CN1935267A - Wound surface active repair material - Google Patents
Wound surface active repair material Download PDFInfo
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- CN1935267A CN1935267A CNA2005101049162A CN200510104916A CN1935267A CN 1935267 A CN1935267 A CN 1935267A CN A2005101049162 A CNA2005101049162 A CN A2005101049162A CN 200510104916 A CN200510104916 A CN 200510104916A CN 1935267 A CN1935267 A CN 1935267A
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- wound surface
- repair material
- surface active
- wound
- active repair
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/18—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing inorganic materials
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/28—Polysaccharides or their derivatives
Abstract
The present invention relates to a material for repairing surface of wound. It is mainly formed from the following components: hyaluronic acid, silicone dioxide, sodium oxide, calcium oxide and phosphorus pentoxide.
Description
Technical field
The present invention relates to a kind of vulnerary material, be meant especially, vulnerary Wound surface active repair material.
Background technology
In the prior art, can be divided into traditional dressing, the dressing of animal class, synthetic dressing, biological dressing, medicines dressing and the fixing dressing of using for curing the dressing that wound adopted according to material and purposes, research about dressing has obtained very big progress in recent ten years, but the dressing of prior art, 1. can not well absorb wound exudate, safeguard the wound surface temperature,, initiatively promote wound healing for wound healing provides good local environment; 2. can not safeguard blood circulation and oxygen branch that wound is an amount of, suppress blood vessel endothelium swelling, and hindered angiogenic growth; 3. the wound that is difficult to heal that wound healing after dressing particularly of the prior art heals for treatment diabetic ulcer, decubital ulcer, empyrosis gynecological cervical erosion, leprosy and unknown cause cause, its treatment effect is poor, and cure rate is very low; The wound healing that prior art causes slowly reaches obstinate, gives the patient no matter on the Cong Jing Zhong, has still all brought huge misery on the health, and the while has also been strengthened the expenditure of medical expense, has brought many inconvenience to the patient.
Summary of the invention
The purpose of this invention is to provide a kind of Wound surface active repair material, by the repair materials among the present invention, can effectively promote angiogenic growth, improve the damage local microcirculation, promote effects such as cell proliferation and growth factor expression, promote wound healing, reduce cicatrization, to remedy the deficiencies in the prior art.
Wound surface active repair material of the present invention, mainly form by following composition:
Hyaluronic acid, silicon dioxide, sodium oxide, calcium oxide, phosphorus pentoxide.
Described main component is formed by following weight ratio:
Hyaluronic acid 3-40%;
Silicon dioxide 20-45%;
Sodium oxide 6-20%;
Calcium oxide 8-25%;
Phosphorus pentoxide 2-7%.
The composition stable of the Wound surface active repair material that the present invention proposes, with silicon dioxide, sodium oxide, calcium oxide, mix after pulverize with phosphorus pentoxide, its particle diameter is not more than 300um, and then and the Wound surface active repair material made after being mixed in proportion of hyaluronic acid, can make powdery, paste and bolt shape by reprocessing.
Wound surface active repair material of the present invention can be used for treating diabetic ulcer decubital ulcer pressure ulcer, skin and mucosal ulcer and the circumscribed II degree of erosive pathological changes III degree burn and scald, the wound surface that various operations and surgery cause, the wound surface that can not sew up the I phase, the operative incision of failing on schedule to heal, gynecological's cervical erosion, the wound healing after the leprosy healing, the wound that is difficult to heal that unknown cause causes.
One embodiment of the present of invention, its main component is formed by following weight ratio:
Hyaluronic acid 30%;
Silicon dioxide 33%;
Sodium oxide 16%;
Calcium oxide 18%;
Phosphorus pentoxide 3%.
The Wound surface active repair material that the present invention relates to, because it has unique surface activity, when it contacts with the soft tissue wound surface, can improve local oxygen and press and pH value, and form stronger surface negative charge, adsorbing fiber albumen, collagen protein and cell, it can promote the quick formation of calcium and phosphorus layer, stablizes these albumen and cell in wound surface, thereby promotes the healing of wound surface.For effect and the effect of verifying above-mentioned Wound surface active repair material, patent applicant of the present invention has carried out clinical verification in an Affiliated Hospital of medical university of China after the approval of the relevant department of country.
Now clinical observation result is summarized as follows:
1. case is selected:
(1) case inclusion criteria
1. the mucocutaneous or soft tissue ulcers sexually transmitted disease (STD) change of indication: A; The mucocutaneous erosive pathological changes of B; The traumatic wound surface that C can not sew up the I phase, the operative incision of failing on schedule to heal; Circumscribed II degree and III degree are scalded or burn wound;
2. the age is 12-85 year, outpatient service and inpatient all can, the men and women does not limit.
(2) case culling level
1. observation period less than 4 all persons;
2. use other method person of changing dressings in the observation period instead.
2. test method:
(1) MethodsThe cases enrolled is divided into test group and matched group, two groups of case ages, the state of an illness and wound surface situations are similar.The case that a plurality of wound surface are arranged can select a wound surface to treat observation, and other wound surface method is routinely changed dressings, and can adopt own control.
(2) wound surface is handled
1. test group: according to a conventional method wound surface is carried out disinfection, remove dirt and slough, simultaneously coated with Wound surface active repair material, every day or change every other day once; Can put into insulin in the diabetics wound surface, other patient takes the circumstances into consideration to put into gentamycin according to the wound surface situation, or the saline soak, or the ointment ribbon gauze drain etc.; After first with material 72 hours, 1 week, 2 weeks, 3 weeks, respectively wound surface was assessed in 4 weeks.
2. matched group: carry out as stated above not adding Wound surface active repair material by medicine, same test group of wound surface evaluation time.
3. observation period: 4 weeks.
4. viewing duration can not swash incarnant special medicine for external use with other system, but can be according to circumstances to the suitable debridement of wound surface.
3. observation index
(1) wound surface exudate: do not have to divide a secret thing 0, a little exudate+, obvious exudate ++.
(2) wound surface granulation tissue: the growth of no meat, the dark atrophy of granulation color or pale edema, that the granulation color is red, fine particulate touches is easily hemorrhage.
(3) the granulation speed of growth: calculate the granulation speed of growth according to the wound surface change in depth, and represent with percentage ratio.
(4) wound healing rate: calculate healing rate according to the wound surface area degree that reduces, represent with percentage ratio.
(5) respectively look into one time routine blood test, hepatic and renal function, plasma protein and blood glucose when finishing with reaching before the material to observe.
4. curative effect determinate standard: curative effect is divided into recovery from illness, produce effects, effective, invalid level Four.
(1) recovery from illness: wound surface heals fully;
(2) produce effects: wound surface row secretions, granulation is fresh, and the speed of growth and healing rate are greater than 60%.
(3) effective: a little oozes out wound surface, and granulation is fresh, the speed of growth and healing rate 20-60%.
(4) invalid: wound surface oozes out obviously, and no granulation growth or granulation are stale, and the speed of growth and healing rate are less than 20%.
5. untoward reaction criterion
Viewing duration, with patient plant the main suit unusually by certainly relevant, may be relevant, have nothing to do certainly, may have nothing to do, can't estimate Pyatyi evaluation.
6. result of the test
(1) the selected situation of case
Selected case 50 examples of observing, test group 43 examples, wherein 4 weeks of 2 example observation period less thaies and eliminate actual test group 41 examples of finishing, matched group 7 examples.
Test group 41 examples, 49.9 years old mean age; Matched group 7 examples, 48.7 years old mean age.Two groups of case basic conditions see Table 1 to table 5.
Table 1 a liang group case sex distributes
| Group | The male | The women | The total number | ||
| Number | Ratio | Number | Ratio | ||
| Test group | 30 | 73.2％ | 11 | 26.8％ | 41 |
| Matched group | 5 | 71.4％ | 2 | 28.6％ | 7 |
Table 2 liang group case age distribution
| Age | 12- | 21- | 31- | 41- | 51- | 61- | 71- | 81- |
| Test group | 3 | 3 | 6 | 9 | 8 | 7 | 2 | 3 |
| Matched group | 2 | 2 | 1 | 2 |
Table 3 liang group case protopathy is because of analyzing
| Protopathy | Test group | Matched group |
| Pemphigus also infects | 6 | 1 |
| Vasculitis | 2 | |
| Diabetes | 6 | 2 |
| Operation or non-healing wounds | 5 | 2 |
| Drug allergy | 5 | 1 |
| Scald | 4 | |
| Decubital ulcer | 3 | |
| Electric burn | 2 | |
| Infect | 1 | |
| Eczema | 1 | |
| Hot crush injury | 1 | 1 |
| Systemic lupus erythematosus (sle) | 1 | |
| Agnogenio | 4 |
The wound surface size relatively before the table 4 liang group treatment
| Wound surface area (cm 2) | The wound surface degree of depth (cm) | |
| Test group | 22.97 | 0.75 |
| Matched group | 10.75 | 0.55 |
Table 5 liang group case wound surface bacteria cultivation results
| Test group | Matched group | |
| Gold Portugal bacterium | 4 | 2 |
| Enterococcus | 2 | 1 |
| The G+ corynebacterium | 1 | |
| Hemolytic streptococcus | 1 | |
| Bacillus pyocyaneus | 1 | |
| Enterobacter cloacae | 1 | |
| Epidermis Portugal coccus | 4 | 2 |
Table 6 wound surface exudate relatively
| Before the test | After the test | |||||
| 72 hours | 1 week | 2 weeks | 3 weeks | 4 weeks | ||
| + ++ add up to | + ++ add up to | + ++ add up to | + ++ add up to | + ++ add up to | + ++ add up to | |
| Test group | 17 23 97.6％ | 21 12 80.5％ | 19 4 62.2％ | 11 0 50％ | 6 0 35.3％ | 4 0 50％ |
| Matched group | 1 6 100％ | 1 6 100％ | 2 5 100％ | 6 0 85.7％ | 4 1 83.3％ | 3 0 75％ |
Granulation tissue situation in table 7 wound surface
| Project | Test group | Matched group | ||
| Before the test | +(％) | 9(21.9) | 0(0) | |
| ++(％) | 2(4.9) | 2(28.6) | ||
| After the test | 72 hours | +(％) | 14(34.1) | 1(14.3) |
| ++(％) | 9(21.9) | 2(28.6) | ||
| 1 week | +(％) | 8(21.6) | 3(42.9) | |
| ++(％) | 24(64.9) | 1(14.3) | ||
| 2 weeks | +(％) | 5(22.7) | 5(71.4) | |
| ++(％) | 17(77.3) | 2(28.6) | ||
| 3 weeks | +(％) | 3(18.8) | 2(33.3) | |
| ++(％) | 13(81.3) | 4(66.6) | ||
| 4 weeks | +(％) | 1(12.5) | 2(66.7) | |
| ++(％) | 7(87.5) | 1(33.3) |
The table 8 wound surface granulation tissue speed of growth relatively
| 72 hours | 1 week | 2 weeks | 3 weeks | 4 weeks | |||||||
| n | ％ | n | ％ | n | ％ | n | ％ | n | ％ | ||
| Test group | ≥ 20％ | 11 | 26.8 | 36 | 87.8 | 35 | 97.2 | 19 | 100 | 17 | 100 |
| ≥ 60％ | 0 | 0 | 1 | 14.3 | 6 | 85.7 | 6 | 785.7 | 6 | 100 | |
| Matched group | ≥ 20％ | 0 | 0 | 1 | 14.3 | 6 | 85.7 | 6 | 85.7 | 6 | 100 |
| ≥ 60％ | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 42.9 | 4 | 66.7 | |
(2) therapeutic effect
1. wound surface exudate: medication after 72 hours the wound surface exudate promptly reduce, 1 week the back obviously reduce, contrast effect sees Table 6.
2. wound surface granulation tissue situation
72 hours wound surface granulation tissuies of medication begin growth, and the fresh granulation tissue in 1 week back increases, and relatively sees Table 7 with matched group.
3. the granulation tissue speed of growth
72 hours wound surface granulation tissuies of medication begin growth, and the back speed of growth quickening of 1 week significantly better than matched group, sees Table 8.
4. wound healing rate
Use Wound surface active repair material wound surface area after 72 hours and begin to dwindle, dwindle in 2 weeks fastest, 2 week the back speed tend towards stability.Matched group wound surface area when 1 week begins to dwindle, and dwindles quickening during 3 weeks, reaches the test group level during 4 weeks, sees Table 9.
Table 9 wound surface area dwindles situation
| 72 hours | 1 week | 2 weeks | 3 weeks | 4 weeks | |||||||
| n | ％ | n | ％ | n | ％ | n | ％ | n | ％ | ||
| Test group | ≥ 20％ | 13 | 31.7 | 26 | 63.4 | 32 | 88.9 | 18 | 90.0 | 17 | 100 |
| ≥ 60％ | 1 | 2.4 | 13 | 31.7 | 22 | 61.1 | 12 | 60.0 | 11 | 64.7 | |
| Matched group | ≥ 20％ | 0 | 0 | 2 | 28.6 | 7 | 100 | 7 | 100 | 6 | 100 |
| ≥ 60％ | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 42.9 | 4 | 66.7 | |
5. clinical efficacy
By treating criterion in the testing program, test group accounts for 46.3% when cure rate accounted for for 9.8%, 2 week during 1 week, and other has a customary II phase to sew up the back recovery from illness, accounts for 75.6% when accounting for for 56.1%, 4 week during 3 weeks.Matched group is all not healings of wound surface in 2 weeks, account for 42.9 when cure rate accounted for for 14.3%, 4 week during 3 weeks, are starkly lower than test group, and by effective percentage=recovery from illness+produce effects, two groups of total effectses see Table 10.
(3) untoward reaction situation
This group case is not found serious adverse reaction.Local pain occurs after only having 1 routine foreskin stain infections patient with Wound surface active repair material, and, do not have other untoward reaction along with the part is reduced and alleviated with the Wound surface active repair material amount.Laboratory checking index before and after the test, Non Apparent Abnormality changes, and sees Table 11.
Table 10 liang group clinical efficacy relatively
| Recovery from illness | Produce effects | Effectively | Invalid | Total effects | |||||
| n | ％ | n | ％ | n | ％ | n | ％ | Recovery from illness+produce effects | |
| Test group | 31 | 75.6 | 3 | 7.3 | 6 | 14.6 | 0 | 0 | 82.9％ |
| Matched group | 3 | 42.9 | 2 | 28.6 | 2 | 28.6 | 0 | 0 | 71.4％ |
The present invention proves by experiment, is Wound surface active repair material of the present invention, can promote the healing of soft tissue wound surface, and total effective rate is 82.9%, and the wound surface cure rate is 75.6%, and obvious effective rate is 7.3%; Wound surface active repair material can reduce wound surface energy exudate significantly, promotes the granulation tissue growth, adopts this material to have the case wound surface granulation tissue more than 64.9% fresh after one week, and the case more than 69.4% was arranged after 2 weeks, and the granulation speed of growth is more than 60%; In effect, account for 75.6% when accounting for for 56.1%, 4 week when accounting for for 46.3%, 3 week when cure rate was 9.8%, 2 week during 1 week, significantly better than the conventional change dressing of matched group to the soft tissue wound healing;
The present invention finds no toxic and side effects in experiment, Wound surface active repair material of the present invention has significant therapeutic effect to the healing that promotes the soft tissue wound surface, and without any side effects.
Model case 1
Patient XXX woman 45 years old suffers from pemphigus vulgaris, and half a year, the whole skin erythema plays vesicle companion erosion, ooze out obviously, and visible oral mucosa, the gums position is the rotten to the corn face companion of lamellar infection on a large scale, and sharp ache can not be taken food, and is difficult to stand; Be coated with Wound surface active repair material outward, once a day, pain relief after the week, the wound surface granulation tissue is fresh, oozes out minimizing, and skin lesion obviously dwindles, and pain obviously alleviate after two weeks, the healing of wound surface bone dry.
Table 11 lab testing result
| Project | Test group | Matched group | |
| Before the test | Hb | 129.2 | 117 |
| WBC | 8.5×10 9 | 5.5×10 9 | |
| ALT | 31.8 | 23.9 | |
| BUN | 5.6 | 4.9 | |
| Cr | 77 | 71.7 | |
| T | 65.8 | 59 | |
| A | 39.4 | 37 | |
| G | 6.5 | 6.8 | |
| After the test | Hb | 126.1 | 111.7 |
| WBC | 7.8×10 9 | 5.9×10 9 | |
| ALT | 35.3 | 29 | |
| BUN | 5.9 | 5.3 | |
| Cr | 77.4 | 68.6 | |
| T | 67.7 | 58 | |
| A | 4.03 | 36.1 | |
| G | 5.4 | 4.9 |
Model case 2
Patient XXX male 54 years old is because of heating, the red and swollen first quarter moon in back, and quiet antibiotic, poor effect was in hospital in February, 1998, and there is 18 * 10cm at the back of having a medical check-up when being admitted to hospital
2Size is red and swollen, fluctuation, chemical examination leukocyte 19.1 * 10
9/ L, fasting glucose 13.5mmol/L, diagnosing diabetes and back carbuncle, give incision and drainage, begin 5 days more purulences that are of exudate, routine is changed dressings to add and is used Wound surface active repair material, and the beginning exudate reduced in the 6th day, simultaneously with coating Wound surface active repair material behind the hydrogen peroxide flushing wound surface, change every day once, patient's wound surface freshen up, the granulation tissue growth is very fast, interrupted suture after two weeks, 4 all produce effects are taken out stitches and are left hospital.
Model case 3
Patient XXX man 12 years old went to a doctor after 6 hours because of electrically contacting wound in 98 years, and admission examination, the right hand are slapped surface, the 5th head of metacarpal bone position the III degree 3 * 4cm of burn wound
2, the right leg lateral surface III degree 6 * 12cm of burn wound
2, the right parietotemporal region scalp of head III degree burn, the row right hand palm, right leg skin grafting surgery after 6 days, head III degree wound surface is cut crust, wound surface 11 * 20cm
2, reach periosteum deeply, skull exposure 5 * 6cm is arranged
2Ooze out obviously, postoperative beginning in 1 day external Wound surface active repair material, look the every 1-3 of wound surface situation days conversion materials 1 time, exposing the cranium edge after 1 week has a little granulation tissue growth, and exudate obviously reduces after 2 weeks, pH value raises, the granulation tissue rate of growth reaches 37.5%, and wound healing rate 22.73% is because of the water injection rate deficiency of heeling-in dilator, so the scalp wound surface continues to use Wound surface active repair material, the granulation tissue rate of growth reaches 100% after 4 weeks.
Model case 4
Patient XXX, the woman, 73 years old, be in hospital in 19 days because of the cerebral hemorrhage postoperative, the patient was found stupor in the bathroom by the people before 22 days, and back shoulder and skin of buttock are scalded and pressurized festers, the back routine of being admitted to hospital is changed dressings, but wound surface is not healed always, after change routine into and change dressings and add the SDAg external application, oily yarn drain, poor effect, begin the external Wound surface active repair material and change dressings after being admitted to hospital 30 days, healing speed is obviously accelerated, and right shoulder wound surface is not dark, 4 weeks i.e. healing fully, the buttocks wound surface is darker, and the granulation color is dark, and it is fresh to add the routine 1 week back granulation tissue of changing dressings with Wound surface active repair material, growth is very fast, wound healing reaches more than 85% after 4 weeks, changes dressings significantly better than conventional method, and does not have any untoward reaction.
Model case 5
Patient XXX, the man, 65 years old, examine over 2 months because of the diabrosis of foreskin glans penis skin, have a medical check-up: the glans penis dorsal part has a 0.8 * 1.5cm
2Root has a 2.0 * 0.5cm in the ulcer, foreskin
2Ulcer, ulcer degree of depth 0.2cm once used 1: antibiotic medicine such as 5000PP washout and oral PPA, DeGrain, after use Wound surface active repair material instead, every day 1 time, exudate disappears after 3 days, and wound surface begins to dwindle, granulation tissue is fresh during 1 week, ulcer healed fully when wound surface dwindled for 50%, 2 week, did not have any untoward reaction.
