CN1613461A - Arthralgia removing pills and their preparation - Google Patents
Arthralgia removing pills and their preparation Download PDFInfo
- Publication number
- CN1613461A CN1613461A CN 200310103525 CN200310103525A CN1613461A CN 1613461 A CN1613461 A CN 1613461A CN 200310103525 CN200310103525 CN 200310103525 CN 200310103525 A CN200310103525 A CN 200310103525A CN 1613461 A CN1613461 A CN 1613461A
- Authority
- CN
- China
- Prior art keywords
- weight portion
- rhizoma curcumae
- chinese medicine
- rhizoma
- medicine composition
- 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
Links
- 239000006187 pill Substances 0.000 title claims abstract description 7
- 238000002360 preparation method Methods 0.000 title claims description 20
- 208000006820 Arthralgia Diseases 0.000 title description 2
- 239000003814 drug Substances 0.000 claims abstract description 34
- 241000218176 Corydalis Species 0.000 claims abstract description 32
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims abstract description 23
- 239000007788 liquid Substances 0.000 claims abstract description 14
- 206010058019 Cancer Pain Diseases 0.000 claims abstract description 11
- 239000003826 tablet Substances 0.000 claims abstract description 5
- 239000002775 capsule Substances 0.000 claims abstract description 4
- 239000000843 powder Substances 0.000 claims description 45
- 241001057584 Myrrha Species 0.000 claims description 30
- 241000180649 Panax notoginseng Species 0.000 claims description 30
- 235000003143 Panax notoginseng Nutrition 0.000 claims description 30
- 239000000341 volatile oil Substances 0.000 claims description 27
- 238000001035 drying Methods 0.000 claims description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 239000007864 aqueous solution Substances 0.000 claims description 18
- 238000004821 distillation Methods 0.000 claims description 18
- 239000000706 filtrate Substances 0.000 claims description 18
- 241001250596 Pleione Species 0.000 claims description 14
- 239000008187 granular material Substances 0.000 claims description 11
- 229920000858 Cyclodextrin Polymers 0.000 claims description 9
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 claims description 9
- 238000000605 extraction Methods 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- 238000004321 preservation Methods 0.000 claims description 9
- 238000004064 recycling Methods 0.000 claims description 9
- 238000010992 reflux Methods 0.000 claims description 9
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 9
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 229940079593 drug Drugs 0.000 claims description 5
- 239000003937 drug carrier Substances 0.000 claims description 5
- 239000004615 ingredient Substances 0.000 claims description 4
- 239000002552 dosage form Substances 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 14
- 239000002245 particle Substances 0.000 abstract description 4
- 206010012335 Dependence Diseases 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 3
- 240000007311 Commiphora myrrha Species 0.000 abstract description 2
- 235000006965 Commiphora myrrha Nutrition 0.000 abstract description 2
- 235000007265 Myrrhis odorata Nutrition 0.000 abstract description 2
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 abstract 1
- 229940116229 borneol Drugs 0.000 abstract 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 abstract 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- 208000002193 Pain Diseases 0.000 description 23
- 206010028980 Neoplasm Diseases 0.000 description 6
- 230000000202 analgesic effect Effects 0.000 description 6
- 239000008280 blood Substances 0.000 description 6
- 210000004369 blood Anatomy 0.000 description 6
- 208000024891 symptom Diseases 0.000 description 6
- 201000011510 cancer Diseases 0.000 description 5
- 230000001737 promoting effect Effects 0.000 description 5
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 description 4
- 231100000957 no side effect Toxicity 0.000 description 4
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 description 3
- 230000004087 circulation Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229940127240 opiate Drugs 0.000 description 3
- 238000012856 packing Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 208000019790 abdominal distention Diseases 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000017531 blood circulation Effects 0.000 description 2
- 229960004126 codeine Drugs 0.000 description 2
- 208000010877 cognitive disease Diseases 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 235000012907 honey Nutrition 0.000 description 2
