CN105944083A - Compound nursing agent for treating fibromyalgia syndrome and preparation method of compound nursing agent - Google Patents
Compound nursing agent for treating fibromyalgia syndrome and preparation method of compound nursing agent Download PDFInfo
- Publication number
- CN105944083A CN105944083A CN201610287019.8A CN201610287019A CN105944083A CN 105944083 A CN105944083 A CN 105944083A CN 201610287019 A CN201610287019 A CN 201610287019A CN 105944083 A CN105944083 A CN 105944083A
- Authority
- CN
- China
- Prior art keywords
- parts
- nursing agent
- fibromyalgia syndrome
- compound recipe
- agent
- 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.)
- Pending
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1825—Fibroblast growth factor [FGF]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/357—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4525—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7135—Compounds containing heavy metals
- A61K31/714—Cobalamins, e.g. cyanocobalamin, i.e. vitamin B12
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/724—Cyclodextrins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Marine Sciences & Fisheries (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention discloses a compound nursing agent for treating fibromyalgia syndrome and a preparation method of the compound nursing agent. The compound nursing agent consists of the following ingredients: cyclobenzaprine, amitriptyline, paroxetine, baclofen, propantheline, S-adenosylmethionine, nardosinone, celecoxib, lornoxicam, a basic fibroblast growth factor, methycobal, tryptophan, maltodextrin and casein phosphopeptides. The compound nursing agent disclosed by the invention has functions of diminishing inflammation and relieving pain, soothing liver and relieving depression, dispelling wind and eliminating dampness, clearing and activating channels and collaterals, relieving spasms and improving patients' sleep; and based upon clinical verification, the compound nursing agent is relatively high in cure rate on the fibromyalgia syndrome, good in treatment effect, remarkable in curative effect, low in toxic and side effects and free from clinical adverse reactions, and the compound nursing agent has good values and prospects of clinical popularization and application.
Description
Technical field
The present invention relates to internal medicine nursing medication field, be specifically related to a kind of for treating answering of fibromyalgia syndrome
Side's nursing agent and preparation method thereof.
Background technology
Fibromyalgia syndrome (fibromyalgia syndrome, FS) is a kind of nonarticular rheumatism, clinical table
It is now musculoskeletal system many places pain and a deadlock, and has pressure pain point at privileged sites.Fibromyalgia syndrome can
Being secondary to wound, various rheumatisms, such as osteoarthritis (osteoarthritis, OA), rheumatoid arthritis
(rheumatoid arthritis, RA) and various non-rheumatism (such as hypothyroidism, malignant tumor) etc..This
Fibrid muscle pain syndrome is referred to as secondary fibromyalgia syndrome (secondary fibromyalgia
Syndromen), as without other illness, the most referred to as primary fibromyalgia syndrome (primary
fibromyagia syndrome)。
It is mainly characterized by chronic widely, symmetrical musculoskeletal pain, may often be such that the muscle skeleton pain disabled
Pain is with unable, with the pressure pain point that multiple symmetry are widely distributed.Can and whole body fatigue stiff with morning, anxiety,
Mental symptom, sleep disorder or chronic insomnia, the nocturnal myoclonus such as melancholy, frightened, grind one's teeth in sleep, morning is stiff, occipitalia
Jumping pain, feel dizzy, cognitive defect and of short duration amnesia etc..It addition, also have feeling of numbness, twinge
Sense, brothers' paraesthesia, gastrointestinal symptoms and bladder disorders are the most common, have a strong impact on the quality of life of patient.FMS
Occur at each age level, but 25~the age bracket of 45 years old, the sickness rate of women is seven times of male.
FMS can cause individual quality of life and somatic function by heavy damage, and its degree can be closed with rheumatic
Joint inflammation is compared.
Fibromyalgia syndrome is a kind of idiopathic disease, and its Pathophysiology is failed to understand so far, the therefore treatment to it
Method is also few, and current treatment is directed generally to improve sleep state, lowers the sensitivity of pain sensation sensory receptor,
Improve muscle blood flow etc..
Summary of the invention
Present invention solves the technical problem that and be to provide a kind of compound recipe nursing agent for treating fibromyalgia syndrome
And preparation method thereof.
A kind of compound recipe nursing agent for treating fibromyalgia syndrome, including the composition of following weight portion: amine benzene
Cycloheptene 16~32 parts, amitriptyline 12~23 parts, paroxetine 10~19 parts, baclofen 8~14 parts, general
Lu Benxin 7.5~13.5 parts, S-adenosylmethionine 6~12 parts, the glycosides new ketone 4 of pine~11 parts, celecoxib 2~9
Part, lornoxicam 1~5 parts, basic fibroblast growth factor 0.5~1.5 parts, cobinamide 0.1~0.7 part,
Tryptophan 18~23 parts, maltodextrin 24~56 parts, phosphopeptide caseinate 34~56 parts.
Further, described amitriptyline is the derivant of dibenzocycloheptene, is to pass through micro passage reaction
It is synthesized.Micro passage reaction is that multistep reaction continuous feed in the case of need not separate is produced
Thing, not only greatly simplifies operating procedure, saves time and personnel;And improve product quality and life
Produce cost.
Further, the described new ketone of glycosides pine is to be extracted by the dry root and rhizome of Valerianaceae plant Radix Et Rhizoma Nardostachyos Batal
A kind of flavone compound gone out, concrete extraction process is with the dry rhizome of Radix Et Rhizoma Nardostachyos as raw material, dry, pulverize,
It is subsequently adding the mixed enzyme enzymolysis of cellulase and pectase, then with ultrasonic extraction 2~3 times, collects ultrasonic
Extracting solution and medicinal residues, and medicinal residues distilled water decocting in water again is extracted, collect aqueous extract, merge twice extraction
Liquid, is subsequently adding petroleum ether and with ultrasonic extraction, finally uses column chromatography, and collects eluent, concentrates,
It is dried, obtains nardosinone;It has calmness, epilepsy, antidepressant, rush nerve growth, improves cognitive energy
Power, protecting myocardial cell, blood pressure lowering, the antibacterial and multiple pharmacologically active such as malaria, antitumor.
Another technical scheme of the present invention is: provide a kind of compound recipe nursing for treating fibromyalgia syndrome
The preparation method of agent, detailed process is: by described proportioning by prohe tatriene, amitriptyline, paroxetine,
The new ketone of baclofen, probanthine, S-adenosylmethionine, glycosides pine, celecoxib, lornoxicam, alkalescence become
Fibroblast growth factor, cobinamide, tryptophan, maltodextrin, phosphopeptide caseinate mix, and are subsequently adding
The antioxidant of 0.1~0.3 part, the filler of 245~324 parts, the disintegrating agent of 2~4 parts, the lubricant of 3~6 parts,
Being placed in blender stirring 20~30min, rotating speed is 400~500r/min, obtains described compound recipe nursing agent.
Further, described compound recipe nursing agent is made sheet by pelletize, tabletting, 10~15 DEG C of low temperature sterilizations
Agent.
Further, described antioxidant is: plant polyphenol or tocopherol, and antioxidant can protect medicine
Go bad from oxidative damage, and there is in human body alimentary canal antioxidation, prevent digestive tract generation oxygen
Change damage, it is ensured that medicine at utmost plays drug effect.
Further, described filler is: pregelatinized Starch, and pregelatinized Starch good fluidity has bonding concurrently
And dilution function, and compressibility is good, can increase the mechanical strength of tablet, reduces the breakage rate adding man-hour, and can
Strengthen the stability of medicine preferentially to combine moisture, do not react with principal agent.
Further, described disintegrating agent is: crospolyvinylpyrrolidone;Crospolyvinylpyrrolidone has
There are hygroscopicity, easy mobility, the strongest expansion character and the complexing power with multiclass material, in medical industry
It is mainly used as the disintegrating agent of tablet, and crospolyvinylpyrrolidone also can improve capillary activity and hydration energy
Power.
Further, described wetting agent is: magnesium stearate, and magnesium stearate has good mobility, makes pressure
Can feed smoothly and slice during sheet, and reduce sticking and reducing and rub between granule and granule, tablet and nib wall
Wiping power, makes unilateral smooth and beautiful appearance.
Compared with prior art, beneficial effects of the present invention is embodied in: the compound recipe nursing agent of the present invention has antiinflammatory
Analgesia, dispersing the stagnated live-QI to relieve the stagnation of QI, expelling wind and removing dampness, dredge the meridian passage, solution spasm, the effect of patient sleeps improved, wherein amine
The new ketone of phenyl ring heptene, amitriptyline, paroxetine, glycosides pine has antidepressant, improves patient sleeps, releases flesh
The effect of spasm;Baclofen, probanthine, S-adenosylmethionine, basic fibroblast growth factor are mainly done
Disturb excitatory neurotransmitter release, the conduction between suppression spinal cord synapse, dredge the meridian passage, trophic nerve;Plug carrys out former times
Cloth, lornoxicam anti-inflammatory and antalgic;Main cobinamide, tryptophan, maltodextrin, phosphopeptide caseinate master
To prevent patient from side reaction occurring during taking medicine as nutrient substance in conjunction with other drug composition, and
The immunity of patient, beneficially patient can be improved recover rapidly.And the present invention is according to clinical verification to fibromyalgia
Syndrome cure rate is higher, and good absorbing effect is evident in efficacy, and toxic and side effects is little, without clinical adverse, tool
There are good clinic popularization and application values and prospect.
Detailed description of the invention
Embodiment 1: the present embodiment prepares the sheet of a kind of compound recipe nursing agent for treating fibromyalgia syndrome
Agent, including the composition of following weight portion: prohe tatriene 16 parts, amitriptyline 12 parts, paroxetine 10
Part, the new ketone 4 parts of baclofen 8 parts, probanthine 7.5 parts, S-adenosylmethionine 6 parts, glycosides pine, plug come
Former times cloth 2 parts, lornoxicam 1 part, basic fibroblast growth factor 0.5 part, cobinamide 0.1 part, color ammonia
Acid 18 parts, maltodextrin 24 parts, phosphopeptide caseinate 34 parts.
Wherein, described amitriptyline is the derivant of dibenzocycloheptene, is to be reacted by micro passage reaction
Synthesis.Micro passage reaction is that multistep reaction continuous feed in the case of need not separate obtains product, no
But greatly simplifie operating procedure, save time and personnel;And improve product quality and production cost.
Wherein, the described new ketone of glycosides pine is to be extracted by the dry root and rhizome of Valerianaceae plant Radix Et Rhizoma Nardostachyos Batal
A kind of flavone compound, concrete extraction process is with the dry rhizome of Radix Et Rhizoma Nardostachyos as raw material, dry, pulverize, so
Rear addition cellulase and the mixed enzyme enzymolysis of pectase, then use ultrasonic extraction 2 times, collects supersound extraction
Liquid, and medicinal residues distilled water decocting in water again is extracted, collect aqueous extract, merge twice extracting solution, then add
Enter petroleum ether and with ultrasonic extraction, finally use column chromatography, collect eluent, concentrate, be dried, obtain
Nardosinone;It has calmness, epilepsy, antidepressant, rush nerve growth, improves cognitive competence, the protection heart
Myocyte, blood pressure lowering, the antibacterial and multiple pharmacologically active such as malaria, antitumor.
The preparation side of a kind of compound recipe nursing agent tablet for treating fibromyalgia syndrome prepared by the present embodiment
Method, detailed process is: by described proportioning by prohe tatriene, amitriptyline, paroxetine, baclofen, general
The new ketone of Lu Benxin, S-adenosylmethionine, glycosides pine, celecoxib, lornoxicam, basic fibroblast growth because of
Son, cobinamide, tryptophan, maltodextrin, phosphopeptide caseinate mix, and are subsequently adding 0.1 part anti-
Oxidant, the filler of 245 parts, the disintegrating agent of 2 parts, the lubricant of 3 parts, be placed in blender stirring 20min,
Rotating speed is 400r/min, obtains described compound recipe nursing agent, then by pelletize, tabletting, 10 DEG C of low temperature sterilizations
Make tablet, every 0.5g.
Wherein, described antioxidant is: plant polyphenol, and antioxidant can protect the drug against oxidative damage
And go bad, and there is in human body alimentary canal antioxidation, prevent digestive tract generation oxidative damage, it is ensured that
Medicine at utmost plays drug effect.
Wherein, described filler is: pregelatinized Starch, pregelatinized Starch good fluidity, has bonding concurrently with dilute
Release function, and compressibility is good, the mechanical strength of tablet can be increased, reduce the breakage rate adding man-hour, Ke Yiyou
First combine moisture and strengthen the stability of medicine, do not react with principal agent.
Wherein, described disintegrating agent is: crospolyvinylpyrrolidone;Crospolyvinylpyrrolidone has suction
Moist, easy mobility, the strongest expansion character and the complexing power with multiclass material, main in medical industry
As the disintegrating agent of tablet, and crospolyvinylpyrrolidone also can improve capillary activity and hydratability.
Wherein, described wetting agent is: magnesium stearate, and magnesium stearate has good mobility, when making tabletting
Can feed smoothly and slice, and reduce sticking and reduce frictional force between granule and granule, tablet and nib wall,
Make unilateral smooth and beautiful appearance.
Usage and dosage: three times a day, each 2, one after each meal.
Embodiment 2: the present embodiment prepares the sheet of a kind of compound recipe nursing agent for treating fibromyalgia syndrome
Agent, including the composition of following weight portion: prohe tatriene 24 parts, amitriptyline 17.5 parts, paroxetine 14.5
Part, the new ketone 7.5 parts of baclofen 11 parts, probanthine 10.5 parts, S-adenosylmethionine 9 parts, glycosides pine,
Celecoxib 5.5 parts, lornoxicam 3 parts, basic fibroblast growth factor 1 part, cobinamide 0.4 part,
Tryptophan 20.5 parts, maltodextrin 40 parts, phosphopeptide caseinate 45 parts.
Wherein, described amitriptyline is the derivant of dibenzocycloheptene, is to be reacted by micro passage reaction
Synthesis.Micro passage reaction is that multistep reaction continuous feed in the case of need not separate obtains product, no
But greatly simplifie operating procedure, save time and personnel;And improve product quality and production cost.
Wherein, the described new ketone of glycosides pine is to be extracted by the dry root and rhizome of Valerianaceae plant Radix Et Rhizoma Nardostachyos Batal
A kind of flavone compound, concrete extraction process is with the dry rhizome of Radix Et Rhizoma Nardostachyos as raw material, dry, pulverize, so
Rear addition cellulase and the mixed enzyme enzymolysis of pectase, then use ultrasonic extraction 2 times, collects supersound extraction
Liquid and medicinal residues, and medicinal residues distilled water decocting in water again is extracted, collect aqueous extract, merge twice extracting solution,
It is subsequently adding petroleum ether and with ultrasonic extraction, finally uses column chromatography, collect eluent, concentrate, be dried,
Obtain nardosinone;It has calmness, epilepsy, antidepressant, rush nerve growth, improves cognitive competence, guarantor
Protect myocardial cell, blood pressure lowering, the antibacterial and multiple pharmacologically active such as malaria, antitumor.
The preparation side of a kind of compound recipe nursing agent tablet for treating fibromyalgia syndrome prepared by the present embodiment
Method, detailed process is: by described proportioning by prohe tatriene, amitriptyline, paroxetine, baclofen, general
The new ketone of Lu Benxin, S-adenosylmethionine, glycosides pine, celecoxib, lornoxicam, basic fibroblast growth because of
Son, cobinamide, tryptophan, maltodextrin, phosphopeptide caseinate mix, and are subsequently adding 0.2 part anti-
Oxidant, the filler of 284.5 parts, the disintegrating agent of 3 parts, the lubricant of 4.5 parts, be placed in blender stirring
25min, rotating speed is 450r/min, obtains described compound recipe nursing agent, then by pelletize, tabletting, 12.5 DEG C
Low temperature sterilization makes tablet, every 0.5g.
Wherein, described antioxidant is: plant polyphenol, and antioxidant can protect the drug against oxidative damage
And go bad, and there is in human body alimentary canal antioxidation, prevent digestive tract generation oxidative damage, it is ensured that
Medicine at utmost plays drug effect.
Wherein, described filler is: pregelatinized Starch, pregelatinized Starch good fluidity, has bonding concurrently with dilute
Release function, and compressibility is good, the mechanical strength of tablet can be increased, reduce the breakage rate adding man-hour, Ke Yiyou
First combine moisture and strengthen the stability of medicine, do not react with principal agent.
Wherein, described disintegrating agent is: crospolyvinylpyrrolidone;Crospolyvinylpyrrolidone has suction
Moist, easy mobility, the strongest expansion character and the complexing power with multiclass material, main in medical industry
As the disintegrating agent of tablet, and crospolyvinylpyrrolidone also can improve capillary activity and hydratability.
Wherein, described wetting agent is: magnesium stearate, and magnesium stearate has good mobility, when making tabletting
Can feed smoothly and slice, and reduce sticking and reduce frictional force between granule and granule, tablet and nib wall,
Make unilateral smooth and beautiful appearance.
Usage and dosage: three times a day, each 2, one after each meal.
Embodiment 3: the present embodiment prepares the sheet of a kind of compound recipe nursing agent for treating fibromyalgia syndrome
Agent, including the composition of following weight portion: prohe tatriene 32 parts, amitriptyline 23 parts, paroxetine 19
Part, the new ketone 11 parts of baclofen 14 parts, probanthine 13.5 parts, S-adenosylmethionine 12 parts, glycosides pine,
Celecoxib 9 parts, lornoxicam 5 parts, basic fibroblast growth factor 1.5 parts, cobinamide 0.7 part,
Tryptophan 23 parts, maltodextrin 56 parts, phosphopeptide caseinate 56 parts.
Wherein, described amitriptyline is the derivant of dibenzocycloheptene, is to be reacted by micro passage reaction
Synthesis.Micro passage reaction is that multistep reaction continuous feed in the case of need not separate obtains product, no
But greatly simplifie operating procedure, save time and personnel;And improve product quality and production cost.
Wherein, the described new ketone of glycosides pine is to be extracted by the dry root and rhizome of Valerianaceae plant Radix Et Rhizoma Nardostachyos Batal
A kind of flavone compound, concrete extraction process is with the dry rhizome of Radix Et Rhizoma Nardostachyos as raw material, dry, pulverize, so
Rear addition cellulase and the mixed enzyme enzymolysis of pectase, then use ultrasonic extraction 3 times, collects supersound extraction
Liquid and medicinal residues, and medicinal residues distilled water decocting in water again is extracted, collect aqueous extract, merge twice extracting solution,
It is subsequently adding petroleum ether and with ultrasonic extraction, finally uses column chromatography, collect eluent, concentrate, be dried,
Obtain nardosinone;It has calmness, epilepsy, antidepressant, rush nerve growth, improves cognitive competence, guarantor
Protect myocardial cell, blood pressure lowering, the antibacterial and multiple pharmacologically active such as malaria, antitumor.
The preparation side of a kind of compound recipe nursing agent tablet for treating fibromyalgia syndrome prepared by the present embodiment
Method, detailed process is: by described proportioning by prohe tatriene, amitriptyline, paroxetine, baclofen, general
The new ketone of Lu Benxin, S-adenosylmethionine, glycosides pine, celecoxib, lornoxicam, basic fibroblast growth because of
Son, cobinamide, tryptophan, maltodextrin, phosphopeptide caseinate mix, and are subsequently adding 0.3 part anti-
Oxidant, the filler of 324 parts, the disintegrating agent of 4 parts, the lubricant of 6 parts, be placed in blender stirring 30min,
Rotating speed is 500r/min, obtains described compound recipe nursing agent, then by pelletize, tabletting, 15 DEG C of low temperature sterilizations
Make tablet, every 0.5g.
Wherein, described antioxidant is: tocopherol, antioxidant can protect the drug against oxidative damage and
Rotten, and there is in human body alimentary canal antioxidation, prevent digestive tract generation oxidative damage, it is ensured that medicine
Product at utmost play drug effect.
Wherein, described filler is: pregelatinized Starch, pregelatinized Starch good fluidity, has bonding concurrently with dilute
Release function, and compressibility is good, the mechanical strength of tablet can be increased, reduce the breakage rate adding man-hour, Ke Yiyou
First combine moisture and strengthen the stability of medicine, do not react with principal agent.
Wherein, described disintegrating agent is: crospolyvinylpyrrolidone;Crospolyvinylpyrrolidone has suction
Moist, easy mobility, the strongest expansion character and the complexing power with multiclass material, main in medical industry
As the disintegrating agent of tablet, and crospolyvinylpyrrolidone also can improve capillary activity and hydratability.
