CA3198558A1 - Adjuvants de reduction d'interactions non specifiques entre des conjugues polymeres fluorescents et des cellules d'un echantillon biologique - Google Patents
Adjuvants de reduction d'interactions non specifiques entre des conjugues polymeres fluorescents et des cellules d'un echantillon biologiqueInfo
- Publication number
- CA3198558A1 CA3198558A1 CA3198558A CA3198558A CA3198558A1 CA 3198558 A1 CA3198558 A1 CA 3198558A1 CA 3198558 A CA3198558 A CA 3198558A CA 3198558 A CA3198558 A CA 3198558A CA 3198558 A1 CA3198558 A1 CA 3198558A1
- Authority
- CA
- Canada
- Prior art keywords
- betaine
- alkyl
- salt
- group
- polymer
- 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.)
- Pending
Links
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- 238000000034 method Methods 0.000 claims abstract description 60
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- 239000002888 zwitterionic surfactant Substances 0.000 claims abstract description 30
- 229920000642 polymer Polymers 0.000 claims description 234
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 115
- -1 dihydroxyethyl Chemical group 0.000 claims description 88
- 125000000217 alkyl group Chemical group 0.000 claims description 83
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- 239000000178 monomer Substances 0.000 claims description 59
- 125000003118 aryl group Chemical group 0.000 claims description 58
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- 150000003839 salts Chemical class 0.000 claims description 37
- XXPBFNVKTVJZKF-UHFFFAOYSA-N dihydrophenanthrene Natural products C1=CC=C2CCC3=CC=CC=C3C2=C1 XXPBFNVKTVJZKF-UHFFFAOYSA-N 0.000 claims description 34
- 125000005647 linker group Chemical group 0.000 claims description 31
- 125000005842 heteroatom Chemical group 0.000 claims description 30
- 150000002148 esters Chemical class 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 claims description 26
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- 239000012491 analyte Substances 0.000 claims description 24
- 125000001072 heteroaryl group Chemical group 0.000 claims description 24
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 23
- 125000000524 functional group Chemical group 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- 125000003545 alkoxy group Chemical group 0.000 claims description 21
- 229920006395 saturated elastomer Polymers 0.000 claims description 21
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 19
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- 125000004104 aryloxy group Chemical group 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 18
- 150000001412 amines Chemical class 0.000 claims description 16
- 125000001188 haloalkyl group Chemical group 0.000 claims description 16
- 210000000265 leukocyte Anatomy 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 13
- 230000003247 decreasing effect Effects 0.000 claims description 13
- 150000002367 halogens Chemical class 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 239000011734 sodium Substances 0.000 claims description 13
- 150000003573 thiols Chemical class 0.000 claims description 13
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- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 12
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 11
- 150000007942 carboxylates Chemical class 0.000 claims description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 229910052708 sodium Inorganic materials 0.000 claims description 11
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
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- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 125000001769 aryl amino group Chemical group 0.000 claims description 8
- 229940094506 lauryl betaine Drugs 0.000 claims description 8
- 239000003755 preservative agent Substances 0.000 claims description 8
- 230000002335 preservative effect Effects 0.000 claims description 8
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 7
- 150000001336 alkenes Chemical class 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims description 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 7
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 7
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims description 7
- ZKWJQNCOTNUNMF-QXMHVHEDSA-N 2-[dimethyl-[3-[[(z)-octadec-9-enoyl]amino]propyl]azaniumyl]acetate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O ZKWJQNCOTNUNMF-QXMHVHEDSA-N 0.000 claims description 6
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 claims description 6
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 6
- 159000000001 potassium salts Chemical class 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 102000008394 Immunoglobulin Fragments Human genes 0.000 claims description 5
- 108010021625 Immunoglobulin Fragments Proteins 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 5
- 125000005677 ethinylene group Chemical class [*:2]C#C[*:1] 0.000 claims description 5
- 235000013336 milk Nutrition 0.000 claims description 5
- 210000004080 milk Anatomy 0.000 claims description 5
- 239000008267 milk Substances 0.000 claims description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- 229940124272 protein stabilizer Drugs 0.000 claims description 5
- 108700004121 sarkosyl Proteins 0.000 claims description 5
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 5
- 108010077895 Sarcosine Proteins 0.000 claims description 4
- RNOAANRGEYCUQZ-UHFFFAOYSA-N azido acetate Chemical compound CC(=O)ON=[N+]=[N-] RNOAANRGEYCUQZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000003446 ligand Substances 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000003107 substituted aryl group Chemical group 0.000 claims description 4
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 4
- XOMRRQXKHMYMOC-NRFANRHFSA-N (3s)-3-hexadecanoyloxy-4-(trimethylazaniumyl)butanoate Chemical compound CCCCCCCCCCCCCCCC(=O)O[C@@H](CC([O-])=O)C[N+](C)(C)C XOMRRQXKHMYMOC-NRFANRHFSA-N 0.000 claims description 3
- FPVJYHHGNGJAPC-UHFFFAOYSA-N 2-[3-(decanoylamino)propyl-dimethylazaniumyl]acetate Chemical compound CCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O FPVJYHHGNGJAPC-UHFFFAOYSA-N 0.000 claims description 3
- OTKWLUKIHNEGIG-UHFFFAOYSA-N 2-[3-(hexadecanoylamino)propyl-dimethylazaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O OTKWLUKIHNEGIG-UHFFFAOYSA-N 0.000 claims description 3
- ZMXWTYDZWPGTOM-LKAWRWRFSA-N 2-[3-[[(z,12r)-12-hydroxyoctadec-9-enoyl]amino]propyl-dimethylazaniumyl]acetate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O ZMXWTYDZWPGTOM-LKAWRWRFSA-N 0.000 claims description 3
- QEJSCTLHIOVBLH-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)-octadecylazaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCCCC[N+](CCO)(CCO)CC([O-])=O QEJSCTLHIOVBLH-UHFFFAOYSA-N 0.000 claims description 3
- NPKLJZUIYWRNMV-UHFFFAOYSA-N 2-[decyl(dimethyl)azaniumyl]acetate Chemical compound CCCCCCCCCC[N+](C)(C)CC([O-])=O NPKLJZUIYWRNMV-UHFFFAOYSA-N 0.000 claims description 3
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- SUZKAIPUWCLPCH-UHFFFAOYSA-N 2-[dimethyl-[3-(octanoylamino)propyl]azaniumyl]acetate Chemical group CCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O SUZKAIPUWCLPCH-UHFFFAOYSA-N 0.000 claims description 3
- UIJMHOVIUFGSNF-UHFFFAOYSA-N 2-[dimethyl-[3-(undec-10-enoylamino)propyl]azaniumyl]acetate Chemical compound [O-]C(=O)C[N+](C)(C)CCCNC(=O)CCCCCCCCC=C UIJMHOVIUFGSNF-UHFFFAOYSA-N 0.000 claims description 3
- SQXSZTQNKBBYPM-UHFFFAOYSA-N 2-[docosyl(dimethyl)azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CC([O-])=O SQXSZTQNKBBYPM-UHFFFAOYSA-N 0.000 claims description 3
- TYIOVYZMKITKRO-UHFFFAOYSA-N 2-[hexadecyl(dimethyl)azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)CC([O-])=O TYIOVYZMKITKRO-UHFFFAOYSA-N 0.000 claims description 3
- IXOCGRPBILEGOX-UHFFFAOYSA-N 3-[3-(dodecanoylamino)propyl-dimethylazaniumyl]-2-hydroxypropane-1-sulfonate Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)CS([O-])(=O)=O IXOCGRPBILEGOX-UHFFFAOYSA-N 0.000 claims description 3
- CNIGBCBFYDWQHS-QXMHVHEDSA-N 3-[dimethyl-[3-[[(z)-octadec-9-enoyl]amino]propyl]azaniumyl]-2-hydroxypropane-1-sulfonate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCC[N+](C)(C)CC(O)CS([O-])(=O)=O CNIGBCBFYDWQHS-QXMHVHEDSA-N 0.000 claims description 3
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- QGCUAFIULMNFPJ-UHFFFAOYSA-N Myristamidopropyl betaine Chemical compound CCCCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O QGCUAFIULMNFPJ-UHFFFAOYSA-N 0.000 claims description 3
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- G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
- G01N33/56966—Animal cells
- G01N33/56972—White blood cells
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/58—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
- G01N33/582—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances with fluorescent label
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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- C08G2261/12—Copolymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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- C08G2261/312—Non-condensed aromatic systems, e.g. benzene
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
- C08G2261/314—Condensed aromatic systems, e.g. perylene, anthracene or pyrene
- C08G2261/3142—Condensed aromatic systems, e.g. perylene, anthracene or pyrene fluorene-based, e.g. fluorene, indenofluorene, or spirobifluorene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/34—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
- C08G2261/342—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing only carbon atoms
- C08G2261/3422—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing only carbon atoms conjugated, e.g. PPV-type
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- Zoology (AREA)
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- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Abstract
La divulgation concerne des procédés et des compositions de réduction ou d'élimination d'une liaison non spécifique d'au moins un conjugué de colorant à des cellules d'un échantillon biologique. Un conjugué de colorant est mis en contact avec au moins un tensioactif zwitterionique ou anionique avant, pendant ou après mise en contact du conjugué de colorant avec un échantillon de sang, ce qui conduit à une liaison non spécifique sensiblement réduite du conjugué de colorant à des cellules de l'échantillon biologique.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202063113703P | 2020-11-13 | 2020-11-13 | |
| US63/113,703 | 2020-11-13 | ||
| PCT/US2021/059254 WO2022104147A1 (fr) | 2020-11-13 | 2021-11-12 | Adjuvants de réduction d'interactions non spécifiques entre des conjugués polymères fluorescents et des cellules d'un échantillon biologique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3198558A1 true CA3198558A1 (fr) | 2022-05-19 |
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|---|---|---|---|
| CA3198558A Pending CA3198558A1 (fr) | 2020-11-13 | 2021-11-12 | Adjuvants de reduction d'interactions non specifiques entre des conjugues polymeres fluorescents et des cellules d'un echantillon biologique |
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| Country | Link |
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| EP (1) | EP4244625A1 (fr) |
| JP (1) | JP2023550721A (fr) |
| CN (1) | CN116997797A (fr) |
| AU (1) | AU2021380843A1 (fr) |
| CA (1) | CA3198558A1 (fr) |
| WO (1) | WO2022104147A1 (fr) |
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| ES2936226T3 (es) | 2016-04-15 | 2023-03-15 | Beckman Coulter Inc | Macromoléculas fotoactivas y usos de las mismas |
| US20240270971A1 (en) * | 2021-05-04 | 2024-08-15 | Beckman Coulter, Inc. | Uv-absorbing polymers, compositions and uses thereof |
| CN117255832A (zh) * | 2021-05-04 | 2023-12-19 | 贝克曼库尔特有限公司 | 紫外吸收聚合物、组合物及其用途 |
| CN115873082A (zh) * | 2022-12-26 | 2023-03-31 | 苏州优逸兰迪生物科技有限公司 | 一种pe/荧光串联染料及其制备方法与标记抗体的方法 |
| CN117024294B (zh) * | 2023-08-22 | 2025-06-24 | 山东金智瑞新材料发展有限公司 | 一种孪尾型甜菜碱表面活性剂、制备方法及压裂液 |
| WO2025064842A1 (fr) * | 2023-09-21 | 2025-03-27 | Beckman Coulter, Inc. | Colorants pontés par dihydrophénanthrène (dhp) destinés à être utilisés en cytométrie en flux |
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| US4486530A (en) | 1980-08-04 | 1984-12-04 | Hybritech Incorporated | Immunometric assays using monoclonal antibodies |
| CA1306194C (fr) * | 1985-08-20 | 1992-08-11 | A. Charles Morgan, Jr. | Utilisation de molecules amphipatiques pour la scintigraphie et therapie au moyen de conjugues des anticorps monoclonaux ou polyclonaux |
| EA007652B1 (ru) | 2002-06-20 | 2006-12-29 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | Способ обнаружения и анализа полинуклеотидов с помощью светособирающих полихромофоров |
| US20040101909A1 (en) | 2002-08-20 | 2004-05-27 | Hema-Quebec, 2535 Boul. Laurier, Ste-Foy, Quebec, Canada G1V 4M3 | Purification of polyreactive autoantibodies and uses thereof |
| US8354249B2 (en) | 2005-08-11 | 2013-01-15 | Omrix Biopharmaceuticals Ltd. | Intravenous immunoglobulin composition |
| US8158444B2 (en) | 2006-10-06 | 2012-04-17 | Sirigen, Inc. | Fluorescent methods and materials for directed biomarker signal amplification |
| US20100150942A1 (en) | 2008-12-03 | 2010-06-17 | Cantor Thomas L | Affinity purified human polyclonal antibodies and methods of making and using them |
| US9034658B2 (en) * | 2009-11-23 | 2015-05-19 | The General Hospital Corporation | Microfluidic devices for the capture of biological sample components |
| JP6073684B2 (ja) | 2010-01-19 | 2017-02-01 | シリゲン セカンド リミテッド | 指向性バイオマーカーシグナル増幅のための新規の試薬 |
| US20130108619A1 (en) | 2011-11-02 | 2013-05-02 | Isaac Melamed | Intravenous immunoglobulin processing, diagnostic, and treatment systems and methods |
| US20130177574A1 (en) | 2012-01-11 | 2013-07-11 | Paul I. Terasaki Foundation Laboratory | ANTI-HLA CLASS-Ib ANTIBODIES MIMIC IMMUNOREACTIVITY AND IMMUNOMODULATORY FUNCTIONS OF INTRAVENOUS IMMUNOGLOBULIN (IVIg) USEFUL AS THERAPEUTIC IVIg MIMETICS AND METHODS OF THEIR USE |
| CN107207874A (zh) | 2015-03-12 | 2017-09-26 | 贝克顿·迪金森公司 | 聚合物bodipy染料及其使用方法 |
| EP3268434A4 (fr) | 2015-03-12 | 2019-03-27 | Becton, Dickinson and Company | Colorants polymères absorbant les ultraviolets et leurs procédés d'utilisation |
| ES2936226T3 (es) | 2016-04-15 | 2023-03-15 | Beckman Coulter Inc | Macromoléculas fotoactivas y usos de las mismas |
| CN120820389A (zh) | 2016-04-22 | 2025-10-21 | 贝克顿·迪金森公司 | 多重聚合染料装置及其使用方法 |
| CN109562379A (zh) | 2016-06-20 | 2019-04-02 | 拜克门寇尔特公司 | 用于染料共轭试剂的干燥过程 |
| CN119306927A (zh) | 2016-07-11 | 2025-01-14 | 贝克顿·迪金森公司 | 可激发蓝色的水溶剂化聚合物染料 |
| KR20230159629A (ko) | 2016-12-12 | 2023-11-21 | 벡톤 디킨슨 앤드 컴퍼니 | 수용성 중합체 염료 |
| WO2018148098A2 (fr) | 2017-02-08 | 2018-08-16 | Becton, Dickinson And Company | Dispositifs réactifs pour du colorant séché et leurs procédés de fabrication et d'utilisation |
| CN113396006A (zh) | 2018-11-13 | 2021-09-14 | 贝克顿·迪金森公司 | 干燥试剂滤网及其制造和使用方法 |
| US11584825B2 (en) | 2018-12-14 | 2023-02-21 | Beckman Coulter, Inc. | Polymer dye modification and applications |
-
2021
- 2021-11-12 AU AU2021380843A patent/AU2021380843A1/en active Pending
- 2021-11-12 EP EP21824154.5A patent/EP4244625A1/fr active Pending
- 2021-11-12 WO PCT/US2021/059254 patent/WO2022104147A1/fr not_active Ceased
- 2021-11-12 JP JP2023528434A patent/JP2023550721A/ja active Pending
- 2021-11-12 CN CN202180088861.8A patent/CN116997797A/zh active Pending
- 2021-11-12 CA CA3198558A patent/CA3198558A1/fr active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| WO2022104147A1 (fr) | 2022-05-19 |
| EP4244625A1 (fr) | 2023-09-20 |
| JP2023550721A (ja) | 2023-12-05 |
| CN116997797A (zh) | 2023-11-03 |
| AU2021380843A1 (en) | 2023-06-15 |
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