CN104587470B - Pharmaceutical composition for promoting bone healing after osteoportic fracture operations and application of pharmaceutical composition - Google Patents

Pharmaceutical composition for promoting bone healing after osteoportic fracture operations and application of pharmaceutical composition Download PDF

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CN104587470B
CN104587470B CN201510088461.3A CN201510088461A CN104587470B CN 104587470 B CN104587470 B CN 104587470B CN 201510088461 A CN201510088461 A CN 201510088461A CN 104587470 B CN104587470 B CN 104587470B
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statinses
pharmaceutical composition
ketorolac tromethamine
knitting
lovastatin
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CN104587470A (en
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杨林
曾萍
周迎锋
张超
马超
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First Affiliated Hospital of Xinxiang Medical University
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First Affiliated Hospital of Xinxiang Medical University
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Abstract

The invention discloses a pharmaceutical composition for promoting bone healing after osteoportic fracture operations and application of the pharmaceutical composition. The pharmaceutical composition comprises statins and ketorolac tromethamine, wherein the statins are selected from one or more of simvastatin, lovastatin and atorvastatin. The pharmaceutical composition has the advantages of improving the bone mass of osteoporosis patients to a greater extent and accelerating the healing of osteoportic fracture to improve the mechanical property.

Description

A kind of pharmaceutical composition for promoting the postoperative knitting of osteoporotic fracture and its application
Technical field
The invention belongs to pharmaceutical technology field, and in particular to a kind of pharmaceutical composition for after fracture operation and its promoting Enter the application of the aspects such as the postoperative knitting of osteoporotic fracture.
Background technology
Osteoporosis (osteoporosis, OP) are a kind of general bone metabolism diseases, and it is with bone amount in unit volume Reduce, bone trabecula number is reduced, cortical bone is thinning, osseous tissue fine structure is destroyed, medullary cavity is broadening, bone fragility increases and is fractured Dangerous probability increase is characterized, and is current clinical commonly encountered diseases, frequently-occurring disease.Fracture is osteoporosis most serious consequence, and is sent out Normal indolence is compared after bone growth promoting folding.At present, the whole world about has more than 200,000,000 patients with osteoporosis, fracture caused by its institute 33% is accounted in women more than 50 years old, male is 20%.The medicine of traditional treatment osteoporosis has:Anti- bone resorption medicine is double Phosphate, calcitonin, calcium vitamin D and its metabolite;The medicine of promoting bone growing --- fluoride.
In recent years, have scholar to find under study for action, statinses can reduce the loss of bone amount, prevent the generation of fracture with And the healing of acceleration fracture.Statinses are the inhibitor of 3-hydroxyl-3-methylglutaryl coenzyme A A, reduce the life of cholesterol Into, while interleukin product can be decomposed, the generation of cytokine being reduced, research finds that statinses can also be by promoting The gene expression of bone morphogenetic protein (bone morphogenetic protein2, BMP-2), acts on osteoblast increasing Plus the mechanism such as the expression of Bone Gla protein (OPG) gene is reaching increase bone amount, improve the purpose of bone density.
Although many research confirms that statinses have ossification potential, systemic administration reaches the medicine of osseous tissue Thing concentration is too low, and skeletonization effect is limited (von Stechow D, Fish S, Yahalom D, et al.Does simvastatin stimulate bone formation in vivo[J]BMC Musculoskelet Disord,2003,4:8.);If increased Plus dosage, then unacceptable toxic and side effects occur.Drug combination provides new thinking to solve this problem (Abdul-Majeed S,Mohamed N,Soelaiman IN.Effects of tocotrienoland lovastatin combination on osteoblast and osteoclast activity in estrogen-deficient Osteoporosis [J] .Evid Based Complement Alternat Med, 2012,2012:960742.).
At present, osteoporosis or union of osteoportic fracture aspect are at home and abroad treated, is not yet found with Statins Medicine is combined the medicine as main active with ketorolac tromethamine.
The content of the invention
Statinses can be used to controlling raising bone density, but it is dense that the medicine of osseous tissue is reached after being administered due to mode by oral administration Low, and toxic and side effects that heavy dose of administration brings are spent, therefore limits statinses application in this respect.The present inventor It was unexpectedly observed that while fracture surgery is eased pain using ketorolac tromethamine, it can significantly increase statin in clinical application Class medicine promotes the curative effect of the postoperative knitting of osteoporotic fracture.
In the research of further animal experiment, inventor has found to be greatly lowered after statinses dosage, coughs up with ketone Sour trometamol drug combination has the synergism for promoting the postoperative knitting of osteoporotic fracture.For this purpose, the present inventor with Ketorolac tromethamine with low dose statinses as active component, so as to provide a kind of good effect, toxic and side effects Low pharmaceutical composition and its in the application for promoting the aspects such as the postoperative knitting of osteoporotic fracture.Its specific technical scheme It is as follows:
A kind of pharmaceutical composition for promoting the postoperative knitting of osteoporotic fracture, it contains statinses and ketorolac Trometamol.Preferably, the active component of pharmaceutical composition as described above is made up of statinses and ketorolac tromethamine.
It is further preferred that statinses of the present invention are selected from simvastatin, lovastatin and atorvastatin One or more of calcium.When described statinses are simvastatins, the quality of simvastatin and ketorolac tromethamine Than for (2-10):1;It is preferred that simvastatin is (4-6) with the mass ratio of ketorolac tromethamine:1.When described statinses When being lovastatin, lovastatin is (1-5) with the mass ratio of ketorolac tromethamine:1;It is preferred that lovastatin and Ketoralac ammonia The mass ratio of butantriol is (2-3):1.When described statinses are Atorvastatin calciums, Atorvastatin calcium is coughed up with ketone The mass ratio of sour trometamol is (0.1-0.8):1;It is preferred that Atorvastatin calcium is with the mass ratio of ketorolac tromethamine (0.2-0.4):1.
There is, therefore of the present invention rush few, easy to implement easy to Local delivery of fracturing due to being administered systemically The pharmaceutical composition for entering the postoperative knitting of osteoporotic fracture is oral formulations, and described oral formulations include tablet, capsule Agent, granule, dry suspension, oral liquid.These oral formulations can add pharmaceuticss on the basis of above-mentioned active component Upper available adjuvant, such as includes but are not limited to filler, disintegrating agent, lubricant, binding agent, by the routine system of this area Agent technique is prepared from.In most preferably example of formulations of the invention, the oral formulations described in per unit contain Lip river and cut down him Spit of fland 5mg, ketorolac tromethamine 2mg.
The present inventor selects castration osteoporosis model, this model to be mainly used in post menopausal and old age in animal experiment Property osteoporosis research, due to rat natural life-span be 2~3 years, female rats at 6~9 months enter osteogenesis Resting stage, there are some researches show that 8-9 is all after rat excision ovary, skeleton may occur in which that bone metabolism is enlivened, and bone conversion strengthens, spongy bone The biochemical indicator for obvious bone loss, bone density value and bone metabolism occur goes out and significantly sexually revises.This characteristic is preferably The bone loss state of high conversion type osteoporosis when having imitated people's normal menopause, therefore, the female rats of castration are current public affairs The ideal animals model of the research primary osteoporosis recognized.Found by this test, the bone density of ovariectomized rat is reduced, Result of the test shows that ketorolac tromethamine can significantly increase low dose of statinses and increase bone amount, improves the effect of bone density Really, that is, bone loss caused by ovary excision is offset, is maintained Jie Jin normal thighbone density, so as to maintaining Bones morphology, improving Osteoplastic speed aspect has significant curative effect, and then promotes the postoperative knitting of osteoporotic fracture.
Based on animal experiment and the result of clinical practice, the second object of the present invention is to provide statinses and ketorolac The pharmaceutical applications of trometamol;I.e.:Statinses are being made with the compositionss of ketorolac tromethamine composition as active component For the application in the medicine for promoting the postoperative knitting of osteoporotic fracture;Or, statinses and ketorolac tromethamine Application of the compositionss of composition as active component in the medicine for preparing treatment osteoporosis;Or, statinses with Application of the compositionss of ketorolac tromethamine composition as active component in the osteoporotic medicine of preventing and treating diabeticss.
