CN100415226C - Electrolyte replenisher for treating hypopotassaemia hypomagnesemia and its uses - Google Patents
Electrolyte replenisher for treating hypopotassaemia hypomagnesemia and its uses Download PDFInfo
- Publication number
- CN100415226C CN100415226C CNB2005100460769A CN200510046076A CN100415226C CN 100415226 C CN100415226 C CN 100415226C CN B2005100460769 A CNB2005100460769 A CN B2005100460769A CN 200510046076 A CN200510046076 A CN 200510046076A CN 100415226 C CN100415226 C CN 100415226C
- Authority
- CN
- China
- Prior art keywords
- magnesium
- aspartic acid
- aspartate hydrochloride
- hypomagnesemia
- treatment
- 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.)
- Active
Links
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The present invention relates to an electrolyte replenishing agent for treating hypokalemia and hypomagnesemia and an application thereof. The electrolyte replenishing agent comprises a medicament prepared by using magnesium aspartate hydrochloride acid and potassium aspartate as active ingredients, wherein the weight ratio of the magnesium aspartate hydrochloride acid to the potassium aspartate is 1: 0.1 to 10. The electrolyte replenishing agent of the present invention is a medicine compound which can replenish potassium ions and magnesium ions in a human body, can not break the original non-dissociative acid-base metabolism balance in cells, and can enhance the bioavailability of the potassium ions and the magnesium ions in the human body.
Description
Technical field
The present invention relates to treat the medicine of hypokalemia and hypomagnesemia, specifically a kind of electrolyte replenisher for the treatment of the hypokalemia hypomagnesemia, it can be used for treating cardiovascular disease, acute and chronic hepatic insufficiency.
Background technology
Cardiovascular disease has become the No.1 formidable enemy of human health.According to World Health Organization's statistics, cardiovascular disease seizes 1,200 ten thousand people's life every year, and this numeral is near 1/4th of the total death toll of world population.Over past ten years, along with the development of Medical Technology means, cardiovascular mortality rate descends to some extent, but still is positioned at the first place of the cause of death, and the human existence quality in serious threat.Along with the development of society, owing to reason and smokings such as environmental pollution, stress be excessive, bad life style such as drink, the people who suffers from hepatopathy is also more and more.Wherein representational hepatopathy comprises acute and chronic hepatitis, liver cirrhosis and hyperbilirubinemia etc.Serious liver dysfunction that hepatopathy causes and concurrent complication, the social problem that has developed into the serious harm health of people at present.In recent years, medicine clinical research confirms that above-mentioned two kinds of body system dysfunctions are all relevant with the low magnesium of the low potassium of human body.
Magnesium is important cation in the body, be the prothetic group of multiple enzymatic reaction in the body, and participate in the biological metabolism of protein, fat, saccharide etc. and the ion transport of oxidative phosphorylation and cell membrane, so magnesium is almost relevant with all importances of vital movement.The circulatory function obstacle that hypomagnesemia causes comprises arrhythmia, congestive heart failure, hypertension etc., and the liver systemic-function obstacle that hypomagnesemia causes comprises acute and chronic hepatitis, liver cirrhosis, hyperbilirubinemia etc.At present, the systemic-function obstacle that causes of clinical use head injury treated with magnesium preparation hypomagnesemia.Magnesium preparation commonly used has magnesium chloride, magnesium sulfate, Magnesium Aminosuccinate.Magnesium chloride intramuscular injection meeting causes pain, and life-time service can cause the fibre modification reaction, and is inactive, and magnesium sulfate easily causes diarrhoea in using, and now substitutes with Magnesium Aminosuccinate.Also find in the clinical practice Magnesium Aminosuccinate because its molecular structure is big, the space structure complexity, molecular weight is big, causes degree of absorbing poor.Because the structure of Aspartic Acid magnesium alkaline-earth metal is formed, acid-base balance in the destructible body causes alkalosis when using for a long time or in a large number simultaneously.Therefore, press in clinical and develop degree of absorbing height, effectively the Mg supplementation ion does not destroy the equilibrated medicine of acid-base metabolism in the body.
Summary of the invention
The object of the present invention is to provide that a kind of degree of absorbing is good, the electrolyte replenisher and the application thereof of the treatment hypokalemia hypomagnesemia that can take for a long time.
For achieving the above object, the technical solution used in the present invention is:
A kind of electrolyte replenisher for the treatment of the hypokalemia hypomagnesemia comprises that Magnesium aspartate hydrochloride and aspartic acid are the medicament that active ingredient is made, and the weight ratio of Magnesium aspartate hydrochloride and aspartic acid is 1: 0.1-10; Be preferably 1: 0.2-6; Be preferably 1: 0.5-3.
Medicament of the present invention can be made into said any stable dosage form on the pharmaceuticss such as tablet, capsule, granule, oral liquid, liquid drugs injection, aseptic powder injection, transfusion, makes things convenient for patient's medication of different conditions.
Electrolyte replenisher of the present invention can be used for preparing in the pharmaceutical composition of blood circulation that treatment causes by hypokalemia hypomagnesemia or liver systemic-function obstacle.