Wound surface active repair material of the present invention, can stimulate epidermis cell and form fibrocellular dividing a word with a hyphen at the end of a line, propagation, differentiation, thereby satisfied the requirement that quick synthetic substrate and epidermis cover, reduce the newborn circulation resistance of repairing blood vessel, hinder granulocytic deposition, suppress blood vessel endothelium swelling, reduce cell debris in endovascular accumulation, reduce microvascular blood resistance and thromboembolism incidence rate greatly, improve local microcirculation thereby play, tissue repair, have the effect of the angiogenic growth of promotion, the formation of blood vessel is for the survival and the form of regenerating tissues, important function has been played in further differentiation on the function; Wound surface active repair material, can be used for treating diabetic ulcer, decubital ulcer, pressure ulcer, the wound surface that skin and mucosal ulcer and erosive pathological changes, circumscribed II degree and III degree burn and scald, various operation and wound cause, the wound surface that can not sew up the I phase, the wound that is difficult to heal that wound healing, the unknown cause after the operative incision of failing on schedule to heal, gynecological's cervical erosion, the leprosy healing causes.Second embodiment of the present invention, its main component is formed by following weight ratio:
Hyaluronic acid 3%
Silicon dioxide 45%;
Sodium oxide 20%;
Calcium oxide 25%;
Phosphorus pentoxide 7%.
Clinical observation result is as follows
Model case 6
60 years old man of patient XXX causes right leg ulcer, area 2 * 12cm owing to suffer from diabetes
2, degree of depth 0.5cm is through using the product of above prescription, the back recovery from illness of 6 week of treatment.
Model case 7
44 years old man of patient XXX causes ulcer of scrotum, area 3 * 1cm owing to take Coritab
2, degree of depth 0.3cm, the course of disease 3 days, 4 week of the product of prescription treatment back recovery from illness more than using.
Model case 8
37 years old man of patient XXX is because drug allergy causes the glans penis skin erosion, area 3 * 3cm
2, degree of depth 0.2cm is with product recovery from illness after 4 weeks of treatment of above prescription.
The 3rd embodiment of the present invention, its main component is formed by following weight ratio:
Hyaluronic acid 40%
Silicon dioxide 28%;
Sodium oxide 20%;
Calcium oxide 10%;
Phosphorus pentoxide 2%.
Clinical observation result is as follows:
Model case 9
66 years old man of patient XXX is because diabetes cause left external malleolus ulcer, area 3 * 4cm
2, degree of depth 15cm, the course of disease 3 months is with 6 week of the product treatment back recovery from illness of above prescription.
Model case 10
The glans penis erosion that patient XXX 34 men cause owing to drug allergy, area 1.5 * 2.0cm
2, degree of depth 0.1cm in 1 week of the course of disease, uses 4 week of the product treatment back recovery from illness of above prescription.
Model case 11
Patient XXX 65 years old man is owing to the agnogenio glans penis ulcer that occurs, pathological changes 2 places, area 1.5 * 0.6cm
2With 2.0 * 0.5cm
2, degree of depth 0.2cm uses 4 week of the product treatment back recovery from illness of above prescription.
Model case 12
The back scald causes right shoulder ulcer, area 3 * 5cm to patient XXX 73 woman because accident is fainted
2, degree of depth 1cm, the course of disease 54 days is used the product treatment back 6 week recovery from illness of above prescription.
Wound surface active repair material of the present invention, it can make Powdered, paste and bolt shape, and that makes Powderedly is to require no macroscopic impurity in the white fine powder end; Paste is white, and is tasteless; The bolt shape is white duckbill bolt.
Claims (4)
1. Wound surface active repair material, mainly form by following composition:
Hyaluronic acid, silicon dioxide, sodium oxide, calcium oxide, phosphorus pentoxide.
2. Wound surface active repair material according to claim 1 is characterized in that: described main component is formed by following weight ratio:
Hyaluronic acid 3-40%;
Silicon dioxide 20-45%;
Sodium oxide 6-20%;
Calcium oxide 8-25%;
Phosphorus pentoxide 2-7%.
3. Wound surface active repair material according to claim 1 is characterized in that: the form of this material is powdery, paste or bolt shape.
