IE45208L - Neutralizing agent. - Google Patents
Neutralizing agent.Info
- Publication number
- IE45208L IE45208L IE771120A IE112077A IE45208L IE 45208 L IE45208 L IE 45208L IE 771120 A IE771120 A IE 771120A IE 112077 A IE112077 A IE 112077A IE 45208 L IE45208 L IE 45208L
- Authority
- IE
- Ireland
- Prior art keywords
- acid
- antacid
- group
- antacid agent
- agent
- Prior art date
Links
- 230000003472 neutralizing effect Effects 0.000 title abstract 2
- 239000003159 antacid agent Substances 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 abstract 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 abstract 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 abstract 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 abstract 1
- QXKAIJAYHKCRRA-JJYYJPOSSA-N D-arabinonic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C(O)=O QXKAIJAYHKCRRA-JJYYJPOSSA-N 0.000 abstract 1
- AEMOLEFTQBMNLQ-YMDCURPLSA-N D-galactopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-YMDCURPLSA-N 0.000 abstract 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 1
- 239000001263 FEMA 3042 Substances 0.000 abstract 1
- DSLZVSRJTYRBFB-UHFFFAOYSA-N Galactaric acid Natural products OC(=O)C(O)C(O)C(O)C(O)C(O)=O DSLZVSRJTYRBFB-UHFFFAOYSA-N 0.000 abstract 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 abstract 1
- 229920002230 Pectic acid Polymers 0.000 abstract 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 abstract 1
- 229920002873 Polyethylenimine Polymers 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 abstract 1
- 239000000783 alginic acid Substances 0.000 abstract 1
- 235000010443 alginic acid Nutrition 0.000 abstract 1
- 229960001126 alginic acid Drugs 0.000 abstract 1
- 229920000615 alginic acid Polymers 0.000 abstract 1
- 150000004781 alginic acids Chemical class 0.000 abstract 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 abstract 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 abstract 1
- 239000001530 fumaric acid Substances 0.000 abstract 1
- DSLZVSRJTYRBFB-DUHBMQHGSA-N galactaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O DSLZVSRJTYRBFB-DUHBMQHGSA-N 0.000 abstract 1
- 210000004211 gastric acid Anatomy 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000001630 malic acid Substances 0.000 abstract 1
- 235000011090 malic acid Nutrition 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000001814 pectin Substances 0.000 abstract 1
- 235000010987 pectin Nutrition 0.000 abstract 1
- 229920001277 pectin Polymers 0.000 abstract 1
- 239000010318 polygalacturonic acid Substances 0.000 abstract 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 abstract 1
- 229940033123 tannic acid Drugs 0.000 abstract 1
- 235000015523 tannic acid Nutrition 0.000 abstract 1
- 229920002258 tannic acid Polymers 0.000 abstract 1
- 239000011975 tartaric acid Substances 0.000 abstract 1
- 235000002906 tartaric acid Nutrition 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/785—Polymers containing nitrogen
-
- 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)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Control Of Combustion (AREA)
- Manufacturing Of Printed Circuit Boards (AREA)
Abstract
The invention is a gastric acid neutralizing antacid agent in liquid form which comprises an aqueous solution of a water-soluble polyethyleneimine, at least one taste improving acid selected from the group consisting of alginic acid, polygalacturonic acid, galacturonic acid, pectin, tannic acid, arabic acid, galactaric acid, and glutaric acid, and at least one acid selected from the group consisting of tartaric acid, fumaric acid, phosphoric acid, acetic acid, citric acid, succinic acid, and malic acid, the latter in such an amount that pH is 4 to 11, and a process for preparing the antacid agent. The antacid agent overcomes various disadvantages of previously known antacid agents containing aluminum hydroxide.
