JP2000516985A - カスケードポリマー表面形成コンビナトリアル法 - Google Patents
カスケードポリマー表面形成コンビナトリアル法Info
- Publication number
- JP2000516985A JP2000516985A JP10511785A JP51178598A JP2000516985A JP 2000516985 A JP2000516985 A JP 2000516985A JP 10511785 A JP10511785 A JP 10511785A JP 51178598 A JP51178598 A JP 51178598A JP 2000516985 A JP2000516985 A JP 2000516985A
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- monomer
- layer
- functional groups
- mixture
- 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
- 238000000034 method Methods 0.000 title claims abstract description 35
- 229920000642 polymer Polymers 0.000 title claims abstract description 24
- 230000015572 biosynthetic process Effects 0.000 title description 8
- 239000000178 monomer Substances 0.000 claims abstract description 52
- 239000000758 substrate Substances 0.000 claims abstract description 51
- 239000000203 mixture Substances 0.000 claims abstract description 39
- 125000000524 functional group Chemical group 0.000 claims abstract description 35
- 239000010410 layer Substances 0.000 claims abstract description 30
- 239000012948 isocyanate Substances 0.000 claims abstract description 25
- 239000002344 surface layer Substances 0.000 claims abstract description 15
- 150000002513 isocyanates Chemical class 0.000 claims description 24
- 230000000295 complement effect Effects 0.000 claims description 8
- 125000006239 protecting group Chemical group 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000010511 deprotection reaction Methods 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 4
- 239000008241 heterogeneous mixture Substances 0.000 claims description 2
- 239000000412 dendrimer Substances 0.000 description 15
- 229920000736 dendritic polymer Polymers 0.000 description 15
- 238000000576 coating method Methods 0.000 description 7
- 238000010276 construction Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000012804 iterative process Methods 0.000 description 3
- 239000000693 micelle Substances 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 125000005592 polycycloalkyl group Polymers 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000006557 surface reaction Methods 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 238000006845 Michael addition reaction Methods 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 244000209710 Samanea saman Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 229920000333 poly(propyleneimine) Polymers 0.000 description 1
- 125000003367 polycyclic group Polymers 0.000 description 1
- 229920005554 polynitrile Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- -1 polysiloxanes Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C40—COMBINATORIAL TECHNOLOGY
- C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
- C40B40/00—Libraries per se, e.g. arrays, mixtures
- C40B40/04—Libraries containing only organic compounds
- C40B40/14—Libraries containing macromolecular compounds and not covered by groups C40B40/06 - C40B40/12
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/71—Monoisocyanates or monoisothiocyanates
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/71—Monoisocyanates or monoisothiocyanates
- C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
-
- 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
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/003—Dendrimers
-
- C—CHEMISTRY; METALLURGY
- C40—COMBINATORIAL TECHNOLOGY
- C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
- C40B50/00—Methods of creating libraries, e.g. combinatorial synthesis
- C40B50/08—Liquid phase synthesis, i.e. wherein all library building blocks are in liquid phase or in solution during library creation; Particular methods of cleavage from the liquid support
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/11—Compounds covalently bound to a solid support
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/70—Nanostructure
- Y10S977/754—Dendrimer, i.e. serially branching or "tree-like" structure
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Structural Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1. 基体上の分岐鎖モノマー混合物をデンドリマー化することにより、該基体上 に表面層を形成する方法であって、該モノマーが不均一な官能基化分岐鎖及び均 一な該基体に対する結合を有する、上記方法。 2. 該デンドリマー化工程がさらに、イソシアネートベースの結合を介して基体 上の分岐鎖モノマーの混合物をデンドリマー化する工程である、請求項1に記載 の方法。 能基の混合物であり、少なくとも幾つかの前記保護官能基はコンプリメンタリー な保護基を有し、かつ-CONH-結合を基体表面と各モノマーとの間に形成する。) の化合物からなるモノマー混合物を基体表面と反応させ、及びコンプリメンタリ ーな保護基を脱保護して不均一な脱保護官能基の混合物を反映する不均一な表面 層を与える工程である、請求項2に記載の方法。 4. 全ての保護官能基がコンプリメンタリーな保護基を有し、該脱保護工程がさ らにモノマー層の全ての官能基を脱保護する工程である、請求項3に記載の方法 。 5. 該モノマー混合物中の少なくとも一つのモノマーが該脱保護工程の際に脱保 護されないことを特徴とする、請求項3に記載の方法。 6. モノマーの第二層をモノマー混合物の該第一層上にデンドリマー化する工程 をさらに含み、脱保護されない該モノマーは反応せずに残って、第一デンドリマ ー化層の脱保護官能基とのみ反応しかつ結合する第二層を与える、請求項5に記 載の方法。 7. 該分岐鎖モノマーが安定な三官能基化イソシアネートである、請求項1に記 載の方法。 8. 該デンドリマー化工程がさらに、所定比の成分の官能基を有するモノマーと 基体とを反応させ、かつ同一の所定比の官能基の混合物からなるモノマーの層を 含むデンドリマー化表面を形成する工程である、請求項1に記載の方法。 9. 表面を含む基体と、不均一な官能基からなりかつ該基体に均一に結合する少 なくとも一つのデンドリマー化表面層とから実質的になるカスケードポリマーコ ート分子。 10. 官能基が脱保護され該基体に以下の式の結合により結合している、請求項 9に記載の分子。 11. 該基体が安定な三官能基化イソシアネートから誘導される基から選択され る表面基を含む、請求項10に記載の分子。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/705,905 | 1996-08-28 | ||
US08/705,905 US5886126A (en) | 1996-08-28 | 1996-08-28 | Combinatorial method of forming cascade polymer surfaces |
PCT/US1997/014914 WO1998008885A1 (en) | 1996-08-28 | 1997-08-25 | Combinatorial method of forming cascade polymer surfaces |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006075728A Division JP2006188717A (ja) | 1996-08-28 | 2006-03-17 | カスケードポリマー表面形成コンビナトリアル法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000516985A true JP2000516985A (ja) | 2000-12-19 |
JP2000516985A5 JP2000516985A5 (ja) | 2005-04-07 |
Family
ID=24835434
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10511785A Pending JP2000516985A (ja) | 1996-08-28 | 1997-08-25 | カスケードポリマー表面形成コンビナトリアル法 |
JP2006075728A Pending JP2006188717A (ja) | 1996-08-28 | 2006-03-17 | カスケードポリマー表面形成コンビナトリアル法 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006075728A Pending JP2006188717A (ja) | 1996-08-28 | 2006-03-17 | カスケードポリマー表面形成コンビナトリアル法 |
Country Status (8)
Country | Link |
---|---|
US (1) | US5886126A (ja) |
EP (1) | EP0922062B1 (ja) |
JP (2) | JP2000516985A (ja) |
AT (1) | ATE283301T1 (ja) |
AU (1) | AU4235497A (ja) |
CA (1) | CA2264035C (ja) |
DE (1) | DE69731752T2 (ja) |
WO (1) | WO1998008885A1 (ja) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3866809B2 (ja) * | 1996-12-19 | 2007-01-10 | 松下電器産業株式会社 | 有機膜及びその製造方法 |
US7250534B1 (en) | 1999-07-27 | 2007-07-31 | University Of South Florida | Performance of energy storage devices: potential areas for dendritic chemistry involvement |
US7448258B2 (en) * | 1999-10-29 | 2008-11-11 | Avery Dennison Corporation | High throughput screening for moisture barrier characteristics of materials |
JP5305553B2 (ja) | 2000-10-12 | 2013-10-02 | ユニバーシティー オブ ロチェスター | 癌細胞の増殖を阻害する組成物 |
US20020146684A1 (en) * | 2001-04-09 | 2002-10-10 | Meldal Morten Peter | One dimensional unichemo protection (UCP) in organic synthesis |
DE10158149A1 (de) * | 2001-11-28 | 2003-06-18 | Bayer Ag | Silangruppen enthaltende Polymere |
CN1856504B (zh) | 2002-02-06 | 2010-12-29 | 史戴西思技术有限公司 | 抗梗塞分子 |
WO2003093452A2 (en) * | 2002-02-26 | 2003-11-13 | University Of Utah Research Foundation | Variants of nedd4l associated with hypertension and viral budding |
EP1575992A4 (en) | 2002-08-05 | 2007-02-21 | Univ Rochester | CHIMERIC PROTEINS WITH PROTEIN TRANSDUCTION FIELD / DOMAINE DESAMINASE, ASSOCIATED COMPOUNDS AND CORRESPONDING USES |
US20050106068A1 (en) * | 2003-11-18 | 2005-05-19 | Abdul Malik | Sol-gel dendron separation and extraction capillary column |
CN103983772A (zh) | 2005-04-05 | 2014-08-13 | 康宁股份有限公司 | 一种测定刺激事件对细胞产生的影响的方法 |
EP2371843B1 (en) | 2005-05-19 | 2014-09-17 | THE GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by the Secretary, Department of Health and Human Services | Functional epitopes of streptococcus pneumoniae psaA antigen and uses thereof |
EP2392645A1 (en) | 2005-10-14 | 2011-12-07 | MUSC Foundation For Research Development | Targeting PAX2 for the induction of DEFB1-mediated tumor immunity and cancer therapy |
US8080534B2 (en) | 2005-10-14 | 2011-12-20 | Phigenix, Inc | Targeting PAX2 for the treatment of breast cancer |
PL1940916T3 (pl) * | 2005-10-25 | 2017-07-31 | Starpharma Pty Limited | Związki wielocząsteczkowe o kontrolowanej stechiometrii |
JP5926475B2 (ja) | 2006-09-21 | 2016-05-25 | ユニバーシティー オブ ロチェスター | 筋緊張性ジストロフィーのためのタンパク質置換治療に関する組成物および方法 |
US8999317B2 (en) | 2006-11-01 | 2015-04-07 | University Of Rochester | Methods and compositions related to the structure and function of APOBEC3G |
WO2008098182A1 (en) | 2007-02-08 | 2008-08-14 | University Of Utah Research Foundation | Methods and compositions related to inhibition of viral entry |
CA2734322A1 (en) * | 2008-08-15 | 2010-02-18 | Georgetown University | Na channels, disease, and related assays and compositions |
US20120070443A1 (en) | 2008-12-02 | 2012-03-22 | University Of Utah Research Foundation | Pde1 as a target therapeutic in heart disease |
WO2011022502A1 (en) | 2009-08-18 | 2011-02-24 | Georgetown University | Boronic acid compositions and methods related to cancer |
US20110081293A1 (en) | 2009-10-07 | 2011-04-07 | Sanford-Burnham Medical Research Institute | Methods and compositions related to clot-binding lipid compounds |
JP2013515008A (ja) | 2009-12-18 | 2013-05-02 | サンフォード−バーナム メディカル リサーチ インスティテュート | 凝血塊結合化合物に関連する方法および組成物 |
WO2012135385A1 (en) | 2011-03-28 | 2012-10-04 | University Of Utah Research Foundation | Methods and compositions related to inhibition of viral entry |
US20200209241A1 (en) | 2017-09-15 | 2020-07-02 | Arizona Board Of Regents On Behalf Of Arizona State University | Methods of classifying response to immunotherapy for cancer |
WO2021067550A1 (en) | 2019-10-02 | 2021-04-08 | Arizona Board Of Regents On Behalf Of Arizona State University | Methods and compositions for identifying neoantigens for use in treating and preventing cancer |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5610268A (en) * | 1992-01-13 | 1997-03-11 | Dsm N.V. | Dendritic macromolecule and the preparation thereof |
US5414075A (en) * | 1992-11-06 | 1995-05-09 | Bsi Corporation | Restrained multifunctional reagent for surface modification |
-
1996
- 1996-08-28 US US08/705,905 patent/US5886126A/en not_active Expired - Lifetime
-
1997
- 1997-08-25 CA CA002264035A patent/CA2264035C/en not_active Expired - Fee Related
- 1997-08-25 AT AT97940611T patent/ATE283301T1/de not_active IP Right Cessation
- 1997-08-25 EP EP97940611A patent/EP0922062B1/en not_active Expired - Lifetime
- 1997-08-25 JP JP10511785A patent/JP2000516985A/ja active Pending
- 1997-08-25 DE DE69731752T patent/DE69731752T2/de not_active Expired - Fee Related
- 1997-08-25 WO PCT/US1997/014914 patent/WO1998008885A1/en active IP Right Grant
- 1997-08-25 AU AU42354/97A patent/AU4235497A/en not_active Abandoned
-
2006
- 2006-03-17 JP JP2006075728A patent/JP2006188717A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0922062A4 (en) | 1999-11-10 |
WO1998008885A1 (en) | 1998-03-05 |
DE69731752T2 (de) | 2005-12-22 |
AU4235497A (en) | 1998-03-19 |
EP0922062B1 (en) | 2004-11-24 |
DE69731752D1 (de) | 2004-12-30 |
CA2264035A1 (en) | 1998-03-05 |
JP2006188717A (ja) | 2006-07-20 |
EP0922062A1 (en) | 1999-06-16 |
US5886126A (en) | 1999-03-23 |
CA2264035C (en) | 2007-10-23 |
ATE283301T1 (de) | 2004-12-15 |
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