CN101703667A - Brown red medicament for treating traumatic injuries and preparation method thereof - Google Patents

Brown red medicament for treating traumatic injuries and preparation method thereof Download PDF

Info

Publication number
CN101703667A
CN101703667A CN200910225965A CN200910225965A CN101703667A CN 101703667 A CN101703667 A CN 101703667A CN 200910225965 A CN200910225965 A CN 200910225965A CN 200910225965 A CN200910225965 A CN 200910225965A CN 101703667 A CN101703667 A CN 101703667A
Authority
CN
China
Prior art keywords
preparation
parts
concentrated solution
weight
medicine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN200910225965A
Other languages
Chinese (zh)
Other versions
CN101703667B (en
Inventor
邬威尧
吕竹芬
苏志伟
谢清春
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sinopharm Group Feng Liao Xing Foshan Pharmaceutical Co Ltd
Original Assignee
Foshan Feng Liao Xing Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from CNA2009100399504A external-priority patent/CN101564487A/en
Application filed by Foshan Feng Liao Xing Pharmaceutical Co Ltd filed Critical Foshan Feng Liao Xing Pharmaceutical Co Ltd
Priority to CN200910225965XA priority Critical patent/CN101703667B/en
Publication of CN101703667A publication Critical patent/CN101703667A/en
Application granted granted Critical
Publication of CN101703667B publication Critical patent/CN101703667B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Medicinal Preparation (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

The invention discloses a brown red medicament for treating traumatic injuries and a preparation method thereof and belongs to the technical field of Chinese medicaments. The medicament is cataplasm prepared from concentrates of ethanol extracts of 39 to 49 weight parts of safflowers, 39 to 49 weight parts of cutch, 39 to 49 weight parts of tangkuei tail, 17 to 27 weight parts of alum, 39 to 49 weight parts of sappan wood, 39 to 49 weight parts of asparagus, 39 to 49 weight parts of frankincense, 39 to 49 weight parts of benzoin, 39 to 49 weight parts of commiphora molmol and 39 to 49 weight parts of dragon's blood and pharmaceutically acceptable matrix materials. The preparation method comprises: (1) the preparation of the concentrates of the ethanol extracts; (2) the preparation of the matrix materials; and (3) the preparation of the cataplasm. The medicament of the invention has the advantages of small skin simulation, quick absorption and more convenient use and can be used for treating fall wounds, muscles and bones injuries, accumulated stasis, pain with swelling and other symptoms.