Wherein, described wetting agent is: magnesium stearate, and magnesium stearate has good mobility, when making tabletting
Can feed smoothly and slice, and reduce sticking and reduce frictional force between granule and granule, tablet and nib wall,
Make unilateral smooth and beautiful appearance.
Usage and dosage: three times a day, each 2, one after each meal.
Present invention application in fibromyalgia syndrome:
One. animal toxicity test:
1. animal selects and is administered: choose the mice 60 of health, then by mice at the environment of subzero 20 DEG C
Middle raising one day, then raises one day in the environment of 20 DEG C, and cold and heat succeed each other raising one month, promotes mice
Have the phenomenon of muscular spasm, tic of the limbs, then mice is randomly divided into 4 groups, often group 15, respectively
It is designated as A group, B group, C group, D group.Then ABC group takes the tablet of the embodiment of the present invention 1~3 preparation,
Dose is taken by the amount of embodiment requirement;D group takes the embodiment of the present invention 2 by 4 times of embodiment requirement dose
The tablet of preparation.Each group gastric infusion respectively, three times a day, successive administration 10 days.
2. test data statistics and result: after off-test, the muscular spasm situation of tri-groups of mices of ABC disappears, and takes out
Phenomenon of jerking no longer occurs, each group mice activity increases, and then dissects D group mice, and mice has no any device
Official is excessive and organ injury occur due to dose, therefore, the compound preparation of the present invention is safe and effective, and poison is secondary
Act on little.
Two. clinical treatment is verified
1, case selection: select the fibromyalgia syndrome patient 80 example clinical observation that certain hospital makes a definite diagnosis, patient
Age 21~64 years old, 39.5 years old mean age, patient is randomly divided into four groups, often organizes 20 people, Qi Zhongzhi
Treatment group has 3 groups, matched group 1 group, and patient's qualifications and record of service are basically identical, without significant difference, have comparability.
2, Therapeutic Method: treatment group patient takes the tablet of the embodiment of the present invention 1~3 preparation respectively, and dose is pressed
The dose that embodiment specifies;Matched group take sell on the market of equivalent for treating fibromyalgia syndrome
Medicine, three times a day, takes medicine 20 days continuously.
3, observation index
Use VAS scale to judge the pain degree (0~10.0 as painless, and 10 is the most bitterly) of muscle, observe simultaneously
Patient muscle's pain, dysfunction and sleep state, carry out efficacy evaluation after 3 courses for the treatment of.
4, efficacy determination
(1) cure: the clinical symptoms such as myalgia, whole body tenderness, sleep disorder, fatigue and anxiety disappear substantially
Losing, physical recovery is healthy, does not affect orthobiosis.
(2) taking a turn for the better: the symptoms such as myalgia, whole body tenderness are substantially alleviated, pain substantially alleviates, sleep disorder,
The clinical symptoms such as fatigue and anxiety substantially alleviate.
(3) invalid: symptom is with treating front no significant difference.
5. therapeutic outcome: before and after each group patient treatment outcome and treatment, pain VAS is measured and is compared as follows table:
Group | Cure | Take a turn for the better | Invalid | Effective percentage/% | VAS before treatment | VAS after treatment |
Embodiment 1 | 16 | 2 | 2 | 90 | 10 | 7 |
Embodiment 2 | 18 | 1 | 1 | 95 | 10 | 5 |
Embodiment 3 | 17 | 1 | 2 | 90 | 10 | 6 |
Matched group | 15 | 1 | 4 | 80 | 10 | 8 |
6. conclusion: from above-mentioned clinical treatment case, compound recipe nursing agent prepared by the present invention has good clinic
Effect, its effective percentage reaches 90%, and relatively matched group is high, can effectively treat fibromyalgia syndrome, and curative effect shows
Writing, side effect is little.
Although the present invention being described and illustrated with reference to its specific embodiments, but those skilled in the art will appreciate that
Arrive, without departing from the spirit and scope of the present invention it can be variously modified, revise and replace.