Described circulatory function obstacle typically refers to cardiovascular disease (as: arrhythmia, congestive heart failure, hypertension); Liver systemic-function obstacle typically refers to acute and chronic hepatic insufficiency (as: acute and chronic hepatitis, liver cirrhosis, hyperbilirubinemia).
One of active ingredient in the electrolyte replenisher of the present invention Magnesium aspartate hydrochloride (being abbreviated as MAH) is equimolar hydrochloric acid and Aspartic Acid, the bonded hydrate of magnesium ion, and molecular formula is (C
4H
6ClNO
4) Mg * 3H
2O, molecular weight are 245.90.
The Magnesium aspartate hydrochloride chemical structural formula is as follows:
(molecular formula is C with Magnesium Aminosuccinate
8H
12N
2MgO
8, molecular weight is 288.50) compare, replaced the Aspartic Acid of a part in the Magnesium Aminosuccinate by a part hydrochloric acid, space conformation changes, and the change macromolecular structure is small molecule structure, and molecular weight reduces, and is easy to pass through cell membrane; Aspartic Acid and three water molecules in the while Magnesium aspartate hydrochloride, hydrophilic increases, and is convenient to intracellular transport.
The Magnesium Aminosuccinate structural formula is as follows:
The 1mol Magnesium aspartate hydrochloride contains Aspartic Acid, Cl, Mg and the 3mol H of equimolecular quantity
2O, on percentage by weight, chemical compound comprises 53.7% Aspartic Acid, 14.4%Cl, 9.9%Mg, 22%H
2O.Because its favourable composition, Magnesium aspartate hydrochloride is verified, and oral or parenteral administration can not destroy the acid-base metabolism balance.
Magnesium ion in the Magnesium aspartate hydrochloride can participate in formation and the release of ATP, chloride ion directly acts on myocardial cell in conjunction with magnesium ion, alleviate of the contraction of various mediators to blood vessel, the chamber that slows down conduction, prolong the absolute refractory period of cell, reduce the cell self-disciplining, have good antiarrhythmic effect.In addition, calcium overload takes place under the situation that magnesium deficiency and extracellular magnesium are blocked in a large number easily, and too much consume ATP, Magnesium aspartate hydrochloride can activate Ca
2+, activate ATP enzyme, Ca in the prevention cell
2+Over loading.
In addition, magnesium ion also has the effect of the potassium of guarantor.Magnesium can be regulated the interior extracellular concentration of cell of potassium to a great extent, and the storage of potassium is stayed, energy delivery all needs magnesium.Clinical research proves that low magnesium makes potassium can not enter the depolarization cell, influences the resting potential of myocardial cell membrane, inspires diversity conduction and reentry phenomenon, forms serious arrhythmia easily.
Another active ingredient in the electrolyte replenisher of the present invention is an aspartic acid.Be the chemical compound of Aspartic Acid and potassium hydroxide reaction generation, its chemical name is: L-2-Potassium Aminosuccinate, molecular formula are C
4H
6KNO
41/2H
2O, molecular weight are 180.20; Aspartic acid be clinical in a kind of potassium salt commonly used, be mainly used in prevention and treatment hypokalemia.Through zoopery and clinical trial certificate, Aspartic Acid plays an important role in tricarboxylic acid cycle as the precursor of oxaloacetic acid in the body, and participates in ornithine cycle, makes ammonia and carbon dioxide in conjunction with generating the urea element.The affinity of pair cell is strong, and the carrier that can be used as potassium, magnesium ion helps it to enter in the cell, improves potassium, magnesium ion concentration in the cell, quickens the hepatocyte tricarboxylic acid cycle, to improving liver function, reducing serum bilirubin level and have certain effect.Potassium ion has multiple physiological function, and it participates in the metabolism of cell, keeps the capacity and the osmotic pressure of intracellular fluid, keeps neural impulse and nervimuscular irritability.In addition, potassium can also be kept myocardial contraction, improves the contractility of cardiac muscle fiber, and cardiac muscle is had protective effect.
The aspartic acid structural formula is as follows:
Used aspartic acid is left-handed aspartic acid in the compositions, and aspartic acid has left-handed and two kinds of structures of dextrorotation, and left-handed have physiologically active, a dextrorotation non-activity.
The present invention a kind ofly can either effectively replenish the potassium magnesium ion, does not destroy acid-base metabolism balance in the body again, and significantly improves the compound drug of degree of absorbing in the potassium magnesium ion body.Result of study is found, Magnesium aspartate hydrochloride and aspartic acid are combined, and by the mutual promoting action of two kinds of medicaments, unexpectedly produces synergistic therapeutic action, significantly improves potassium magnesium ion biological degree in vivo; Simultaneously,, do not influence acid-base balance in the body, avoided alkalotic generation owing to contain the magnesium and the chlorine of five equilibrium subnumber in the Magnesium aspartate hydrochloride structure composition.
The specific embodiment
Further specify the present invention below by embodiment and application examples, but these embodiment and application examples just to the explanation the present invention, protection scope of the present invention is not subjected to the restriction of this example.
