ZA200809725B - Preparation of antibody-or antibody-fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof - Google Patents
Preparation of antibody-or antibody-fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereofInfo
- Publication number
- ZA200809725B ZA200809725B ZA2008/09725A ZA200809725A ZA200809725B ZA 200809725 B ZA200809725 B ZA 200809725B ZA 2008/09725 A ZA2008/09725 A ZA 2008/09725A ZA 200809725 A ZA200809725 A ZA 200809725A ZA 200809725 B ZA200809725 B ZA 200809725B
- Authority
- ZA
- South Africa
- Prior art keywords
- antibody
- fragment
- therapeutic
- preparation
- systemic administration
- Prior art date
Links
- 239000000032 diagnostic agent Substances 0.000 title 1
- 229940039227 diagnostic agent Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 238000007910 systemic administration Methods 0.000 title 1
- 229940124597 therapeutic agent Drugs 0.000 title 1
- 230000001225 therapeutic effect Effects 0.000 title 1
Classifications
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- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/42—Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
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- 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
- A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A—HUMAN NECESSITIES
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
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- A61K47/6843—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a material from animals or humans
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- A61K47/6905—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a colloid or an emulsion
- A61K47/6911—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a colloid or an emulsion the form being a liposome
- A61K47/6913—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a colloid or an emulsion the form being a liposome the liposome being modified on its surface by an antibody
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- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/18—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes
- A61K49/1806—Suspensions, emulsions, colloids, dispersions
- A61K49/1812—Suspensions, emulsions, colloids, dispersions liposomes, polymersomes, e.g. immunoliposomes
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- A61K9/127—Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
- A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes or liposomes coated or grafted with polymers
- A61K9/1272—Non-conventional liposomes, e.g. PEGylated liposomes or liposomes coated or grafted with polymers comprising non-phosphatidyl surfactants as bilayer-forming substances, e.g. cationic lipids or non-phosphatidyl liposomes coated or grafted with polymers
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Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Dispersion Chemistry (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Neurosurgery (AREA)
- Virology (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Biophysics (AREA)
- Dermatology (AREA)
- Radiology & Medical Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Zoology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Inorganic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- AIDS & HIV (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80016306P | 2006-05-15 | 2006-05-15 | |
| US84435206P | 2006-09-14 | 2006-09-14 | |
| PCT/US2007/011407 WO2007142781A1 (en) | 2006-05-15 | 2007-05-11 | Preparation of antibody or an antibody fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200809725B true ZA200809725B (en) | 2010-02-24 |
Family
