USRE33086E - Process for manufacturing effervescent granules and tablets and high efficiency granulation tower for such process - Google Patents
Process for manufacturing effervescent granules and tablets and high efficiency granulation tower for such process Download PDFInfo
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- USRE33086E USRE33086E US07/071,991 US7199187A USRE33086E US RE33086 E USRE33086 E US RE33086E US 7199187 A US7199187 A US 7199187A US RE33086 E USRE33086 E US RE33086E
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- United States
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- 238000000034 method Methods 0.000 title claims abstract description 46
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 16
- 239000008187 granular material Substances 0.000 title claims description 32
- 238000005469 granulation Methods 0.000 title claims description 30
- 230000003179 granulation Effects 0.000 title claims description 30
- 238000001035 drying Methods 0.000 claims abstract description 27
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 239000012530 fluid Substances 0.000 claims abstract description 9
- 239000007938 effervescent tablet Substances 0.000 claims abstract 6
- 238000001291 vacuum drying Methods 0.000 claims abstract 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 41
- 239000002994 raw material Substances 0.000 claims description 27
- 230000005484 gravity Effects 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 19
- 238000003860 storage Methods 0.000 claims description 16
- 239000000843 powder Substances 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 229960004106 citric acid Drugs 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 6
- NZZLTKHBCHMMOJ-UHFFFAOYSA-N 2-acetyloxybenzoic acid;urea Chemical compound NC(N)=O.CC(=O)OC1=CC=CC=C1C(O)=O NZZLTKHBCHMMOJ-UHFFFAOYSA-N 0.000 claims description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 235000013905 glycine and its sodium salt Nutrition 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- 238000009736 wetting Methods 0.000 claims description 5
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims description 4
- 229960004543 anhydrous citric acid Drugs 0.000 claims description 4
- 238000010907 mechanical stirring Methods 0.000 claims description 4
- 229960005489 paracetamol Drugs 0.000 claims description 4
- 230000001105 regulatory effect Effects 0.000 claims description 4
- CVHZOJJKTDOEJC-UHFFFAOYSA-M 1,1-dioxo-1,2-benzothiazol-3-olate Chemical compound C1=CC=C2C([O-])=NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-M 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 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 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 230000001687 destabilization Effects 0.000 claims description 3
- 239000000600 sorbitol Substances 0.000 claims description 3
- 238000005303 weighing Methods 0.000 claims description 3
- 239000011668 ascorbic acid Substances 0.000 claims description 2
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 claims description 2
- 238000007907 direct compression Methods 0.000 claims description 2
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 14
- FMWMHQWEJMHRIO-UHFFFAOYSA-N C(N)(O)=O.C(CC(O)(C(=O)O)CC(=O)O)(=O)O Chemical compound C(N)(O)=O.C(CC(O)(C(=O)O)CC(=O)O)(=O)O FMWMHQWEJMHRIO-UHFFFAOYSA-N 0.000 claims 2
- 238000011109 contamination Methods 0.000 claims 2
- 229960000878 docusate sodium Drugs 0.000 claims 1
- AKEKKCGPLHMFCI-UHFFFAOYSA-L potassium sodium hydrogen carbonate Chemical compound [Na+].[K+].OC([O-])=O.OC([O-])=O AKEKKCGPLHMFCI-UHFFFAOYSA-L 0.000 claims 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 claims 1
- CLJTZNIHUYFUMR-UHFFFAOYSA-M sodium;hydrogen carbonate;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound [Na+].OC([O-])=O.OC(=O)CC(O)(C(O)=O)CC(O)=O CLJTZNIHUYFUMR-UHFFFAOYSA-M 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000007664 blowing Methods 0.000 description 3
- 238000005243 fluidization Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 230000001960 triggered effect Effects 0.000 description 3
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- 229960001138 acetylsalicylic acid Drugs 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- 239000001509 sodium citrate Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YKXUOESQDCXGIW-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylic acid;2-(trimethylazaniumyl)acetate Chemical compound C[N+](C)(C)CC(O)=O.OC(=O)CC(O)(C(O)=O)CC([O-])=O YKXUOESQDCXGIW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 239000004429 Calibre Substances 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- KBAUFVUYFNWQFM-UHFFFAOYSA-N Doxylamine succinate Chemical compound OC(=O)CCC(O)=O.C=1C=CC=NC=1C(C)(OCCN(C)C)C1=CC=CC=C1 KBAUFVUYFNWQFM-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 229960002609 betaine citrate Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 229960005008 doxylamine succinate Drugs 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- RCIJACVHOIKRAP-UHFFFAOYSA-N sodium;1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound [Na+].CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC RCIJACVHOIKRAP-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 229940038773 trisodium citrate Drugs 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 238000005550 wet granulation Methods 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0002—Galenical forms characterised by the drug release technique; Application systems commanded by energy
- A61K9/0007—Effervescent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/16—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by suspending the powder material in a gas, e.g. in fluidised beds or as a falling curtain
Definitions
- the present invention relates to an improved process for manufacturing effervescent mixtures and tablets containing in particular active principles for pharmaceutical use.
- this technique presents the drawback of necessitating the transfer of the filler, after step (1), from the mixer to the drier. Consequently, the effervescent reaction triggered off in the mixer cannot be mastered with total precision as its interruption, which occurs in step (2) in the drier, depends on the time for emptying and transferring the filler towards the drier, which time varies from one batch to the following.
- FIG. 1 shows the apparatus, and in particular the granulator-drier, used for the tests referred to hereinbelow according to one variant embodiment of the invention.
- FIG. 2 schematically shows the arrangement of apparatus according to another variant of the invention in a production tower.
- FIG. 1 a granulator-drier operating entirely in fluid bed is used.
- Granulator-driers of the type which will be described hereinafter have been known for a long time.
- the process of granulation also enables mixtures of powders of homogeneous chemical composition to be obtained by using fluidization.
- Granulation consists in a fixation by chemical bond of the particles of sodium bicarbonate and of citric acid. These chemical bonds are obtained by an addition of a defined quantity of demineralized water which provokes a partial effervescent reaction with the formation of mono-, di- or trisodium citrate. These molecules of sodium citrate are considered as bridges bonding the particles of sodium bicarbonate and the particles of citric acid and give the mixture the physical properties of compressibility.
- aqueous solvent water or wetting solution
- the .[.proces.]. .Iadd.process .Iaddend.of granulation-drying is applicable in particular to the production of an excipient type effervescent mixture on which the active principles and lubricants are added in a subsequent operation; by way of example, we shall cite the parameters defined for buffered effervescent aspirin, for which a wet-process granulation is effected on 3 compounds: sodium bicarbonate, citric acid and possibly glycocoll (binding agent).
- the invention enables a process of production employing a vacuum to be carried out in particularly .[.effective manner.]. .Iadd.efficient.Iaddend.. This technique makes it possible:
- a further original feature of the invention resides in the fact that the apparatus have been grouped together in a vertical production tower.
- the process for producing effervescent granules intended for compression is characterized by the creation of a tower 1 in which the following operations are carried out:
- Operations 1 to 6 occur vertically downwardly, transfers taking place by gravity and being dustfree.
- the interest resides in the fact that the 3 operations of point 3 (mixing, granulation, drying) can be automated from the standpoint of monitoring of the process.
- operations 1 to 5 in their chronological sequence may be automated.
- Such automatization renders the process economical from the standpoint of manpower (about 1 t/hr. for 2 persons) by elimination of the interruptions between the operations.
- the apparatus serving for mixing-granulation-drying is composed of a perfectly sealed tank, provided with a system of mechanical stirring for mixing the incorporated powders and equipped with lump-breaking cutters which divide the agglomerates formed by the solvent during wetting.
- This tank must also comprise:
- thermometric probe All the mechanical or physical elements intervening in the successive operations of granulation-drying are monitored by thermometric probe, by measurement of amperage and vacuum.
- an apparatus of the adapted DVT Lodige type is suitable.
- a further originality of the invention resides in the use of a heat exchange hopper for cooling the granules.
- Examples 1 to 4 relate to the first variant, and I and II to the second variant of the invention.
- Air temperature 64° C.
- the solvent is always sprayed on the powders in suspension in air, which makes it possible to increase the exchange surface between the base particles and the acid particles; at this stage of operation, the output and spray time must be monitored.
- the rate of flow of air is to be monitored so as to avoid too great a turbulence of the powders in the cavity of the apparatus, which would render the particles fragile.
- Granulation on granulator-drier of an effervescent mixture containing a plurality of active principles Granulation on granulator-drier of an effervescent mixture containing a plurality of active principles.
- Air temperature 64° C.
- the different raw materials mentioned above are successively incorporated in the mixer 4 without taking into account any physical incompatibilities existing therebetween.
- the premix is effected in 3 minutes. During this period of time, the temperature of the powder is raised by introducing a heat-exchange liquid in the double jacket of the mixer.
- the solvent is a mixture of water/sodium dioctylsulfosuccinate.
- Granulation is effected under atmospheric pressure for 5 minutes.
- This operation lasts about 37 minutes, stoppage of drying being triggered off by monitoring the residual humidity of the powder.
- thermolabile active products not to be destabilized
- the calcium carbasalate will be stored in one of hoppers 2. It will then be pre-weighed at 3 and incorporated in the mixer-granulator-drier 4.
- the automation of the tower makes it possible to eliminate the functions of mixing and granulation and to conserve only the drying function of apparatus 4.
- the auxiliary constituents aroma, PEG and ammonium saccharinate, are added into the band mixer.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Preparation (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Glanulating (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
______________________________________ Formula of granulation ______________________________________ Paracetamol 28 kg Monosodium carbonate 100 kg Monopotassium carbonate 3.740 kg Sorbitol 25.500 kg Anhydrous citric acid 73.000 kg Ascorbic acid 17.000 kg TOTAL 247.24 kg ______________________________________
______________________________________
Disodium sulfate 20.200 kg
Sodium bromide 7.100 kg
Disodium phosphate
13.800 kg
Monosodium carbonate
101.000 kg
Anhydrous citric acid
89.000 kg
______________________________________
______________________________________
Monosodium carbonate
108.000 kg
Anhydrous citric acid
14.500 kg
Betaine citrate 142.000 kg
______________________________________
Claims (9)
- citric acid..]. .Iadd.10. A process for the manufacture of effervescent tablets from a plurality of powdered raw materials, with the avoidance of external contamination, said process comprising the steps of:(a) storing said powdered raw materials in storage hoppers;(b) transferring said raw materials downwardly by gravity to a granulator-vacuum-dryer device, introducing into said granulator-vacuum dryer device a granulation agent in an amount effective to wet form wet granules and drying under vacuum said wet granules therein to obtain dried granules;(c) evacuating the dried granules by gravity from said granulator-vacuum dryer, transferring them downwardly by gravity to a cooler and cooling said dried granules to a temperature at which destabilization is impeded; and(d) transferring said dried and cooled granules downwardly by gravity to a storage container;said process being carried out in an enclosed vertically arranged apparatus
- array. .Iaddend. .Iadd.11. The process of claim 10, wherein the raw materials are individually subjected to said steps (a), (b) and (c), then mixed together and subjected to direct compression. .Iaddend. .Iadd.12. The process of claim 10, wherein the raw materials are pre-mixed within said granulator-vacuum-dryer device. .Iaddend. .Iadd.13. The process of claim 10, wherein said granulation agent is a solvent selected from the group consisting of demineralized water an aqueous wetting solutions. .Iaddend. .Iadd.14. The process of claim 10, wherein said granulation agent is a solution of dioctylsulfosuccinate in water. .Iaddend.
- .Iadd. The process of claim 10, wherein after drying and cooling, the dried and cooled raw materials are transferred by gravity to a calibration device. .Iaddend. .Iadd.16. The process of claim 15, wherein after calibration, said dried, cooled and calibrated raw materials are transferred by gravity to a band mixer. .Iaddend. .Iadd.17. The process according to claim 10, wherein the raw materials are weighed before any treatment. .Iaddend. .Iadd.18. The process of claim 10, wherein said dryer has a jacket for a heat exchange fluid and during said drying step (b), said raw materials are subjected to mechanical stirring with lump-breaking cutters, a vacuum is created and a granulation agent introduced by aspiration, the temperature being regulated by circulating a heat-exchange fluid in said jacket. .Iaddend. .Iadd.19. The process of claim 10, wherein the raw materials comprise:effervescent mixture:sodium bicarbonatecitric acidand the granulation agent is demineralized water. .Iaddend. .Iadd.20. The process of claim 19, wherein the effervescent mixture contains glycocoll. .Iaddend. .Iadd.21. The process of claim 10, wherein the raw materials comprise:paracetamolmonosodium carbonatemonopotassium carbonatesorbitolanhydrous citric acidascorbic acidand the granulation agent is a solution of sodium dioctylsulfosuccinate in
- water. .Iaddend. .Iadd.22. The process of claim 10, wherein the raw materials in powder form are as follows:calcium carbasalate1ysine carbamatecitric acid .Iaddend. .Iadd.23. The process of claim 10, wherein the raw materials are as follows:calcium carbasalate1ysine carbamatecitric acidaromaPEG (polyethyleneglycol)
- ammonium saccharinate. .Iaddend. .Iadd.24. A process for the manufacture of effervescent tablets from a plurality of powered raw materials, with the avoidance of external contamination, said process comprising the steps of:(a) storing said powdered raw materials in storage hoppers;(b) transferring said raw materials downwardly by gravity to a mixer-granulator-dryer device, mixing said raw materials, introducing into said mixer-granulator-dryer device a granulation agent, mixing the raw materials and the granulation agent under substantially atmospheric pressure for a period of time sufficient to achieve formation of wet granules and drying under vacuum said wet granules in said mixer-granulator-dryer device to obtain dried granules;(c) evacuating the dried granules by gravity from said granulator-vacuum dryer, transferring them downwardly by gravity to a cooler and cooling said dried granules to a temperature at which destabilization is impeded; and(d) transferring said dried and cooled granules downwardly by gravity to a storage container;said process being carried out in an enclosed vertically arranged apparatus
- array. .Iaddend. .Iadd.25. The process of claim 24, wherein the granulation agent is introduced by spraying or by aspiration under partial vacuum. .Iaddend. .Iadd.26. The process of claim 24, wherein there is introduced one to six weight percent of granulation agent. .Iaddend. .Iadd.27. The process of claim 24, which is automated. .Iaddend.
- .Iadd. A vertically disposed apparatus array for the manufacture of effervescent tablets, said apparatus array constituting a tower and comprising in vertically descending order:(a) storage hopper means positioned near the top of said tower for the storage of raw materials;(b) granulation and vacuum drying means including means for introducing a granulation agent to wet form wet granules and means for eliminating humidity from said wet granules to obtain dried granules;(c) cooling means for lowering the temperature of said dried granules, and(d) at least one storage container for dried and cooled granules:said apparatus comprising also means for feeding material by gravity from said storage hopper means to said granulation-vacuum drying means, means for evacuating said dried granules by gravity from said granulation-vacuum-drying means and feeding them by gravity to said cooling means, and means for transferring granules by gravity from said cooling means to said storage container or containers. .Iaddend.
- .Iadd. The apparatus of claim 28, further comprising calibrating means for calibrating the materials after they leave said cooler. .Iaddend. .Iadd.30. The apparatus of claim 29, further comprising a band mixer for mixing the materials after they leave said calibrating means. .Iaddend. .Iadd.31. The apparatus of claim 30, further comprising weighing means for weighing said raw materials before any treatment. .Iaddend. .Iadd.32. The apparatus of claim 29, wherein said drying device comprises mixing means comprising a system of mechanical stirring with lump-breaking cutters, means for introducing a granulation agent by creation of a vacuum or a spraying system supplied by a pump, means for regulating the temperature comprising a double jacket for circulating heat-exchange fluid, and vacuum means for creating vacuum. .Iaddend. .Iadd.33. A vertically disposed apparatus array for the manufacture of effervescent tablets, said apparatus array constituting a tower and comprising in vertically descending order:(a) storage hopper means positioned near the top of said tower for the storage of raw materials;(b) a mixer-granulator-dryer device having mixing means, means for introducing a granulation agent, means for subjecting said mixer-granulator-dryer device to substantially atmospheric pressure at least during granulation and means for eliminating humidity from said wet granules material under vacuum to obtain dried granules;(c) cooling means for lowering the temperature of the dried granules, and(d) at least one storage container for dried and cooled granules;said apparatus comprising also means for feeding material by gravity from said storage hopper means to said mixer-granulator-dryer device, means for evacuating said dried granules by gravity from said mixer-granulator-dryer device and feeding them by gravity to said cooling means, and means for transferring said granules by gravity from said cooling means to said
- storage container or containers. .Iaddend. .Iadd.34. The apparatus array of claim 33, wherein said mixing means comprise mechanical stirring means with lump-breaking cutters, said means for introducing a granulation agent comprises means for creating a vacuum or spraying system means supplied by a pump; and said mixer-granulator-dryer device includes means for regulating the temperature comprising a double jacket for circulating heat-exchange fluid, and vacuum means for creating vacuum. .Iaddend.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR82-21476 | 1982-12-21 | ||
| FR8221476A FR2537872B1 (en) | 1982-12-21 | 1982-12-21 | PROCESS FOR THE MANUFACTURE OF EFFERVESCENT TABLETS |
| FR838319143A FR2555439B1 (en) | 1983-11-30 | 1983-11-30 | PROCESS AND APPARATUS FOR MANUFACTURING GRANULES AND EFFERVESCENT TABLETS |
| FR83-19143 | 1983-11-30 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06643980 Reissue | 1983-12-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE33086E true USRE33086E (en) | 1989-10-10 |
Family
ID=26223202
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/643,980 Ceased US4614648A (en) | 1982-12-21 | 1983-12-20 | Process for manufacturing effervescent granules and tablets |
| US07/071,991 Expired - Lifetime USRE33086E (en) | 1982-12-21 | 1987-07-10 | Process for manufacturing effervescent granules and tablets and high efficiency granulation tower for such process |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/643,980 Ceased US4614648A (en) | 1982-12-21 | 1983-12-20 | Process for manufacturing effervescent granules and tablets |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US4614648A (en) |
| EP (1) | EP0162043B1 (en) |
| JP (1) | JPH07100653B2 (en) |
| KR (1) | KR900007312B1 (en) |
| AT (1) | AT394492B (en) |
| CA (1) | CA1209040A (en) |
| CH (1) | CH664491A5 (en) |
