CN103251594A - Repaglinide/metformin combo tablet - Google Patents
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- CN103251594A CN103251594A CN2013102199299A CN201310219929A CN103251594A CN 103251594 A CN103251594 A CN 103251594A CN 2013102199299 A CN2013102199299 A CN 2013102199299A CN 201310219929 A CN201310219929 A CN 201310219929A CN 103251594 A CN103251594 A CN 103251594A
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Abstract
The invention relates to a repaglinide/metformin combo tablet, particularly a pharmaceutical composition in the form of a tablet, which comprises the following components in parts by weight: 500 parts of metformin hydrochloride, 0.5-5 parts of repaglinide and 10-200 parts of medicinal auxiliary materials. The medicinal auxiliary materials include, but are not limited to filler, disintegrant, binding agent, alkali and lubricant. The invention also relates to a method for preparing the pharmaceutical composition. The pharmaceutical composition provided by the invention has favorable pharmaceutical properties.
Description
Technical field
The invention belongs to medical technical field, be specifically related to a kind of by repaglinide and the metformin tablet medicine composition and method of making the same as active ingredient.
Background technology
Repaglinide (English name Repaglinide), its chemical name is: S (+)-2-ethyoxyl-4-{2-[(3-methyl isophthalic acid-(2-(piperidino) phenyl) butyl) amino]-the 2-oxoethyl } benzoic acid.Molecular formula: C27H36N2O4, molecular weight: 452.59, its structural formula is as follows:
Repaglinide is benzoic acid derivative, the non-sulfonylurea Drugs Promoting Insulin Secretion, be rapidly new oral hypoglycemic medicine of a kind of effect, be combined with the 36KDA protein-specific on the potassium-channel of dependency ATP outside the d cell film, potassium channel is closed, the D cell depolarization, calcium channel is open, and flow of calcium ions promotes insulin secretion, its effect is faster than sulfonylurea, therefore hypoglycemic activity is fast after the meal.
Metformin (Metformin), its hydrochlorate commonly used clinically, i.e. metformin hydrochloride, chemistry 1,1-Dimethylbiguanide hydrochloride by name, its structural formula is as follows:
Metformin is the biguanides hypoglycemic drug, is a kind of common medicine that is used for the treatment of non-insulin-depending type (II type) diabetes.Because it can obviously reduce the blood glucose of diabetics, and can reduce the danger of the relevant vascular complication of diabetes, reduce the incidence rate that impaired glucose tolerance patients develops into diabetes, and side effect is less, in the global type 2 diabetes mellitus treatment guide of the up-to-date promulgation of IDF in 2005, in the prevention and treatment of diabetes, the effect of metformin is extremely paid attention to.Metformin hypoglycemic medicine mechanism of action comprises: 1. promote surrounding tissue cell (muscle etc.) to the utilization of glucose; 2. suppress gluconeogenesis function of liver, therefore reduce glycogen output; 8. suppress intestinal wall cellular uptake glucose, different from insulin action, namely this product without obvious hypoglycemic activity, therefore, does not generally cause hypoglycemia to the normal person without the effect that impels lipogenesis.Metformin can be used for diet-treated only unsatisfied non-insulin-dependent diabetes mellitus people, especially overweight people, with this class medicine hypoglycemic activity is arranged not only, also slimming effect may be arranged.Metformin accounts for respectively 25% and 28% of all oral antidiabetic drug at the sales volume of Europe and the U.S..Over nearly 10 years, medical circle has had new cognition gradually to the pharmacological action of metformin and its some advantage in the clinical treatment diabetes, and particularly it is that sulfonylureas drugs for diabetes is unexistent in the effect that improves aspect the insulin resistant.Because its blood sugar reducing function does not rely on insulin, it is by the glyconeogenesis that suppresses liver and impels the periphery insulin target tissue to the picked-up utilization of glucose, to improve the insulin sensitivity of body.Metformin hydrochloride can reduce diabetes patient's hyperglycemia, but blood glucose is reduced again.Therefore, use separately metformin not have hypoglycemic reaction.Therefore, metformin now become gently, moderate type 2 diabetes mellitus patient's, particularly obese patient first-selected curative.There are some researches show, metformin can increase the secretion of glucagon kind polypeptide-1 (GLP-1), GLP-1 can promote the insulin secretion of type 2 diabetes mellitus patient glucose mediation, the glucagon suppression secretion, promote that hepatic glycogen is synthetic and reduce glycogen output, improve the B cell function, alleviate hyperinsulinemia.
The document of Gu Ming (metformin and repaglinide (NovoNorm) use in conjunction is known from experience [J]. the healthy digest in China and foreign countries, 2008 08 month the 8th phase of the 5th volume) thinks in, the co-administrated metformin repaglinide namely has synergism, the side reactions such as hypoglycemia, body weight increase are increased, hepatic and renal function is also harmless, therefore be safety, effectively reach the good combined treatment of toleration, be worthy to be popularized.
The repaglinide of FDA approval Novo Nordisk Co.,Ltd (Novo Nordisk)/metformin Compound Tablet (PrandiMet) listing is used for the treatment of type 2 diabetes mellitus.The dosage specification of this compound tablet is repaglinide/metformin hydrochloride 1mg/500mg or 2mg/500mg.This tablet be first also be so far unique quick-acting short secretion medicine repaglinide of getting permission to go on the market and the dose formulations of euglycemic agent metformin hydrochloride.The repaglinide of this compound tablet 1mg/500mg and 2mg/500mg and corresponding dosage and metformin hydrochloride single medicine preparation coupling bioequivalence similar temperament.
The control successful that two medicines share HbAlc, FPG and 2hPG is higher than alone repaglinide or alone metformin hydrochloride.Repaglinide and metformin have share synergism, for the type 2 diabetes mellitus patient of oral other antidiabetic drug unsatisfactory curative effects, can select two medicines to share.
(Chinese patent application numbers 200780036006.2, Nuo Wo-Nuo Disike) discloses a kind of pharmaceutical preparation that comprises metformin and repaglinide to CN101516347A.This invention relates to pharmaceutical composition, comprise repaglinide, it is unit dosage forms in conjunction with metformin or its salt, wherein the preformulation of repaglinide with have before metformin or its salt mix with the irrelevant dissolution characteristic of pH value with less than about 25% relative humidity; With choose any one kind of them or multiple pharmaceutically acceptable excipient, also relate to its preparation method.
CN101756971A (Chinese patent application numbers 200810224002.3, moral crowd is perfectly sound) a kind of oral solid drug composition that contains metformin hydrochloride and repaglinide disclosed, it contains pharmaceutically acceptable carrier, its preparation technology is simple, efficiently solve sliver, simultaneously repaglinide content uniformity, dissolution are good, are used for the treatment of type ii diabetes.This solid composite medicament contains metformin hydrochloride and pharmaceutically acceptable carrier that repaglinide and particle diameter D90 are 10um-200um.
