EP0968133A1 - Carbonate basique de magnesium et d'aluminium, son procede de fabrication et son utilisation comme composition pharmaceutique destinee au traitement de l'acidite gastrique - Google Patents
Carbonate basique de magnesium et d'aluminium, son procede de fabrication et son utilisation comme composition pharmaceutique destinee au traitement de l'acidite gastriqueInfo
- Publication number
- EP0968133A1 EP0968133A1 EP98966416A EP98966416A EP0968133A1 EP 0968133 A1 EP0968133 A1 EP 0968133A1 EP 98966416 A EP98966416 A EP 98966416A EP 98966416 A EP98966416 A EP 98966416A EP 0968133 A1 EP0968133 A1 EP 0968133A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- whose
- compound
- magnesium carbonate
- pharmaceutical composition
- spectrum shows
- 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.)
- Withdrawn
Links
- UJOHNXQDVUADCG-UHFFFAOYSA-L aluminum;magnesium;carbonate Chemical compound [Mg+2].[Al+3].[O-]C([O-])=O UJOHNXQDVUADCG-UHFFFAOYSA-L 0.000 title claims abstract description 7
- 210000002784 stomach Anatomy 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 5
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 35
- 238000000113 differential scanning calorimetry Methods 0.000 claims abstract description 7
- 238000002441 X-ray diffraction Methods 0.000 claims abstract description 6
- 238000001228 spectrum Methods 0.000 claims abstract description 5
- 238000002329 infrared spectrum Methods 0.000 claims abstract description 4
- 238000002425 crystallisation Methods 0.000 claims abstract description 3
- 230000008025 crystallization Effects 0.000 claims abstract description 3
- 239000011777 magnesium Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 4
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 4
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- 235000017557 sodium bicarbonate Nutrition 0.000 claims 1
- 229940069428 antacid Drugs 0.000 abstract description 7
- 239000003159 antacid agent Substances 0.000 abstract description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 6
- 230000001458 anti-acid effect Effects 0.000 abstract description 6
- 239000003814 drug Substances 0.000 abstract description 3
- 241001465754 Metazoa Species 0.000 description 15
- MTEOMEWVDVPTNN-UHFFFAOYSA-E almagate Chemical compound O.O.[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Al+3].[O-]C([O-])=O MTEOMEWVDVPTNN-UHFFFAOYSA-E 0.000 description 12
- 229960004612 almagate Drugs 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 10
- 238000012360 testing method Methods 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- OAASZOYKRKXUCK-UHFFFAOYSA-K O.O.O.[OH-].C([O-])([O-])=O.[Mg+2].[Al+3] Chemical compound O.O.O.[OH-].C([O-])([O-])=O.[Mg+2].[Al+3] OAASZOYKRKXUCK-UHFFFAOYSA-K 0.000 description 7
- 230000002178 gastroprotective effect Effects 0.000 description 7
- 229920001817 Agar Polymers 0.000 description 6
- 239000008272 agar Substances 0.000 description 6
- 241000700159 Rattus Species 0.000 description 5
- 230000002496 gastric effect Effects 0.000 description 4
- 210000001156 gastric mucosa Anatomy 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 230000009858 acid secretion Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 230000003902 lesion Effects 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 238000013223 sprague-dawley female rat Methods 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 244000248349 Citrus limon Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 208000007882 Gastritis Diseases 0.000 description 1
- 206010048714 Gastroduodenitis Diseases 0.000 description 1
- 206010017982 Gastrointestinal necrosis Diseases 0.000 description 1
- 206010019909 Hernia Diseases 0.000 description 1
- 206010020601 Hyperchlorhydria Diseases 0.000 description 1
- YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 206010030216 Oesophagitis Diseases 0.000 description 1
- 241000700157 Rattus norvegicus Species 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 210000000683 abdominal cavity Anatomy 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- LHPJBAIYHPWIOT-UHFFFAOYSA-K aluminum;magnesium;carbonate;hydroxide Chemical compound [OH-].[Mg+2].[Al+3].[O-]C([O-])=O LHPJBAIYHPWIOT-UHFFFAOYSA-K 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000012926 crystallographic analysis Methods 0.000 description 1
