EP1917004A2 - Verfahren zur einschleusung von therapeutischen substanzen in zellen - Google Patents
Verfahren zur einschleusung von therapeutischen substanzen in zellenInfo
- Publication number
- EP1917004A2 EP1917004A2 EP06775877A EP06775877A EP1917004A2 EP 1917004 A2 EP1917004 A2 EP 1917004A2 EP 06775877 A EP06775877 A EP 06775877A EP 06775877 A EP06775877 A EP 06775877A EP 1917004 A2 EP1917004 A2 EP 1917004A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- nanoparticles
- cells
- pharmaceutical composition
- acid
- composition according
- 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.)
- Withdrawn
Links
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Definitions
- pharmacologically acceptable carriers excipients and / or solvents
- the usual in galenics (pharmaceutical technology) substances can be used, with liquid pharmaceutical compositions are preferred.
- Increasing the activity is understood to mean that the same amount of therapeutically active substance, especially anticancer agent, exhibits enhanced activity in the presence of the nanoparticles, rather than in their absence.
- Such a positively polarizable and / or positively ionizable coating can be obtained by coating the nanoparticles with positively polarizable and / or positively ionizable substances.
- Such substances may contain, for example, amino groups or protonatable nitrogen atoms which are present in protonated form at the corresponding pH.
- this coating consists of monomeric aminosilanes, e.g. 3-aminopropyltriethoxysilane, 2-aminoethyl-3-aminopropyltrimethoxysilane, trimethoxysilylpropyldiethylenetriamine or N- (6-aminohexyl) -3-aminopropyltrimethoxysilane, which are polycondensed to obtain the required stability by known methods.
- a suitable method is described for example in DE 19614136 A or DE 19515820 A.
- poly-barrier or copolymers based on ⁇ -hydroxycarboxylic acids such as polylactic acid, polylactides, polyglycolic acid, polyglycolides and copolymers thereof.
- polyols e.g., polyethylene glycol
- polyacid such as e.g. Polyacrylic acids as well as carbohydrates and sugars, especially dextrans.
- polyclonal, antibodies, monoclonal antibodies, humanized antibodies, human antibodies, chimeric antibodies, recombinant antibodies, bispecific antibodies, antibody fragments, aptamers, Fab can be synthesized on the surface of the nanoparticles or on the outer layer or shell of the nanoparticles. Fragments, Fc fragments, peptides, peptidomimetics, gap mers, ribozymes, CpG oligomers, DNA Zyme, riboswitches and / or lipids coupled and / or attached and / or stored.
- the compounds are designed in such a way that they recognize certain cells, for example tumor cells, and further increase the cell discrimination of the nanoparticles.
- Methotrexate, 5-fluorouracil, 6-thioguanine, 6-mercaptopurine, fludarabine, cladribine, pentostatin, gemcitabine, cytarabine, azathioprine, raltitrexed, capecitabine, cytosine arabinoside, tioguanine and mercaptopurine may be cited as examples of antimetabolites (antimetabolic agents).
- the class of alkaloids and podophyllotoxins include, but are not limited to, vincristine, vinblastine, vindesine, etoposide, and teniposide.
- platinum-containing compounds can be used according to the invention. Examples of platinum-containing compounds are cisplatin, carboplatin and oxaliplatin.
- To the microtubule inhibitors include, for example alkaloids, such as vinca alkaloids (vincristine, vinblastine, vindesine, Venorelbin) and paclitaxel (Taxol ®), as well as derivatives of paclitaxel.
- Examples of topoisomerase inhibitors include etoposide, teniposide, camptothecin, topotecan and irinotecan.
- osteoplastic carcinoma osteosarcoma, ovarian carcinoma, pancreatic carcinoma, penile cancer, plasmocytoma, squamous cell carcinoma of the head and neck, prostate cancer, pharyngeal cancer, rectal carcinoma, retinoblastoma, vaginal cancer, thyroid carcinoma, Schneeberger disease, esophageal cancer, spinal, T-cell lymphoma (Mycosis fungoides), Thymoma, tubal carcinoma, tumors of the eye, urethral cancer, urological tumors, urothelial carcinoma, vulvar cancer, wart involvement, soft tissue tumors, soft tissue sarcoma, Wilms tumor, cervical carcinoma and tongue cancer.
- FIG. 3 shows RUSIRS1 cells 24h after addition of mitomycin in 0.9% NaCl
- FIG. 6 shows RUSIRS1 cells 48h after addition of mitomycin in 0.9% NaCl + nanoparticles
- FIG. 11 shows WiDr cells after 72 hours as a control with cefamandole but without nanoparticles
- the 7 cell lines were a) glioblastoma-human cell line RUSIRS1, b) mammary carcinoma cell lines BT20, c) cell carcinoma Zellline WiDr, d) bronchial carcinoma cells NSCLC, e) rectal carcinoma Cells and f) prostate carcinoma Zellline DU 145 with the active ingredients mentioned in Table 1 in vitro.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Inorganic Chemistry (AREA)
- Nanotechnology (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Optics & Photonics (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dermatology (AREA)
- Medical Informatics (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biotechnology (AREA)
- Dispersion Chemistry (AREA)
- Radiology & Medical Imaging (AREA)
- Biophysics (AREA)
- General Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK10012394.2T DK2266544T3 (en) | 2005-08-19 | 2006-08-21 | Method of incorporating therapeutic substances into cells |
| EP10012394.2A EP2266544B1 (de) | 2005-08-19 | 2006-08-21 | Verfahren zur einschleusung von therapeutischen substanzen in zellen |
| PL10012394T PL2266544T3 (pl) | 2005-08-19 | 2006-08-21 | Sposób wprowadzania substancji terapeutycznych do komórek |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005039579.1A DE102005039579B4 (de) | 2005-08-19 | 2005-08-19 | Verfahren zur Einschleusung von therapeutischen Substanzen in Zellen |
| US71140705P | 2005-08-26 | 2005-08-26 | |
| PCT/DE2006/001453 WO2007019845A2 (de) | 2005-08-19 | 2006-08-21 | Verfahren zur einschleusung von therapeutischen substanzen in zellen |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10012394.2A Division EP2266544B1 (de) | 2005-08-19 | 2006-08-21 | Verfahren zur einschleusung von therapeutischen substanzen in zellen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1917004A2 true EP1917004A2 (de) | 2008-05-07 |
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ID=39676367
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP06775877A Withdrawn EP1917004A2 (de) | 2005-08-19 | 2006-08-21 | Verfahren zur einschleusung von therapeutischen substanzen in zellen |
| EP10012394.2A Active EP2266544B1 (de) | 2005-08-19 | 2006-08-21 | Verfahren zur einschleusung von therapeutischen substanzen in zellen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10012394.2A Active EP2266544B1 (de) | 2005-08-19 | 2006-08-21 | Verfahren zur einschleusung von therapeutischen substanzen in zellen |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US20080187595A1 (pl) |
| EP (2) | EP1917004A2 (pl) |
| JP (1) | JP5512968B2 (pl) |
| KR (2) | KR20080034925A (pl) |
| CN (2) | CN102716068A (pl) |
| AU (1) | AU2006281783B2 (pl) |
| BR (1) | BRPI0614835A2 (pl) |
| CA (1) | CA2619278C (pl) |
| DE (1) | DE102005039579B4 (pl) |
| DK (1) | DK2266544T3 (pl) |
| ES (1) | ES2635493T3 (pl) |
| IL (1) | IL189079A (pl) |
| PL (1) | PL2266544T3 (pl) |
| PT (1) | PT2266544T (pl) |
| RU (1) | RU2480201C2 (pl) |
| WO (1) | WO2007019845A2 (pl) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| WO2021124028A1 (es) | 2019-12-18 | 2021-06-24 | Universidad De Guadalajara | Nanopartículas para el tratamiento del cáncer |
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| AU2006281783B2 (en) | 2011-07-14 |
| RU2480201C2 (ru) | 2013-04-27 |
| CA2619278A1 (en) | 2007-02-02 |
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