Embodiment 1
1. tablet formulation: Magnesium aspartate hydrochloride 100g
Aspartic acid 10g
Starch 380g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 100g, aspartic acid 10g and starch 380g mixing pulverizing, add starch slurry 10g mixing and make soft material, 14 or 16 mesh sieve granulations, oven dry, granulate, tabletting, coating, packing get final product.Usage: oral, one time 1,2 times on the one.One month is a course of treatment.
Embodiment 2
1. tablet formulation: Magnesium aspartate hydrochloride 42.5g
Aspartic acid 425g
Starch 120g
Make 2000
2. preparation technology: get Magnesium aspartate hydrochloride 42.5g, aspartic acid 425g and starch 120g mixing pulverizing, add starch slurry 10g mixing and make soft material, 14 or 16 mesh sieve granulations, oven dry, granulate, tabletting, coating, packing get final product.Usage: oral, one time 1,2 times on the one.One month is a course of treatment.
Embodiment 3
1. tablet formulation: Magnesium aspartate hydrochloride 40g
Aspartic acid 20g
Starch 30g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 40g, aspartic acid 20g and starch 30g mixing pulverizing, add starch slurry 10g mixing and make soft material, 14 or 16 mesh sieve granulations, oven dry, granulate, tabletting, coating, packing get final product.Usage: oral, one time 1,2 times on the one.One month is a course of treatment.
Embodiment 4
1. tablet formulation: Magnesium aspartate hydrochloride 180g
Aspartic acid 180g
Starch 130g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 180g, aspartic acid 180g and starch 130g mixing pulverizing, add starch slurry 10g mixing and make soft material, 14 or 16 mesh sieve granulations, oven dry, granulate, tabletting, coating, packing get final product.Usage: oral, one time 1,2 times on the one.One month is a course of treatment.
Embodiment 5
1. tablet formulation: Magnesium aspartate hydrochloride 12g
Aspartic acid 60g
Starch 168g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 12g, aspartic acid 60g starch 168g mixing pulverizing, add starch slurry 10g mixing and make soft material, 14 or 16 mesh sieve granulations, oven dry, granulate, tabletting, coating, packing get final product.Usage: oral, one time 1,2 times on the one.One month is a course of treatment.
Embodiment 6
1. transfusion is write out a prescription:
Magnesium aspartate hydrochloride 2500g
Aspartic acid 250g
Sodium chloride 35g
Make 1000 bottles
2. preparation technology: get Magnesium aspartate hydrochloride 2500g, aspartic acid 250g, add water for injection 800ml stirring and dissolving, other gets sodium chloride 35g and adds injection water 200ml stirring and dissolving, and above-mentioned two kinds of solution are mixed, add needle-use activated carbon 200g, stir, filter, transfer pH to 5-7, add water for injection to 250000ml, use filtering with microporous membrane, fill is in 250ml hard infusion bottle, and sterilization promptly.Usage: intravenous drip, a 250ml, 1 time on the one.2 weeks were a course of treatment.
Embodiment 7
1. transfusion is write out a prescription:
Magnesium aspartate hydrochloride 320g
Aspartic acid 1600g
Sodium chloride 35g
Make 1000 bottles
2. preparation technology: get Magnesium aspartate hydrochloride 320g, aspartic acid 1600g, add water for injection 800ml stirring and dissolving, other gets sodium chloride 35g and adds injection water 200ml stirring and dissolving, and above-mentioned two kinds of solution are mixed, add needle-use activated carbon 200g, stir, filter, transfer pH to 5-7, add water for injection to 100000ml, use filtering with microporous membrane, fill is in 100ml hard infusion bottle, and sterilization promptly.Usage: intravenous drip, a 100ml, 1 time on the one.2 weeks were a course of treatment.
Embodiment 8
1. capsule is write out a prescription:
Magnesium aspartate hydrochloride 23.8g
Aspartic acid 238g
Microcrystalline Cellulose 5g
Starch 35g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 23.8g, aspartic acid 238g, microcrystalline Cellulose 5g and starch 35g mixing pulverizing, add polyvinylpolypyrrolidone 10g again and make disintegrating agent, mixing, the capsule of packing into No. 1, packing gets final product.Usage: oral, one time 1,2 times on the one, one month is a course of treatment.
Embodiment 9
1. capsule is write out a prescription:
Magnesium aspartate hydrochloride 110g
Aspartic acid 55g
Microcrystalline Cellulose 5g
Starch 30g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 110g, aspartic acid 55g, microcrystalline Cellulose 5g and starch 30g mixing pulverizing, add polyvinylpolypyrrolidone 10g again and make disintegrating agent, mixing, the capsule of packing into No. 1, packing gets final product.Usage: oral, one time 1,2 times on the one, one month is a course of treatment.
Embodiment 10
1. capsule is write out a prescription:
Magnesium aspartate hydrochloride 25g
Aspartic acid 25g
Microcrystalline Cellulose 5g
Starch 45g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 25g, aspartic acid 25g, microcrystalline Cellulose 5g and starch 45g mixing pulverizing, add polyvinylpolypyrrolidone 10g again and make disintegrating agent, mixing, the capsule of packing into No. 1, packing gets final product.Usage: oral, one time 1,2 times on the one, one month is a course of treatment.
Embodiment 11
1. liquid drugs injection is write out a prescription
Magnesium aspartate hydrochloride 2340g
Aspartic acid 234g
Make 1000
2. preparation process: get Magnesium aspartate hydrochloride 2340g, aspartic acid 234g, add water for injection 1000ml stirring and dissolving, transfer pH to 5-7, add needle-use activated carbon 2g, filter, add water for injection to 2000ml, fill, sealing by fusing, sterilization, lamp inspection, packing is promptly.Usage: intravenous drip, a 2ml, once-a-day.3 weeks were a course of treatment.
Embodiment 12
1. liquid drugs injection is write out a prescription
Magnesium aspartate hydrochloride 550g
Aspartic acid 5500g
Make 1000
2. preparation process: get Magnesium aspartate hydrochloride 550g, aspartic acid 5500g, add water for injection 1000ml stirring and dissolving, transfer pH to 5-7, add needle-use activated carbon 2g, filter, add water for injection to 10000ml, fill, sealing by fusing, sterilization, lamp inspection, packing is promptly.Usage: intravenous drip, a 10ml, once-a-day.3 weeks were a course of treatment.
Embodiment 13
1. liquid drugs injection is write out a prescription
Magnesium aspartate hydrochloride 650g
Aspartic acid 3250g
Make 1000
2. preparation process: get Magnesium aspartate hydrochloride 650g, aspartic acid 3250g, add water for injection 1000ml stirring and dissolving, transfer pH to 5-7, add needle-use activated carbon 2g, filter, add water for injection to 20000ml, fill, sealing by fusing, sterilization, lamp inspection, packing is promptly.Usage: intravenous drip, a 20ml, once-a-day.3 weeks were a course of treatment.
Embodiment 14
1. oral liquid is write out a prescription
Magnesium aspartate hydrochloride 910g
Aspartic acid 910g
Sorbic acid 10g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 910g, aspartic acid 910g, sorbic acid 10g makes antiseptic, adds distilled water 200ml and dissolves, filters, and mends distilled water again to 50000ml, filtration, fill, sterilization, lamp inspection, packing are promptly.Usage: oral, a 10-20ml, one time 3 times.One month is a course of treatment.
Embodiment 15
1. oral liquid is write out a prescription
Magnesium aspartate hydrochloride 480g
Aspartic acid 240g
Sorbic acid 5g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 480g, aspartic acid 240g, sorbic acid 5g makes antiseptic, adds distilled water 200ml and dissolves, filters, and mends distilled water again to 100000ml, filtration, fill, sterilization, lamp inspection, packing are promptly.Usage: oral, a 10-20ml, one time 3 times.One month is a course of treatment.
Embodiment 16
1. the powder pin is write out a prescription:
Magnesium aspartate hydrochloride 2000g
Aspartic acid 200g
Mannitol 100g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 2000g, aspartic acid 200g, add water for injection 1000ml stirring and dissolving, proppant mannitol 200g adds injection water 200ml stirring and dissolving, above-mentioned two kinds of solution are mixed, add needle-use activated carbon 150g, stir, filter, transfer pH to 5-7, add water for injection, use filtering with microporous membrane to 10000ml, fill, through pre-freeze, freezing, heat up, the insulation rear pressing cover promptly.Usage: intravenous drip, one time 1, a twice-daily.3 weeks were a course of treatment.
Embodiment 17
1. the powder pin is write out a prescription:
Magnesium aspartate hydrochloride 540g
Aspartic acid 270g
Mannitol 100g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 540g, aspartic acid 270g, add water for injection 1000ml stirring and dissolving, proppant mannitol 200g adds injection water 200ml stirring and dissolving, above-mentioned two kinds of solution are mixed, add needle-use activated carbon 150g, stir, filter, transfer pH to 5-7, add water for injection, use filtering with microporous membrane to 10000ml, fill, through pre-freeze, freezing, heat up, the insulation rear pressing cover promptly.Usage: intravenous drip, one time 1, a twice-daily.3 weeks were a course of treatment.
Embodiment 18
1. the powder pin is write out a prescription:
Magnesium aspartate hydrochloride 30g
Aspartic acid 300g
Mannitol 100g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 30g, aspartic acid 300g, add water for injection 1000ml stirring and dissolving, proppant mannitol 100g adds injection water 200ml stirring and dissolving, above-mentioned two kinds of solution are mixed, add needle-use activated carbon 150g, stir, filter, transfer pH to 5-7, add water for injection, use filtering with microporous membrane to 20000ml, fill, through pre-freeze, freezing, heat up, the insulation rear pressing cover promptly.Usage: intravenous drip, one time 1, a twice-daily.3 weeks were a course of treatment.
Embodiment 19
1. the powder pin is write out a prescription:
Magnesium aspartate hydrochloride 350g
Aspartic acid 350g
Mannitol 100g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 350g, aspartic acid 350g, add water for injection 1000ml stirring and dissolving, proppant mannitol 100g adds injection water 200ml stirring and dissolving, above-mentioned two kinds of solution are mixed, add needle-use activated carbon 150g, stir, filter, transfer pH to 5-7, add water for injection, use filtering with microporous membrane to 20000ml, fill, through pre-freeze, freezing, heat up, the insulation rear pressing cover promptly.Usage: intravenous drip, one time 1, a twice-daily.3 weeks were a course of treatment.
Embodiment 20
1. the powder pin is write out a prescription:
Magnesium aspartate hydrochloride 480g
Aspartic acid 2400g
Mannitol 100g
Make 1000
2. preparation technology: get Magnesium aspartate hydrochloride 480g, aspartic acid 2400g, add water for injection 1000ml stirring and dissolving, proppant mannitol 100g adds injection water 200ml stirring and dissolving, above-mentioned two kinds of solution are mixed, add needle-use activated carbon 150g, stir, filter, transfer pH to 5-7, add water for injection, use filtering with microporous membrane to 20000ml, fill, through pre-freeze, freezing, heat up, the insulation rear pressing cover promptly.Usage: intravenous drip, one time 1, a twice-daily.3 weeks were a course of treatment.
Embodiment 21-28
Present composition prescription is referring to table 1, and its preparation technology is identical with the preparation of compositions process of embodiment 1-20 same dosage form.
Table 1
Embodiment 29-40
Present composition prescription is referring to table 2, and its preparation technology is identical with the preparation of compositions process of embodiment 1-20 same dosage form.
Table 2
Application examples 1 present composition is for the rat acute toxicity test
Experiment material:
The 1st group: Magnesium aspartate hydrochloride and aspartic acid compositions (weight ratio is 1: 1.5);
The 2nd group: Magnesium aspartate hydrochloride;
The 3rd group: aspartic acid;
The 4th group: matched group.
Experimental technique: every group is used dd is that (body weight is 15 ± 1g) each 10 to male mice, and oral administration is confirmed fatality rate respectively.To respectively organize the consumption respectively administration of medicament by every kg body weight 500mg, 100mg, 20mg and 0mg in the experiment material, number goes out the dead number of animals in 4 week backs, calculates fatality rate, the results are shown in Table 3.
Table 3 dd is the acute toxicity that male mice gives pharmaceutical composition of the present invention
| Animal groups | Dosage (mg/kg) | Number of animals | Death toll | Mortality rate (%) |
| The 1st group (Magnesium aspartate hydrochloride and aspartic acid) | 500 | 10 | 0 | 0 |
| The 2nd group (Magnesium aspartate hydrochloride) | 100 | 10 | 0 | 0 |
| The 3rd group (aspartic acid) | 20 | 10 | 0 | 0 |
| The 4th group (matched group) | 0 | 10 | 0 | 0 |
As above shown in the table 3, the contrast experiment of the acute toxicity by compositions (Magnesium aspartate hydrochloride and aspartic acid) and Magnesium aspartate hydrochloride, aspartic acid as can be known, the dosage of compositions increases, but the mortality rate no change illustrates that pharmaceutical composition of the present invention is safety, avirulent medicament.
Application examples 2 present compositions are for the rat long term toxicity test
Experiment material:
1. be subjected to the reagent thing: Magnesium aspartate hydrochloride and aspartic acid compositions (weight ratio is 1: 1) dosage is: the 1st group: 500mg/Kg; The 2nd group: 100mg/Kg; The 3rd group: 20mg/Kg; The 4th group of (matched group): 0mg/Kg;
2. laboratory animal: Wistar rat, each 40 of male and female, body weight 90-120g, 6-8 age in week;
Experimental technique:
1. each Wistar rat of 40 of male and female is divided into 4 groups, each 20 of every group of male and female are observed a week before the administration, and animal activity, feed, feces etc. are no abnormal, the body weight normal growth.
2. give the dosage that 4 groups of rats are subjected to reagent thing 1-4 group respectively, administering mode is for replacing in rat abdominal cavity both sides drug administration by injection every day 1 time, continuous 4 weeks.
3. situations such as animal activity, hair, feces and food-intake, body weight gain after the observation administration after 4 weeks of administration and drug withdrawal recovered for 2 weeks, are measured hematology and blood parameters, internal organs weight in wet base, organ coefficient, and are carried out histopathologic examination.
Experimental result is summarized as follows:
(1) general symptom: in all each groups of experiment male and female, do not find animal dead or that frequently die on one's deathbed.Compare with matched group, food-intake, weight increase amount, amount of drinking water, feces etc. are not seen significant change.
(2) hematology: each organizes index and matched group compares there was no significant difference.
(3) blood biochemical is learned: each dosage group and matched group be there was no significant difference relatively.
(4) system's postmortem: the administration phase and convalescent period internal organs show no obvious abnormalities.
(5) internal organs weight in wet base and organ coefficient: internal organs weight in wet base and organ coefficient and matched group be there was no significant difference relatively.
(6) histopathologic examination: internal organs histopathologic examination there is no obvious change.