In a word, pharmaceutical composition of the invention adopts statinses and ketorolac tromethamine use in conjunction, not only more The bone amount of sufferers of osteoporosis face is improve to limits, the healing of osteoporotic fracture is also accelerated on this basis, improved Its mechanical property.In addition, the using dosage of statinses is reduced, so that the expense of patient medication is reduced, while reducing The toxic and side effects of statinses, increased the safety of medication and the compliance of patient.
Specific embodiment
Further describe the present invention with reference to specific embodiment, advantages of the present invention and feature will be with description and It is apparent.It should be understood that the embodiment is only exemplary, any restriction is not constituted to protection scope of the present invention.This Art personnel should be understood that the details of technical scheme and form can be carried out without departing from the spirit of the invention Modification is replaced, but these modifications or replacement each fall within protection scope of the present invention.
Embodiment 1:Lovastatin is combined impact test of the ketorolac tromethamine to castration osteoporotic fracture model
7 monthly age cleaning grade SD rats 40 are chosen, female, 280~320g of weight is randomly divided into sham operated rats, model Matched group, lovastatin group, ketorolac tromethamine group, therapeutic alliance group, 8 per group.
In addition to sham operated rats, other each group row bilateral ovaries enucleation, step is:Rat is pressed with 10% chloral hydrate 2m1/kg weight intraperitoneal injection of anesthesia, row abdominal cavity center stringer otch, is about 3cm after preserved skin, successively cuts, and exposes intraperitoneal Internal organs, metraterm is found with aseptic cotton carrier to both sides respectively, and excision completely is attached to the bilateral ovaries tissue of metraterm, and Stump is ligatured with silk thread, thoroughly hemostasis, return to receive and successively close otch after abdominal viscera.It is postoperative to give the unit of penicillin 800,000, Intramuscular injection, 2 times/d, continuous 3d.
After bilateral ovaries enucleation, freedom is movable and takes food 2 months, then the sawed-off art of each group rats underwent femur, and step is: Then 10% chloral hydrate 2mL/kg intraperitoneal anesthesias, bilateral femur stage casing row stringer otch respectively, cut skin, subcutaneous tissue and Deep fascia, separates exposure femur in spatium intermusculare.Periosteum is cut in femur midpoint, the sawed-off femur of row uses immediately diameter 1.2mm Intramedullary needle is fixed, and otch is closed successively.It is postoperative to give the unit of penicillin 800,000, intramuscular injection, 2 times/d, continuous 3d.
The sawed-off postoperative freely activity of femur and feed, while sham operated rats and model control group give physiology salt by 2mL/kg Water gavage;Lovastatin group (Lov groups) gavage gives lovastatin 10mg/kg;Ketorolac tromethamine group (Keto groups) gavage Give ketorolac tromethamine 2mg/kg;Therapeutic alliance group (Lov-Keto groups) gavage gives lovastatin 5mg/kg and ketorolac Trometamol 2mg/kg Combination interventions, once a day.After continuous gavage gives corresponding tested material 6 weeks, each group Rat Right is taken respectively Side whole femur, determines bone mineral density of proximal femur on Dual-energy X-rays absorptionmetry.In addition, taking the right side femur row of all rats Three-point bending test, fulcrum span is 20mm, central vertical (femur with load at an angle of 90) imposed load, speed 10mm/min, Maximum load is directly obtained in software.
The bone density and peak load of each group osteoporotic fracture rat model of table 1 compares
Model control group compares with sham operated rats,*P < 0.05,**P < 0.01;
Each administration group compares with model control group,#P < 0.05,##P < 0.01;
Lov-Keto groups compare with Lov groups,$P < 0.05,$$P < 0.01;
Lov-Keto groups compare with Keto groups,&P < 0.05,&&P < 0.01.
By the result of the test of table 1, after administration terminates, the bone density of each group osteoporotic fracture rat model and Peak load comparative result shows, compares with sham operated rats that the bone density and peak load of model control group significantly decline (P < 0.01), illustrate that castration osteoporosis model is replicated successfully;Compared with model control group, bone of the Keto groups to rat fracture Density and peak load have not significant impact (P > 0.05), and the peak load and bone density of Lov groups have certain increase, but bone The increase of density does not have significant difference (P > 0.05);And the bone density and peak load of Lov-Keto groups have significance Improve, either compare model control group or single medicine group (Lov groups, Keto groups), it there are significant difference (P < 0.05 or P < 0.01);This show lovastatin group combination ketorolac tromethamine can with it is synergitic quickening bone ore deposit composition sedimentation rate, Bone density is improved, so as to the healing for promoting to fracture.

