CN102940677B - Medicine composition for treating diabetic foot - Google Patents

Medicine composition for treating diabetic foot Download PDF

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Publication number
CN102940677B
CN102940677B CN201210428581.XA CN201210428581A CN102940677B CN 102940677 B CN102940677 B CN 102940677B CN 201210428581 A CN201210428581 A CN 201210428581A CN 102940677 B CN102940677 B CN 102940677B
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parts
diabetic foot
medicine
treatment
pharmaceutical composition
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CN201210428581.XA
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CN102940677A (en
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李文军
张太君
张玲
成建国
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Chengdu Yilukang Medical Technology & Service Co Ltd
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Chengdu Yilukang Medical Technology & Service Co Ltd
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Abstract

The invention discloses a medicine composition for treating diabetic foot, comprising Rhodiola sachalinensis, Eupolyphaga, aspongopus and liquorice. The medicine composition disclosed herein has low price and no side effect.

Description

The pharmaceutical composition for the treatment of diabetic foot
Technical field
The present invention relates to a kind of medicine for the treatment of diabetes, relate to specifically a kind of pharmaceutical composition for the treatment of diabetic foot.
Background technology
Diabetes are that China's sickness rate is high, endanger one of serious epidemic diseases.According to statistics, the mortality rate of diabetic complication is only second to cardiovascular diseases, cerebrovascular and tumor, occupies the 4th.Diabetes mellitus in China patient quantity has approached 4,000 ten thousand people, occupies third place in the world, compares with 0.7% of the eighties in 20th century, has increased by 5 times.
Diabetics is because the concentration of glucose in blood is too high, human body defensive ability/resistance ability declines, the supply of blood flow of lower limb and foot is not enough, causes foot to resist the decline of infection and wound self-healing ability, once wound, ulcer and infection appear in foot or lower limb, as treatment not in time, often be difficult to healing, a slight wound will prolongedly not healed, and wound scope expands fast, even downright bad, the amputation of finally having to.
Diabetic foot is most commonly in long, the long-term bad middle-aged and elderly people of glycemic control of diabetes medical history, is one of diabetes severe complication, and sickness rate 15%~20%, is the main cause that amputation disables.It is numbness that the diabetic foot initial stage shows, send out cool, sensory capacity reduces, easily injured, shallow table wound is difficult for healing etc., often easily out in the cold, and later stage deterioration is very fast, probably in one week, faces amputation.
Therapeutic Method major control blood glucose, blood fat and the blood pressure of the diabetic foot of doctor trained in Western medicine aspect treatment at present, improve blood circulation, improves peripheral neuropathy, uses antibiotic anti-infective therapy, changing dressings of ulcer wound surface processed etc.Chemical drugs does not also have the special medicine for diabetic foot, and general treatment method is conservative symptomatic treatment, and conventional chemicals has obvious side effect simultaneously, and diabetics needs lifelong medication, and long-term prescription can exert an adverse impact to health.
Diabetic foot claims again diabetic gangrene, belongs to the traditional Chinese medical science " necrosis " category together with thromboangiitis obliterans, atherosclerotic occlusive disease.Chinese medicine thinks that this disease is mainly deficiency of both QI and YIN, obstruction of collaterals by blood stasis, QI and blood can not sensible extremity due to.Adopt the Chinese medicine of suiting the medicine to the illness can reduce patient's blood viscosity, increase LBF, remove the damage factor of blood capillary and local organization, make local blood for improving, be conducive to diabetic gangrene's recovery.Although Chinese medicine verification treatment diabetic foot has certain advantage, but there is no at present specially for diabetic foot, be used for the treatment of the Chinese patent medicine listing of diabetic foot, substantially just lean on doctor for the interim prescription of different patients, do not there is the general directive significance of clinical practice.
Summary of the invention
The object of the present invention is to provide a kind of pharmaceutical composition diabetic foot, determined curative effect for the treatment of.This medicine composite for curing diabetic foot is with strong points, and curative effect is better, and side effect is little, and safety is good.
To achieve these goals, technical scheme provided by the invention is:
Treat a pharmaceutical composition for diabetic foot, it is to be the medicament that medicinal raw material is made by Radix Rhodiolae, eupolyphaga, Aspongopus and Radix Glycyrrhizae.
The weight proportion of pharmaceutical composition of the present invention medicine material used can be: Radix Rhodiolae 5-20 part, eupolyphaga 1-12 part, Aspongopus 1-6 part, Radix Glycyrrhizae 2-5 part.
More preferably the proportioning of pharmaceutical composition of the present invention medicine material used is: Radix Rhodiolae 8-15 part, eupolyphaga 4-8 part, Aspongopus 2-4 part, Radix Glycyrrhizae 1-3 part.
The best proportioning of pharmaceutical composition of the present invention medicine material used is: 12 parts of Radix Rhodiolaes, 6 parts of eupolyphaga, 3 parts of Aspongopuss, 2 parts, Radix Glycyrrhizae
The pharmaceutical composition of above-mentioned treatment diabetic foot can be made each crude drug after treatment according to conventional formulation method the medicine of any one dosage form suitable on pharmaceutics, preferably granulation agent, tablet, hard capsule, oral liquid, soft capsule, drop pill etc.
According to the needs of the various drug forms of preparation, medicine of the present invention also can add suitable pharmaceutic adjuvant in preparation process, as starch, dextrin, microcrystalline cellulose, amylum pregelatinisatum, magnesium stearate, micropowder silica gel, sucrose, carboxymethyl starch sodium etc.
Compared with prior art, the invention has the beneficial effects as follows: the present invention's various raw medicinal materials used are the Chinese crude drug that meets country or provincial standard regulation.The present invention treats in the pharmaceutical composition of diabetic foot, and Radix Rhodiolae is cold in nature, and sweet-puckery flavor is attributed to lung meridian, heart channel.Benefiting QI for activating blood circulation, promotes blood circulation and relievings asthma.Eupolyphaga salty in the mouth, cold in nature, return Liver Channel.Removing blood stasis, reunion of fractured tendons and bones.Aspongopus salty in the mouth, warm in nature, inducing diuresis for treating stranguria syndrome, promoting the circulation of QI to relieve pain, warming the kidney to invigorate YANG.The invigorating middle warmer of Radix Glycyrrhizae QI invigorating, the function of heat-clearing and toxic substances removing, the mediation property of medicine.Above 4 taste Chinese medicine composition application, have Synergistic function, are used for the treatment of diabetic foot, determined curative effect, through clinical research, show, it is better that medicine of the present invention is used for the treatment of diabetic foot curative effect, and total effective rate reaches more than 90%, can dwindle wound surface area, reduce amputation rate, shorten and treat the course for the treatment of.And do not find obvious side effect and untoward reaction.