ID=38801787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA2008/09725A ZA200809725B (en) | 2006-05-15 | 2008-11-14 | Preparation of antibody-or antibody-fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US9034330B2 (OSRAM) |
| EP (1) | EP2023897A4 (OSRAM) |
| JP (1) | JP2009537526A (OSRAM) |
| KR (2) | KR20140135267A (OSRAM) |
| AU (1) | AU2007257357B2 (OSRAM) |
| CA (1) | CA2652222A1 (OSRAM) |
| IL (1) | IL195216A (OSRAM) |
| MX (1) | MX2008014362A (OSRAM) |
| WO (1) | WO2007142781A1 (OSRAM) |
| ZA (1) | ZA200809725B (OSRAM) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9034330B2 (en) * | 1999-02-22 | 2015-05-19 | Georgetown University | Preparation of antibody or an antibody fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof |
| US8450302B2 (en) * | 2002-08-02 | 2013-05-28 | Ab Science | 2-(3-aminoaryl) amino-4-aryl-thiazoles and their use as c-kit inhibitors |
| KR20140038288A (ko) | 2012-09-19 | 2014-03-28 | 조지타운 유니버시티 | 표적화된 리포솜 |
| US20140120157A1 (en) | 2012-09-19 | 2014-05-01 | Georgetown University | Targeted liposomes |
| CA2901616A1 (en) | 2013-03-14 | 2014-10-02 | Georgetown University | Treatment for exposure to nerve agent |
| CN108350450B (zh) * | 2015-11-09 | 2022-07-05 | 国立大学法人京都工艺纤维大学 | 人血清来源的IgG多克隆抗体的分离剂、以及使用其的人血清来源的IgG多克隆抗体的分离方法 |
| WO2020077039A1 (en) * | 2018-10-12 | 2020-04-16 | Synergene Therapeutics, Inc. | Methods for reducing side effects of immunotherapy |
| WO2022040435A1 (en) * | 2020-08-19 | 2022-02-24 | The Board Of Regents Of The University Of Texas System | Nanodrugs for targeted drug delivery and use thereof |
| WO2022226513A1 (en) * | 2021-04-21 | 2022-10-27 | University Of Florida Research Foundation, Inc. | Enzymatically-cleavable glycidyl methacrylate hyaluronic acid |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4429008B1 (en) | 1981-12-10 | 1995-05-16 | Univ California | Thiol reactive liposomes |
| US4946778A (en) * | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| US5688488A (en) * | 1989-04-03 | 1997-11-18 | Purdue Research Foundation | Composition and method for tumor imaging |
| AU642980B2 (en) | 1990-03-21 | 1993-11-04 | Quest International B.V. | Ultilization of enzymes |
| US6099842A (en) * | 1990-12-03 | 2000-08-08 | The United States Of America As Represented By The Department Of Health And Human Services | Recombinant immunotoxin composed of a single chain antibody reacting with the human transferrin receptor and diptheria toxin |
| US5705655A (en) | 1992-12-17 | 1998-01-06 | Megabios Corporation | Amphiphilic nitrogen containing imidazolinium derivative compounds and uses |
| AU696881B2 (en) | 1994-06-22 | 1998-09-24 | Megabios Corporation | Cationic amphiphiles |
| US5786214A (en) * | 1994-12-15 | 1998-07-28 | Spinal Cord Society | pH-sensitive immunoliposomes and method of gene delivery to the mammalian central nervous system |
| FR2730637B1 (fr) * | 1995-02-17 | 1997-03-28 | Rhone Poulenc Rorer Sa | Composition pharmaceutique contenant des acides nucleiques, et ses utilisations |
| AU6113396A (en) * | 1995-06-14 | 1997-01-15 | Regents Of The University Of California, The | Novel high affinity human antibodies to tumor antigens |
| JPH09110722A (ja) * | 1995-10-20 | 1997-04-28 | Toray Ind Inc | 抗腫瘍活性物質の腫瘍細胞内導入用イムノリポソーム及びその調製法 |
| US6077834A (en) | 1996-02-09 | 2000-06-20 | Cheng; Pi-Wan | Receptor ligand-facilitated delivery of biologically active molecules |
| US6210707B1 (en) * | 1996-11-12 | 2001-04-03 | The Regents Of The University Of California | Methods of forming protein-linked lipidic microparticles, and compositions thereof |
| CA2271325A1 (en) * | 1996-11-12 | 1998-05-22 | The Regents Of The University Of California | Preparation of stable formulations of lipid-nucleic acid complexes for efficient in vivo delivery |
| AU759164C (en) | 1997-11-19 | 2007-03-29 | Georgetown University | Targeted liposome gene delivery |
| US6794128B2 (en) * | 1998-04-24 | 2004-09-21 | The Regents Of The University Of California | Methods of selecting internalizing antibodies |
| WO1999059643A2 (en) | 1998-05-20 | 1999-11-25 | Sdg, Inc. | Liposomal delivery complex |
| US6693086B1 (en) * | 1998-06-25 | 2004-02-17 | National Jewish Medical And Research Center | Systemic immune activation method using nucleic acid-lipid complexes |
| US20030022854A1 (en) * | 1998-06-25 | 2003-01-30 | Dow Steven W. | Vaccines using nucleic acid-lipid complexes |
| WO2000015649A1 (en) | 1998-09-11 | 2000-03-23 | Thomas Jefferson University | METHODS OF INHIBITING SMOOTH MUSCLE CELL PROLIFERATION AND PREVENTING RESTENOSIS WITH A VECTOR EXPRESSING RB2/p130 |
| PT1811036E (pt) | 1999-02-22 | 2011-07-11 | Univ Georgetown | Imunolipossomas dirigidos por fragmento de anticorpo para distribuição sistémica de genes |
| US7780882B2 (en) * | 1999-02-22 | 2010-08-24 | Georgetown University | Simplified and improved method for preparing an antibody or an antibody fragment targeted immunoliposome for systemic administration of a therapeutic or diagnostic agent |
| US9034330B2 (en) * | 1999-02-22 | 2015-05-19 | Georgetown University | Preparation of antibody or an antibody fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof |
| CN1448183A (zh) * | 2002-04-04 | 2003-10-15 | 深圳市生尔易实业发展有限责任公司 | 一种肿瘤特异性靶向给药系统及其在制备治疗肿瘤药物中的应用 |
| CN1798545B (zh) * | 2003-06-04 | 2013-06-05 | 乔治敦大学 | 改良脂质体复合物的稳定性和保存期的方法 |
| JP2005306865A (ja) * | 2004-03-25 | 2005-11-04 | Japan Science & Technology Agency | ホウ酸基含有シス−スチルベン化合物及びその製造方法、並びに、ホウ酸基含有トランス−スチルベン化合物及びその製造方法 |
| JP4593961B2 (ja) | 2004-04-20 | 2010-12-08 | Thk株式会社 | 直動案内用広速度域グリース組成物及びこれを用いた直動案内装置 |
| WO2005117876A1 (en) * | 2004-06-01 | 2005-12-15 | University Of Virginia Patent Foundation | Dual small molecule inhibitors of cancer and angiogenesis |
-
2007
- 2007-05-11 US US11/798,296 patent/US9034330B2/en not_active Expired - Fee Related
- 2007-05-11 KR KR1020147031229A patent/KR20140135267A/ko not_active Ceased
- 2007-05-11 JP JP2009510991A patent/JP2009537526A/ja active Pending
- 2007-05-11 CA CA002652222A patent/CA2652222A1/en not_active Abandoned
- 2007-05-11 WO PCT/US2007/011407 patent/WO2007142781A1/en not_active Ceased
- 2007-05-11 AU AU2007257357A patent/AU2007257357B2/en not_active Ceased
- 2007-05-11 EP EP07809069A patent/EP2023897A4/en not_active Withdrawn
- 2007-05-11 KR KR1020087030321A patent/KR101573928B1/ko not_active Expired - Fee Related
- 2007-05-11 MX MX2008014362A patent/MX2008014362A/es active IP Right Grant
-
2008
- 2008-11-11 IL IL195216A patent/IL195216A/en active IP Right Grant
- 2008-11-14 ZA ZA2008/09725A patent/ZA200809725B/en unknown
-
2015
- 2015-04-24 US US14/695,841 patent/US9480750B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2023897A4 (en) | 2013-04-03 |
| JP2009537526A (ja) | 2009-10-29 |
| KR20090016022A (ko) | 2009-02-12 |
| US9480750B2 (en) | 2016-11-01 |
| AU2007257357A1 (en) | 2007-12-13 |
| US20150224201A1 (en) | 2015-08-13 |
| AU2007257357B2 (en) | 2010-08-26 |
| CA2652222A1 (en) | 2007-12-13 |
| US9034330B2 (en) | 2015-05-19 |
| KR20140135267A (ko) | 2014-11-25 |
| WO2007142781A1 (en) | 2007-12-13 |
| IL195216A (en) | 2017-06-29 |
| US20070231378A1 (en) | 2007-10-04 |
| MX2008014362A (es) | 2008-11-27 |
| IL195216A0 (en) | 2009-09-22 |
| KR101573928B1 (ko) | 2015-12-03 |
| EP2023897A1 (en) | 2009-02-18 |
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