Description

A kind of Jiehong medicine for injuries from falls and preparation method thereof
Technical field
The present invention relates to a kind of Chinese medicine preparation, more particularly, it relate to a kind of be used for the treatment of get injured by a fall, the Jiehong medicine for injuries from falls of diseases such as bones and muscles injury, long-pending swelling due to stasis, the invention still further relates to above-mentioned medicaments preparation method.
Background technology
Soft tissue injury is commonly encountered diseases, a frequently-occurring disease clinically, and worldwide, its sickness rate is only second to flu.Particularly be engaged in amusement, sports, or blue-collar philtrum, seldom do not suffering soft tissue injury.Soft tissue injury is meant that various causative factors of injury act on body and cause the disease of a series of pathological changes of soft tissue, and its pathological change is a principal character with local acute inflammation and reparation.Clinical local swelling, pain, dysfunction, the livid purple ecchymosis etc. of mainly showing as.Be divided into two kinds of acute injury (acute trauma) and chronic injuries (chronic trauma), and chronic injury is come by the acute injury transformation often, so acute soft tissue injury need obtain in time, effectively treatment.Modern medicine has the main Therapeutic Method of acute soft tissue injury: wrapping, partial closure, physical therapy etc., and these method curative effects are not good enough, and rehabilitation duration is longer.The medicine for external use of treatment acute soft tissue injury based on apply ointment or plaster, ointment, plaster, medicine loose, these medicines are again mainly based on conventional dosage forms, exist dosage form to fall behind and use inconvenience, positions such as trunk are difficult for wrapping up deficiencies such as the medicated clothing of firmly, easily making dirty, waste medicine, hindered further and promoted the use, also seek and treat acute soft tissue injury with medicinal herb spray, but its complicated process of preparation, reasons such as cost costliness have hindered further popularization.
Chinese medicine " exhausts red traumatic injury ", and the side mainly is made up of Sanguis Draxonis, Flos Carthami, Olibanum, Myrrha, Aloe, Radix Angelicae Sinensis, catechu, Lignum Sappan etc., generally use, be used to get injured by a fall bones and muscles injury with tincture, diseases such as long-pending swelling due to stasis, treatment has remarkable advantages and unique curative effect to soft tissue injury.But also there are two big subject matters at present in it: the one, and preparation process is backward relatively, and using dosage once is bigger, and local irritation is arranged, and has reduced patient's compliance, and quality standard is perfect inadequately, has limited its further developing in market; The 2nd, exhaust red traumatic injury tincture when patient uses, put the affected part on the skin after must soaking medicinal liquid with Cotton Gossypii, and to attach affected part and to make lasting soak behind the gauze infiltration medicinal liquid, again because the solvent volatility of tincture is strong, easily dry, in order to keep moistening, patient must add medicinal liquid at any time, equally also reduce patient's compliance, restricted its clinical practice.Having become this sick problem demanding prompt solution of treatment so study the modern preparation of external evident in efficacy, lasting, easy to use, also is an important topic of modernization of cmm.
Summary of the invention
The technical problem to be solved in the present invention is the above-mentioned deficiency at prior art, provides diseases such as a kind of more effectively treatment is got injured by a fall, bones and muscles injury, long-pending swelling due to stasis, the Jiehong medicine for injuries from falls little to skin irritation, that drug absorption fast, use is convenient.
Another technical problem that the present invention will solve provides a kind of preparation method of above-mentioned novel Jiehong medicine for injuries from falls.
Last technical scheme of the present invention is such: a kind of Jiehong medicine for injuries from falls, be the cataplasma of being made by the ethanol extraction concentrated solution and the receptible host material of pharmaceutics of 39~49 parts on Flos Carthami, 39~49 parts in catechu, 39~49 parts of Radix Angelicae Sinensis, 17~27 parts of Alumens, 39~49 parts of Lignum Sappans, 39~49 parts of Aloes, 39~49 parts of Olibanums, 39~49 parts of Benzoinumes, 39~49 parts of Myrrhas, 39~49 parts of Sanguis Draxonis, above-mentioned deal is a weight portion.
Further, a kind of Jiehong medicine for injuries from falls of the present invention, its preferred plan is the cataplasma of being made by the ethanol extraction concentrated solution of 44 parts on Flos Carthami, 44 parts in catechu, 44 parts of Radix Angelicae Sinensis, 22 parts of Alumens, 44 parts of Lignum Sappans, 44 parts of Aloes, 44 parts of Olibanums, 44 parts of Benzoinumes, 44 parts of Myrrhas, 44 parts of Sanguis Draxonis and the receptible host material of pharmaceutics, and above-mentioned deal is a weight portion.
