CN1686493A - Medicine for treating gynecopathy inflammation and its preparation method - Google Patents
Medicine for treating gynecopathy inflammation and its preparation method Download PDFInfo
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Abstract
A Chinese medicine for treating gynecologic inflammation is proportionally prepared from 10 Chinese-medicinal materials including Chinese angelica root, sphatholobus stem, zanthoxylum nitidum, persimmon leaf, etc. Its preparing process is also disclosed.
Description
Technical field:
The present invention relates to a kind of clearing heat and expelling damp that has, gynecologic medicine preparation of adjusting meridian and stopping leukorrhea effect and preparation method thereof,
Technical background:
Gynecological's internal genitalia inflammation comprises adnexitis, pelvic inflammatory disease, the other cellulites in palace, endometritis etc., is gynecological's common frdquently encountered disease.Doctor trained in Western medicine adopts antibiotic therapy and physical therapy, but because the adhesion of inflammation focus hypertrophy, drug absorption is bad, and because the appearance of Resistant strain make antibiotic curative effect have a greatly reduced quality, and side effect is many, recurrence easily.
The traditional Chinese medical science is included it in disease categories such as " leukorrhagia ", " dysmenorrhea ", " tumor abdominal mass ".Patient or because of insufficiency of the spleen, or because of suffering from a deficiency of the kidney, insufficiency of the spleen can not fortune, suffer from a deficiency of the kidney and can not gasify, and cause endogenous dampness, or through row puerperal, in the vessels of the uterus inanition, exogenous damp is taken advantage of a weak point.Its pathogenesis mostly is invades in damp and hot, pents up the uterus vessels of the uterus.If the damp and hot multiple abscess part of the body cavity below the umbilicus, housing the bladder, kidneys and bowels, then see profuse leukorrhea, yellow skin, matter thickness, or as the bean dregs sample, or as the pus sample, frowziness, or mix symptom such as color is " leukorrhagia "; If damp and hot retardance QI and blood, disorder of movement of QI dashes and appoints impairedly, then can send out and is menoxenia; The knot if damp and hot and QI and blood are fought is then sent out and is the leprosy abdominal mass.Therefore, always not from damp and hot, it is main adopting clearing heat and expelling damp in the treatment, is aided with the promoting flow of QI and blood pain relieving.
Used FUYANJING JIAONANG has clearing heat and expelling damp, the promoting the circulation of QI to relieve pain function at present.Can attack heresy, take into account again and set upright, in can removing dampness and detoxicating, be aided with the spleen invigorating invigorating the liver and kidney, make heresy go and just do not hinder.Treatment leukorrheal diseases or leprosy abdominal mass are inflammation such as women's adnexitis, father-in-law chamber inflammation of primary symptom, no matter be acute inflammation or chronic inflammatory disease, no matter be the type of invading in the noxious dampness, still no matter invade type in the noxious dampness, be ascites of liver meridian damp-heat type, or the Liver and kidney deficiency, all obtain satisfied effect, total effective rate reaches 98.2%.Modern pharmacology experimental results show that this product has antiinflammation preferably, and does not have obvious toxic-side effects, is worth clinical application.But capsule is because volume is bigger, and dosage accuracy is lower, and its quality stability is descended.
Summary of the invention:
The objective of the invention is to: a kind of smaller volume is provided, taking convenience, and steady quality, dosage is Tabules more accurately, overcoming above-mentioned shortcoming, and provides many a kind of selections for patient and clinician.
The present invention is achieved in that in 1000 dosage units, it is mainly made by following Chinese medicine raw materials by weight proportion, 50～200 parts of Radix Picriae felterrae, 200～600 parts of Elephantopus scaber L., 120～400 parts of Radix Angelicae Sinensis, 200～600 parts of Caulis Spatholobis, 200～600 parts of Radix Zanthoxylis, 200～600 parts of Herba Thlaspis, 200～800 parts of Herba Fici Simplicissimae, 200～600 parts of Radix calophylli membranacei, 200～600 parts of Folium Kaki, 50～200 parts in Radix Picriae felterrae powder.
Wherein the consumption of crude drug is: 125 parts of Radix Picriae felterrae, 375 parts of Elephantopus scaber L., 250 parts of Radix Angelicae Sinensis, 375 parts of Caulis Spatholobis, 375 parts of Radix Zanthoxylis, 375 parts of Herba Thlaspis, 500 parts of Herba Fici Simplicissimae, 375 parts of Radix calophylli membranacei, 375 parts of Folium Kaki, 125 parts in Radix Picriae felterrae powder.
