FI106723B - Menetelmä nanopartikkelien valmistamiseksi - Google Patents
Menetelmä nanopartikkelien valmistamiseksi Download PDFInfo
- Publication number
- FI106723B FI106723B FI935869A FI935869A FI106723B FI 106723 B FI106723 B FI 106723B FI 935869 A FI935869 A FI 935869A FI 935869 A FI935869 A FI 935869A FI 106723 B FI106723 B FI 106723B
- Authority
- FI
- Finland
- Prior art keywords
- nanoparticles
- polymer
- copolymer
- process according
- solution
- Prior art date
Links
- 239000002105 nanoparticle Substances 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims abstract description 27
- 238000002360 preparation method Methods 0.000 title claims abstract description 10
- 229920000642 polymer Polymers 0.000 claims abstract description 43
- 239000000243 solution Substances 0.000 claims abstract description 26
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims abstract description 12
- 229920001451 polypropylene glycol Polymers 0.000 claims abstract description 10
- 239000007864 aqueous solution Substances 0.000 claims abstract description 9
- 239000003960 organic solvent Substances 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 3
- 239000003223 protective agent Substances 0.000 claims abstract description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 20
- 229920001577 copolymer Polymers 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 18
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N Lactic Acid Natural products CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 235000014655 lactic acid Nutrition 0.000 claims description 5
- 239000004310 lactic acid Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 150000002012 dioxanes Chemical class 0.000 claims description 2
- 150000002576 ketones Chemical group 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 230000003381 solubilizing effect Effects 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 150000002170 ethers Chemical class 0.000 claims 1
- 238000001556 precipitation Methods 0.000 abstract description 4
- 238000000935 solvent evaporation Methods 0.000 abstract 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 13
- 239000004626 polylactic acid Substances 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 239000002245 particle Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical group CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 239000003638 chemical reducing agent Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000001376 precipitating effect Effects 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- ACTOXUHEUCPTEW-BWHGAVFKSA-N 2-[(4r,5s,6s,7r,9r,10r,11e,13e,16r)-6-[(2s,3r,4r,5s,6r)-5-[(2s,4r,5s,6s)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-10-[(2s,5s,6r)-5-(dimethylamino)-6-methyloxan-2-yl]oxy-4-hydroxy-5-methoxy-9,16-dimethyl-2-o Chemical compound O([C@H]1/C=C/C=C/C[C@@H](C)OC(=O)C[C@@H](O)[C@@H]([C@H]([C@@H](CC=O)C[C@H]1C)O[C@H]1[C@@H]([C@H]([C@H](O[C@@H]2O[C@@H](C)[C@H](O)[C@](C)(O)C2)[C@@H](C)O1)N(C)C)O)OC)[C@@H]1CC[C@H](N(C)C)[C@@H](C)O1 ACTOXUHEUCPTEW-BWHGAVFKSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 239000004187 Spiramycin Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229960001294 spiramycin Drugs 0.000 description 2
- 229930191512 spiramycin Natural products 0.000 description 2
- 235000019372 spiramycin Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5107—Excipients; Inactive ingredients
- A61K9/513—Organic macromolecular compounds; Dendrimers
- A61K9/5146—Organic macromolecular compounds; Dendrimers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides
- A61K9/5153—Polyesters, e.g. poly(lactide-co-glycolide)
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5192—Processes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/664—Polyesters containing oxygen in the form of ether groups derived from hydroxy carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/14—Powdering or granulating by precipitation from solutions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2371/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2371/02—Polyalkylene oxides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Nanotechnology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Veterinary Medicine (AREA)
- Optics & Photonics (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Preparation (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Electroluminescent Light Sources (AREA)
- Aiming, Guidance, Guns With A Light Source, Armor, Camouflage, And Targets (AREA)
- Rear-View Mirror Devices That Are Mounted On The Exterior Of The Vehicle (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9108042A FR2678178A1 (fr) | 1991-06-28 | 1991-06-28 | Procede de preparation de nanoparticules. |
| FR9108042 | 1991-06-28 | ||
| FR9200582 | 1992-01-21 | ||
| PCT/FR1992/000582 WO1993000388A1 (fr) | 1991-06-28 | 1992-06-25 | Procede de preparation de nanoparticules |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI935869A0 FI935869A0 (fi) | 1993-12-27 |
| FI935869L FI935869L (fi) | 1993-12-27 |
| FI106723B true FI106723B (fi) | 2001-03-30 |
Family
ID=9414445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI935869A FI106723B (fi) | 1991-06-28 | 1993-12-27 | Menetelmä nanopartikkelien valmistamiseksi |
Country Status (14)
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5543158A (en) * | 1993-07-23 | 1996-08-06 | Massachusetts Institute Of Technology | Biodegradable injectable nanoparticles |
| US5565215A (en) * | 1993-07-23 | 1996-10-15 | Massachusettes Institute Of Technology | Biodegradable injectable particles for imaging |
| FR2721510B1 (fr) * | 1994-06-22 | 1996-07-26 | Rhone Poulenc Rorer Sa | Nanoparticules filtrables dans des conditions stériles. |
| US6007845A (en) * | 1994-07-22 | 1999-12-28 | Massachusetts Institute Of Technology | Nanoparticles and microparticles of non-linear hydrophilic-hydrophobic multiblock copolymers |
| US5611344A (en) * | 1996-03-05 | 1997-03-18 | Acusphere, Inc. | Microencapsulated fluorinated gases for use as imaging agents |
| JPH11322948A (ja) * | 1998-05-08 | 1999-11-26 | Nof Corp | 高分子微粒子およびその製造方法 |
| DE19839212C2 (de) | 1998-08-28 | 2002-05-23 | Celanese Ventures Gmbh | Verfahren zur Herstellung von sphärischen Nanopartikeln, die ganz oder teilweise aus mindestens einem wasserunlöslichen linearen Polysaccharid bestehen |
| CA2309575A1 (en) | 2000-05-26 | 2001-11-26 | James E. Guillet | Internally cross-linked macromolecules |
| US8012457B2 (en) | 2004-06-04 | 2011-09-06 | Acusphere, Inc. | Ultrasound contrast agent dosage formulation |
| JP5398112B2 (ja) * | 2005-10-27 | 2014-01-29 | 東レ株式会社 | 生分解性粒子およびその製造方法 |
| FR2936722B1 (fr) * | 2008-10-07 | 2013-11-22 | Nanolege Inc | Materiaux nanocomposites et procede de fabrication par nanoprecipitation. |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8416234D0 (en) * | 1984-06-26 | 1984-08-01 | Ici Plc | Biodegradable amphipathic copolymers |
| FR2608988B1 (fr) * | 1986-12-31 | 1991-01-11 | Centre Nat Rech Scient | Procede de preparation de systemes colloidaux dispersibles d'une substance, sous forme de nanoparticules |
-
1991
- 1991-06-28 FR FR9108042A patent/FR2678178A1/fr active Granted
-
1992
- 1992-06-25 DK DK92913337.9T patent/DK0591331T3/da active
- 1992-06-25 CA CA002102185A patent/CA2102185C/fr not_active Expired - Lifetime
- 1992-06-25 EP EP92401789A patent/EP0520889A1/fr active Pending
- 1992-06-25 ES ES92913337T patent/ES2084363T3/es not_active Expired - Lifetime
- 1992-06-25 WO PCT/FR1992/000582 patent/WO1993000388A1/fr active IP Right Grant
- 1992-06-25 JP JP50136793A patent/JP3228742B2/ja not_active Expired - Lifetime
- 1992-06-25 MX MX9203354A patent/MX9203354A/es unknown
- 1992-06-25 DE DE69209074T patent/DE69209074T2/de not_active Expired - Lifetime
- 1992-06-25 EP EP92913337A patent/EP0591331B1/fr not_active Expired - Lifetime