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
- 229960005489 paracetamol Drugs 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000012795 verification Methods 0.000 description 2
- USSIQXCVUWKGNF-UHFFFAOYSA-N 6-(dimethylamino)-4,4-diphenylheptan-3-one Chemical compound C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 USSIQXCVUWKGNF-UHFFFAOYSA-N 0.000 description 1
- 206010002198 Anaphylactic reaction Diseases 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- 241000208229 Burseraceae Species 0.000 description 1
- 241000846172 Cremastra appendiculata Species 0.000 description 1
- 206010014080 Ecchymosis Diseases 0.000 description 1
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000008896 Opium Substances 0.000 description 1
- 241000208343 Panax Species 0.000 description 1
- 241000218180 Papaveraceae Species 0.000 description 1
- 208000001647 Renal Insufficiency Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 230000036783 anaphylactic response Effects 0.000 description 1
- 208000003455 anaphylaxis Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 210000000038 chest Anatomy 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000002651 drug therapy Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000007661 gastrointestinal function Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 230000023597 hemostasis Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 201000006370 kidney failure Diseases 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000005906 menstruation Effects 0.000 description 1
- 229960001797 methadone Drugs 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- 229960001027 opium Drugs 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000012109 statistical procedure Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Landscapes
- Medicines Containing Plant Substances (AREA)
Abstract
A Chinese medicine in the form of particles; tablet, capsule, pill, or oral liquid for treating cancer pain is prepared from 7 Chinese-medicinal materials including corydalis tuber, notogniseng, myrrh, borneol, etc. Its advantages are high curative effect and durability, and no addiction and toxic by-effect.
Description
[invention field]
The present invention relates to a kind of Chinese medicine composition, is a kind of Chinese medicine composition that is used for the treatment of cancer pain specifically, the invention still further relates to the preparation method of this Chinese medicine composition.
[background technology]
Show that according to the Ministry of Public Health statistics Chinese annual cancer patient increases progressively with the million people, just have one family to be subjected to the harm of tumor disease in per 200 families.Wherein pain is an insoluble problem as cancer patient's serious symptoms always.Three stage therapies are recommended to use to the treatment of cancer pain by World Health Organization (WHO), mild pain uses the non-opium antalgica, as acetaminophen, aspirin etc., moderate pain then uses weak opiates antalgica, as codeine, paracetamol ﹠ codeine etc., severe pain is then used strong opiates antalgica, as morphine, methadone etc.Though these strong opiates antalgicas can the respite patient suffering, use continuously easily to produce side effect such as cumulative toxicity and dependency, if improper use more can jeopardize health of human body,
In view of the medicine and the method that not have at present better effectively to treat cancer pain, so a kind of Chinese medicine for oral administration that can effectively treat cancer pain and have no side effect of demand still.The inventor develops a kind of Chinese medicine composition that can effectively treat cancer pain and have no side effect, thereby has finished the present invention through animal experiment and clinical verification repeatedly for many years.
[summary of the invention]
Goal of the invention
Purpose of the present invention just provides a kind of Chinese medicine composition that can effectively treat cancer pain.This medicine has the effect of regulating qi to disperse stagnation, removing obstruction in the collateral to relieve pain, can be used for costalgia, pain heavy treatment at night that qi depression to blood stasis causes, to the treatment cancerous pain have that analgesic effect is good, long action time, no addiction and toleration, the characteristics that have no side effect.
Another object of the present invention just provides the preparation method of this Chinese medicine composition.