Wherein also be added with adjuvant disintegrating agent 0.5-5 part, lubricant 0.2-1 part.
Described disintegrating agent is cross-linking sodium carboxymethyl cellulose (CC-Na), crospolyvinylpyrrolidone (PVPP), crosslinked carboxymethyl fecula sodium (CCMS-Na) or low-substituted hydroxypropyl cellulose (L-HPC), preferred crosslinked carboxymethyl fecula sodium (CCMS-Na); Lubricant is magnesium stearate or micropowder silica gel, preferred magnesium stearate.
Described preparation is a tablet.
Its preparation method is: nine flavors in the prescription, and half of Radix Picriae felterrae is ground into fine powder, and remaining Radix Picriae felterrae and other eight flavors medical materials decoct with water twice, add 10 times of amounts of water for the first time, decocted 3 hours, and added 8 times of amounts of water for the second time, decocted collecting decoction 2 hours, filter, filtrate is condensed into the thick paste shape, adds the Radix Picriae felterrae fine powder, mixing, drying is pulverized, and granulates drying, granulate adds disintegrating agent, lubricant, tabletting, coating, packing, promptly.
Preparation of the present invention has clearing heat and expelling damp, withers through the function of leukorrhagia stopping.Below beneficial effect by clinical experiment explanation medicine of the present invention.
The clinical research result of the chronic pelvic inflammatory disease of controlling 120 examples be reported as follows:
1 clinical data
1.1 selected 180 examples of physical data are the out-patient, are divided into treatment group and matched group at random.
Wherein 120 examples are organized in treatment, 18～48 years old age, year mean age (31.76～7.09); Course of disease June～84 months, average course of disease (32.90～19.02) month; State of an illness scoring 7.5～21 minutes, average (14.54 ± 3.51) are divided.Matched group 60 examples, 21～48 years old age, year mean age (32.38 ± 7.45); Average course of disease (34.00～21.03) moon: state of an illness scoring 8～21.5 minutes, average (13.95 ± 3.33) are divided.2 groups of patients there was no significant difference (P＞0.05) aspect age, the course of disease and the state of an illness has comparability.
2 treatments and observation, statistical method
2.1 Therapeutic Method
It is oral that 2.1.1 the treatment group gives the present invention, and each 3, every day 3 times.
2.1.2 matched group is taken FUKE QIANJIN PIAN (main component is Radix Rosae Laevigatae, Radix Flemingiae Philippinensis, Radix Angelicae Sinensis, Fructus Zanthoxyli Dissiti, Herba Andrographis, Caulis Mahoniae, Radix Codonopsis, Caulis Spatholobi etc., is produced by zhuzhou,hunan pharmaceutical factory), and is each 6, every with 3 times.2 groups was 11 courses of treatment with 20 days all.General treatment is judged curative effect 3 courses of treatment.
2.2 observation index (1) health giving quality is observed: clinical symptoms, gynecologial examination, B ultrasonic, hemorheology, nail fold microcirculation.(2) safety is observed; Inspections such as routine blood test, routine urinalysis, hepatic and renal function.
2.3 statistical procedures The data SPSS medical statistics software is added up, result (x ± s) expression.Measurement data adopts the t check, and enumeration data adopts the x2 check.
3 therapeutic outcomes
3.1 the clinical efficacy treatment is organized in 120 examples, 73 examples of fully recovering, produce effects 21 examples, effective 22 examples, invalid 4 examples, total effective rate 96.67%; In matched group 60 examples, 2 examples of fully recovering, produce effects 16 examples, effective 30 examples, invalid 12 examples, total effective rate 80.00%.2 groups relatively have highly significant difference (P＜0.0005), and treatment group curative effect obviously is better than matched group.
3.2 the symptom integral situation of change sees Table 1 before and after the treatment.As known from Table 1,2 groups of treatment front and back symptom integral all have highly significant difference (P＜0.0005); Compare 2 groups of treatment backs, and the treatment group descends more obvious than matched group symptom integral, and highly significant difference (P＜0.0005) is arranged.