Such as, due to the change of responding ability of the people of treated particular condition, beyond preferred dose as explained above
Effective dose may be suitable for.Similarly, it was observed that pharmacology respond may basis and rely on selected given activity
Compound or whether there is pharmaceutical carrier and preparation type and mode of administration used and become, according to the mesh of the present invention
And practice be contemplated in result this kind of expection change or difference.Therefore, the invention is intended to only by following patent
The scope required limits and these claim should be explained in rational degree as broadly as possible.
Claims (9)
1. the compound recipe nursing agent being used for treating fibromyalgia syndrome, it is characterised in that described compound recipe protects
Reason agent includes the composition of following weight portion: prohe tatriene 16~32 parts, amitriptyline 12~23 parts, Paro west
Spit of fland 10~19 parts, baclofen 8~14 parts, probanthine 7.5~13.5 parts, S-adenosylmethionine 6~12 parts,
The new ketone 4 of glycosides pine~11 parts, celecoxib 2~9 parts, lornoxicam 1~5 parts, basic fibroblast growth factor 0.5~1.5
Part, cobinamide 0.1~0.7 part, tryptophan 18~23 parts, maltodextrin 24~56 parts, casein phosphoric acid
Peptide 34~56 parts.
A kind of compound recipe nursing agent for treating fibromyalgia syndrome, its feature
Being, described amitriptyline is the derivant of dibenzocycloheptene, is to be synthesized by micro passage reaction
's.
A kind of compound recipe nursing agent for treating fibromyalgia syndrome, its feature
Being, the described new ketone of glycosides pine is the one extracted by the dry root and rhizome of Valerianaceae plant Radix Et Rhizoma Nardostachyos Batal
Flavone compound.
A kind of compound recipe nursing agent for treating fibromyalgia syndrome, its feature
Being, preparation method is: by described proportioning by prohe tatriene, amitriptyline, paroxetine, baclofen,
Probanthine, S-adenosylmethionine, glycosides pine new ketone, celecoxib, lornoxicam, basic fibroblast growth
The factor, cobinamide, tryptophan, maltodextrin, phosphopeptide caseinate mix, and are subsequently adding 0.1~0.3
The antioxidant of part, the filler of 245~324 parts, the disintegrating agent of 2~4 parts, the lubricant of 3~6 parts, be placed in
Stirring 20~30min in blender, rotating speed is 400~500r/min, obtains described compound recipe nursing agent.
A kind of preparation side of the compound recipe nursing agent for treating fibromyalgia syndrome
Method, it is characterised in that described compound recipe nursing agent is made by pelletize, tabletting, 10~15 DEG C of low temperature sterilizations
Tablet.
A kind of preparation side of the compound recipe nursing agent for treating fibromyalgia syndrome
Method, it is characterised in that described antioxidant is: plant polyphenol or tocopherol.
A kind of preparation side of the compound recipe nursing agent for treating fibromyalgia syndrome
Method, it is characterised in that described filler is: pregelatinized Starch.
A kind of preparation side of the compound recipe nursing agent for treating fibromyalgia syndrome
Method, it is characterised in that described disintegrating agent is: crospolyvinylpyrrolidone.
