CS265231B2 - Process for preparing effervescent copulated preparates with anacid effect - Google Patents
Process for preparing effervescent copulated preparates with anacid effect Download PDFInfo
- Publication number
- CS265231B2 CS265231B2 CS87355A CS35587A CS265231B2 CS 265231 B2 CS265231 B2 CS 265231B2 CS 87355 A CS87355 A CS 87355A CS 35587 A CS35587 A CS 35587A CS 265231 B2 CS265231 B2 CS 265231B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- methyl
- mixture
- sodium
- effervescent
- tablets
- Prior art date
Links
- 230000000694 effects Effects 0.000 title claims description 8
- 238000004519 manufacturing process Methods 0.000 title description 8
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 72
- 239000000203 mixture Substances 0.000 claims description 69
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 68
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 34
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 31
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 30
- 229910052708 sodium Inorganic materials 0.000 claims description 30
- 239000011734 sodium Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 27
- 238000003756 stirring Methods 0.000 claims description 25
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 24
- 238000001035 drying Methods 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000001569 carbon dioxide Substances 0.000 claims description 12
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 12
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 5
- 238000006386 neutralization reaction Methods 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 230000008878 coupling Effects 0.000 claims description 2
- 238000010168 coupling process Methods 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 239000003826 tablet Substances 0.000 description 38
- 229960001380 cimetidine Drugs 0.000 description 26
- CCGSUNCLSOWKJO-UHFFFAOYSA-N cimetidine Chemical compound N#CNC(=N/C)\NCCSCC1=NC=N[C]1C CCGSUNCLSOWKJO-UHFFFAOYSA-N 0.000 description 26
- 238000003860 storage Methods 0.000 description 18
- -1 sulfotidine Chemical compound 0.000 description 16
- 229960004106 citric acid Drugs 0.000 description 15
- 239000000047 product Substances 0.000 description 14
- 238000002156 mixing Methods 0.000 description 11
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 11
- 239000004299 sodium benzoate Substances 0.000 description 11
- 235000010234 sodium benzoate Nutrition 0.000 description 11
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 10
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 229960004543 anhydrous citric acid Drugs 0.000 description 9
- 239000003485 histamine H2 receptor antagonist Substances 0.000 description 9
- 230000002829 reductive effect Effects 0.000 description 9
- OFFPEAOWWDXZOY-UHFFFAOYSA-N 2-methyl-1-[2-[(5-methyl-1h-imidazol-4-yl)methylsulfanyl]ethyl]guanidine Chemical compound CN=C(N)NCCSCC=1N=CNC=1C OFFPEAOWWDXZOY-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 229960002908 cimetidine hydrochloride Drugs 0.000 description 7
- QJHCNBWLPSXHBL-UHFFFAOYSA-N cimetidine hydrochloride Chemical compound [H+].[Cl-].N#C/N=C(/NC)NCCSCC=1N=CNC=1C QJHCNBWLPSXHBL-UHFFFAOYSA-N 0.000 description 7
- 239000007857 degradation product Substances 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 238000004128 high performance liquid chromatography Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 6
- 239000007938 effervescent tablet Substances 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- 239000011343 solid material Substances 0.000 description 6
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
- ZKPZQFVHCXIQJS-UHFFFAOYSA-N [amino-[methyl-[2-[(5-methyl-1h-imidazol-4-yl)methylsulfanyl]ethyl]amino]methylidene]urea Chemical compound NC(=O)\N=C(\N)N(C)CCSCC=1N=CNC=1C ZKPZQFVHCXIQJS-UHFFFAOYSA-N 0.000 description 5
