DD211056A5 - Mikroemulsionen - Google Patents

Mikroemulsionen Download PDF

Info

Publication number: DD211056A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; water; active substance; optionally; weight
Prior art date: 1982-09-25

Application number

DD83255092A

Other languages

German (de)

English (en)

Inventor

Heinz Hausmann

Heinz-Josef Niessen

Heinz-Otto Horstmann

Original Assignee

Bayer Ag

Priority date (The priority date 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 date listed.)

1982-09-25

Filing date

1983-09-23

Publication date

1984-07-04

1983-09-23 Application filed by Bayer Ag filed Critical Bayer Ag

1984-07-04 Publication of DD211056A5 publication Critical patent/DD211056A5/de

Links

239000004530 micro-emulsion Substances 0.000 title claims abstract description 37
239000013543 active substance Substances 0.000 claims abstract description 26
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
239000000203 mixture Substances 0.000 claims abstract description 17
239000003960 organic solvent Substances 0.000 claims abstract description 16
239000002904 solvent Substances 0.000 claims abstract description 16
239000000654 additive Substances 0.000 claims abstract description 11
241000607479 Yersinia pestis Species 0.000 claims abstract description 8
239000003995 emulsifying agent Substances 0.000 claims abstract description 7
238000000034 method Methods 0.000 claims abstract description 7
150000001875 compounds Chemical class 0.000 claims abstract description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
-1 oxypropylene unit Chemical group 0.000 claims description 18
229920000151 polyglycol Polymers 0.000 claims description 16
239000010695 polyglycol Substances 0.000 claims description 16
125000002877 alkyl aryl group Chemical group 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 9
238000003756 stirring Methods 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 7
125000006353 oxyethylene group Chemical group 0.000 claims description 6
238000002360 preparation method Methods 0.000 claims description 6
150000001768 cations Chemical class 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 2
239000008240 homogeneous mixture Substances 0.000 claims description 2
238000003898 horticulture Methods 0.000 claims 1
239000004480 active ingredient Substances 0.000 description 15
239000000126 substance Substances 0.000 description 12
239000000839 emulsion Substances 0.000 description 7
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
239000007788 liquid Substances 0.000 description 6
239000002562 thickening agent Substances 0.000 description 5
239000003905 agrochemical Substances 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
IQAXZJZTCMIPCX-UHFFFAOYSA-L calcium;4-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1.CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 IQAXZJZTCMIPCX-UHFFFAOYSA-L 0.000 description 3
239000003814 drug Substances 0.000 description 3
229940079593 drug Drugs 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000012456 homogeneous solution Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 2
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical group C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical group OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
239000000975 dye Substances 0.000 description 2
238000004945 emulsification Methods 0.000 description 2
238000009472 formulation Methods 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 1
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
ITNHXUMPVZZZBT-UHFFFAOYSA-N 2-(1h-benzimidazol-2-yl)-7h-purine Chemical compound C1=CC=C2NC(C=3N=C4N=CNC4=CN=3)=NC2=C1 ITNHXUMPVZZZBT-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
PCWGTDULNUVNBN-UHFFFAOYSA-N 4-methylpentan-1-ol Chemical compound CC(C)CCCO PCWGTDULNUVNBN-UHFFFAOYSA-N 0.000 description 1
YJEGIQBEXCSBLN-UHFFFAOYSA-N C(C)OOP(OC1=CC=C(C=C1)[N+](=O)[O-])(O)=S Chemical compound C(C)OOP(OC1=CC=C(C=C1)[N+](=O)[O-])(O)=S YJEGIQBEXCSBLN-UHFFFAOYSA-N 0.000 description 1
ULSLJYXHZDTLQK-UHFFFAOYSA-N Coumatetralyl Chemical compound C1=CC=CC2=C1OC(=O)C(C1C3=CC=CC=C3CCC1)=C2O ULSLJYXHZDTLQK-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
BABJTMNVJXLAEX-UHFFFAOYSA-N Triamiphos Chemical compound N1=C(N)N(P(=O)(N(C)C)N(C)C)N=C1C1=CC=CC=C1 BABJTMNVJXLAEX-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
KVXNKFYSHAUJIA-UHFFFAOYSA-N acetic acid;ethoxyethane Chemical compound CC(O)=O.CCOCC KVXNKFYSHAUJIA-UHFFFAOYSA-N 0.000 description 1
239000012868 active agrochemical ingredient Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
229910052784 alkaline earth metal 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
239000008346 aqueous phase Substances 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
238000004049 embossing Methods 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229960002809 lindane Drugs 0.000 description 1
230000007774 longterm Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
WSGCRAOTEDLMFQ-UHFFFAOYSA-N nonan-5-one Chemical compound CCCCC(=O)CCCC WSGCRAOTEDLMFQ-UHFFFAOYSA-N 0.000 description 1
235000010292 orthophenyl phenol Nutrition 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000012071 phase Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
229960005235 piperonyl butoxide Drugs 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
- 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
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
- A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of compounds

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Dispersion Chemistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Toxicology (AREA)
Environmental Sciences (AREA)
Wood Science & Technology (AREA)
Biophysics (AREA)
Materials Engineering (AREA)
Organic Chemistry (AREA)
Molecular Biology (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Epidemiology (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Medicinal Preparation (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

DD83255092A 1982-09-25 1983-09-23 Mikroemulsionen DD211056A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19823235612 DE3235612A1 (de)	1982-09-25	1982-09-25	Mikroemulsionen

Publications (1)

Publication Number	Publication Date
DD211056A5 true DD211056A5 (de)	1984-07-04

Family

ID=6174194

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD83255092A DD211056A5 (de)	1982-09-25	1983-09-23	Mikroemulsionen

Country Status (13)

Country	Link
EP (1)	EP0107009A3 (fr)
JP (1)	JPS5980321A (fr)
KR (1)	KR840005648A (fr)
AU (1)	AU1929383A (fr)
BR (1)	BR8305232A (fr)
CA (1)	CA1209361A (fr)
DD (1)	DD211056A5 (fr)
DE (1)	DE3235612A1 (fr)
DK (1)	DK437883A (fr)
ES (1)	ES8501638A1 (fr)
IL (1)	IL69776A0 (fr)
NZ (1)	NZ205688A (fr)
ZA (1)	ZA837087B (fr)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
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ZW3486A1 (en) *	1985-03-12	1986-10-01	Bayer Ag	Macroemulsions
ZW3586A1 (en) *	1985-03-12	1986-06-11	Bayer Ag	Macroemulsions
DE3707711A1 (de) *	1987-03-11	1988-09-22	Hoechst Ag	Oel-in-wasser-emulsionen, verfahren zu deren herstellung und deren verwendung
GB8822936D0 (en) *	1988-09-30	1988-11-09	Nc Dev Inc	Pesticidal control
GB8822937D0 (en) *	1988-09-30	1988-11-09	Nc Dev Inc	Chemical formulations
WO1990003112A1 (fr) *	1987-03-30	1990-04-05	Nc Development, Inc.	Lutte antiparasitaire
CA1301642C (fr) *	1987-03-30	1992-05-26	Howard Bernard Dawson	Formulations chimiques
HU199234B (en) *	1987-05-18	1990-02-28	Chinoin Gyogyszer Es Vegyeszet	Microemulsion composition comprising phosphoric acid ester or thiophosphoric acid ester as active ingredient
US4954338A (en) *	1987-08-05	1990-09-04	Rohm And Haas Company	Microbicidal microemulsion
US6007840A (en) *	1988-09-16	1999-12-28	Novartis Ag	Pharmaceutical compositions comprising cyclosporins
KR0148748B1 (ko)	1988-09-16	1998-08-17	장 크라메르, 한스 루돌프 하우스	사이클로스포린을 함유하는 약학조성물
HU204393B (en) *	1988-12-22	1992-01-28	Chinoin Gyogyszer Es Vegyeszet	Insecticide aqouos solutions containing piretroides as active components and microemulsion compositions containing former solutions
FR2673075B1 (fr) *	1991-02-22	1998-12-31	Rhone Poulenc Chimie	Microemulsions de pyrethrouides et leur utilisation.
US6262022B1 (en)	1992-06-25	2001-07-17	Novartis Ag	Pharmaceutical compositions containing cyclosporin as the active agent
HK1004520A1 (en)	1992-05-13	1998-11-27	Novartis Ag	Ophthalmic compositions containing a cyclosporin
PT589843E (pt)	1992-09-25	2002-04-29	Novartis Ag	Composicoes farmaceuticas contendo ciclosporinas
US5444078A (en) *	1993-10-01	1995-08-22	Rohm And Haas Company	Fully water-dilutable microemulsions
SK164796A3 (en)	1994-11-03	1997-06-04	Dresden Arzneimittel	Novel cyclosporine preparation forms for oral administration of and process for producing them
GB2306965B (en)	1995-11-06	1999-09-01	American Cyanamid Co	Aqueous spray compositions
DE19544507B4 (de)	1995-11-29	2007-11-15	Novartis Ag	Cyclosporin enthaltende Präparate
SK285019B6 (sk)	1997-01-30	2006-04-06	Novartis Ag	Tvrdá želatínová tobolka
DE19752552A1 (de)	1997-11-27	1999-06-02	Hoechst Schering Agrevo Gmbh	Tensidsysteme für flüssige wässrige Zubereitungen
