메뉴 건너뛰기




Volumn 22, Issue 11, 2011, Pages 2199-2209

Regenerative biomaterials that "click": Simple, aqueous-based protocols for hydrogel synthesis, surface immobilization, and 3D patterning

Author keywords

[No Author keywords available]

Indexed keywords

BIOMATERIALS; BIOMIMETIC PROCESSES; COPPER COMPOUNDS; CYCLOADDITION; HYDROGELS; SCAFFOLDS; SCAFFOLDS (BIOLOGY); TISSUE REGENERATION;

EID: 81255143206     PISSN: 10431802     EISSN: 15204812     Source Type: Journal    
DOI: 10.1021/bc200281k     Document Type: Review
Times cited : (179)

References (85)
  • 1
    • 0027595948 scopus 로고
    • Tissue engineering
    • Langer, R. and Vacanti, J. P. (1993) Tissue engineering Science 260, 920-926 (Pubitemid 23209960)
    • (1993) Science , vol.260 , Issue.5110 , pp. 920-926
    • Langer, R.1    Vacanti, J.P.2
  • 2
    • 0042061223 scopus 로고    scopus 로고
    • Hydrogels for tissue engineering: Scaffold design variables and applications
    • DOI 10.1016/S0142-9612(03)00340-5
    • Drury, J. L. and Mooney, D. J. (2003) Hydrogels for tissue engineering: scaffold design variables and applications Biomaterials 24, 4337-4351 (Pubitemid 36960132)
    • (2003) Biomaterials , vol.24 , Issue.24 , pp. 4337-4351
    • Drury, J.L.1    Mooney, D.J.2
  • 3
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C., Finn, M. G., and Sharpless, K. B. (2001) Click chemistry: diverse chemical function from a few good reactions Angew. Chem., Int. Ed. 40, 2004-2021
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 4
    • 71249129936 scopus 로고    scopus 로고
    • Synthesis and applications of biomedical and pharmaceutical polymers via click chemistry methodologies
    • van Dijk, M., Rijkers, D. T. S., Liskamp, R. M. J., van Nostrun, C. F., and Hennink, W. E. (2009) Synthesis and applications of biomedical and pharmaceutical polymers via click chemistry methodologies Bioconjugate Chem. 20, 2001-2016
    • (2009) Bioconjugate Chem. , vol.20 , pp. 2001-2016
    • Van Dijk, M.1    Rijkers, D.T.S.2    Liskamp, R.M.J.3    Van Nostrun, C.F.4    Hennink, W.E.5
  • 5
    • 77949812304 scopus 로고    scopus 로고
    • Marrying click chemistry with polymerization: Expanding the scope of polymeric materials
    • Golas, P. L. and Matyjaszewski, K. (2009) Marrying click chemistry with polymerization: expanding the scope of polymeric materials Chem. Soc. Rev. 39, 1338-1354
    • (2009) Chem. Soc. Rev. , vol.39 , pp. 1338-1354
    • Golas, P.L.1    Matyjaszewski, K.2
  • 6
    • 34547482973 scopus 로고    scopus 로고
    • Clicking polymers: A straightforward approach to novel macromolecular architectures
    • Fournier, D., Hoogenboom, R., and Schubert, U. S. (2007) Clicking polymers: a straightforward approach to novel macromolecular architectures Chem. Soc. Rev. 36, 1369-1380
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1369-1380
    • Fournier, D.1    Hoogenboom, R.2    Schubert, U.S.3
  • 7
    • 33846703461 scopus 로고    scopus 로고
    • Click chemistry in polymer and materials science
    • Binder, W. H. and Sachsenhofer, R. (2007) Click chemistry in polymer and materials science Macromol. Rapid Commun. 28, 15-24
    • (2007) Macromol. Rapid Commun. , vol.28 , pp. 15-24
    • Binder, W.H.1    Sachsenhofer, R.2
  • 8
    • 84981800416 scopus 로고
    • Cycloadditions - Defintion, classification, and characterization
    • Huisgen, R. (1968) Cycloadditions - defintion, classification, and characterization Angew. Chem., Int. Ed. Engl. 7, 321-328
    • (1968) Angew. Chem., Int. Ed. Engl. , vol.7 , pp. 321-328
    • Huisgen, R.1
  • 9
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on solid phase: [1,2,3]-Triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
    • DOI 10.1021/jo011148j
    • Tornoe, C. W., Christensen, C., and Meldal, M. (2002) Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides J. Org. Chem. 67, 3057-3064 (Pubitemid 34457265)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.9 , pp. 3057-3064
    • Tornoe, C.W.1    Christensen, C.2    Meldal, M.3
  • 10
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • DOI 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