| DE (1) | DE3390423C2 (en) |
| DK (1) | DK163565C (en) |
| EG (1) | EG17260A (en) |
| ES (1) | ES8603753A1 (en) |
| GB (1) | GB2146244B (en) |
| GR (1) | GR81352B (en) |
| IT (1) | IT1175295B (en) |
| MA (1) | MA19980A1 (en) |
| NL (1) | NL193488C (en) |
| PT (1) | PT77864B (en) |
| SE (1) | SE457416B (en) |
| WO (1) | WO1984002468A1 (en) |
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|---|---|---|---|---|
| US5298261A (en) * | 1992-04-20 | 1994-03-29 | Oregon Freeze Dry, Inc. | Rapidly distintegrating tablet |
| US5348745A (en) * | 1989-05-09 | 1994-09-20 | Miles Inc. | Aqueous granulation solution and a method of tablet granulation |
| US5503846A (en) * | 1993-03-17 | 1996-04-02 | Cima Labs, Inc. | Base coated acid particles and effervescent formulation incorporating same |
| US5997901A (en) | 1998-10-22 | 1999-12-07 | Mills; Robert G. | Method of manufacturing scented molded products |
| US6620433B2 (en) | 2000-11-03 | 2003-09-16 | Laboratorios Belmac, S.A. | Dispersible and soluble galenic paracetamol formulation, method for its preparation and its applications |
| US20090135666A1 (en) * | 2005-02-09 | 2009-05-28 | Satoru Watano | Kneading and granulating machine |
| US7568297B2 (en) * | 2006-04-10 | 2009-08-04 | Woodhaven Capital Corp. | Grain drying aeration system |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1209040A (en) * | 1982-12-21 | 1986-08-05 | Jean Bru | Manufacture of effervescent granules or tablets |
| US4904478A (en) * | 1983-08-11 | 1990-02-27 | Mission Pharmacal Company | Slow-release sodium fluoride tablet and method for treatment of osteoporosis |
| DE3440288C2 (en) * | 1984-11-05 | 1987-03-12 | Gergely, Gerhard, Dr.-Ing., Wien | Pharmaceutical preparation containing ibuprofen and process for its preparation |
| US4772467A (en) * | 1985-02-19 | 1988-09-20 | Board Of Regents, U T Systems | Osteoporosis inhibition by dietary calcium supplementation |
| US4851221A (en) * | 1985-02-19 | 1989-07-25 | Mission Pharmacal Company | Liquid calcium supplementation from readily soluble mixtures of calcium compound and citric acid |
| GB2174004B (en) * | 1985-04-23 | 1988-11-30 | American Cyanamid Co | Pharmaceutical tablet preparations |
| IT1209667B (en) * | 1985-11-12 | 1989-08-30 | Zambon Spa | EFFEVERSCENT COMPOSITION ANALGESIC ADAPTITY. |
| US4814177A (en) * | 1986-03-18 | 1989-03-21 | Board Of Regents, University Of Texas System | Ultradense and more soluble and bioavailable preparations of calcium citrate |
| DE3767998D1 (en) * | 1986-12-20 | 1991-03-14 | Boehringer Mannheim Gmbh | MEDICINAL PRODUCTS CONTAINING CLODRONATE AND METHOD FOR THE PRODUCTION THEREOF. |
| CA2009326C (en) * | 1989-05-09 | 1998-01-27 | Lawrence J. Daher | Aqueous granulation solution and a method of tablet granulation |
| USRE35447E (en) * | 1989-05-16 | 1997-02-11 | J. M. Huber Corporation | Endothermic blowing agents for strengthening weld lines in molded thermoplastic resins and products |
| US5302455A (en) * | 1989-05-16 | 1994-04-12 | J. M. Huber Corporation | Endothermic blowing agents compositions and applications |
| US5250224A (en) * | 1989-05-16 | 1993-10-05 | J. M. Huber Corporation | Foamed products containing endothermic blowing agents and processes |
| US5009810A (en) * | 1989-05-16 | 1991-04-23 | J. M. Huber Corporation | Endothermic blowing agents compositions and applications |
| US5317044A (en) * | 1989-05-16 | 1994-05-31 | J. M. Huber Corporation | Endothermic blowing agents for surface migration of components in foamed products, compositions and applications |
| US5252618A (en) * | 1989-05-16 | 1993-10-12 | J. M. Huber Corporation | Endothermic blowing agents for strengthening weld lines in molded thermoplastic resins and products |
| US5009809A (en) * | 1989-05-16 | 1991-04-23 | J. M. Huber Corporation | High temperature endothermic blowing agents compositions and applications |
| USRE35368E (en) * | 1989-05-16 | 1996-10-29 | J. M. Huber Corporation | Endothermic blowing agents for surface migration of components in foamed products, compositions and applications |
| US5106534A (en) * | 1989-05-16 | 1992-04-21 | J. M. Huber Corporation | Endothermic blowing agents compositions and applications |
| US5137655A (en) * | 1989-05-16 | 1992-08-11 | J. M. Huber Corporation | High temperature endothermic blowing agents compositions and applications |
| US5252213A (en) * | 1989-06-20 | 1993-10-12 | University Of Washington | Dry dialysate composition |
| US5234963A (en) * | 1992-05-13 | 1993-08-10 | Gaia Research | Production of encapsulated chemical foaming concentrates |
| EP0673644A1 (en) * | 1994-03-18 | 1995-09-27 | E-PHARMA TRENTO S.p.A. | Process and plant for preparation of effervescent granules |
| DE19734431A1 (en) * | 1997-08-08 | 1999-02-11 | Glatt Process Technology Gmbh | Method and device for working up a solution or solid suspension containing thermally labile components |
| DE19931708A1 (en) | 1999-07-08 | 2001-01-18 | Bayer Ag | Process for the preparation of rapidly disintegrating solid pharmaceutical preparations |
| FR2796841B1 (en) * | 1999-07-28 | 2003-08-15 | Lipha | NEW PROCESS FOR THE PRODUCTION OF EFFERVESCENT MIXTURES AND THE TABLETS THEREOF |
| RU2257891C1 (en) * | 2003-12-31 | 2005-08-10 | ООО "Фармстандарт-Фитофарм-НН" | Method for preparing composition as carbonated tablet |
| JP5467751B2 (en) * | 2008-09-29 | 2014-04-09 | 小林製薬株式会社 | Amino acid-containing solid composition with suppressed protein coagulation action |
| WO2013081567A1 (en) * | 2011-12-02 | 2013-06-06 | Mahmut Bilgic | Effervescent antipsychotic formulations |
| RU2706727C2 (en) | 2014-09-17 | 2019-11-20 | Стирлайф Индия Прайвит Лимитед | Effervescent compositions and methods for production and use thereof |
| US11219594B2 (en) | 2015-12-12 | 2022-01-11 | Steerlife India Private Limited | Effervescent compositions of metformin and processes for preparation thereof |
| DE102016218135A1 (en) | 2016-09-21 | 2018-03-22 | Robert Bosch Gmbh | Production module for the production of solid dosage forms |
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|---|---|---|---|---|
| US2463962A (en) * | 1947-05-17 | 1949-03-08 | Fearn Lab Inc | Product for producing effervescing carbonated beverages |
| US2497057A (en) * | 1950-02-07 | Toilet bowl -gleanee | ||
| US2877159A (en) * | 1957-04-26 | 1959-03-10 | Ciba Pharm Prod Inc | Method for preparing tablet granulations |
| DE1060093B (en) * | 1957-04-26 | 1959-06-25 | Ciba Geigy | New method for the production of tablet granules |
| US2985562A (en) * | 1958-03-27 | 1961-05-23 | Warner Lambert Pharmaceutical | Effervescent compositions |
| US2999293A (en) * | 1957-09-12 | 1961-09-12 | Warner Lambert Pharmaceutical | Process of granulating effervescent materials |
| US3401216A (en) * | 1964-01-09 | 1968-09-10 | Bristol Myers Co | Methods for preparing pharmaceutical compositions |
| US3480185A (en) * | 1966-06-20 | 1969-11-25 | Johnson & Johnson | Charged effervescing agent and medicament dispensing metering valve-actuated aerosol container producing a dose of medicament and carbonation in water |
| FR2092893A1 (en) * | 1970-06-29 | 1972-01-28 | Bru Jean | |
| US3773922A (en) * | 1971-04-06 | 1973-11-20 | Fr Dev Rech Sofrader | Method for the manufacture of effervescent tablets |
| US3903255A (en) * | 1971-05-17 | 1975-09-02 | Rohm & Haas | Effervescent potassium chloride tablet |
| US3946996A (en) * | 1972-04-18 | 1976-03-30 | Barmag Barmer Maschinenfabrik Aktiengesellschaft | Mixing and granulating apparatus |
| US4093710A (en) * | 1976-07-07 | 1978-06-06 | Sandoz, Inc. | Rapid dissolving effervescent granules |
| US4153678A (en) * | 1978-07-17 | 1979-05-08 | American Cyanamid Company | Levamisole effervescent tablets |
| EP0011489A1 (en) * | 1978-11-16 | 1980-05-28 | Beecham Group Plc | An analgesic effervescent powder and process for its preparation |
| US4267164A (en) * | 1980-01-31 | 1981-05-12 | Block Drug Company Inc. | Effervescent stannous fluoride tablet |
| EP0076340A1 (en) * | 1981-10-06 | 1983-04-13 | Gerhard Dr. Gergely | Process for manufacturing effervescent granules which may be transformed, when required, into effervescent tablets |
| AT372299B (en) * | 1980-12-15 | 1983-09-26 | Gergely Gerhard | DEVICE FOR PRODUCING THE DESIRED CASE FOR EQUIPMENT TO BE PROCESSED SHOWER GRANULES |
| US4614648A (en) * | 1982-12-21 | 1986-09-30 | Jean Bru | Process for manufacturing effervescent granules and tablets |
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| FR2132521A1 (en) * | 1971-04-06 | 1972-11-24 | Sofrader Sa | Effervescent tablets prdn - by controlled drying in effervescent granule formation |
| FR2154323A1 (en) * | 1971-09-29 | 1973-05-11 | Sofrader Sa | Effervescent tablets prdn - by controlled drying in effervescent granule formation |
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1983
- 1983-12-19 CA CA000443701A patent/CA1209040A/en not_active Expired
- 1983-12-20 CH CH4062/84A patent/CH664491A5/en not_active IP Right Cessation
- 1983-12-20 JP JP59500291A patent/JPH07100653B2/en not_active Expired - Lifetime
- 1983-12-20 DE DE3390423T patent/DE3390423C2/en not_active Expired - Lifetime
- 1983-12-20 EP EP84900064A patent/EP0162043B1/en not_active Expired
- 1983-12-20 GB GB08427318A patent/GB2146244B/en not_active Expired
- 1983-12-20 NL NL8320404A patent/NL193488C/en not_active IP Right Cessation
- 1983-12-20 AT AT0908083A patent/AT394492B/en not_active IP Right Cessation
- 1983-12-20 GR GR73291A patent/GR81352B/el unknown
- 1983-12-20 WO PCT/FR1983/000253 patent/WO1984002468A1/en active IP Right Grant
- 1983-12-20 PT PT77864A patent/PT77864B/en unknown
- 1983-12-20 US US06/643,980 patent/US4614648A/en not_active Ceased
- 1983-12-21 ES ES528271A patent/ES8603753A1/en not_active Expired
- 1983-12-21 IT IT68331/83A patent/IT1175295B/en active
- 1983-12-21 KR KR1019830006082A patent/KR900007312B1/en not_active Expired
- 1983-12-21 EG EG79483A patent/EG17260A/en active
- 1983-12-21 MA MA20201A patent/MA19980A1/en unknown
-
1984
- 1984-08-20 SE SE8404142A patent/SE457416B/en not_active IP Right Cessation
- 1984-08-20 DK DK397984A patent/DK163565C/en not_active IP Right Cessation
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| US2877159A (en) * | 1957-04-26 | 1959-03-10 | Ciba Pharm Prod Inc | Method for preparing tablet granulations |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5348745A (en) * | 1989-05-09 | 1994-09-20 | Miles Inc. | Aqueous granulation solution and a method of tablet granulation |
| US5298261A (en) * | 1992-04-20 | 1994-03-29 | Oregon Freeze Dry, Inc. | Rapidly distintegrating tablet |
| US5503846A (en) * | 1993-03-17 | 1996-04-02 | Cima Labs, Inc. | Base coated acid particles and effervescent formulation incorporating same |
| US5997901A (en) | 1998-10-22 | 1999-12-07 | Mills; Robert G. | Method of manufacturing scented molded products |
| US6620433B2 (en) | 2000-11-03 | 2003-09-16 | Laboratorios Belmac, S.A. | Dispersible and soluble galenic paracetamol formulation, method for its preparation and its applications |
| US20090135666A1 (en) * | 2005-02-09 | 2009-05-28 | Satoru Watano | Kneading and granulating machine |
| US8721167B2 (en) * | 2005-02-09 | 2014-05-13 | Shinagawa Machinery Works Co., Ltd. | Kneading and granulating machine |
| US7568297B2 (en) * | 2006-04-10 | 2009-08-04 | Woodhaven Capital Corp. | Grain drying aeration system |
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