Claims (9)

1. a kind of pharmaceutical composition for promoting the postoperative knitting of osteoporotic fracture, it is characterised in that described drug regimen Thing contains statinses and ketorolac tromethamine, and described statinses are selected from simvastatin, lovastatin and atropic Cut down statin calcium one or more.
2. the pharmaceutical composition of the postoperative knitting of osteoporotic fracture is promoted according to claim 1, it is characterised in that institute The statinses stated are simvastatins, and simvastatin is (2-10) with the mass ratio of ketorolac tromethamine:1.
3. the pharmaceutical composition of the postoperative knitting of osteoporotic fracture is promoted according to claim 1, it is characterised in that institute The statinses stated are lovastatins, and lovastatin is (1-5) with the mass ratio of ketorolac tromethamine:1.
4. the pharmaceutical composition of the postoperative knitting of osteoporotic fracture is promoted according to claim 1, it is characterised in that institute The statinses stated are Atorvastatin calciums, and Atorvastatin calcium is (0.1-0.8) with the mass ratio of ketorolac tromethamine: 1。
5. the pharmaceutical composition of the postoperative knitting of osteoporotic fracture is promoted according to any one of claim 1-4, and it is special Levy and be, it is oral formulations, described oral formulations include tablet, capsule, granule, dry suspension, oral liquid.
6. the pharmaceutical composition of the postoperative knitting of osteoporotic fracture is promoted according to claim 5, it is characterised in that every Oral formulations described in one unit contain lovastatin 5mg, ketorolac tromethamine 2mg.
7. statinses are preparing promotion osteoporotic with the compositionss of ketorolac tromethamine composition as active component Application in the medicine of fracture surgery knitting, described statinses cut down him selected from simvastatin, lovastatin and atropic One or more of spit of fland calcium.
8. statinses are preparing treatment osteoporosis with the compositionss of ketorolac tromethamine composition as active component Medicine in application, the one kind or many of described statinses selected from simvastatin, lovastatin and Atorvastatin calcium Kind.
9. statinses are preparing preventing and treating diabeticss with the compositionss of ketorolac tromethamine composition as active component Application in osteoporotic medicine, described statinses are selected from simvastatin, lovastatin and Atorvastatin calcium One or more.
CN201510088461.3A 2015-02-26 2015-02-26 Pharmaceutical composition for promoting bone healing after osteoportic fracture operations and application of pharmaceutical composition Expired - Fee Related CN104587470B (en)

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CN106333977B (en) * 2015-07-06 2020-02-21 陕西天奎生物医药科技有限公司 Natural pharmaceutical composition for treating osteoporotic fracture and/or osteoarthritis and application thereof
CN105726532A (en) * 2016-02-03 2016-07-06 张少峰 Simvastatin composition and application thereof in preparation of medicine for treating osteoporotic fracture
AU2022331738A1 (en) * 2021-08-18 2024-02-29 Orthotreat Ltd. Composition of β-caryophyllene and a statin, and methods of using same

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