    • Rostovtsev, V. V., Green, L. G., Fokin, V. V., and Sharpless, K. B. (2002) A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes Angew. Chem., Int. Ed. 41, 2596-2599 (Pubitemid 34803480)
    • (2002) Angewandte Chemie - International Edition , vol.41 , Issue.14 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 11
  • 12
    • 9344227358 scopus 로고    scopus 로고
    • A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems
    • DOI 10.1021/ja044996f
    • Agard, N. J., Prescher, J. A., and Bertozzi, C. R. (2004) A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems J. Am. Chem. Soc. 126, 15046-15047 (Pubitemid 39557262)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.46 , pp. 15046-15047
    • Agard, N.J.1    Prescher, J.A.2    Bertozzi, C.R.3
  • 13
    • 50249085119 scopus 로고    scopus 로고
    • Second-generation difluorinated cyclooctynes for cooper-free click chemistry
    • Codelli, J. A., Baskin, J. M., Agard, N. J., and Bertozzi, C. R. (2008) Second-generation difluorinated cyclooctynes for cooper-free click chemistry J. Am. Chem. Soc. 130, 11486-11493
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11486-11493
    • Codelli, J.A.1    Baskin, J.M.2    Agard, N.J.3    Bertozzi, C.R.4
  • 15
    • 84962105974 scopus 로고
    • Synthesen in der hydroaromatischen Reihe
    • Diels, O. and Alder, K. (1928) Synthesen in der hydroaromatischen Reihe Justus Liebigs Ann. Chem. 460, 98-122
    • (1928) Justus Liebigs Ann. Chem. , vol.460 , pp. 98-122
    • Diels, O.1    Alder, K.2
  • 16
    • 0041818406 scopus 로고    scopus 로고
    • Hydrophobic interactions and chemical reactivity
    • Otto, S. and Engberts, J. B. (2003) Hydrophobic interactions and chemical reactivity Org. Biomol. Chem. 1, 2809-2820
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 2809-2820
    • Otto, S.1    Engberts, J.B.2
  • 17
    • 33847085398 scopus 로고
    • Hydrophobic acceleration of Diels-Alder reactions
    • Rideout, D. C. and Breslow, R. J. (1980) Hydrophobic acceleration of Diels-Alder reactions J. Am. Chem. Soc. 102, 7816-7817
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 7816-7817
    • Rideout, D.C.1    Breslow, R.J.2
  • 20
    • 0037122788 scopus 로고    scopus 로고
    • Novel crosslinking methods to design hydrogels
    • DOI 10.1016/S0169-409X(01)00240-X, PII S0169409X0100240X
    • Hennink, W. E. and van Nostrum, C. F. (2002) Novel crosslinking methods to design hydrogels Adv. Drug Delivery Rev. 54, 13-36 (Pubitemid 34075312)
    • (2002) Advanced Drug Delivery Reviews , vol.54 , Issue.1 , pp. 13-36
    • Hennink, W.E.1    Van Nostrum, C.F.2
  • 21
    • 33644952400 scopus 로고    scopus 로고
    • Poly(vinyl alcohol)-based hydrogels formed by "click chemistry"
    • Ossipov, D. A. and Hilborn, J. (2006) Poly(vinyl alcohol)-based hydrogels formed by "click chemistry" Macromolecules 39, 1709-1718
    • (2006) Macromolecules , vol.39 , pp. 1709-1718
    • Ossipov, D.A.1    Hilborn, J.2
  • 23
    • 0025814801 scopus 로고
    • Arginyl-glycyl-aspartic acid (RGD): A cell adhesion motif
    • DSouza, S. E., Ginsberg, M. H., and Plow, E. F. (1991) Arginyl-glycyl-aspartic acid (RGD): a cell adhesion motif Trends Biochem. Sci. 16, 246-250 (Pubitemid 121004445)
    • (1991) Trends in Biochemical Sciences , vol.16 , Issue.1 , pp. 246-250
    • D'Souza, S.E.1    Ginsberg, M.H.2    Plow, E.F.3
  • 24
    • 58249085147 scopus 로고    scopus 로고
    • Biodegradable poly(ethylene glycol)-peptide hydrogels with well-defined structure and properties for cell delivery
    • Liu, S. Q., Ee, P. L. R., Ke, C. Y., Hedrick, J. L., and Yang, Y. Y. (2009) Biodegradable poly(ethylene glycol)-peptide hydrogels with well-defined structure and properties for cell delivery Biomaterials 30, 1453-1461
    • (2009) Biomaterials , vol.30 , pp. 1453-1461
    • Liu, S.Q.1    Ee, P.L.R.2    Ke, C.Y.3    Hedrick, J.L.4    Yang, Y.Y.5
  • 25
    • 77954610157 scopus 로고    scopus 로고
    • Synthesis and characterization of enzymatically biodegradable PEG and peptide-based hydrogels prepared by click chemistry
    • Van Dijk, M., van Nostrum, C. F., Hennink, W. E., Rijkers, D. T. S., and Liskamp, R. M. J. (2010) Synthesis and characterization of enzymatically biodegradable PEG and peptide-based hydrogels prepared by click chemistry Biomacromolecules 11, 1608-1614
    • (2010) Biomacromolecules , vol.11 , pp. 1608-1614
    • Van Dijk, M.1    Van Nostrum, C.F.2    Hennink, W.E.3    Rijkers, D.T.S.4    Liskamp, R.M.J.5
  • 26
    • 33750959643 scopus 로고    scopus 로고
    • Review. Hyaluronan: A powerful tissue engineering tool
    • DOI 10.1089/ten.2006.12.2131
    • Allison, D. D. and Grande-Allen, K. J. (2006) Review. Hyaluronan: a powerful tissue engineering tool Tissue Eng. 12, 2131-2140 (Pubitemid 44734972)
    • (2006) Tissue Engineering , vol.12 , Issue.8 , pp. 2131-2140
    • Allison, D.D.1    Grande-Allen, K.J.2
  • 27
    • 34347325267 scopus 로고    scopus 로고
    • Novel hydrogels via click chemistry: Synthesis and potential biomedical applications
    • DOI 10.1021/bm0700800
    • Crescenzi, V., Cornelio, L., Di Meo, C., Nardecchia, S., and Lamanna, R. (2007) Novel hydrogels via click chemistry: synthesis and potential biomedical applications Biomacromolecules 8, 1844-1850 (Pubitemid 47009962)
    • (2007) Biomacromolecules , vol.8 , Issue.6 , pp. 1844-1850
    • Crescenzi, V.1    Cornelio, L.2    Di Meo, C.3    Nardecchia, S.4    Lamanna, R.5
  • 29
    • 79952187613 scopus 로고    scopus 로고
    • Biological hydrogel synthesized from hyaluronic acid, gelatin and chondroitin sulfate by click chemistry
    • Hu, X., Li, D., Zhou, F., and Gao, C. (2011) Biological hydrogel synthesized from hyaluronic acid, gelatin and chondroitin sulfate by click chemistry Acta Biomater. 7, 1618-1626
    • (2011) Acta Biomater. , vol.7 , pp. 1618-1626
    • Hu, X.1    Li, D.2    Zhou, F.3    Gao, C.4
  • 30
    • 68849096820 scopus 로고    scopus 로고
    • Sequential click reactions for synthesizing and patterning three-dimensional cell microenvironments
    • DeForest, C. A., Polizzotti, B. D., and Anseth, K. S. (2009) Sequential click reactions for synthesizing and patterning three-dimensional cell microenvironments Nat. Mater. 8, 659-664
    • (2009) Nat. Mater. , vol.8 , pp. 659-664
    • Deforest, C.A.1    Polizzotti, B.D.2    Anseth, K.S.3
  • 31
    • 77955694267 scopus 로고    scopus 로고
    • Peptide-functionalized click hydrogels with independently tunable mechanics and chemical functionality for 3D cell culture
    • DeForest, C. A., Sims, E. A., and Anseth, K. S. (2010) Peptide-functionalized click hydrogels with independently tunable mechanics and chemical functionality for 3D cell culture Chem. Mater. 22, 4783-4790
    • (2010) Chem. Mater. , vol.22 , pp. 4783-4790
    • Deforest, C.A.1    Sims, E.A.2    Anseth, K.S.3
  • 32
    • 79951965004 scopus 로고    scopus 로고
    • Spatial and temporal control of the alkyne-azide cycloaddition by photoinitiated Cu(II) reduction
    • Adzima, B. J., Tao, Y., Kloxin, C. J., DeForest, C. A., Anseth, K. S., and Bowman, C. N. (2011) Spatial and temporal control of the alkyne-azide cycloaddition by photoinitiated Cu(II) reduction Nat. Chem. 3, 258-261
    • (2011) Nat. Chem. , vol.3 , pp. 258-261
    • Adzima, B.J.1    Tao, Y.2    Kloxin, C.J.3    Deforest, C.A.4    Anseth, K.S.5    Bowman, C.N.6
  • 33
    • 33747367687 scopus 로고
    • Living/controlled radical polymerization. Transition-metal-catalyzed atom transfer radical polymerization in the presence of a conventional radical initiator
    • Wang, J.-S. and Matyjaszewski, K. (1995) Living/controlled radical polymerization. Transition-metal-catalyzed atom transfer radical polymerization in the presence of a conventional radical initiator Macromolecules 28, 7572-7573
    • (1995) Macromolecules , vol.28 , pp. 7572-7573
    • Wang, J.-S.1    Matyjaszewski, K.2
  • 34
    • 0037056318 scopus 로고    scopus 로고
    • Diels-Alder reactions with novel polymeric dienes and dienophiles: Synthesis of reversibly crosslinked elastomers
    • Gheneim, R., Perez-Berumen, C., and Gandini, A. (2002) Diels-Alder reactions with novel polymeric dienes and dienophiles: synthesis of reversibly crosslinked elastomers Macromolecules 35, 7246-7253
    • (2002) Macromolecules , vol.35 , pp. 7246-7253
    • Gheneim, R.1    Perez-Berumen, C.2    Gandini, A.3
  • 35
