JPS6447381A - Preparation of liposome containing sealed gene - Google Patents
Preparation of liposome containing sealed geneInfo
- Publication number
- JPS6447381A JPS6447381A JP20418387A JP20418387A JPS6447381A JP S6447381 A JPS6447381 A JP S6447381A JP 20418387 A JP20418387 A JP 20418387A JP 20418387 A JP20418387 A JP 20418387A JP S6447381 A JPS6447381 A JP S6447381A
- Authority
- JP
- Japan
- Prior art keywords
- gene
- liposome
- dna
- preparation
- reverse
- 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
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
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
-
- 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
- A61K9/127—Liposomes
- A61K9/1277—Processes for preparing; Proliposomes
-
- 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
- C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
- C12N15/88—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation using microencapsulation, e.g. using amphiphile liposome vesicle
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Wood Science & Technology (AREA)
- General Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Biotechnology (AREA)
- Zoology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Plant Pathology (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
Abstract
PURPOSE:To enable removal of microbial cells with a 0.45mum filter, by adding a polyhydric alcohol at a latter stage of a gene-inclusion process using a reverse- phase evaporation method, thereby efficiently including a DNA in a liposome having a diameter of <=450nm. CONSTITUTION:In the production of a gene-including liposome by a reverse- phase evaporation method, a polyhydric alcohol such as glycerol or ethylene glycol is added at the latter stage of the gene-inclusion process. The liposome suspension obtained by the above process is treated with a Nuclepore filter having an average pore size of 400nm to obtain liposomes composed mainly of those having diameter of 100-400nm. The gene to be included by this process may be a DNA or a recombinant DNA.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20418387A JP2627899B2 (en) | 1987-08-19 | 1987-08-19 | Production method of gene-encapsulated liposome |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20418387A JP2627899B2 (en) | 1987-08-19 | 1987-08-19 | Production method of gene-encapsulated liposome |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6447381A true JPS6447381A (en) | 1989-02-21 |
JP2627899B2 JP2627899B2 (en) | 1997-07-09 |
Family
ID=16486211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20418387A Expired - Lifetime JP2627899B2 (en) | 1987-08-19 | 1987-08-19 | Production method of gene-encapsulated liposome |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2627899B2 (en) |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5589466A (en) * | 1989-03-21 | 1996-12-31 | Vical Incorporated | Induction of a protective immune response in a mammal by injecting a DNA sequence |
US5693622A (en) * | 1989-03-21 | 1997-12-02 | Vical Incorporated | Expression of exogenous polynucleotide sequences cardiac muscle of a mammal |
JP2001502299A (en) * | 1996-09-13 | 2001-02-20 | リポゼン リミテッド | Liposome |
US6214804B1 (en) | 1989-03-21 | 2001-04-10 | Vical Incorporated | Induction of a protective immune response in a mammal by injecting a DNA sequence |
US6228844B1 (en) | 1991-11-12 | 2001-05-08 | Vical Incorporated | Stimulating vascular growth by administration of DNA sequences encoding VEGF |
US6413942B1 (en) | 1989-03-21 | 2002-07-02 | Vical, Inc. | Methods of delivering a physiologically active polypeptide to a mammal |
WO2002079447A2 (en) | 2001-03-30 | 2002-10-10 | Avigenics, Inc. | Avian lysozyme promoter |
US6706694B1 (en) | 1990-03-21 | 2004-03-16 | Vical Incorporated | Expression of exogenous polynucleotide sequences in a vertebrate |
WO2004064750A2 (en) | 2003-01-22 | 2004-08-05 | Duke University | Improved constructs for expressing lysosomal polypeptides |