[SE7606256A]
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE7606256A SE405445B (en) | 1976-06-03 | 1976-06-03 | PROCEDURE FOR THE PREPARATION OF A STOMACH ACID NEUTRALIZING ANTACIDUM IN LIQUID CONTAINING POLYETHYLENIMINE |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE45208L true IE45208L (en) | 1977-12-03 |
| IE45208B1 IE45208B1 (en) | 1982-07-14 |
Family
ID=20328121
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1120/77A IE45208B1 (en) | 1976-06-03 | 1977-05-31 | Neutralizing agent |
Country Status (21)
| Country | Link |
|---|---|
| JP (1) | JPS52148630A (en) |
| AT (1) | AT353406B (en) |
| AU (1) | AU514929B2 (en) |
| BE (1) | BE855349A (en) |
| CA (1) | CA1087094A (en) |
| CS (1) | CS207459B2 (en) |
| DD (1) | DD131345A5 (en) |
| DE (1) | DE2722486A1 (en) |
| DK (1) | DK234077A (en) |
| FI (1) | FI59023C (en) |
| FR (1) | FR2353296A1 (en) |
| GB (1) | GB1539162A (en) |
| HU (1) | HU174584B (en) |
| IE (1) | IE45208B1 (en) |
| LU (1) | LU77480A1 (en) |
| NL (1) | NL7706085A (en) |
| NO (1) | NO771899L (en) |
| NZ (1) | NZ184237A (en) |
| SE (1) | SE405445B (en) |
| SU (1) | SU812156A3 (en) |
| ZA (1) | ZA772913B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5936192B2 (en) * | 2012-10-25 | 2016-06-15 | 学校法人神奈川大学 | Chiral supramolecular crystal, solid catalyst comprising the same, and method for producing chiral supramolecular crystal |
-
1976
- 1976-06-03 SE SE7606256A patent/SE405445B/en unknown
-
1977
- 1977-05-16 ZA ZA00772913A patent/ZA772913B/en unknown
- 1977-05-18 DE DE19772722486 patent/DE2722486A1/en not_active Withdrawn
- 1977-05-24 FI FI771660A patent/FI59023C/en not_active IP Right Cessation
- 1977-05-27 DK DK234077A patent/DK234077A/en unknown
- 1977-05-30 NZ NZ184237A patent/NZ184237A/en unknown
- 1977-05-30 AU AU25612/77A patent/AU514929B2/en not_active Expired
- 1977-05-31 NO NO771899A patent/NO771899L/en unknown
- 1977-05-31 IE IE1120/77A patent/IE45208B1/en unknown
- 1977-06-01 DD DD7700199241A patent/DD131345A5/en unknown
- 1977-06-01 CS CS773612A patent/CS207459B2/en unknown
- 1977-06-01 HU HU77HE737A patent/HU174584B/en unknown
- 1977-06-02 SU SU772490602A patent/SU812156A3/en active
- 1977-06-02 CA CA279,734A patent/CA1087094A/en not_active Expired
- 1977-06-02 FR FR7716916A patent/FR2353296A1/en active Granted
- 1977-06-02 NL NL7706085A patent/NL7706085A/en not_active Application Discontinuation
- 1977-06-02 GB GB23486/77A patent/GB1539162A/en not_active Expired
- 1977-06-03 JP JP6568177A patent/JPS52148630A/en active Pending
- 1977-06-03 LU LU77480A patent/LU77480A1/xx unknown
- 1977-06-03 BE BE178155A patent/BE855349A/en unknown
- 1977-06-03 AT AT393877A patent/AT353406B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FI771660A7 (en) | 1977-12-04 |
| HU174584B (en) | 1980-02-28 |
| DE2722486A1 (en) | 1977-12-22 |
| ATA393877A (en) | 1979-04-15 |
| FR2353296A1 (en) | 1977-12-30 |
| DD131345A5 (en) | 1978-06-21 |
| SE405445B (en) | 1978-12-11 |
| SE7606256L (en) | 1977-12-04 |
| NZ184237A (en) | 1979-10-25 |
| AU2561277A (en) | 1978-12-07 |
| DK234077A (en) | 1977-12-04 |
| AT353406B (en) | 1979-11-12 |
| NO771899L (en) | 1977-12-06 |
| AU514929B2 (en) | 1981-03-05 |
| NL7706085A (en) | 1977-12-06 |
| IE45208B1 (en) | 1982-07-14 |
| FI59023C (en) | 1981-06-10 |
| FR2353296B1 (en) | 1981-01-16 |
| CS207459B2 (en) | 1981-07-31 |
| ZA772913B (en) | 1978-04-26 |
| SU812156A3 (en) | 1981-03-07 |
| BE855349A (en) | 1977-12-05 |
| FI59023B (en) | 1981-02-27 |
| GB1539162A (en) | 1979-01-31 |
| JPS52148630A (en) | 1977-12-10 |
| LU77480A1 (en) | 1978-01-26 |
| CA1087094A (en) | 1980-10-07 |
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