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 5
- 229960001340 histamine Drugs 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- CEYULKASIQJZGP-UHFFFAOYSA-L disodium;2-(carboxymethyl)-2-hydroxybutanedioate Chemical compound [Na+].[Na+].[O-]C(=O)CC(O)(C(=O)O)CC([O-])=O CEYULKASIQJZGP-UHFFFAOYSA-L 0.000 description 4
- 208000000718 duodenal ulcer Diseases 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 102000005962 receptors Human genes 0.000 description 4
- 108020003175 receptors Proteins 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 208000007107 Stomach Ulcer Diseases 0.000 description 3
- 229940069428 antacid Drugs 0.000 description 3
- 239000003159 antacid agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000002552 dosage form Substances 0.000 description 3
- 201000005917 gastric ulcer Diseases 0.000 description 3
- HWPKGOGLCKPRLZ-UHFFFAOYSA-M monosodium citrate Chemical compound [Na+].OC(=O)CC(O)(C([O-])=O)CC(O)=O HWPKGOGLCKPRLZ-UHFFFAOYSA-M 0.000 description 3
- 239000002524 monosodium citrate Substances 0.000 description 3
- 235000018342 monosodium citrate Nutrition 0.000 description 3
- 239000008194 pharmaceutical composition Substances 0.000 description 3
- 210000002381 plasma Anatomy 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- KGQVSZDGKJRBPF-UHFFFAOYSA-N 1-methyl-1-[n'-[2-[(5-methyl-1h-imidazol-4-yl)methylsulfanyl]ethyl]carbamimidoyl]urea Chemical compound NC(=O)N(C)C(N)=NCCSCC=1N=CNC=1C KGQVSZDGKJRBPF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 208000025865 Ulcer Diseases 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000001458 anti-acid effect Effects 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 2
- 230000037058 blood plasma level Effects 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000007911 effervescent powder Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- YECBIJXISLIIDS-UHFFFAOYSA-N mepyramine Chemical compound C1=CC(OC)=CC=C1CN(CCN(C)C)C1=CC=CC=N1 YECBIJXISLIIDS-UHFFFAOYSA-N 0.000 description 2
- 229960000582 mepyramine Drugs 0.000 description 2
- 239000012057 packaged powder Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 230000036470 plasma concentration Effects 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229960003975 potassium Drugs 0.000 description 2
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- 231100000397 ulcer Toxicity 0.000 description 2
- 210000002700 urine Anatomy 0.000 description 2
- HXRSXEDVVARPHP-UDWIEESQSA-N (z)-1-n'-(1,3-benzodioxol-5-ylmethyl)-1-n-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-2-nitroethene-1,1-diamine Chemical compound O1C(CN(C)C)=CC=C1CSCCN\C(=C/[N+]([O-])=O)NCC1=CC=C(OCO2)C2=C1 HXRSXEDVVARPHP-UDWIEESQSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- KEDVUOWPLAHMLZ-UHFFFAOYSA-N 1-cyano-3-[2-[(5-methyl-1h-imidazol-4-yl)methylsulfanyl]ethyl]-2-prop-2-ynylguanidine Chemical compound CC=1NC=NC=1CSCCNC(NC#N)=NCC#C KEDVUOWPLAHMLZ-UHFFFAOYSA-N 0.000 description 1
- CZTPLYMKHNEVHO-UHFFFAOYSA-N 2-[2-[[5-(2-aminopropan-2-yl)furan-2-yl]methylsulfanyl]ethylamino]-5-[(6-methylpyridin-3-yl)methyl]-1h-pyrimidin-6-one Chemical compound C1=NC(C)=CC=C1CC(C(N1)=O)=CN=C1NCCSCC1=CC=C(C(C)(C)N)O1 CZTPLYMKHNEVHO-UHFFFAOYSA-N 0.000 description 1
- GIMNAEMRNXUAQP-UHFFFAOYSA-N 2-[4-(2-methyl-1h-imidazol-5-yl)-1,3-thiazol-2-yl]guanidine Chemical compound N1C(C)=NC=C1C1=CSC(N=C(N)N)=N1 GIMNAEMRNXUAQP-UHFFFAOYSA-N 0.000 description 1
- FSWCCDQGXZITPD-UHFFFAOYSA-N 2-[4-[2-[(5-amino-4-methyl-1,1-dioxo-1,2,4,6-thiatriazin-3-yl)amino]ethylsulfanylmethyl]-1,3-thiazol-2-yl]guanidine Chemical compound CN1C(N)=NS(=O)(=O)N=C1NCCSCC1=CSC(N=C(N)N)=N1 FSWCCDQGXZITPD-UHFFFAOYSA-N 0.000 description 1