CN101822672A (Chinese patent application numbers 200910105692.5, south are full of letter) discloses a kind of compound take metformin hydrochloride and repaglinide as active ingredient and its production and use.This compound is take metformin hydrochloride and repaglinide as medicinal active ingredient, mixes the Pharmaceutical composition that forms with carrier, and can be prepared into slow releasing tablet, slow-releasing granules, slow releasing capsule, conventional tablet, capsule; The oral formulations such as granule, dispersible tablet, chewable tablet, oral cavity disintegration tablet, buccal tablet, liquid capsule, soft capsule, drop pill.This compound is used for type i diabetes or type ii diabetes (non-insulin is according to patience) patient's treatment, and control blood glucose is had synergism.
CN102218064A (Chinese patent application numbers 201110100196.8, Hainan brocade is auspicious) relate to a kind of by repaglinide and metformin as Pharmaceutical composition of active ingredient and preparation method thereof, this Pharmaceutical composition comprises a) medicament active composition repaglinide and metformin and b) pharmaceutic adjuvant; The weight portion of described active constituents of medicine is 0.1～10 part of repaglinide, 100～1500 parts of metformin; Described pharmaceutic adjuvant is filler, disintegrating agent, binding agent, correctives, lubricant and swellability adjuvant; Wherein said repaglinide is the repaglinide crystal.The Pharmaceutical composition that this invention adopts the very little repaglinide crystal of particle diameter and metformin and pharmaceutic adjuvant to be prepared from can be realized the synchronously purpose of release, and because the repaglinide of this invention is the very little crystal of particle diameter, dissolubility has obtained obvious improvement, thereby improved dissolution, improved bioavailability.
But because the repaglinide dissolubility is little, dissolubility in water is 0.005mg/mL, and metformin hydrochloride is water soluble drug, can cause the metformin hydrochloride rate of releasing drug suitable if adopt conventional technique to carry out tabletting, and repaglinide will can not discharge out.And the repaglinide rate of releasing drug is suitable, will lose control of the release of metformin hydrochloride, and cause the prominent of metformin hydrochloride to be released.For this reason, CN101843617A adopts respectively different framework material compacting double-layer sustained release tablets with repaglinide, metformin hydrochloride, obtaining two medicines all has the formulation and technology of suitable rate of releasing drug, perhaps repaglinide, metformin hydrochloride are adopted respectively respectively compressed minitablets of different framework materials, then fill capsule proportionally is to solve the problem of insoluble drug repaglinide and water soluble drug metformin hydrochloride synchronous slow.
Above-mentioned double-layer sustained release tablets or respectively the shortcoming of compressed minitablets be that its preparation is too high to equipment requirements, be difficult to suitability for industrialized production, even product is introduced to the market, also will cause needs of patients payment great number medical expense; And double-layer sustained release tablets can cause tablet hardness excessive in preparation process, affects drug release, and Dual-layer sheet joint face then is difficult to discharge medicine.And because repaglinide is almost insoluble in water, cause the vitro Drug dissolution poor, cause its bioavailability low.
Owing to comprising in the compound tablet of repaglinide and metformin, the weight of two kinds of active component differs greatly, is to need special considerations for the uniformity of the repaglinide of low dosage is uniformity of dosage units; Other repaglinide the poorly soluble and metformin dissolubility is very good, there is larger difference in the two dissolving out capability at tablet, can cause thus after the tablets onset time of two kinds of medicines inconsistent.The problems referred to above all are that those skilled in the art extremely will pay close attention to.The method of the compound tablet of new preparation repaglinide and metformin is still expected to have in this area, and the tablet of expectation the method preparation has the superperformance of one or more aspects.
Summary of the invention
The object of the present invention is to provide the method for the compound tablet of a kind of new preparation repaglinide and metformin, the tablet of expectation the method preparation has the superperformance of one or more aspects.The inventor is unexpectedly discovery, and the compound tablet that comprises repaglinide and metformin that uses specific method to prepare has challenging superior function.Therefore the present invention finds and is accomplished.
For this reason, first aspect present invention provides a kind of pharmaceutical composition, wherein comprises: metformin hydrochloride, repaglinide and pharmaceutic adjuvant.
According to each pharmaceutical composition of first aspect present invention, wherein comprise: the repaglinide of the metformin hydrochloride of 500 weight portions, 0.5～5 weight portion and the pharmaceutic adjuvant of 10～200 weight portions.
According to each pharmaceutical composition of first aspect present invention, wherein comprise: the repaglinide of the metformin hydrochloride of 500 weight portions, 0.5～2.5 weight portion and the pharmaceutic adjuvant of 20～150 weight portions.
According to each pharmaceutical composition of first aspect present invention, wherein said pharmaceutic adjuvant includes but not limited to filler, disintegrating agent, binding agent, alkaline agent, lubricant.
According to each pharmaceutical composition of first aspect present invention, wherein said pharmaceutic adjuvant also comprises solubilizing agent.
According to each pharmaceutical composition of first aspect present invention, wherein, the amount of described disintegrating agent can particularly easily be determined according to existing knowledge and experience during tablet in pharmaceutical compositions according to those skilled in the art.For example the amount of disintegrating agent can be to account for 1%～20% of Pharmaceutical composition gross weight, for example accounts for 5%～15% of Pharmaceutical composition gross weight.Perhaps, for example, for the metformin hydrochloride of per 500 weight portions, the amount of disintegrating agent can be 5～50 weight portions, for example 10～25 weight portions.
According to each pharmaceutical composition of first aspect present invention, wherein, the amount of described binding agent can particularly easily be determined according to existing knowledge and experience during tablet in pharmaceutical compositions according to those skilled in the art.For example the amount of binding agent can be to account for 1%～20% of Pharmaceutical composition gross weight, for example accounts for 1%～15% of Pharmaceutical composition gross weight, for example accounts for 1%～10% of Pharmaceutical composition gross weight.For example the amount of binding agent can be to account for 1%～20% of granulation gross weight, for example accounts for 1%～15% of granulation gross weight, for example accounts for 1%～10% of granulation gross weight.Perhaps, for example, for the metformin hydrochloride of per 500 weight portions, the amount of binding agent can be 5～50 weight portions, for example 10～30 weight portions.
According to each pharmaceutical composition of first aspect present invention, wherein, the amount of described lubricant can particularly easily be determined according to existing knowledge and experience during tablet in pharmaceutical compositions according to those skilled in the art.For example the amount of lubricant can be to account for 0.1%～10% of Pharmaceutical composition gross weight, for example accounts for 0.2%～5% of Pharmaceutical composition gross weight, for example accounts for 0.2%～2.5% of Pharmaceutical composition gross weight.Perhaps, for example, for the metformin hydrochloride of per 500 weight portions, the amount of lubricant can be 2～20 weight portions, for example 3～15 weight portions.
According to each pharmaceutical composition of first aspect present invention, wherein, the amount of described filler can particularly easily be determined according to existing knowledge and experience during tablet in pharmaceutical compositions according to those skilled in the art, particularly can easily determine according to the needs of preparations shaping, such as will usually determining according to the size of tablet, compression molding etc.For example the amount of filler can be to account for 3%～30% of Pharmaceutical composition gross weight, for example accounts for 5%～25% of Pharmaceutical composition gross weight, for example accounts for 5%～20% of Pharmaceutical composition gross weight.Perhaps, for example, for the metformin hydrochloride of per 500 weight portions, the amount of filler can be 15～150 weight portions, for example 25～125 weight portions, for example 50～100 weight portions.
According to each pharmaceutical composition of first aspect present invention, wherein, described " alkaline agent " represents alkaline agent commonly used in the medicine preparation.Being applicable to prepare the alkaline agent that comprises the repaglinide pharmaceutical composition comprises harmless on the physiology in used dosage range at least, be pharmaceutically useful many inorganic or organic bases, such as sodium hydroxide solution, potassium hydroxide solution, ammonia, phosphoric acid uncle sodium (tert-sodium phosphate), diethanolamine, ethylenediamine, N-METHYL-ALPHA-L-GLUCOSAMINE (being meglumine), 1B, trometamol etc.The mol ratio of active substance repaglinide and alkaline agent is preferably about 1:1.0 to 1:10, about 1:1.0 to 1:5 for example, about 1:1.0 to 1:2.5 for example, namely the amount of alkaline agent be 1～10 mole of the repaglinide amount doubly, for example 1～5 mole times, for example 1～2.5 mole times.But more excessive alkali in some cases also may be favourable.Have been found that alkaline agent is useful for the stripping that promotes repaglinide.
According to each pharmaceutical composition of first aspect present invention, wherein, described term " solubilizing agent " represents solubilizing agent commonly used in the medicine preparation.The example that is applicable to prepare the solubilizing agent that comprises the repaglinide pharmaceutical composition comprises poloxamer, tween.In one embodiment, described alkaline agent poloxamer is PLURONICS F87.The character of solubilizing agent and used ratio all are being important aspect the dissolution rate that determines active substance.The amount of solubilizing agent can particularly easily be determined according to existing knowledge and experience during tablet in pharmaceutical compositions according to those skilled in the art.For example, for the repaglinide of per 1 weight portion, the amount of solubilizing agent can be 0.1～10 weight portion, for example 0.1～5 weight portion, for example 0.1～2.5 weight portion, for example 0.1～0.5 weight portion.
According to each pharmaceutical composition of first aspect present invention, wherein, described filler is one or more in Icing Sugar, lactose, amylum pregelatinisatum, corn starch, microcrystalline Cellulose, calcium sulfate, calcium hydrogen phosphate, calcium phosphate, Sorbitol, the mannitol.
According to each pharmaceutical composition of first aspect present invention, wherein, described disintegrating agent is one or more of carboxymethyl starch sodium, low-substituted hydroxypropyl cellulose, crospolyvinylpyrrolidone, sodium carboxymethyl cellulose, cross-linking sodium carboxymethyl cellulose, polyvinylpyrrolidone or low-substituted hydroxypropyl cellulose sodium, polacrilin potassium (polacrillin potassium also is called Po Lakelin potassium).
According to each pharmaceutical composition of first aspect present invention, wherein, described binding agent is one or more in water, polyvidone, ethanol, sodium carboxymethyl cellulose, polyvinylpyrrolidone or the hypromellose.When described binding agent was hypromellose, it was the alcoholic solution of hypromellose, preferred 2.5% hypromellose alcoholic solution.In addition, in the situation that binding agent is water, it is essentially the wetting agent of granulation usefulness, and it is removed in final granule.
According to each pharmaceutical composition of first aspect present invention, wherein, described lubricant is a kind of in magnesium stearate, Macrogol 4000-8000, micropowder silica gel, the Pulvis Talci etc.
According to each pharmaceutical composition of first aspect present invention, wherein, described alkaline agent is selected from meglumine, trometamol.In one embodiment, described alkaline agent is trometamol.In one embodiment, described alkaline agent is trometamol, and comprises calcium hydrogen phosphate in the described filler.
According to each pharmaceutical composition of first aspect present invention, it is tablet or capsule.
According to each pharmaceutical composition of first aspect present invention, it is tablet.
According to each pharmaceutical composition of first aspect present invention, it is tablet, and it is further by coating.In one embodiment, described coating is film coating.
According to each pharmaceutical composition of first aspect present invention, it is unit dose formulations.
According to each pharmaceutical composition of first aspect present invention, it is unit dose formulations, the amount of repaglinide is 0.5～5.0mg in each unit dose formulations, for example is about 0.5mg, 1.0mg, 1.5mg, 2.0mg, 2.5mg, 3.0mg, 4.0mg, 5.0mg.
According to each pharmaceutical composition of first aspect present invention, it is unit dose formulations, and the amount of metformin hydrochloride is 100～1000mg in each unit dose formulations, for example is 400～600mg, for example is about 400mg, 500mg, 600mg.
According to each pharmaceutical composition of first aspect present invention, it is unit dose formulations, and the amount of repaglinide is 0.5～5.0mg in each unit dose formulations, and the amount of metformin hydrochloride is 400～600mg in each unit dose formulations.
According to each pharmaceutical composition of first aspect present invention, it is unit dose formulations, and the amount of repaglinide is 1mg or 2mg in each unit dose formulations, and the amount of metformin hydrochloride is 500mg in each unit dose formulations.
Further, second aspect present invention provides for example method of the described pharmaceutical composition of the arbitrary embodiment of first aspect present invention of pharmaceutical compositions, and the method may further comprise the steps:
(a) each material is crushed to respectively acceptable granularity in the pharmacy (granularity is less than 80 orders usually);
(b) preparation granule I: with repaglinide and alkaline agent, solubilizing agent, (for example the amount of binding agent can be to account for 1%～20% of granulation (namely preparing granule I) gross weight to an amount of binding agent, for example account for 1%～15% of granulation gross weight, for example account for the granulation gross weight 1%～10%) be dissolved in make in an amount of water solution (in invention normally 1/4～3/4 of degree of reaching capacity concentration for most preferably, in the test below the present invention, as not specifying, all make the solution of 2/4 degree of saturation), (its weight for example is 5-50 times of repaglinide to an amount of filler with this spray solution, for example 5-25 doubly, for example 5-15 is doubly) in, abundant mix homogeneously, being dried to moisture is lower than 5% and (for example is lower than 2.5%, particularly moisture is lower than 2%) granule, again this dried particles is ground to form granularity less than the fine powder of 80 orders (for example less than 100 orders), get granule I;
(c) preparation granule II: with metformin hydrochloride, remainder binder, (its weight for example is 0～20% of metformin hydrochloride weight to optional filler, for example 0～10%, for example 0～5%) and an amount of lubricant (its weight for example is 0～10% of metformin hydrochloride weight, for example 0～5%, for example 0～2.5%) mix homogeneously, water is the wetting agent pelletize, and drying gets granule II;
(d) whole mixed and preparations shaping: granule I, granule II, disintegrating agent, surplus lubricant and surplus filler are fully mixed, and the mixture that obtains is pharmaceutical composition of the present invention; Randomly this pharmaceutical composition is packed in the hard capsule case or be pressed into tablet, make the pharmaceutical composition of capsule or tablet.
According to each method of second aspect present invention, wherein, described tablet is further by coating.Coating material is well known to a person skilled in the art, it can be commercial especially, the coating material of the commodity that for example are commercially available Opadry by name.The amount of tablet coating can be according to clothing material composition and easily definite, and when for example using the Opadry film coating, the amount of coating weightening finish can be 2-8%, for example can be 2～6%.
According to each method of second aspect present invention, wherein, filler is calcium hydrogen phosphate described in the step (b).
According to each method of second aspect present invention, wherein, alkaline agent is trometamol described in the step (b).
Unexpectedly found to use trometamol not only can make compound medicament composition keep good stripping stability as alkaline agent, and to help to keep the chemical stability of preparation, this prior art not to have the beneficial effect of instruction fully be beat all fully.Used trometamol can be the product that meets the quality standard of the 5.0 editions 2633 pages trometamol that record of European Pharmacopoeia (TROMETAMOL) in the present invention.
It is unit of association's dosage particles for pharmaceutical composition of the present invention, wherein preferably contain about 0.25 milligram to about 5 milligrams of repaglinides and about 200 milligrams to about 1200 milligrams of metformin or its salt hydrochlorate for example.More preferably, this unit of association's dosage particles contain about 0.5 milligram to about 2.0 milligrams of repaglinides and about 500 milligrams to about 1000 milligrams of metformin or its salt hydrochlorate for example.
In addition, preparation of the present invention shows and the basic similarly dissolution characteristic of the independent product of selling.
The dissolution characteristic of unit dose formulations of the present invention can be in simulated gastric fluid and is measured in the pH scope is several aqueous solutions of 1-7.5.Can use oar method (device 2 among the USP, the device 1 among the Ph.Eur.).The dissolving of repaglinide is strongly to rely on pH value.
Unit dose formulations of the present invention comprises repaglinide preformulation, metformin granule, filler, disintegrating agent and lubricant.
In another aspect of this invention, the method of the patient's that treatment or prevention need this class treatment or prevention hyperglycemia, type 2 diabetes mellitus, impaired glucose tolerance, type 1 diabetes, obesity, hypertension, X syndrome, dyslipidemia, cognitive disorder, arteriosclerosis, myocardial infarction, coronary heart disease and other cardiovascular disorder, apoplexy, enteritis syndrome, dyspepsia and gastric ulcer is provided, has comprised this patient is used the unit dosage forms of the present invention agent of stopping.
In another aspect of this invention, provide the method for progression of disease of type 2 diabetes mellitus that delays or need to prevent the patient of this class treatment, comprised this patient is used unit dosage forms preparation of the present invention.
In another aspect of this invention, provide and in the patient of this class treatment of needs, reduced food intake, reduction beta cell apoptosis, raising Instreptozotocin Induced and beta cell quality (mass), and/or recovery comprises this patient is used unit dosage forms preparation of the present invention the method for the glucose-sensitive of beta cell.
With unit dosage forms preparation for treating of the present invention also can with for example be selected from antidiabetic drug, anti-obesity medicine, appetite stimulator, antihypertensive, treat and/or prevent by diabetes and cause or the medicament of the complication relevant with diabetes and treating and/or preventing by obesity causes or second or more pharmaceutically active substance of the medicament of the complication relevant with obesity and deficiency disorder are combined.
In one embodiment, unit dosage forms preparation of the present invention is for the preparation for the treatment of or the prophylactic agent of hyperglycemia, type 2 diabetes mellitus, impaired glucose tolerance, type 1 diabetes, obesity, hypertension, X syndrome, dyslipidemia, cognitive disorder, arteriosclerosis, myocardial infarction, apoplexy, coronary heart disease and other cardiovascular disorder, enteritis syndrome, dyspepsia and gastric ulcer.
In another embodiment, unit dosage forms preparation of the present invention is for the preparation of the medicine that delays or prevent the progression of disease of type 2 diabetes mellitus to use.
Term used herein " disease treatment " refers to occur the patient's of this disease, symptom or deficiency disorder management and nursing.Therapeutic purposes are antagonism this disease, symptom or deficiency disorders.Treatment comprises uses reactive compound with elimination or controls this disease, symptom or deficiency disorder, and alleviates symptom or the complication relevant with this disease, symptom or deficiency disorder.
Term used herein " disease prevention " referred to before the clinical episodes of this disease management and the nursing to the individuality that the danger that this disease occurs is arranged.The prevention purpose is that the development and comprising of antagonism this disease, symptom or deficiency disorder is used reactive compound with prevention or delayed outbreak and the prevention of symptom or complication or delay the development of relevant disease, symptom or deficiency disorder.
Arbitrary embodiment of applicable equally other the arbitrary embodiment of arbitrary technical characterictic that arbitrary embodiment of either side of the present invention or this either side has or other either side, as long as they can be not conflicting, certainly at where applicable each other, necessary words can be done suitably to modify to individual features.The below is further described with characteristics to various aspects of the present invention.
All documents that the present invention quotes from, their full content is incorporated this paper by reference into, and if the expressed implication of these documents and the present invention when inconsistent, be as the criterion with statement of the present invention.In addition, various terms and phrase that the present invention uses have the general sense of well known to a person skilled in the art, nonetheless, the present invention still wishes at this these terms and phrase to be described in more detail and to explain, the term of mentioning and phrase are as the criterion with the implication that the present invention was explained if any inconsistent with known implication.
One of active component of the present invention repaglinide is almost insoluble in water, dissolubility in water only is 0.005mg/mL, not only cause the vitro Drug dissolution poor, cause its bioavailability low, and because metformin is water soluble drug, can cause the metformin rate of releasing drug suitable if therefore adopt conventional technique to carry out tabletting, repaglinide will can not discharge out.And the repaglinide rate of releasing drug is suitable, will lose control of the release of metformin, and cause the prominent of metformin hydrochloride to be released.Prior art adopts the method for improving technique to solve the problems referred to above, adopts such as CN101843617A and adopts respectively different framework materials to be pressed into the method that double-layer sustained release tablets becomes to be pressed into respectively small pieces repaglinide, metformin hydrochloride.But the method is too high to equipment requirements, is difficult to suitability for industrialized production, and double-layer sustained release tablets can cause tablet hardness excessive in preparation process, affects drug release, and Dual-layer sheet joint face then is difficult to discharge medicine.
