DE2154277A1 - Verfahren zum teilweisen Abbau von Desoxyribonucleinsäure - Google Patents
Verfahren zum teilweisen Abbau von DesoxyribonucleinsäureInfo
- Publication number
- DE2154277A1 DE2154277A1 DE19712154277 DE2154277A DE2154277A1 DE 2154277 A1 DE2154277 A1 DE 2154277A1 DE 19712154277 DE19712154277 DE 19712154277 DE 2154277 A DE2154277 A DE 2154277A DE 2154277 A1 DE2154277 A1 DE 2154277A1
- Authority
- DE
- Germany
- Prior art keywords
- deoxyribonucleic acid
- solution
- viscosity
- partial degradation
- proton
- 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.)
- Granted
Links
- 108020004414 DNA Proteins 0.000 title claims description 18
- 102000053602 DNA Human genes 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 15
- 230000015556 catabolic process Effects 0.000 title claims description 7
- 238000006731 degradation reaction Methods 0.000 title claims description 6
- 150000001447 alkali salts Chemical class 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 8
- 210000001557 animal structure Anatomy 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003456 ion exchange resin Substances 0.000 claims description 2
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 2
- 239000001632 sodium acetate Substances 0.000 claims description 2
- 235000017281 sodium acetate Nutrition 0.000 claims description 2
- 239000002244 precipitate Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 4
- ASJSAQIRZKANQN-CRCLSJGQSA-N 2-deoxy-D-ribose Chemical compound OC[C@@H](O)[C@@H](O)CC=O ASJSAQIRZKANQN-CRCLSJGQSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000003480 fibrinolytic effect Effects 0.000 description 3
- 102000039446 nucleic acids Human genes 0.000 description 3
- 108020004707 nucleic acids Proteins 0.000 description 3
- 150000007523 nucleic acids Chemical class 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 108091034117 Oligonucleotide Proteins 0.000 description 2
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 230000009089 cytolysis Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000010936 aqueous wash Methods 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 239000003527 fibrinolytic agent Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 239000002773 nucleotide Substances 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1003—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Biophysics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Analytical Chemistry (AREA)
- Veterinary Medicine (AREA)
- Plant Pathology (AREA)
- Physics & Mathematics (AREA)
- Microbiology (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT31308/70A IT1043823B (it) | 1970-11-03 | 1970-11-03 | Procedimento per l estrazione di acidi nucleici da organi animali |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2154277A1 true DE2154277A1 (de) | 1972-05-25 |
| DE2154277C2 DE2154277C2 (OSRAM) | 1988-04-07 |
Family
ID=11233430
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712154277 Granted DE2154277A1 (de) | 1970-11-03 | 1971-10-30 | Verfahren zum teilweisen Abbau von Desoxyribonucleinsäure |
| DE19712154278 Pending DE2154278A1 (de) | 1970-11-03 | 1971-10-30 | Verfahren zur Extraktion von Alkalisalzen von Desoxyribonucleinsäure aus tierischen Organen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712154278 Pending DE2154278A1 (de) | 1970-11-03 | 1971-10-30 | Verfahren zur Extraktion von Alkalisalzen von Desoxyribonucleinsäure aus tierischen Organen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3770720A (OSRAM) |
| JP (1) | JPS5229320B1 (OSRAM) |
| DE (2) | DE2154277A1 (OSRAM) |
| FR (2) | FR2131249A5 (OSRAM) |
| GB (2) | GB1367656A (OSRAM) |
| IT (1) | IT1043823B (OSRAM) |
| SE (2) | SE385902B (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4699930A (en) * | 1982-10-12 | 1987-10-13 | Kazuo Suga | Cosmetic composition |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0107161B1 (de) * | 1982-10-26 | 1989-08-09 | CTA Finanz AG | Mittel und Verfahren zur Optimierung der Gewebemasse von Organen innerhalb der genetischen Schwankungsbreite bei Menschen und Tieren |
| IT1170214B (it) * | 1983-09-12 | 1987-06-03 | Crinos Industria Farmaco | Composizione farmaceutica per la cura delle arteriopatie periferiche |
| IT1170215B (it) * | 1983-09-12 | 1987-06-03 | Crinos Industria Farmaco | Composizione farmaceutica per il trattamento di stati di insufficienza renale acuta |