- KEWLVUBYGUZFKX-UHFFFAOYSA-N 2-ethylguanidine Chemical compound CCNC(N)=N KEWLVUBYGUZFKX-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229940124056 Histamine H1 receptor antagonist Drugs 0.000 description 1
- 102000000543 Histamine Receptors Human genes 0.000 description 1
- 108010002059 Histamine Receptors Proteins 0.000 description 1
- 239000004395 L-leucine Substances 0.000 description 1
- 235000019454 L-leucine Nutrition 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
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- 241000124008 Mammalia Species 0.000 description 1
- 206010030201 Oesophageal ulcer Diseases 0.000 description 1
- SMTZFNFIKUPEJC-UHFFFAOYSA-N Roxane Chemical compound CC(=O)OCC(=O)NCCCOC1=CC=CC(CN2CCCCC2)=C1 SMTZFNFIKUPEJC-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical group [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 239000004141 Sodium laurylsulphate Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
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- 239000004480 active ingredient Substances 0.000 description 1
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- 150000001413 amino acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 102000012740 beta Adrenergic Receptors Human genes 0.000 description 1
- 108010079452 beta Adrenergic Receptors Proteins 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- 238000009534 blood test Methods 0.000 description 1
- RIMGDBZXWSGBQN-UHFFFAOYSA-N burimamide Chemical compound CNC(=S)NCCCCC1=CN=C[N]1 RIMGDBZXWSGBQN-UHFFFAOYSA-N 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
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- UZLGHNUASUZUOR-UHFFFAOYSA-L dipotassium;3-carboxy-3-hydroxypentanedioate Chemical compound [K+].[K+].OC(=O)CC(O)(C([O-])=O)CC([O-])=O UZLGHNUASUZUOR-UHFFFAOYSA-L 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 229950007285 etintidine Drugs 0.000 description 1
- 229960001596 famotidine Drugs 0.000 description 1
- XUFQPHANEAPEMJ-UHFFFAOYSA-N famotidine Chemical compound NC(N)=NC1=NC(CSCCC(N)=NS(N)(=O)=O)=CS1 XUFQPHANEAPEMJ-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000012027 fruit salads Nutrition 0.000 description 1
- 210000004211 gastric acid Anatomy 0.000 description 1
- 239000000938 histamine H1 antagonist Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 229960003136 leucine Drugs 0.000 description 1
- 229950000367 lupitidine Drugs 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 229950008866 mifentidine Drugs 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 210000003097 mucus Anatomy 0.000 description 1
- GOZUADYOHPCXLE-UHFFFAOYSA-N n-[4-(1h-imidazol-5-yl)phenyl]-n'-propan-2-ylmethanimidamide Chemical compound C1=CC(NC=NC(C)C)=CC=C1C1=CN=CN1 GOZUADYOHPCXLE-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229960001323 niperotidine Drugs 0.000 description 1
- 229960004872 nizatidine Drugs 0.000 description 1
- SGXXNSQHWDMGGP-IZZDOVSWSA-N nizatidine Chemical compound [O-][N+](=O)\C=C(/NC)NCCSCC1=CSC(CN(C)C)=N1 SGXXNSQHWDMGGP-IZZDOVSWSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
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- 238000002161 passivation Methods 0.000 description 1
- 230000001175 peptic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000002980 postoperative effect Effects 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229960000620 ranitidine Drugs 0.000 description 1
- VMXUWOKSQNHOCA-LCYFTJDESA-N ranitidine Chemical compound [O-][N+](=O)/C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 VMXUWOKSQNHOCA-LCYFTJDESA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229940044551 receptor antagonist Drugs 0.000 description 1
- 239000002464 receptor antagonist Substances 0.000 description 1
- 230000000306 recurrent effect Effects 0.000 description 1