Medicine in vivo infiltration rate is usually determined by the speed of dissolving, medicine in the solid preparation is before being absorbed, must and dissolve the process that then transfers solution to through disintegrate, if medicine is difficult for discharging from preparation or the dissolution velocity of medicine is very slow, then the infiltration rate of said preparation Chinese medicine or degree just might have problems, on the other hand, some pharmacological action is violent, safety index is little, the medicine dissolution rate is too fast rapidly if absorb, and may produce obvious untoward reaction, and the time of keeping drug effect also will shorten, in this case, the dissolution rate of preparation of Chinese medicine be should give control.Among the present invention, repaglinide is water-soluble hardly, and metformin is water-soluble, can exist the metformin dissolution rate suitable if therefore adopt common repaglinide and metformin and pharmaceutic adjuvant to make common tablet, and repaglinide just is difficult for discharging from compound preparation; And the repaglinide dissolution rate is suitable, and metformin is will dissolution rate too fast.The present invention finds the tablet that uses prescription of the present invention to make, and two kinds of active medicines all have good dissolving out capability in acid and neutral dissolution medium, and it is stable all to have a good stripping; In addition, the inventive method is simple, (this complex device is very obvious for drug loss for example not need to use spray-dired complex device, for example the inventive method step (b) prepares granule I, the yield of its active component repaglinide (being that the amount of repaglinide among the granule I is divided by repaglinide inventory gained percent) reaches more than 95%, shows that the drug loss amount is fewer; Yet with reference to CN101516347A (Chinese patent application numbers 200780036006.2, " repaglinide trituration " described in the method Preparation Example 2 of the embodiment 3 of Nuo Wo-Nuo Disike), the yield of repaglinide is 76% only, shows relatively large active component and loses because of preparation technology).
In some examples of the present invention, repaglinide is with described alkaline agent and described calcium hydrogen phosphate preparation granule as filler.
In some examples of the present invention, the gained compound tablet is carried out coating.The coating material that coating is used is the thin film coating material Opadry, and 1000 compound Repaglinide/diformin tablets of the present invention (hydrochloric metformin is 500mg approximately) are approximately used 5.5g Opadry coating powder (Opadry).
Specifically, art for coating comprises preparation and two steps of coating of film-coat solution, and these two its techniques of step are as follows:
The preparation of film-coat solution: the purified water that takes by weighing recipe quantity is put in the agitator tank, open to stir to make liquid level just form whirlpool, at the uniform velocity is added to the Opadry powder of recipe quantity in the whirlpool, after reinforced complete, adjust mixing speed whirlpool is just disappeared, continue to stir 45 minutes, for subsequent use.
Coating: get plain chip and put in the coating pan, open compressed air, start seed-coating machine, coating pan is slowly rotated, and the preheating label is opened spray gun to approximately 40 ℃ the time, coating solution is sprayed onto on the label of rotation, spraying is carried out drying with the hot blast that relaxes simultaneously, and is complete to the coating solution spraying, continues blowing hot-air the coating solvent evaporates is done.
Prepared a kind of of the present invention has following one or more advantages by repaglinide and metformin as Pharmaceutical composition and the described preparation method of active ingredient: (1) prescription rationally, used adjuvant is safe and reliable, has greatly improved patient's drug safety; (2) obtained label outward appearance is good, has simultaneously better dissolving out capability; (3) steady quality is difficult for decomposing and goes bad, and also can not jolt because of transportation produces destruction to tablet; (4) fast disintegrate and disperseing rapidly of described compositions, so that the medicine Uniform Dispersion, the digestive tract local drug concentration is unlikely to too high, thereby has avoided the stimulation that causes because local drug concentration is too high; (5) Pharmaceutical composition provided by the present invention can be realized the synchronously purpose of release, and In Vitro Dissolution is good, and its bioavailability is high.
The specific embodiment
Further specify the present invention below by specific embodiment/experimental example, still, should be understood to, these embodiment and experimental example are only used for the usefulness that specifically describes more in detail, and should not be construed as for limiting in any form the present invention.
The present invention carries out generality and/or concrete description to the material and the test method that use in the test.Although for realizing that the employed many materials of the object of the invention and operational approach are well known in the art, the present invention still does to describe in detail as far as possible at this.It will be apparent to those skilled in the art that hereinafter, if do not specify, material therefor of the present invention and operational approach are well known in the art.
When the present invention hereinafter prepared tablet, the amount that comprises metformin hydrochloride in every was 500mg; And the amount of repaglinide can be easily by in second aspect present invention step (d), carrying out two kinds of granules when mixing, adjust the amount of granule I so that the amount of every middle repaglinide is adjusted into 1mg or 2mg; Hereinafter in the example if no special instructions, the amount that comprises repaglinide in every is adjusted into 2mg.In addition, the amount of the metformin hydrochloride that comprises during every batch of material feeds intake is 500g, and namely every batch of material inventory is 1000 amount of preparation, although the scale with each component in every shows when listing prescription in the following example.
When carrying out test chemical hereinafter, for example to the content of metformin or repaglinide in the compositions of preparation, dissolution, when related substance checks, can use the detection method of these two kind single preparationss of ephedrine, for example can use metformin hydrochloride raw material that two ones of version Chinese Pharmacopoeias in 2010 record and the method for preparation to carry out for metformin, can use repaglinide raw material that two ones of version Chinese Pharmacopoeias in 2010 record and the method for preparation to carry out for repaglinide.These methods are applicable to compound tablet and are unlikely the wherein mensuration of another component of components influence (deducting the chromatographic peak that another active substance produces when measuring the related substance of certain active component), can not be affected because of the existence assay method of metformin when for example using the repaglinide determination of related substances to measure related substance.
The embodiment part: preparation comprises the pharmaceutical composition of metformin and repaglinide
Embodiment 1: pharmaceutical compositions
Prescription:
In the upper table, the amount of trometamol is 1.87 moles times (all doubly representing with mole during the two relative quantity of following calculating) of repaglinide.
Method for making:
(a) each material is crushed to respectively acceptable granularity in the pharmacy (granularity is less than 80 orders);
(b) preparation granule I: repaglinide and alkaline agent, solubilizing agent, binding agent are dissolved in the solution of making 2/4 degree of saturation in an amount of water, (exit is through the syringe of repacking with this spray solution, solution can therefrom spray when outwards pushing) in filler, abundant mix homogeneously, be dried to moisture and be lower than 2% granule, again this dried particles is ground to form granularity less than 80 purpose fine powders, get granule I (the repaglinide yield of granule I is 96.3% in this technique);
(c) preparation granule II: metformin hydrochloride, binding agent, filler and mix lubricant is even, and water is the wetting agent pelletize, is dried to moisture and is lower than 2%, gets granule II;
(d) whole mixed and preparations shaping: granule I, granule II, disintegrating agent, lubricant and filler are fully mixed, and the mixture that obtains is pharmaceutical composition of the present invention.Said composition 1/3 is directly packed into powder/granule in the hard gelatin capsule, every hydrochloric metformin 500mg; Other 2/3 is pressed into tablet, every hydrochloric metformin 500mg; This tablet is designated as Ex1, uses the aluminum-plastic composite membrane bag hermetic package, namely gets the pharmaceutical composition of the present invention (plain sheet) that is tablet, and its test that is used for is hereinafter investigated.
(e) further, with step (d) gained part tablet Opadry coating, every parcel clothing material 15mg (increase weight approximately 2.42%) obtains being the pharmaceutical composition of the present invention of Film coated tablets.
