CA1064903A - Water-soluble acidic saponine - Google Patents
Water-soluble acidic saponineInfo
- Publication number
- CA1064903A CA1064903A CA256,650A CA256650A CA1064903A CA 1064903 A CA1064903 A CA 1064903A CA 256650 A CA256650 A CA 256650A CA 1064903 A CA1064903 A CA 1064903A
- Authority
- CA
- Canada
- Prior art keywords
- escin
- nozzle
- solution
- spray drying
- spray
- 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.)
- Expired
Links
- 230000002378 acidificating effect Effects 0.000 title description 11
- SYXUBXTYGFJFEH-UHFFFAOYSA-N oat triterpenoid saponin Chemical compound CNC1=CC=CC=C1C(=O)OC1C(C=O)(C)CC2C3(C(O3)CC3C4(CCC5C(C)(CO)C(OC6C(C(O)C(OC7C(C(O)C(O)C(CO)O7)O)CO6)OC6C(C(O)C(O)C(CO)O6)O)CCC53C)C)C4(C)CC(O)C2(C)C1 SYXUBXTYGFJFEH-UHFFFAOYSA-N 0.000 title description 3
- 229940011399 escin Drugs 0.000 claims abstract description 40
- 229930186222 escin Natural products 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000001694 spray drying Methods 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 6
- 239000007921 spray Substances 0.000 claims description 5
- 239000011261 inert gas Substances 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 3
- 239000001569 carbon dioxide Substances 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- 238000000605 extraction Methods 0.000 claims description 3
- 235000010181 horse chestnut Nutrition 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 241000157280 Aesculus hippocastanum Species 0.000 claims description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 9
- 238000002360 preparation method Methods 0.000 abstract description 3
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 6
- 239000008298 dragée Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- -1 aliphatic alcohols Chemical class 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection 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
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 241000157282 Aesculus Species 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 206010037549 Purpura Diseases 0.000 description 1
- LBPGGVGNNLPHBO-UHFFFAOYSA-N [N].OC Chemical compound [N].OC LBPGGVGNNLPHBO-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 230000002322 anti-exudative effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 210000004051 gastric juice Anatomy 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 206010034754 petechiae Diseases 0.000 description 1
- 229920000058 polyacrylate Polymers 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
- 239000000126 substance Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/256—Polyterpene radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pain & Pain Management (AREA)
- Biotechnology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Saccharide Compounds (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2530953A DE2530953C2 (de) | 1975-07-11 | 1975-07-11 | Verfahren zur Herstellung von röntgenamorphem Aescin, nach diesem Verfahren erhältliches röntgenamorphes Aescin und dieses enthaltende Arzneimittel |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1064903A true CA1064903A (en) | 1979-10-23 |
Family
ID=5951225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA256,650A Expired CA1064903A (en) | 1975-07-11 | 1976-07-09 | Water-soluble acidic saponine |
Country Status (20)
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1252201B (it) * | 1991-12-12 | 1995-06-05 | Dompe Farmaceutici Spa | S-carbossimetilcisteina sale di lisina monoidrato e procedimento per la sua preparazione. |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE302543C (enrdf_load_stackoverflow) * | ||||
NL301747A (enrdf_load_stackoverflow) * | 1962-12-14 | |||
YU37063B (en) * | 1971-12-06 | 1984-08-31 | Lek Tovarna Farmacevtskih | Process for preparing x-ray amorphous water-sulubleascin |
DE2357226A1 (de) * | 1973-11-16 | 1975-05-28 | Merck Patent Gmbh | Verfahren zur herstellung von wasserloeslichem beta-aescin |
-
1975
- 1975-07-11 DE DE2530953A patent/DE2530953C2/de not_active Expired - Lifetime
-
1976
- 1976-06-30 PT PT65302A patent/PT65302B/pt unknown
- 1976-06-30 FI FI761895A patent/FI62099C/fi not_active IP Right Cessation
- 1976-07-05 BG BG033673A patent/BG27379A3/xx unknown