US6867195B1 (en) | 1989-03-21 | 2005-03-15 | Vical Incorporated | Lipid-mediated polynucleotide administration to reduce likelihood of subject's becoming infected |
WO2006017673A2 (en) | 2004-08-03 | 2006-02-16 | Biogen Idec Ma Inc. | Taj in neuronal function |
WO2006081331A2 (en) | 2005-01-25 | 2006-08-03 | Prolexys Pharmaceuticals, Inc. | Quinoxaline derivatives as antitumor agents |
US7384923B2 (en) | 1999-05-14 | 2008-06-10 | Lipoxen Technologies Limited | Liposomes |
EP1997829A1 (en) | 2001-12-21 | 2008-12-03 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2206720A1 (en) | 2000-04-12 | 2010-07-14 | Human Genome Sciences, Inc. | Albumin fusion proteins |
WO2010096388A2 (en) | 2009-02-18 | 2010-08-26 | Carnegie Mellon University | Quenched dendrimeric dyes for bright detection |
EP2314692A2 (en) | 2003-06-02 | 2011-04-27 | University of Massachusetts | Methods and compositions for enhancing the efficacy and specificity of RNAi |
EP2345720A2 (en) | 2001-07-12 | 2011-07-20 | University of Massachusetts | In vivo production of small interfering RNAs that mediate gene silencing |
WO2011150079A1 (en) | 2010-05-25 | 2011-12-01 | Carnegie Mellon University | Targeted probes of cellular physiology |
EP2441474A1 (en) | 2003-10-17 | 2012-04-18 | Joslin Diabetes Center, Inc. | Methods and compositions for modulating adipocyte function |
EP2629094A1 (en) | 2007-01-24 | 2013-08-21 | Carnegie Mellon University | Optical biosensors |
EP2769732A1 (en) | 2013-02-22 | 2014-08-27 | Sanofi | Serpins: methods of therapeutic beta-cell regeneration and function |
WO2014128257A1 (en) | 2013-02-22 | 2014-08-28 | Sanofi | Serpins: methods of therapeutic beta-cell regeneration and function |
EP2851086A1 (en) | 2013-09-20 | 2015-03-25 | Sanofi | Serpins: methods of therapeutic ß-cell regeneration and function |
WO2017147128A1 (en) | 2016-02-22 | 2017-08-31 | The University Of North Carolina At Chapel Hill | Peptide inhibitors of calcium channels |
US10434177B2 (en) | 2014-11-17 | 2019-10-08 | Carnegie Mellon University | Activatable two-component photosensitizers |
-
1987
- 1987-08-19 JP JP20418387A patent/JP2627899B2/en not_active Expired - Lifetime
Cited By (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6673776B1 (en) | 1989-03-21 | 2004-01-06 | Vical Incorporated | Expression of exogenous polynucleotide sequences in a vertebrate, mammal, fish, bird or human |
US6413942B1 (en) | 1989-03-21 | 2002-07-02 | Vical, Inc. | Methods of delivering a physiologically active polypeptide to a mammal |
US5703055A (en) * | 1989-03-21 | 1997-12-30 | Wisconsin Alumni Research Foundation | Generation of antibodies through lipid mediated DNA delivery |
US6867195B1 (en) | 1989-03-21 | 2005-03-15 | Vical Incorporated | Lipid-mediated polynucleotide administration to reduce likelihood of subject's becoming infected |
US6214804B1 (en) | 1989-03-21 | 2001-04-10 | Vical Incorporated | Induction of a protective immune response in a mammal by injecting a DNA sequence |
US6710035B2 (en) | 1989-03-21 | 2004-03-23 | Vical Incorporated | Generation of an immune response to a pathogen |
US5693622A (en) * | 1989-03-21 | 1997-12-02 | Vical Incorporated | Expression of exogenous polynucleotide sequences cardiac muscle of a mammal |
US5589466A (en) * | 1989-03-21 | 1996-12-31 | Vical Incorporated | Induction of a protective immune response in a mammal by injecting a DNA sequence |
US6706694B1 (en) | 1990-03-21 | 2004-03-16 | Vical Incorporated | Expression of exogenous polynucleotide sequences in a vertebrate |
US6228844B1 (en) | 1991-11-12 | 2001-05-08 | Vical Incorporated | Stimulating vascular growth by administration of DNA sequences encoding VEGF |
EP1254657A2 (en) * | 1996-09-13 | 2002-11-06 | Lipoxen Technologies Limited | Liposomes |
US7790696B2 (en) | 1996-09-13 | 2010-09-07 | Lipoxen Technologies Limited | Cationic liposomes containing immune response generating moieties |
JP2001502299A (en) * | 1996-09-13 | 2001-02-20 | リポゼン リミテッド | Liposome |
US7384923B2 (en) | 1999-05-14 | 2008-06-10 | Lipoxen Technologies Limited | Liposomes |