4. Wound surface active repair material according to claim 1 and 2, it is characterized in that: the silicon dioxide in this repair materials, sodium oxide, calcium oxide, phosphorus pentoxide are mixed after pulverize, its particle diameter is not more than 300um, and then and the Wound surface active repair material made after being mixed in proportion of hyaluronic acid.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005101049162A CN100502953C (en) | 2005-09-22 | 2005-09-22 | Wound surface active repairing material |
| PCT/CN2006/002459 WO2007033591A1 (en) | 2005-09-22 | 2006-09-20 | Active prosthetic material for wounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005101049162A CN100502953C (en) | 2005-09-22 | 2005-09-22 | Wound surface active repairing material |
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| Publication Number | Publication Date |
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| CN1935267A true CN1935267A (en) | 2007-03-28 |
| CN100502953C CN100502953C (en) | 2009-06-24 |
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| CNB2005101049162A Active CN100502953C (en) | 2005-09-22 | 2005-09-22 | Wound surface active repairing material |
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| CN (1) | CN100502953C (en) |
| WO (1) | WO2007033591A1 (en) |
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| CN104258453A (en) * | 2014-09-24 | 2015-01-07 | 湖北华中医用材料有限公司 | Raw material composition of active wound repair material and preparation method of raw material composition |
| CN104324410A (en) * | 2014-09-26 | 2015-02-04 | 湖北华中医用材料有限公司 | Raw material composition of multi-component active wound repair material and preparation method |
| CN105169458A (en) * | 2015-09-25 | 2015-12-23 | 胡方 | Biological activity mineral substance material and application of biological activity mineral substance material to soft tissue anabrosis and long-time erosion wound cell regeneration and melanoma restraining |
| CN109513037A (en) * | 2018-11-14 | 2019-03-26 | 华中科技大学同济医学院附属协和医院 | A kind of submucous layer of small intestine Wound dressing of loaded mesoporous bio-vitric |
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| US5604200A (en) * | 1994-05-02 | 1997-02-18 | Taylor-Mccord; Darlene | Wound therapeutic mixture containing medical grade hyaluronic acid and tissue culture grade plasma-fibronectin in a delivery system that creates a moist environment which simulates in utero healing |
| US6517863B1 (en) * | 1999-01-20 | 2003-02-11 | Usbiomaterials Corporation | Compositions and methods for treating nails and adjacent tissues |
| US6262020B1 (en) * | 2000-02-15 | 2001-07-17 | Alphamed Pharmaceuticals Corp. | Topical wound therapeutic compositions |
| CN1136012C (en) * | 2000-08-07 | 2004-01-28 | 黄玲惠 | Wound dressing and its prepn. |
| US20040265268A1 (en) * | 2001-08-18 | 2004-12-30 | Deepak Jain | Compositions and methods for skin rejuvenation and repair |
-
2005
- 2005-09-22 CN CNB2005101049162A patent/CN100502953C/en active Active
-
2006
- 2006-09-20 WO PCT/CN2006/002459 patent/WO2007033591A1/en active Application Filing
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103260628A (en) * | 2010-10-07 | 2013-08-21 | 成功大学 | Use of hyaluronan for promoting angiogenesis |
| CN104258453A (en) * | 2014-09-24 | 2015-01-07 | 湖北华中医用材料有限公司 | Raw material composition of active wound repair material and preparation method of raw material composition |
| CN104324410A (en) * | 2014-09-26 | 2015-02-04 | 湖北华中医用材料有限公司 | Raw material composition of multi-component active wound repair material and preparation method |
| CN105169458A (en) * | 2015-09-25 | 2015-12-23 | 胡方 | Biological activity mineral substance material and application of biological activity mineral substance material to soft tissue anabrosis and long-time erosion wound cell regeneration and melanoma restraining |
| CN109513037A (en) * | 2018-11-14 | 2019-03-26 | 华中科技大学同济医学院附属协和医院 | A kind of submucous layer of small intestine Wound dressing of loaded mesoporous bio-vitric |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007033591A1 (en) | 2007-03-29 |
| CN100502953C (en) | 2009-06-24 |
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