RU2007141588A - Наночастица, и на ее основе инфузионный раствор и фармацевтическая композици - Google Patents
Наночастица, и на ее основе инфузионный раствор и фармацевтическая композици Download PDFInfo
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- RU2007141588A RU2007141588A RU2007141588/15A RU2007141588A RU2007141588A RU 2007141588 A RU2007141588 A RU 2007141588A RU 2007141588/15 A RU2007141588/15 A RU 2007141588/15A RU 2007141588 A RU2007141588 A RU 2007141588A RU 2007141588 A RU2007141588 A RU 2007141588A
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- nanoparticle according
- active substance
- therapeutically active
- nanoparticle
- rna
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- Medicinal Preparation (AREA)
Abstract
1. Наночастица, связанная с по меньшей мере одним терапевтически активным веществом посредством линкера, содержащего группу, которая является термолабильной, электромагнитно лабильной, фотолабильной, кислотно-лабильной или может интеркалироваться или расщепляться энзиматически, причем освобождение терапевтически активного вещества от наночастицы вызывается, или инициируется, или существенно ускоряется переменным магнитным полем. ! 2. Наночастица по п.1, которая связана с терапевтически активным веществом ковалентной связью. ! 3. Наночастица по п.1, которая связана с терапевтически активным веществом посредством линкера, выбранного из группы, включающей молекулу нуклеиновой кислоты, полипептид, пептидную нуклеиновую кислоту, аптамер, ДНК, РНК, лейфиновый зиппер, олигонуклеотид, олигопептид, биотин, авидин, стептавидин, связь гаптен-антитело или связь биотин-авидин. ! 4. Наночастица по п.1, которая связана посредством линкера, выбранного из группы, включающей конструкцию двуцепочечной нуклеиновой кислоты, двойную спираль, гомо-гибрид или гетеро-гибрид типа ДНК-ДНК, ДНК-РНК, ДНК-ПНК, РНК-РНК, РНК-ПНК или ПНК-ПНК. ! 5. Наночастица по пп.1-4, которая имеет защитную оболочку или покрытие. ! 6. Наночастица по п.5, в которой защитная оболочка или покрытие имеет аминогруппы или карбоксильные группы. ! 7. Наночастица по п.1 или 2, которая связана с терапевтически активным веществом, выбранным из группы, включающей антипролиферативные, антимиграционные, антиангиогенные, противотромбозные, противовоспалительные, цитостатики, цитотоксические, антикоагуляционные, антибактериальные, антивирусные и/или противогрибковые препараты. !
Claims (14)
1. Наночастица, связанная с по меньшей мере одним терапевтически активным веществом посредством линкера, содержащего группу, которая является термолабильной, электромагнитно лабильной, фотолабильной, кислотно-лабильной или может интеркалироваться или расщепляться энзиматически, причем освобождение терапевтически активного вещества от наночастицы вызывается, или инициируется, или существенно ускоряется переменным магнитным полем.
2. Наночастица по п.1, которая связана с терапевтически активным веществом ковалентной связью.
3. Наночастица по п.1, которая связана с терапевтически активным веществом посредством линкера, выбранного из группы, включающей молекулу нуклеиновой кислоты, полипептид, пептидную нуклеиновую кислоту, аптамер, ДНК, РНК, лейфиновый зиппер, олигонуклеотид, олигопептид, биотин, авидин, стептавидин, связь гаптен-антитело или связь биотин-авидин.
4. Наночастица по п.1, которая связана посредством линкера, выбранного из группы, включающей конструкцию двуцепочечной нуклеиновой кислоты, двойную спираль, гомо-гибрид или гетеро-гибрид типа ДНК-ДНК, ДНК-РНК, ДНК-ПНК, РНК-РНК, РНК-ПНК или ПНК-ПНК.
5. Наночастица по пп.1-4, которая имеет защитную оболочку или покрытие.
6. Наночастица по п.5, в которой защитная оболочка или покрытие имеет аминогруппы или карбоксильные группы.