The specific embodiment
Below in conjunction with the specific embodiment, the present invention is described in further detail.
Embodiment 1
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
12 parts of Radix Rhodiolaes, 6 parts of eupolyphaga, 3 parts of Aspongopuss, 2 parts, Radix Glycyrrhizae.
Granulation agent as follows: get the crude drug of described proportioning, add respectively suitable quantity of water, adopt decocting method to extract respectively 2 times, filter, merge 2 times filtrate, by each concentrated solution mix homogeneously, dry after concentrating, after granulation, be distributed into bag and get final product.
Embodiment 2
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
20 parts of Radix Rhodiolaes, 12 parts of eupolyphaga, 6 parts of Aspongopuss, 5 parts, Radix Glycyrrhizae.
Granulation agent as follows: get the crude drug of described proportioning, add respectively suitable quantity of water, adopt decocting method to extract respectively 3 times, filter, merge 3 times filtrate, by each concentrated solution mix homogeneously, dry after concentrating, after granulation, be distributed into bag and get final product.
Embodiment 3
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
8 parts of Radix Rhodiolaes, 4 parts of eupolyphaga, 2 parts of Aspongopuss, 1 part, Radix Glycyrrhizae.
Granulation agent as follows: get the crude drug of described proportioning, add respectively appropriate 70% ethanol, adopt reflux extraction to extract respectively 3 times, filter, merge 3 times filtrate, reclaim ethanol and concentrate after by each concentrated solution mix homogeneously, dry, after granulation, be distributed into bag and get final product.
Embodiment 4
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
5 parts of Radix Rhodiolaes, 1 part of eupolyphaga, 1 part of Aspongopus, 2 parts, Radix Glycyrrhizae.
Granulation agent as follows: get the crude drug of described proportioning, add respectively 80% ethanol of approximately 10 times of amounts, employing percolation extracts, filters, by each concentrated solution mix homogeneously, dry after recovery ethanol also concentrates, and is distributed into bag and get final product after granulation.
Embodiment 5
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
15 parts of Radix Rhodiolaes, 8 parts of eupolyphaga, 4 parts of Aspongopuss, 3 parts, Radix Glycyrrhizae.
Granulation agent as follows: get the crude drug of described proportioning, mix, add suitable quantity of water, adopt decocting method to extract 3 times, filter, merge 3 times filtrate, concentrated, dry, after granulation, be distributed into bag and get final product.
Embodiment 6
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
12 parts of Radix Rhodiolaes, 8 parts of eupolyphaga, 2 parts of Aspongopuss, 3 parts, Radix Glycyrrhizae.
Granulation agent as follows: get the crude drug of described proportioning, mix, add appropriate 65% ethanol, adopt reflux extraction to extract 2 times, filter, merge 2 times filtrate, concentrated, dry, after granulation, be distributed into bag and get final product.
Embodiment 7
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
8 parts of Radix Rhodiolaes, 6 parts of eupolyphaga, 3 parts of Aspongopuss, 1 part, Radix Glycyrrhizae.
Make as follows tablet: get the crude drug of described proportioning, mix, add suitable quantity of water, adopt decocting method to extract 3 times, filter, merges 3 times filtrate, concentrated, dry, the rear tabletting and get final product of granulating.
Embodiment 8
The pharmaceutical composition of the treatment diabetic foot that the present embodiment is enumerated, is comprised of the medicinal raw material of following weight:
14 parts of Radix Rhodiolaes, 4 parts of eupolyphaga, 3 parts of Aspongopuss, 2 parts, Radix Glycyrrhizae.
Make as follows capsule: get the crude drug of described proportioning, mix, add suitable quantity of water, adopt decocting method to extract 2 times, filter, merge 2 times filtrate, concentrated, dry, after granulation, pack in hungry area softgel shell and get final product.
The various embodiments described above medicine, also can be according to other conventional formulation method, by each crude drug of corresponding weight proportion through other extract and the method processing such as purification after, make again the medicine of other dosage form, as: granule, tablet, hard capsule, oral liquid, soft capsule, drop pill, water pill, honeyed pill etc.
In addition, according to the needs of the various drug forms of preparation, the various embodiments described above medicine also can add suitable pharmaceutic adjuvant as magnesium stearate, starch, dextrin, sucrose, microcrystalline Cellulose, hydroxypropyl emthylcellulose, vegetable oil, lecithin, Polyethylene Glycol, propylene glycol, ethyl hydroxybenzoate etc. in preparation process.
For the efficacy and saferry of proof medicine of the present invention, inventor has carried out the clinical research of 100 examples.The research method and the result of the test that adopt are as follows:
The granule of medicine of the present invention for making according to crude drug component and the preparation method of embodiment 1.
Selection is diagnosed as patient's 100 examples of diabetic foot, through scheduling to last the objective clinical observation of system in March.Medicine group all cases of the present invention all meets the diagnostic criteria (draft) of the diabetic foot (acral necrosis) of first national diabetic foot academic conference formulation of Chinese Medical Association.Medicine group case man of the present invention 50 examples, female's 50 examples; Observe 3 months.
Method of administration: every day potion, minutes 3 times are oral.When taking medicine, coordinate following Therapeutic Method: 1. insulinize, makes glycemic control between 7~9mmol/L.2. concurrent infection person, gives antiinflammatory and symptomatic treatment.3. for suffering from sufficient wound surface, do corresponding processing.
Curative effect is sentenced standard: cure: wound surface all healed; Effective: to take a turn for the better two more than rank; Effective: to take a turn for the better 1 more than rank; Invalid: unchanged or gangrenous increasing the weight of.
Observation index comprises following aspect before taking medicine and after taking medicine:
(1) safety indexes: blood pressure, pulse, blood, urine, the large routine of excrement three and electrocardiogram, liver, kidney brake check.
(2) health giving quality index:
A. general curative effect comparison
B. skin ulcer face area, the product representation with greatest length (cm) * Breadth Maximum (cm), if any many places wound surface, records the gross area.
(3) untoward reaction is observed: comprise gastrointestinal reaction, nervous system abnormality, skin allergy etc.
All cases are all carried out efficacy determination after treating 3 months.Result: medicine group of the present invention is cured 40 examples, effective 38 examples, effective 14 examples, invalid 8 examples; Total effective rate 92%.Before treatment, skin ulcer face area is 23.54 ± 17.65, and after treatment, skin ulcer face area is 8.73 ± 5.41, and through paired data t check, P<0.01, has significant difference.In drug administration process, have no obvious adverse reaction, electrocardiogram before and after taking medicine, liver, renal function, blood, routine urinalysis are without significant change.