In above-mentioned a kind of Jiehong medicine for injuries from falls, described ethanol extraction concentrated solution is that extracting solution is concentrated into 25~35% of medical material weight; The weight ratio of described ethanol extraction concentrated solution and host material is 1: 2.0~5.0.
In above-mentioned a kind of Jiehong medicine for injuries from falls, described host material is to be selected from sodium polyacrylate, carbopol, hypromellose, polyvinylpyrrolidone, gelatin, Kaolin, silica gel, dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, 1, the wherein two or more at least mixture of 2-propylene glycol, tartaric acid, tween, distilled water, glycerol, azone.The preferred following material of described host material mixes by weight proportion, 0.01~1 part of 1~5 part of sodium polyacrylate, 1~5 part of carbopol, 1~10 part of Kaolin, 1~10 part in silica gel, 0.01~0.1 part of dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, 1,0.1~1 part of 2-propylene glycol, 0.01~0.1 part in tartaric acid, 10~50 parts of distilled water, 1~10 part of glycerol, 0.1~2 part of azone.
In above-mentioned a kind of Jiehong medicine for injuries from falls, also be added with the unguentum usual auxiliaries of concentrated solution weight 0.1~1% in the described ethanol extraction concentrated solution, described unguentum usual auxiliaries is meant at least a in menthol, Mentholum, Borneolum Syntheticum, azone, eucalyptus oil, Oleum Ricini, the methyl salicylate, with the flexibility, the tolerance to cold that improve medicament or play the Percutaneous absorption enhancer effect.
Back of the present invention one technical scheme is such: a kind of preparation method of Jiehong medicine for injuries from falls, comprise the preparation of (1) ethanol extraction concentrated solution, (2) preparation of the preparation of host material and (3) cataplasma, wherein the preparation method of (1) ethanol extraction concentrated solution is to get Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis to be ground into coarse powder, adopting percolation, make solvent with 60~80% ethanol, is slowly percolation of 1~3ml/min by percolation speed, the ethanol that adds 5 times of amounts of medical material weight is altogether collected percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, with 60~80% alcohol dipping of above-mentioned percolate and 3 times of amounts of medical material 30 days, filter, filtrate decompression is concentrated into 30~40% the concentrated solution that weight is medical material weight; (2) preparation method of host material is that dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, adds sodium polyacrylate, fully grinds well; Tartaric acid is dissolved in the part distilled water, and gradation joins in the said mixture, stirs; The carbopol adding distil water is dissolved into clear solution, adds again in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs promptly; (3) preparation method of cataplasma is to extract concentrated solution and the host material mixed by 1: 2.0~5.0, to stir 10~30 minutes, and coating covers upper protective film, section, and packing is promptly.
In the preparation method of above-mentioned a kind of Jiehong medicine for injuries from falls, described ethanol extraction concentrated solution also can prepare as follows: get Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis and be ground into coarse powder, adopt percolation, make solvent with 60~80% ethanol, by percolation speed is slowly percolation of 1~3ml/min, the ethanol that adds 5 times of amounts of medical material weight is altogether collected percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, add twice of ultrasonic Treatment of 60~80% ethanol that 3 medical materials are doubly measured, two hours for the first time, one hour for the second time, filter, filtrate and above-mentioned percolate merge and be evaporated to 30~40% the concentrated solution that weight is medical material weight, or add the unguentum usual auxiliaries and stir; Can under the situation that guarantees extraction effect, improve extraction efficiency greatly.
The present invention compared with prior art has following advantage:
(1) cataplasma of the present invention adopts water-soluble base and water solublity, fat-soluble medicine intermiscibility good, and the drug loading of host material is big, is fit to very that Chinese medicine is formed minute more, the medication characteristics of heavy dose.
(2) water content is higher in the cataplasma of the present invention, and the keratodermatitis cell hydration is expanded, and more helps drug transdermal and absorbs.
(3) cataplasma breathability of the present invention is poor, to skin vigorous property, the equal tool of moisture retention obviously be better than traditional rubber-emplastrum, and use comfortable, little to skin irritation, can take off advantages such as paste not having pain repeatedly.
The specific embodiment
Below in conjunction with specific embodiment the present invention is described in further detail, but does not constitute any limitation of the invention.
Embodiment 1
One of preparation of ethanol extraction concentrated solution
Component: Flos Carthami 390g, catechu 390g, Radix Angelicae Sinensis 390g, Alumen 170g, Lignum Sappan 390g, Aloe 390g, Olibanum 390g, Benzoinum 390g, Myrrha 390g, Sanguis Draxonis 390g