Additional embodiment 1: with reference to prescription and the method for above-described embodiment 1, different is that wherein the amount of trometamol is regulated, be respectively 0,0.2,0.5,0.75,1.0,1.5,2.0,3.0,4.0,5.0,6.0,8.0,12.0 or 20.0 mole of repaglinide doubly, the plain sheet that obtains is designated as respectively Ex101, Ex102, Ex103, Ex104, Ex105, Ex106, Ex107, Ex108, Ex109, Ex110, Ex111, Ex112, Ex113, Ex114, uses respectively the aluminum-plastic composite membrane bag hermetic package.
Additional embodiment 2: with reference to prescription and the method for above-described embodiment 1, different is that wherein the amount of calcium hydrogen phosphate is regulated, respectively 0,1,2.5,5,7.5,12.5,15,20,30,50 times of weight of repaglinide, the plain sheet that obtains is designated as respectively Ex121, Ex122, Ex123, Ex124, Ex125, Ex126, Ex127, Ex128, Ex129 and Ex130, uses respectively the aluminum-plastic composite membrane bag hermetic package.
Additional embodiment 3: with reference to prescription and the method for above-described embodiment 1, different is that wherein trometamol replaces with meglumine, and its amount is respectively 0.5,1.0,2.0,5.0,10.0 mole times of repaglinide, the plain sheet that obtains is designated as respectively Ex131, Ex132, Ex133, Ex134, Ex135, uses respectively the aluminum-plastic composite membrane bag hermetic package.
Additional embodiment 4: with reference to prescription and the method for above-described embodiment 1, different is that wherein trometamol replaces with 1B, and its amount is respectively 0.5,1.0,2.0,5.0,10.0 mole times of repaglinide, the plain sheet that obtains is designated as respectively Ex136, Ex137, Ex138, Ex139, Ex140, uses respectively the aluminum-plastic composite membrane bag hermetic package.
Additional embodiment 5: with reference to prescription and the method for above-described embodiment 1, different is that wherein calcium hydrogen phosphate replaces with respectively equivalent: calcium phosphate, microcrystalline Cellulose, calcium sulfate, carboxymethyl starch sodium or silicon dioxide, the plain sheet that obtains is designated as respectively Ex141, Ex142, Ex143, Ex144, Ex145, uses respectively the aluminum-plastic composite membrane bag hermetic package.
With reference to CN101516347A (Chinese patent application numbers 200780036006.2, the prescription of description embodiment 2 of Nuo Wo-Nuo Disike) and the method for making of embodiment 3, the plain sheet that obtains is designated as Ex151, with aluminum-plastic composite membrane bag hermetic package (the repaglinide yield is 76.2% when using spray drying method preparation " repaglinide trituration ").
With reference to prescription and the method for making of CN101756971A (Chinese patent application number 200810224002.3, moral crowd is perfectly sound) embodiment 2, the plain sheet that obtains is designated as Ex152, uses the aluminum-plastic composite membrane bag hermetic package.
With reference to CN102218064A (Chinese patent application numbers 201110100196.8, Hainan brocade is auspicious) prescription and the method for making of description example of formulations 5, and be raw material with the repaglinide that embodiment 4 methods wherein make, the plain sheet that obtains is designated as Ex153, uses the aluminum-plastic composite membrane bag hermetic package.
With reference to prescription and the method for CN102319245A (Chinese patent application 201110190175.X) description embodiment 1, the plain sheet that obtains is designated as Ex154, uses the aluminum-plastic composite membrane bag hermetic package.
With reference to prescription and the method for CN103070864A (Chinese patent application number 201210518601.2) description embodiment 3, the plain sheet that obtains is designated as Ex155, uses the aluminum-plastic composite membrane bag hermetic package.
Embodiment 201: prepare pharmaceutical composition of the present invention
With reference to prescription and the method for above-described embodiment 1, different is that the amount of granule I reduces by half when " (d) whole mixed and preparations shaping ", change 12mg into, make the tablet that contains repaglinide 1mg/ metformin hydrochloride 500mg, the plain sheet that obtains is designated as Ex201, uses the aluminum-plastic composite membrane bag hermetic package.
Embodiment 202: prepare pharmaceutical composition of the present invention
Prescription:
With reference to the method for above-described embodiment 1, the plain sheet that obtains is designated as Ex202, uses the aluminum-plastic composite membrane bag hermetic package.
Embodiment 203: prepare pharmaceutical composition of the present invention
Prescription:
With reference to the method for above-described embodiment 1, the plain sheet that obtains is designated as Ex203, uses the aluminum-plastic composite membrane bag hermetic package.
Embodiment 204: prepare pharmaceutical composition of the present invention
Prescription:
With reference to the method for above-described embodiment 1, the plain sheet that obtains is designated as Ex204, uses the aluminum-plastic composite membrane bag hermetic package.
Embodiment 205: prepare pharmaceutical composition of the present invention
Prescription is with embodiment 1, but preparation method carries out to the method for section with reference to the CN103070864A description, and the plain sheet that obtains is designated as Ex205, uses the aluminum-plastic composite membrane bag hermetic package.
Embodiment 206: prepare pharmaceutical composition of the present invention
Prescription is with embodiment 1, but preparation method carries out with reference to the method for CN102319245A description embodiment 1, and the plain sheet that obtains is designated as Ex206, uses the aluminum-plastic composite membrane bag hermetic package.
Test example part: the tablet medicine that comprises metformin and repaglinide that embodiment is above partly prepared
Compositions is carried out pharmaceutical property and is detected
Test example 1: the Performance of pharmaceutical composition---Dissolution Rate Testing
1, the dissolution in the acid medium is investigated: get the tablet medicine compositions that comprises two kinds of components that above each embodiment prepares, carry out according to the second method (oar method) in two appendix XC of Chinese Pharmacopoeia version in 2010 dissolution method.Dissolution medium is the hydrochloric acid solution 900ml of 0.1mol/L, and rotating speed 50rpm is in 20 minutes sampling and measuring dissolution of two kinds of combinations wherein.
2, the dissolution in the neutral medium is investigated: get the tablet medicine compositions that comprises two kinds of components that above each embodiment prepares, carry out according to the second method (oar method) in two appendix XC of Chinese Pharmacopoeia version in 2010 dissolution method.Dissolution medium is potassium dihydrogen phosphate (phosphoric acid or potassium hydroxide regulate pH to the 6.8) 900ml of 0.2mol/L, and rotating speed 50rpm is in 20 minutes sampling and measuring dissolution of two kinds of combinations wherein.
3, result: whole tablets of partly preparing of embodiment above, in acid and neutral two media, all in 94～101% scopes, the demonstration metformin has good dissolving out capability to the dissolution of metformin.For example the dissolution of Ex1 tablet metformin in acid and neutral two media is respectively 97.6% and 95.3%.
Whole tablets of partly preparing of embodiment above, in acid and neutral two media, the dissolution of repaglinide all in 75～98% scopes, shows that repaglinide has good dissolving out capability (stripping of version pharmacopeia repaglinide kind 45min in 2010 is defined as 75%).Particularly Ex1, Ex105, Ex106, Ex107, Ex108, Ex109, Ex110, Ex124, Ex125, Ex126, Ex127, Ex201, Ex202, Ex203, Ex204, Ex205, Ex206 these have the compositions of feature of the present invention, in acid and neutral two media, the dissolution of repaglinide is all in 88～98% scopes.For example the dissolution of Ex1 tablet metformin in acid and neutral two media is respectively 93.1% and 90.6%.
Test example 2: the Performance of pharmaceutical composition---dissolving out capability study on the stability
Accelerated test method: will be above whole tablets of partly preparing of embodiment, use the aluminum-plastic composite membrane bag hermetic package, place under 45 ° of C conditions and place May (can be called for short below " 45 ° of C-5 months ", " May ", " high-temperature treatment " or " high-temperature treatment May "), measure the dissolution (dissolution determination method referring to test example 1) of each sample behind this high-temperature treatment, and compare with the dissolution of respective samples 0 month the time, calculate the dissolution percent change that can be used for characterizing tablet dissolving out capability stability with following formula:
The dissolution percent change more shows that close to 100% sample is better through the stability of high-temperature treatment dissolution performance after May.
The result shows, whole tablets of partly preparing of embodiment above, and in acid and neutral two media, all in 95～105% scopes, the demonstration metformin has good stripping stability to the dissolution percent change of metformin.For example the dissolution percent change of Ex1 tablet metformin in acid and neutral two media is respectively 101.6% and 99.6%.
Whole tablets of partly preparing of embodiment above, in acid and neutral two media, the dissolution percent change of repaglinide demonstrates different situations of change.For Ex1, Ex105, Ex106, Ex107, Ex108, Ex109, Ex110, Ex124, Ex125, Ex126, Ex127, Ex201, Ex202, Ex203, Ex204, Ex205, Ex206, their dissolution percent change in acid medium are all in 94～102% scopes, their dissolution percent change in neutral medium are all in 95～103% scopes, show that these samples all have good dissolution stability, for example the dissolution percent change of Ex1 tablet repaglinide in acid and neutral two media is respectively 97.8% and 99.5%.
For Ex101, Ex102, these samples of Ex103, Ex104, their dissolution percent change in acid medium are all in 72～84% scopes, their dissolution percent change in neutral medium all in 69～83% scopes, show that the dissolution of these samples in two media all has bad stability.For Ex111, Ex112, these samples of Ex113, Ex114, their dissolution percent change in acid medium are all in 92～99% scopes, their dissolution percent change in neutral medium are all in 71～84% scopes, show that the dissolution of these samples in acid medium has good stability, but after the trometamol consumption is excessive, dissolution stability in neutral medium can not be satisfactory, shows that the measurer of trometamol has the specific range of choice in the present composition.
For Ex121, Ex122, these samples of Ex123, their dissolution percent change in acid medium are all in 73～86% scopes, their dissolution percent change in neutral medium all in 70～84% scopes, show that the dissolution of these samples in two media all has bad stability.For Ex128, Ex129, these samples of Ex130, their dissolution percent change in acid medium are all in 68～80% scopes, their dissolution percent change in neutral medium are all in 87～95% scopes, show the dissolution poor stability of these samples in acid medium, but after the calcium hydrogen phosphate consumption is excessive, dissolution stability in acid medium can not be satisfactory, shows that the measurer of calcium hydrogen phosphate has the specific range of choice in the present composition.
For Ex131, Ex132, Ex133, Ex134, Ex135, Ex136, Ex137, Ex138, these samples of Ex139, Ex140, their dissolution percent change in acid medium are all in 67～85% scopes, their dissolution percent change in neutral medium all in 88～95% scopes, show the dissolution poor stability of these samples in acid medium.Show and do not use trometamol and use other alkaline agent instead and can not guarantee that the dissolving out capability of tablet in acid and neutral medium stablize.
These do not use the sample of calcium hydrogen phosphate for Ex141, Ex142, Ex143, Ex144, Ex145, their dissolution percent change in acid medium are all in 71～84% scopes, their dissolution percent change in neutral medium all in 73～83% scopes, show that the dissolution of these samples in two media all has bad stability.
These do not have the sample of feature of the present invention for Ex151, Ex152, Ex153, Ex154, Ex155, their dissolution percent change in acid medium are all in 73～87% scopes, their dissolution percent change in neutral medium all in 68～85% scopes, show that the dissolution of these samples in two media all has bad stability.
Test example 3: the Performance of pharmaceutical composition---related substance inspection
Get the tablet medicine compositions that comprises two kinds of components that above each embodiment prepares, the repaglinide raw material that records according to Chinese Pharmacopoeia two ones of versions in 2010 and the method in the tablet are measured total related substance in the present invention's tablet medicine compositions that above each embodiment prepares.Folk prescription tablet in the pharmacopeia stipulates that total related substance should be less than 1.5%.
After measured, the tablet medicine compositions that comprises two kinds of components that the various embodiments described above prepare is used repaglinide determination of related substances method, and all in 0.15～0.55% scope, for example total related substance of Ex1 is 0.23% to the amount that the result shows total related substance.
Test example 4: the Performance of pharmaceutical composition---related substance study on the stability
Accelerated test method: will be above whole tablets of partly preparing of embodiment, use the aluminum-plastic composite membrane bag hermetic package, place under 45 ° of C conditions and place May (can be called for short below " 45 ° of C-5 months ", " May ", " high-temperature treatment " or " high-temperature treatment May "), measure the total related substance of each sample behind this high-temperature treatment, and compare with total related substance of respective samples 0 month the time, calculate the total related substance percent change that can be used for characterizing tablet chemistry stability with following formula:
Total related substance percent change more close to 100% show sample through high-temperature treatment after May the stability of chemical property better.
Whole tablets of partly preparing of embodiment above, total related substance percent change of repaglinide demonstrates different situations of change.For Ex1, Ex105, Ex106, Ex107, Ex108, Ex109, Ex110, Ex124, Ex125, Ex126, Ex127, Ex201, Ex202, Ex203, Ex204, Ex205, Ex206, their total related substance percent change is all in 97～121% scopes, for example total related substance percent change of Ex1 is 112%, is not obviously increasing through 5 months rear impurities of high-temperature process when showing these samples with respect to 0 month.
For Ex101, Ex102, these samples of Ex103, Ex104, their total related substance percent change is all in 175～245% scopes, and the fewer percent change of trometamol consumption is larger.For Ex111, Ex112, these samples of Ex113, Ex114, their total related substance percent change is all in 165～230% scopes, and the larger percent change of trometamol consumption is larger.These do not use the sample of trometamol for Ex131, Ex132, Ex133, Ex134, Ex135 and Ex136, Ex137, Ex138, Ex139, Ex140, and their total related substance percent change is all in 150～220% scopes.These do not use the sample of trometamol for Ex151, Ex152, Ex153, Ex154, Ex155, and their total related substance percent change is all in 165～230% scopes.As seen, comprise the appropriate amounts of ammonia butantriol for the chemical stability of tablet particularly the chemical stability of repaglinide be useful.