Symptom total mark comparison before and after table 1 treatment group and the treatment of control group (X ± S)
After treating before the treatment of group example number
Treatment organizes 120 14.54 ± 3.51 3.52 ± 4.69
Matched group 60 13.95 ± 3.33 7.49 ± 3.54
Annotate: with compare P＜0.0005 before the treatment
3.3 hemorheology index situation of change treatment group has been observed 30 routine patients' hemorheology index, wherein whole blood viscosity low is cut before and after the treatment, aggregate index, electrophoresis index, plasma viscosity, packed cell volume, K value have significant difference (P＜0.005, P＜0.05, P＜0.001, P＜0.01); Matched group has also been observed 30 routine patients, wherein cut in the whole blood viscosity before and after the treatment, the whole blood viscosity height is cut, aggregate index, K value, reduced viscosity hang down cut, the electrophoresis index has significant difference (P＜0.05, P＜0.001, P＜0.01).Treatment back treatment group plasma viscosity, packed cell volume and matched group relatively have significant difference (P＜0.05) in addition.
3.4 adnexa enclosed mass situation of change treatment group has 51 examples to find the adnexa enclosed mass before and after the treatment of treatment group, all carries out gynecological's routine and ultrasound diagnosis before and after the treatment.In treating 51 examples, recovery from illness (enclosed mass disappearance) 39 examples, (dwindling 1/3～1/2) 10 examples that take a turn for the better, invalid (dwindling below 1/3) 2 examples, total effective rate is 96.08%.
3.5 safety observation treatment group is got 30 examples and do inspections such as routine blood test, routine urinalysis, hepatic and renal function before and after treatment, shows no obvious abnormalities, and proves that the present invention has no adverse reaction to human body.
Modern medicine thinks that the generation of chronic Jia chamber inflammation is relevant with the up infection of genital tract causal agent.Clinical multilist is now suffered from abdominal pain, abdomen weigh down to expand, soreness of waist pain, menoxenia, leukorrhagia, the formation of salt chamber enclosed mass.Main pathology is changed to that the Jia cavity tissue thickens, adhesion, fibrosis.Western medical treatment mainly adopts antibiotic to cooperate Chymetin, placenta interstitial fluid or adrenocortical hormone, but curative effect is unsatisfactory, and prolonged application also can be brought toxic and side effects, and easily produces persister.
Chinese medicine does not have this name of disease, it is belonged to categories such as " leukorrhagia ", " dysmenorrhea ", " stomachache ", " lump in the abdomen " according to clinical manifestation.Pathogenesis is mainly the stasis of blood, heat, the three that wets accumulates uterus, causes dashing and appoints QI-blood circulation not smooth, numbness resistance vessels of the uterus, stagnation of QI and blood may bring about pain.The general stasis of blood is main cause heat, wet taking second place.Based on above understanding to the primary disease pathogenesis, be the rule of treatment with upright " removing blood stasis Qinghua ", the development cost invention.From clinical observation, chronic father-in-law chamber is scorching, and every clinical indices improves through after we's treatment, and sings and symptoms alleviates or disappears, and abnormal indexes such as hemorheology and nail fold microcirculation also make moderate progress.These have proved that all the present invention can improve urn chamber blood stasis, dissolve stasis, promote disappearing of inflammatory lesions tissue and softening, loosen and absorbing of proliferative lesion tissue, practice has proved that also this tablet is a kind of medicine for the treatment of chronic pelvic inflammatory disease safely and effectively, is worth clinical application.
The specific embodiment:
Embodiments of the invention: take by weighing Radix Picriae felterrae 250g, Elephantopus scaber L. 375g, Radix Angelicae Sinensis 250g, Caulis Spatholobi 375g, Radix Zanthoxyli 375g, Herba Thlaspis 375g, Herba Fici Simplicissimae 500g, Radix calophylli membranacei 375g, Folium Kaki 375g, 125g is ground into fine powder with Radix Picriae felterrae, crosses 60～120 mesh sieves, eight flavor medical materials such as remaining Radix Picriae felterrae and Radix Angelicae Sinensis decoct with water twice, add 10 times of amounts of water for the first time, decoct 3 hours, for the second time add 8 times of amounts of water, decocted collecting decoction 2 hours, filter, filtrate is condensed into the thick paste shape, adds the Radix Picriae felterrae fine powder, mixing, dry, powder is rare, granulates drying, granulate, add 0.5g carboxymethyl starch sodium and 0.5g magnesium stearate, 1000 of tablettings, coating, packing, promptly.