FR2787348B1 (fr) *	1998-12-18	2002-06-28	Arcane Ind	Micro-emulsions, procede de preparation et applications
US8328829B2 (en)	1999-08-19	2012-12-11	Covidien Lp	High capacity debulking catheter with razor edge cutting window
US7713279B2 (en)	2000-12-20	2010-05-11	Fox Hollow Technologies, Inc.	Method and devices for cutting tissue
US7708749B2 (en)	2000-12-20	2010-05-04	Fox Hollow Technologies, Inc.	Debulking catheters and methods
US6299622B1 (en)	1999-08-19	2001-10-09	Fox Hollow Technologies, Inc.	Atherectomy catheter with aligned imager
ATE499054T1 (de)	2000-12-20	2011-03-15	Fox Hollow Technologies Inc	Verkleinerungskatheter
US8246640B2 (en)	2003-04-22	2012-08-21	Tyco Healthcare Group Lp	Methods and devices for cutting tissue at a vascular location
JP4025735B2 (ja) *	2003-08-21	2007-12-26	ロームアンドハースカンパニー	水性系を処理する方法
DE102005049765A1 (de) *	2005-10-18	2007-04-19	Forschungszentrum Jülich GmbH	Verfahren zur Effizienzsteigerung von Tensiden, zur Aufweitung des Temperaturfensters, zur Unterdrückung lamellarer Mesophasen in Mikroemulsionen mittels Additiven, sowie Mikroemulsionen
US20070276419A1 (en)	2006-05-26	2007-11-29	Fox Hollow Technologies, Inc.	Methods and devices for rotating an active element and an energy emitter on a catheter
EP1891855A1 (fr) *	2006-08-05	2008-02-27	Bayer CropScience AG	Concentrés nouveaux de microémulsion
US8784440B2 (en)	2008-02-25	2014-07-22	Covidien Lp	Methods and devices for cutting tissue
JP5555242B2 (ja)	2008-10-13	2014-07-23	コヴィディエンリミテッドパートナーシップ	カテーテルシャフトを操作するデバイスおよび方法
AU2010241801B2 (en)	2009-04-29	2013-04-11	Covidien Lp	Methods and devices for cutting and abrading tissue
BRPI1010595A2 (pt)	2009-05-14	2017-05-16	Tyco Healthcare	cateteres de aterectomia facilmente limpaveis e metodos para uso
WO2011068932A1 (fr)	2009-12-02	2011-06-09	Fox Hollow Technologies, Inc.	Procédés et dispositifs de coupe de tissu
RU2520801C2 (ru)	2009-12-11	2014-06-27	ТАЙКО ХЕЛСКЕА ГРУП эЛПи	Устройство для съема материала с улучшенной эффективностью захвата и способы применения
CN102946815B (zh)	2010-06-14	2015-07-15	科维蒂恩有限合伙公司	材料移除装置
RU2539720C2 (ru)	2010-10-28	2015-01-27	Ковидиен Лп	Устройство для удаления материала и способ применения
KR101518151B1 (ko)	2010-11-11	2015-05-06	코비디엔 엘피	촬영용 가요성 디벌킹 카테터와, 사용 및 제조 방법
US8992717B2 (en)	2011-09-01	2015-03-31	Covidien Lp	Catheter with helical drive shaft and methods of manufacture
US9532844B2 (en)	2012-09-13	2017-01-03	Covidien Lp	Cleaning device for medical instrument and method of use
US9943329B2 (en)	2012-11-08	2018-04-17	Covidien Lp	Tissue-removing catheter with rotatable cutter
WO2015200702A1 (fr)	2014-06-27	2015-12-30	Covidien Lp	Dispositif de nettoyage pour cathéter, et cathéter le comprenant
US10314667B2 (en)	2015-03-25	2019-06-11	Covidien Lp	Cleaning device for cleaning medical instrument
US10292721B2 (en)	2015-07-20	2019-05-21	Covidien Lp	Tissue-removing catheter including movable distal tip
WO2018013721A1 (fr)	2016-07-12	2018-01-18	Monsanto Technology Llc	Compositions pesticides

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DE824949C (de) *	1948-11-26	1951-12-17	Bayer Ag	Emulgier- und Dispergiermittel
GB1215108A (en) *	1969-03-25	1970-12-09	Sanyo Chemical Ind Ltd	Emulsifiers and emulsifiable toxicant compositions
DE2041480C3 (de) *	1970-08-20	1974-05-02	Vyzkumny Ustav Agrochemickej Technologie, Pressburg (Tschechoslowakei)	Nichtionogene oberflächenaktive Verbindungen auf der Basis von PoIyglykoläthern benzylierter Phenole
DE2053356B2 (de) *	1970-10-30	1978-09-21	Basf Ag, 6700 Ludwigshafen	Zwei-Komponenten-Emulgatorsystem für die Formulierung von Pflanzenschutzmitteln