- 1976-07-07 GB GB28233/76A patent/GB1550845A/en not_active Expired
- 1976-07-07 SU SU762377645A patent/SU786857A3/ru active
- 1976-07-08 YU YU1670/76A patent/YU41812B/xx unknown
- 1976-07-08 ZA ZA764065A patent/ZA764065B/xx unknown
- 1976-07-08 AU AU15729/76A patent/AU510463B2/en not_active Expired
- 1976-07-09 HU HU76MA2797A patent/HU174603B/hu not_active IP Right Cessation
- 1976-07-09 CS CS764567A patent/CS208184B2/cs unknown
- 1976-07-09 CA CA256,650A patent/CA1064903A/en not_active Expired
- 1976-07-10 RO RO7686932A patent/RO70354A/ro unknown
- 1976-07-10 ES ES449748A patent/ES449748A1/es not_active Expired
- 1976-07-10 PL PL1976191114A patent/PL99028B1/pl unknown
- 1976-07-12 JP JP51082846A patent/JPS5234915A/ja active Granted
- 1976-07-12 FR FR7621313A patent/FR2316961A1/fr active Granted
- 1976-07-12 BE BE168849A patent/BE844053A/xx not_active IP Right Cessation
- 1976-07-12 PH PH18678A patent/PH13989A/en unknown
-
1981
- 1981-07-16 HK HK336/81A patent/HK33681A/xx unknown
-
1986
- 1986-12-22 JP JP61304058A patent/JPS6366127A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0336808B2 (enrdf_load_stackoverflow) | 1991-06-03 |
YU41812B (en) | 1988-02-29 |
DE2530953A1 (de) | 1977-01-27 |
JPS6221765B2 (enrdf_load_stackoverflow) | 1987-05-14 |
AU510463B2 (en) | 1980-06-26 |
BG27379A3 (bg) | 1979-10-12 |
FI62099C (fi) | 1982-11-10 |
PL99028B1 (pl) | 1978-06-30 |
HU174603B (hu) | 1980-02-28 |
AU1572976A (en) | 1978-01-12 |
GB1550845A (en) | 1979-08-22 |
FR2316961A1 (fr) | 1977-02-04 |
PT65302A (de) | 1976-07-01 |
JPS5234915A (en) | 1977-03-17 |
SU786857A3 (ru) | 1980-12-07 |
ZA764065B (en) | 1977-07-27 |
PT65302B (de) | 1977-12-13 |
FI62099B (fi) | 1982-07-30 |
PH13989A (en) | 1980-11-28 |
FR2316961B1 (enrdf_load_stackoverflow) | 1984-04-20 |
CS208184B2 (en) | 1981-08-31 |
BE844053A (fr) | 1977-01-12 |
YU167076A (en) | 1983-06-30 |
JPS6366127A (ja) | 1988-03-24 |
DE2530953C3 (de) | 1994-07-07 |
HK33681A (en) | 1981-07-24 |
RO70354A (ro) | 1982-03-24 |
ES449748A1 (es) | 1977-08-16 |
DE2530953C2 (de) | 1994-07-07 |
FI761895A7 (enrdf_load_stackoverflow) | 1977-01-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2094054C1 (ru) | Способ получения обедненного пестицидами концентрата биологически активного вещества из растений | |
Funayama et al. | Kukoamine B, a spermine alkaloid from Lycium chinense | |
Meurer et al. | Hydroxycinnamic acid spermidine amides from pollen of Corylus avellana L. | |
JPS55167226A (en) | Analgesic and antinflammatory agent, and its preparation | |
CA1064903A (en) | Water-soluble acidic saponine | |
Cárdenas et al. | The analgesic activity of Hedyosmum bonplandianum: flavonoid glycosides | |
US4238518A (en) | Process for the preparation of a stable Beta vulgaris extract | |
Zhang et al. | Glycolipids from Mirabilis himalaica | |
Sciuto et al. | Biosynthesis of amaranthin in Celosia plumosa | |
Asomaning et al. | Pyrano-and dihydrofurano-isoflavones from Milletia thonningii | |
EP0932409B1 (en) | A method for producing an extract from valeriana officinalis containing high levels of valerenic acid | |
US4132782A (en) | Method for suppressing herpes simplex virus | |
El Abbadi et al. | New alkaloids of Chiococca alba | |
US6197307B1 (en) | Method for producing high activity extracts from harpagophytum procumbens | |
Galeffi et al. | N, N-dimethyl-5-methoxytryptamine, a component of a dart poison of the Yanoama Indians | |
GB1559275A (en) | Process for the preparation of a stable beta vulgaris extrct | |
Pérez et al. | The monoterpene 9-hydroxythymol from Bahia schaffneri var. aristata | |
Abe et al. | Identification of auxin-active substances as ethyl chlorogenate and indolyl-3-acetic acid in immature seeds of Helianthus annuus | |
KR820002108B1 (ko) | 수용성 산성 사포닌의 제조 방법 | |
US2963401A (en) | Rimocidin and methods for its recovery | |
Asante‐Poku et al. | Site of decomposition of methyl bromide in cocoa beans | |
GB970894A (en) | Analgesic preparation | |
GB1219345A (en) | Pharmacologically effective substance and process for isolating it | |
GB2317613A (en) | A method for producing an extract from paeonia containing high levels of paeoniflorin | |
Howard et al. | Hydrolysis of diacetylcycloserine. In vitro and in vivo studies |