EP2206720A1 (en) | 2000-04-12 | 2010-07-14 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2357008A1 (en) | 2000-04-12 | 2011-08-17 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2311872A1 (en) | 2000-04-12 | 2011-04-20 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2295456A1 (en) | 2000-04-12 | 2011-03-16 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2213743A1 (en) | 2000-04-12 | 2010-08-04 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2216409A1 (en) | 2000-04-12 | 2010-08-11 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2298355A2 (en) | 2000-04-12 | 2011-03-23 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2236152A1 (en) | 2000-04-12 | 2010-10-06 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2267026A1 (en) | 2000-04-12 | 2010-12-29 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2275557A1 (en) | 2000-04-12 | 2011-01-19 | Human Genome Sciences, Inc. | Albumin fusion proteins |
WO2002079447A2 (en) | 2001-03-30 | 2002-10-10 | Avigenics, Inc. | Avian lysozyme promoter |
EP2345720A2 (en) | 2001-07-12 | 2011-07-20 | University of Massachusetts | In vivo production of small interfering RNAs that mediate gene silencing |
EP2360251A2 (en) | 2001-07-12 | 2011-08-24 | University of Massachusetts | In vivo production of small interfering RNAs that mediate gene silencing |
EP2261250A1 (en) | 2001-12-21 | 2010-12-15 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2277888A2 (en) | 2001-12-21 | 2011-01-26 | Human Genome Sciences, Inc. | Fusion proteins of albumin and erythropoietin |
EP2277910A1 (en) | 2001-12-21 | 2011-01-26 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP1997829A1 (en) | 2001-12-21 | 2008-12-03 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP2277889A2 (en) | 2001-12-21 | 2011-01-26 | Human Genome Sciences, Inc. | Fusion proteins of albumin and interferon beta |
WO2004064750A2 (en) | 2003-01-22 | 2004-08-05 | Duke University | Improved constructs for expressing lysosomal polypeptides |
US9873868B2 (en) | 2003-01-22 | 2018-01-23 | Duke University | Constructs for expressing lysosomal polypeptides |
EP2314692A2 (en) | 2003-06-02 | 2011-04-27 | University of Massachusetts | Methods and compositions for enhancing the efficacy and specificity of RNAi |
EP2441474A1 (en) | 2003-10-17 | 2012-04-18 | Joslin Diabetes Center, Inc. | Methods and compositions for modulating adipocyte function |
EP2329714A1 (en) | 2004-08-03 | 2011-06-08 | Biogen Idec MA Inc. | Influence of TAJ in the neuronal functions |
WO2006017673A2 (en) | 2004-08-03 | 2006-02-16 | Biogen Idec Ma Inc. | Taj in neuronal function |
WO2006081331A2 (en) | 2005-01-25 | 2006-08-03 | Prolexys Pharmaceuticals, Inc. | Quinoxaline derivatives as antitumor agents |
EP2629094A1 (en) | 2007-01-24 | 2013-08-21 | Carnegie Mellon University | Optical biosensors |
WO2010096388A2 (en) | 2009-02-18 | 2010-08-26 | Carnegie Mellon University | Quenched dendrimeric dyes for bright detection |
WO2011150079A1 (en) | 2010-05-25 | 2011-12-01 | Carnegie Mellon University | Targeted probes of cellular physiology |
US9995679B2 (en) | 2010-05-25 | 2018-06-12 | Carnegie Mellon University | Targeted probes of cellular physiology |
WO2014128257A1 (en) | 2013-02-22 | 2014-08-28 | Sanofi | Serpins: methods of therapeutic beta-cell regeneration and function |
EP2769732A1 (en) | 2013-02-22 | 2014-08-27 | Sanofi | Serpins: methods of therapeutic beta-cell regeneration and function |
EP2851086A1 (en) | 2013-09-20 | 2015-03-25 | Sanofi | Serpins: methods of therapeutic ß-cell regeneration and function |
US10434177B2 (en) | 2014-11-17 | 2019-10-08 | Carnegie Mellon University | Activatable two-component photosensitizers |
US10946098B2 (en) | 2014-11-17 | 2021-03-16 | Carnegie Mellon University | Activatable two-component photosensitizers |
WO2017147128A1 (en) | 2016-02-22 | 2017-08-31 | The University Of North Carolina At Chapel Hill | Peptide inhibitors of calcium channels |
Also Published As
Publication number | Publication date |
---|---|
JP2627899B2 (en) | 1997-07-09 |
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