7. Наночастица по п.1 или 2, которая связана с терапевтически активным веществом, выбранным из группы, включающей антипролиферативные, антимиграционные, антиангиогенные, противотромбозные, противовоспалительные, цитостатики, цитотоксические, антикоагуляционные, антибактериальные, антивирусные и/или противогрибковые препараты.
8. Наночастица по п.7, которая связана с терапевтически активным веществом, выбранным из группы, включающей актиномицин D, аметантрон, 9-аминокамфотецин, аминоглутетимид, амсакрин, анастрозол, антагонисты пуриновых и пиримидиновых оснований, антрациклины, ингибиторы ароматазы, аспарагиназу, антиэстрогены, бендамустин, бексаротен, биолимус А9, блеомицин, бузерелин, бусульфан, калихеамицины, камптотецин, производные камптотецина, капецитабин, карбоплатин, кармустин, хлорамбуцил, цисплатин, кладрибин, циклофосфамид, цитарабин, цитозинарабинозид, ал килирующие цитостатики, дакарбазин, да ктиномицин, даунорубицин, 5'-деокси-5-фторуридин, доцетаксел, доксорубицин (адриамицин), доксорубицин липо, эпирубицин, эстрамустин, этопозид, эксеместан, флударабин, фтороурацил, антагонисты фолиевой кислоты, форместан, гемцитабин, глюкокортикоиды, гозерелин, гормоны и гормональные антагонисты, гикамтин, гидроксимочевина, идарубицин, ифосфамид, иматиниб, иринотекан, детрозол, левпрорелин, ломустин, майтанзиноиды, мелфалан, меркаптопурин, метотрексат, милтефозин, митомицины, митоподозид, антимитотические агенты, митоксантрон, нимустин, оксалиплатин, оксазафосфорины, паклитаксел, пентостатин, производные подофиллотоксина, прокарбазин, рапамицин, родомицин D, тамоксифен, темозоломид, тенипозид, тестолактон, тиотепа, тиогуанин, ингибиторы топоизомеразы, топотекан, треосульфан, третиноин, трипторелин, трофосфамиды, алкалоиды барвинка, винбластин, винкристин, виндезин, винорелбин, цитостатически активные антибиотики.
9. Наночастица по п.7, которая связана с терапевтически активным веществом, выбранным из группы, включающей нуклеиновые кислоты, аминокислоты, пептиды, протеины, углеводы, липиды, гликопротеины, гликаны или липопротеины, причем вышеуказанные вещества имеют антипролиферативные, антимиграционные, антиангиогенные, противотромбозные, противовоспалительные, цитостатические, цитотоксические, антикоагуляционные, антибактериальные, антивирусные и/или противогрибковые свойства.
10. Наночастица по п.1 или 2, которая состоит из суперпарамагнитных оксидов железа или из чистого железа, имеющего оксидный слой.
11. Наночастица по п.1 или 2, которая связана с сенсибилизатором, радиосенсибилизатором и/или усилителем в качестве дополнения к обычным способам лечения рака.
12. Наночастица по п.1 или 2, которая связана своей поверхностью с моноклональными антителами или соответственно фрагментами антител и/или аптамеров.
13. Инфузионный раствор, содержащий наночастицы по пп.1-12.
14. Применение наночастиц по пп.1-12 в качестве компонента для приготовления фармацевтической композиции для лечения и/или профилактики пролиферативных заболеваний, рака и бактериальных инфекций.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005016873.6 | 2005-04-12 | ||
| DE102005016873A DE102005016873A1 (de) | 2005-04-12 | 2005-04-12 | Nanopartikel-Wirstoff-Konjugate |
| US67510005P | 2005-04-27 | 2005-04-27 | |
| US60/675,100 | 2005-04-27 | ||
| PCT/DE2006/000653 WO2006108405A2 (de) | 2005-04-12 | 2006-04-12 | Nanopartikel-wirkstoff-konjugate |
Publications (3)
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| RU2007141588A true RU2007141588A (ru) | 2009-05-20 |
| RU2490027C2 RU2490027C2 (ru) | 2013-08-20 |
| RU2490027C9 RU2490027C9 (ru) | 2013-09-27 |
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| RU2007141588/15A RU2490027C9 (ru) | 2005-04-12 | 2006-04-12 | Магнитная наночастица для лечения и/или профилактики рака, на ее основе инфузионный раствор и фармацевтическая композиция |
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| EP (1) | EP1871423B9 (ru) |
| JP (1) | JP5037490B2 (ru) |
| KR (3) | KR20130098441A (ru) |
| CN (1) | CN101247836B (ru) |
| AU (1) | AU2006233483B2 (ru) |
| BR (1) | BRPI0610220A2 (ru) |
| CA (1) | CA2603734C (ru) |
| DE (2) | DE102005016873A1 (ru) |
| DK (1) | DK1871423T3 (ru) |
| ES (1) | ES2392346T3 (ru) |
| IL (1) | IL186521A (ru) |
| MX (1) | MX2007012670A (ru) |
| NZ (1) | NZ561928A (ru) |
| RU (1) | RU2490027C9 (ru) |
| WO (1) | WO2006108405A2 (ru) |
| ZA (1) | ZA200708692B (ru) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2431472C2 (ru) * | 2009-09-24 | 2011-10-20 | Российская Федерация, От Имени Которой Выступает Министерство Образования И Науки Российской Федерации | Способ получения наночастиц магнетита, стабилизированных биосовместимым полимером, имеющим функциональные формильные группы |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITRM20030376A1 (it) | 2003-07-31 | 2005-02-01 | Univ Roma | Procedimento per l'isolamento e l'espansione di cellule staminali cardiache da biopsia. |
| US11660317B2 (en) | 2004-11-08 | 2023-05-30 | The Johns Hopkins University | Compositions comprising cardiosphere-derived cells for use in cell therapy |
| EP1919507A2 (en) * | 2005-08-04 | 2008-05-14 | Thomas William Rademacher | Nanoparticles comprising antibacterial ligands |
| DE102005039579B4 (de) | 2005-08-19 | 2022-06-30 | Magforce Ag | Verfahren zur Einschleusung von therapeutischen Substanzen in Zellen |
| CA2651763A1 (en) * | 2006-05-17 | 2007-11-29 | Board Of Regents Of The Nevada System Of Higher Education On Behalf Of T He University Of Nevada | Magnetorheological fluids and therapeutic uses thereof |
| US8466154B2 (en) | 2006-10-27 | 2013-06-18 | The Board Of Regents Of The University Of Texas System | Methods and compositions related to wrapping of dehydrons |
| US20080213377A1 (en) * | 2006-12-08 | 2008-09-04 | Bhatia Sangeeta N | Delivery of Nanoparticles and/or Agents to Cells |
| CA2671806A1 (en) * | 2006-12-08 | 2008-06-19 | Austin M. Derfus | Remotely triggered release from heatable surfaces |
| BRPI0808635B1 (pt) * | 2007-03-07 | 2022-06-07 | Abraxis Bioscience, Llc | Uso de uma composição farmacêutica compreendendo nanopartículas que compreendem rapamicina ou um seu derivado e uma proteína veículo, composição para uso em um método de tratamento de câncer em um indivíduo, forma de dosagem unitária para o referido tratamento, e kit |
| DE102007011702A1 (de) * | 2007-03-08 | 2008-09-11 | Rheinische Friedrich-Wilhelms Universität | Aptamer-basierte Reagenzien |
| KR101010100B1 (ko) | 2007-06-28 | 2011-01-24 | (주)미래생명공학연구소 | 나노 입자를 이용한 유전자도입 배아 줄기세포의 제조 방법 |
| DE102008003615A1 (de) | 2008-01-09 | 2009-07-16 | Magforce Nanotechnologies Ag | Magnetische Transducer |
| DE102008008522A1 (de) | 2008-02-11 | 2009-08-13 | Magforce Nanotechnologies Ag | Implantierbare Nanopartikel-enthaltende Produkte |
| US8236284B1 (en) | 2008-04-02 | 2012-08-07 | University Of Central Florida Research Foundation, Inc. | Multimodal, multifunctional polymer coated nanoparticles |
| US8697098B2 (en) | 2011-02-25 | 2014-04-15 | South Dakota State University | Polymer conjugated protein micelles |
| JP5526324B2 (ja) * | 2008-07-15 | 2014-06-18 | 独立行政法人物質・材料研究機構 | 薬物が結合可能な光応答性薬物輸送体 |
| AU2008361497B2 (en) * | 2008-09-04 | 2014-07-17 | Takeshi Kobayashi | Methods and kits for hyperthermia and CTLA4 inhibitory therapy |
| MX2011002847A (es) * | 2008-09-19 | 2011-04-07 | Activus Pharma Co Ltd | Polvo de compuesto organico combinado para uso medico y metodo de produccion y suspension del mismo. |
| EP2189539B2 (en) * | 2008-11-21 | 2018-06-13 | Chimera Biotec GmbH | Conjugate complexes for analyte detection |
| ES2381022T3 (es) * | 2008-12-19 | 2012-05-22 | Biolitec Ag | Nanopartículas de fosfato de calcio como vehículo de colorantes para la terapia fotodinámica |
| WO2010074675A1 (en) * | 2008-12-23 | 2010-07-01 | Board Of Regents Of The University Of Texas System | Inflammation targeting particles |
| US20100233270A1 (en) | 2009-01-08 | 2010-09-16 | Northwestern University | Delivery of Oligonucleotide-Functionalized Nanoparticles |
| US20100294952A1 (en) * | 2009-01-15 | 2010-11-25 | Northwestern University | Controlled agent release and sequestration |
| WO2010091183A2 (en) * | 2009-02-04 | 2010-08-12 | The Regents Of The University Of Colorado, A Body Corporate | Non-invasive detection of complement-mediated inflammation using cr2-targeted nanoparticles |
| US8911766B2 (en) * | 2009-06-26 | 2014-12-16 | Abbott Cardiovascular Systems Inc. | Drug delivery compositions including nanoshells for triggered drug release |
| EP2490723A1 (en) * | 2009-10-19 | 2012-08-29 | University Of Louisville Research Foundation, Inc. | Nanoparticles for drug delivery |
| ES2600229T3 (es) * | 2009-11-12 | 2017-02-07 | Helmholtz-Zentrum Geesthacht Zentrum für Material- und Küstenforschung GmbH | Nanopartículas magnéticas biocompatibles para el tratamiento de glioblastomas |
| ES2539588T3 (es) | 2009-11-18 | 2015-07-02 | Nanobacterie | Tratamiento de cáncer o tumor inducido por la liberación de calor generado por diversas cadenas de magnetosomas extraídas de bacterias magnetotácticas y sometidas a un campo magnético alterno |
| DE102009058769A1 (de) | 2009-12-16 | 2011-06-22 | MagForce Nanotechnologies AG, 10589 | Temperaturabhängige Aktivierung von katalytischen Nukleinsäuren zur kontrollierten Wirkstofffreisetzung |
| US8226985B2 (en) | 2010-01-28 | 2012-07-24 | International Business Machines Corporation | Surface modified nanoparticles, methods of their preparation, and uses thereof for gene and drug delivery |
| US20110206611A1 (en) * | 2010-02-24 | 2011-08-25 | Genisphere, Llc | DNA Dendrimers as Thermal Ablation Devices |
| US9845457B2 (en) | 2010-04-30 | 2017-12-19 | Cedars-Sinai Medical Center | Maintenance of genomic stability in cultured stem cells |
| US9249392B2 (en) | 2010-04-30 | 2016-02-02 | Cedars-Sinai Medical Center | Methods and compositions for maintaining genomic stability in cultured stem cells |
| CA2816121C (en) | 2010-11-01 | 2017-06-13 | Syracuse University | System and method for delivery of dna-binding chemotherapy drugs using nanoparticles |
| EP2646818A4 (en) * | 2010-11-30 | 2016-09-21 | Univ Illinois | SILICANANOPARTIKELKONJUGATE |
| CA2828255A1 (en) | 2011-02-25 | 2012-08-30 | South Dakota State University | Protein nanocarriers for topical delivery |
| CA2828253C (en) | 2011-02-25 | 2016-10-18 | South Dakota State University | Polymer conjugated protein micelles |
| RU2568344C2 (ru) | 2011-03-10 | 2015-11-20 | Магфорс Аг | Компьютеризованное средство имитационного моделирования для предоставления помощи в планировании термотерапии |
| FR2974815B1 (fr) | 2011-05-06 | 2014-01-10 | Univ Paris Curie | Utilisation d'au moins un agent chelatant introduit dans le milieu de culture de bacteries magnetotactiques pour stimuler la croissance de ces bacteries |
| US9408912B2 (en) | 2011-08-10 | 2016-08-09 | Magforce Ag | Agglomerating magnetic alkoxysilane-coated nanoparticles |
| DE102011112898A1 (de) * | 2011-09-08 | 2013-03-14 | Charité - Universitätsmedizin Berlin | Nanopartikuläres Phosphatadsorbens basierend auf Maghämit oder Maghämit/Magnetit, dessen Herstellung und Verwendungen |
| KR101337684B1 (ko) | 2011-10-17 | 2013-12-30 | 성균관대학교산학협력단 | 표적지향 및 치료가 가능한 다기능성 핵산 기반 항암제, 이의 제조 방법 및 이를 포함하는 항암제 조성물 |
| CN102539760A (zh) * | 2012-02-11 | 2012-07-04 | 刘�东 | 具有体外肿瘤靶向作用的经叶酸配体修饰的氧化铁纳米颗粒与其制备方法及体外评价方法 |
| US9393306B2 (en) | 2012-04-24 | 2016-07-19 | The Board Of Regents Of The University Of Oklahoma | Singlet oxygen-labile linkers and methods of production and use thereof |
| WO2013184527A1 (en) | 2012-06-05 | 2013-12-12 | Capricor, Inc. | Optimized methods for generation of cardiac stem cells from cardiac tissue and their use in cardiac therapy |
| JP6433896B2 (ja) | 2012-08-13 | 2018-12-05 | シーダーズ−サイナイ・メディカル・センターCedars−Sinai Medical Center | 組織再生のためのエキソソームおよびマイクロリボ核酸 |
| WO2014107419A1 (en) * | 2013-01-02 | 2014-07-10 | The Johns Hopkins University | Use of oscillating gradients of high magnetic field for specific destruction of cells labeled with magnetic nanoparticles |
| WO2014124329A1 (en) | 2013-02-08 | 2014-08-14 | University Of Louisville Research Foundation, Inc. | Nanoparticles for drug delivery |
| HK1220888A1 (zh) * | 2013-03-15 | 2017-05-19 | Georgia State University Research Foundation, Inc. | 用於将治疗剂和显像剂递送至窦和中耳的组合物和方法 |
| KR101465626B1 (ko) * | 2013-05-23 | 2014-12-10 | 고려대학교 산학협력단 | 바이오틴을 포함하는 표적 특이적 항암 약물 전구체 |
| RU2550955C1 (ru) * | 2013-12-11 | 2015-05-20 | Общество с ограниченной ответственностью "Уральский центр биофармацевтических технологий | Способ электрохимического иммуноанализа для определения вирусов/антигенов вирусов |
| US10464955B2 (en) * | 2014-02-28 | 2019-11-05 | Hangzhou Dac Biotech Co., Ltd. | Charged linkers and their uses for conjugation |
| RU2563369C1 (ru) * | 2014-02-28 | 2015-09-20 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Московский государственный университет имени М.В. Ломоносова" (МГУ) | Способ ферримагнито-термохимиотерапии злокачественных опухолей комбинациями магнитоуправляемых нанопрепаратов с визуализацией онкогенеза, определением терапии, предпочтительной в режиме реального времени, и мониторингом результатов лечения в эксперименте |
| RU2561294C1 (ru) * | 2014-05-08 | 2015-08-27 | Федеральное государственное бюджетное учреждение "Ростовский научно-исследовательский онкологический институт" Министерства здравоохранения Российской Федерации | Способ торможения роста лимфосаркомы плисса в эксперименте |
| ES2725948T3 (es) | 2014-06-04 | 2019-09-30 | Exicure Inc | Suministro multivalente de inmunomoduladores mediante ácidos nucleicos esféricos liposomales para aplicaciones profilácticas o terapéuticas |
| RU2581946C2 (ru) * | 2014-07-10 | 2016-04-20 | Федеральное государственное бюджетное учреждение "Ростовский научно-исследовательский онкологический институт" Министерства здравоохранения Российской Федерации | Способ лечения рака мочевого пузыря |
| JP6878274B2 (ja) | 2014-10-03 | 2021-05-26 | シーダーズ−サイナイ・メディカル・センターCedars−Sinai Medical Center | 筋ジストロフィーの処置における心筋球由来細胞およびこのような細胞によって分泌されたエキソソーム |
| EP3310342A4 (en) * | 2015-06-16 | 2019-03-06 | The Trustees of the University of Pennsylvania | INORGANIC RETARD PARTICLES WITH FAST ACTIVE LOAD |
| US11260027B2 (en) | 2015-07-29 | 2022-03-01 | Musc Foundation For Research Development | Donor organ pre-treatment formulation |
| EP3393490A4 (en) * | 2015-12-15 | 2019-11-20 | Icahn School of Medicine at Mount Sinai | METHOD FOR TREATING A CLOSED INFLAMMATORY REACTION WITH TOPOISOMERASE L-INHIBITORS |
| US10765881B2 (en) | 2016-01-08 | 2020-09-08 | University Of Florida Research Foundation, Inc. | Magnetic particle conjugates and methods of activating cell signaling |
| WO2017123662A1 (en) | 2016-01-11 | 2017-07-20 | Cedars-Sinai Medical Center | Cardiosphere-derived cells and exosomes secreted by such cells in the treatment of heart failure with preserved ejection fraction |
| WO2017210652A1 (en) | 2016-06-03 | 2017-12-07 | Cedars-Sinai Medical Center | Cdc-derived exosomes for treatment of ventricular tachyarrythmias |
| WO2018039629A2 (en) | 2016-08-25 | 2018-03-01 | Northwestern University | Micellar spherical nucleic acids from thermoresponsive, traceless templates |
| EP3515459A4 (en) | 2016-09-20 | 2020-08-05 | Cedars-Sinai Medical Center | CELLS DERIVED FROM CARDIOSPHERES AND THEIR EXTRACELLULAR VESICLES TO DELAY OR REVERSE AGING AND AGE-RELATED DISORDERS |
| CA3059910A1 (en) | 2017-04-19 | 2018-10-25 | Cedars-Sinai Medical Center | Methods and compositions for treating skeletal muscular dystrophy |
| RU2657545C1 (ru) * | 2017-08-17 | 2018-06-14 | Максим Артемович Абакумов | Лекарственный препарат для лечения рака молочной железы |
| KR102141220B1 (ko) * | 2017-11-30 | 2020-08-05 | 한국생산기술연구원 | 친수성 또는 소수성 약물을 제어하는 다공성 나노입자의 콜로이드화 |
| EP3727351A4 (en) | 2017-12-20 | 2021-10-06 | Cedars-Sinai Medical Center | MANIPULATED EXTRACELLULAR VESICLES FOR ENHANCED RELEASE INTO TISSUE |
| WO2019152549A1 (en) | 2018-02-05 | 2019-08-08 | Cedars-Sinai Medical Center | Methods for therapeutic use of exosomes and y-rnas |
| CN109374558A (zh) * | 2018-12-11 | 2019-02-22 | 山东吉威医疗制品有限公司 | 一种无聚合物药物涂层洗脱支架体外释放度的测定方法 |
| CN110623942B (zh) * | 2019-09-30 | 2020-09-22 | 武汉大学 | 一种全反式维甲酸纳米药物制剂、其制备方法及应用 |
| AU2020370342A1 (en) * | 2019-10-22 | 2022-05-19 | Otomagnetics, Inc. | Lipid coated iron oxide nanoparticles for otitis media |
| KR20220133893A (ko) | 2020-01-31 | 2022-10-05 | 매그포스 아게 | 자성 알콕시실란-코팅된 금속 함유 나노입자를 포함하는 페이스트 |
| CN111554501A (zh) * | 2020-04-28 | 2020-08-18 | 天津大学 | 磁性吸附细菌和孢子的超顺磁性镍纳米颗粒的制备方法 |
| DE102020116859A1 (de) | 2020-06-26 | 2021-12-30 | Pharma Development Holding Gmbh | Liposomen |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2662539B1 (fr) * | 1990-05-23 | 1994-09-30 | Centre Nat Rech Scient | Procede d'obtention de supports magnetiques finement divises par modification controlee de la surface de particules precurseurs magnetiques chargees et produits obtenus. |
| DE4117782C2 (de) | 1991-05-28 | 1997-07-17 | Diagnostikforschung Inst | Nanokristalline magnetische Eisenoxid-Partikel, Verfahren zu ihrer Herstellung sowie diagnostische und/oder therapeutische Mittel |
| US5411730A (en) * | 1993-07-20 | 1995-05-02 | Research Corporation Technologies, Inc. | Magnetic microparticles |
| DE4428851C2 (de) * | 1994-08-04 | 2000-05-04 | Diagnostikforschung Inst | Eisen enthaltende Nanopartikel, ihre Herstellung und Anwendung in der Diagnostik und Therapie |
| US6147205A (en) * | 1995-12-15 | 2000-11-14 | Affymetrix, Inc. | Photocleavable protecting groups and methods for their use |
| DE19614136A1 (de) * | 1996-04-10 | 1997-10-16 | Inst Neue Mat Gemein Gmbh | Verfahren zur Herstellung agglomeratfreier nanoskaliger Eisenoxidteilchen mit hydrolysebeständigem Überzug |
| DE19624426A1 (de) * | 1996-06-19 | 1998-01-02 | Christian Bergemann | Magnetische Flüssigkeiten für den Transport von diagnostisch oder therapeutisch wirksamen Substanzen |
| DE19726282A1 (de) | 1997-06-20 | 1998-12-24 | Inst Neue Mat Gemein Gmbh | Nanoskalige Teilchen mit einem von mindestens zwei Schalen umgebenen eisenoxid-haltigen Kern |
| AU727730B2 (en) * | 1997-06-25 | 2000-12-21 | Earl P. Burke Jr. | Easy mount stirrup |
| US6645464B1 (en) * | 1998-07-30 | 2003-11-11 | James F. Hainfeld | Loading metal particles into cell membrane vesicles and metal particular use for imaging and therapy |
| CA2384429A1 (en) * | 1999-09-14 | 2001-03-22 | Michael K. Bahr | Magnetic nanoparticles having biochemical activity, method for the production thereof and their use |
| JP2002010471A (ja) * | 2000-06-19 | 2002-01-11 | Yazaki Corp | 過電流遮断装置 |
| JP2002090366A (ja) * | 2000-09-14 | 2002-03-27 | Rikogaku Shinkokai | フェライトを固定した生体特異的親和性キャリヤとその製造方法 |
| DE10059151C2 (de) * | 2000-11-29 | 2003-10-16 | Christoph Alexiou | Magnetische Partikel zur zielgerichteten regionalen Therapie und Verwendung derselben |
| ATE388691T1 (de) * | 2001-07-10 | 2008-03-15 | Univ North Carolina State | Träger zur freisetzung von nanopartikeln |
| US7074175B2 (en) * | 2001-07-25 | 2006-07-11 | Erik Schroeder Handy | Thermotherapy via targeted delivery of nanoscale magnetic particles |
| US20060057192A1 (en) * | 2001-09-28 | 2006-03-16 | Kane Patrick D | Localized non-invasive biological modulation system |
| CA2476888A1 (en) | 2002-02-01 | 2003-08-14 | Vanderbilt University | Targeted drug delivery methods |
| US20050084539A1 (en) * | 2002-02-04 | 2005-04-21 | Hiroshi Handa | Organic substance having ferrite bonded thereto and process for producing the same |
| JP2004305055A (ja) | 2003-04-04 | 2004-11-04 | Hitachi Maxell Ltd | 磁性複合粒子およびその製造方法 |
| KR100612734B1 (ko) | 2003-04-30 | 2006-08-18 | 함승주 | 자기성 물질 및 치료제를 생분해성 고분자로 캡슐화한자기성 나노입자를 함유하는 조성물 |
| JP2005060221A (ja) * | 2003-07-31 | 2005-03-10 | Rikogaku Shinkokai | 有機物質とフェライトとの複合材料とその製造方法 |
| DE10350248A1 (de) | 2003-10-28 | 2005-06-16 | Magnamedics Gmbh | Thermosensitive, biokompatible Polymerträger mit veränderbarer physikalischer Struktur für die Therapie, Diagnostik und Analytik |
| WO2005065282A2 (en) | 2003-12-31 | 2005-07-21 | The Regents Of The University Of California | Remote magnetically induced treatment of cancer |
| WO2005070471A2 (en) * | 2004-01-20 | 2005-08-04 | Alnis Biosciences, Inc. | Articles comprising magnetic material and bioactive agents |
| KR100604976B1 (ko) * | 2004-09-03 | 2006-07-28 | 학교법인연세대학교 | 다작용기 리간드로 안정화된 수용성 나노입자 |
| CA2600370A1 (en) * | 2005-03-14 | 2006-09-14 | Board Of Regents Of The University Of Texas System | Bioactive fus1 peptides and nanoparticle-polypeptide complexes |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| RU2431472C2 (ru) * | 2009-09-24 | 2011-10-20 | Российская Федерация, От Имени Которой Выступает Министерство Образования И Науки Российской Федерации | Способ получения наночастиц магнетита, стабилизированных биосовместимым полимером, имеющим функциональные формильные группы |
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| EP1871423A2 (de) | 2008-01-02 |
| KR20080007323A (ko) | 2008-01-18 |
| AU2006233483B2 (en) | 2009-07-16 |
| DE112006001565A5 (de) | 2008-03-27 |
| EP1871423B1 (de) | 2012-08-01 |
| NZ561928A (en) | 2010-10-29 |
| WO2006108405A3 (de) | 2007-02-01 |
| KR20120101727A (ko) | 2012-09-14 |
| AU2006233483A1 (en) | 2006-10-19 |
| DK1871423T3 (da) | 2012-10-29 |
| US20080268061A1 (en) | 2008-10-30 |
| CA2603734A1 (en) | 2006-10-19 |
| RU2490027C9 (ru) | 2013-09-27 |
| DE102005016873A1 (de) | 2006-10-19 |
| BRPI0610220A2 (pt) | 2012-09-25 |
| RU2490027C2 (ru) | 2013-08-20 |
| WO2006108405A2 (de) | 2006-10-19 |
| CN101247836B (zh) | 2013-07-10 |
| CA2603734C (en) | 2012-06-05 |
| IL186521A0 (en) | 2008-01-20 |
| JP2008536837A (ja) | 2008-09-11 |
| JP5037490B2 (ja) | 2012-09-26 |
| ZA200708692B (en) | 2009-01-28 |
| CN101247836A (zh) | 2008-08-20 |
| ES2392346T3 (es) | 2012-12-07 |
| WO2006108405B1 (de) | 2007-04-05 |
| MX2007012670A (es) | 2008-01-28 |
| US9345768B2 (en) | 2016-05-24 |
| KR20130098441A (ko) | 2013-09-04 |
| IL186521A (en) | 2013-03-24 |
| EP1871423B9 (de) | 2014-09-10 |
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