- 229960003320 roxatidine Drugs 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 229950010224 tuvatidine Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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- PCHQDTOLHOFHHK-UHFFFAOYSA-L zinc;hydrogen carbonate Chemical compound [Zn+2].OC([O-])=O.OC([O-])=O PCHQDTOLHOFHHK-UHFFFAOYSA-L 0.000 description 1
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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Cosmetics (AREA)
- Peptides Or Proteins (AREA)
- Processing Of Solid Wastes (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines Containing Plant Substances (AREA)
- Saccharide Compounds (AREA)
- Compounds Of Unknown Constitution (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8600839A FR2593065B1 (fr) | 1986-01-22 | 1986-01-22 | Couples effervescents, compositions effervescentes d'antagonistes h2 de l'histamine les contenant et leur preparation. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS35587A2 CS35587A2 (en) | 1988-12-15 |
| CS265231B2 true CS265231B2 (en) | 1989-10-13 |
Family
ID=9331358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS87355A CS265231B2 (en) | 1986-01-22 | 1987-01-19 | Process for preparing effervescent copulated preparates with anacid effect |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US4824664A (de) |
| EP (1) | EP0233853B1 (de) |
| JP (2) | JPH0669964B2 (de) |
| KR (1) | KR950002883B1 (de) |
| CN (1) | CN1032841C (de) |
| AT (1) | ATE56356T1 (de) |
| AU (1) | AU599071B2 (de) |
| BG (1) | BG50924A3 (de) |
| CA (1) | CA1299583C (de) |
| CS (1) | CS265231B2 (de) |
| DD (1) | DD285720A5 (de) |
| DE (1) | DE3764816D1 (de) |
| DK (1) | DK30087A (de) |
| EG (1) | EG18194A (de) |
| ES (1) | ES2017531B3 (de) |
| FI (1) | FI90941C (de) |
| FR (1) | FR2593065B1 (de) |
| GR (1) | GR3001150T3 (de) |
| HU (1) | HU196305B (de) |
| IE (1) | IE59652B1 (de) |
| IL (1) | IL81313A (de) |
| MX (1) | MX9203546A (de) |
| NO (1) | NO173972C (de) |
| NZ (1) | NZ218895A (de) |
| OA (1) | OA08464A (de) |
| PH (1) | PH25292A (de) |
| PL (1) | PL154164B1 (de) |
| PT (1) | PT84148B (de) |
| SU (1) | SU1605913A3 (de) |
| TN (1) | TNSN87005A1 (de) |
| ZA (1) | ZA87433B (de) |
| ZW (1) | ZW587A1 (de) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR960011236B1 (ko) * | 1987-05-08 | 1996-08-21 | 스미스 클라인 앤드 프렌취 라보라토리스 리미티드 | 제약학적 조성물 및 고체 제형 |
| GB8730011D0 (en) * | 1987-12-23 | 1988-02-03 | Smithkline Dauelsberg | Pharmaceutical compositions |
| YU120988A (en) * | 1988-06-23 | 1990-06-30 | Lek Tovarna Farmacevtskih | Process for preparing new dispersion pills of cimetidine |
| FR2633181B1 (fr) * | 1988-06-24 | 1992-01-10 | Glaxo Lab Sa | Composition pharmaceutique a base de ranitidine et son procede de preparation |
| NZ230701A (en) * | 1988-09-20 | 1992-01-29 | Glaxo Group Ltd | Pharmaceutical compositions comprising ranitidine, alginic acid and a carbonate or bicarbonate |
| US5275823A (en) * | 1989-04-27 | 1994-01-04 | Smith Kline & French Laboratories Ltd. | Pharmaceutical compositions |
| US5348745A (en) * | 1989-05-09 | 1994-09-20 | Miles Inc. | Aqueous granulation solution and a method of tablet granulation |
| FR2648710B1 (fr) * | 1989-06-23 | 1994-01-14 | Glaxo Sa Laboratoires | Composition pharmaceutique a base de ranitidine et son procede de preparation |
| DE4027927A1 (de) * | 1990-09-04 | 1992-03-05 | Bayer Ag | Brausekomponente und verfahren zu ihrer herstellung |
| AU639137B2 (en) * | 1990-09-21 | 1993-07-15 | Merrell Dow Pharmaceuticals Inc. | Superior tasting pharmaceutical composition having porous particles and the process of preparing such pharmaceutical composition |
| GB9027827D0 (en) * | 1990-12-21 | 1991-02-13 | Glaxo Laboratoires | Pharmaceutical compositions |
| CA2055661A1 (en) * | 1990-12-21 | 1992-06-22 | Manley A. Paulos | Treatment of upset stomach associated with heartburn, sour stomach or acid indigestion with an effervescent h2 blocker formulation |