Preparation method: getting Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis and be ground into coarse powder, adopt percolation, make solvent with 60% ethanol, is slowly percolation of 1ml/min by percolation speed, adds the ethanol of 5 times of amounts of medical material weight altogether, the collection percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, and with 60% alcohol dipping of above-mentioned percolate and 3 times of amounts of medical material 30 days, filtration, it is 30% of medical material weight that filtrate decompression is concentrated into weight, about 1100g.
Embodiment 2
Two of the preparation of ethanol extraction concentrated solution
Component: Flos Carthami 440g, catechu 440g, Radix Angelicae Sinensis 440g, Alumen 220g, Lignum Sappan 440g, Aloe 440g, Olibanum 440g, Benzoinum 440g, Myrrha 440g, Sanguis Draxonis 440g
Preparation method: getting Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis and be ground into coarse powder, adopt percolation, make solvent with 70% ethanol, is slowly percolation of 2ml/min by percolation speed, adds the ethanol of 5 times of amounts of medical material weight altogether, the collection percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, with 70% alcohol dipping of above-mentioned percolate and 3 times of amounts of medical material 30 days, filter, it is 35% of medical material weight that filtrate decompression is concentrated into weight, about 1460g adds the 12.5g eucalyptus oil then and mixes.
Embodiment 3
Three of the preparation of ethanol extraction concentrated solution
Component: Flos Carthami 490g, catechu 490g, Radix Angelicae Sinensis 490g, Alumen 270g, Lignum Sappan 490g, Aloe 490g, Olibanum 490g, Benzoinum 490g, Myrrha 490g, Sanguis Draxonis 490g
Preparation method: getting Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis and be ground into coarse powder, adopt percolation, make solvent with 80% ethanol, is slowly percolation of 3ml/min by percolation speed, adds the ethanol of 5 times of amounts of medical material weight altogether, the collection percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, with 80% alcohol dipping of above-mentioned percolate and 3 times of amounts of medical material 30 days, filter, it is 40% of medical material weight that filtrate decompression is concentrated into weight, about 1870g adds menthol 2g then and mixes.
Embodiment 4
Four of the preparation of ethanol extraction concentrated solution
Component: Flos Carthami 440g, catechu 440g, Radix Angelicae Sinensis 440g, Alumen 220g, Lignum Sappan 440g, Aloe 440g, Olibanum 440g, Benzoinum 440g, Myrrha 440g, Sanguis Draxonis 440g
Preparation method: getting Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis and be ground into coarse powder, adopt percolation, make solvent with 70% ethanol, is slowly percolation of 2ml/min by percolation speed, adds the ethanol of 5 times of amounts of weight altogether, the collection percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, 70% ethanol that adds medical material 3 amounts, with twice of ultrasonic Treatment, two hours for the first time, one hour for the second time, filter, be 35% of medical material weight with being evaporated to weight after filtrate and the percolate merging, about 1360g adds menthol 2g then and mixes.
Embodiment 5
One of medicaments preparation
The extract 3.5g that extracting solution concentrated solution: embodiment 1 is prepared.
Host material: sodium polyacrylate (NP-700) 0.9g, Kaolin 4.5g, ethylenediaminetetraacetic acid 0.15g, dihydroxyaluminum aminoacetate 0.03g, 1,2-propylene glycol 0.3g, tartaric acid 0.03g, glycerol 4.5g, azone 0.6g, distilled water 8g.
The host material preparation: dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, add sodium polyacrylate, fully grind well; Tartaric acid is dissolved in the part distilled water, joins at twice in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs standby.
Medicaments preparation: the extracting solution concentrated solution is added in the preparation host material, and stirring grinds well, and this mixture stand is applied on the non-woven fabrics, and horizontal positioned covers upper protective film, and section packs room temperature and places, and gets final product.
Usage and consumption: be affixed on the affected part, paste every day one.
Embodiment 6
Two of medicaments preparation
The extract 4.4g that extracting solution concentrated solution: embodiment 2 is prepared.
Host material: sodium polyacrylate (NP-700) 0.6g, Kaolin 3g, ethylenediaminetetraacetic acid 0.1g, dihydroxyaluminum aminoacetate 0.025g, 1,2-propylene glycol 0.2g, tartaric acid 0.025g, glycerol 3.5g, azone 0.45g, distilled water 6.5g.
The host material preparation: dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, add sodium polyacrylate, fully grind well; Tartaric acid is dissolved in the part distilled water, joins at twice in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs standby.
Medicaments preparation: the extracting solution concentrated solution is added in the preparation host material, and stirring grinds well, and this mixture stand is applied on the non-woven fabrics, and horizontal positioned covers upper protective film, and section packs room temperature and places, and gets final product.
Usage and consumption: be affixed on the affected part, paste every day one.
Embodiment 7
Three of medicaments preparation
The extract 5.7g that extracting solution concentrated solution: embodiment 3 is prepared.