- 230000013872 defecation Effects 0.000 description 1
- 230000008260 defense mechanism Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 229940008099 dimethicone Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 208000007784 diverticulitis Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 208000006881 esophagitis Diseases 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000008368 mint flavor Substances 0.000 description 1
- 230000036651 mood Effects 0.000 description 1
- 230000037023 motor activity Effects 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 235000008476 powdered milk Nutrition 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 210000001187 pylorus Anatomy 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/06—Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
- A61K33/10—Carbonates; Bicarbonates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
- C01F7/78—Compounds containing aluminium, with or without oxygen or hydrogen, and containing two or more other elements
- C01F7/784—Layered double hydroxide, e.g. comprising nitrate, sulfate or carbonate ions as intercalating anions
- C01F7/785—Hydrotalcite
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/77—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by unit-cell parameters, atom positions or structure diagrams
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
- C01P2002/82—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by IR- or Raman-data
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
- C01P2002/88—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by thermal analysis data, e.g. TGA, DTA, DSC
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/50—Agglomerated particles
Definitions
- the compound of this invention is prepared by reacting aluminum hydroxide with magnesium hydroxide and sodium acid carbonate in an aqueous medium at the boiling temperature of the mixture.
- the stoichiometric ratio of aluminum hydroxide to magnesium hydroxide should be 1:2.
- the sodium acid carbonate is used in a molar excess, in such a way that the medium pH ranges between 9 and 11.
- the crystalline cell volume is 183 A 3 and the X-ray diffraction spectrum shows the following d(A) values: 7.597; 3.798; 2.6202; 2.5698; 2.5322; 2.2830; 1.93545; 1.72447; 1.62930; 1.52289; 1.49318; 1.46002; 1.41351; 1.38528 and 1.31011 (Table 1).
- H. K. L Sites of the reticular parameters of the compound (elemental cell) that allow to assign a triplet of indices or integers (H. K. L) to each line of diffraction.
- 2- ⁇ Angular variable that shows the angular position where the line of diffraction (H. K. L) appears on the diagram. If the elemental cell of the compound and the triplet (H. K. L) are known, the theoretical position, which should coincide with the observed one, can be calculated (obs.: observed; cal . : calculated) .
- Intensity It provides the height of the diffraction line, which is characteristic of the atomic positions in the crystalline cell, in contrast to the angular position, which is characteristic of the size of the crystalline cell.
- aluminum magnesium carbonates are already known to be used as antacids in therapeutics.
- aluminum magnesium carbonates those prepared in accordance with US Patents Nos . 3,539,306 and 3,650,704 (hydrotalcyte [TalcidTM] of the formula Al 2 Mg 6 (OH) 16 CO 3 .4H 2 0) , US Patents Nos. 4,447,417 and 4,560,545 (almagate [AlmaxTM and AlmaxTM Forte] of the formula Al 2 g s (OH) (C0 3 ) 2 .4H 2 0, and US Patent No. 4,539,195 (compound of the formula Al 2 Mg 6 (OH) 12 (C0 3 ) 3 .xH 2 0) can be used.
- the compound of the present invention (I) is different from the compounds disclosed in the aforesaid patents and does not turn to be obvious despite the similarity between their chemical formulas.
- the compound (I) has a unique crystalline structure as evidenced by its X-ray diffraction spectrum (Table 1) .
- the DSC thermogram shows the presence of a properly structured unique compound ( Figure 2) .
- the compound of this invention has antacid properties and also exhibits an advantageous superior gastroprotective activity over known compounds.
- Irwin test The technique described by R.A. Turner ⁇ Screening Methods in Pharmacology, 1965, p. 27-34. Academic Press, New York and London) was employed.
- the compound of Example 1 and almagate were orally administered to Swiss mice of either sex at doses of 0.3 , 1 and 3 g/kg in a volume of 30 mL/kg. None of the three doses tested induced changes in the parameters assessed (awareness and mood, reflexes, motor activity, CNS excitation, muscle tone, optical signs, secretory-excretory signs, general signs, acute mortality and delayed mortality) in either group, and the absence of changes in the defecation and mortality should be emphasized. Therefore, Irwin test revealed the safety of the compound of Example 1 and almagate.
- Antacid activi ty Measurement of the antacid activity was performed in female Wistar rats, weighing 140 - 160 g. The animals were housed in metabolism cages and fasted from 24 h before the experiment to 1 h before the start of experiment but with free access to water. The animals were anesthetized with a mixture of Ketolar (91 mg/kg) and Tiazine (3.6 mg/kg) and then laparotomized; the pylorus was carefully ligated and the abdominal cavity was closed using a sterile suture (H. Shay et al . "Gastroenterology", 1954, 5_, 43-61). Three hours after the pyloric ligature, test drugs were given orally to the conscious animals.
- One group of 10 animals received the compound of Example 1 in 0.25% Bacto-agar suspension at a dose of 125 mg/kg and another group of 10 animals at a dose of 62.5 mg/kg; a control group of 10 animals dosed with 10 mL/kg of 0.25% Bacto-agar was used. Similarly, the experiment was repeated with almagate at the same doses and using the same number of animals; a new control group of 10 animals was given the same dose of Bacto-agar as in the experiment with the compound of Example 1. Sixty minutes after the administration, the animals were sacrificed, the gastric contents was collected and volume was determined.
- Gastroprotective activi ty To measure the gastroprotective activity the experimental method of ethanol -induced gastric necrosis described by A. Robert et al . ( Gastroenterology, 1979, 21(3), 433-443) was employed. The experiment was carried out in female Sprague-Dawley rats weighing 180-200 g which were fasted since 24 h before the start of experiment. The compound of this invention was compared to almagate in the same manner as in the preceding test. The compound of Example 1 was administered in a 0.25% Bacto-agar suspension. Both test products were administered orally at doses of 100 and 50 mg/kg. Simultaneously, a control group received 0.25% Bacto-agar. After 30 minutes, the animals were given absolute ethanol at a dose of 1 mL/rat. Sixty minutes after ethanol administration, the animals were sacrificed and the length of lesions in the gastric mucosa measured. The results obtained are tabulated in Table 3.
- the compound of this invention is characterized by inhibiting the stomach acid secretion, minimizing the aggressive factors on the gastric mucosa and, in addition, exhibiting a surprising gastroprotective action.
- the gastroprotection afforded by the compound of this invention has a higher potency and longer duration than almagate, which advantageously results in a much more effective improvement of the defense mechanisms of gastric mucosa.
- the therapeutic application of the compound of this invention is as an antacid and gastroprotector, and can be administered to treat hyperchlorhydria, gastritis, gastroduodenitis, dyspepsia, esophagitis, diverticulitis, hyatal hernia, gastric and duodenal ulcers, gastric post-operated patients, vagotomized patients and, in general, to alleviate all those disturbances or episodes causing increased acidity in the stomach.
- the compound of this invention mixed with suitable carriers can be administered orally at daily doses ranging from 250 mg to 10 g, preferably between 1 and 6 g, in the form of suspensions, granules, tablets, capsules, powders, coated tablets and the like.
- Example 1 Aluminum magnesium carbonate hydroxide trihyrate Al 2 Mg ask(OH) 12 C0.3H 2 0) (I)
- This suspension may be inserted in 100 -mL containers or in unidose 15 -mL sachets containing 1.5 g of active ingredient.
- Example 3 Preparation of a dispersible granulate of aluminum magnesium carbonate hydroxide trihydrate
- Formulation per 5 g of granulate aluminum magnesium carbonate hydroxide trihydrate 1.50 g dimethylpolysiloxane 0.20 g sorbitol powder 1.00 g sodium saccharin 0.01 g polyvinylpyrrolidone K-25 0.03 g butylhydroxytoluene 0.0005 g lemon flavour 0.0050 g skim powdered milk q.s 5.0000 g
- This granulate is placed in unidose sachets for its dispersion in water.
- These tablets may be inserted in aluminium tubes or blister and are dissolved in the mouth or chewed.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Geology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
L'invention concerne un nouveau carbonate basique de magnésium et d'aluminium, de formule Al2Mg4(OH)12CO3.3H2O (I) et à cristallisation rhomboédrique, dont les paramètres réticulaires sont a = b = 3,046 Å; c = 22,79 Å; α = β = 90°; η = 120° et dont le volume cellulaire est égal à 183 A3; dont le spectre de diffraction des rayons X présente les valeurs d(Å) suivantes: 7,597; 3,798; 2,6202; 2,5698; 2,5322; 2,2830; 1,93545; 1,72447; 1,62930; 1,52289; 1,49318; 1,46002; 1,41351; 1,38528 et 1,31011; dont le spectre infrarouge présente des bandes caractéristiques à 1361 et 449 cm-1 (figure 1) et dont l'analyse enthalpique différentielle (DSC) est illustrée par la figure 2. Ce composé est utile en thérapeutique en tant qu'antiacide et gastroprotecteur.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9702717 | 1997-12-30 | ||
| ES009702717A ES2133136B1 (es) | 1997-12-30 | 1997-12-30 | Nuevo carbonato basico de aluminio y magnesio. |
| PCT/EP1998/008498 WO1999035088A1 (fr) | 1997-12-30 | 1998-12-29 | Carbonate basique de magnesium et d'aluminium, son procede de fabrication et son utilisation comme composition pharmaceutique destinee au traitement de l'acidite gastrique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0968133A1 true EP0968133A1 (fr) | 2000-01-05 |
Family
ID=8301660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP98966416A Withdrawn EP0968133A1 (fr) | 1997-12-30 | 1998-12-29 | Carbonate basique de magnesium et d'aluminium, son procede de fabrication et son utilisation comme composition pharmaceutique destinee au traitement de l'acidite gastrique |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP0968133A1 (fr) |
| JP (1) | JP2001516328A (fr) |
| KR (1) | KR20000075839A (fr) |
| AR (1) | AR007232A1 (fr) |
| AU (1) | AU742544B2 (fr) |
| BR (1) | BR9807275A (fr) |
| CA (1) | CA2282361A1 (fr) |
| ES (1) | ES2133136B1 (fr) |
| IL (1) | IL131573A0 (fr) |
| NO (1) | NO994160D0 (fr) |
| PA (1) | PA8464401A1 (fr) |
| PL (1) | PL335464A1 (fr) |
| RU (1) | RU2168464C1 (fr) |
| WO (1) | WO1999035088A1 (fr) |
| ZA (1) | ZA9811216B (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4338470B2 (ja) * | 2003-08-12 | 2009-10-07 | 日鉄鉱業株式会社 | ハイドロタルサイト粒子及びその製造方法 |
| CA2579421C (fr) * | 2004-10-20 | 2013-06-11 | Sakai Chemical Industry Co., Ltd. | Hydrotalcite et composition de resine synthetique |
| RU2540635C2 (ru) * | 2012-11-22 | 2015-02-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Национальный минерально-сырьевой университет "Горный" | Способ получения гидрокарбоалюминатов щелочноземельных металлов из природного магнийсодержащего сырья |
| CN108159072A (zh) * | 2017-12-04 | 2018-06-15 | 上海裕英生物医药科技有限公司 | 铝镁加的制备工艺 |
| RU2678007C1 (ru) * | 2017-12-05 | 2019-01-22 | Федеральное государственное бюджетное учреждение науки Федеральный исследовательский центр "Кольский научный центр Российской академии наук" (ФИЦ КНЦ РАН) | Способ получения слоистого гидроксида магния и алюминия |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0476489A1 (fr) * | 1990-09-11 | 1992-03-25 | Haldor Topsoe A/S | Procédé et catalyseur pour la préparation de composés aromatiques |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3539306A (en) * | 1966-07-25 | 1970-11-10 | Kyowa Chem Ind Co Ltd | Process for the preparation of hydrotalcite |
| US4904457A (en) * | 1974-03-30 | 1990-02-27 | Aluminum Company Of America | Synthetic hydrotalcite |
| GB1598375A (en) * | 1978-02-17 | 1981-09-16 | Anphar Sa | Aluminium magnesium carbonate |
| DE3306822C2 (de) * | 1983-02-26 | 1985-01-03 | Giulini Chemie Gmbh, 6700 Ludwigshafen | Kristallines, basisches Aluminium-Magnesium-Carbonat |
| US5364828A (en) * | 1992-10-21 | 1994-11-15 | Minerals Technologies | Spheroidal aggregate of platy synthetic hydrotalcite |
| EP0776317B1 (fr) * | 1994-08-15 | 1999-11-03 | Aluminum Company Of America | Synthese d'hydrotalcite et de composes apparentes, a partir de deux poudres |
| DE19503522A1 (de) * | 1995-02-03 | 1996-08-08 | Rwe Dea Ag | Herstellung gemischter schichtförmig aufgebauter Metallhydroxide sowie deren Metalloxide |
-
1997
- 1997-12-30 ES ES009702717A patent/ES2133136B1/es not_active Expired - Lifetime
-
1998
- 1998-12-08 ZA ZA9811216A patent/ZA9811216B/xx unknown
- 1998-12-10 PA PA19988464401A patent/PA8464401A1/es unknown
- 1998-12-29 EP EP98966416A patent/EP0968133A1/fr not_active Withdrawn
- 1998-12-29 CA CA002282361A patent/CA2282361A1/fr not_active Abandoned
- 1998-12-29 JP JP53563199A patent/JP2001516328A/ja active Pending
- 1998-12-29 BR BR9807275-7A patent/BR9807275A/pt unknown
- 1998-12-29 AU AU22767/99A patent/AU742544B2/en not_active Ceased
- 1998-12-29 AR ARP980106727A patent/AR007232A1/es unknown
- 1998-12-29 PL PL98335464A patent/PL335464A1/xx unknown
- 1998-12-29 KR KR1019997007914A patent/KR20000075839A/ko not_active Ceased
- 1998-12-29 IL IL13157398A patent/IL131573A0/xx unknown
- 1998-12-29 WO PCT/EP1998/008498 patent/WO1999035088A1/fr not_active Ceased
- 1998-12-29 RU RU99120777/12A patent/RU2168464C1/ru active
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1999
- 1999-08-27 NO NO994160A patent/NO994160D0/no not_active Application Discontinuation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0476489A1 (fr) * | 1990-09-11 | 1992-03-25 | Haldor Topsoe A/S | Procédé et catalyseur pour la préparation de composés aromatiques |
Also Published As
| Publication number | Publication date |
|---|---|
| ES2133136B1 (es) | 2000-04-01 |
| RU2168464C1 (ru) | 2001-06-10 |
| AU742544B2 (en) | 2002-01-03 |
| JP2001516328A (ja) | 2001-09-25 |
| ZA9811216B (en) | 1999-07-14 |
| WO1999035088A1 (fr) | 1999-07-15 |
| NO994160L (no) | 1999-08-27 |
| PA8464401A1 (es) | 2000-09-29 |
| AU2276799A (en) | 1999-07-26 |
| ES2133136A1 (es) | 1999-08-16 |
| NO994160D0 (no) | 1999-08-27 |
| CA2282361A1 (fr) | 1999-07-15 |
| BR9807275A (pt) | 2000-05-02 |
| KR20000075839A (ko) | 2000-12-26 |
| PL335464A1 (en) | 2000-04-25 |
| AR007232A1 (es) | 1999-10-27 |
| IL131573A0 (en) | 2001-01-28 |
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