| US5468504A (en) * | 1990-12-21 | 1995-11-21 | Laboratoires Glaxo S.A. | Effervescent pharmaceutical compositions |
| CA2061520C (en) * | 1991-03-27 | 2003-04-22 | Lawrence J. Daher | Delivery system for enhanced onset and increased potency |
| DE59201238D1 (de) * | 1991-07-01 | 1995-03-02 | Gerhard Gergely | Reaktionsdotierte brausesysteme. |
| ES2079743T3 (es) * | 1991-07-01 | 1996-01-16 | Gergely Gerhard | Tableta para chupar o masticar. |
| GB9127150D0 (en) * | 1991-12-20 | 1992-02-19 | Smithkline Beecham Plc | Novel treatment |
| FR2685199A1 (fr) * | 1991-12-24 | 1993-06-25 | Stirnweiss Charles | Procede de fabrication d'un granule effervescent et dispositif pour la mise en óoeuvre de ce procede. |
| EP0574624B1 (de) * | 1992-06-17 | 1997-09-10 | Laboratoires Glaxo Sa | Arzneimittel |
| US5503846A (en) * | 1993-03-17 | 1996-04-02 | Cima Labs, Inc. | Base coated acid particles and effervescent formulation incorporating same |
| IL112779A (en) * | 1994-03-01 | 1999-11-30 | Gergely Gerhard | Granular product or tablet containing an efferescent system and an active pharmaceutical substance and its preparation |
| US6274172B1 (en) | 1995-07-05 | 2001-08-14 | Smithkline Beecham Laboratoires Pharmaceutiques | Therapeutic effervescent compositions |
| FR2736264B1 (fr) * | 1995-07-05 | 1997-09-26 | Smithkline Beecham Lab | Couples effervescents, formulations pharmaceutiques les contenant, et leur utilisation en therapeutique |
| SE512835C2 (sv) * | 1996-01-08 | 2000-05-22 | Astrazeneca Ab | Doseringsform innehållande en mångfald enheter alla inneslutande syralabil H+K+ATPas-hämmare |
| US5989588A (en) * | 1996-10-04 | 1999-11-23 | Merck & Co., Inc. | Methods and compositions for preventing and treating heartburn |
| US5728401A (en) * | 1997-04-16 | 1998-03-17 | Ranbaxy Laboratories, Ltd. | Effervescent ranitidine formulations |
| US6165506A (en) * | 1998-09-04 | 2000-12-26 | Elan Pharma International Ltd. | Solid dose form of nanoparticulate naproxen |
| RU2160601C1 (ru) * | 1999-11-18 | 2000-12-20 | Закрытое акционерное общество "Межрегиональный центр "Адаптоген" | Растворимая шипучая лекарственная композиция с растительным экстрактом |
| US6264984B1 (en) | 1999-12-06 | 2001-07-24 | Bristol-Myers Squibb Company | Effervescent histamine H2 antagonist composition |
| US6554139B1 (en) * | 2000-06-01 | 2003-04-29 | Parker-Hannifin Corporation | Extension and locking assembly for dripless element, and container therefore |
| US6426111B1 (en) | 2000-06-02 | 2002-07-30 | Gerald Phillip Hirsch | Effervescent mixtures and methods of making |
| US8216610B2 (en) * | 2004-05-28 | 2012-07-10 | Imaginot Pty Ltd. | Oral paracetamol formulations |
| JP2008500288A (ja) * | 2004-05-28 | 2008-01-10 | イメイジノット ピーティーワイ エルティーディー | 経口治療用化合物の供給系 |
| EP3449928A1 (de) * | 2005-11-28 | 2019-03-06 | Imaginot Pty Ltd. | Abgabesystem für eine orale therapeutische verbindung |
| EP1983827A4 (de) | 2006-02-01 | 2013-07-10 | Stuart L Weg | Verwendung von antifungalen zusammensetzungen für die behandlung von erkrankungen des oberen magen-darm-trakts |
| CA3018828C (en) | 2014-09-17 | 2021-05-11 | Steerlife India Private Limited | Effervescent composition and method of making it |
| WO2017098481A1 (en) | 2015-12-12 | 2017-06-15 | Steerlife India Private Limited | Effervescent compositions of metformin and processes for preparation thereof |
| US10383810B2 (en) | 2016-03-31 | 2019-08-20 | L'oreal | Inhibiting color fading with layer-by-layer films |
| US10357668B2 (en) | 2016-03-31 | 2019-07-23 | L'oreal | Inhibiting color fading with layer-by-layer films |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1764996A (en) * | 1928-04-12 | 1930-06-17 | Squibb & Sons Inc | Stable effervescent composition |