Host material: sodium polyacrylate (NP-700) 0.6g, carbopol (
Figure G200910225965XD0000051
Ultrez21) 0.3g, Kaolin 4g, ethylenediaminetetraacetic acid 0.12g, dihydroxyaluminum aminoacetate 0.03g, 1,2-propylene glycol 0.25g, tartaric acid 0.02g, glycerol 4g, azone 0.5g, distilled water 6g.
The host material preparation: dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, add sodium polyacrylate, fully grind well; Tartaric acid is dissolved in the part distilled water, joins at twice in the said mixture, stir; The carbopol adding distil water is dissolved into clear solution, adds in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs standby.
Medicaments preparation: the extracting solution concentrated solution is added in the preparation host material, and stirring grinds well, and this mixture stand is applied on the non-woven fabrics, and horizontal positioned covers upper protective film, and section packs room temperature and places, and gets final product.
Usage and consumption: be affixed on the affected part, paste every day one.
Embodiment 8
Four of medicaments preparation
The extract 4.4g that extracting solution concentrated solution: embodiment 4 is prepared.
Host material: sodium polyacrylate (NP-700) 0.6g, carbopol (
Figure G200910225965XD0000052
980NF) 0.2g, Kaolin 3.5g, ethylenediaminetetraacetic acid 0.15g, dihydroxyaluminum aminoacetate 0.03g, 1,2-propylene glycol 0.5g, tartaric acid 0.02g, glycerol 3.5g, azone 0.4g, distilled water 7g.
The host material preparation: dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, add sodium polyacrylate, fully grind well; Tartaric acid is dissolved in the part distilled water, joins at twice in the said mixture, stir; The carbopol adding distil water is dissolved into clear solution, adds in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs standby.
Medicaments preparation: the extracting solution concentrated solution is added in the preparation host material, and stirring grinds well, and this mixture stand is applied on the non-woven fabrics, and horizontal positioned covers upper protective film, and section packs room temperature and places, and gets final product.
Usage and consumption: be affixed on the affected part, paste every day one.
Experimental example 1
The present invention exhausts the skin irritation experimental study of red traumatic injury cataplasma
1. exhaust of the influence of red traumatic injury cataplasma single-dose to rabbit intact skin and damaged skin.
4 of new zealand purebred rabbits, each 2 of intact skin and damaged skins, 24h loses hair or feathers with 8% sodium sulfide before the administration, about 15cm * the 10cm of area, divide two districts about spinal column, the left side is the check plot for right side, administration district, amassing at depilation administration district veneer is the cataplasma of 7.5cm * 5cm, of the same area cataplasma that contains substrate pasted on the right side, removes cataplasma behind medicine and the contact skin 24h, observes the dermoreaction situation, record 1h, 24h, 48h, 72h, have or not erythema, edema, protuberance, burnt silly form etc., and the dermoreaction intensity of every animal marked, medicine observed to the skin irritation situation.Then medicine-feeding part and contrast position are cut respectively, put into 10% formalin and do the pathology histological examination.Damaged skin scratches epidermis with knife blade, the degree of being with the oozing of blood, and other are with the intact skin irritant test.
1.1 skin irritation reaction standards of grading and skin irritation intensity standards of grading
Table 5 skin irritation reaction standards of grading
Figure G200910225965XD0000061
Table 6 skin irritation intensity evaluation standard
The average product score value Estimate
??0~0.49 Nonirritant
The average product score value Estimate
??0.5~2.99 Slight zest
??3~5.99 The moderate zest
??6.0~8.0 Strong and stimulating
Annotate: the reaction meansigma methods: (erythema forms total points+edema and forms total points)/total number of animals
1.2 exhaust of the influence of red traumatic injury cataplasma single-dose to rabbit intact skin and damaged skin stimulation
Table 7 exhausts the influence that red traumatic injury cataplasma single-dose stimulates the rabbit intact skin
Figure G200910225965XD0000071
The influence that table 8 cataplasma single-dose stimulates the rabbit damaged skin
Figure G200910225965XD0000072
1.3 conclusion: rabbit intact skin and the test of damaged skin dose all do not have erythema, edema forms, and skin irritation intensity shows tentatively that less than 0.5 medicine is to the skin nonirritant.
2. exhaust of the influence of red traumatic injury cataplasma multiple dosing to rabbit intact skin and damaged skin stimulation
4 of new zealand purebred rabbits, medicine-feeding part is a skin of back, after 24h uses the surgical scissors cropping before the medicine, lose hair or feathers with 8% sodium sulfide, about 15cm * the 10cm of area divides into intact skin check plot, damaged skin check plot, intact skin administration district, 4 zones, damaged skin administration district with the back part of animal depilation at random, and each region area is 7.5cm * 5cm, epidermis scratches with knife blade, the degree of being with the oozing of blood in damaged skin check plot and damaged skin administration district.Apply and be subjected to reagent thing, substrate in the administration district, once a day, successive administration 7 days, behind the last coating 24 hours with warm water cleaning medicine and substrate, in 1h, 24h, 72h observes the dermoreaction situation, observes to have or not erythema, edema, protuberance, burnt silly formation etc., and reference standard is tested with acute irritation, dermoreaction intensity to every animal is marked, and observes medicine to the skin irritation situation.
Table 9 exhausts red traumatic injury cataplasma successive administration to rabbit skin irritation situation
Group ??1h ??24h ??48h ??72h
The intact skin check plot ??0 ??0 ??0 ??0
The intact skin medicament region ??0 ??0 ??0 ??0
Group ??1h ??24h ??48h ??72h
The damaged skin check plot ??0 ??0 ??0 ??0
The damaged skin medicament region ??0 ??0 ??0 ??0
Conclusion: the rabbit one or many is coated with after exhausting red traumatic injury cataplasma, skin irritation reactions such as erythema, edema all do not occur, illustrates that this exhausts red traumatic injury cataplasma is safe.
Experimental example 2
The clinical observation that exhausts red traumatic injury cataplasma treatment closed soft tissue injury of the present invention
1, physical data
Select the closed injury of extremity soft tissue, local pain, swelling, handicapped out-patient 200 examples, at 18~60 years old age, the injured time was the object of observation at 4 days with interior case.The course of disease surpasses 4 days, and the injury skin injury merges except fracture, osteofascial compartment syndrome or other the pathological changes persons.
2, primary symptom criterion
Pain: slight, pain perception is arranged, do not influence routine work with movable; Moderate, pain acid is expanded and is felt, can adhere to routine work and life; Severe, sharp ache is difficult to stand, and influences routine work and life.
Swelling: slight, the colour of skin changes, and the swelling degree is higher than normal skin 1mm~3mm; Moderate, the colour of skin changes, and the swelling degree is higher than between normal skin 4mm~6mm; Severe, the colour of skin changes, and as seen smooth bright or livid purple, the swelling degree is higher than normal skin 5mm~10mm.
The functional activity scope: good (+), in more than 1/2 of normal range; In (++), normal range 1/2~1/3 between; Difference (+++), in below 1/3 of normal range.
3, grouping
The object of observation is divided into 2 groups at random.120 examples are organized in treatment, use to exhaust red traumatic injury cataplasma treatment affected part, and matched group 80 examples are used 701 DIEDA ZHENTONG GAO treatment affected part, and once a day, be 15 days the full course of treatment.Two groups of patients' situation is as follows:
Table 10 liang group medication therapentic part distribution situation
The position Treatment group (male 83 examples, women 37 examples)/routine number Matched group (male 55 examples, women 25 examples)/routine number
Elbow joint ??8 ??5
Carpal joint ??15 ??9
Knee joint ??32 ??17
Shank ??11 ??6
Ankle joint ??39 ??27
Foot ??15 ??16
The position Treatment group (male 83 examples, women 37 examples)/routine number Matched group (male 55 examples, women 25 examples)/routine number
Add up to ??120 ??80
4, treatment is analyzed
4.1 criterion of therapeutical effect
Recovery from illness: 1 course of treatment of the drug of topical application, pain, swelling disappear, and the movable function scope is normal;
Produce effects: 1 course of treatment of the drug of topical application, pain, swelling obviously alleviate or disappear, and the movable function scope transfers (+) to by (+++);
Effectively: 1 course of treatment of the drug of topical application, pain, swelling alleviate, and the movable function scope transfers (++) to by (+++);
Invalid: 1 course of treatment of the drug of topical application, local symptom does not have improvement.
4.2, efficacy result judges and efficacy assessment standard that according to primary symptom it is as follows that the therapeutic outcome of two groups of cases is added up respectively:
The comparison of average onset time (d) after the table 11 liang group medication (x ± s)
Symptom and sign Treatment group (n=120) Matched group (n=80) The P value
Pain ??1.45±0.60 ??2.87±0.78 ??<0.01
Swelling ??2.33±0.80 ??3.55±0.70 ??<0.01
Dysfunction ??2.89±0.82 ??4.30±1.41 ??<0.01
The comparison of table 12 liang group transference cure time (d) (x ± s)
Symptom and sign Treatment group (n) Matched group (n) The P value
Pain ??8.90±1.60(120) ??12.98±1.88(80) ??<0.01
Swelling ??9.23±1.95(118) ??11.76±2.14(77) ??<0.01
Dysfunction ??9.38±1.66(108) ??12.05±2.12(53) ??<0.01
Table 13 liang group is soft hinders the total therapeutic outcome of patient relatively
Group The example number Recovery from illness (%) Produce effects (%) Effectively (%) Invalid (%) Total effective rate (%)
The treatment group ??120 ??78(65.0) ??29(24.2) ??10(8.3) ??2(1.7) ??98.3
Matched group ??80 ??12(15.0) ??18(25.0) ??36(45.0) ??12(15.0) ??85.0
Two groups of total effective rates compare, and the treatment group is 98.3%, and matched group is 85.0%, two group and learns statistics by statistics that there is significant difference in P<0.05, two a group total effective rate, illustrates that treatment group total effective rate is apparently higher than matched group.