    • 64549086668 scopus 로고    scopus 로고
    • Rheological and chemical analysis of reverse gelation in a covalently crosslinked Diels-Alder polymer network
    • Adzima, B. J., Aguirre, H. A., Kloxin, C. J., Scott, T. F., and Bowman, C. N. (2008) Rheological and chemical analysis of reverse gelation in a covalently crosslinked Diels-Alder polymer network Macromolecules 41, 9112-9117
    • (2008) Macromolecules , vol.41 , pp. 9112-9117
    • Adzima, B.J.1    Aguirre, H.A.2    Kloxin, C.J.3    Scott, T.F.4    Bowman, C.N.5
  • 36
    • 0036500524 scopus 로고    scopus 로고
    • A thermally re-mendable cross-linked polymeric material
    • DOI 10.1126/science.1065879
    • Chen, X., Dam, M. A., Ono, K., Mal, A., Shen, H., Nutt, S. R., Sheran, K., and Wudl, F. (2002) A thermally re-mendable crosslinked polymeric material Science 295, 1698-1702 (Pubitemid 34202902)
    • (2002) Science , vol.295 , Issue.5560 , pp. 1698-1702
    • Chen, X.1    Dam, M.A.2    Ono, K.3    Mal, A.4    Shen, H.5    Nutt, S.R.6    Sheran, K.7    Wudl, F.8
  • 37
    • 33846142171 scopus 로고    scopus 로고
    • Controlling dispersion and migration of particulate additives with block copolymers and Diels-Alder chemistry
    • DOI 10.1021/la0624541
    • Costanzo, P. J., Demaree, J. D., and Beyer, F. L. (2006) Controlling dispersion and migration of particulate additives with block copolymers and Diels-Alder chemistry Langmuir 22, 10251-10257 (Pubitemid 46079314)
    • (2006) Langmuir , vol.22 , Issue.24 , pp. 10251-10257
    • Costanzo, P.J.1    Demaree, J.D.2    Beyer, F.L.3
  • 38
    • 0025421807 scopus 로고
    • Reversible gelation of polyoxazoline by means of Diels-alder reaction
    • Chujo, Y., Sada, K., and Saegusa, T. (1990) Reversible gelation of polyoxazoline by means of Diels-Alder reaction Macromolecules 23, 2636-2641 (Pubitemid 21734774)
    • (1990) Macromolecules , vol.23 , Issue.10 , pp. 2636-2641
    • Chujo Yoshiki1    Sada Kazuki2    Saegusa Takeo3
  • 39
    • 66049125068 scopus 로고    scopus 로고
    • Thermosensitive hydrogels synthesized by fast Diels-Alder reactions in water
    • Wei, H.-L., Yang, Z., and Shen, Y.-M. (2009) Thermosensitive hydrogels synthesized by fast Diels-Alder reactions in water Polymer 50, 2836-2840
    • (2009) Polymer , vol.50 , pp. 2836-2840
    • Wei, H.-L.1    Yang, Z.2    Shen, Y.-M.3
  • 40
    • 78650877095 scopus 로고    scopus 로고
    • Diels-Alder reaction in water for straightforward preparation of thermoresponsive hydrogels
    • Wei, H.-L., Yang, J., Chu, H.-J., Yang, Z., Ma, C.-C., and Yao, K. (2011) Diels-Alder reaction in water for straightforward preparation of thermoresponsive hydrogels J. Appl. Polym. Sci. 120, 974-980
    • (2011) J. Appl. Polym. Sci. , vol.120 , pp. 974-980
    • Wei, H.-L.1    Yang, J.2    Chu, H.-J.3    Yang, Z.4    Ma, C.-C.5    Yao, K.6
  • 41
    • 66049125068 scopus 로고    scopus 로고
    • Thermosensitive hydrogels synthesized by fast Diels-Alder reactions in water
    • Wei, H.-L., Yang, Z., and Shen, Y.-M. (2009) Thermosensitive hydrogels synthesized by fast Diels-Alder reactions in water Polymer 50, 2836-2840
    • (2009) Polymer , vol.50 , pp. 2836-2840
    • Wei, H.-L.1    Yang, Z.2    Shen, Y.-M.3
  • 42
    • 79955412522 scopus 로고    scopus 로고
    • Diels-Alder click crosslinked hyaluronic acid hydrogels for tissue engineering
    • Nimmo, C. M., Owen, S. C., and Shoichet, M. S. (2011) Diels-Alder click crosslinked hyaluronic acid hydrogels for tissue engineering Biomacromolecules 12, 824-830
    • (2011) Biomacromolecules , vol.12 , pp. 824-830
    • Nimmo, C.M.1    Owen, S.C.2    Shoichet, M.S.3
  • 43
    • 0037209905 scopus 로고    scopus 로고
    • A hydrogel prepared by in situ cross-linking of a thiol-containing poly(ethylene glycol)-based copolymer: A new biomaterial for protein drug delivery
    • DOI 10.1016/S0142-9612(02)00227-2, PII S0142961202002272
    • Qui, B., Stefanos, S., Ma, J., Lalloo, A., Perry, B. A., Leibowitz, M. J., Sinko, P. J., and Stein, S. (2003) A hydrogel prepared by in situ crosslinking of a thiol-containing poly(ethylene glycol)-based copolymer: a new biomaterial for protein drug delivery Biomaterials 24, 11-18 (Pubitemid 35300198)
    • (2003) Biomaterials , vol.24 , Issue.1 , pp. 11-18
    • Qiu, B.1    Stefanos, S.2    Ma, J.3    Lalloo, A.4    Perry, B.A.5    Leibowitz, M.J.6    Sinko, P.J.7    Stein, S.8
  • 46
    • 79955390959 scopus 로고    scopus 로고
    • Biodegradable and biocompatible synthetic saccharide-peptide hydrogels for three-dimensional stem cell culture
    • Chawla, K., Yu, T.-B., Liao, S. W., and Guan, Z. (2011) Biodegradable and biocompatible synthetic saccharide-peptide hydrogels for three-dimensional stem cell culture Biomacromolecules 12, 560-567
    • (2011) Biomacromolecules , vol.12 , pp. 560-567
    • Chawla, K.1    Yu, T.-B.2    Liao, S.W.3    Guan, Z.4
  • 47
    • 34249866545 scopus 로고    scopus 로고
    • Rapidly in situ-forming degradable hydrogels from dextram triols through Michael addition
    • DOI 10.1021/bm061191m
    • Hiemstra, C., van der Aa, L. J., Zhang, Z., Dijkstra, P. J., and Feijen, J. (2007) Rapidly in situ-forming degradable hydrogels from dextran thiols through Michael addition Biomacromolecules 8, 1548-1556 (Pubitemid 46865127)
    • (2007) Biomacromolecules , vol.8 , Issue.5 , pp. 1548-1556
    • Hiemstra, C.1    Van Der Aa, L.J.2    Zhong, Z.3    Dijkstra, P.J.4    Feijen, J.5
  • 48
  • 49
    • 79952101791 scopus 로고    scopus 로고
    • The performance of human mesenchymal stem cells encapsulated in cell-degradable polymer-peptide hydrogels
    • Anderson, S. B., Lin, C.-C., Kuntzler, D. V., and Anseth, K. S. (2011) The performance of human mesenchymal stem cells encapsulated in cell-degradable polymer-peptide hydrogels Biomaterials 32, 3564-74
    • (2011) Biomaterials , vol.32 , pp. 3564-3574
    • Anderson, S.B.1    Lin, C.-C.2    Kuntzler, D.V.3    Anseth, K.S.4
  • 50
    • 66249090167 scopus 로고    scopus 로고
    • Using "click" chemistry to prepare SAM substrates to study stem cell adhesion
    • Hudalla, G. A. and Murphy, W. L. (2009) Using "click" chemistry to prepare SAM substrates to study stem cell adhesion Langmuir 25, 5737-5746
    • (2009) Langmuir , vol.25 , pp. 5737-5746
    • Hudalla, G.A.1    Murphy, W.L.2
  • 51
    • 0032496959 scopus 로고    scopus 로고
    • 3OH groups to characterize long-term attachment of bovine capillary endothelial cells to surfaces
    • DOI 10.1021/ja972467o
    • Roberts, C., Chen, C. S., Mrksich, M., Martichonok, V., Ingber, D. E., and Whitesides, G. M. (1998) Using mixed self-assembled monolayers presenting RGD and (EG)3OH groups to characterize long-term attachement of bovine capillary endothelial cells to surfaces J. Am. Chem. Soc. 120, 6548-6555 (Pubitemid 28345220)
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.26 , pp. 6548-6555
    • Roberts, C.1    Chen, C.S.2    Mrksich, M.3    Martichonok, V.4    Ingber, D.E.5    Whitesides, G.M.6
  • 53
    • 70449394185 scopus 로고    scopus 로고
    • Patterning discrete stem cell culture environments via localized self-assembled monolayer replacement
    • Koepsel, J. T. and Murphy, W. L. (2009) Patterning discrete stem cell culture environments via localized self-assembled monolayer replacement Langmuir 25, 12825-12834
    • (2009) Langmuir , vol.25 , pp. 12825-12834
    • Koepsel, J.T.1    Murphy, W.L.2
  • 54
    • 0033557842 scopus 로고    scopus 로고
    • A strategy for the generation of surfaces presenting ligands for studies of binding based on an active ester as a common reactive intermediate: A surface plasmon resonance study
    • Lahiri, J., Isaacs, L., Tien, J., and Whitesides, G. M. (1999) A strategy for the generation of surfaces presenting ligands for studies of binding based on an active ester as a common reactive intermediate: a surface plasmon resonance study Anal. Chem. 71, 777-790
    • (1999) Anal. Chem. , vol.71 , pp. 777-790
    • Lahiri, J.1    Isaacs, L.2    Tien, J.3    Whitesides, G.M.4
  • 55
    • 0037418506 scopus 로고    scopus 로고
    • Maleimide-functionalized self-assembled monolayers for the preparation of peptide and carbohydrate biochips
    • Houseman, B. T., Gawalt, E. S., and Mrksich, M. (2003) Maleimide-functionalized self-assembled monolayers for the preparation of peptide and carbohydrate biochips Langmuir 19, 1522-1531
    • (2003) Langmuir , vol.19 , pp. 1522-1531
    • Houseman, B.T.1    Gawalt, E.S.2    Mrksich, M.3
  • 56
    • 70249112218 scopus 로고    scopus 로고
    • Orthogonal transformations on solid substrates: Efficient avenues to surface modification
    • Nebhani, L. and Barner-Kowollik, C. (2009) Orthogonal transformations on solid substrates: efficient avenues to surface modification Adv. Mater. 21, 3442-3468
    • (2009) Adv. Mater. , vol.21 , pp. 3442-3468
    • Nebhani, L.1    Barner-Kowollik, C.2
  • 57
    • 34250646279 scopus 로고    scopus 로고
    • Universal gradient substrates for "click" biofunctionalization
    • DOI 10.1002/adma.200602221
    • Gallant, N. D., Lavery, K. A., Amis, E. J., and Becker, M. L. (2007) Universal gradient substrates for "click" biofunctionalization Adv. Mater. 19, 965-969 (Pubitemid 46942295)
    • (2007) Advanced Materials , vol.19 , Issue.7 , pp. 965-969
    • Gallant, N.D.1    Lavery, K.A.2    Amis, E.J.3    Becker, M.L.4
  • 58
    • 61849100392 scopus 로고    scopus 로고
    • Click chemistry functionalized polymeric nanoparticles target corneal epithelial cells through RGD-cell surface receptors
    • Lu, J., Shi, M., and Shoichet, M. S. (2009) Click chemistry functionalized polymeric nanoparticles target corneal epithelial cells through RGD-cell surface receptors Bioconjugate Chem. 20, 87-94
    • (2009) Bioconjugate Chem. , vol.20 , pp. 87-94
    • Lu, J.1    Shi, M.2    Shoichet, M.S.3
  • 59
    • 73249137506 scopus 로고    scopus 로고
    • The use of immobilized osteogenic growth peptide on gradient substrates synthesized via click chemistry to enhance MC3T3-E1 osteoblast proliferation
    • Moore, N. M., Lin, N. J., Gallant, N. D., and Becker, M. L. (2010) The use of immobilized osteogenic growth peptide on gradient substrates synthesized via click chemistry to enhance MC3T3-E1 osteoblast proliferation Biomaterials 31, 1604-1611
    • (2010) Biomaterials , vol.31 , pp. 1604-1611
    • Moore, N.M.1    Lin, N.J.2    Gallant, N.D.3    Becker, M.L.4
  • 60
    • 2942739131 scopus 로고    scopus 로고
    • Osteogenic growth peptide modulates fracture callus structural and mechanical properties
    • DOI 10.1016/j.bone.2004.03.025, PII S8756328204001292
    • Gabet, Y., Muller, R., Regev, E., Sela, J., Shteyer, A., Salisbury, K., Chorev, M., and Bab, I. (2004) Osteogenic growth peptide modulates fracture callus structural and mechanical properties Bone 35, 65-73 (Pubitemid 38789149)
    • (2004) Bone , vol.35 , Issue.1 , pp. 65-73
    • Gabet, Y.1    Muller, R.2    Regev, E.3    Sela, J.4    Shteyer, A.5    Salisbury, K.6    Chorev, M.7    Bab, I.8
  • 61
    • 4444324951 scopus 로고    scopus 로고
    • Polytrizaoles as copper(I)-stabilizing ligands in catalysis
    • Chan, T. R., Hilgraf, R., Sharpless, K. B., and Fokin, V. V. (2004) Polytrizaoles as copper(I)-stabilizing ligands in catalysis Org. Lett. 6, 2853-2855
    • (2004) Org. Lett. , vol.6 , pp. 2853-2855
    • Chan, T.R.1    Hilgraf, R.2    Sharpless, K.B.3    Fokin, V.V.4
  • 62
    • 77951689718 scopus 로고    scopus 로고
    • Immobilization of peptides with distinct biological activities onto stem cell culture substrates using orthogonal chemistries
    • Hudalla, G. A. and Murphy, W. L. (2010) Immobilization of peptides with distinct biological activities onto stem cell culture substrates using orthogonal chemistries Langmuir 26, 6449-6456
    • (2010) Langmuir , vol.26 , pp. 6449-6456
    • Hudalla, G.A.1    Murphy, W.L.2
  • 63
    • 0033526361 scopus 로고    scopus 로고
    • Diels-Alder reaction for the selective immobilization of protein to electroactive self-assembled monolayers
    • DOI 10.1021/ja983529t
    • Yousaf, M. N. and Mrksich, M. (1999) Diels-Alder reaction for the selective immobilization of protein to electroactive self-assembled monolayers J. Am. Chem. Soc. 121, 4286-4287 (Pubitemid 29220308)
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.17 , pp. 4286-4287
    • Yousaf, M.N.1    Mrksich, M.2
  • 64
    • 31544446908 scopus 로고    scopus 로고
    • Carbohydrate and protein immobilization onto solid surfaces by sequential Diels-Alder and azide-alkyne cycloadditions
    • DOI 10.1021/bc0502311
