RU2016132482A - Магнитные наночастицы, функционализированные пирокатехином, их получение и применение - Google Patents
Магнитные наночастицы, функционализированные пирокатехином, их получение и применение Download PDFInfo
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- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 title claims 3
- 239000002122 magnetic nanoparticle Substances 0.000 title claims 3
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 5
- 210000004027 cell Anatomy 0.000 claims 5
- 239000002105 nanoparticle Substances 0.000 claims 4
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 208000023275 Autoimmune disease Diseases 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- 210000001744 T-lymphocyte Anatomy 0.000 claims 2
- 229920000249 biocompatible polymer Polymers 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
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- 238000002054 transplantation Methods 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims 1
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Claims (22)
1. Магнитные наночастицы, поверхность которых функционализирована пирокатехином, концевая часть молекулы которого не связана с поверхностью частицы и обеспечивает гидрофобную реакционноспособность, причем указанные магнитные частицы состоят из магнетитовых наночастиц.
2. Конструкция, содержащая множество наночастиц по п. 1, инкапсулированных в биологически совместимом полимерном матриксе, в котором необязательно диспергированы молекулы вещества, обладающего терапевтическим действием.
3. Конструкция по п. 2, дополнительно содержащая также множество золотых наностержней.
4. Конструкция по п. 2, в которой указанный биологически совместимый полимерный матрикс состоит из сополимеров, способных к биологической деградации.
5. Конструкция по п. 5, в которой указанные сополимеры, способные к биологической деградации, выбраны из способных к биологической деградации наномицелл, сложных полиэфиров, полиуретанов, поликарбонатов и поли(глутаминовой) кислоты, полиэфирамина и полибензилглутамата.
6. Конструкция по п. 5, в которой указанные способные к биологической деградации наномицеллы состоят из поли(молочной-со-гликолевой) кислоты и полиэтиленгликолькарбоксилата (PLGA-b-PEG-COOH), описываемого формулой (I)
где m=[117-330]; n=[117-330]; р=[60-100].
7. Конструкция по п. 2, в которой указанные вещества, обладающие терапевтическим действием, выбраны из противораковых агентов, скэвенджеров пероксинитрита; ингибиторов супероксиддисмутазы; ретиноидов; цитокинов; аспирина.
8. Конструкция по п. 6, в которой концевая карбоксильная группа фрагмента PEG-COOH в мицеллах дополнительно функционализирована моноклональными антителами, белками, пептидами или иными активными молекулами, представляющими интерес с точки зрения специфичного распознавания по чрезмерной экспрессии в клетках.
9. Конструкция по п. 8, в которой указанные антитела выбраны из hEGR, hEGFR, IgG, moAb.
10. Способ получения конструкции по п. 2, в котором
раствор полимера в органическом растворителе, смешанный с суспензией наночастиц, покрытых органическим связующим агентом, в том же растворителе, и
водный раствор Na2HPO4 (1 мМ)
смешивают в постоянном потоке в смесителе при периодическом или непрерывном синтезе.
11. Способ получения конструкций по п. 7, в котором концевую карбоксильную группу фрагмента PEG-COOH активируют, чтобы способствовать последующей реакции этерификации концевых аминогрупп.
12. Клетки иммунной системы человека, содержащие конструкции по п. 2.
13. Клетки по п. 12, в котором указанные клетки иммунной системы человека выбраны из Т-лимфоцитов, моноцитов, макрофагов, дендритных клеток, натуральных киллеров (NK-клеток), В-лимфоцитов, нейтрофильных гранулоцитов, эозинофильных гранулоцитов, базофильных гранулоцитов, гамма-дельта Т-лимфоцитов.
14. Применение наночастиц по п. 1 и конструкций по п. 2 для гипертермического лечения.
15. Применение клеток по п. 12 для диагностирования рака, дегенеративных заболеваний, заболеваний центральной нервной системы, сердечно-сосудистых заболеваний головного мозга, инфекционных и аутоиммунных заболеваний, и состояний, связанных с трансплантацией, а также для лечения опухолей, сердечно-сосудистых заболеваний головного мозга, дегенеративных заболеваний (например, болезни Альцгеймера), инфекционных заболеваний, состояний, связанных с трансплантацией, цирроза печени и других состояний, характеризующихся образованием и прорастанием соединительной ткани, расстройств, сопровождающихся повторными выкидышами, внутриутробной гибели плода, неонатальных заболеваний, врожденных и приобретенных расстройств свертывания крови, генетически обусловленных заболеваний, аутоиммунных заболеваний и, наконец, для облегчения боли.
16. Применение магнитных наночастиц по п. 1 в качестве средства для визуализации при магнитно-резонансной томографии.
17. Применение наночастиц по п. 3, содержащих наностержни, для диагностирования и лечения опухолевых заболеваний.
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BR112016015810A2 (pt) | 2017-08-08 |
EP3092012A1 (en) | 2016-11-16 |
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DK3092012T3 (da) | 2019-09-02 |
IL246665A0 (en) | 2016-08-31 |
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US10888630B2 (en) | 2021-01-12 |
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JP6590809B2 (ja) | 2019-10-16 |
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US20230330273A1 (en) | 2023-10-19 |
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US20160331850A1 (en) | 2016-11-17 |
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CA2935858C (en) | 2022-06-21 |
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