| US2147743A (en) * | 1938-08-05 | 1939-02-21 | Baker Chem Co J T | Pharmaceutical preparation |
| FR1484202A (fr) * | 1965-07-05 | 1967-06-09 | Andreu Sa Dr | Procédé de préparation d'un composé acide pour compositions effervescentes |
| ES315494A1 (es) * | 1965-07-05 | 1966-02-01 | Serra Jorge Miquel | Un procedimiento para la preparaciën de un componente acido para composiciones efervescentes |
| AT307616B (de) * | 1969-05-02 | 1973-05-25 | Biochemie Gmbh | Verfahren zur Herstellung einer Brausezubereitung |
| US3887700A (en) * | 1969-11-28 | 1975-06-03 | Aspro Nicholas Ltd | Analgesic formulations |
| FR2092893B1 (de) * | 1970-06-29 | 1973-07-13 | Bru Jean | |
| FR2132521A1 (en) * | 1971-04-06 | 1972-11-24 | Sofrader Sa | Effervescent tablets prdn - by controlled drying in effervescent granule formation |
| AU528310B2 (en) * | 1978-11-16 | 1983-04-21 | Beecham Group Plc | Composition of paracetamol and metoclopramide |
| US4289751A (en) * | 1979-06-29 | 1981-09-15 | Merck & Co., Inc. | Effervescent enteric-coated formulation of soluble form of erythromycin and therapeutic use thereof |
| US4522943A (en) * | 1981-05-18 | 1985-06-11 | Bristol-Myers Company | Chemical compounds |
| US4503051A (en) * | 1981-05-18 | 1985-03-05 | Bristol-Myers Company | Substituted 3-cyclobutene-1,2-diones, pharmaceutical compositions thereof and methods of use |
| HU185457B (en) * | 1981-09-25 | 1985-02-28 | Richter Gedeon Vegyeszet | Process for preparating cimetidine-z |
-
1986
- 1986-01-22 FR FR8600839A patent/FR2593065B1/fr not_active Expired
-
1987
- 1987-01-12 NZ NZ218895A patent/NZ218895A/xx unknown
- 1987-01-19 ZW ZW5/87A patent/ZW587A1/xx unknown
- 1987-01-19 PH PH8734738A patent/PH25292A/en unknown
- 1987-01-19 CS CS87355A patent/CS265231B2/cs unknown
- 1987-01-19 PL PL1987263720A patent/PL154164B1/pl unknown
- 1987-01-19 FI FI870199A patent/FI90941C/fi not_active IP Right Cessation
- 1987-01-20 JP JP62013273A patent/JPH0669964B2/ja not_active Expired - Lifetime
- 1987-01-20 NO NO870243A patent/NO173972C/no unknown
- 1987-01-20 HU HU87156A patent/HU196305B/hu not_active IP Right Cessation
- 1987-01-20 IE IE12087A patent/IE59652B1/en not_active IP Right Cessation
- 1987-01-20 IL IL81313A patent/IL81313A/xx not_active IP Right Cessation
- 1987-01-20 OA OA59046A patent/OA08464A/xx unknown
- 1987-01-20 DK DK030087A patent/DK30087A/da not_active Application Discontinuation
- 1987-01-20 PT PT84148A patent/PT84148B/pt active IP Right Revival
- 1987-01-20 ES ES87870007T patent/ES2017531B3/es not_active Expired - Lifetime
- 1987-01-20 AT AT87870007T patent/ATE56356T1/de not_active IP Right Cessation
- 1987-01-20 DE DE8787870007T patent/DE3764816D1/de not_active Expired - Fee Related
- 1987-01-20 US US07/004,725 patent/US4824664A/en not_active Expired - Lifetime
- 1987-01-20 EP EP87870007A patent/EP0233853B1/de not_active Expired - Lifetime
- 1987-01-21 BG BG078136A patent/BG50924A3/bg unknown
- 1987-01-21 ZA ZA87433A patent/ZA87433B/xx unknown
- 1987-01-21 EG EG3587A patent/EG18194A/xx active
- 1987-01-21 KR KR1019870000450A patent/KR950002883B1/ko not_active Expired - Fee Related
- 1987-01-21 SU SU874028841A patent/SU1605913A3/ru active
- 1987-01-21 CN CN87100378A patent/CN1032841C/zh not_active Expired - Fee Related
- 1987-01-21 AU AU67899/87A patent/AU599071B2/en not_active Expired
- 1987-01-21 CA CA000527782A patent/CA1299583C/en not_active Expired - Lifetime
- 1987-01-21 DD DD87299383A patent/DD285720A5/de not_active IP Right Cessation
- 1987-01-22 TN TNTNSN87005A patent/TNSN87005A1/fr unknown
-
1990
- 1990-11-30 GR GR90401017T patent/GR3001150T3/el unknown
-
1992
- 1992-06-26 MX MX9203546A patent/MX9203546A/es unknown
-
1994
- 1994-01-26 JP JP6007012A patent/JPH08175976A/ja not_active Ceased
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