1982
- 1982-09-25 DE DE19823235612 patent/DE3235612A1/de not_active Withdrawn
1983
- 1983-09-14 EP EP83109051A patent/EP0107009A3/fr not_active Withdrawn
- 1983-09-20 AU AU19293/83A patent/AU1929383A/en not_active Abandoned
- 1983-09-21 IL IL69776A patent/IL69776A0/xx unknown
- 1983-09-22 NZ NZ205688A patent/NZ205688A/en unknown
- 1983-09-23 KR KR1019830004459A patent/KR840005648A/ko not_active Ceased
- 1983-09-23 BR BR8305232A patent/BR8305232A/pt unknown
- 1983-09-23 DD DD83255092A patent/DD211056A5/de unknown
- 1983-09-23 ES ES525901A patent/ES8501638A1/es not_active Expired
- 1983-09-23 CA CA000437476A patent/CA1209361A/fr not_active Expired
- 1983-09-23 DK DK437883A patent/DK437883A/da not_active Application Discontinuation
- 1983-09-23 ZA ZA837087A patent/ZA837087B/xx unknown
- 1983-09-24 JP JP58175224A patent/JPS5980321A/ja active Pending

Also Published As

Publication number	Publication date
IL69776A0 (en)	1983-12-30
AU1929383A (en)	1984-03-29
ES525901A0 (es)	1984-12-01
ZA837087B (en)	1984-05-30
ES8501638A1 (es)	1984-12-01
JPS5980321A (ja)	1984-05-09
DK437883A (da)	1984-03-26
BR8305232A (pt)	1984-05-02
DE3235612A1 (de)	1984-03-29
KR840005648A (ko)	1984-11-16
CA1209361A (fr)	1986-08-12
NZ205688A (en)	1985-08-30
DK437883D0 (da)	1983-09-23
EP0107009A2 (fr)	1984-05-02
EP0107009A3 (fr)	1985-07-10

Publication	Publication Date	Title
DD211056A5 (de)	1984-07-04	Mikroemulsionen
EP0062181B1 (fr)	1985-06-05	Emulsions du type huile dans l'eau, procédé pour leur préparation et leur utilisation
EP0297207A2 (fr)	1989-01-04	Emulsions huile-dans-l'eau, procédé de leur préparation et de leur utilisation
EP0407874B1 (fr)	1995-01-18	Agents antimoussants pour agents mouillants liquides et produits liquides peu moussants protecteurs de plantes
EP0257286B1 (fr)	1992-07-08	Microémulsions aqueuses concentrées
DE4013930A1 (de)	1990-11-08	Fluessige konzentrierte zusammensetzungen auf der basis von n-phosphonomethylglycin
DE60008125T2 (de)	2004-07-01	Pestizidformulierungen die als oberflächenaktive verbindungen phosphat-ester und alkoxylierte lignosulfonate enthalten
EP0197293B1 (fr)	1988-12-21	Macro-émulsions
WO1999008517A1 (fr)	1999-02-25	Microemulsions
DE68922097T2 (de)	1995-11-02	Pflanzenschutz-mikroemulsionszusammensetzung.
DE4108871A1 (de)	1992-09-24	Waessrige formulierung von prochloraz, ihre herstellung und ihre verwendung
EP0669800B1 (fr)	1998-09-30	Emulsions huile dans eau
EP0074329B1 (fr)	1988-09-28	Concentrés aqueux de pesticides
EP0224846A1 (fr)	1987-06-10	Emulsions aqueuses de pesticides
AT398402B (de)	1994-12-27	Wasserverdünnbares holzschutzmittelkonzentrat und daraus hergestelltes mittel zum konservieren von holz und holzwerkstoffen und verfahren zu seiner herstellung
EP0196463A1 (fr)	1986-10-08	Macro-émulsions
EP0085922B1 (fr)	1986-03-05	Agent herbicide
EP0107023A1 (fr)	1984-05-02	Formulations aqueuses homogènes
DE69626201T2 (de)	2003-10-23	Pestizide formulierungen und verfahren zur deren herstellung
EP0735815A1 (fr)	1996-10-09	Emulsions huile dans l'eau
DE69916615T2 (de)	2004-08-19	Flüssigformulierung
EP1221837B1 (fr)	2004-04-14	Nouvelles formulations liquides
DE3508642A1 (de)	1986-09-18	Makroemulsionen
DE3508643A1 (de)	1986-09-18	Makroemulsionen
EP0443405A1 (fr)	1991-08-28	Emulsions concentrées aqueuses de néophanes et azanéophanes pour l'utilisation à la protection des plantes