Claims (6)
1. preparation for the treatment of gynecological inflammation, it is characterized in that: in 1000 dosage units, it is mainly made by following Chinese medicine raw materials by weight proportion, 50～200 parts of Radix Picriae felterrae, 200～600 parts of Elephantopus scaber L., 120～400 parts of Radix Angelicae Sinensis, 200～600 parts of Caulis Spatholobis, 200～600 parts of Radix Zanthoxylis, 200～600 parts of Herba Thlaspis, 200～800 parts of Herba Fici Simplicissimae, 200～600 parts of Radix calophylli membranacei, 200～600 parts of Folium Kaki, 50～200 parts in Radix Picriae felterrae powder.
2. preparation according to claim 1 is characterized in that: wherein the consumption of crude drug is: 125 parts of Radix Picriae felterrae, 375 parts of Elephantopus scaber L., 250 parts of Radix Angelicae Sinensis, 375 parts of Caulis Spatholobis, 375 parts of Radix Zanthoxylis, 375 parts of Herba Thlaspis, 500 parts of Herba Fici Simplicissimae, 375 parts of Radix calophylli membranacei, 375 parts of Folium Kaki, 125 parts in Radix Picriae felterrae powder.
3. preparation according to claim 1 and 2 is characterized in that: wherein also be added with adjuvant disintegrating agent 0.5-5 part, lubricant 0.2-1 part.
4. preparation according to claim 3, it is characterized in that: described disintegrating agent is cross-linking sodium carboxymethyl cellulose (CC-Na), crospolyvinylpyrrolidone (PVPP), crosslinked carboxymethyl fecula sodium (CCMS-Na) or low-substituted hydroxypropyl cellulose (L-HPC), preferred crosslinked carboxymethyl fecula sodium (CCMS-Na); Lubricant is magnesium stearate or micropowder silica gel, preferred magnesium stearate.
5. preparation according to claim 1 is characterized in that: described preparation is a tablet.
6. preparation method of preparation according to claim 1 is characterized in that: nine flavors in the prescription, and 50% of Radix Picriae felterrae is ground into fine powder, and remaining Radix Picriae felterrae decocts with water twice with other eight medical materials of distinguishing the flavor of, for the first time add 10 times of amounts of water, decocted 3 hours, add 8 times of amounts of water for the second time, decocted 2 hours, collecting decoction filters, and filtrate is condensed into the thick paste shape, adds the Radix Picriae felterrae fine powder, mixing, drying is pulverized, and granulates, drying, granulate adds disintegrating agent, lubricant, tabletting, coating, packing, promptly.
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| Application Number | Priority Date | Filing Date | Title |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101804121A (en) * | 2010-05-26 | 2010-08-18 | 安徽华佗国药股份有限公司 | Medicine for treating gynecologic diseases and preparation method thereof |
| CN103110738A (en) * | 2012-12-17 | 2013-05-22 | 广西梧州制药（集团）股份有限公司 | Traditional Chinese medicine composition for treating gynecologic inflammation and preparation method thereof |
| CN103169806A (en) * | 2011-12-23 | 2013-06-26 | 杨文龙 | Fuyanjing oral preparation and preparation method thereof |
-
2005
- 2005-04-11 CN CN 200510200230 patent/CN100353964C/en active Active
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101804121A (en) * | 2010-05-26 | 2010-08-18 | 安徽华佗国药股份有限公司 | Medicine for treating gynecologic diseases and preparation method thereof |
| CN103169806A (en) * | 2011-12-23 | 2013-06-26 | 杨文龙 | Fuyanjing oral preparation and preparation method thereof |
| CN103169806B (en) * | 2011-12-23 | 2014-10-29 | 杨文龙 | Fuyanjing oral preparation and preparation method thereof |
| CN103110738A (en) * | 2012-12-17 | 2013-05-22 | 广西梧州制药（集团）股份有限公司 | Traditional Chinese medicine composition for treating gynecologic inflammation and preparation method thereof |
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| CN100353964C (en) | 2007-12-12 |
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Address after: 553400 Guizhou city of Liupanshui province Liuzhi Mu Gang Industrial Park B District No. 6 Patentee after: Sunflower Pharmaceutical Group (Guizhou) macro wonder Co., Ltd. Address before: 550001 No. 4 Yong Feng Road, Guizhou, Guiyang Patentee before: Guizhou Hongqi Pharmaceutical Co. Ltd. |
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