parts of volatile oil, 16 parts of beta-sitosterol, 15 parts of camelliaside, 14 parts of cyproheptadine, 10 parts of flavonoid glycosides, 5.3 parts of purple taro extract, 4.2 parts of wild sesame extract, 3.6 parts of lycopodium pine extract, 0.16 parts of vitamin C, 0.11 parts of vitamin P .

[0023] The preparation method of the oral preparation for treating the urticaria is as follows: extracting the weight components of paeonol, lentinan, betulinic acid, tannin, beta-sitosterol, camellin, cyproheptadine, flavonoid glycosides and purple taro 15min of 300r / min rotation speed with a mixer, the obtained mixture was pulverized into fine powder with an ultrafine pulverizer, passed through a 200-mesh sieve, and then the volatile oil Spray directly on the fine powder, then add 12 par...

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PUM

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Abstract

The invention discloses an orally-taken preparation for treating urticaria and a preparation method thereof. The orally-taken preparation for treating urticaria is prepared from, by weight, paeonol, lentinan, betulinic acid, tannin, volatile oil, beta-sitosterol, tea saponin, cyproheptadine, flavonoid glycosides, colocasia tonoimo extract, boehmeria siamensis craib extract, lycopodium phlegmaria L. extract, vitamin C and vitamin P. The orally-taken preparation combines western medicine and effective constituents of the traditional Chinese medicine extract, has the effects of dispelling wind, relieving itching, clearing away heat and toxic materials, tonifying the spleen, eliminating dampness and resisting to bacteria, infection and allergy, meanwhile can regulate immunocompetence of the human body and lower the side effects of medicine, can be used for treating urticaria which attacks repeatedly and is remarkable in treatment effect.

Description

technical field [0001] The invention relates to the technical field of medication for urticaria, in particular to an oral preparation for treating urticaria and a preparation method thereof. Background technique [0002] Skin disease has always been one of the frequently-occurring diseases that plague people's health. It is characterized by mild onset, high morbidity, and difficulty in curing it repeatedly. It is also related to factors such as season, climate, living environment, diet, and family history. It is changeable and complicated, and 75% of patients can't even find the cause of the disease, so it is difficult to cure it, such as dermatitis, eczema, urticaria, prickly heat, tinea pedis, etc. Among them, urticaria is a common multiple skin disease and is a disease of skin allergic allergic reaction. It is a localized edema reaction due to dilation and increased permeability of small blood vessels in the skin and mucous membranes, usually within 2 to 24 hours. It sub...

Claims

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Application Information

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IPC IPC(8): A61K36/8884A61P17/00A61K31/715A61K31/575A61K31/56A61K31/4418A61K31/375A61K31/12A61K31/7048A61K31/7024
CPCA61K36/8884A61K9/1652A61K31/12A61K31/375A61K31/4418A61K31/56A61K31/575A61K31/7024A61K31/7048A61K31/715A61K36/11A61K36/185A61K2300/00
Inventor 于群杜乐栋
Owner 于群
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