Technical scheme
The object of the present invention is achieved like this:
The present invention treats the Chinese medicine composition of cancer pain, it is characterized in that the preparation raw material (in weight portion) of the contained active component of this Chinese medicine composition is as follows:
Rhizoma Corydalis 471-601 part Radix Notoginseng 257-386 part Myrrha 257-386 part
Rhizoma Curcumae Longae 257-386 part Pseudobulbus Cremastrae Seu Pleiones 257-386 part Rhizoma Curcumae 257-386 part
Borneolum Syntheticum 6-16 part
Preferably, medicine material consumption of the present invention is as follows in weight portion:
Rhizoma Corydalis 493-589 part Radix Notoginseng 278-365 part Myrrha 278-365 part
Rhizoma Curcumae Longae 278-365 part Pseudobulbus Cremastrae Seu Pleiones 278-365 part Rhizoma Curcumae 278-365 part
Borneolum Syntheticum 8-13 part
More preferably, medicine material consumption of the present invention is as follows by weight:
320 parts of 320 parts of Myrrhas of 533 portions of Radix Notoginseng of Rhizoma Corydalis
320 parts of 320 parts of Rhizoma Curcumae of 320 parts of Pseudobulbus Cremastrae Seu Pleioness of Rhizoma Curcumae Longae
11 parts of Borneolum Syntheticums
The source and the effect thereof of the Chinese crude drug that technique scheme is mentioned are as follows:
Rhizoma Corydalis: be the dry tuber of papaveraceae plant corydalis, invigorate blood circulation, promoting the circulation of QI, analgesic effect.
Radix Notoginseng: be the dry root of panax araliaceae plant, have the hemostasis of becoming silted up of loosing, the effect of subduing swelling and relieving pain.
Myrrha: the oleo-gum-resin for Burseraceae shrub or dungarunga myrrh or other bdellium plant skin zone wounds ooze out has promoting blood circulation to relieve pain, the effect of granulation promoting.
Rhizoma Curcumae Longae: be the dry rhizome of zingiberaceous plant Rhizoma Curcumae Longae, can the removing blood stasis circulation of qi promoting, inducing menstruation to relieve menalgia.
Pseudobulbus Cremastrae Seu Pleiones: the dry pseudobulb for the orchid Cremastra appendiculata has the effect of heat-clearing and toxic substances removing, dissipating phlegm and resolving masses.
Rhizoma Curcumae: be the dry rhizome of zingiberaceous plant Rhizoma Curcumae, have the circulation of qi promoting removing blood stasis, removing food stagnancy analgesic effect.
Borneolum Syntheticum:, have the refreshment of having one's ideas straightened out, the effect of clearing away heat to alleviate pain for water white transparency or the crisp crystallization of white translucent lamellar.
The effective ingredient of Chinese medicine composition of the present invention is according to comprising that the method for following each processing step obtains:
(a) Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, with 60-95 volume % ethanol water heating and refluxing extraction three times, each 1-3 hour, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol;
(b) Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 1-3 hour at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying;
(c) above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 1-3 hour, collecting decoction, filter and the aqueous solution after the distillation in filtrate and the above-mentioned steps (b) merged, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps (a) in the clear paste merging, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps
(b) fine powder of volatile oil inclusion complex is evenly mixed in, makes various dosage forms with pharmaceutically acceptable carrier or excipient then, promptly obtains Chinese medicine composition of the present invention.
The described concentration of alcohol of step in the above-mentioned preparation method (a) is preferably 80%, preferably make a living by weight 6 times of dose of alcoholic solution consumption.
Prescription of the present invention is through the above-mentioned steps preparation, can make various pharmaceutical formulations such as granule, capsule, tablet, pill, oral liquid or the like with pharmaceutically acceptable carrier or excipient composition.Wherein said pharmaceutically acceptable carrier or excipient are selected according to different dosage forms.These used carriers or excipient all are easy to determine for the those of ordinary skill of pharmaceutical field, also are conspicuous.
Beneficial effect
Chinese medicine composition of the present invention has the effect of regulating qi to disperse stagnation, removing obstruction in the collateral to relieve pain, can be used for bloated, the pain heavy treatment at night of costalgia, rib that qi depression to blood stasis causes, to the treatment cancerous pain have that analgesic effect is good, long action time, no addiction and toleration, characteristics such as have no side effect, be suitable for taking for a long time.Medicine of the present invention is easy to take, evident in efficacy, be a kind of medicine of ideal treatment cancer pain.
[specific embodiment]
Below in conjunction with specific embodiment the present invention is elaborated.
Embodiment 1:The preparation of granule of the present invention
Rhizoma Corydalis 533 weight portion Radix Notoginseng 320 weight portion Myrrhas 320 weight portions
Rhizoma Curcumae Longae 320 weight portion Pseudobulbus Cremastrae Seu Pleioness 320 weight portion Rhizoma Curcumae 320 weight portions
Borneolum Syntheticum 11 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in Myrrha, the fine powder of the volatile oil inclusion complex of Rhizoma Curcumae Longae and Rhizoma Curcumae is evenly mixed, adds the correctives steviosin and granulates, with the particle drying of preparation, packing.
Below in conjunction with specific embodiment the present invention is elaborated.
Embodiment 2:The preparation of granule of the present invention
Rhizoma Corydalis 471 weight portion Radix Notoginseng 257 weight portion Myrrhas 257 weight portions
Rhizoma Curcumae Longae 257 weight portion Pseudobulbus Cremastrae Seu Pleioness 257 weight portion Rhizoma Curcumae 257 weight portions
Borneolum Syntheticum 6 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in Myrrha, the fine powder of the volatile oil inclusion complex of Rhizoma Curcumae Longae and Rhizoma Curcumae is evenly mixed, adds the correctives steviosin and granulates, with the particle drying of preparation, packing.
Below in conjunction with specific embodiment the present invention is elaborated.
Embodiment 3:The preparation of granule of the present invention
Rhizoma Corydalis 601 weight portion Radix Notoginseng 386 weight portion Myrrhas 386 weight portions
Rhizoma Curcumae Longae 386 weight portion Pseudobulbus Cremastrae Seu Pleioness 386 weight portion Rhizoma Curcumae 386 weight portions
Borneolum Syntheticum 16 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in Myrrha, the fine powder of the volatile oil inclusion complex of Rhizoma Curcumae Longae and Rhizoma Curcumae is evenly mixed, adds the correctives steviosin and granulates, with the particle drying of preparation, packing.
Embodiment 4:The preparation of capsule of the present invention
Rhizoma Corydalis 533 weight portion Radix Notoginseng 320 weight portion Myrrhas 320 weight portions
Rhizoma Curcumae Longae 320 weight portion Pseudobulbus Cremastrae Seu Pleioness 320 weight portion Rhizoma Curcumae 320 weight portions
Borneolum Syntheticum 11 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in the fine powder of volatile oil inclusion complex of Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae evenly mixed, incapsulate then.
Embodiment 5:The preparation of tablet of the present invention
Rhizoma Corydalis 533 weight portion Radix Notoginseng 320 weight portion Myrrhas 320 weight portions
Rhizoma Curcumae Longae 320 weight portion Pseudobulbus Cremastrae Seu Pleioness 320 weight portion Rhizoma Curcumae 320 weight portions
Borneolum Syntheticum 11 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in Myrrha, the fine powder of the volatile oil inclusion complex of Rhizoma Curcumae Longae and Rhizoma Curcumae is mixed evenly, makes wet granular, tabletting with preparation tablet excipient commonly used such as starch etc. then.
Embodiment 6:The preparation of pill of the present invention
Rhizoma Corydalis 533 weight portion Radix Notoginseng 320 weight portion Myrrhas 320 weight portions
Rhizoma Curcumae Longae 320 weight portion Pseudobulbus Cremastrae Seu Pleioness 320 weight portion Rhizoma Curcumae 320 weight portions
Borneolum Syntheticum 11 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in Myrrha, the fine powder of the volatile oil inclusion complex of Rhizoma Curcumae Longae and Rhizoma Curcumae is evenly mixed, adds refined honey then and makes small honey pill or big honeyed pills.
Embodiment 7:Oral liquid of the present invention
Rhizoma Corydalis 533 weight portion Radix Notoginseng 320 weight portion Myrrhas 320 weight portions
Rhizoma Curcumae Longae 320 weight portion Pseudobulbus Cremastrae Seu Pleioness 320 weight portion Rhizoma Curcumae 320 weight portions
Borneolum Syntheticum 11 weight portions
Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, and with 80 volume % ethanol water heating and refluxing extraction three times, each 2 hours, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol; Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, and the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 2 hours at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying; Above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 2 hours, collecting decoction, filter and with the merging of the aqueous solution after the distillation in filtrate and the above-mentioned steps, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps in the clear paste of Rhizoma Corydalis and Radix Notoginseng merge, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps in Myrrha, the fine powder of the volatile oil inclusion complex of Rhizoma Curcumae Longae and Rhizoma Curcumae is evenly mixed, adds correctives Mel and diluent water then and makes oral liquid.
Below by testing the effect of further Chinese medicine composition.
Experimental example 1:The clinical trial of Chinese medicine composition of the present invention
The case choice criteria:
1, checks, is diagnosed as cancer person through X line, CT, B ultrasonic, blood biochemical, seroimmunity, MRI,, need Drug therapy person with pain in conjunction with medical history, clinical symptoms and sign.
2, Chinese medical discrimination is a qi depression to blood stasis disease, localized pain, and pain night is heavy, and is uncomfortable in chest with abdominal distention, the kind sigh, dark tongue quality or ecchymosis is arranged, stringy and thready pulse or weak pulse.
3, the age is at 18-65 between year.
4, estimate that existence is person more than 3 months.
5, stop using put, chemotherapy is more than one week, pain does not have alleviation person.
Get rid of the case standard:
1, non-above-mentioned cancer patient.
2, with severe cardiac, liver, renal insufficiency person.
3, treatment was used other analgesic and analgesic person in preceding 24 hours.
4, cognitive disorder or disturbance of consciousness person are arranged.
5, just carrying out the chemicotherapy person.
Test method:
1, adopts random packet, counter point.
2, verify routine number: 60 examples are organized in treatment, matched group 60 examples.
3, treatment group medication: product granule of the present invention, oral, each 10 grams, every day 3 times.
4, the course of treatment: 7 days, and tried the patient during the clinical verification and can not adopt other relevant treatment simultaneously.
5, medication did not have alleviation person as pain in 3 days, invalid case.
Curative effect index:
1, observation index: to the influence of blood pressure, breathing, heart rate; To neural influence; Gastrointestinal function is influenced; Anaphylaxis.
2, the observation of pain: mild pain; Moderate pain; Severe pain.
3, tcm symptom is observed: abdominal distention; Pain is heavy night; Breast is vexed; The kind sigh;
Curative effect determinate standard:
1, clinic control: treat the back symptom and disappear substantially.
2, produce effects: treat the back symptom and obviously improve.
3, effective: as to treat the back doing well,improving.
4, invalid: clinical symptoms no change or do not reach effective standard.
Result of the test: the every data to clinical trial are carried out statistical procedures, general enumeration data X 2 test, and measurement data is checked with t, and the level data data is analyzed with Ridit.Concrete data see the following form.
Table 1 cancer pain remission effect synopsis
The example number | Transference cure | Manifest alleviation | The slight alleviation | Do not alleviate | Remission rate | |
Granule of the present invention | ????61 | ????7 | ????15 | ????24 | ????15 | ????75.41% |
Above data show that Chinese medicine of the present invention is 75.41% to terminal cancer case syndrome remission rate, and disappearance rate is that 11.48% alleviation degree is good, the remission rate height.
Claims (6)
1. Chinese medicine composition that is used for the treatment of cancer pain, it is made up of effective ingredient or effective ingredient and pharmaceutically acceptable carrier, it is characterized in that its contained effective ingredient made by following bulk drugs:
Rhizoma Corydalis 471-601 weight portion Radix Notoginseng 257-386 weight portion
Myrrha 257-386 weight portion Rhizoma Curcumae Longae 257-386 weight portion
Pseudobulbus Cremastrae Seu Pleiones 257-386 weight portion Rhizoma Curcumae 257-386 weight portion
Borneolum Syntheticum 6-16 weight portion.
2. according to the Chinese medicine composition described in the claim 1, be characterised in that preparation raw materials of effective components medicine and consumption thereof are:
Rhizoma Corydalis 493-589 weight portion Radix Notoginseng 278-365 weight portion
Myrrha 278-365 weight portion Rhizoma Curcumae Longae 278-365 weight portion
Pseudobulbus Cremastrae Seu Pleiones 278-365 weight portion Rhizoma Curcumae 278-365 weight portion
Borneolum Syntheticum 8-13 weight portion.
3. according to the Chinese medicine composition described in the claim 1, wherein prepare raw materials of effective components medicine and consumption thereof and be:
Rhizoma Corydalis 533 weight portion Radix Notoginseng 320 weight portion Myrrhas 320 weight portions
Rhizoma Curcumae Longae 320 weight portion Pseudobulbus Cremastrae Seu Pleioness 320 weight portion Rhizoma Curcumae 320 weight portions
Borneolum Syntheticum 11 weight portions.
4. according to any one described Chinese medicine composition among the claim 1-3, it is granule, capsule, tablet, pill or oral liquid.
5. according to the preparation method of any one described Chinese medicine composition among the claim 1-4, it comprises:
(a) Rhizoma Corydalis and Radix Notoginseng powder are broken into coarse powder, with 60-95 volume % ethanol water heating and refluxing extraction three times, each 1-3 hour, merge extractive liquid, also filtered, and relative density is the clear paste of 1.02-1.05 60 ℃ the time with being concentrated into behind the filtrate recycling ethanol;
(b) Myrrha, Rhizoma Curcumae Longae and Rhizoma Curcumae are extracted volatile oil, the aqueous solution after distillation device is in addition collected, and volatile oil is mixed with Borneolum Syntheticum, carries out inclusion with cyclodextrin and water then, stirs 1-3 hour at 60 ℃, and cold preservation is spent the night, and filters, and is ground into fine powder after the cold drying;
(c) above-mentioned medicinal residues and Pseudobulbus Cremastrae Seu Pleiones are decocted with water three times, each 1-3 hour, collecting decoction, filter and the aqueous solution after the distillation in filtrate and the above-mentioned steps (b) merged, be concentrated into that relative density is the clear paste of 1.02-1.05 in the time of 60 ℃, then with above-mentioned steps (a) in the clear paste merging, relative density is the thick paste of 1.20-1.25 when being concentrated into 60 ℃, through drying under reduced pressure, resulting dry thing is crushed to fine powder, again with above-mentioned steps
(b) fine powder of volatile oil inclusion complex is evenly mixed in, makes various dosage forms with pharmaceutically acceptable carrier or excipient then, promptly obtains Chinese medicine composition of the present invention.
6. preparation method according to claim 5 is characterized in that the described concentration of alcohol of step (a) is 80%, make a living by weight 6 times of dose of alcoholic solution consumption.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB200310103525XA CN1304045C (en) | 2003-11-06 | 2003-11-06 | Arthralgia removing pills and their preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB200310103525XA CN1304045C (en) | 2003-11-06 | 2003-11-06 | Arthralgia removing pills and their preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1613461A true CN1613461A (en) | 2005-05-11 |
CN1304045C CN1304045C (en) | 2007-03-14 |
Family
ID=34756712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB200310103525XA Expired - Fee Related CN1304045C (en) | 2003-11-06 | 2003-11-06 | Arthralgia removing pills and their preparation |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1304045C (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104399011A (en) * | 2014-12-16 | 2015-03-11 | 孔馨苑 | Traditional Chinese medicine combination for treating esophageal cancer pain and preparation method thereof |
CN107335011A (en) * | 2017-07-14 | 2017-11-10 | 烟台市中医医院 | Treat the external application Chinese medicine compound preparation of cancer pain |
CN115381912A (en) * | 2022-09-23 | 2022-11-25 | 湖南省中医药研究院附属医院 | External traditional Chinese medicine compound preparation for reducing cancer pain and preparation method thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1042799C (en) * | 1993-03-03 | 1999-04-07 | 高贵 | Blood-activating analgetic plaster for tumour |
-
2003
- 2003-11-06 CN CNB200310103525XA patent/CN1304045C/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104399011A (en) * | 2014-12-16 | 2015-03-11 | 孔馨苑 | Traditional Chinese medicine combination for treating esophageal cancer pain and preparation method thereof |
CN107335011A (en) * | 2017-07-14 | 2017-11-10 | 烟台市中医医院 | Treat the external application Chinese medicine compound preparation of cancer pain |
CN107335011B (en) * | 2017-07-14 | 2020-10-23 | 侯爱画 | External traditional Chinese medicine compound preparation for treating cancer pain |
CN115381912A (en) * | 2022-09-23 | 2022-11-25 | 湖南省中医药研究院附属医院 | External traditional Chinese medicine compound preparation for reducing cancer pain and preparation method thereof |
CN115381912B (en) * | 2022-09-23 | 2024-02-13 | 湖南省中医药研究院 | External traditional Chinese medicine compound preparation for reducing cancer pain and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN1304045C (en) | 2007-03-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1861163A (en) | Traditional Chinese medicine composition for treating kidney-yang deficiency and deficiency of vital energy and blood, its prepn. process | |
CN1228071C (en) | Medicament for treating cervical spondylosis and preparation method thereof | |
CN1857615A (en) | Medicine for treating hepatitis and cholecystitis and its preparing method and application | |
CN1876144A (en) | A Chinese medicine for treating skin disease of fur-bearing animal and preparation process thereof | |
CN1304045C (en) | Arthralgia removing pills and their preparation | |
CN1262951A (en) | Medicine for curing arthralgia-syndrome resulted from wind,cold and dampness and its preparation method | |
CN1864730A (en) | A cancer-treating medicine | |
CN1053587C (en) | Chinese patent drug | |
CN1186067C (en) | Medicine for curing acute injury of muscle and tendon and its preparation method | |
CN1254267C (en) | Medicine for treating gastral cavity pain and its preparation method | |
CN1304027C (en) | Bone nourishing and rheumatic treating pills and their preparation | |
CN101032540A (en) | Medicine composition for curing arthritis and the preparing method and purpose thereof | |
CN1140071A (en) | Anticancer drug and preparing method thereof | |
CN1899439A (en) | Chinese medicine composition for treating goat and its use | |
CN1304043C (en) | Longhedan pills and their preparation | |
CN1899387A (en) | Method for preventing and treating child convulsion and its preparing method | |
CN1840101A (en) | Chinese medicine with wind-dispelling damp-eliminating, collaterals-dredging, coldness-expelling pain-relieving functions and preparation process thereof | |
CN1176689C (en) | Medicine for treating primary dysmenorrhea and its prepn | |
CN1471954A (en) | Chinese medicine for withdrawal of drug dependence | |
CN1261156C (en) | Medicine for treating chronic gastroenteritis and colitis | |
CN101066291A (en) | Chinese medicine composition for transquilizing, warming Yang, benefiting Qi and nourishing heart and its prepn | |
CN1281252C (en) | Medicinal composition for treating urinary lithiasis and its preparing method | |
CN1299752C (en) | Traditional Chinese medicine capsule for treating urinary calculus and its prepn. method | |
CN1274353C (en) | Medication for curing children's infantile malnutrition and preparation method | |
CN1907315A (en) | Orthopaedics disease treating and preventing medicinal composition |
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 | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070314 |
|
CF01 | Termination of patent right due to non-payment of annual fee |