A kind of preparation side of the compound recipe nursing agent for treating fibromyalgia syndrome
Method, it is characterised in that described wetting agent is: magnesium stearate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610287019.8A CN105944083A (en) | 2016-05-03 | 2016-05-03 | Compound nursing agent for treating fibromyalgia syndrome and preparation method of compound nursing agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610287019.8A CN105944083A (en) | 2016-05-03 | 2016-05-03 | Compound nursing agent for treating fibromyalgia syndrome and preparation method of compound nursing agent |
Publications (1)
Publication Number | Publication Date |
---|---|
CN105944083A true CN105944083A (en) | 2016-09-21 |
Family
ID=56913408
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610287019.8A Pending CN105944083A (en) | 2016-05-03 | 2016-05-03 | Compound nursing agent for treating fibromyalgia syndrome and preparation method of compound nursing agent |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105944083A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1678585A (en) * | 2002-06-28 | 2005-10-05 | 欧洲凯尔特公司 | Therapeutic agents useful for treating pain |
CN101484152A (en) * | 2006-06-08 | 2009-07-15 | 舒沃茨药物股份公司 | Therapeutic combination for painful medical conditions |
CN101657193A (en) * | 2007-03-09 | 2010-02-24 | 切尔西治疗公司 | The droxidopa and the pharmaceutical composition thereof that are used for the treatment of fibromyalgia |
CN102266563A (en) * | 2011-07-13 | 2011-12-07 | 赵磊 | Compound analgesic composition and preparation method thereof |
CN105056133A (en) * | 2015-08-21 | 2015-11-18 | 孙丕磊 | Traditional Chinese medicine pills for treating fibromyalgia syndrome and preparing method of traditional Chinese medicine pills |
-
2016
- 2016-05-03 CN CN201610287019.8A patent/CN105944083A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1678585A (en) * | 2002-06-28 | 2005-10-05 | 欧洲凯尔特公司 | Therapeutic agents useful for treating pain |
CN101484152A (en) * | 2006-06-08 | 2009-07-15 | 舒沃茨药物股份公司 | Therapeutic combination for painful medical conditions |
CN101657193A (en) * | 2007-03-09 | 2010-02-24 | 切尔西治疗公司 | The droxidopa and the pharmaceutical composition thereof that are used for the treatment of fibromyalgia |
CN102266563A (en) * | 2011-07-13 | 2011-12-07 | 赵磊 | Compound analgesic composition and preparation method thereof |
CN105056133A (en) * | 2015-08-21 | 2015-11-18 | 孙丕磊 | Traditional Chinese medicine pills for treating fibromyalgia syndrome and preparing method of traditional Chinese medicine pills |
Non-Patent Citations (2)
Title |
---|
徐健: "帕罗西汀和阿米替林治疗原发性纤维肌痛综合征的疗效和安全性对照研究", 《中国心理卫生杂志》 * |
高崎: "帕罗西汀与阿米替林治疗原发性纤维肌痛综合征的临床价值分析", 《中国医药指南》 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104523865B (en) | Medicine for treating breast diseases | |
CN102526640B (en) | Pantoprazole sodium medicine compound and preparation technology thereof | |
CN104524247B (en) | One treats migrainous medical composition and its use | |
CN103705789A (en) | Pharmaceutical composition for treating cerebral hemorrhage | |
CN101596302A (en) | A kind of treatment treating coronary heart disease and angina pectoris and preparation method thereof | |
CN103784893B (en) | A kind of medicine for the treatment of cerebral apoplexy sequela | |
CN105944083A (en) | Compound nursing agent for treating fibromyalgia syndrome and preparation method of compound nursing agent | |
CN101244181B (en) | Plaster for bone paralysis with function of qufengshengshi, blood circulation activating and stasis removing, and removing the obstruction in the channels to relieve pain, and preparation thereof | |
CN101518582A (en) | Traditional Chinese medicine cream for treating bone fracture diseases and preparation method thereof | |
CN104474173B (en) | A kind of medicine for treating facioplegia | |
CN102552742B (en) | Medicine for treating scapulohumeral periarthritis and rheumatism | |
US11684631B2 (en) | Method of treating cancer with composition of traditional Chinese medicine and its preparation method thereof | |
CN102319330A (en) | Traditional Chinese medicine cataplasma for treating hyperosteogeny and preparation method thereof | |
CN106581468A (en) | Preparation method of traditional Chinese medicine capable of treating gastric ulcer | |
CN101422489A (en) | Traditional Chinese medicine preparation for treating adenocarcinoma | |
CN105832885A (en) | Traditional Chinese medicine composition for treating insomnia | |
CN104306811B (en) | A kind of Chinese medicine composition for treating children's psoriasis vulgaris | |
CN104740038B (en) | One kind treats prostatitic Chinese medicine | |
CN103251851B (en) | Internal and external traditional Chinese medicine formulation for treating rheumatic and rheumatoid diseases | |
CN102000297B (en) | Traditional Chinese medical composition for treating coronary heart disease | |
CN102940671A (en) | Medicine composition for treating diabetic foot | |
CN101979010A (en) | Chinese medicament for treating metrorrhagia | |
CN101653495A (en) | Chinese traditional medicine for curing insomnia | |
CN106177562A (en) | The Chinese medicine composition that a kind for the treatment of is had blood in stool | |
CN106139032A (en) | A kind of Chinese medicine composition treating diabetes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20160921 |