Test example 5: the Performance of pharmaceutical composition---the uniformity of dosage units of repaglinide in the tablet
With reference to the Determination of Content Uniformity method in two repaglinides that record of version Chinese Pharmacopoeia in 2010, measure the uniformity of dosage units of repaglinide in Ex1, Ex105, Ex106, Ex107, Ex108, Ex109, Ex110, Ex124, Ex125, Ex126, Ex127, Ex201, Ex202, Ex203, Ex204, Ex205, these tablets of Ex206, the A+1.80S value that the result shows these samples is all less than 12.0 (pharmacopeia regulation should A+1.80S≤15.0), for example the A+1.80S=8.7 of Ex1.Show that the present invention uses better simply method to obtain the good tablet content uniformity.
Claims (10)
1. a pharmaceutical composition wherein comprises: the repaglinide of the metformin hydrochloride of 500 weight portions, 0.5～5 weight portion and the pharmaceutic adjuvant of 10～200 weight portions.
2. according to claim 1 pharmaceutical composition, wherein said pharmaceutic adjuvant includes but not limited to filler, disintegrating agent, binding agent, alkaline agent, lubricant.
3. according to claim 1 to 2 pharmaceutical composition, wherein said pharmaceutic adjuvant also comprises solubilizing agent.
4. according to claim 1 to 3 pharmaceutical composition, wherein:
For the metformin hydrochloride of per 500 weight portions, the amount of disintegrating agent can be 5～50 weight portions, for example 10～25 weight portions;
For the metformin hydrochloride of per 500 weight portions, the amount of binding agent can be 5～50 weight portions, for example 10～30 weight portions;
For the metformin hydrochloride of per 500 weight portions, the amount of lubricant can be 2～20 weight portions, for example 3～15 weight portions; And/or
For the metformin hydrochloride of per 500 weight portions, the amount of filler can be 15～150 weight portions, for example 25～125 weight portions, for example 50～100 weight portions.
5. according to claim 1 to 4 pharmaceutical composition, wherein, described alkaline agent is selected from sodium hydroxide solution, potassium hydroxide solution, ammonia, phosphoric acid uncle sodium, diethanolamine, ethylenediamine, meglumine, 1B, trometamol etc.; Further, the mol ratio of repaglinide and alkaline agent is preferably about 1:1.0 to 1:10, for example about 1:1.0 to 1:5, for example about 1:1.0 to 1:2.5.
6. according to claim 1 to 5 pharmaceutical composition, wherein,
Described solubilizing agent is selected from poloxamer, tween;
Described filler is selected from one or more in Icing Sugar, lactose, amylum pregelatinisatum, corn starch, microcrystalline Cellulose, calcium sulfate, calcium hydrogen phosphate, calcium phosphate, Sorbitol, the mannitol.
Described disintegrating agent is selected from one or more of carboxymethyl starch sodium, low-substituted hydroxypropyl cellulose, crospolyvinylpyrrolidone, sodium carboxymethyl cellulose, cross-linking sodium carboxymethyl cellulose, polyvinylpyrrolidone or low-substituted hydroxypropyl cellulose sodium, polacrilin potassium;
Described binding agent is selected from one or more in water, polyvidone, ethanol, sodium carboxymethyl cellulose, polyvinylpyrrolidone or the hypromellose; And/or
Described lubricant is selected from a kind of in magnesium stearate, Macrogol 4000-8000, micropowder silica gel, the Pulvis Talci etc.
7. according to claim 1 to 6 pharmaceutical composition, wherein, described alkaline agent is selected from meglumine, trometamol; And/or, comprise calcium hydrogen phosphate in the described filler.
8. according to claim 1 to 7 pharmaceutical composition, it is tablet or capsule; Be preferably tablet; It is randomly further by coating.In one embodiment, described coating is film coating.
9. according to claim 1 to 8 pharmaceutical composition, it is unit dose formulations, and the amount of repaglinide is 0.5～5.0mg in each unit dose formulations, and the amount of metformin hydrochloride is 100～1000mg in each unit dose formulations.
10. prepare the method for each described pharmaceutical composition of claim 1 to 9, the method may further comprise the steps:
(a) each material is crushed to respectively acceptable granularity in the pharmacy;
(b) preparation granule I: repaglinide and alkaline agent, solubilizing agent, an amount of binding agent are dissolved in an amount of water and make solution, with this spray solution in an amount of filler, abundant mix homogeneously, be dried to moisture and be lower than 5% granule, again this dried particles is ground to form granularity less than 80 purpose fine powders, get granule I;
(c) preparation granule II: metformin hydrochloride, remainder binder, optional filler and an amount of mix lubricant is even, and water is the wetting agent pelletize, and drying gets granule II;
(d) whole mixed and preparations shaping: granule I, granule II, disintegrating agent, surplus lubricant and surplus filler are fully mixed, and the mixture that obtains is pharmaceutical composition of the present invention; Randomly this pharmaceutical composition is packed in the hard capsule case or be pressed into tablet, make the pharmaceutical composition of capsule or tablet.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103877049A (en) * | 2014-04-04 | 2014-06-25 | 白玲强 | Tablet containing fenofibrate and preparation technology thereof |
| CN106109428A (en) * | 2016-07-22 | 2016-11-16 | 江苏豪森药业集团有限公司 | The preparation process of repaglinide metformin |
| CN106176718A (en) * | 2016-08-03 | 2016-12-07 | 上海延安药业有限公司 | Compound recipe canagliflozin diformin tablet |
| CN115154432A (en) * | 2022-07-22 | 2022-10-11 | 北京惠之衡生物科技有限公司 | Repaglinide tablet and preparation method thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101516347A (en) * | 2006-09-29 | 2009-08-26 | 诺沃-诺迪斯克有限公司 | Pharmaceutical formulation comprising metformin and repaglinide |
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2013
- 2013-06-04 CN CN201310219929.9A patent/CN103251594B/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101516347A (en) * | 2006-09-29 | 2009-08-26 | 诺沃-诺迪斯克有限公司 | Pharmaceutical formulation comprising metformin and repaglinide |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103877049A (en) * | 2014-04-04 | 2014-06-25 | 白玲强 | Tablet containing fenofibrate and preparation technology thereof |
| CN106109428A (en) * | 2016-07-22 | 2016-11-16 | 江苏豪森药业集团有限公司 | The preparation process of repaglinide metformin |
| CN106109428B (en) * | 2016-07-22 | 2019-06-21 | 江苏豪森药业集团有限公司 | The preparation process of Repaglinide melbine |
| CN106176718A (en) * | 2016-08-03 | 2016-12-07 | 上海延安药业有限公司 | Compound recipe canagliflozin diformin tablet |
| CN115154432A (en) * | 2022-07-22 | 2022-10-11 | 北京惠之衡生物科技有限公司 | Repaglinide tablet and preparation method thereof |
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