Claims (1)

1. a pharmaceutical composition for the treatment of diabetic foot, is characterized in that: it is to be the medicament that medicinal raw material is made by Radix Rhodiolae, eupolyphaga, Aspongopus and Radix Glycyrrhizae; The weight portion proportioning of described crude drug is 12 parts of Radix Rhodiolaes, 6 parts of eupolyphaga, 3 parts of Aspongopuss, 2 parts, Radix Glycyrrhizae; The preparation method of described pharmaceutical composition adds respectively suitable quantity of water for getting crude drug, adopts decocting method to extract respectively 2 times, filters, and merges 2 times filtrate, by each concentrated solution mix homogeneously, dry after concentrating, and is distributed into bag after granulation.
CN201210428581.XA 2012-10-31 2012-10-31 Medicine composition for treating diabetic foot Expired - Fee Related CN102940677B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104800425A (en) * 2015-04-23 2015-07-29 杨孝良 External Chinese herbal compound applying liquid for treating diabetic foot ulcer

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116327688A (en) * 2023-04-04 2023-06-27 普联东俪(烟台)生物科技有限公司 Stem cell gel for treating diabetic foot

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
《诺迪康胶囊治疗糖尿病足64 例临床研究》;裴晏民;《中国当代医药》;20101031(第28期);第49,50页 *
糖尿病足的中医药治疗进展;赵立沙等;《国医论坛》;20060320(第02期);第53-55页 *
裴晏民.《诺迪康胶囊治疗糖尿病足64 例临床研究》.《中国当代医药》.2010,(第28期),第49-50页. *
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104800425A (en) * 2015-04-23 2015-07-29 杨孝良 External Chinese herbal compound applying liquid for treating diabetic foot ulcer

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