Claims (10)

1. Jiehong medicine for injuries from falls, it is characterized in that it being the cataplasma of being made by the ethanol extraction concentrated solution and the receptible host material of pharmaceutics of 39~49 parts on Flos Carthami, 39~49 parts in catechu, 39~49 parts of Radix Angelicae Sinensis, 17~27 parts of Alumens, 39~49 parts of Lignum Sappans, 39~49 parts of Aloes, 39~49 parts of Olibanums, 39~49 parts of Benzoinumes, 39~49 parts of Myrrhas, 39~49 parts of Sanguis Draxonis, above-mentioned deal is a weight portion.
2. a kind of Jiehong medicine for injuries from falls according to claim 1, it is characterized in that it being the cataplasma of being made by the ethanol extraction concentrated solution and the receptible host material of pharmaceutics of 44 parts on Flos Carthami, 44 parts in catechu, 44 parts of Radix Angelicae Sinensis, 22 parts of Alumens, 44 parts of Lignum Sappans, 44 parts of Aloes, 44 parts of Olibanums, 44 parts of Benzoinumes, 44 parts of Myrrhas, 44 parts of Sanguis Draxonis, above-mentioned deal is a weight portion.
3. a kind of Jiehong medicine for injuries from falls according to claim 1 is characterized in that described ethanol extraction concentrated solution is that extracting solution is concentrated into 30~40% of medical material weight.
4. a kind of Jiehong medicine for injuries from falls according to claim 3, the weight ratio that it is characterized in that described ethanol extraction concentrated solution and host material is 1: 2.0~5.0.
5. according to claim 1 or 2 or 4 described a kind of Jiehong medicine for injuries from falls, it is characterized in that described host material is to be selected from sodium polyacrylate, carbopol, hypromellose, polyvinylpyrrolidone, gelatin, Kaolin, silica gel, dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, 1, the wherein two or more at least mixture of 2-propylene glycol, tartaric acid, tween, distilled water, glycerol, azone.
6. a kind of Jiehong medicine for injuries from falls according to claim 5, it is characterized in that described host material is to be mixed by weight proportion by following material, 0.01~1 part of 1~5 part of sodium polyacrylate, 1~5 part of carbopol, 1~10 part of Kaolin, 1~10 part in silica gel, 0.01~0.1 part of dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, 1,0.1~1 part of 2-propylene glycol, 0.01~0.1 part in tartaric acid, 10~50 parts of distilled water, 1~10 part of glycerol, 0.1~2 part of azone.
7. according to claim 1 or 2 or 3 described a kind of Jiehong medicine for injuries from falls, it is characterized in that also being added with in the described ethanol extraction concentrated solution unguentum usual auxiliaries of concentrated solution weight 0.1~1%, described unguentum usual auxiliaries is meant at least a in menthol, Mentholum, Borneolum Syntheticum, azone, eucalyptus oil, Oleum Ricini, the methyl salicylate; Described host material is to be mixed by weight proportion by following material, 0.01~1 part of 1~5 part of sodium polyacrylate, 1~5 part of carbopol, 1~10 part of Kaolin, 1~10 part in silica gel, 0.01~0.1 part of dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, 1,0.1~1 part of 2-propylene glycol, 0.01~0.1 part in tartaric acid, 10~50 parts of distilled water, 1~10 part of glycerol, 0.1~2 part of azone.
8. the preparation method of the described a kind of Jiehong medicine for injuries from falls of claim 6, it is characterized in that comprising the preparation of (1) ethanol extraction concentrated solution, (2) preparation of the preparation of host material and (3) cataplasma, wherein the preparation method of (1) ethanol extraction concentrated solution is to get Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis to be ground into coarse powder, adopting percolation, make solvent with 60~80% ethanol, is slowly percolation of 1~3ml/min by percolation speed, the ethanol that adds 5 times of amounts of medical material weight is altogether collected percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, with 60~80% alcohol dipping of above-mentioned percolate and 3 times of amounts of medical material 30 days, filter, filtrate decompression is concentrated into 30~40% the concentrated solution that weight is medical material weight; (2) preparation method of host material is that dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, adds sodium polyacrylate, fully grinds well; Tartaric acid is dissolved in the part distilled water, and gradation joins in the said mixture, stirs; The carbopol adding distil water is dissolved into clear solution, adds again in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs promptly; (3) preparation method of cataplasma is to extract concentrated solution and the host material mixed by 1: 2.0~5.0, to stir 10~30 minutes, and coating covers upper protective film, section, and packing is promptly.
9. the preparation method of the described a kind of Jiehong medicine for injuries from falls of claim 7, it is characterized in that comprising the preparation of (1) ethanol extraction concentrated solution, (2) preparation of the preparation of host material and (3) cataplasma, wherein the preparation method of (1) ethanol extraction concentrated solution is to get Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis to be ground into coarse powder, adopting percolation, make solvent with 60~80% ethanol, is slowly percolation of 1~3ml/min by percolation speed, the ethanol that adds 5 times of amounts of medical material weight is altogether collected percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, with 60~80% alcohol dipping of above-mentioned percolate and 3 times of amounts of medical material 30 days, filter, filtrate decompression is concentrated into 30~40% the concentrated solution that weight is medical material weight, adds the unguentum usual auxiliaries at last and stirs; (2) preparation method of host material is that dihydroxyaluminum aminoacetate, ethylenediaminetetraacetic acid, glycerol and Kaolin is evenly mixed, adds sodium polyacrylate, fully grinds well; Tartaric acid is dissolved in the part distilled water, and gradation joins in the said mixture, stirs; The carbopol adding distil water is dissolved into clear solution, adds again in the said mixture, stir; Add azone, 1 at last, the 2-propylene glycol stirs promptly; (3) preparation method of cataplasma is to extract concentrated solution and the host material mixed by 1: 2.0~5.0, to stir 10~30 minutes, and coating covers upper protective film, section, and packing is promptly.
10. according to Claim 8 or the preparation method of 9 described a kind of Jiehong medicine for injuries from falls, the preparation method that it is characterized in that described ethanol extraction concentrated solution is to get Flos Carthami, Lignum Sappan, Radix Angelicae Sinensis to be ground into coarse powder, adopt percolation, make solvent with 60~80% ethanol, by percolation speed is slowly percolation of 1~3ml/min, the ethanol that adds 5 times of amounts of medical material is altogether collected percolate; All the other catechu, Alumen, Aloe, Olibanum, Benzoinum, Myrrha, Sanguis Draxonis seven flavors are ground into coarse powder, add twice of ultrasonic Treatment of 60~80% ethanol of 3 times of amounts of medical material, two hours for the first time, one hour for the second time, filter, filtrate and above-mentioned percolate merge and be evaporated to 30~40% the concentrated solution that weight is medical material weight, or add the unguentum usual auxiliaries and stir.
CN200910225965XA 2009-06-03 2009-11-21 Brown red medicament for treating traumatic injuries and preparation method thereof Active CN101703667B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN200910225965XA CN101703667B (en) 2009-06-03 2009-11-21 Brown red medicament for treating traumatic injuries and preparation method thereof