| IT1206341B (it) * | 1984-02-16 | 1989-04-14 | Crinos Industria Farmaco | Composizione farmaceutica per il trattamento dell'ischemia acuta del miocardio. |
| IT1187833B (it) * | 1985-12-12 | 1987-12-23 | Farmigea Spa | Procedimento per l ottenimento di polidesossiribonucleotidi non informazionali sostanzialmente puri e dotati di attivita biologiche e prodotto relativo |
| IT1190313B (it) * | 1986-04-17 | 1988-02-16 | Crinos Industria Farmaco | Procedimento per l'ottenimento di polidesossiribonucleotidi chimicamente definiti e riproducibili e prodotto farmacologicamente attivo risultante |
| IT1212143B (it) | 1987-06-26 | 1989-11-08 | Crinos Industria Farmaco | Composizione ad attivita'tricogena. |
| IT1222701B (it) * | 1987-09-23 | 1990-09-12 | Crinos Industria Farmaco | Composizione ad uso topico avente attivita' tricogena,antiforfora ed antiseborroica |
| IT1223322B (it) * | 1987-10-23 | 1990-09-19 | Crinos Industria Farmaco | Metodo per prevenire la formazione di coaguli sanguigni nel circuito extracorporeo di apparecchi di dialisi a composizione utile per esso |
| IT1231509B (it) * | 1989-09-07 | 1991-12-07 | Crinos Industria Farmaco | Composizione farmceutica ad uso topico per la terapia della fragilita' capillare. |
| US5977083A (en) * | 1991-08-21 | 1999-11-02 | Burcoglu; Arsinur | Method for using polynucleotides, oligonucleotides and derivatives thereof to treat various disease states |
| US6699985B2 (en) * | 1991-08-21 | 2004-03-02 | Arsinur Burcoglu | Method of treating HIV infection and related secondary infections thereof |
| IT1252174B (it) * | 1991-12-09 | 1995-06-05 | Crinos Industria Farmaco | Oligodesossimibonucleotidi ad attivita' antiischemica e procedimenti per il loro ottenimento |
| US7683035B1 (en) | 1999-02-23 | 2010-03-23 | Qiagen, Gmbh | Method of stabilizing and/or isolating nucleic acids |
| EP1059092B1 (en) | 1999-06-08 | 2005-12-07 | Gentium S.p.A. | Use of complexes among cationic liposomes and polydeoxyribonucleotides as medicaments |
| US6323743B1 (en) * | 1999-08-24 | 2001-11-27 | Tresness Irrevocable Patent Trust | Electronic filter assembly |
| US8771663B2 (en) * | 2000-04-18 | 2014-07-08 | Gentium Spa | Formulation having mobilising activity |
| EP1147777A1 (en) | 2000-04-18 | 2001-10-24 | Crinos Industria Farmacobiologica S.p.A. | Combination of defibrotide and G-CSF and its use to activate haematopoietic progenitors |
| ITMI20031714A1 (it) * | 2003-09-05 | 2005-03-06 | Gentium Spa | Formazioni ad azione antitumorale. |
| MX2007010754A (es) * | 2005-03-03 | 2007-11-07 | Gentium Spa | Defibrotide y/u oligodeoxiribonucleotidos para tratar tumores dependientes de angiogenesis. |
| EP1872787A1 (en) * | 2006-06-27 | 2008-01-02 | Gentium S.p.A. | Use of defibrotide for the inhibition of heparanase |
| EP1982722A1 (en) * | 2007-04-16 | 2008-10-22 | Gentium S.p.A. | Use of oligotide for the treatment of renal diseases |
| EP2103689A1 (en) * | 2008-03-19 | 2009-09-23 | Gentium S.p.A. | Synthetic phosphodiester oligonucleotides and therapeutical uses thereof |
| CN107007617A (zh) | 2010-11-12 | 2017-08-04 | 真蒂奥姆责任有限公司 | 去纤维蛋白多核苷酸用于预防和/或治疗移植物抗宿主病(gvhd) |
| CA2874960C (en) | 2012-06-22 | 2021-05-18 | Gentium S.P.A. | Euglobulin-based method for determining the biological activity of defibrotide |
| EP3026122A1 (en) | 2014-11-27 | 2016-06-01 | Gentium S.p.A. | Cellular-based method for determining the potency of defibrotide |
| EP3661484A1 (en) | 2017-08-03 | 2020-06-10 | Jazz Pharmaceuticals Ireland Limited | Formulations comprising a nucleic acid in a high concentration |
| WO2019200251A1 (en) | 2018-04-12 | 2019-10-17 | Jazz Pharmaceuticals, Inc. | Defibrotide for the prevention and treatment of cytokine release syndrome and neurotoxicity associated with immunodepletion |
| US20220023533A1 (en) | 2018-12-07 | 2022-01-27 | Jazz Phrmaceticals Ireland Limited | Subcutaneous delivery of high concentration formulations |
| EP4110287A1 (en) | 2020-02-28 | 2023-01-04 | Jazz Pharmaceuticals Ireland Limited | Delivery of low viscosity formulations |
| US20230086833A1 (en) | 2020-04-17 | 2023-03-23 | Jazz Pharmaceuticals Ireland Limited | Defibrotide treatment for the prevention of organ rejection and injury |
| WO2022234101A1 (en) | 2021-05-06 | 2022-11-10 | Jazz Pharmaceuticals Ireland Limited | Defibrotide for the treatment and prevention of acute respiratory distress syndrome |
-
1970
- 1970-11-03 IT IT31308/70A patent/IT1043823B/it active