    • Sun, X.-L., Stabler, C. L., Cazalis, C. S., and Chaikof, E. L. (2006) Carbohydrate and protein immobilization onto solid surfaces by sequential Diels-Alder and azide-alkyne cycloadditions Bioconjugate Chem. 17, 52-57 (Pubitemid 43157584)
    • (2006) Bioconjugate Chemistry , vol.17 , Issue.1 , pp. 52-57
    • Sun, X.-L.1    Stabler, C.L.2    Cazalis, C.S.3    Chaikof, E.L.4
  • 67
    • 0032587329 scopus 로고    scopus 로고
    • Zinc-catalyted sulfur alkylation: Insights from protein farnesyltransferase
    • DOI 10.1016/S1367-5931(99)80030-1
    • Hightower, K. E. and Fierk, C. A. (1999) Zing-catalyzed sulfur alkylation: insights from protein farnesyltransferase Curr. Opin. Chem. Biol. 3, 176-181 (Pubitemid 29145784)
    • (1999) Current Opinion in Chemical Biology , vol.3 , Issue.2 , pp. 176-181
    • Hightower, K.E.1    Fierke, C.A.2
  • 68
    • 53149108926 scopus 로고    scopus 로고
    • The effect of immobilized platelet derived growth factor AA on neural stem/progenitor cell differentiation on cell-adhesive hydrogels
    • Aizawa, Y., Leipzig, N., Zahir, T., and Shoichet, M. (2008) The effect of immobilized platelet derived growth factor AA on neural stem/progenitor cell differentiation on cell-adhesive hydrogels Biomaterials 29, 4676-4683
    • (2008) Biomaterials , vol.29 , pp. 4676-4683
    • Aizawa, Y.1    Leipzig, N.2    Zahir, T.3    Shoichet, M.4
  • 69
    • 77956191683 scopus 로고    scopus 로고
    • The use of vascular endothelial growth factor functionalized agarose to guide pluripotent stem cell aggregates toward blood progenitor cells
    • Rahman, N., Purpura, K. A., Wylie, R. G., Zandstra, P. W., and Shoichet, M. S. (2010) The use of vascular endothelial growth factor functionalized agarose to guide pluripotent stem cell aggregates toward blood progenitor cells Biomaterials 31, 8262-8270
    • (2010) Biomaterials , vol.31 , pp. 8262-8270
    • Rahman, N.1    Purpura, K.A.2    Wylie, R.G.3    Zandstra, P.W.4    Shoichet, M.S.5
  • 70
    • 77950193801 scopus 로고    scopus 로고
    • Functional immobilization of interferon-gamma induces neuronal differentiation of neural stem cells
    • Leipzig, N. D., Xu, C., Zahir, T., and Shoichet, M. S. (2010) Functional immobilization of interferon-gamma induces neuronal differentiation of neural stem cells J. Biomed. Mater. Res., Part A 93, 625-633
    • (2010) J. Biomed. Mater. Res., Part A , vol.93 , pp. 625-633
    • Leipzig, N.D.1    Xu, C.2    Zahir, T.3    Shoichet, M.S.4
  • 71
    • 33749543445 scopus 로고    scopus 로고
    • Anisotropic three-dimensional peptide channels guide neurite outgrowth within a biodegradable hydrogel matrix
    • DOI 10.1088/1748-6041/1/3/011, PII S1748604106284924, 011
    • Musoke-Zawedde, P. and Shoichet, M. S. (2006) Anisotropic three-dimensional peptide channels guide neurite outgrowth within a biodegradable hydrogel matrix Biomed. Mater. 1, 162-169 (Pubitemid 44529342)
    • (2006) Biomedical Materials , vol.1 , Issue.3 , pp. 162-169
    • Musoke-Zawedde, P.1    Shoichet, M.S.2
  • 72
    • 1842731242 scopus 로고    scopus 로고
    • A photolabile hydrogel for guided three-dimensional cell growth and migration
    • Luo, Y. and Shoichet, M. S. (2004) A photolabile hydrogel for guided three-dimensional cell growth and migration Nat. Mater. 3, 249-253
    • (2004) Nat. Mater. , vol.3 , pp. 249-253
    • Luo, Y.1    Shoichet, M.S.2
  • 73
    • 42749097087 scopus 로고    scopus 로고
    • Three-dimensional micropatterning of bioactive hydrogels via two-photo laser scanning photolithography for guided 3D cell migration
    • Lee, S. H., Moon, J. J., and West, J. L. (2008) Three-dimensional micropatterning of bioactive hydrogels via two-photo laser scanning photolithography for guided 3D cell migration Biomaterials 29, 2962-2968
    • (2008) Biomaterials , vol.29 , pp. 2962-2968
    • Lee, S.H.1    Moon, J.J.2    West, J.L.3
  • 74
    • 43149124584 scopus 로고    scopus 로고
    • Three-dimensional biochemical patterning of click-based composite hydrogels via thiolene photopolymerization
    • DOI 10.1021/bm7012636
    • Polizzotti, B. D., Fairbanks, B. D., and Anseth, K. S. (2008) Three-dimensional biochemical patterning of click-based composite hydrogels via thiolene photopolymerization Biomacromolecules 9, 1084-1087 (Pubitemid 351639558)
    • (2008) Biomacromolecules , vol.9 , Issue.4 , pp. 1084-1087
    • Polizzotti, B.D.1    Fairbanks, B.D.2    Anseth, K.S.3
  • 75
    • 39149135546 scopus 로고    scopus 로고
    • Three-dimensional chemical patterning of transparent hydrogels
    • DOI 10.1021/cm071158m
    • Wosnick, J. H. and Shoichet, M. S. (2008) Three-dimensional chemical patterning of transparent hydrogels Chem. Mater. 20, 55-60 (Pubitemid 351256711)
    • (2008) Chemistry of Materials , vol.20 , Issue.1 , pp. 55-60
    • Wosnick, J.H.1    Shoichet, M.S.2
  • 76
    • 78449273142 scopus 로고    scopus 로고
    • Endothelial cell guidance in 3D patterned scaffolds
    • Aizawa, Y., Wylie, R., and Shoichet, M. (2010) Endothelial cell guidance in 3D patterned scaffolds Adv. Mater. 22, 4831-4835
    • (2010) Adv. Mater. , vol.22 , pp. 4831-4835
    • Aizawa, Y.1    Wylie, R.2    Shoichet, M.3
  • 77
    • 77951936291 scopus 로고    scopus 로고
    • Fabrication of maleimide containing thiol reactive hydrogels via Diels-Alder/Retro-Diels-Alder strategy
    • Kosif, I., Park, Eun-Ju, P., Sanyal, R., and Sanyal, A. (2010) Fabrication of maleimide containing thiol reactive hydrogels via Diels-Alder/Retro-Diels-Alder strategy Macromolecules 43, 4140-4148
    • (2010) Macromolecules , vol.43 , pp. 4140-4148
    • Kosif, I.1    Park Eun-Ju, P.2    Sanyal, R.3    Sanyal, A.4
  • 78
    • 33646008877 scopus 로고    scopus 로고
    • Copper in medicine: Homeostasis, chelation therapy and antitumor drug design
    • Wang, T. and Guo, Z. J. (2006) Copper in medicine: homeostasis, chelation therapy and antitumor drug design Curr. Med. Chem. 13, 525-537
    • (2006) Curr. Med. Chem. , vol.13 , pp. 525-537
    • Wang, T.1    Guo, Z.J.2
  • 79
    • 77949823784 scopus 로고    scopus 로고
    • Thiol-click chemistry: A multifaceted toolbox for small molecule and polymer synthesis
    • Hoyle, C. E., Lowe, A. B., and Bowman, C. N. (2010) Thiol-click chemistry: a multifaceted toolbox for small molecule and polymer synthesis Chem. Soc. Rev. 39, 1355-1387
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1355-1387
    • Hoyle, C.E.1    Lowe, A.B.2    Bowman, C.N.3
  • 80
    • 36049017974 scopus 로고    scopus 로고
    • Thio-click modification of poly[2-(3-butenyl)-2-oxazoline]
    • DOI 10.1021/ma071357r
    • Gress, A., Volkel, A., and Schlaad, H. (2007) Thio-click modification of poly[2-(3-butenyl)-2-oxazoline] Macromolecules 40, 7928-7933 (Pubitemid 350099696)
    • (2007) Macromolecules , vol.40 , Issue.22 , pp. 7928-7933
    • Gress, A.1    Volkel, A.2    Schlaad, H.3
  • 81
    • 0001685645 scopus 로고
    • Reactions of mercaptans with acrylic and methacrylic derivatives
    • Hurd, C. D. and Gershbein, L. L. (1947) Reactions of mercaptans with acrylic and methacrylic derivatives J. Am. Chem. Soc. 69, 2328-2335
    • (1947) J. Am. Chem. Soc. , vol.69 , pp. 2328-2335
    • Hurd, C.D.1    Gershbein, L.L.2
  • 84
    • 61649106062 scopus 로고    scopus 로고
    • Thiol-yne photopolymerizations: Novel mechanism, kinetics, and step-growth formation of highly cross-linked networks
    • Fairbanks, B. D., Scott, T. F., Kloxin, C. J., Anseth, K. S., and Bowman, C. N. (2008) Thiol-yne photopolymerizations: novel mechanism, kinetics, and step-growth formation of highly cross-linked networks Macrimolecules 42, 211-217
    • (2008) Macrimolecules , vol.42 , pp. 211-217
    • Fairbanks, B.D.1    Scott, T.F.2    Kloxin, C.J.3    Anseth, K.S.4    Bowman, C.N.5
  • 85
    • 81255130671 scopus 로고    scopus 로고
    • Three-dimensional, spatially-controlled simultaneous patterning of multiple growth factors in hydrogels
    • accepted
    • Wylie, R. G., Ahsan, S., Aizawa, Y., Maxwell, K. L., Morshead, C. M., and Shoichet, M. S. (2011) Three-dimensional, spatially-controlled simultaneous patterning of multiple growth factors in hydrogels. Nat. Mater., accepted.
    • (2011) Nat. Mater.
    • Wylie, R.G.1    Ahsan, S.2    Aizawa, Y.3    Maxwell, K.L.4    Morshead, C.M.5    Shoichet, M.S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.