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN200910039950.4 2009-06-03
CNA2009100399504A CN101564487A (en) 2009-06-03 2009-06-03 Jiehong medicine for injuries from falls and preparation method thereof
CN200910225965XA CN101703667B (en) 2009-06-03 2009-11-21 Brown red medicament for treating traumatic injuries and preparation method thereof

Publications (2)

Publication Number Publication Date
CN101703667A true CN101703667A (en) 2010-05-12
CN101703667B CN101703667B (en) 2012-10-03

Family

ID=42373965

Family Applications (1)

Application Number Title Priority Date Filing Date
CN200910225965XA Active CN101703667B (en) 2009-06-03 2009-11-21 Brown red medicament for treating traumatic injuries and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101703667B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103071134A (en) * 2013-01-28 2013-05-01 广西玉林大金大药业有限公司 External preparation for treating rheumatic arthrodynia and traumatic pain and swelling and preparation method thereof
CN104623167A (en) * 2015-01-19 2015-05-20 杨怀强 Traditional Chinese medicine plaster for treating neck-shoulder and lumbocrural pain
CN105251037A (en) * 2015-11-19 2016-01-20 赵岱 Bandage for treating scalds and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103071134A (en) * 2013-01-28 2013-05-01 广西玉林大金大药业有限公司 External preparation for treating rheumatic arthrodynia and traumatic pain and swelling and preparation method thereof
CN104623167A (en) * 2015-01-19 2015-05-20 杨怀强 Traditional Chinese medicine plaster for treating neck-shoulder and lumbocrural pain
CN104623167B (en) * 2015-01-19 2018-12-04 杨怀强 It is a kind of for treating the traditional Chinese medicine plaster of neck-shoulder pain, lumbago and leg pain
CN105251037A (en) * 2015-11-19 2016-01-20 赵岱 Bandage for treating scalds and preparation method thereof

Also Published As

Publication number Publication date
CN101703667B (en) 2012-10-03

Similar Documents

Publication Publication Date Title
EP2362777B1 (en) Use of pharmaceutical compositions in preparing pharmaceuticals for treating diabetic ulcer
CN104306358B (en) Antipruritic scar liniment of dispelling
CN101773551B (en) External-use medicine composition of traditional Mongolian medicine for curing soft tissue injury
CN108186711A (en) Promote the pharmaceutical composition of wound healing
CN101703667B (en) Brown red medicament for treating traumatic injuries and preparation method thereof
CN101564487A (en) Jiehong medicine for injuries from falls and preparation method thereof
CN110974861A (en) Blumea balsamifera oil liposome
CN105497537A (en) Medicine composition with skin whitening and tendering functions and preparing method thereof
CN115381912A (en) External traditional Chinese medicine compound preparation for reducing cancer pain and preparation method thereof
CN101744873A (en) Externally used liquid preparation containing only iridoid glycoside and application thereof
CN108403932A (en) A kind of Chinese medicine compound prescription external preparation and its preparation method and application for treating steroid dependent dermatitis
US11154583B2 (en) Composition and method of skin relief cream useful for eczema, psoriasis, lipoma, burn wounds, scars, keloids, shingles, dry skin disorders, and skin allergies
CN110721274B (en) External antipruritic and preparation method thereof
ES2932359T3 (en) Formulation based on N-acetylcysteine and urea for the treatment of dermatological disorders
CN114177160A (en) Foot patch for treating dental ulcer and preparation method thereof
CN111759905A (en) Cataplasm for treating osteoarthritis and preparation method thereof
CN1251753C (en) Externally-applied medicine composition for treating mastoproliferation and its prepn
CN114246926B (en) External traditional Chinese medicine composition for treating skin warts and preparation method and application thereof
CN111658716A (en) Hydrogel magnetic therapy traditional Chinese medicine plaster and preparation method thereof
CN1171628C (en) Ointment for eliminating macula and its preparation method
CN114886981B (en) Traditional Chinese medicine composition and application thereof in preparation of neck-shoulder lumbocrural pain medicines
CN108853293B (en) Compound essential oil for treating hemorrhoids and preparation method and use method thereof
CN101940652A (en) Chinese medicinal liniment for treating psoriasis, multiple kinds of stubborn dermatitis and pruritus
CN101926859B (en) Chinese medicinal composition
CN109806321B (en) A Chinese medicinal composition, its preparation method and application in preparing medicine for treating trauma

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee

Owner name: FENG LIAOXING (FOSHAN) PHARMACEUTICAL CO., LTD. OF

Free format text: FORMER NAME: FOSHAN FENGLIAOXING PHARMACEUTICAL CO., LTD.

CP01 Change in the name or title of a patent holder

Address after: Chancheng District of Guangdong city in Foshan Province, the 528000 Florida Highway No. 35 of

Patentee after: Sinopharm group (Foshan) Pharmaceutical Co., Ltd.

Address before: Chancheng District of Guangdong city in Foshan Province, the 528000 Florida Highway No. 35 of

Patentee before: Foshan Fengliaoxing Pharmaceutical Co., Ltd.