Table 4 Wistar rat gives the acute toxicity of pharmaceutical composition of the present invention
| Animal groups | Dosage (mg/kg) | Number of animals | Death toll | Mortality rate (%) |
| The 1st group | 500 | 20 | 0 | 0 |
| The 2nd group | 100 | 20 | 0 | 0 |
| The 3rd group | 20 | 20 | 0 | 0 |
| The 4th group (matched group) | 0 | 20 | 0 | 0 |
Can conclude by above experimental result, with Magnesium aspartate hydrochloride and continuous 4 weeks of aspartic acid compositions in the experiment of rat abdominal cavity administration, at maximum concentration is in the administration group of 500mg/kg, do not observe the toxicity that needs special record, therefore compositions of the present invention is safe combination drug.
Blood Mg before and after application examples 3 these compositionss of clinical practice
2+, blood K
+Change relatively (the arrhythmia curative effect relatively)
Data and method:
1. case is selected:
Patients with arrhythmia (the low potassium of companion, hypomagnesemia) 50 examples; (physical signs of hypokalemia is serum potassium concentration＜3.5mEq/L; the physical signs of hypomagnesemia for the blood plasma magnesium density be＜0.7mmol/L); wherein male 38 examples, women 12 examples; be divided into 2 groups at random; there was no significant differences (P＞0.05) such as 2 groups of ages, sex, the cause of disease, arrhythmia type have comparability.
2. Therapeutic Method:
The 1st group gives Magnesium Aminosuccinate, the 2nd group of compositions (1: 1.1) that gives Magnesium aspartate hydrochloride and aspartic acid, and once a day, 14 days is a course of treatment.
3. observation of curative effect
Inquire patient's clinical symptoms and untoward reaction every day, recorded heart rate, the rhythm of the heart are done routine electrocardiogram every day one time.All carry out complete physical examination before all patient's medications and after the medication, do 24 hr Ambulatory EKG Monitoring inspections, and blood potassium, blood magnesium determination are done in blood drawing.
4. efficacy assessment standard
Produce effects: premature beat disappears or reduces＞90%; Effectively: premature beat reduces 50%～90%; Invalid: as early to reduce＜50% or no change; Total effective rate=obvious effective rate+effective percentage.
Experimental result
1. two groups of medication bleeding from anus Mg
2+, blood K
+Change (referring to table 5)
The 1st group of medication bleeding from anus potassium does not have significant change, P＞0.05, and blood magnesium has significance to change P＜0.001; The 2nd group of medication bleeding from anus potassium has significance to change, P＜0.001, and blood magnesium has significance to change P＜0.001; The 1st group and the 2nd group is compared after the medication, and blood magnesium, blood potassium concentration all have significance to improve.Set of applications compound group is described than using Magnesium Aminosuccinate group blood Mg
2+, blood K
+Improve fast.
Blood Mg before and after two groups of medicines of table 5 clinical practice
2+, blood K
+Change
| Concentration of blood kalium mmol/L | Blood magnesium density mmol/L | |
| Before the medication | 3.26±0.18 | 0.53±0.04 |
| After the 1st group of medication | 3.27±0.12 | 0.80±0.05 |
| After the 2nd group of medication | 4.46±0.25 | 0.97±0.06 |
(annotate: normal human's concentration of blood kalium is 3.5～5mmol/L, and the blood magnesium density is 0.79～1.05mmol/L)
2. arrhythmia curative effect (referring to table 6)
Table 6 liang group medicine arrhythmia curative effect is (%) relatively
| Group | The example number | Produce effects | Effectively | Invalid | Total effective rate |
| The 1st group | 25 | 8(32) | 8(32) | 9(36) | 16(64) |
| The 2nd group | 25 | 16(64) | 5(20) | 4(16) | 21(84) |
By experimental result as can be seen, treatment arrhythmia compositions group (the 2nd group) total effective rate illustrates that apparently higher than Magnesium Aminosuccinate group (the 1st group) the ARR curative effect of compositions group (the 2nd group) treatment is better.
Application examples 4 stability tests
1. acceleration test
Investigation project and method: get this composition tablet (1: 1.05), put 40 ℃ ± 2 ℃, relative humidity and be in 75% ± 5% the calorstat, take a sample when placing 0,1,2,3,6 the end of month, according to " Pharmacopoeia of People's Republic of China 2000 editions " standard inspection, project is appearance luster, acid-base value, solution colour and clarity, loss on drying, catabolite and content, its experimental result such as following table:
Table 7 acceleration test is investigated the result
| Time | Appearance luster | Acid-base value | Solution colour and clarity | Loss on drying | Catabolite | Content |
| 0 | The white circular piece | 6.5 | Up to specification | Up to specification | Do not detect | 0.1％ |
| 1 | No abnormal variation | 6.5 | Up to specification | Up to specification | Do not detect | 0.23％ |
| 2 | No abnormal variation | 6.4 | Up to specification | Up to specification | Do not detect | 0.15％ |
| 3 | No abnormal variation | 6.3 | Up to specification | Up to specification | Do not detect | 0.09％ |
| 6 | No abnormal variation | 6.4 | Up to specification | Up to specification | Do not detect | 0.12％ |
2. chronicity test
Investigation project and method: get this composition tablet, put 25 ℃ ± 2 ℃, relative humidity and be in 60% ± 10% the calorstat, take a sample when placing 0,3,9,12,18 the end of month, according to " Pharmacopoeia of People's Republic of China 2000 editions " standard inspection, project is appearance luster, acid-base value, solution colour and clarity, loss on drying, catabolite and content, its experimental result such as following table:
Table 8 long term test is investigated the result
| Time | Appearance luster | Acid-base value | Solution colour and clarity | Loss on drying | Catabolite | Content |
| 0 | The white circular piece | 6.7 | Up to specification | Up to specification | Do not detect | 0.2％ |
| 3 | No abnormal variation | 6.8 | Up to specification | Up to specification | Do not detect | 0.1％ |
| 9 | No abnormal variation | 6.6 | Up to specification | Up to specification | Do not detect | 0.11％ |
| 12 | No abnormal variation | 6.7 | Up to specification | Up to specification | Do not detect | 0.15％ |
| 18 | No abnormal variation | 6.5 | Up to specification | Up to specification | Do not detect | 0.13％ |
By above result of the test as can be known, the significance variation does not all take place through the every investigation index in acceleration test and chronicity test back in this compositions, illustrates that this compositions is unusual stable compositions.
Compare with motassium magnessium aspartate
1. improve soon the length of holding time with dosage blood drug level.
Because chloride chemical compound is better than sulfate and aspartate, in zoopery, take motassium magnessium aspartate and this compositions of same dose, it is fast that the result shows that the blood drug level of this compositions group improves, the length of holding time, metabolism is slower.
Table 9 serum potassium magnesium density is (mmol/L) relatively
A: be present composition group B: the motassium magnessium aspartate group
2. toxicity relatively
The toxicity test of Magnesium aspartate hydrochloride shows that it has very high safety.Single oral administration in the experiment of rat, mice and Canis familiaris L., the LD of Magnesium aspartate hydrochloride
50Be respectively 6.8,6.9,4.5g/kg, the LD of its corresponding magnesium
50Be respectively 660,670,440Mg
2+/ kg.On the other hand, because the trap height of Magnesium aspartate hydrochloride, the use amount that reaches equal therapeutic effect is low than Magnesium Aminosuccinate, so also reduced the caused neurovirulent generation of practical application Aspartic Acid simultaneously.
3. side reaction relatively
As everyone knows, the pH value of extracellular fluid is by the concentration of soda acid and the decision of its degree of dissociation.Provide a large amount of alkali metal and alkaline-earth metal easily to cause alkalosis, easily cause acidosis and take a large amount of hydrochlorates, sulfate, phosphate.The clinical medium-term and long-term motassium magnessium aspartate of using easily causes alkalosis, cause the patient neuromuscular dysfunction to occur such as nervomuscular irritability increases and tetany, and central nervous system dysfunction such as symptoms such as dysphoria, mental disorder and delirium, and the Magnesium aspartate hydrochloride in this compositions is owing to contain the magnesium and the chlorine of five equilibrium subnumber, life-time service do not influence acid-base balance, even can not cause alkalosis yet.Particularly in many complex disease application of model,, have only the magnesium salt of chloride that the protective effect of heart is just arranged as the unbalance type of acid-base metabolism
4. curative effect relatively
The effect of motassium magnessium aspartate and this composition therapeuticing disease compares, and this compositions is more remarkable to the improvement of symptom, short treating period, the length of holding time.
Two groups of Drug therapy arrhythmia curative effects relatively
| Group | n | The course of treatment (d) | Produce effects | Effectively | Invalid | Effectively total |
| The A group | 85 | 11 | 41(48.2) | 32(37.6) | 12(14.1) | 73(85.9) |
| The B group | 66 | 14 | 23(35.4) | 15(23.1) | 28(43.1) | 37(58.5) |
A: be present composition group B: the motassium magnessium aspartate group
Claims (6)
1. electrolyte replenisher for the treatment of the hypokalemia hypomagnesemia, it is characterized in that: comprise that Magnesium aspartate hydrochloride and aspartic acid are the medicament that active ingredient is made, the weight ratio of Magnesium aspartate hydrochloride and aspartic acid is 1: 0.1-10.
2. the electrolyte replenisher of treatment hypokalemia hypomagnesemia according to claim 1 is characterized in that: the weight ratio of described Magnesium aspartate hydrochloride and aspartic acid is 1: 0.2-6.
3. the electrolyte replenisher of treatment hypokalemia hypomagnesemia according to claim 1 is characterized in that: the weight ratio of described Magnesium aspartate hydrochloride and aspartic acid is 1: 0.5-3.
4. the application of the electrolyte replenisher of a treatment hypokalemia hypomagnesemia as claimed in claim 1 in the pharmaceutical composition of preparation treatment blood circulation or liver systemic-function obstacle.
5. the application of the electrolyte replenisher of a treatment hypokalemia hypomagnesemia as claimed in claim 1 in the pharmaceutical composition of preparation treatment blood circulation or liver systemic-function obstacle, it is characterized in that: described circulatory function obstacle is meant cardiovascular disease.
6. the application of the electrolyte replenisher of a treatment hypokalemia hypomagnesemia as claimed in claim 1 in the pharmaceutical composition of preparation treatment blood circulation or liver systemic-function obstacle, it is characterized in that: described liver systemic-function obstacle is meant the acute and chronic hepatic insufficiency.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100460769A CN100415226C (en) | 2005-03-23 | 2005-03-23 | Electrolyte replenisher for treating hypopotassaemia hypomagnesemia and its uses |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100460769A CN100415226C (en) | 2005-03-23 | 2005-03-23 | Electrolyte replenisher for treating hypopotassaemia hypomagnesemia and its uses |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1836655A CN1836655A (en) | 2006-09-27 |
| CN100415226C true CN100415226C (en) | 2008-09-03 |
Family
ID=37014249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100460769A Active CN100415226C (en) | 2005-03-23 | 2005-03-23 | Electrolyte replenisher for treating hypopotassaemia hypomagnesemia and its uses |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100415226C (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101921309B (en) * | 2009-06-12 | 2013-04-17 | 沈阳药联科技创新有限公司 | L-cystyl-2-L-aspartic tripeptide and derivatives, preparation method and application thereof |
| CN105795278A (en) * | 2014-12-27 | 2016-07-27 | 辽宁药联制药有限公司 | Beverage containing potassium aspartate and preparation method thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6579905B1 (en) * | 2001-11-19 | 2003-06-17 | Mcmains Michael B. | Method for the prevention or treatment of hypomagnesemia in pediatric patients and in patients with G-tubes or NG-tubes |
-
2005
- 2005-03-23 CN CNB2005100460769A patent/CN100415226C/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6579905B1 (en) * | 2001-11-19 | 2003-06-17 | Mcmains Michael B. | Method for the prevention or treatment of hypomagnesemia in pediatric patients and in patients with G-tubes or NG-tubes |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1836655A (en) | 2006-09-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101926779A (en) | Gemcitabine solid lipid nanospheres, preparation method thereof and use thereof | |
| CN100493514C (en) | Composite medicine of creatine phosphate sodium and magnesium salt | |
| CN100415226C (en) | Electrolyte replenisher for treating hypopotassaemia hypomagnesemia and its uses | |
| CN105832763A (en) | Medicine composition containing sodium L-ascorbate and preparing method of medicine composition | |
| JP3622985B2 (en) | How to increase magnesium absorption and prevent atherosclerosis | |
| CN101524355B (en) | Compound preparation of antituberculosis medicaments, and preparation method thereof | |
| JP2009526086A (en) | Drug for treating diseases caused by hyperphosphatemia and method for producing the same | |
| CN101474195B (en) | Medicament composition for treating cardiac and cerebral vascular disease | |
| CN100534998C (en) | Preparation and application of fructose-1, 6-diphosphate-calcium salt | |
| CN101091715A (en) | Composition of medication for treating cardiovascular diseases and cerebrovascular diseases | |
| CN109091500A (en) | A kind of children's compound electrolyte glucose injection and preparation method thereof | |
| US20130022673A1 (en) | Enhancement of magnesium uptake in mammals | |
| CN109010362A (en) | A kind of children's compound electrolyte glucose injection and preparation method thereof | |
| CN101780091B (en) | Medical composition containing ivabradine and ranolazine | |
| CN101234104A (en) | Pharmaceutical composition containing lipoic acid and mecobalamin and preparation thereof | |
| CN101012240A (en) | Creatine phosphate arginine salt and preparing method thereof | |
| CN102125558A (en) | Compound sodium levofolinate fluorouracil antineoplastic medicament | |
| CN107737108B (en) | A kind of combination of oral medication for treating Pathogenesis of Post-infarction Ventricular Remodeling | |
| CN114948944B (en) | Application of composition containing sulbactam sodium sulfate and amiodarone in preparation of drugs for treating arrhythmia | |
| CN102210694A (en) | Oral amifostine preparation and preparation method thereof | |
| CN101548985A (en) | Compound antihypertensive drug and preparation method thereof | |
| CN100408047C (en) | Medicinal composition of fructose diphosphate sodium and magnesium salt | |
| CN102406616B (en) | Montmorillonite combined propranolol sustained-release dry suspension, preparation method thereof and preparation method of Na-montmorillonite used in propranolol sustained-release dry suspension | |
| KR20040032821A (en) | Method for Reducing Muscle Fatigue through Administration of Adenosine Triphosphate | |
| WO2003061568A2 (en) | Methods and therapeutic compositions in the treatment of advanced cancer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: LIAONING YAOLIAN PHARMACEUTICAL CO., LTD. Free format text: FORMER OWNER: SHENYANG YAOLIAN TECHNOLOGICAL INNOVATION CO., LTD. Effective date: 20120521 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| COR | Change of bibliographic data |
Free format text: CORRECT: ADDRESS; FROM: 110004 SHENYANG, LIAONING PROVINCE TO: 117004 BENXI, LIAONING PROVINCE |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20120521 Address after: 117004 Liaoning city of Benxi province Benxi Cladrastis Road Economic Development Zone 122A Patentee after: Liaoning Pharma-Union Pharmaceutical Co., Ltd. Address before: 110004 Liaoning province Shenyang City Street Heping District Longquan Road No. 15 building 178 room bertram Patentee before: Shenyang Yaolian Technology Innovation Co., Ltd. |