-
1971
- 1971-10-29 SE SE7113830A patent/SE385902B/xx unknown
- 1971-10-29 SE SE7113831A patent/SE385376B/xx unknown
- 1971-10-30 DE DE19712154277 patent/DE2154277A1/de active Granted
- 1971-10-30 DE DE19712154278 patent/DE2154278A1/de active Pending
- 1971-11-02 FR FR7139257A patent/FR2131249A5/fr not_active Expired
- 1971-11-02 FR FR7139256A patent/FR2131248A5/fr not_active Expired
- 1971-11-02 US US00194919A patent/US3770720A/en not_active Expired - Lifetime
- 1971-11-03 GB GB5104871A patent/GB1367656A/en not_active Expired
- 1971-11-03 GB GB5104771A patent/GB1366647A/en not_active Expired
- 1971-11-04 JP JP46087235A patent/JPS5229320B1/ja active Pending
Non-Patent Citations (3)
| Title |
|---|
| Methods in Enzymology, Vol.XII, Part B, 1968, S.97-99 * |
| Z.Naturf. 23b, 1968, S.11176-1183 * |
| Z.Naturf. 24b, 1969, S.106-109 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4699930A (en) * | 1982-10-12 | 1987-10-13 | Kazuo Suga | Cosmetic composition |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2131249A5 (OSRAM) | 1972-11-10 |
| DE2154278A1 (de) | 1972-05-25 |
| SE385376B (sv) | 1976-06-28 |
| DE2154277C2 (OSRAM) | 1988-04-07 |
| GB1366647A (en) | 1974-09-11 |
| SE385902B (sv) | 1976-07-26 |
| IT1043823B (it) | 1980-02-29 |
| GB1367656A (en) | 1974-09-18 |
| US3770720A (en) | 1973-11-06 |
| JPS5229320B1 (OSRAM) | 1977-08-01 |
| FR2131248A5 (OSRAM) | 1972-11-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2154277C2 (OSRAM) | ||
| DE68917009T2 (de) | Sulfaminoderivate von Chondroitinsulfat, Dermatansulfat und Hyaluronsäure und ihre pharmakologischen Eigenschaften. | |
| DE3118588C2 (de) | Verfahren zur Herstellung eines injizierbaren hochreinen Chondroitinpolysulfates, hiernach erhältliches Produkt und pharmazeutische Zusammensetzung | |
| DE2834702C2 (OSRAM) | ||
| DE2604481C2 (OSRAM) | ||
| DE3689375T2 (de) | Verfahren zur Herstellung von substantiell reinen nicht für Transpiration geeigneten Polydesoxyribonukleotiden mit biologischen Aktivitäten und respektives Produkt. | |
| DE1443665A1 (de) | Komplex Eisen-hydriertes Dextran und Herstellungsverfahren hierfuer | |
| DE2133572C2 (de) | Verfahren zur Herstellung von Pektinen mit einem Methoxylgehalt von etwa 4,5 bis 7% und einem Molekulargewicht von mindestens 120 000 | |
| DE602004007784T2 (de) | Verfahren zur herstellung von heparin in fester form | |
| DE1642612A1 (de) | Die Verwendung von Erythrozyten zur Gewinnung bzw.Isolierung eines Plasminogen-Aktivators | |
| DE938502C (de) | Verfahren zur Herstellung einer kolloidalen Eisenzubereitung | |
| DE2806515A1 (de) | Amorphes heparin-natrium und verfahren zu dessen herstellung | |
| DE916848C (de) | Verfahren zur Herstellung von Dextran-Produkten fuer pharmazeutische und therapeutische Praeparate | |
| DE1908353C3 (de) | Verfahren zur Herstellung von Amylopektinsulfaten | |
| DE720109C (de) | Verfahren zur Herstellung einer hochkonzentrierten Loesung eines stabilen Hochviskosen, teilweise verseiften Celluloseacetats | |
| DE1768362A1 (de) | Dextranderivat und Verfahren zu seiner Herstellung | |
| DE936594C (de) | Verfahren zur Herstellung von Dextranabbauprodukten fuer pharmazeutische Zwecke | |
| DE711886C (de) | Verfahren zur Herstellung plastischer Massen | |
| DE660752C (de) | Verfahren zur Herstellung eines mit Wasser leicht ausziehbares Pektin enthaltenden Praeparates | |
| DE1595865A1 (de) | Nicotindextran- und carboxylierte Methyldextran-Ester und Verfahren zur Herstellung derselben | |
| DE935843C (de) | Verfahren zur Herstellung eines blutgerinnungshemmenden Mittels | |
| AT155811B (de) | Verfahren zur fortlaufenden Herstellung von gebrauchsfertigem Polyvinylchlorid. | |
| AT114021B (de) | Verfahren zur Behandlung von Cellulosederivative enthaltender Essigsäure. | |
| AT70784B (de) | Verfahren zur Herstellung von Gallussäure aus Galläpfeln. | |
| DE1242202B (de) | Verfahren zur Herstellung von antilipaemisch wirksamen Alkalisalzen von Dextranschwefelsaeureestern |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8127 | New person/name/address of the applicant |
Owner name: CRINOS INDUSTRIA FARMACOBIOLOGIA S.P.A., VILLA GUA |
|
| 8128 | New person/name/address of the agent |
Representative=s name: SCHOENWALD, K., DR.-ING. FUES, J., DIPL.-CHEM. DR. |
|
| 8125 | Change of the main classification |
Ipc: A61K 31/70 |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition |