RU2003112701A - CYCLOPEPTIDES, METHOD FOR PRODUCING THEM AND APPLICATION AS AN INHIBITORS OR ACTIVATORS OF ANTIOGENESIS - Google Patents

CYCLOPEPTIDES, METHOD FOR PRODUCING THEM AND APPLICATION AS AN INHIBITORS OR ACTIVATORS OF ANTIOGENESIS

Info

Publication number
RU2003112701A
RU2003112701A RU2003112701/04A RU2003112701A RU2003112701A RU 2003112701 A RU2003112701 A RU 2003112701A RU 2003112701/04 A RU2003112701/04 A RU 2003112701/04A RU 2003112701 A RU2003112701 A RU 2003112701A RU 2003112701 A RU2003112701 A RU 2003112701A
Authority
RU
Russia
Prior art keywords
lle
gln
pro
gly
lys
Prior art date
Application number
RU2003112701/04A
Other languages
Russian (ru)
Other versions
RU2249599C2 (en
Inventor
Наташа БЕС
Андреа БИКФАЛЬВИ
Жерар ДЕЛЕРИ
Original Assignee
Коммиссариат А Л`Энержи Атомик
Юниверсите Виктор Сегалан Бордо 2
Юниверсите Бордо 1
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from FR0012654A external-priority patent/FR2814744B1/en
Application filed by Коммиссариат А Л`Энержи Атомик, Юниверсите Виктор Сегалан Бордо 2, Юниверсите Бордо 1 filed Critical Коммиссариат А Л`Энержи Атомик
Publication of RU2003112701A publication Critical patent/RU2003112701A/en
Application granted granted Critical
Publication of RU2249599C2 publication Critical patent/RU2249599C2/en

Links

Claims (23)

1. Циклопептид общей формулы цикло(Р1-Arg-lle-Lys-Pro-His-R2), причем указанный полипептид выбран из числа следующих соединений:1. The cyclopeptide of the General formula cyclo (P 1 -Arg-lle-Lys-Pro-His-R 2 ), and the specified polypeptide is selected from among the following compounds: Р11: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:5,P11: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 5, P16: цикло(Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:8,P16: cyclo (Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 8, P17: цикло(Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:9,P17: Cyclo (Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 9, P19: цикло(Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:10,P19: cyclo (Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 10, P20: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO:11,P20: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO: 11, P23: цикло(DPhe-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO:13,P23: Cyclo (DPhe-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO: 13, P24: цикло(Gly-Arg-lle-Lys-Pro-His) SEQ ID NO:25,P24: cyclo (Gly-Arg-lle-Lys-Pro-His) SEQ ID NO: 25, а также соединений P11, P20 и P23, у которых DPhe заменен на DTyr.as well as compounds P11, P20 and P23, in which DPhe is replaced by DTyr. 2. Фармацевтическая композиция для ингибирования ангиогенеза, включающая циклопептид, выбранный из числа следующих циклопептидов:2. A pharmaceutical composition for inhibiting angiogenesis, comprising a cyclopeptide selected from the following cyclopeptides: Р11: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:5,P11: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 5, P16: цикло(Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:8,P16: cyclo (Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 8, P17: цикло(Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:9,P17: Cyclo (Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 9, P19: цикло(Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:10,P19: cyclo (Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 10, P20: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO:11,P20: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO: 11, P23: цикло(DPhe-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO:13,P23: Cyclo (DPhe-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO: 13, P24: цикло(Gly-Arg-lle-Lys-Pro-His) SEQ ID NO:25,P24: cyclo (Gly-Arg-lle-Lys-Pro-His) SEQ ID NO: 25, а также циклопептидов P11, P20 и P23, у которых DPhe заменен на DTyr.as well as cyclopeptides P11, P20 and P23, in which DPhe is replaced by DTyr. 3. Фармацевтическая композиция для активации ангиогенеза, включающая два идентичных или различных циклопептида, конъюгированных с фармацевтически приемлемым органическим соединением, причем циклопептиды выбирают из числа следующих циклопептидов:3. A pharmaceutical composition for activating angiogenesis, comprising two identical or different cyclopeptides conjugated to a pharmaceutically acceptable organic compound, the cyclopeptides being selected from the following cyclopeptides: Р11: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:5,P11: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 5, Р16: цикло(Arg-lle-Lys-Pro-His-Gln-Gly) SEQIDNO:8,P16: cyclo (Arg-lle-Lys-Pro-His-Gln-Gly) SEQIDNO: 8, P17: цикло(Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQIDNO:9,P17: Cyclo (Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQIDNO: 9, P19: цикло(Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:10,P19: cyclo (Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 10, P20: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO:11,P20: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO: 11, P23: цикло(DPhe-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO:13,P23: Cyclo (DPhe-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO: 13, P24: цикло(Gly-Arg-lle-Lys-Pro-His) SEQ ID NO:25,P24: cyclo (Gly-Arg-lle-Lys-Pro-His) SEQ ID NO: 25, а также циклопептидов P11, P20 и P23, у которых DPhe заменен на DTyr.as well as cyclopeptides P11, P20 and P23, in which DPhe is replaced by DTyr. 4. Система, включающая циклопептид по любому из пп.1-3, ковалентно связанный с органической ножкой-спейсером.4. A system comprising a cyclopeptide according to any one of claims 1 to 3, covalently linked to an organic spacer leg. 5. Система по п.4, в которой органическая ножка-спейсер ковалентно связана с подложкой.5. The system of claim 4, wherein the organic spacer leg is covalently bonded to the substrate. 6. Система, включающая два циклопептида по любому из пп.1-3, ковалентно связанные с органическим соединением.6. A system comprising two cyclopeptides according to any one of claims 1 to 3, covalently linked to an organic compound. 7. Система по п.6, в которой расстояние между двумя циклопептидами таково, что при приведении системы в контакт с клетками, экспрессирующими рецепторы фактора роста эпителия сосудов (VEGF), она позволяет димеризоваться указанным рецепторам.7. The system of claim 6, wherein the distance between the two cyclopeptides is such that when the system is brought into contact with cells expressing receptors for vascular epithelial growth factor (VEGF), it allows these receptors to dimerize. 8. Система по любому из пп.6 и 7, в которой органическое соединение ковалентно связано с подложкой при помощи органической ножки-спейсера.8. The system according to any one of claims 6 and 7, in which the organic compound is covalently bonded to the substrate using an organic spacer leg. 9. Система, включающая твердую подложку, на которой циклопептиды по любому из пп.1-3 присоединены ковалентными связями, причем каждый из циклопептидов связан с подложкой при помощи органической ножки-спейсера.9. A system comprising a solid support on which the cyclopeptides according to any one of claims 1 to 3 are attached by covalent bonds, each of the cyclopeptides being connected to the support using an organic spacer leg. 10. Система по любому из пп.4-9, в которой ножка-спейсер включает цепь углеводорода, фторуглерода, простого полиэфира, полиэтиленгликоля, полиамина, полиамида, сложного полиэфира, полисилоксана или их комбинацию, имеющую функциональные группы на каждом конце для образования ковалентной связи, с одной стороны, с циклопептидом, а с другой - с подложкой.10. The system according to any one of claims 4 to 9, in which the spacer leg includes a chain of a hydrocarbon, fluorocarbon, polyester, polyethylene glycol, polyamine, polyamide, polyester, polysiloxane or a combination thereof having functional groups at each end to form a covalent bond on the one hand with a cyclopeptide, and on the other with a substrate. 11. Система по любому из пп.4-10, в которой органическая ножка-спейсер дополнительно включает группировку, подверженную расщеплению какой-либо ферментативной системой.11. The system according to any one of claims 4 to 10, in which the organic spacer leg further comprises a moiety susceptible to cleavage by any enzymatic system. 12. Система по п.11, в которой органическая ножка-спейсер дополнительно включает биологически активное соединение.12. The system of claim 11, wherein the organic spacer leg further comprises a biologically active compound. 13. Система по любому из пп.5, 8 и 9, в которой подложка представляет собой органическое или неорганическое твердое вещество.13. The system according to any one of paragraphs.5, 8 and 9, in which the substrate is an organic or inorganic solid. 14. Система по любому из пп.5, 8 и 9, в которой подложка представляет собой органический полимер в твердом виде или в виде геля.14. The system according to any one of paragraphs.5, 8 and 9, in which the substrate is an organic polymer in solid form or in the form of a gel. 15. Система по п.14, в которой органический полимер является биосовместимым, биодеградируемым полимером или не является биосовместимым, биодеградируемым полимером.15. The system of claim 14, wherein the organic polymer is a biocompatible, biodegradable polymer or is not a biocompatible, biodegradable polymer. 16. Система по п.15, в которой органический полимер выбран из числа полиэтилентерефталата, сополимеров винилиденфторида и гексафторпропилена, поливиниловых спиртов, полигидроксиэтилметакрилатов, полисахаридов и их сополимеров.16. The system of claim 15, wherein the organic polymer is selected from polyethylene terephthalate, copolymers of vinylidene fluoride and hexafluoropropylene, polyvinyl alcohols, polyhydroxyethyl methacrylates, polysaccharides and their copolymers. 17. Фармацевтическая композиция для ингибирования ангиогенеза, включающая систему по любому из пп.4 и 5, в которой циклопептид выбран из числа следующих циклопептидов:17. A pharmaceutical composition for inhibiting angiogenesis, comprising a system according to any one of claims 4 and 5, wherein the cyclopeptide is selected from the following cyclopeptides: Р11: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:5,P11: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 5, P16: цикло(Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:8,P16: cyclo (Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 8, P17: цикло(Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:9,P17: Cyclo (Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 9, P19: цикло(Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:10,P19: cyclo (Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 10, P20: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO:11,P20: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO: 11, P23: цикло(DTyr-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO:13,P23: Cyclo (DTyr-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO: 13, Р24: цикло(Gly-Arg-lle-Lys-Pro-His) SEQ ID NO:25,P24: cyclo (Gly-Arg-lle-Lys-Pro-His) SEQ ID NO: 25, а также циклопептидов P11, P20 и Р23, у которых DPhe заменен на DTyr.as well as cyclopeptides P11, P20 and P23, in which DPhe is replaced by DTyr. 18. Система для активации ангиогенеза по любому из пп.6-8, в которой циклопептид выбран из числа следующих циклопептидов:18. A system for activating angiogenesis according to any one of claims 6 to 8, in which the cyclopeptide is selected from the following cyclopeptides: Р11: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:5,P11: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 5, P16: цикло(Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:8,P16: cyclo (Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 8, P17: цикло(Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO:9,P17: Cyclo (Pro-Arg-lle-Lys-Pro-His-Gln-Gly) SEQ ID NO: 9, P19: цикло(Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO:10,P19: cyclo (Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly-Glu) SEQ ID NO: 10, P20: цикло(DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO:11,P20: cyclo (DPhe-Pro-Gln-lle-Met-Arg-lle-Lys-Pro-His-Gln-Gly-Gln-His-lle-Gly) SEQ ID NO: 11, P23: цикло(DTyr-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO:13,P23: Cyclo (DTyr-Pro-Arg-lle-Lys-Pro-His-Gln) SEQ ID NO: 13, P24: цикло(Gly-Arg-lle-Lys-Pro-His) SEQ ID NO:25,P24: cyclo (Gly-Arg-lle-Lys-Pro-His) SEQ ID NO: 25, а также циклопептидов P11, P20 и P23, у которых DPhe заменен на DTyr.as well as cyclopeptides P11, P20 and P23, in which DPhe is replaced by DTyr. 19. Способ получения системы по любому из пп.14-16, который заключается в облучении подложки, сделанной из органического полимера, ионизирующим излучением, плазмой или пучком фотонов по определенным участкам подложки, а затем в прививке органических ножек-спейсеров по этим участкам подложки.19. A method of obtaining a system according to any one of paragraphs.14-16, which consists in irradiating a substrate made of an organic polymer, ionizing radiation, a plasma or a photon beam in certain areas of the substrate, and then inoculating organic spacer legs on these sections of the substrate. 20. Способ по п.19, в котором облучение проводится через маску.20. The method according to claim 19, in which the irradiation is carried out through a mask. 21. Способ по п.19, в котором ионизирующее излучение представляет собой пучок электронов или быстрых тяжелых ионов.21. The method according to claim 19, in which the ionizing radiation is a beam of electrons or fast heavy ions. 22. Способ по п.19, в котором циклопептиды присоединяют к органическим ножкам-спейсерам до прививки к подложке.22. The method according to claim 19, in which the cyclopeptides are attached to the organic spacer legs before grafting to the substrate. 23. Способ по п.19, дополнительно включающий стадию присоединения циклопептидов к органическим ножкам-спейсерам после их прививки к подложке.23. The method according to claim 19, further comprising the step of attaching the cyclopeptides to the organic spacer legs after they are grafted onto the substrate.
RU2003112701/04A 2000-10-04 2001-10-02 Cyclopeptides, method for production thereof and uses as angiogenesis inhibitors or activators RU2249599C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0012654A FR2814744B1 (en) 2000-10-04 2000-10-04 CYCLOPEPTIDES, THEIR PREPARATION PROCESS AND THEIR USE AS ANGIOGENESIS INHIBITOR OR ACTIVATOR
FR0012654 2000-10-04

Publications (2)

Publication Number Publication Date
RU2003112701A true RU2003112701A (en) 2004-12-10
RU2249599C2 RU2249599C2 (en) 2005-04-10

Family

ID=8854977

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2003112701/04A RU2249599C2 (en) 2000-10-04 2001-10-02 Cyclopeptides, method for production thereof and uses as angiogenesis inhibitors or activators

Country Status (15)

Country Link
US (2) US7199100B2 (en)
EP (1) EP1328546B1 (en)
JP (1) JP4303958B2 (en)
AT (1) ATE354589T1 (en)
AU (2) AU2001293948B2 (en)
CA (1) CA2424506A1 (en)
DE (1) DE60126802T2 (en)
DK (1) DK1328546T3 (en)
ES (1) ES2282293T3 (en)
FR (1) FR2814744B1 (en)
IL (1) IL155117A0 (en)
NO (1) NO20031377L (en)
NZ (1) NZ525069A (en)
RU (1) RU2249599C2 (en)
WO (1) WO2002028895A2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7261876B2 (en) 2002-03-01 2007-08-28 Bracco International Bv Multivalent constructs for therapeutic and diagnostic applications
US8623822B2 (en) * 2002-03-01 2014-01-07 Bracco Suisse Sa KDR and VEGF/KDR binding peptides and their use in diagnosis and therapy
US7211240B2 (en) * 2002-03-01 2007-05-01 Bracco International B.V. Multivalent constructs for therapeutic and diagnostic applications
US7794693B2 (en) 2002-03-01 2010-09-14 Bracco International B.V. Targeting vector-phospholipid conjugates
US20050100963A1 (en) 2002-03-01 2005-05-12 Dyax Corporation KDR and VEGF/KDR binding peptides and their use in diagnosis and therapy
WO2004078778A2 (en) * 2003-03-03 2004-09-16 Dyax Corp. PEPTIDES THAT SPECIFICALLY BIND HGF RECEPTOR (cMet) AND USES THEREOF
ES2340885T3 (en) * 2006-01-17 2010-06-10 N.V. Organon SELECTIVE ENZYMATIC HYDROLYSIS OF TERC-BUTILIC ESTERS C PEPTIDES TERMINAL.
US8227413B2 (en) 2006-10-19 2012-07-24 Ramot At Tel-Aviv University Ltd. Compositions and methods for inducing angiogenesis
US8741850B2 (en) * 2009-07-24 2014-06-03 Advanced Accelerator Applications S.A. Compounds modulators of VEGF activity and uses thereof
FR2969999B1 (en) 2011-01-03 2013-02-08 Commissariat Energie Atomique CONJUGATE, PROCESS FOR PREPARING THE SAME AND USES THEREOF
JP6758022B2 (en) * 2012-09-03 2020-09-23 国立大学法人 東京大学 Vascular endothelial cell growth factor receptor inhibitor peptide
CN103724290B (en) * 2013-11-15 2015-04-29 浙江大学 Cyclopeptide compound clavatustide A as well as producing strain, preparation method and application thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4310643A1 (en) * 1993-04-01 1994-10-06 Merck Patent Gmbh Cyclic adhesion inhibitors
EP0844252A3 (en) * 1996-11-15 1998-07-08 Remacle, José Cyclic peptides bearing a tail designed for subsequent chemical coupling and process for preparing same
CA2320339A1 (en) * 1998-02-11 1999-08-19 Resolution Pharmaceuticals Inc. Angiogenesis targeting molecules
KR20010102556A (en) * 1999-03-11 2001-11-15 추후제출 Compositions and methods for treating cancer and hyperproliferative disorders

Similar Documents

Publication Publication Date Title
RU2003112701A (en) CYCLOPEPTIDES, METHOD FOR PRODUCING THEM AND APPLICATION AS AN INHIBITORS OR ACTIVATORS OF ANTIOGENESIS
US5262451A (en) Multifunctional thrombo-resistant coatings and methods of manufacture
Itoh et al. Hydroxyapatite-coated tendon chitosan tubes with adsorbed laminin peptides facilitate nerve regeneration in vivo
US5342693A (en) Multifunctional thrombo-resistant coating and methods of manufacture
US5182317A (en) Multifunctional thrombo-resistant coatings and methods of manufacture
Kharbikar et al. Modulating the foreign body response of implants for diabetes treatment
Gardner et al. Biomaterials-based modulation of the immune system
US5573916A (en) Immunogenic constructs comprising b-cell and t-cell epitopes on common carrier
US8986713B2 (en) Medical device capable of being compacted and expanded having anti-thrombin III binding activity
Karamdoust et al. Preparation of antibacterial surfaces by hyperthermal hydrogen induced cross-linking of polymer thin films
AR002255A1 (en) A COMPOSITION THAT INCLUDES A FORMULATION OF MICROFLUIDIZED ANTIGEN AND USES OF SUCH FORMULATION.
Dai et al. Surface and interface control of polymeric biomaterials, conjugated polymers, and carbon nanotubes
DE69329735D1 (en) PEPTIDE HYDROCARBON CONJUGATES WHICH T-CELL IMMUNITY
CA2398668A1 (en) Delivery systems using preformed biodegradable polymer compositions and methods
US7824672B2 (en) Method for coating living cells
US20140273148A1 (en) Methods and compositions involving fibrillizing polypeptides for nanofibers
US20080089919A1 (en) Immobilized Biologically Active Entities Having a High Degree of Biological Activity
Zarubova et al. Biomaterial-based immunoengineering to fight COVID-19 and infectious diseases
JP2011502631A5 (en)
Kidane et al. Surface modification of polyethylene terephthalate using PEO-polybutadiene-PEO triblock copolymers
US6961610B2 (en) Branched polyethylene oxide terminated biomedical polymers and their use in biomedical devices
EP1328546B1 (en) Cyclic peptides, method for preparing same and use as angiogenesis inhibitor or activator
JP2010070615A (en) Crosslinked polymer composition for surface treatment of support
CN101411899B (en) Vascular undercoat stent
Bromberg et al. Bioactive surfaces via immobilization of self-assembling polymers onto hydrophobic materials