- 1992-06-25 AT AT92913337T patent/ATE135385T1/de active
- 1992-07-01 IE IE922109A patent/IE72509B1/en not_active IP Right Cessation
-
1993
- 1993-12-01 NO NO934359A patent/NO308313B1/no not_active IP Right Cessation
- 1993-12-27 FI FI935869A patent/FI106723B/fi not_active IP Right Cessation
-
1996
- 1996-03-14 GR GR950403440T patent/GR3019308T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX9203354A (es) | 1992-12-01 |
| FI935869A0 (fi) | 1993-12-27 |
| WO1993000388A1 (fr) | 1993-01-07 |
| FI935869L (fi) | 1993-12-27 |
| NO934359L (no) | 1993-12-01 |
| EP0520889A1 (fr) | 1992-12-30 |
| JP3228742B2 (ja) | 2001-11-12 |
| EP0591331A1 (fr) | 1994-04-13 |
| DE69209074D1 (de) | 1996-04-18 |
| NO934359D0 (no) | 1993-12-01 |
| DK0591331T3 (da) | 1996-04-01 |
| ATE135385T1 (de) | 1996-03-15 |
| JPH06508867A (ja) | 1994-10-06 |
| CA2102185C (fr) | 2003-07-22 |
| FR2678178B1 (enrdf_load_stackoverflow) | 1995-01-13 |
| FR2678178A1 (fr) | 1992-12-31 |
| IE922109A1 (en) | 1992-12-30 |
| NO308313B1 (no) | 2000-08-28 |
| EP0591331B1 (fr) | 1996-03-13 |
| CA2102185A1 (fr) | 1992-12-29 |
| ES2084363T3 (es) | 1996-05-01 |
| DE69209074T2 (de) | 1996-09-05 |
| IE72509B1 (en) | 1997-04-23 |
| GR3019308T3 (en) | 1996-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FI109576B (fi) | Nanopartikkeleita, joilla on retikuloendoteelijärjestelmän toimesta pidentynyt sieppausaika | |
| US5766635A (en) | Process for preparing nanoparticles | |
| FI106723B (fi) | Menetelmä nanopartikkelien valmistamiseksi | |
| JP3523821B2 (ja) | 薬物が封入されたポリマーミセルの製造方法および該ポリマーミセル組成物 | |
| EP1279682B1 (en) | Amphiphilic biodegradable block copolymers and self-assembled polymer aggregates formed from the same in aqueous milieu | |
| Gao et al. | Synthesis of a biodegradable tadpole-shaped polymer via the coupling reaction of polylactide onto mono (6-(2-aminoethyl) amino-6-deoxy)-β-cyclodextrin and its properties as the new carrier of protein delivery system | |
| IE83404B1 (en) | Polyethylene-polylactic acid block copolymer nanoparticles | |
| US20040138095A1 (en) | Colloidal suspension of nanoparticles based on an amphiphilic copolymer | |
| Vandorpe et al. | Long circulating biodegradable poly (phosphazene) nanoparticles surface modified with poly (phosphazene)-poly (ethylene oxide) copolymer | |
| SK26096A3 (en) | Contrasting agent, method of manufacture thereof and application | |
| EA036522B1 (ru) | Фармацевтическая композиция, пригодная для лиофилизации, содержащая множество терапевтических частиц | |
| PL173254B1 (pl) | Środek farmaceutyczny w postaci koloidalnej zawiesiny nanokapsułek i sposób wytwarzania środka farmaceutycznego w postaci koloidalnej zawiesiny nanokapsułek | |
| JP2000507934A (ja) | 有効成分の担体として使用できる複合ゲル微粒子、その製造法、およびその使用 | |
| US20100247654A1 (en) | Stable micelles formed with diblock copolymers of critical micelle concentration copolymer and temperature-sensitive copolymer | |
| US20040048782A1 (en) | Colloidal suspension of submicronic particles for carrying hydrophilic active principles (insulin) and method for preparing same | |
| KR20040021760A (ko) | 약물 담지능력이 우수한 블록 공중합체 미셀 조성물 | |
| US20100254939A1 (en) | Graft copolymers as drug delivery systems | |
| US20050043481A1 (en) | Material consisting of at least a biodegradable polymer and cyclodextrins | |
| CN103739852B (zh) | mPEG接枝α-玉米醇溶蛋白聚合物及其制备方法 | |
| Leiske et al. | Mission ImPOxable–or the unknown utilization of non-toxic poly (2-oxazoline) s as cryoprotectants and surfactants at the same time | |
| JP2020512448A (ja) | ポリ（オキサゾリン）安定化剤を含有する有機ポリマー粒子および有機ポリマー粒子の安定化のためのポリ（オキサゾリン）の使用 | |
| KR102688912B1 (ko) | pH 반응성 마이크로 입자 및 이를 이용한 암질환 치료용 약학 조성물 | |
| KR100987693B1 (ko) | 폴리(에틸렌 글리콜)-ｂ-[폴리(Ｌ-세린)-ｇ-폴리(Ｄ,Ｌ-락티드)]의 블록공중합체 및 이를 이용한 약물전달체용 나노입자의 제조 방법 | |
| KR100261466B1 (ko) | 생분해성나노파티클및이의제조방법 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MA | Patent expired |