CH631893A5 - Stabile waessrige oder waessrig-alkoholische loesung von fettloeslichen parfuemoelen oder arzneimitteln. - Google Patents
Stabile waessrige oder waessrig-alkoholische loesung von fettloeslichen parfuemoelen oder arzneimitteln. Download PDFInfo
- Publication number
- CH631893A5 CH631893A5 CH1061277A CH1061277A CH631893A5 CH 631893 A5 CH631893 A5 CH 631893A5 CH 1061277 A CH1061277 A CH 1061277A CH 1061277 A CH1061277 A CH 1061277A CH 631893 A5 CH631893 A5 CH 631893A5
- Authority
- CH
- Switzerland
- Prior art keywords
- oil
- aqueous
- hydroxyalkyl
- fat
- weight
- Prior art date
Links
- 239000003921 oil Substances 0.000 title claims description 31
- 239000002304 perfume Substances 0.000 title claims description 24
- 229940126601 medicinal product Drugs 0.000 title claims description 3
- 230000001476 alcoholic effect Effects 0.000 title description 4
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 27
- -1 hydroxyalkyl ester Chemical class 0.000 claims description 14
- 150000001408 amides Chemical class 0.000 claims description 11
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 29
- 239000000243 solution Substances 0.000 description 20
- 239000002904 solvent Substances 0.000 description 16
- 239000003814 drug Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 7
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 235000019501 Lemon oil Nutrition 0.000 description 3
- 235000019502 Orange oil Nutrition 0.000 description 3
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000007046 ethoxylation reaction Methods 0.000 description 3
- 239000010501 lemon oil Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000010502 orange oil Substances 0.000 description 3
- 150000002924 oxiranes Chemical group 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 150000003722 vitamin derivatives Chemical class 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000010627 cedar oil Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000001734 eugenia caryophyllata l. bud oleoresin Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 2
- 235000019477 peppermint oil Nutrition 0.000 description 2
- 239000010665 pine oil Substances 0.000 description 2
- 239000001738 pogostemon cablin oil Substances 0.000 description 2
- 239000010668 rosemary oil Substances 0.000 description 2
- 229940058206 rosemary oil Drugs 0.000 description 2
- 230000003381 solubilizing effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 235000019155 vitamin A Nutrition 0.000 description 2
- 239000011719 vitamin A Substances 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000010617 anise oil Substances 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000010642 eucalyptus oil Substances 0.000 description 1
- 229940044949 eucalyptus oil Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000010643 fennel seed oil Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 235000019717 geranium oil Nutrition 0.000 description 1
- 239000010648 geranium oil Substances 0.000 description 1
- 239000001469 lavandula hydrida abrial herb oil Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000013558 reference substance Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012438 synthetic essential oil Substances 0.000 description 1
- 239000010678 thyme oil Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/45—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
-
- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762639293 DE2639293A1 (de) | 1976-09-01 | 1976-09-01 | Stabile waessrige oder waessrig-alkoholische loesungen von fettloeslichen parfuemoelen oder arzneimitteln |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH631893A5 true CH631893A5 (de) | 1982-09-15 |
Family
ID=5986874
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1061277A CH631893A5 (de) | 1976-09-01 | 1977-08-31 | Stabile waessrige oder waessrig-alkoholische loesung von fettloeslichen parfuemoelen oder arzneimitteln. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4170655A (Direct) |
| AT (1) | AT354635B (Direct) |
| BE (1) | BE858273A (Direct) |
| CH (1) | CH631893A5 (Direct) |
| DE (1) | DE2639293A1 (Direct) |
| FR (1) | FR2363324A1 (Direct) |
| GB (1) | GB1582028A (Direct) |
| IT (1) | IT1085014B (Direct) |
| NL (1) | NL7708880A (Direct) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2913467A1 (de) * | 1979-04-04 | 1980-10-16 | Henkel Kgaa | Stabile waessrige oder waessrig-alkoholische loesungen von fettloeslichen parfuemoelen |
| US4292211A (en) * | 1980-07-31 | 1981-09-29 | Shaw Mudge & Company | Fragrance dispersant composition |
| ATE109963T1 (de) * | 1990-07-11 | 1994-09-15 | Quest Int | Parfümierte strukturierte emulsionen in körperpflegemitteln. |
| EP0572080B1 (en) | 1992-05-29 | 1995-11-15 | Quest International B.V. | Aqueous perfume oil microemulsions |
| EP0571677A1 (en) * | 1992-05-29 | 1993-12-01 | Unilever Plc | Aqueous parfume oil microemulsions |
| US5585343A (en) * | 1993-11-02 | 1996-12-17 | Givaudan-Roure Corporation | Low VOC perfume formulations |
| US20030129253A1 (en) * | 2002-01-03 | 2003-07-10 | Milley Christopher J. | Stable aqueous suspension |
| DE102004054036A1 (de) * | 2004-11-05 | 2006-05-11 | Cognis Ip Management Gmbh | Verwendung von alkoxylierten Hydroxycarbonsäureestern zur Lösungsvermittlung von Parfümölen in Wasser |
| EP4124334A1 (en) | 2021-07-30 | 2023-02-01 | V. Mane Fils | Transparent aqueous perfume composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2991296A (en) * | 1959-02-26 | 1961-07-04 | Oscar L Scherr | Method for improving foam stability of foaming detergent composition and improved stabilizers therefor |
| US3102114A (en) * | 1961-04-03 | 1963-08-27 | Komori Saburo | Polyoxyethylene derivatives of esters of sucrose with long-chain fatty acids |
| CH467069A (de) * | 1964-05-28 | 1969-01-15 | Ciba Geigy | Hautpflegemittel |
| FR2003231A1 (Direct) | 1968-03-05 | 1969-11-07 | Monsanto Co | |
| DE2019839A1 (de) * | 1969-04-28 | 1970-11-05 | Ferrosan As | Stabile,klare,wasserdispergierbare bzw.-verduennbare,Vitamin-A enthaltende Loesung und Verfahren zu ihrer Herstellung |
| FR2264522A1 (en) * | 1974-03-22 | 1975-10-17 | Rouchy Maurice | Vitamin F cpds having surface active properties - comprise linoleic, linolenic and arachidonic acid radical joined via O or N to polyalcohols |
-
1976
- 1976-09-01 DE DE19762639293 patent/DE2639293A1/de not_active Withdrawn
-
1977
- 1977-08-11 NL NL7708880A patent/NL7708880A/xx not_active Application Discontinuation
- 1977-08-19 US US05/826,044 patent/US4170655A/en not_active Expired - Lifetime
- 1977-08-25 GB GB35628/77A patent/GB1582028A/en not_active Expired
- 1977-08-25 IT IT26931/77A patent/IT1085014B/it active
- 1977-08-31 BE BE180568A patent/BE858273A/xx unknown
- 1977-08-31 CH CH1061277A patent/CH631893A5/de not_active IP Right Cessation
- 1977-08-31 AT AT628077A patent/AT354635B/de not_active IP Right Cessation
- 1977-09-01 FR FR7726574A patent/FR2363324A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2363324B1 (Direct) | 1983-05-06 |
| NL7708880A (nl) | 1978-03-03 |
| IT1085014B (it) | 1985-05-28 |
| ATA628077A (de) | 1979-06-15 |
| BE858273A (fr) | 1978-02-28 |
| FR2363324A1 (fr) | 1978-03-31 |
| DE2639293A1 (de) | 1978-03-02 |
| GB1582028A (en) | 1980-12-31 |
| AT354635B (de) | 1979-01-25 |
| US4170655A (en) | 1979-10-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |