메뉴 건너뛰기




Volumn 37, Issue 1, 2012, Pages 18-37

ATRP in the design of functional materials for biomedical applications

Author keywords

Atom Transfer Radical Polymerization (ATRP); Bioactive surfaces; Bioconjugation; Biomaterials; Biomedical engineering; Block copolymers; Drug delivery; Functionality; Imaging; Nanogels; Nanoparticles; Polymer grafting; Polymeric micelles; Tissue engineering

Indexed keywords

BIOMATERIALS; BIOMEDICAL ENGINEERING; BLOCK COPOLYMERS; CONTROLLED DRUG DELIVERY; CROSSLINKING; DESIGN; DIAGNOSIS; DRUG DELIVERY; FREE RADICAL REACTIONS; FUNCTIONAL MATERIALS; FUNCTIONAL POLYMERS; IMAGING TECHNIQUES; MACROMOLECULES; MEDICAL APPLICATIONS; NANOPARTICLES; NANOSTRUCTURED MATERIALS; POLYMERIZATION; TARGETED DRUG DELIVERY; TISSUE; TISSUE ENGINEERING;

EID: 80455173858     PISSN: 00796700     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.progpolymsci.2011.08.001     Document Type: Review
Times cited : (514)

References (286)
  • 1
    • 0027595948 scopus 로고
    • Tissue engineering
    • R. Langer, and J.P. Vacanti Tissue engineering Science 260 1993 920 926 (Pubitemid 23209960)
    • (1993) Science , vol.260 , Issue.5110 , pp. 920-926
    • Langer, R.1    Vacanti, J.P.2
  • 2
    • 0038387390 scopus 로고    scopus 로고
    • The dawning era of polymer therapeutics
    • DOI 10.1038/nrd1088
    • R. Duncan The dawning era of polymer therapeutics Nat Rev Drug Discov 2 2003 347 360 (Pubitemid 37361705)
    • (2003) Nature Reviews Drug Discovery , vol.2 , Issue.5 , pp. 347-360
    • Duncan, R.1
  • 3
    • 1842484779 scopus 로고    scopus 로고
    • Designing materials for biology and medicine
    • DOI 10.1038/nature02388
    • R. Langer, and D.A. Tirrell Designing materials for biology and medicine Nature 428 2004 487 492 (Pubitemid 38480528)
    • (2004) Nature , vol.428 , Issue.6982 , pp. 487-492
    • Langer, R.1    Tirrell, D.A.2
  • 4
    • 4644237284 scopus 로고    scopus 로고
    • Materials science - Smart biomaterials
    • D.G. Anderson, J.A. Burdick, and R. Langer Materials science - smart biomaterials Science 305 2004 1923 1924
    • (2004) Science , vol.305 , pp. 1923-1924
    • Anderson, D.G.1    Burdick, J.A.2    Langer, R.3
  • 6
    • 70450186565 scopus 로고    scopus 로고
    • Sequence control in polymer synthesis
    • J.F. Lutz, and N. Badi Sequence control in polymer synthesis Chem Soc Rev 38 2009 3383 3390
    • (2009) Chem Soc Rev , vol.38 , pp. 3383-3390
    • Lutz, J.F.1    Badi, N.2
  • 7
    • 0037039862 scopus 로고    scopus 로고
    • Third-generation biomedical materials
    • L.L. Hench, and J.M. Polak Third-generation biomedical materials Science 295 2002 1014 1017
    • (2002) Science , vol.295 , pp. 1014-1017
    • Hench, L.L.1    Polak, J.M.2
  • 8
    • 0021690284 scopus 로고
    • Surface-active biomaterials
    • L.L. Hench, and J. Wilson Surface-active biomaterials Science 226 1984 630 636 (Pubitemid 15202145)
    • (1984) Science , vol.226 , Issue.4675 , pp. 630-636
    • Hench, L.L.1    Wilson, J.2
  • 9
    • 69249207273 scopus 로고    scopus 로고
    • Precision polymers: Monodisperse, monomer-sequence-defined segments to target future demands of polymers in medicine
    • L. Hartmann, and H.G. Borner Precision polymers: monodisperse, monomer-sequence-defined segments to target future demands of polymers in medicine Adv Mater 21 2009 3425 3431
    • (2009) Adv Mater , vol.21 , pp. 3425-3431
    • Hartmann, L.1    Borner, H.G.2
  • 10
    • 78651431186 scopus 로고    scopus 로고
    • Precision Polymers - Modern tools to understand and program macromolecular interactions
    • H.G. Borner Precision Polymers - modern tools to understand and program macromolecular interactions Macromol Rapid Commun 32 2011 115 126
    • (2011) Macromol Rapid Commun , vol.32 , pp. 115-126
    • Borner, H.G.1
  • 11
    • 0006278227 scopus 로고
    • Controlled living radical polymerization - Atom-transfer radical polymerization in the presence of transition-metal complexes
    • J.S. Wang, and K. Matyjaszewski Controlled living radical polymerization - atom-transfer radical polymerization in the presence of transition-metal complexes J Am Chem Soc 117 1995 5614 5615
    • (1995) J Am Chem Soc , vol.117 , pp. 5614-5615
    • Wang, J.S.1    Matyjaszewski, K.2
  • 12
    • 0035470133 scopus 로고    scopus 로고
    • Atom transfer radical polymerization
    • DOI 10.1021/cr940534g
    • K. Matyjaszewski, and J.H. Xia Atom transfer radical polymerization Chem Rev 101 2001 2921 2990 (Pubitemid 35377809)
    • (2001) Chemical Reviews , vol.101 , Issue.9 , pp. 2921-2990
    • Matyjaszewski, K.1    Xia, J.2
  • 13
    • 33846841153 scopus 로고    scopus 로고
    • Controlled/living radical polymerization: Features, developments, and perspectives
    • DOI 10.1016/j.progpolymsci.2006.11.002, PII S007967000600133X, 50 Years of Living Polymerization
    • W.A. Braunecker, and K. Matyjaszewski Controlled/living radical polymerization: features, developments, and perspectives Prog Polym Sci 32 2007 93 146 (Pubitemid 46201961)
    • (2007) Progress in Polymer Science (Oxford) , vol.32 , Issue.1 , pp. 93-146
    • Braunecker, W.A.1    Matyjaszewski, K.2
  • 14
    • 67949112461 scopus 로고    scopus 로고
    • Nanostructured functional materials prepared by atom transfer radical polymerization
    • K. Matyjaszewski, and N. Tsarevsky Nanostructured functional materials prepared by atom transfer radical polymerization Nat Chem 1 2009 276 288
    • (2009) Nat Chem , vol.1 , pp. 276-288
    • Matyjaszewski, K.1    Tsarevsky, N.2
  • 15
    • 77955428224 scopus 로고    scopus 로고
    • Transition metal catalysts for controlled radical polymerization
    • F. di Lena, and K. Matyjaszewski Transition metal catalysts for controlled radical polymerization Prog Polym Sci 35 2010 959 1021
    • (2010) Prog Polym Sci , vol.35 , pp. 959-1021
    • Di Lena, F.1    Matyjaszewski, K.2
  • 16
    • 0035304692 scopus 로고    scopus 로고
    • Functional polymers by atom transfer radical polymerization
    • DOI 10.1016/S0079-6700(01)00003-X, PII S007967000100003X
    • V. Coessens, T. Pintauer, and K. Matyjaszewski Functional polymers by atom transfer radical polymerization Prog Polym Sci 26 2001 337 377 (Pubitemid 32427643)
    • (2001) Progress in Polymer Science (Oxford) , vol.26 , Issue.3 , pp. 337-377
    • Coessens, V.1    Pintauer, T.2    Matyjaszewski, K.3
  • 17
    • 0034782358 scopus 로고    scopus 로고
    • Synthesis of nanocomposite organic/inorganic hybrid materials using controlled/"living" radical polymerization
    • DOI 10.1021/cm011065j
    • J. Pyun, and K. Matyjaszewski Synthesis of nanocomposite organic/inorganic hybrid materials using controlled/"living" radical polymerization Chem Mater 13 2001 3436 3448 (Pubitemid 32999283)
    • (2001) Chemistry of Materials , vol.13 , Issue.10 , pp. 3436-3448
    • Pyun, J.1    Matyjaszewski, K.2
  • 18
    • 0029254795 scopus 로고
    • Polymerization of methyl methacrylate with the carbon tetrachloride/dichlorotris-(triphenylphosphine)ruthenium(II)/methylaluminum bis(2,6-di-tert-butylphenoxide) initiating system: Possibility of living radical polymerization
    • M. Kato, M. Kamigaito, M. Sawamoto, and T. Higashimura Polymerization of methyl methacrylate with the carbon tetrachloride/dichlorotris- (triphenylphosphine)ruthenium(II)/methylaluminum bis(2,6-di-tert-butylphenoxide) initiating system: possibility of living radical polymerization Macromolecules 28 1995 1721 1723
    • (1995) Macromolecules , vol.28 , pp. 1721-1723
    • Kato, M.1    Kamigaito, M.2    Sawamoto, M.3    Higashimura, T.4
  • 19
    • 85078684020 scopus 로고    scopus 로고
    • Transition metal catalysis in controlled radical polymerization: Atom transfer radical polymerization
    • K. Matyjaszewski Transition metal catalysis in controlled radical polymerization: atom transfer radical polymerization Chem Eur J 5 1999 3095 3102 (Pubitemid 129611754)
    • (1999) Chemistry - A European Journal , vol.5 , Issue.11 , pp. 3095-3102
    • Matyjaszewski, K.1
  • 20
    • 0001367322 scopus 로고    scopus 로고
    • Living radical polymerization based on transition metal complexes
    • M. Sawamoto, and M. Kamigaito Living radical polymerization based on transition metal complexes Trends Polym Sci 4 1996 371 377
    • (1996) Trends Polym Sci , vol.4 , pp. 371-377
    • Sawamoto, M.1    Kamigaito, M.2
  • 21
    • 0035781198 scopus 로고    scopus 로고
    • Metal-catalyzed living radical polymerization
    • DOI 10.1021/cr9901182
    • M. Kamigaito, T. Ando, and M. Sawamoto Metal-catalyzed living radical polymerization Chem Rev 101 2001 3689 3745 (Pubitemid 35373047)
    • (2001) Chemical Reviews , vol.101 , Issue.12 , pp. 3689-3745
    • Kamigaito, M.1    Ando, T.2    Sawamoto, M.3
  • 22
    • 1642587720 scopus 로고    scopus 로고
    • Kinetics of living radical polymerization
    • A. Goto, and T. Fukuda Kinetics of living radical polymerization Prog Polym Sci 29 2004 329 385
    • (2004) Prog Polym Sci , vol.29 , pp. 329-385
    • Goto, A.1    Fukuda, T.2
  • 25
    • 52449132647 scopus 로고    scopus 로고
    • Ab initio evaluation of the thermodynamic and electrochemical properties of alkyl halides and radicals and their mechanistic implications for Atom Transfer Radical Polymerization
    • C.Y. Lin, M.L. Coote, A. Gennaro, and K. Matyjaszewski Ab initio evaluation of the thermodynamic and electrochemical properties of alkyl halides and radicals and their mechanistic implications for Atom Transfer Radical Polymerization J Am Chem Soc 130 2008 12762 12774
    • (2008) J Am Chem Soc , vol.130 , pp. 12762-12774
    • Lin, C.Y.1    Coote, M.L.2    Gennaro, A.3    Matyjaszewski, K.4
  • 26
    • 34447107134 scopus 로고    scopus 로고
    • "Green:atom transfer radical polymerization: From process design to preparation of well-defined environmentally friendly polymeric materials
    • DOI 10.1021/cr050947p
    • N.V. Tsarevsky, and K. Matyjaszewski "Green" Atom Transfer Radical Polymerization: from process design to preparation of well-defined environmentally friendly polymeric materials Chem Rev 107 2007 2270 2299 (Pubitemid 47029094)
    • (2007) Chemical Reviews , vol.107 , Issue.6 , pp. 2270-2299
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 27
    • 77951892435 scopus 로고    scopus 로고
    • ATRP of MMA in polar solvents catalyzed by FeBr2 without additional ligand
    • Y. Wang, and K. Matyjaszewski ATRP of MMA in polar solvents catalyzed by FeBr2 without additional ligand Macromolecules 43 2010 4003 4005
    • (2010) Macromolecules , vol.43 , pp. 4003-4005
    • Wang, Y.1    Matyjaszewski, K.2
  • 28
    • 79952765311 scopus 로고    scopus 로고
    • ATRP of MMA catalyzed by (FeBr2)-Br-II in the presence of triflate anions
    • Y. Wang, and K. Matyjaszewski ATRP of MMA catalyzed by (FeBr2)-Br-II in the presence of triflate anions Macromolecules 44 2011 1226 1228
    • (2011) Macromolecules , vol.44 , pp. 1226-1228
    • Wang, Y.1    Matyjaszewski, K.2
  • 30
    • 19944385275 scopus 로고    scopus 로고
    • Activator generated by electron transfer for atom transfer radical polymerization
    • DOI 10.1021/ma047389l
    • W. Jakubowski, and K. Matyjaszewski Activator generated by electron transfer for Atom Transfer Radical Polymerization Macromolecules 38 2005 4139 4146 (Pubitemid 40751129)
    • (2005) Macromolecules , vol.38 , Issue.10 , pp. 4139-4146
    • Jakubowski, W.1    Matyjaszewski, K.2
  • 31
    • 34247388537 scopus 로고    scopus 로고
    • Grafting from surfaces for "everyone": ARGET ATRP in the presence of air
    • DOI 10.1021/la063402e
    • K. Matyjaszewski, H. Dong, W. Jakubowski, J. Pietrasik, and A. Kusumo Grafting from surfaces for "Everyone": ARGET ATRP in the presence of air Langmuir 23 2007 4528 4531 (Pubitemid 46643185)
    • (2007) Langmuir , vol.23 , Issue.8 , pp. 4528-4531
    • Matyjaszewski, K.1    Hongchen, D.2    Jakubowski, W.3    Pietrasik, J.4    Kusumo, A.5
  • 32
    • 33746284320 scopus 로고    scopus 로고
    • Activators regenerated by electron transfer for atom-transfer radical polymerization of (meth)acrylates and related block copolymers
    • DOI 10.1002/anie.200600272
    • W. Jakubowski, and K. Matyjaszewski Activators regenerated by electron transfer for atom-transfer radical polymerization of (meth)acrylates and related block copolymers Angew Chem Int Edit 45 2006 4482 4486 (Pubitemid 44105616)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.27 , pp. 4482-4486
    • Jakubowski, W.1    Matyjaszewski, K.2
  • 37
    • 0037124473 scopus 로고    scopus 로고
    • Introduction and overview of peptide and protein pegylation
    • DOI 10.1016/S0169-409X(02)00020-0, PII S0169409X02000200
    • F.M. Veronese, and J.M. Harris Preface - introduction and overview of peptide and protein pegylation Adv Drug Deliver Rev 54 2002 453 456 (Pubitemid 34615541)
    • (2002) Advanced Drug Delivery Reviews , vol.54 , Issue.4 , pp. 453-456
    • Veronese, F.M.1    Harris, J.M.2
  • 38
    • 0037362655 scopus 로고    scopus 로고
    • Effect of pegylation on pharmaceuticals
    • DOI 10.1038/nrd1033
    • J.M. Harris, and R.B. Chess Effect of PEGylation on pharmaceuticals Nat Rev Drug Discov 2 2003 214 221 (Pubitemid 37361666)
    • (2003) Nature Reviews Drug Discovery , vol.2 , Issue.3 , pp. 214-221
    • Milton Harris, J.1    Chess, R.B.2
  • 39
    • 0025015189 scopus 로고
    • Polymer micelles as novel drug carrier: Adriamycin-conjugated poly(ethylene glycol)-poly(aspartic acid) block copolymer
    • M. Yokoyama, M. Miyauchi, N. Yamada, T. Okano, Y. Sakurai, K. Kataoka, and S. Inoue Polymer micelles as novel drug carrier - Adriamycin-conjugated poly(ethylene glycol) poly(aspartic acid) block copolymer J Control Release 11 1990 269 278 (Pubitemid 20070104)
    • (1990) Journal of Controlled Release , vol.11 , Issue.1-3 , pp. 269-278
    • Yokoyama, M.1    Miyauchi, M.2    Yamada, N.3    Okanao, T.4    Sakurai, Y.5    Kataoka, K.6    Inoue, S.7
  • 41
    • 34547870488 scopus 로고    scopus 로고
    • Living radical polymerization as a tool for the synthesis of polymer-protein/peptide bioconjugates
    • DOI 10.1002/marc.200700112
    • J. Nicolas, G. Mantovani, and D.M. Haddleton Living radical polymerization as a tool for the synthesis of polymer-protein/peptide bioconjugates Macromol Rapid Commun 28 2007 1083 1111 (Pubitemid 47252039)
    • (2007) Macromolecular Rapid Communications , vol.28 , Issue.10 , pp. 1083-1111
    • Nicolas, J.1    Mantovani, G.2    Haddleton, D.M.3
  • 42
    • 37249018985 scopus 로고    scopus 로고
    • Modern trends in polymer bioconjugates design
    • DOI 10.1016/j.progpolymsci.2007.07.005, PII S0079670007000974
    • J. Lutz, and H. Borner Modern trends in polymer bioconjugates design Prog Polym Sci 33 2008 1 39 (Pubitemid 350266041)
    • (2008) Progress in Polymer Science (Oxford) , vol.33 , Issue.1 , pp. 1-39
    • Lutz, J.-F.1    Borner, H.G.2
  • 43
    • 77649179434 scopus 로고    scopus 로고
    • Stability of responsive polymer-protein bioconjugates
    • A.K. Shakya, H. Sami, A. Srivastava, and A. Kumar Stability of responsive polymer-protein bioconjugates Prog Polym Sci 35 2010 459 486
    • (2010) Prog Polym Sci , vol.35 , pp. 459-486
    • Shakya, A.K.1    Sami, H.2    Srivastava, A.3    Kumar, A.4
  • 44
    • 33646255225 scopus 로고    scopus 로고
    • Polymer-drug conjugates: Progress in polymeric prodrugs
    • J. Khandare, and T. Minko Polymer-drug conjugates: progress in polymeric prodrugs Prog Polym Sci 31 2006 359 397
    • (2006) Prog Polym Sci , vol.31 , pp. 359-397
    • Khandare, J.1    Minko, T.2
  • 45
    • 0017388651 scopus 로고
    • Effect of covalent attachment of polyethylene glycol on immunogenicity and circulating life of bovine liver catalase
    • A. Abuchowski, J.R. Mccoy, N.C. Palczuk, T. Vanes, and F.F. Davis Effect of covalent attachment of polyethylene-glycol on immunogenicity and circulating life of bovine liver catalase J Biol Chem 252 1977 3582 3586 (Pubitemid 8116088)
    • (1977) Journal of Biological Chemistry , vol.252 , Issue.11 , pp. 3582-3586
    • Abuchowski, A.1    McCoy, J.R.2    Palczuk, N.C.3
  • 46
    • 6344287483 scopus 로고    scopus 로고
    • A new approach to bioconjugates for proteins and peptides ("pegylation") utilising living radical polymerisation
    • DOI 10.1039/b407712a
    • F. Lecolley, L. Tao, G. Mantovani, I. Durkin, S. Lautru, and D.M. Haddleton A new approach to bioconjugates for proteins and peptides ("pegylation") utilising living radical polymerisation Chem Commun 2004 2026 2027 (Pubitemid 39389495)
    • (2004) Chemical Communications , Issue.18 , pp. 2026-2027
    • Lecolley, F.1    Tao, L.2    Mantovani, G.3    Durkin, I.4    Lautru, S.5    Haddleton, D.M.6
  • 47
    • 31544452783 scopus 로고    scopus 로고
    • Preparation of ideal PEG analogues with a tunable thermosensitivity by controlled radical copolymerization of 2-(2-methoxyethoxy)ethyl methacrylate and oligo(ethylene glycol) methacrylate
    • DOI 10.1021/ma0517042
    • J.F. Lutz, and A. Hoth Preparation of ideal PEG analogues with a tunable thermosensitivity by controlled radical copolymerization of 2-(2-methoxyethoxy) ethyl methacrylate and oligo(ethylene glycol) methacrylate Macromolecules 39 2006 893 896 (Pubitemid 43164604)
    • (2006) Macromolecules , vol.39 , Issue.2 , pp. 893-896
    • Lutz, J.-F.1    Hoth, A.2
  • 48
    • 33646462613 scopus 로고    scopus 로고
    • Inverse miniemulsion ATRP: A new method for synthesis and functionalization of well-defined water-soluble/cross-linked polymeric particles
    • J.K. Oh, C.B. Tang, H.F. Gao, N.V. Tsarevsky, and K. Matyjaszewski Inverse miniemulsion ATRP: a new method for synthesis and functionalization of well-defined water-soluble/cross-linked polymeric particles J Am Chem Soc 128 2006 5578 5584
    • (2006) J Am Chem Soc , vol.128 , pp. 5578-5584
    • Oh, J.K.1    Tang, C.B.2    Gao, H.F.3    Tsarevsky, N.V.4    Matyjaszewski, K.5
  • 49
    • 36949017070 scopus 로고    scopus 로고
    • Biocompatible, thermoresponsive, and biodegradable: Simple preparation of "All-in-one" biorelevant polymers
    • DOI 10.1021/ma7021474
    • J. Lutz, J. Andrieu, S. Uzgun, C. Rudolph, and S. Agarwal Biocompatible, thermoresponsive, and biodegradable: simple preparation of "all-in- one" biorelevant polymers Macromolecules 40 2007 8540 8543 (Pubitemid 350241352)
    • (2007) Macromolecules , vol.40 , Issue.24 , pp. 8540-8543
    • Lutz, J.-F.1    Andrieu, J.2    Uzgun, S.3    Rudolph, C.4    Agarwal, S.5
  • 50
    • 38349100697 scopus 로고    scopus 로고
    • ATRP synthesis of thermally responsive molecular brushes from oligo(ethylene oxide) methacrylates
    • S.-I. Yamamoto, J. Pietrasik, and K. Matyjaszewski ATRP synthesis of thermally responsive molecular brushes from oligo(ethylene oxide) methacrylates Macromolecules 40 2007 9348 9353
    • (2007) Macromolecules , vol.40 , pp. 9348-9353
    • Yamamoto, S.-I.1    Pietrasik, J.2    Matyjaszewski, K.3
  • 51
    • 54849403875 scopus 로고    scopus 로고
    • Temperature- and pH-responsive dense copolymer brushes prepared by ATRP
    • S.-I. Yamamoto, J. Pietrasik, and K. Matyjaszewski Temperature- and pH-responsive dense copolymer brushes prepared by ATRP Macromolecules 41 2008 7013 7020
    • (2008) Macromolecules , vol.41 , pp. 7013-7020
    • Yamamoto, S.-I.1    Pietrasik, J.2    Matyjaszewski, K.3
  • 52
    • 77649210916 scopus 로고    scopus 로고
    • Ultralow-fouling, functionalizable, and hydrolyzable zwitterionic materials and their derivatives for biological applications
    • S.Y. Jiang, and Z.Q. Cao Ultralow-fouling, functionalizable, and hydrolyzable zwitterionic materials and their derivatives for biological applications Adv Mater 22 2010 920 932
    • (2010) Adv Mater , vol.22 , pp. 920-932
    • Jiang, S.Y.1    Cao, Z.Q.2
  • 53
    • 57349183204 scopus 로고    scopus 로고
    • A switchable biocompatible polymer surface with self-sterilizing and nonfouling capabilities
    • G. Cheng, H. Xite, Z. Zhang, S.F. Chen, and S.Y. Jiang A switchable biocompatible polymer surface with self-sterilizing and nonfouling capabilities Angew Chem Int Edit 47 2008 8831 8834
    • (2008) Angew Chem Int Edit , vol.47 , pp. 8831-8834
    • Cheng, G.1    Xite, H.2    Zhang, Z.3    Chen, S.F.4    Jiang, S.Y.5
  • 54
    • 78649445138 scopus 로고    scopus 로고
    • Functionalizable and nonfouling zwitterionic carboxybetaine hydrogels with a carboxybetaine dimethacrylate crosslinker
    • L.R. Carr, H. Xue, and S.Y. Jiang Functionalizable and nonfouling zwitterionic carboxybetaine hydrogels with a carboxybetaine dimethacrylate crosslinker Biomaterials 32 2011 961 968
    • (2011) Biomaterials , vol.32 , pp. 961-968
    • Carr, L.R.1    Xue, H.2    Jiang, S.Y.3
  • 55
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • H.C. Kolb, M.G. Finn, and K.B. Sharpless Click chemistry: diverse chemical function from a few good reactions Angew Chem Int Edit 40 2001 2004 2021
    • (2001) Angew Chem Int Edit , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 56
    • 33749664981 scopus 로고    scopus 로고
    • Combining ATRP and ̈click" chemistry: A promising platform toward functional biocompatible polymers and polymer bioconjugates
    • DOI 10.1021/ma061557n
    • J. Lutz, H. Borner, and K. Weichenhan Combining ATRP and "click" chemistry: a promising platform toward functional biocompatible polymers and polymer bioconjugates Macromolecules 39 2006 6376 6383 (Pubitemid 44555078)
    • (2006) Macromolecules , vol.39 , Issue.19 , pp. 6376-6383
    • Lutz, J.-F.1    Borner, H.G.2    Weichenhan, K.3
  • 57
    • 33846703461 scopus 로고    scopus 로고
    • 'Click' chemistry in polymer and materials science
    • DOI 10.1002/marc.200600625
    • W. Binder, and R. Sachsenhofer 'Click' chemistry in polymer and materials science Macromol Rapid Commun 28 2007 15 54 (Pubitemid 46192085)
    • (2007) Macromolecular Rapid Communications , vol.28 , Issue.1 , pp. 15-54
    • Binder, W.H.1    Sachsenhofer, R.2
  • 58
    • 54749104711 scopus 로고    scopus 로고
    • 'Click' chemistry in polymer and material science: An update
    • W. Binder, and R. Sachsenhofer 'Click' chemistry in polymer and material science: an update Macromol Rapid Commun 29 2008 952 981
    • (2008) Macromol Rapid Commun , vol.29 , pp. 952-981
    • Binder, W.1    Sachsenhofer, R.2
  • 60
    • 43249099890 scopus 로고    scopus 로고
    • In vivo imaging of membrane-associated glycans in developing zebrafish
    • DOI 10.1126/science.1155106
    • S.T. Laughlin, J.M. Baskin, S.L. Amacher, and C.R. Bertozzi In vivo imaging of membrane-associated glycans in developing zebrafish Science 320 2008 664 667 (Pubitemid 351928348)
    • (2008) Science , vol.320 , Issue.5876 , pp. 664-667
    • Laughlin, S.T.1    Baskin, J.M.2    Amacher, S.L.3    Bertozzi, C.R.4
  • 63
    • 4544241038 scopus 로고    scopus 로고
    • Atom transfer radical polymerization with polypeptide initiators: A general approach to block copolymers of sequence-defined polypeptides and synthetic polymers
    • H. Rettig, E. Krause, and H.G. Borner Atom transfer radical polymerization with polypeptide initiators: a general approach to block copolymers of sequence-defined polypeptides and synthetic polymers Macromol Rapid Commun 25 2004 1251 1256
    • (2004) Macromol Rapid Commun , vol.25 , pp. 1251-1256
    • Rettig, H.1    Krause, E.2    Borner, H.G.3
  • 64
    • 30744438588 scopus 로고    scopus 로고
    • Sequence-defined polypeptide-polymer conjugates utilizing reversible addition fragmentation transfer radical polymerization
    • DOI 10.1021/ma0519415
    • M.G.J. ten Cate, H. Rettig, K. Bernhardt, and H.G. Borner Sequence-defined polypeptide-polymer conjugates utilizing reversible addition fragmentation transfer radical polymerization Macromolecules 38 2005 10643 10649 (Pubitemid 43099312)
    • (2005) Macromolecules , vol.38 , Issue.26 , pp. 10643-10649
    • Ten Cate, M.G.J.1    Rettig, H.2    Bernhardt, K.3    Borner, H.G.4
  • 65
    • 38349091736 scopus 로고    scopus 로고
    • Designed amino acid ATRP initiators for the synthesis of biohybrid materials
    • R.M. Broyer, G.M. Quaker, and H.D. Maynard Designed amino acid ATRP initiators for the synthesis of biohybrid materials J Am Chem Soc 130 2008 1041 1047
    • (2008) J Am Chem Soc , vol.130 , pp. 1041-1047
    • Broyer, R.M.1    Quaker, G.M.2    Maynard, H.D.3
  • 66
    • 2542551131 scopus 로고    scopus 로고
    • Determination of the bioavailability of biotin conjugated onto shell cross-linked (SCK) nanoparticles
    • DOI 10.1021/ja039647k
    • K. Qi, Q. Ma, E. Remsen, C. Clark, and K. Wooley Determination of the bioavailability of biotin conjugated onto shell cross-linked (SCK) nanoparticles J Am Chem Soc 126 2004 6599 6607 (Pubitemid 38701760)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.21 , pp. 6599-6607
    • Qi, K.1    Ma, Q.2    Remsen, E.E.3    Clark Jr., C.G.4    Wooley, K.L.5
  • 67
    • 26944463809 scopus 로고    scopus 로고
    • One-step synthesis of low polydispersity, biotinylated poly(N- isopropylacrylamide) by ATRP
    • DOI 10.1039/b507912h
    • D. Bontempo, R.C. Li, T. Ly, C.E. Brubaker, and H.D. Maynard One-step synthesis of low polydispersity, biotinylated poly(N-isopropylacrylamide) by ATRP Chem Commun 2005 4702 4704 (Pubitemid 41475759)
    • (2005) Chemical Communications , Issue.37 , pp. 4702-4704
    • Bontempo, D.1    Li, R.C.2    Ly, T.3    Brubaker, C.E.4    Maynard, H.D.5
  • 68
    • 28844501733 scopus 로고    scopus 로고
    • Synthesis of uniform protein-polymer conjugates
    • DOI 10.1021/bm050428w
    • B. Lele, H. Murata, K. Matyjaszewski, and A. Russell Synthesis of uniform protein-polymer conjugates Biomacromolecules 6 2005 3380 3387 (Pubitemid 41764102)
    • (2005) Biomacromolecules , vol.6 , Issue.6 , pp. 3380-3387
    • Lele, B.S.1    Murata, H.2    Matyjaszewski, K.3    Russell, A.J.4
  • 69
    • 18644377228 scopus 로고    scopus 로고
    • Streptavidin as a macroinitiator for polymerization: In situ protein-polymer conjugate formation
    • DOI 10.1021/ja042230+
    • D. Bontempo, and H.D. Maynard Streptavidin as a macroinitiator for polymerization: in situ protein-polymer conjugate formation J Am Chem Soc 127 2005 6508 6509 (Pubitemid 40664138)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.18 , pp. 6508-6509
    • Bontempo, D.1    Maynard, H.D.2
  • 71
    • 55349127434 scopus 로고    scopus 로고
    • Biotin-, pyrene-, and GRGDS-functionalized polymers and nanogels via ATRP and end group modification
    • D. Siegwart, J. Oh, H. Gao, S. Bencherif, F. Perineau, and A. Bohaty Biotin-, pyrene-, and GRGDS-functionalized polymers and nanogels via ATRP and end group modification Macromol Chem Phys 209 2008 2180 2193
    • (2008) Macromol Chem Phys , vol.209 , pp. 2180-2193
    • Siegwart, D.1    Oh, J.2    Gao, H.3    Bencherif, S.4    Perineau, F.5    Bohaty, A.6
  • 72
    • 70349339238 scopus 로고    scopus 로고
    • In situ growth of a stoichiometric PEG-like conjugate at a protein's N-terminus with significantly improved pharmacokinetics
    • W. Gao, W. Liu, J. Mackay, M. Zalutsky, E. Toone, and A. Chilkoti In situ growth of a stoichiometric PEG-like conjugate at a protein's N-terminus with significantly improved pharmacokinetics Proc Natl Acad Sci USA 106 2009 15231 15236
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 15231-15236
    • Gao, W.1    Liu, W.2    MacKay, J.3    Zalutsky, M.4    Toone, E.5    Chilkoti, A.6
  • 73
    • 78049256803 scopus 로고    scopus 로고
    • In situ growth of a PEG-like polymer from the C terminus of an intein fusion protein improves pharmacokinetics and tumor accumulation
    • W.P. Gao, W.G. Liu, T. Christensen, M.R. Zalutsky, and A. Chilkoti In situ growth of a PEG-like polymer from the C terminus of an intein fusion protein improves pharmacokinetics and tumor accumulation Proc Natl Acad Sci USA 107 2010 16432 16437
    • (2010) Proc Natl Acad Sci USA , vol.107 , pp. 16432-16437
    • Gao, W.P.1    Liu, W.G.2    Christensen, T.3    Zalutsky, M.R.4    Chilkoti, A.5
  • 76
    • 27844566629 scopus 로고    scopus 로고
    • Biomimetic anchor for surface-initiated polymerization from metal substrates
    • DOI 10.1021/ja0532638
    • X. Fan, L. Lin, J. Dalsin, and P. Messersmith Biomimetic anchor for surface-initiated polymerization from metal substrates J Am Chem Soc 127 2005 15843 15847 (Pubitemid 41643294)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.45 , pp. 15843-15847
    • Fan, X.1    Lin, L.2    Dalsin, J.L.3    Messersmith, P.B.4
  • 77
    • 0033154074 scopus 로고    scopus 로고
    • Novel initiators for atom transfer radical and ring-opening polymerization: A new general method for the preparation of thiol-functional polymers
    • G. Carrot, J. Hilborn, J.L. Hedrick, and M. Trollss Novel initiators for atom transfer radical and ring-opening polymerization: a new general method for the preparation of thiol-functional polymers Macromolecules 32 1999 5171 5173
    • (1999) Macromolecules , vol.32 , pp. 5171-5173
    • Carrot, G.1    Hilborn, J.2    Hedrick, J.L.3    Trollss, M.4
  • 79
    • 11144225434 scopus 로고    scopus 로고
    • Biological-synthetic hybrid block copolymers: Combining the best from two worlds
    • H.A. Klok Biological-synthetic hybrid block copolymers: combining the best from two worlds J Polym Sci Part A: Polym Chem 43 2005 1 17
    • (2005) J Polym Sci Part A: Polym Chem , vol.43 , pp. 1-17
    • Klok, H.A.1
  • 81
    • 0142119372 scopus 로고    scopus 로고
    • Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change
    • DOI 10.1002/anie.200250653
    • Y. Bae, S. Fukushima, A. Harada, and K. Kataoka Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: polymeric micelles that are responsive to intracellular pH change Angew Chem Int Edit 42 2003 4640 4643 (Pubitemid 37271305)
    • (2003) Angewandte Chemie - International Edition , vol.42 , Issue.38 , pp. 4640-4643
    • Bae, Y.1    Fukushima, S.2    Harada, A.3    Kataoka, K.4
  • 82
    • 33750960634 scopus 로고    scopus 로고
    • Supramolecular assemblies of block copolymers in aqueous media as nanocontainers relevant to biological applications
    • DOI 10.1016/j.progpolymsci.2006.09.004, PII S0079670006000888
    • A. Harada, and K. Kataoka Supramolecular assemblies of block copolymers in aqueous media as nanocontainers relevant to biological applications Prog Polym Sci 31 2006 949 982 (Pubitemid 44738012)
    • (2006) Progress in Polymer Science (Oxford) , vol.31 , Issue.11 , pp. 949-982
    • Harada, A.1    Kataoka, K.2
  • 83
    • 33746307391 scopus 로고    scopus 로고
    • Nanostructured devices based on block copolymer assemblies for drug delivery: Designing structures for enhanced drug function
    • N. Nishiyama, and K. Kataoka Nanostructured devices based on block copolymer assemblies for drug delivery: designing structures for enhanced drug function Adv Polym Sci 193 2006 67 101
    • (2006) Adv Polym Sci , vol.193 , pp. 67-101
    • Nishiyama, N.1    Kataoka, K.2
  • 84
    • 77956156055 scopus 로고    scopus 로고
    • Fabrication of micellar nanoparticles for drug delivery through the self-assembly of block copolymers
    • Z.L. Tyrrell, Y. Shen, and M. Radosz Fabrication of micellar nanoparticles for drug delivery through the self-assembly of block copolymers Prog Polym Sci 35 2010 1128 1143
    • (2010) Prog Polym Sci , vol.35 , pp. 1128-1143
    • Tyrrell, Z.L.1    Shen, Y.2    Radosz, M.3
  • 85
    • 33644937518 scopus 로고    scopus 로고
    • Proton diffusion across membranes of vesicles of poly(styrene-b-acrylic acid) diblock copolymers
    • J. Wu, and A. Eisenberg Proton diffusion across membranes of vesicles of poly(styrene-b-acrylic acid) diblock copolymers J Am Chem Soc 128 2006 2880 2884
    • (2006) J Am Chem Soc , vol.128 , pp. 2880-2884
    • Wu, J.1    Eisenberg, A.2
  • 87
    • 18444392735 scopus 로고    scopus 로고
    • Birth of a new macromolecular architecture: Dendrimers as quantized building blocks for nanoscale synthetic polymer chemistry
    • DOI 10.1016/j.progpolymsci.2005.01.007, PII S0079670005000043, Dendrimers and Dendritic Polymers
    • D.A. Tomalia Birth of a new macromolecular architecture: dendrimers as quantized building blocks for nanoscale synthetic polymer chemistry Prog Polym Sci 30 2005 294 324 (Pubitemid 40642933)
    • (2005) Progress in Polymer Science (Oxford) , vol.30 , Issue.3-4 , pp. 294-324
    • Tomalia, D.A.1
  • 88
    • 25844461769 scopus 로고    scopus 로고
    • Target-specific cellular uptake of PLGA nanoparticles coated with poly(L-lysine)-poly(ethylene glycol)-folate conjugate
    • DOI 10.1021/la0502084
    • S.H. Kim, J.H. Jeong, K.W. Chun, and T.G. Park Target-specific cellular uptake of PLGA nanoparticles coated with poly(l-lysine)-poly(ethylene glycol)-folate conjugate Langmuir 21 2005 8852 8857 (Pubitemid 41396646)
    • (2005) Langmuir , vol.21 , Issue.19 , pp. 8852-8857
    • Kim, S.H.1    Jeong, J.H.2    Chun, K.W.3    Park, T.G.4
  • 90
    • 0023581602 scopus 로고
    • Applications of thermally reversible polymers and hydrogels in therapeutics and diagnostics
    • DOI 10.1016/0168-3659(87)90083-6
    • A.S. Hoffman Applications of thermally reversible polymers and hydrogels in therapeutics and diagnostics J Control Release 6 1987 297 305 (Pubitemid 18017739)
    • (1987) Journal of Controlled Release , vol.6 , Issue.SPEC.NO. , pp. 297-305
    • Hoffman, A.S.1
  • 91
    • 41349093105 scopus 로고    scopus 로고
    • The development of microgels/nanogels for drug delivery applications
    • J. Oh, R. Drumright, D. Siegwart, and K. Matyjaszewski The development of microgels/nanogels for drug delivery applications Prog Polym Sci 33 2008 448 477
    • (2008) Prog Polym Sci , vol.33 , pp. 448-477
    • Oh, J.1    Drumright, R.2    Siegwart, D.3    Matyjaszewski, K.4
  • 92
    • 71749101556 scopus 로고    scopus 로고
    • Biopolymer-based microgels/nanogels for drug delivery applications
    • J.K. Oh, D.I. Lee, and J.M. Park Biopolymer-based microgels/nanogels for drug delivery applications Prog Polym Sci 34 2009 1261 1282
    • (2009) Prog Polym Sci , vol.34 , pp. 1261-1282
    • Oh, J.K.1    Lee, D.I.2    Park, J.M.3
  • 93
    • 79960391102 scopus 로고    scopus 로고
    • Polymer vectors via controlled/living radical polymerization for gene delivery
    • F. Xu, and W. Yang Polymer vectors via controlled/living radical polymerization for gene delivery Prog Polym Sci 36 2011 1099 1131
    • (2011) Prog Polym Sci , vol.36 , pp. 1099-1131
    • Xu, F.1    Yang, W.2
  • 94
    • 77956187410 scopus 로고    scopus 로고
    • Hydrophobic modifications of cationic polymers for gene delivery
    • Z. Liu, Z. Zhang, C. Zhou, and Y. Jiao Hydrophobic modifications of cationic polymers for gene delivery Prog Polym Sci 35 2010 1144 1162
    • (2010) Prog Polym Sci , vol.35 , pp. 1144-1162
    • Liu, Z.1    Zhang, Z.2    Zhou, C.3    Jiao, Y.4
  • 95
    • 77649339137 scopus 로고    scopus 로고
    • Non-viral polyplexes: Scaffold mediated delivery for gene therapy
    • S. O'Rorke, M. Keeney, and A. Pandit Non-viral polyplexes: scaffold mediated delivery for gene therapy Prog Polym Sci 35 2010 441 458
    • (2010) Prog Polym Sci , vol.35 , pp. 441-458
    • O'Rorke, S.1    Keeney, M.2    Pandit, A.3
  • 96
    • 68549126855 scopus 로고    scopus 로고
    • Block copolymer micelles for delivery of cancer therapy: Transport at the whole body, tissue and cellular levels
    • A.S. Mikhail, and C. Allen Block copolymer micelles for delivery of cancer therapy: transport at the whole body, tissue and cellular levels J Control Release 138 2009 214 223
    • (2009) J Control Release , vol.138 , pp. 214-223
    • Mikhail, A.S.1    Allen, C.2
  • 97
    • 72549089193 scopus 로고    scopus 로고
    • Polymeric supramolecular systems for drug delivery
    • H.-J. Yoon, and W.-D. Jang Polymeric supramolecular systems for drug delivery J Mater Chem 20 2010 211 222
    • (2010) J Mater Chem , vol.20 , pp. 211-222
    • Yoon, H.-J.1    Jang, W.-D.2
  • 98
    • 33750281612 scopus 로고    scopus 로고
    • Cross-linked block copolymer micelles: Functional nanostructures of great potential and versatility
    • DOI 10.1039/b514858h
    • R. O'Reilly, C. Hawker, and K. Wooley Cross-linked block copolymer micelles: functional nanostructures of great potential and versatility Chem Soc Rev 35 2006 1068 1083 (Pubitemid 44611720)
    • (2006) Chemical Society Reviews , vol.35 , Issue.11 , pp. 1068-1083
    • O'Reilly, R.K.1    Hawker, C.J.2    Wooley, K.L.3
  • 99
    • 36249004431 scopus 로고    scopus 로고
    • Solvent induced morphologies of poly(methyl methacrylate-b-ethylene oxide-b-methyl methacrylate) triblock copolymers synthesized by atom transfer radical polymerization
    • DOI 10.1016/j.polymer.2007.10.009, PII S003238610700969X
    • D.J. Siegwart, W. Wu, M. Mandalaywala, M. Tamir, T. Sarbu, M.S. Silverstein, T. Kowalewski, J.O. Hollinger, and K. Matyjaszewski Solvent induced morphologies of poly(methyl methacrylate-b-ethylene oxide-b-methyl methacrylate) triblock copolymers synthesized by atom transfer radical polymerization Polymer 48 2007 7279 7290 (Pubitemid 350137423)
    • (2007) Polymer , vol.48 , Issue.25 , pp. 7279-7290
    • Siegwart, D.J.1    Wu, W.2    Mandalaywala, M.3    Tamir, M.4    Sarbu, T.5    Silverstein, M.S.6    Kowalewski, T.7    Hollinger, J.O.8    Matyjaszewski, K.9
  • 101
    • 77957559065 scopus 로고    scopus 로고
    • Polysaccharide-containing block copolymers: Synthesis, properties and applications of an emerging family of glycoconjugates
    • C. Schatz, and S. Lecommandoux Polysaccharide-containing block copolymers: synthesis, properties and applications of an emerging family of glycoconjugates Macromol Rapid Commun 31 2010 1664 1684
    • (2010) Macromol Rapid Commun , vol.31 , pp. 1664-1684
    • Schatz, C.1    Lecommandoux, S.2
  • 102
    • 78249284337 scopus 로고    scopus 로고
    • Modification of polysaccharides through Controlled/Living Radical Polymerization grafting - Towards the generation of high performance hybrids
    • M. Tizzotti, A. Charlot, E. Fleury, M. Stenzel, and J. Bernard Modification of polysaccharides through Controlled/Living Radical Polymerization grafting - towards the generation of high performance hybrids Macromol Rapid Commun 31 2010 1751 1772
    • (2010) Macromol Rapid Commun , vol.31 , pp. 1751-1772
    • Tizzotti, M.1    Charlot, A.2    Fleury, E.3    Stenzel, M.4    Bernard, J.5
  • 103
    • 0034208950 scopus 로고    scopus 로고
    • Well-defined oligosaccharide-terminated polymers from living radical polymerization
    • D. Haddleton, and K. Ohno Well-defined oligosaccharide-terminated polymers from living radical polymerization Biomacromolecules 1 2000 152 156
    • (2000) Biomacromolecules , vol.1 , pp. 152-156
    • Haddleton, D.1    Ohno, K.2
  • 104
    • 34447629377 scopus 로고    scopus 로고
    • Synthesis of ATRP-induced dextran-b-polystyrene diblock copolymers and preliminary investigation of their self-assembly in water
    • DOI 10.1039/b706248f
    • C. Houga, J.-F. Le Meins, R. Borsali, D. Taton, and Y. Gnanou Synthesis of ATRP-induced dextran-b-polystyrene diblock copolymers and preliminary investigation of their self-assembly in water Chem Commun 2007 3063 3065 (Pubitemid 47087718)
    • (2007) Chemical Communications , Issue.29 , pp. 3063-3065
    • Houga, C.1    Meins, J.-F.L.2    Borsali, R.3    Taton, D.4    Gnanou, Y.5
  • 106
    • 0035964535 scopus 로고    scopus 로고
    • Structural control of poly(methyl methacrylate)-g-poly(lactic acid) graft copolymers by atom transfer radical polymerization (ATRP)
    • DOI 10.1021/ma0105791
    • H. Shinoda, and K. Matyjaszewski Structural control of poly(methyl methacrylate)-g-poly(lactic acid) graft copolymers by atom transfer radical polymerization (ATRP) Macromolecules 34 2001 6243 6248 (Pubitemid 34217133)
    • (2001) Macromolecules , vol.34 , Issue.18 , pp. 6243-6248
    • Shinoda, H.1    Matyjaszewski, K.2
  • 107
    • 11144268181 scopus 로고    scopus 로고
    • Controlled ring-opening polymerization of lactide and glycolide
    • DOI 10.1021/cr040002s
    • O. Dechy-Cabaret, B. Martin-Vaca, and D. Bourissou Controlled ring-opening polymerization of lactide and glycolide Chem Rev 104 2004 6147 6176 (Pubitemid 40025736)
    • (2004) Chemical Reviews , vol.104 , Issue.12 , pp. 6147-6176
    • Dechy-Cabaret, O.1    Martin-Vaca, B.2    Bourissou, D.3
  • 108
    • 17044431562 scopus 로고    scopus 로고
    • Block and random copolymers as surfactants for dispersion polymerization. I. synthesis via atom transfer radical polymerization and ring-opening polymerization
    • DOI 10.1002/pola.20629
    • W. Jakubowski, J.-F. Lutz, S. Slomkowski, and K. Matyjaszewski Block and random copolymers as surfactants for dispersion polymerization. I. Synthesis via atom transfer radical polymerization and ring-opening polymerization J Polym Sci Part A: Polym Chem 43 2005 1498 1510 (Pubitemid 40496623)
    • (2005) Journal of Polymer Science, Part A: Polymer Chemistry , vol.43 , Issue.7 , pp. 1498-1510
    • Jakubowski, W.1    Lutz, J.-F.2    Slomkowski, S.3    Matyjaszewski, K.4
  • 109
    • 50249188910 scopus 로고    scopus 로고
    • Atom Transfer Radical Polymerization of tulipalin A: A naturally renewable monomer
    • J. Mosnacek, and K. Matyjaszewski Atom Transfer Radical Polymerization of tulipalin A: a naturally renewable monomer Macromolecules 41 2008 5509 5511
    • (2008) Macromolecules , vol.41 , pp. 5509-5511
    • Mosnacek, J.1    Matyjaszewski, K.2
  • 110
    • 79953036136 scopus 로고    scopus 로고
    • Thermoresponsive star triblock copolymers by combination of ROP and ATRP: From micelles to hydrogels
    • W. Zhu, A. Nese, and K. Matyjaszewski Thermoresponsive star triblock copolymers by combination of ROP and ATRP: from micelles to hydrogels J Polym Sci Part A: Polym Chem 49 2011 1942 1952
    • (2011) J Polym Sci Part A: Polym Chem , vol.49 , pp. 1942-1952
    • Zhu, W.1    Nese, A.2    Matyjaszewski, K.3
  • 111
    • 54749106138 scopus 로고    scopus 로고
    • Sustained release of drugs dispersed in polymer nanoparticles
    • G.B. Jacobson, R. Shinde, C.H. Contag, and R.N. Zare Sustained release of drugs dispersed in polymer nanoparticles Angew Chem Int Edit 47 2008 7880 7882
    • (2008) Angew Chem Int Edit , vol.47 , pp. 7880-7882
    • Jacobson, G.B.1    Shinde, R.2    Contag, C.H.3    Zare, R.N.4
  • 112
    • 33847417136 scopus 로고    scopus 로고
    • Preparation and characterization of poly (2-methacryloyloxyethyl phosphorylcholine)-block-poly(D,L-lactide) polymer nanoparticles
    • DOI 10.1002/pola.21741
    • G.-H. Hsiue, C.-L. Lo, C.-H. Cheng, C.-P. Lin, C.-K. Huang, and H.-H. Chen Preparation and characterization of poly(2-methacryloyloxyethyl phosphorylcholine)-block-poly(d,l-lactide) polymer nanoparticles J Polym Sci Part A: Polym Chem 45 2007 688 698 (Pubitemid 46346454)
    • (2007) Journal of Polymer Science, Part A: Polymer Chemistry , vol.45 , Issue.4 , pp. 688-698
    • Hsiue, G.-H.1    Lo, C.-L.2    Cheng, C.-H.3    Lin, C.-P.4    Huang, C.-K.5    Chen, H.-H.6
  • 113
    • 66149135977 scopus 로고    scopus 로고
    • Amphiphilic poly(d- or l-lactide)-b-poly(N,N-dimethylamino-2-ethyl methacrylate) block copolymers: Controlled synthesis, characterization, and stereocomplex formation
    • M. Spasova, L. Mespouille, O. Coulembier, D. Paneva, N. Manolova, I. Rashkov, and P. Dubois Amphiphilic poly(d- or l-lactide)-b-poly(N,N- dimethylamino-2-ethyl methacrylate) block copolymers: controlled synthesis, characterization, and stereocomplex formation Biomacromolecules 10 2009 1217 1223
    • (2009) Biomacromolecules , vol.10 , pp. 1217-1223
    • Spasova, M.1    Mespouille, L.2    Coulembier, O.3    Paneva, D.4    Manolova, N.5    Rashkov, I.6    Dubois, P.7
  • 114
    • 76249095948 scopus 로고    scopus 로고
    • Poly(dl-lactide)-b-poly(N,N-dimethylamino-2-ethyl methacrylate): Synthesis, characterization, micellization behavior in aqueous solutions, and encapsulation of the hydrophobic drug dipyridamole
    • N. Karanikolopoulos, M. Zamurovic, M. Pitsikalis, and N. Hadjichristidis Poly(dl-lactide)-b-poly(N,N-dimethylamino-2-ethyl methacrylate): synthesis, characterization, micellization behavior in aqueous solutions, and encapsulation of the hydrophobic drug dipyridamole Biomacromolecules 11 2010 430 438
    • (2010) Biomacromolecules , vol.11 , pp. 430-438
    • Karanikolopoulos, N.1    Zamurovic, M.2    Pitsikalis, M.3    Hadjichristidis, N.4
  • 115
    • 76249086258 scopus 로고    scopus 로고
    • Biocompatible and pH-responsive triblock copolymer mPEG-b-PCL-b-PDMAEMA: Synthesis, self-assembly, and application
    • W. Zhang, J. He, Z. Liu, P. Ni, and X. Zhu Biocompatible and pH-responsive triblock copolymer mPEG-b-PCL-b-PDMAEMA: synthesis, self-assembly, and application J Polym Sci Part A: Polym Chem 48 2010 1079 1091
    • (2010) J Polym Sci Part A: Polym Chem , vol.48 , pp. 1079-1091
    • Zhang, W.1    He, J.2    Liu, Z.3    Ni, P.4    Zhu, X.5
  • 116
    • 68549096373 scopus 로고    scopus 로고
    • Poly(lactide)-block-poly(HEMA) block copolymers: An orthogonal one-pot combination of ROP and ATRP, using a bifunctional initiator
    • F.F. Wolf, N. Friedemann, and H. Frey Poly(lactide)-block-poly(HEMA) block copolymers: an orthogonal one-pot combination of ROP and ATRP, using a bifunctional initiator Macromolecules 42 2009 5622 5628
    • (2009) Macromolecules , vol.42 , pp. 5622-5628
    • Wolf, F.F.1    Friedemann, N.2    Frey, H.3
  • 117
    • 43049154835 scopus 로고    scopus 로고
    • Pentablock copolymers of poly(ethylene glycol), poly((2-dimethyl amino)ethyl methacrylate) and poly(2-hydroxyethyl methacrylate) from consecutive atom transfer radical polymerizations for non-viral gene delivery
    • F.-J. Xu, H. Li, J. Li, Z. Zhang, E.-T. Kang, and K.-G. Neoh Pentablock copolymers of poly(ethylene glycol), poly((2-dimethyl amino)ethyl methacrylate) and poly(2-hydroxyethyl methacrylate) from consecutive atom transfer radical polymerizations for non-viral gene delivery Biomaterials 29 2008 3023 3033
    • (2008) Biomaterials , vol.29 , pp. 3023-3033
    • Xu, F.-J.1    Li, H.2    Li, J.3    Zhang, Z.4    Kang, E.-T.5    Neoh, K.-G.6
  • 118
    • 23044520307 scopus 로고    scopus 로고
    • Synthesis of amphiphilic block copolymers with well-defined glycopolymer segment by atom transfer radical polymerization
    • Z.C. Li, Y.Z. Liang, G.Q. Chen, and F.M. Li Synthesis of amphiphilic block copolymers with well-defined glycopolymer segment by atom transfer radical polymerization Macromol Rapid Commun 21 2000 375 380
    • (2000) Macromol Rapid Commun , vol.21 , pp. 375-380
    • Li, Z.C.1    Liang, Y.Z.2    Chen, G.Q.3    Li, F.M.4
  • 119
    • 0036433930 scopus 로고    scopus 로고
    • Synthesis of low polydispersity, controlled-structure sugar methacrylate polymers under mild conditions without protecting group chemistry
    • R. Narain, and S.P. Armes Synthesis of low polydispersity, controlled-structure sugar methacrylate polymers under mild conditions without protecting group chemistry Chem Commun 2002 2776 2777 (Pubitemid 35375675)
    • (2002) Chemical Communications , Issue.23 , pp. 2776-2777
    • Narain, R.1    Armes, S.P.2
  • 120
    • 0345257129 scopus 로고    scopus 로고
    • Synthesis and aqueous solution properties of novel sugar methacrylate-based homopolymers and block copolymers
    • DOI 10.1021/bm034166e
    • R. Narain, and S.P. Armes Synthesis and aqueous solution properties of novel sugar methacrylate-based homopolymers and block copolymers Biomacromolecules 4 2003 1746 1758 (Pubitemid 37455589)
    • (2003) Biomacromolecules , vol.4 , Issue.6 , pp. 1746-1758
    • Narain, R.1    Armes, S.P.2
  • 121
    • 0037781968 scopus 로고    scopus 로고
    • Direct synthesis and aqueous solution properties of well-defined cyclic sugar methacrylate polymers
    • R. Narain, and S.P. Armes Direct synthesis and aqueous solution properties of well-defined cyclic sugar methacrylate polymers Macromolecules 36 2003 4675 4678
    • (2003) Macromolecules , vol.36 , pp. 4675-4678
    • Narain, R.1    Armes, S.P.2
  • 122
    • 0347985280 scopus 로고    scopus 로고
    • Synthetic and biological polymers-merging the interface
    • D. Cunliffe, S. Pennadam, and C. Alexander Synthetic and biological polymers-merging the interface Eur Polym J 40 2004 5 25
    • (2004) Eur Polym J , vol.40 , pp. 5-25
    • Cunliffe, D.1    Pennadam, S.2    Alexander, C.3
  • 123
    • 0037426512 scopus 로고    scopus 로고
    • Sugar-coated amphiphilic block copolymer micelles from living radical polymerization: Recognition by immobilized lectins
    • L. Bes, S. Angot, A. Limer, and D.M. Haddleton Sugar-coated amphiphilic block copolymer micelles from living radical polymerization: recognition by immobilized lectins Macromolecules 36 2003 2493 2499
    • (2003) Macromolecules , vol.36 , pp. 2493-2499
    • Bes, L.1    Angot, S.2    Limer, A.3    Haddleton, D.M.4
  • 124
    • 33846172660 scopus 로고    scopus 로고
    • Responsive polymers at the biology/materials science interface
    • DOI 10.1002/adma.200502640
    • C. Alexander, and K.M. Shakesheff Responsive polymers at the biology/materials science interface Adv Mater 18 2006 3321 3328 (Pubitemid 46080237)
    • (2006) Advanced Materials , vol.18 , Issue.24 , pp. 3321-3328
    • Alexander, C.1    Shakesheff, K.M.2
  • 125
    • 34547561267 scopus 로고    scopus 로고
    • Physical stimuli-responsive polymeric micelles for anti-cancer drug delivery
    • DOI 10.1016/j.progpolymsci.2007.05.009, PII S0079670007000640, Polymers in Biomedical Applications
    • N. Rapoport Physical stimuli-responsive polymeric micelles for anti-cancer drug delivery Prog Polym Sci 32 2007 962 990 (Pubitemid 47198285)
    • (2007) Progress in Polymer Science (Oxford) , vol.32 , Issue.8-9 , pp. 962-990
    • Rapoport, N.1
  • 126
    • 73749088453 scopus 로고    scopus 로고
    • Stimuli-responsive nanoparticles, nanogels and capsules for integrated multifunctional intelligent systems
    • M. Motornov, Y. Roiter, I. Tokarev, and S. Minko Stimuli-responsive nanoparticles, nanogels and capsules for integrated multifunctional intelligent systems Prog Polym Sci 35 2010 174 211
    • (2010) Prog Polym Sci , vol.35 , pp. 174-211
    • Motornov, M.1    Roiter, Y.2    Tokarev, I.3    Minko, S.4
  • 127
    • 77952537515 scopus 로고    scopus 로고
    • Synthesis and micellization of pH/temperature-responsive double-hydrophilic diblock copolymers polyphosphoester-block-poly[2- (dimethylamino)ethyl methacrylate] prepared via ROP and ATRP
    • X. Liu, P. Ni, J. He, and M. Zhang Synthesis and micellization of pH/temperature-responsive double-hydrophilic diblock copolymers polyphosphoester-block-poly[2-(dimethylamino)ethyl methacrylate] prepared via ROP and ATRP Macromolecules 43 2010 4771 4781
    • (2010) Macromolecules , vol.43 , pp. 4771-4781
    • Liu, X.1    Ni, P.2    He, J.3    Zhang, M.4
  • 128
    • 63849224294 scopus 로고    scopus 로고
    • Synthesis and characterization of pH sensitive poly(glycidol)-b-poly(4- vinylpyridine) block copolymers
    • S. Mendrek, A. Mendrek, H.-J. Adler, A. Dworak, and D. Kuckling Synthesis and characterization of pH sensitive poly(glycidol)-b-poly(4-vinylpyridine) block copolymers J Polym Sci Part A: Polym Chem 47 2009 1782 1794
    • (2009) J Polym Sci Part A: Polym Chem , vol.47 , pp. 1782-1794
    • Mendrek, S.1    Mendrek, A.2    Adler, H.-J.3    Dworak, A.4    Kuckling, D.5
  • 129
    • 61849097305 scopus 로고    scopus 로고
    • Acid-sensitive polymeric micelles based on thermoresponsive block copolymers with pendent cyclic orthoester groups
    • X. Huang, F. Du, J. Cheng, Y. Dong, D. Liang, S. Ji, S.-S. Lin, and Z. Li Acid-sensitive polymeric micelles based on thermoresponsive block copolymers with pendent cyclic orthoester groups Macromolecules 42 2009 783 790
    • (2009) Macromolecules , vol.42 , pp. 783-790
    • Huang, X.1    Du, F.2    Cheng, J.3    Dong, Y.4    Liang, D.5    Ji, S.6    Lin, S.-S.7    Li, Z.8
  • 130
    • 20444460701 scopus 로고    scopus 로고
    • A new design for light-breakable polymer micelles
    • DOI 10.1021/ja0521019
    • J. Jiang, X. Tong, and Y. Zhao A new design for light-breakable polymer micelles J Am Chem Soc 127 2005 8290 8291 (Pubitemid 40828140)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.23 , pp. 8290-8291
    • Jiang, J.1    Tong, X.2    Zhao, Y.3
  • 131
    • 33746362871 scopus 로고    scopus 로고
    • Toward photocontrolled release using light-dissociable block copolymer micelles
    • DOI 10.1021/ma060142z
    • J. Jiang, X. Tong, D. Morris, and Y. Zhao Toward photocontrolled release using light-dissociable block copolymer micelles Macromolecules 39 2006 4633 4640 (Pubitemid 44114097)
    • (2006) Macromolecules , vol.39 , Issue.13 , pp. 4633-4640
    • Jiang, J.1    Tong, X.2    Morris, D.3    Zhao, Y.4
  • 136
    • 33847693626 scopus 로고    scopus 로고
    • Polymer micelles stabilization on demand through reversible photo-cross-linking
    • DOI 10.1021/ma062493j
    • J. Jiang, B. Qi, M. Lepage, and Y. Zhao Polymer micelles stabilization on demand through reversible photo-cross-linking Macromolecules 40 2007 790 792 (Pubitemid 46383723)
    • (2007) Macromolecules , vol.40 , Issue.4 , pp. 790-792
    • Jiang, J.1    Qi, B.2    Lepage, M.3    Zhao, Y.4
  • 137
    • 67650470426 scopus 로고    scopus 로고
    • Photoresponsive nanogels based on photocontrollable cross-links
    • J. He, X. Tong, and Y. Zhao Photoresponsive nanogels based on photocontrollable cross-links Macromolecules 42 2009 4845 4852
    • (2009) Macromolecules , vol.42 , pp. 4845-4852
    • He, J.1    Tong, X.2    Zhao, Y.3
  • 138
    • 79961140159 scopus 로고    scopus 로고
    • Reductively degradable polyester-based block copolymers prepared by facile polycondensation and ATRP: Synthesis, degradation, and aqueous micellization
    • A. Nelson-Mendez, S. Aleksanian, M. Oh, H.-S. Lim, and J.K. Oh Reductively degradable polyester-based block copolymers prepared by facile polycondensation and ATRP: synthesis, degradation, and aqueous micellization Soft Matter 7 2011 7441 7452
    • (2011) Soft Matter , vol.7 , pp. 7441-7452
    • Nelson-Mendez, A.1    Aleksanian, S.2    Oh, M.3    Lim, H.-S.4    Oh, J.K.5
  • 139
    • 67650366854 scopus 로고    scopus 로고
    • A general method for the synthesis and isolation of well-defined core cross-linked multistar assemblies: A route toward enhanced pH-responsive polymers
    • J.F. Tan, A. Blencowe, T.K. Goh, I.T.M. Dela Cruz, and G.G. Qiao A general method for the synthesis and isolation of well-defined core cross-linked multistar assemblies: a route toward enhanced pH-responsive polymers Macromolecules 42 2009 4622 4631
    • (2009) Macromolecules , vol.42 , pp. 4622-4631
    • Tan, J.F.1    Blencowe, A.2    Goh, T.K.3    Dela Cruz, I.T.M.4    Qiao, G.G.5
  • 140
    • 80054000128 scopus 로고    scopus 로고
    • New thiol-reponsive mono-cleavable block copolymer micelles labeled with single disulfides
    • doi:10.1002/marc.201100372
    • Khorsand Sourkohi B, Schmidt R, Oh JK. New thiol-reponsive mono-cleavable block copolymer micelles labeled with single disulfides. Macromol Rapid Commun, doi:10.1002/marc.201100372.
    • Macromol Rapid Commun
    • Khorsand Sourkohi, B.1    Schmidt, R.2    Oh, J.K.3
  • 141
    • 0000103356 scopus 로고    scopus 로고
    • Nanogels and microgels: The new polymeric materials playground
    • N.B. Graham, and A. Cameron Nanogels and microgels: the new polymeric materials playground Pure Appl Chem 70 1998 1271 1275 (Pubitemid 128486994)
    • (1998) Pure and Applied Chemistry , vol.70 , Issue.6 , pp. 1271-1275
    • Graham, N.B.1    Cameron, A.2
  • 142
    • 33745600550 scopus 로고    scopus 로고
    • Microgel, nanogel and hydrogel-hydrogel semi-IPN composites for biomedical applications: Synthesis and characterization
    • DOI 10.1007/s00396-006-1489-4
    • N. Sahiner, W.T. Godbey, G.L. McPherson, and V.T. John Microgel, nanogel and hydrogel-hydrogel semi-IPN composites for biomedical applications: synthesis and characterization Colloid Polym Sci 284 2006 1121 1129 (Pubitemid 43983975)
    • (2006) Colloid and Polymer Science , vol.284 , Issue.10 , pp. 1121-1129
    • Sahiner, N.1    Godbey, W.T.2    McPherson, G.L.3    John, V.T.4
  • 143
    • 33644628244 scopus 로고    scopus 로고
    • Preparation and characterization of photo-cross-linked thermosensitive PNIPAAm nanogels
    • D. Kuckling, C.D. Vo, H.J.P. Adler, A. Voelkel, and H. Coelfen Preparation and characterization of photo-cross-linked thermosensitive PNIPAAm nanogels Macromolecules 39 2006 1585 1591
    • (2006) Macromolecules , vol.39 , pp. 1585-1591
    • Kuckling, D.1    Vo, C.D.2    Adler, H.J.P.3    Voelkel, A.4    Coelfen, H.5
  • 144
  • 145
    • 79955463389 scopus 로고    scopus 로고
    • Polymer nanoparticles: Preparation techniques and size-control parameters
    • J.P. Rao, and K.E. Geckeler Polymer nanoparticles: preparation techniques and size-control parameters Prog Polym Sci 36 2011 887 913
    • (2011) Prog Polym Sci , vol.36 , pp. 887-913
    • Rao, J.P.1    Geckeler, K.E.2
  • 146
    • 0023450012 scopus 로고
    • Effect of molecular weight (Mw) of N-(2-hydroxypropyl)methacrylamide copolymers on body distribution and rate of excretion after subcutaneous, intraperitoneal, and intravenous administration to rats
    • L.W. Seymour, R. Duncan, J. Strohalm, and J. Kopecek Effect of molecular weight (Mw) of N-(2-hydroxypropyl)methacrylamide copolymers on body distribution and rate of excretion after subcutaneous, intraperitoneal, and intravenous administration to rats J Biomed Mater Res Part A 21 1987 1341 1358
    • (1987) J Biomed Mater Res Part A , vol.21 , pp. 1341-1358
    • Seymour, L.W.1    Duncan, R.2    Strohalm, J.3    Kopecek, J.4
  • 147
    • 51049090204 scopus 로고    scopus 로고
    • Nanoparticle therapeutics: An emerging treatment modality for cancer
    • M.E. Davis, Z. Chen, and D.M. Shin Nanoparticle therapeutics: an emerging treatment modality for cancer Nat Rev Drug Discov 7 2008 771 782
    • (2008) Nat Rev Drug Discov , vol.7 , pp. 771-782
    • Davis, M.E.1    Chen, Z.2    Shin, D.M.3
  • 149
    • 41349093552 scopus 로고    scopus 로고
    • Intracellular delivery of nanogel-quantum dot hybrid nanoparticles into human periodontal ligament cells
    • T. Fukui, H. Kobayashi, U. Hasegawa, T. Nagasawa, K. Akiyoshi, and I. Ishikawa Intracellular delivery of nanogel-quantum dot hybrid nanoparticles into human periodontal ligament cells Drug Metab Lett 1 2007 131 135
    • (2007) Drug Metab Lett , vol.1 , pp. 131-135
    • Fukui, T.1    Kobayashi, H.2    Hasegawa, U.3    Nagasawa, T.4    Akiyoshi, K.5    Ishikawa, I.6
  • 150
    • 0141743466 scopus 로고    scopus 로고
    • Biodegradable magnetic gel: Synthesis and characterization
    • DOI 10.1007/s00396-003-0916-z
    • J. Chatterjee, Y. Haik, and C.J. Chen Biodegradable magnetic gel: synthesis and characterization Colloid Polym Sci 281 2003 892 896 (Pubitemid 37161621)
    • (2003) Colloid and Polymer Science , vol.281 , Issue.9 , pp. 892-896
    • Chatterjee, J.1    Haik, Y.2    Chen, C.J.3
  • 151
    • 2342457069 scopus 로고    scopus 로고
    • Surface-modified superparamagnetic nanoparticles for drug delivery: Preparation, characterization, and cytotoxicity studies
    • K. Gupta Ajay, and S. Wells Surface-modified superparamagnetic nanoparticles for drug delivery: preparation, characterization, and cytotoxicity studies IEEE Trans Nanobiosci 3 2004 66 73
    • (2004) IEEE Trans Nanobiosci , vol.3 , pp. 66-73
    • Gupta Ajay, K.1    Wells, S.2
  • 152
    • 33846346179 scopus 로고    scopus 로고
    • Microgels loaded with gold nanorods: Photothermally triggered volume transitions under physiological conditions
    • DOI 10.1021/la061596s
    • M. Das, N. Sanson, D. Fava, and E. Kumacheva Microgels loaded with gold nanorods: photothermally triggered volume transitions under physiological conditions Langmuir 23 2007 196 201 (Pubitemid 46129724)
    • (2007) Langmuir , vol.23 , Issue.1 , pp. 196-201
    • Das, M.1    Sanson, N.2    Fava, D.3    Kumacheva, E.4
  • 153
    • 0031188392 scopus 로고    scopus 로고
    • Nitroxide-controlled free-radical copolymerization of vinyl and divinyl monomers. Evaluation of pendant-vinyl reactivity
    • N. Ide, and T. Fukuda Nitroxide-controlled free-radical copolymerization of vinyl and divinyl monomers. Evaluation of pendant-vinyl reactivity Macromolecules 30 1997 4268 4271 (Pubitemid 127567537)
    • (1997) Macromolecules , vol.30 , Issue.15 , pp. 4268-4271
    • Ide, N.1    Fukuda, T.2
  • 154
    • 17444413755 scopus 로고    scopus 로고
    • Combining atom transfer radical polymerization and disulfide/thiol redox chemistry: A route to well-defined (bio)degradable polymeric materials
    • DOI 10.1021/ma050020r
    • N.V. Tsarevsky, and K. Matyjaszewski Combining Atom Transfer Radical Polymerization and disulfide/thiol redox chemistry: a route to well-defined (bio)degradable polymeric materials Macromolecules 38 2005 3087 3092 (Pubitemid 40541211)
    • (2005) Macromolecules , vol.38 , Issue.8 , pp. 3087-3092
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 155
    • 31544469769 scopus 로고    scopus 로고
    • pH- and temperature-responsive hydrogels from crosslinked triblock copolymers prepared via consecutive atom transfer radical polymerizations
    • DOI 10.1016/j.biomaterials.2006.01.003, PII S0142961206000123
    • F. Xu, E. Kang, and K. Neoh pH- and temperature-responsive hydrogels from crosslinked triblock copolymers prepared via consecutive atom transfer radical polymerizations Biomaterials 27 2006 2787 2797 (Pubitemid 43165747)
    • (2006) Biomaterials , vol.27 , Issue.14 , pp. 2787-2797
    • Xu, F.-J.1    Kang, E.-T.2    Neoh, K.-G.3
  • 156
    • 33846355644 scopus 로고    scopus 로고
    • Synthesis and in situ atomic force microscopy characterization of temperature-responsive hydrogels based on poly(2-(dimethylamino)ethyl methacrylate) prepared by atom transfer radical polymerization
    • DOI 10.1021/la061683k
    • J. Huang, B. Cusick, J. Pietrasik, L. Wang, T. Kowalewski, Q. Lin, and K. Matyjaszewski Synthesis and in situ atomic force microscopy characterization of temperature-responsive hydrogels based on poly(2-(dimethylamino)ethyl methacrylate) prepared by Atom Transfer Radical Polymerization Langmuir 23 2007 241 249 (Pubitemid 46129730)
    • (2007) Langmuir , vol.23 , Issue.1 , pp. 241-249
    • Huang, J.1    Cusick, B.2    Pietrasik, J.3    Wang, L.4    Kowalewski, T.5    Lin, Q.6    Matyjaszewski, K.7
  • 157
    • 36049023754 scopus 로고    scopus 로고
    • Determination of gel point during atom transfer radical copolymerization with cross-linker
    • DOI 10.1021/ma071324b
    • H. Gao, K. Min, and K. Matyjaszewski Determination of gel point during atom transfer radical copolymerization with cross-linker Macromolecules 40 2007 7763 7770 (Pubitemid 350099677)
    • (2007) Macromolecules , vol.40 , Issue.22 , pp. 7763-7770
    • Gao, H.1    Min, K.2    Matyjaszewski, K.3
  • 158
    • 42449144281 scopus 로고    scopus 로고
    • Synthesis of polyacrylate networks by ATRP: Parameters influencing experimental gel points
    • DOI 10.1021/ma702823b
    • H. Gao, W. Li, and K. Matyjaszewski Synthesis of polyacrylate networks by ATRP: parameters influencing experimental gel points Macromolecules 41 2008 2335 2340 (Pubitemid 351569188)
    • (2008) Macromolecules , vol.41 , Issue.7 , pp. 2335-2340
    • Gao, H.1    Li, W.2    Matyjaszewski, K.3
  • 159
    • 70349964697 scopus 로고    scopus 로고
    • Atom transfer radical polymerization in aqueous dispersed media
    • K. Min, and K. Matyjaszewski Atom transfer radical polymerization in aqueous dispersed media Cent Eur J Chem 7 2009 657 674
    • (2009) Cent Eur J Chem , vol.7 , pp. 657-674
    • Min, K.1    Matyjaszewski, K.2
  • 160
    • 66549093495 scopus 로고    scopus 로고
    • Influence of initiation efficiency and polydispersity of primary chains on gelation during atom transfer radical copolymerization of monomer and cross-linker
    • W. Li, H. Gao, and K. Matyjaszewski Influence of initiation efficiency and polydispersity of primary chains on gelation during atom transfer radical copolymerization of monomer and cross-linker Macromolecules 42 2009 927 932
    • (2009) Macromolecules , vol.42 , pp. 927-932
    • Li, W.1    Gao, H.2    Matyjaszewski, K.3
  • 161
    • 62849103818 scopus 로고    scopus 로고
    • Synthesis of functional polymers with controlled architecture by CRP of monomers in the presence of cross-linkers: From stars to gels
    • H. Gao, and K. Matyjaszewski Synthesis of functional polymers with controlled architecture by CRP of monomers in the presence of cross-linkers: from stars to gels Prog Polym Sci 34 2009 317 350
    • (2009) Prog Polym Sci , vol.34 , pp. 317-350
    • Gao, H.1    Matyjaszewski, K.2
  • 162
    • 68049109546 scopus 로고    scopus 로고
    • Star polymers via cross-linking amphiphilic macroinitiators by AGET ATRP in aqueous media
    • W. Li, and K. Matyjaszewski Star polymers via cross-linking amphiphilic macroinitiators by AGET ATRP in aqueous media J Am Chem Soc 131 2009 10378 10379
    • (2009) J Am Chem Soc , vol.131 , pp. 10378-10379
    • Li, W.1    Matyjaszewski, K.2
  • 163
    • 77953299415 scopus 로고    scopus 로고
    • Dual-reactive surfactant used for synthesis of functional nanocapsules in miniemulsion
    • W. Li, J.A. Yoon, and K. Matyjaszewski Dual-reactive surfactant used for synthesis of functional nanocapsules in miniemulsion J Am Chem Soc 132 2010 7823 7825
    • (2010) J Am Chem Soc , vol.132 , pp. 7823-7825
    • Li, W.1    Yoon, J.A.2    Matyjaszewski, K.3
  • 164
    • 34248567083 scopus 로고    scopus 로고
    • Biodegradable nanogels prepared by atom transfer radical polymerization as potential drug delivery carriers: Synthesis, biodegradation, in vitro release, and bioconjugation
    • DOI 10.1021/ja069150l
    • J.K. Oh, D.J. Siegwart, Lee H-i, G. Sherwood, L. Peteanu, J.O. Hollinger, K. Kataoka, and K. Matyjaszewski Biodegradable nanogels prepared by atom transfer radical polymerization as potential drug delivery carriers: synthesis, biodegradation, in vitro release, and bioconjugation J Am Chem Soc 129 2007 5939 5945 (Pubitemid 46748500)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.18 , pp. 5939-5945
    • Jung, K.O.1    Siegwart, D.J.2    Lee, H.-I.3    Sherwood, G.4    Peteanu, L.5    Hollinger, J.O.6    Kataoka, K.7    Matyjaszewski, K.8
  • 165
    • 36649034654 scopus 로고    scopus 로고
    • Synthesis and biodegradation of nanogels as delivery carriers for carbohydrate drugs
    • DOI 10.1021/bm070381+
    • J.K. Oh, D.J. Siegwart, and K. Matyjaszewski Synthesis and biodegradation of nanogels as delivery carriers for carbohydrate drugs Biomacromolecules 8 2007 3326 3331 (Pubitemid 350193730)
    • (2007) Biomacromolecules , vol.8 , Issue.11 , pp. 3326-3331
    • Oh, J.K.1    Siegwart, D.J.2    Matyjaszewski, K.3
  • 166
    • 68849097626 scopus 로고    scopus 로고
    • Cellular uptake of functional nanogels prepared by inverse miniemulsion ATRP with encapsulated proteins, carbohydrates, and gold nanoparticles
    • D. Siegwart, A. Srinivasan, S. Bencherif, A. Karunanidhi, J. Oh, S. Vaidya, R. Jin, J. Hollinger, and K. Matyjaszewski Cellular uptake of functional nanogels prepared by inverse miniemulsion ATRP with encapsulated proteins, carbohydrates, and gold nanoparticles Biomacromolecules 10 2009 2300 2309
    • (2009) Biomacromolecules , vol.10 , pp. 2300-2309
    • Siegwart, D.1    Srinivasan, A.2    Bencherif, S.3    Karunanidhi, A.4    Oh, J.5    Vaidya, S.6    Jin, R.7    Hollinger, J.8    Matyjaszewski, K.9
  • 167
    • 63849191100 scopus 로고    scopus 로고
    • AGET ATRP in water and inverse miniemulsion: A facile route for preparation of high-molecular-weight biocompatible brush-like polymers
    • J. Oh, F. Perineau, B. Charleux, and K. Matyjaszewski AGET ATRP in water and inverse miniemulsion: a facile route for preparation of high-molecular-
    • (2009) J Polym Sci Part A: Polym Chem , vol.47 , pp. 1771-1781
    • Oh, J.1    Perineau, F.2    Charleux, B.3    Matyjaszewski, K.4
  • 168
    • 79151469086 scopus 로고    scopus 로고
    • Chemical reactions of polymer crosslinking and post-crosslinking at room and medium temperature
    • G. Tillet, B. Boutevin, and B. Ameduri Chemical reactions of polymer crosslinking and post-crosslinking at room and medium temperature Prog Polym Sci 36 2010 191 217
    • (2010) Prog Polym Sci , vol.36 , pp. 191-217
    • Tillet, G.1    Boutevin, B.2    Ameduri, B.3
  • 169
    • 15744383376 scopus 로고    scopus 로고
    • Preparation of hydrogel nanoparticles by atom transfer radical polymerization of N-isopropylacrylamide in aqueous media using PEG macro-initiator
    • DOI 10.1016/j.polymer.2005.02.009, PII S0032386105001412
    • K.H. Kim, J. Kim, and W.H. Jo Preparation of hydrogel nanoparticles by atom transfer radical polymerization of N-isopropylacrylamide in aqueous media using PEG macro-initiator Polymer 46 2005 2836 2840 (Pubitemid 40417845)
    • (2005) Polymer , vol.46 , Issue.9 , pp. 2836-2840
    • Kim, K.H.1    Kim, J.2    Jo, W.H.3
  • 170
    • 33744471389 scopus 로고    scopus 로고
    • Preparation of poly(oligo(ethylene glycol) monomethyl ether methacrylate) by homogeneous aqueous AGET ATRP
    • DOI 10.1021/ma060258v
    • J.K. Oh, K. Min, and K. Matyjaszewski Preparation of poly(oligo(ethylene glycol) monomethyl ether methacrylate) by homogeneous aqueous AGET ATRP Macromolecules 39 2006 3161 3167 (Pubitemid 43798059)
    • (2006) Macromolecules , vol.39 , Issue.9 , pp. 3161-3167
    • Oh, J.K.1    Min, K.2    Matyjaszewski, K.3
  • 171
    • 0030765707 scopus 로고    scopus 로고
    • Cysteine and glutathione secretion in response to protein disulfide bond formation in the ER
    • DOI 10.1126/science.277.5332.1681
    • S. Carelli, A. Ceriotti, A. Cabibbo, G. Fassina, M. Ruvo, and R. Sitia Cysteine and glutathione secretion in response to protein disulfide bond formation in the ER Science 277 1997 1681 1684 (Pubitemid 27446233)
    • (1997) Science , vol.277 , Issue.5332 , pp. 1681-1684
    • Carelli, S.1    Ceriotti, A.2    Cabibbo, A.3    Fassina, G.4    Ruvo, M.5    Sitia, R.6
  • 172
    • 0030973631 scopus 로고    scopus 로고
    • The glutathione level of retinal Muller glial cells is dependent on the high-affinity sodium-dependent uptake of glutamate
    • W. Reichelt, J. StabelBurow, T. Pannicke, H. Weichert, and U. Heinemann The glutathione level of retinal Muller glial cells is dependent on the high-affinity sodium-dependent uptake of glutamate Neuroscience 77 1997 1213 1224
    • (1997) Neuroscience , vol.77 , pp. 1213-1224
    • Reichelt, W.1    Stabelburow, J.2    Pannicke, T.3    Weichert, H.4    Heinemann, U.5
  • 174
    • 33746217408 scopus 로고    scopus 로고
    • A new class of biochemically degradable, stimulus-responsive triblock copolymer gelators
    • DOI 10.1002/anie.200600324
    • C. Li, J. Madsen, S. Armes, and A. Lewis A new class of biochemically degradable, stimulus-responsive triblock copolymer gelators Angew Chem Int Edit 45 2006 3510 3513 (Pubitemid 44098970)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.21 , pp. 3510-3513
    • Li, C.1    Madsen, J.2    Armes, S.P.3    Lewis, A.L.4
  • 176
    • 4043156991 scopus 로고    scopus 로고
    • Magnetic nanoparticle design for medical diagnosis and therapy
    • S. Mornet, S. Vasseur, F. Grasset, and E. Duguet Magnetic nanoparticle design for medical diagnosis and therapy J Mater Chem 14 2004 2161 2175
    • (2004) J Mater Chem , vol.14 , pp. 2161-2175
    • Mornet, S.1    Vasseur, S.2    Grasset, F.3    Duguet, E.4
  • 177
    • 0032141569 scopus 로고    scopus 로고
    • Atom transfer radical polymerization and the synthesis of polymeric materials
    • T.E. Patten, and K. Matyjaszewski Atom-transfer radical polymerization and the synthesis of polymeric materials Adv Mater 10 1998 901 915 (Pubitemid 128539708)
    • (1998) Advanced Materials , vol.10 , Issue.12 , pp. 901-915
    • Patten, T.E.1    Matyjaszewski, K.2
  • 178
    • 46749132642 scopus 로고    scopus 로고
    • Multifunctional magnetic nanoparticles for targeted imaging and therapy
    • J.R. McCarthy, and R. Weissleder Multifunctional magnetic nanoparticles for targeted imaging and therapy Adv Drug Deliver Rev 60 2008 1241 1251
    • (2008) Adv Drug Deliver Rev , vol.60 , pp. 1241-1251
    • McCarthy, J.R.1    Weissleder, R.2
  • 179
    • 0034614210 scopus 로고    scopus 로고
    • Particle control of emulsion by membrane emulsification and its applications
    • T. Nakashima, M. Shimizu, and M. Kukizaki Particle control of emulsion by membrane emulsification and its applications Adv Drug Deliver Rev 45 2000 47 56
    • (2000) Adv Drug Deliver Rev , vol.45 , pp. 47-56
    • Nakashima, T.1    Shimizu, M.2    Kukizaki, M.3
  • 180
    • 79955471462 scopus 로고    scopus 로고
    • RAFT/MADIX polymers for the preparation of polymer/inorganic nanohybrids
    • M. Beija, J.-D. Marty, and M. Destarac RAFT/MADIX polymers for the preparation of polymer/inorganic nanohybrids Prog Polym Sci 36 2011 845 886
    • (2011) Prog Polym Sci , vol.36 , pp. 845-886
    • Beija, M.1    Marty, J.-D.2    Destarac, M.3
  • 181
    • 78649721117 scopus 로고    scopus 로고
    • Iron oxide-based superparamagnetic polymeric nanomaterials: Design, preparation, and biomedical application
    • J.K. Oh, and J.M. Park Iron oxide-based superparamagnetic polymeric nanomaterials: design, preparation, and biomedical application Prog Polym Sci 36 2011 168 189
    • (2011) Prog Polym Sci , vol.36 , pp. 168-189
    • Oh, J.K.1    Park, J.M.2
  • 182
    • 0012392952 scopus 로고    scopus 로고
    • Semiconductor nanocrystals as fluorescent biological labels
    • DOI 10.1126/science.281.5385.2013
    • M. Bruchez Jr., M. Moronne, P. Gin, S. Weiss, and A.P. Alivisatos Semiconductor nanocrystals as fluorescent biological labels Science 281 1998 2013 2016 (Pubitemid 28475485)
    • (1998) Science , vol.281 , Issue.5385 , pp. 2013-2016
    • Bruchez Jr., M.1    Moronne, M.2    Gin, P.3    Weiss, S.4    Alivisatos, A.P.5
  • 183
    • 33747502183 scopus 로고    scopus 로고
    • Quantum dots in biological and biomedical research: Recent progress and present challenges
    • DOI 10.1002/adma.200500786
    • J.M. Klostranec, and W.C.W. Chan Quantum dots in biological and biomedical research: recent progress and present challenges Adv Mater 18 2006 1953 1964 (Pubitemid 44259247)
    • (2006) Advanced Materials , vol.18 , Issue.15 , pp. 1953-1964
    • Klostranec, J.M.1    Chan, W.C.W.2
  • 184
    • 54749138351 scopus 로고    scopus 로고
    • Semiconductor quantum dots for bioanalysis
    • R. Gill, M. Zayats, and I. Willner Semiconductor quantum dots for bioanalysis Angew Chem Int Edit 47 2008 7602 7625
    • (2008) Angew Chem Int Edit , vol.47 , pp. 7602-7625
    • Gill, R.1    Zayats, M.2    Willner, I.3
  • 185
    • 80455144189 scopus 로고    scopus 로고
    • Semiconductor quantum dots for molecular and cellular imaging
    • A.M. Smith, and S. Nie Semiconductor quantum dots for molecular and cellular imaging Bionanotechnology 2009 233 242
    • (2009) Bionanotechnology , pp. 233-242
    • Smith, A.M.1    Nie, S.2
  • 186
    • 77957763445 scopus 로고    scopus 로고
    • Surface modification of colloidal CdX-based quantum dots for biomedical applications
    • J.K. Oh Surface modification of colloidal CdX-based quantum dots for biomedical applications J Mater Chem 20 2010 8433 8445
    • (2010) J Mater Chem , vol.20 , pp. 8433-8445
    • Oh, J.K.1
  • 187
    • 0000939999 scopus 로고
    • Synthesis and characterization of nearly monodisperse CdE (E = sulfur, selenium, tellurium) semiconductor nanocrystallites
    • C.B. Murray, D.J. Norris, and M.G. Bawendi Synthesis and characterization of nearly monodisperse CdE (E = sulfur, selenium, tellurium) semiconductor nanocrystallites J Am Chem Soc 115 1993 8706 8715
    • (1993) J Am Chem Soc , vol.115 , pp. 8706-8715
    • Murray, C.B.1    Norris, D.J.2    Bawendi, M.G.3
  • 188
    • 0000592050 scopus 로고    scopus 로고
    • The band edge luminescence of surface modified CdSe nanocrystallites: Probing the luminescing state
    • M. Kuno, J.K. Lee, B.O. Dabbousi, F.V. Mikulec, and M.G. Bawendi The band edge luminescence of surface modified CdSe nanocrystallites: probing the luminescing state J Chem Phys 106 1997 9869 9882 (Pubitemid 127626951)
    • (1997) Journal of Chemical Physics , vol.106 , Issue.23 , pp. 9869-9882
    • Kuno, M.1    Lee, J.K.2    Dabbousi, B.O.3    Mikulec, F.V.4    Bawendi, M.G.5
  • 189
    • 0032566763 scopus 로고    scopus 로고
    • Quantum dot bioconjugates for ultrasensitive nonisotopic detection
    • DOI 10.1126/science.281.5385.2016
    • W.C. Chan, and S. Nie Quantum dot bioconjugates for ultrasensitive nonisotopic detection Science 281 1998 2016 2018 (Pubitemid 28475486)
    • (1998) Science , vol.281 , Issue.5385 , pp. 2016-2018
    • Chan, W.C.W.1    Nie, S.2
  • 191
    • 0348087040 scopus 로고    scopus 로고
    • Long-term multiple color imaging of live cells using quantum dot bioconjugates
    • DOI 10.1038/nbt767
    • J.K. Jaiswal, H. Mattoussi, J.M. Mauro, and S.M. Simon Long-term multiple color imaging of live cells using quantum dot bioconjugates Nat Biotechnol 21 2003 47 51 (Pubitemid 36055826)
    • (2003) Nature Biotechnology , vol.21 , Issue.1 , pp. 47-51
    • Jaiswal, J.K.1    Mattoussi, H.2    Mauro, J.M.3    Simon, S.M.4
  • 194
    • 3042601649 scopus 로고    scopus 로고
    • Surface passivation of luminescent colloidal quantum dots with poly(dimethylaminoethly methacrylate) through a ligand exchange process
    • DOI 10.1021/ja0489339
    • X.-S. Wang, T.E. Dykstra, M.R. Salvador, I. Manners, G.D. Scholes, and M.A. Winnik Surface passivation of luminescent colloidal quantum dots with poly(dimethylaminoethyl methacrylate) through a ligand exchange process J Am Chem Soc 126 2004 7784 7785 (Pubitemid 38812762)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.25 , pp. 7784-7785
    • Wang, X.-S.1    Dykstra, T.E.2    Salvador, M.R.3    Manners, I.4    Scholes, G.D.5    Winnik, M.A.6
  • 195
    • 33744490151 scopus 로고    scopus 로고
    • Surface modification of CdSe and CdSe/ZnS semiconductor nanocrystals with poly(N,N-dimethylaminoethyl methacrylate)
    • DOI 10.1021/ma0525740
    • M. Wang, J.K. Oh, T.E. Dykstra, X. Lou, G.D. Scholes, and M.A. Winnik Surface modification of CdSe and CdSe/ZnS semiconductor nanocrystals with poly(N,N-dimethylaminoethyl methacrylate) Macromolecules 39 2006 3664 3672 (Pubitemid 43798246)
    • (2006) Macromolecules , vol.39 , Issue.10 , pp. 3664-3672
    • Wang, M.1    Oh, J.K.2    Dykstra, T.E.3    Lou, X.4    Scholes, G.D.5    Winnik, M.A.6
  • 196
    • 34548287406 scopus 로고    scopus 로고
    • Water-soluble CdSe quantum dots passivated by a multidentate diblock copolymer
    • DOI 10.1021/ma070553v
    • M. Wang, N. Felorzabihi, G. Guerin, J.C. Haley, G.D. Scholes, and M.A. Winnik Water-soluble CdSe quantum dots passivated by a multidentate diblock copolymer Macromolecules 40 2007 6377 6384 (Pubitemid 47329085)
    • (2007) Macromolecules , vol.40 , Issue.17 , pp. 6377-6384
    • Wang, M.1    Felorzabihi, N.2    Guerin, G.3    Haley, J.C.4    Sechloes, G.D.5    Winnik, M.A.6
  • 197
    • 33746306163 scopus 로고    scopus 로고
    • Colloidal CdSe nanocrystals passivated by a dye-labeled multidentate polymer: Quantitative analysis by size-exclusion chromatography
    • DOI 10.1002/anie.200502538
    • M. Wang, T.E. Dykstra, X. Lou, M.R. Salvador, G.D. Scholes, and M.A. Winnik Colloidal CdSe nanocrystals passivated by a dye-labeled multidentate polymer: quantitative analysis by size-exclusion chromatography Angew Chem Int Edit 45 2006 2221 2224 (Pubitemid 44105147)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.14 , pp. 2221-2224
    • Wang, M.1    Dykstra, T.E.2    Lou, X.3    Salvador, M.R.4    Scholes, G.D.5    Winnik, M.A.6
  • 198
    • 33846004215 scopus 로고    scopus 로고
    • One-pot synthesis of PEGylated ultrasmall iron-oxide nanoparticles and their in vivo evaluation as magnetic resonance imaging contrast agents
    • DOI 10.1021/bm0607527
    • J.-F. Lutz, S. Stiller, A. Hoth, L. Kaufner, U. Pison, and R. Cartier One-pot synthesis of PEGylated ultrasmall iron-oxide nanoparticles and their in vivo evaluation as magnetic resonance imaging contrast agents Biomacromolecules 7 2006 3132 3138 (Pubitemid 46039971)
    • (2006) Biomacromolecules , vol.7 , Issue.11 , pp. 3132-3138
    • Lutz, J.-F.1    Stiller, S.2    Hoth, A.3    Kaufner, L.4    Pison, U.5    Cartier, R.6
  • 200
    • 35349005887 scopus 로고    scopus 로고
    • 4 nanoparticles: Synthesis, characterization and cellular uptake
    • DOI 10.1016/j.biomaterials.2007.08.039, PII S0142961207006989
    • 4 nanoparticles: synthesis, characterization and cellular uptake Biomaterials 28 2007 5426 5436 (Pubitemid 47610690)
    • (2007) Biomaterials , vol.28 , Issue.36 , pp. 5426-5436
    • Fan, Q.-L.1    Neoh, K.-G.2    Kang, E.-T.3    Shuter, B.4    Wang, S.-C.5
  • 201
    • 0141521850 scopus 로고    scopus 로고
    • 3@polystyrene core-shell nanoparticles
    • DOI 10.1021/nl034211o
    • 3@polystyrene core-shell nanoparticles Nano Lett 3 2003 789 793 (Pubitemid 37140600)
    • (2003) Nano Letters , vol.3 , Issue.6 , pp. 789-793
    • Wang, Y.1    Teng, X.2    Wang, J.-S.3    Yang, H.4
  • 202
    • 33744476694 scopus 로고    scopus 로고
    • Magnetic thermoresponsive core-shell nanoparticles
    • DOI 10.1021/ma060006u
    • T. Gelbrich, M. Feyen, and A.M. Schmidt Magnetic thermoresponsive core-shell nanoparticles Macromolecules 39 2006 3469 3472 (Pubitemid 43798094)
    • (2006) Macromolecules , vol.39 , Issue.9 , pp. 3469-3472
    • Gelbrich, T.1    Feyen, M.2    Schmidt, A.M.3
  • 203
    • 2442677848 scopus 로고    scopus 로고
    • Cross-linking the linear polymeric chains in the ATRP synthesis of iron oxide/polystyrene core/shell nanoparticles
    • G. Li, J. Fan, R. Jiang, and Y. Gao Cross-linking the linear polymeric chains in the ATRP synthesis of iron oxide/polystyrene core/shell nanoparticles Chem Mater 16 2004 1835 1837
    • (2004) Chem Mater , vol.16 , pp. 1835-1837
    • Li, G.1    Fan, J.2    Jiang, R.3    Gao, Y.4
  • 204
    • 12944259208 scopus 로고    scopus 로고
    • Polymers at interfaces: Using atom transfer radical polymerization in the controlled growth of homopolymers and block copolymers from silicon surfaces in the absence of untethered sacrificial initiator
    • DOI 10.1021/ma991146p
    • K. Matyjaszewski, P.J. Miller, N. Shukla, B. Immaraporn, A. Gelman, B.B. Luokala, T.M. Siclovan, G. Kickelbick, T. Vallant, H. Hoffmann, and T. Pakula Polymers at interfaces: using Atom Transfer Radical Polymerization in the controlled growth of homopolymers and block copolymers from silicon surfaces in the absence of untethered sacrificial initiator Macromolecules 32 1999 8716 8724 (Pubitemid 30533926)
    • (1999) Macromolecules , vol.32 , Issue.26 , pp. 8716-8724
    • Matyjaszewski, K.1    Miller, P.J.2    Shukla, N.3    Immaraporn, B.4    Gelman, A.5    Luokala, B.B.6    Siclovan, T.M.7    Kickelbick, G.8    Vallant, T.9    Hoffmann, H.10    Pakula, T.11
  • 207
    • 33847696914 scopus 로고    scopus 로고
    • Functionalization of iron oxide magnetic nanoparticles with poly(methyl methacrylate) brushes via grafting-from atom transfer radical polymerization
    • DOI 10.1002/pola.21854
    • I. Garcia, N.E. Zafeiropoulos, A. Janke, A. Tercjak, A. Eceiza, M. Stamm, and I. Mondragon Functionalization of iron oxide magnetic nanoparticles with poly(methyl methacrylate) brushes via grafting-from atom transfer radical polymerization J Polym Sci Part A: Polym Chem 45 2007 925 932 (Pubitemid 46384392)
    • (2007) Journal of Polymer Science, Part A: Polymer Chemistry , vol.45 , Issue.5 , pp. 925-932
    • Garcia, I.1    Zafeiropoulos, N.E.2    Janke, A.3    Tercjak, A.4    Eceiza, A.5    Stamm, M.6    Mondracon, I.7
  • 208
    • 42649115430 scopus 로고    scopus 로고
    • A novel approach to magneto-responsive polymeric gels assisted by iron nanoparticles as nano cross-linkers
    • DOI 10.1039/b717721f
    • M. Czaun, L. Hevesi, M. Takafuji, and H. Ihara A novel approach to magneto-responsive polymeric gels assisted by iron nanoparticles as nano cross-linkers Chem Commun 2008 2124 2126 (Pubitemid 351601252)
    • (2008) Chemical Communications , Issue.18 , pp. 2124-2126
    • Czaun, M.1    Hevesi, L.2    Takafuji, M.3    Ihara, H.4
  • 209
    • 33645505356 scopus 로고    scopus 로고
    • Cellular response to magnetic nanoparticles "pEGylated" via surface-initiated Atom Transfer Radical Polymerization
    • F. Hu, K.G. Neoh, L. Cen, and E.-T. Kang Cellular response to magnetic nanoparticles "PEGylated" via surface-initiated Atom Transfer Radical Polymerization Biomacromolecules 7 2006 809 816
    • (2006) Biomacromolecules , vol.7 , pp. 809-816
    • Hu, F.1    Neoh, K.G.2    Cen, L.3    Kang, E.-T.4
  • 210
    • 33744939999 scopus 로고    scopus 로고
    • Antibiofouling polymer-coated superparamagnetic iron oxide nanoparticles as potential magnetic resonance contrast agents for in vivo cancer imaging
    • DOI 10.1021/ja061529k
    • H. Lee, E. Lee, D.K. Kim, N.K. Jang, Y.Y. Jeong, and S. Jon Antibiofouling polymer-coated superparamagnetic iron oxide nanoparticles as potential magnetic resonance contrast agents for in vivo cancer imaging J Am Chem Soc 128 2006 7383 7389 (Pubitemid 43849141)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.22 , pp. 7383-7389
    • Lee, H.1    Lee, E.2    Kim, D.K.3    Jang, N.K.4    Jeong, Y.Y.5    Jon, S.6
  • 211
    • 79151477116 scopus 로고    scopus 로고
    • Dye-labelled polymer chains at specific sites: Synthesis by living/controlled polymerization
    • M. Beija, M.-T. Charreyre, and J.M.G. Martinho Dye-labelled polymer chains at specific sites: synthesis by living/controlled polymerization Prog Polym Sci 36 2011 568 602
    • (2011) Prog Polym Sci , vol.36 , pp. 568-602
    • Beija, M.1    Charreyre, M.-T.2    Martinho, J.M.G.3
  • 212
    • 35548999721 scopus 로고    scopus 로고
    • Thermally cross-linked superparamagnetic iron oxide nanoparticles: Synthesis and application as a dual imaging probe for cancer in vivo
    • DOI 10.1021/ja072210i
    • H. Lee, M.K. Yu, S. Park, S. Moon, J.J. Min, Y.Y. Jeong, H.-W. Kang, and S. Jon Thermally cross-linked superparamagnetic iron oxide nanoparticles: synthesis and application as a dual imaging probe for cancer in vivo J Am Chem Soc 129 2007 12739 12745 (Pubitemid 350004485)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.42 , pp. 12739-12745
    • Lee, H.1    Mi, K.Y.2    Park, S.3    Moon, S.4    Jung, J.M.5    Yong, Y.J.6    Kang, H.-W.7    Jon, S.8
  • 213
    • 65649145703 scopus 로고    scopus 로고
    • Synthesis of folic acid functionalized PLLA-b-PPEGMA nanoparticles for cancer cell targeting
    • F. Hu, K.G. Neoh, and E.-T. Kang Synthesis of folic acid functionalized PLLA-b-PPEGMA nanoparticles for cancer cell targeting Macromol Rapid Commun 30 2009 609 614
    • (2009) Macromol Rapid Commun , vol.30 , pp. 609-614
    • Hu, F.1    Neoh, K.G.2    Kang, E.-T.3
  • 214
    • 69849115212 scopus 로고    scopus 로고
    • Thermally responsive PM(EO)2MA magnetic microgels via Activators Generated by Electron Transfer Atom Transfer Radical Polymerization in miniemulsion
    • H. Dong, V. Mantha, and K. Matyjaszewski Thermally responsive PM(EO)2MA magnetic microgels via Activators Generated by Electron Transfer Atom Transfer Radical Polymerization in miniemulsion Chem Mater 21 2009 3965 3972
    • (2009) Chem Mater , vol.21 , pp. 3965-3972
    • Dong, H.1    Mantha, V.2    Matyjaszewski, K.3
  • 215
    • 79955481486 scopus 로고    scopus 로고
    • Thermosensitive core-shell microgels: From colloidal model systems to nanoreactors
    • Y. Lu, and M. Ballauff Thermosensitive core-shell microgels: from colloidal model systems to nanoreactors Prog Polym Sci 36 2011 767 792
    • (2011) Prog Polym Sci , vol.36 , pp. 767-792
    • Lu, Y.1    Ballauff, M.2
  • 217
    • 80051746315 scopus 로고    scopus 로고
    • Designing three-dimensional materials at the interface to biology
    • R. Gentsch, and H.G. Borner Designing three-dimensional materials at the interface to biology Adv Polym Sci 140 2011 163 193
    • (2011) Adv Polym Sci , vol.140 , pp. 163-193
    • Gentsch, R.1    Borner, H.G.2
  • 218
    • 67649381653 scopus 로고    scopus 로고
    • Bioactive surfaces and biomaterials via atom transfer radical polymerization
    • F. Xu, K. Neoh, and E. Kang Bioactive surfaces and biomaterials via atom transfer radical polymerization Prog Polym Sci 34 2009 719 761
    • (2009) Prog Polym Sci , vol.34 , pp. 719-761
    • Xu, F.1    Neoh, K.2    Kang, E.3
  • 219
    • 80051755368 scopus 로고    scopus 로고
    • Smart polymer surfaces: Concepts and applications in biosciences
    • E. Wischerhoff, N. Badi, A. Laschewsky, and J.-F. Lutz Smart polymer surfaces: concepts and applications in biosciences Adv Polym Sci 40 2011 1 33
    • (2011) Adv Polym Sci , vol.40 , pp. 1-33
    • Wischerhoff, E.1    Badi, N.2    Laschewsky, A.3    Lutz, J.-F.4
  • 221
    • 0033743374 scopus 로고    scopus 로고
    • Controlled grafting of a well-defined glycopolymer on a solid surface by surface-initiated Atom Transfer Radical Polymerization
    • M. Ejaz, K. Ohno, Y. Tsujii, and T. Fukuda Controlled grafting of a well-defined glycopolymer on a solid surface by surface-initiated Atom Transfer Radical Polymerization Macromolecules 33 2000 2870 2874
    • (2000) Macromolecules , vol.33 , pp. 2870-2874
    • Ejaz, M.1    Ohno, K.2    Tsujii, Y.3    Fukuda, T.4
  • 222
    • 53149096922 scopus 로고    scopus 로고
    • Ultra low fouling zwitterionic polymers with a biomimetic adhesive group
    • G. Li, G. Cheng, H. Xue, S. Chen, F. Zhang, and S. Jiang Ultra low fouling zwitterionic polymers with a biomimetic adhesive group Biomaterials 29 2008 4592 4597
    • (2008) Biomaterials , vol.29 , pp. 4592-4597
    • Li, G.1    Cheng, G.2    Xue, H.3    Chen, S.4    Zhang, F.5    Jiang, S.6
  • 223
    • 77949566695 scopus 로고    scopus 로고
    • Synthetic polymers with quaternary nitrogen atoms: Synthesis and structure of the most used type of cationic polyelectrolytes
    • W. Jaeger, J. Bohrisch, and A. Laschewsky Synthetic polymers with quaternary nitrogen atoms: synthesis and structure of the most used type of cationic polyelectrolytes Prog Polym Sci 35 2010 511 577
    • (2010) Prog Polym Sci , vol.35 , pp. 511-577
    • Jaeger, W.1    Bohrisch, J.2    Laschewsky, A.3
  • 224
    • 34249895273 scopus 로고    scopus 로고
    • Antibacterial polypropylene via surface-initiated atom transfer radical polymerization
    • DOI 10.1021/bm061236j
    • J. Huang, H. Murata, R. Koepsel, A. Russell, and K. Matyjaszewski Antibacterial polypropylene via surface-initiated atom transfer radical polymerization Biomacromolecules 8 2007 1396 1399 (Pubitemid 46865108)
    • (2007) Biomacromolecules , vol.8 , Issue.5 , pp. 1396-1399
    • Huang, J.1    Murata, H.2    Koepsel, R.R.3    Russell, A.J.4    Matyjaszewski, K.5
  • 225
    • 0141726814 scopus 로고    scopus 로고
    • ATRP synthesis of amphiphilic random, gradient, and block copolymers of 2-(dimethylamino)ethly methacrylate and n-butyl methacrylate in aqueous media
    • DOI 10.1021/bm034126a
    • S.B. Lee, A.J. Russell, and K. Matyjaszewski ATRP synthesis of amphiphilic random, gradient, and block copolymers of 2-(dimethylamino)ethyl methacrylate and n-butyl methacrylate in aqueous media Biomacromolecules 4 2003 1386 1393 (Pubitemid 37184656)
    • (2003) Biomacromolecules , vol.4 , Issue.5 , pp. 1386-1393
    • Lee, S.B.1    Russell, A.J.2    Matyjaszewski, K.3
  • 226
    • 2542512315 scopus 로고    scopus 로고
    • Permanent, nonleaching antibacterial surfaces, 1. Synthesis by atom transfer radical polymerization
    • DOI 10.1021/bm034352k
    • S.B. Lee, R.R. Koepsel, S.W. Morley, K. Matyjaszewski, Y. Sun, and A.J. Russell Permanent, nonleaching antibacterial surfaces. 1. Synthesis by Atom Transfer Radical Polymerization Biomacromolecules 5 2004 877 882 (Pubitemid 38702260)
    • (2004) Biomacromolecules , vol.5 , Issue.3 , pp. 877-882
    • Lee, S.B.1    Koepsel, R.R.2    Morley, S.W.3    Matyjaszewski, K.4    Sun, Y.5    Russell, A.J.6
  • 227
    • 34548049706 scopus 로고    scopus 로고
    • Permanent, non-leaching antibacterial surfaces-2: How high density cationic surfaces kill bacterial cells
    • DOI 10.1016/j.biomaterials.2007.06.012, PII S0142961207004681
    • H. Murata, R. Koepsel, K. Matyjaszewski, and A. Russell Permanent, non-leaching antibacterial surfaces. 2. How high density cationic surfaces kill bacterial cells Biomaterials 28 2007 4870 4879 (Pubitemid 47285332)
    • (2007) Biomaterials , vol.28 , Issue.32 , pp. 4870-4879
    • Murata, H.1    Koepsel, R.R.2    Matyjaszewski, K.3    Russell, A.J.4
  • 228
    • 47349095473 scopus 로고    scopus 로고
    • Nonleaching antibacterial glass surfaces via "grafting onto": The effect of the number of quaternary ammonium groups on biocidal activity
    • J. Huang, R.R. Koepsel, H. Murata, W. Wu, S.B. Lee, and T. Kowalewski Nonleaching antibacterial glass surfaces via "grafting onto": the effect of the number of quaternary ammonium groups on biocidal activity Langmuir 24 2008 6785 6795
    • (2008) Langmuir , vol.24 , pp. 6785-6795
    • Huang, J.1    Koepsel, R.R.2    Murata, H.3    Wu, W.4    Lee, S.B.5    Kowalewski, T.6
  • 229
    • 0023637601 scopus 로고
    • New perspectives in cell adhesion: RGD and integrins
    • E. Ruoslahti, and M.D. Pierschbacher New perspectives in cell-adhesion: RGD and integrins Science 238 1987 491 497 (Pubitemid 17147032)
    • (1987) Science , vol.238 , Issue.4826 , pp. 491-497
    • Ruoslahti, E.1    Pierschbacher, M.D.2
  • 230
    • 0023609864 scopus 로고
    • Influence of stereochemistry of the sequence Arg-Gly-Asp-Xaa on binding specificity in cell adhesion
    • M.D. Pierschbacher, and E. Ruoslahti Influence of stereochemistry of the sequence Arg-Gly-Asp-Xaa on binding-specificity in cell-adhesion J Biol Chem 262 1987 17294 17298 (Pubitemid 18032201)
    • (1987) Journal of Biological Chemistry , vol.262 , Issue.36 , pp. 17294-17298
    • Pierschbacher, M.D.1    Ruoslahti, E.2
  • 231
    • 0031034352 scopus 로고    scopus 로고
    • Integrin-ligand binding properties govern cell migration speed through cell-substratum adhesiveness
    • DOI 10.1038/385537a0
    • S.P. Palecek, J.C. Loftus, M.H. Ginsberg, D.A. Lauffenburger, and A.F. Horwitz Integrin-ligand binding properties govern cell migration speed through cell-substratum adhesiveness Nature 385 1997 537 540 (Pubitemid 27074672)
    • (1997) Nature , vol.385 , Issue.6616 , pp. 537-540
    • Palecek, S.P.1    Loftust, J.C.2    Ginsberg, M.H.3    Lauffenburger, D.A.4    Horwitz, A.F.5
  • 232
    • 0034629303 scopus 로고    scopus 로고
    • Three-dimensional migration of neurites is mediated by adhesion site density and affinity
    • DOI 10.1074/jbc.275.10.6813
    • J.C. Schense, and J.A. Hubbell Three-dimensional migration of neurites is mediated by adhesion site density and affinity J Biol Chem 275 2000 6813 6818 (Pubitemid 30146220)
    • (2000) Journal of Biological Chemistry , vol.275 , Issue.10 , pp. 6813-6818
    • Schense, J.C.1    Hubbell, J.A.2
  • 234
    • 0034769388 scopus 로고    scopus 로고
    • Effect of RGD coating on osteocompatibility of PLGA-polymer disks in a rat tibial wound
    • DOI 10.1002/1097-4636(200111)57:2<224::AID-JBM1162>3.0.CO;2-F
    • K. Eid, E. Chen, L. Griffith, and J. Glowacki Effect of RGD coating on osteocompatibility of PLGA-polymer disks in a rat tibial wound J Biomed Mater Res 57 2001 224 231 (Pubitemid 32988501)
    • (2001) Journal of Biomedical Materials Research , vol.57 , Issue.2 , pp. 224-231
    • Eid, K.1    Chen, E.2    Griffith, L.3    Glowacki, J.4
  • 235
    • 0034893617 scopus 로고    scopus 로고
    • Nanoscale clustering of RGD peptides at surfaces using comb polymers. 1. Synthesis and characterization of comb thin films
    • DOI 10.1021/bm005584b
    • D.J. Irvine, A.M. Mayes, and L.G. Griffith Nanoscale clustering of RGD peptides at surfaces using comb polymers. 1. Synthesis and characterization of comb thin films Biomacromolecules 2 2001 85 94 (Pubitemid 32707478)
    • (2001) Biomacromolecules , vol.2 , Issue.1 , pp. 85-94
    • Irvine, D.J.1    Mayes, A.M.2    Griffith, L.G.3
  • 236
    • 0034899970 scopus 로고    scopus 로고
    • Nanoscale clustering of RGD peptides at surfaces using comb polymers. 2. Surface segregation of comb polymers in polylactide
    • DOI 10.1021/bm015510f
    • D.J. Irvine, A.V.G. Ruzette, A.M. Mayes, and L.G. Griffith Nanoscale clustering of RGD peptides at surfaces using comb polymers. 2. Surface segregation of comb polymers in polylactide Biomacromolecules 2 2001 545 556 (Pubitemid 32717070)
    • (2001) Biomacromolecules , vol.2 , Issue.2 , pp. 545-556
    • Irvine, D.J.1    Ruzette, A.-V.G.2    Mayes, A.M.3    Griffith, L.G.4
  • 237
    • 68549090562 scopus 로고    scopus 로고
    • Nanostructured hybrid hydrogels prepared by a combination of atom transfer radical polymerization and free radical polymerization
    • S.A. Bencherif, D.J. Siegwart, A. Srinivasan, F. Horkay, J.O. Hollinger, N.R. Washburn, and K. Matyjaszewski Nanostructured hybrid hydrogels prepared by a combination of atom transfer radical polymerization and free radical polymerization Biomaterials 30 2009 5270 5278
    • (2009) Biomaterials , vol.30 , pp. 5270-5278
    • Bencherif, S.A.1    Siegwart, D.J.2    Srinivasan, A.3    Horkay, F.4    Hollinger, J.O.5    Washburn, N.R.6    Matyjaszewski, K.7
  • 238
    • 0025294059 scopus 로고
    • Synthesis and application of thermally reversible heterogels for drug delivery
    • DOI 10.1016/0168-3659(90)90071-Z
    • L.C. Dong, and A.S. Hoffman Synthesis and application of thermally reversible heterogels for drug delivery J Control Release 13 1990 21 31 (Pubitemid 20221198)
    • (1990) Journal of Controlled Release , vol.13 , Issue.1 , pp. 21-31
    • Dong, L.-C.1    Hoffman, A.S.2
  • 239
    • 0004991063 scopus 로고
    • Poly(N-isopropylacrylamide) - Experiment, theory and application
    • H.G. Schild Poly(N-isopropylacrylamide) - experiment, theory and application Prog Polym Sci 17 1992 163 249
    • (1992) Prog Polym Sci , vol.17 , pp. 163-249
    • Schild, H.G.1
  • 240
    • 4644254366 scopus 로고    scopus 로고
    • Copolymers of N-alkylacrylamides as thermosensitive hydrogels
    • X.X. Zhu, D. Avoce, H.Y. Liu, and A. Benrebouh Copolymers of N-alkylacrylamides as thermosensitive hydrogels Macromol Symp 207 2004 187 191
    • (2004) Macromol Symp , vol.207 , pp. 187-191
    • Zhu, X.X.1    Avoce, D.2    Liu, H.Y.3    Benrebouh, A.4
  • 241
    • 53549085990 scopus 로고    scopus 로고
    • Synthesis, characterization, and in vitro cell culture viability of degradable poly(N-isopropylacrylamide-co-5,6-benzo-2-methylene-1,3-dioxepane)- based polymers and crosslinked gels
    • D. Siegwart, S. Bencherif, A. Srinivasan, J. Hollinger, and K. Matyjaszewski Synthesis, characterization, and in vitro cell culture viability of degradable poly(N-isopropylacrylamide-co-5,6-benzo-2-methylene-1,3-dioxepane) -based polymers and crosslinked gels J Biomed Mater Res Part A 87A 2008 345 358
    • (2008) J Biomed Mater Res Part A , vol.87 A , pp. 345-358
    • Siegwart, D.1    Bencherif, S.2    Srinivasan, A.3    Hollinger, J.4    Matyjaszewski, K.5
  • 242
    • 79955471240 scopus 로고    scopus 로고
    • Polymers prepared using cleavable initiators: Synthesis, characterization and degradation
    • M.D. Rikkou, and C.S. Patrickios Polymers prepared using cleavable initiators: synthesis, characterization and degradation Prog Polym Sci 36 2011 1079 1097
    • (2011) Prog Polym Sci , vol.36 , pp. 1079-1097
    • Rikkou, M.D.1    Patrickios, C.S.2
  • 246
    • 0038103612 scopus 로고    scopus 로고
    • Synthesis of degradable poly(methyl methacrylate) via ATRP: Atom transfer radical ring-opening copolymerization of 5-methylene-2-phenyl-1,3-dioxolan-4- one and methyl methacrylate
    • I.S. Chung, and K. Matyjaszewski Synthesis of degradable poly(methyl methacrylate) via ATRP: atom transfer radical ring-opening copolymerization of 5-methylene-2-phenyl-1,3-dioxolan-4-one and methyl methacrylate Macromolecules 36 2003 2995 2998
    • (2003) Macromolecules , vol.36 , pp. 2995-2998
    • Chung, I.S.1    Matyjaszewski, K.2
  • 247
    • 0001604536 scopus 로고
    • Free-radical ring-opening polymerization of 4,7-dimethyl-2-methylene-1,3- dioxepane and 5,6-benzo-2-methylene-1,3-dioxepane
    • W.J. Bailey, Z. Ni, and S.R. Wu Free-radical ring-opening polymerization of 4,7-dimethyl-2-methylene-1,3-dioxepane and 5,6-benzo-2-methylene-1,3- dioxepane Macromolecules 15 1982 711 714
    • (1982) Macromolecules , vol.15 , pp. 711-714
    • Bailey, W.J.1    Ni, Z.2    Wu, S.R.3
  • 248
    • 0034818924 scopus 로고    scopus 로고
    • "Living" free radical ring-opening polymerization of 5,6-benzo-2-methylene-1,3-dioxepane using the atom transfer radical polymerization method
    • J.Y. Yuan, C.Y. Pan, and B.Z. Tang "Living" free radical ring-opening polymerization of 5,6-benzo-2-methylene-1,3-dioxepane using the atom transfer radical polymerization method Macromolecules 34 2001 211 214
    • (2001) Macromolecules , vol.34 , pp. 211-214
    • Yuan, J.Y.1    Pan, C.Y.2    Tang, B.Z.3
  • 249
    • 27844481629 scopus 로고    scopus 로고
    • Synthesis and characterization of copolymers of 5,6-benzo-2-methylene-1, 3- dioxepane and n-butyl acrylate
    • DOI 10.1016/j.polymer.2005.09.048, PII S0032386105013832
    • J.Y. Huang, R. Gil, and K. Matyjaszewski Synthesis and characterization of copolymers of 5,6-benzo-2-methylene-1, 3-dioxepane and n-butyl acrylate Polymer 46 2005 11698 11706 (Pubitemid 41653365)
    • (2005) Polymer , vol.46 , Issue.25 , pp. 11698-11706
    • Huang, J.1    Gil, R.2    Matyjaszewski, K.3
  • 250
    • 0037426483 scopus 로고    scopus 로고
    • Homopolymers and random copolymers of 5,6-benzo-2-methylene-1,3-dioxepane and methyl methacrylate: Structural characterization using 1D and 2D NMR
    • H. Wickel, S. Agarwal, and A. Greiner Homopolymers and random copolymers of 5,6-benzo-2-methylene-1,3-dioxepane and methyl methacrylate: structural characterization using 1D and 2D NMR Macromolecules 36 2003 2397 2403
    • (2003) Macromolecules , vol.36 , pp. 2397-2403
    • Wickel, H.1    Agarwal, S.2    Greiner, A.3
  • 251
    • 0042976444 scopus 로고    scopus 로고
    • Synthesis and characterization of copolymers of 5,6-benzo-2-methylene-1, 3-dioxepane and styrene
    • H. Wickel, and S. Agarwal Synthesis and characterization of copolymers of 5,6-benzo-2-methylene-1,3-dioxepane and styrene Macromolecules 36 2003 6152 6159
    • (2003) Macromolecules , vol.36 , pp. 6152-6159
    • Wickel, H.1    Agarwal, S.2
  • 252
    • 34547779576 scopus 로고    scopus 로고
    • Synthesis, characterization, and properties evaluation of poly[(N-isopropylacrylamide)-co-ester]s
    • DOI 10.1002/macp.200600484
    • L.Q. Ren, and S. Agarwal Synthesis, characterization, and properties evaluation of poly[(N-isopropylacrylamide)-co-ester]s Macromol Chem Phys 208 2007 245 253 (Pubitemid 47233661)
    • (2007) Macromolecular Chemistry and Physics , vol.208 , Issue.3 , pp. 245-253
    • Ren, L.1    Agarwal, S.2
  • 253
    • 79151483825 scopus 로고    scopus 로고
    • Synthesis of well-defined star-branched polymers by stepwise iterative methodology using living anionic polymerization
    • T. Higashihara, M. Hayashi, and A. Hirao Synthesis of well-defined star-branched polymers by stepwise iterative methodology using living anionic polymerization Prog Polym Sci 36 2011 323 375
    • (2011) Prog Polym Sci , vol.36 , pp. 323-375
    • Higashihara, T.1    Hayashi, M.2    Hirao, A.3
  • 254
    • 0037137351 scopus 로고    scopus 로고
    • Reversible redox cleavage/coupling of polystyrene with disulfide or thiol groups prepared by atom transfer radical polymerization
    • DOI 10.1021/ma021061f
    • N. Tsarevsky, and K. Matyjaszewski Reversible redox cleavage/coupling of polystyrene with disulfide or thiol groups prepared by atom transfer radical polymerization Macromolecules 35 2002 9009 9014 (Pubitemid 35421925)
    • (2002) Macromolecules , vol.35 , Issue.24 , pp. 9009-9014
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 255
    • 0033877980 scopus 로고    scopus 로고
    • Using atom transfer radical polymerization to amplify monolayers of initiators patterned by microcontact printing into polymer brushes for pattern transfer
    • DOI 10.1021/ma991264c
    • R.R. Shah, D. Merreceyes, M. Husemann, I. Rees, N.L. Abbott, C.J. Hawker, and J.L. Hedrick Using atom transfer radical polymerization to amplify monolayers of initiators patterned by microcontact printing into polymer brushes for pattern transfer Macromolecules 33 2000 597 605 (Pubitemid 30541891)
    • (2000) Macromolecules , vol.33 , Issue.2 , pp. 597-605
    • Shah, R.R.1    Merreceyes, D.2    Husemann, M.3    Rees, I.4    Abbott, N.L.5    Hawker, C.J.6    Hedrick, J.L.7
  • 256
    • 9644254051 scopus 로고    scopus 로고
    • Cysteine-reactive polymers synthesized by atom transfer radical polymerization for conjugation to proteins
    • D. Bontempo, K. Heredia, B. Fish, and H. Maynard Cysteine-reactive polymers synthesized by atom transfer radical polymerization for conjugation to proteins J Am Chem Soc 126 2004 15372 15373 (Pubitemid 39577459)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.47 , pp. 15372-15373
    • Bontempo, D.1    Heredia, K.L.2    Fish, B.A.3    Maynard, H.D.4
  • 257
    • 26944465370 scopus 로고    scopus 로고
    • Synthesis and chemical degradation of branched vinyl polymers prepared via ATRP: Use of a cleavable disulfide-based branching agent
    • DOI 10.1021/ma051121s
    • Y. Li, and S.P. Armes Synthesis and chemical degradation of branched vinyl polymers prepared via ATRP: use of a cleavable disulfide-based branching agent Macromolecules 38 2005 8155 8162 (Pubitemid 41476077)
    • (2005) Macromolecules , vol.38 , Issue.20 , pp. 8155-8162
    • Li, Y.1    Armes, S.P.2
  • 258
    • 22944482156 scopus 로고    scopus 로고
    • Synthesis of degradable miktoarm star copolymers via atom transfer radical polymerization
    • DOI 10.1021/ma0503099
    • H. Gao, N. Tsarevsky, and K. Matyjaszewski Synthesis of degradable miktoarm star copolymers via atom transfer radical polymerization Macromolecules 38 2005 5995 6004 (Pubitemid 41048613)
    • (2005) Macromolecules , vol.38 , Issue.14 , pp. 5995-6004
    • Gao, H.1    Tsarevsky, N.V.2    Matyjaszewski, K.3
  • 259
    • 33745548631 scopus 로고    scopus 로고
    • Synthesis and peptide-induced degradation of biocompatible fibers based on highly branched poly(2-hydroxyethyl methacrylate)
    • DOI 10.1002/adma.200600314
    • L. Wang, C.M. Li, A.J. Ryan, and S.P. Armes Synthesis and peptide-induced degradation of biocompatible fibers based on highly branched poly(2-hydroxyethyl methacrylate) Adv Mater 18 2006 1566 1570 (Pubitemid 43979521)
    • (2006) Advanced Materials , vol.18 , Issue.12 , pp. 1566-1570
    • Wang, L.1    Li, C.2    Ryan, A.J.3    Armes, S.P.4
  • 260
    • 11444260400 scopus 로고    scopus 로고
    • Synthesis of hydroxy-telechelic poly(methyl acrylate) and polystyrene by atom transfer radical coupling
    • DOI 10.1021/ma0484375
    • T. Sarbu, K.-Y. Lin, J. Spanswick, R.R. Gil, D.J. Siegwart, and K. Matyjaszewski Synthesis of hydroxy-telechelic poly(methyl acrylate) and polystyrene by Atom Transfer Radical Coupling Macromolecules 37 2004 9694 9700 (Pubitemid 40079953)
    • (2004) Macromolecules , vol.37 , Issue.26 , pp. 9694-9700
    • Sarbu, T.1    Lin, K.-Y.2    Spanswick, J.3    Gil, R.R.4    Siegwart, D.J.5    Matyjaszewski, K.6
  • 261
    • 2442665592 scopus 로고    scopus 로고
    • Polystyrene with designed molecular weight distribution by atom transfer radical coupling
    • T. Sarbu, K.Y. Lin, J. Ell, D.J. Siegwart, J. Spanswick, and K. Matyjaszewski Polystyrene with designed molecular weight distribution by atom transfer radical coupling Macromolecules 37 2004 3120 3127
    • (2004) Macromolecules , vol.37 , pp. 3120-3127
    • Sarbu, T.1    Lin, K.Y.2    Ell, J.3    Siegwart, D.J.4    Spanswick, J.5    Matyjaszewski, K.6
  • 262
    • 79151476163 scopus 로고    scopus 로고
    • Telechelic polymers by living and controlled/living polymerization methods
    • M.A. Tasdelen, M.U. Kahveci, and Y. Yagci Telechelic polymers by living and controlled/living polymerization methods Prog Polym Sci 36 2011 455 567
    • (2011) Prog Polym Sci , vol.36 , pp. 455-567
    • Tasdelen, M.A.1    Kahveci, M.U.2    Yagci, Y.3
  • 263
    • 18744368194 scopus 로고    scopus 로고
    • Step-growth "click" coupling of telechelic polymers prepared by atom transfer radical polymerization
    • DOI 10.1021/ma050370d
    • N.V. Tsarevsky, B.S. Sumerlin, and K. Matyjaszewski Step-growth "click" coupling of telechelic polymers prepared by atom transfer radical polymerization Macromolecules 38 2005 3558 3561 (Pubitemid 40672479)
    • (2005) Macromolecules , vol.38 , Issue.9 , pp. 3558-3561
    • Tsarevsky, N.V.1    Sumerlin, B.S.2    Matyjaszewski, K.3
  • 264
    • 6344233861 scopus 로고    scopus 로고
    • Design of biodegradable amphiphilic polymers: Well-defined amphiphilic polyphosphates with hydrophilic graft chains via ATRP
    • Y. Iwasaki, and K. Akiyoshi Design of biodegradable amphiphilic polymers: well-defined amphiphilic polyphosphates with hydrophilic graft chains via ATRP Macromolecules 37 2004 7637 7642
    • (2004) Macromolecules , vol.37 , pp. 7637-7642
    • Iwasaki, Y.1    Akiyoshi, K.2
  • 265
    • 32344440800 scopus 로고    scopus 로고
    • Room-temperature polycondensation of dicarboxylic acids and diols catalyzed by water-stable lewis acids
    • DOI 10.1295/polymj.37.946
    • A. Takasu, Y. Iio, T. Mimura, and T. Hirabayashi Room-temperature polycondensation of dicarboxylic acids and diols catalyzed by water-stable lewis acids Polym J 37 2005 946 953 (Pubitemid 43219888)
    • (2005) Polymer Journal , vol.37 , Issue.12 , pp. 946-953
    • Takasu, A.1    Iio, Y.2    Mimura, T.3    Hirabayashi, T.4
  • 266
    • 72449181386 scopus 로고    scopus 로고
    • Synthesis of hyperbranched degradable polymers by atom transfer radical (co)polymerization of inimers with ester or disulfide groups
    • N.V. Tsarevsky, J. Huang, and K. Matyjaszewski Synthesis of hyperbranched degradable polymers by atom transfer radical (co)polymerization of inimers with ester or disulfide groups J Polym Sci Part A: Polym Chem 47 2009 6839 6851
    • (2009) J Polym Sci Part A: Polym Chem , vol.47 , pp. 6839-6851
    • Tsarevsky, N.V.1    Huang, J.2    Matyjaszewski, K.3
  • 267
    • 0037065707 scopus 로고    scopus 로고
    • Atom transfer radical polymerization from cellulose fibers at ambient temperature
    • DOI 10.1021/ja016582h
    • A. Carlmark, and E. Malmstrom Atom transfer radical polymerization from cellulose fibers at ambient temperature J Am Chem Soc 124 2002 900 901 (Pubitemid 34130963)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.6 , pp. 900-901
    • Carlmark, A.1    Malmstrom, E.2
  • 268
    • 0344394325 scopus 로고    scopus 로고
    • ATRP grafting from cellulose fibers to create block-copolymer grafts
    • DOI 10.1021/bm030046v
    • A. Carlmark, and E.E. Malmstrom ATRP grafting from cellulose fibers to create block-copolymer grafts Biomacromolecules 4 2003 1740 1745 (Pubitemid 37455588)
    • (2003) Biomacromolecules , vol.4 , Issue.6 , pp. 1740-1745
    • Carlmark, A.1    Malmstrom, E.E.2
  • 269
    • 33646380840 scopus 로고    scopus 로고
    • Surface modification of natural substrates by atom transfer radical polymerization
    • DOI 10.1002/app.23457
    • J. Lindqvist, and E. Malmstrom Surface modification of natural substrates by atom transfer radical polymerization J Appl Polym Sci 100 2006 4155 4162 (Pubitemid 43666815)
    • (2006) Journal of Applied Polymer Science , vol.100 , Issue.5 , pp. 4155-4162
    • Lindqvist, J.1    Malmstrom, E.2
  • 270
    • 27644500123 scopus 로고    scopus 로고
    • Densely grafting copolymers of ethyl cellulose through atom transfer radical polymerization
    • DOI 10.1002/pola.20908
    • D.W. Shen, H. Yu, and Y. Huang Densely grafting copolymers of ethyl cellulose through atom transfer radical polymerization J Polym Sci Part A: Polym Chem 43 2005 4099 4108 (Pubitemid 41561797)
    • (2005) Journal of Polymer Science, Part A: Polymer Chemistry , vol.43 , Issue.18 , pp. 4099-4108
    • Shen, D.1    Hui, Y.U.2    Huang, Y.3
  • 271
    • 0037711361 scopus 로고    scopus 로고
    • Synthesis of a well-defined Chitosan Graft Poly(methoxy polyethyleneglycol methacrylate) by Atom transfer radical polymerization polymerization
    • DOI 10.1002/app.12001
    • K. El Tahlawy, and S.M. Hudson Synthesis of a well-defined chitosan graft poly(methoxy polyethyleneglycol methacrylate) by atom transfer radical polymerization J Appl Polym Sci 89 2003 901 912 (Pubitemid 36663537)
    • (2003) Journal of Applied Polymer Science , vol.89 , Issue.4 , pp. 901-912
    • El Tahlawy, K.1    Hudson, S.M.2
  • 272
    • 29444445972 scopus 로고    scopus 로고
    • Enhanced and selective adsorption of mercury ions on chitosan beads grafted with polyacrylamide via surface-initiated atom transfer radical polymerization
    • DOI 10.1021/la051551b
    • N. Li, R.B. Bai, and C.K. Liu Enhanced and selective adsorption of mercury ions on chitosan beads grafted with polyacrylamide via surface-initiated atom transfer radical polymerization Langmuir 21 2005 11780 11787 (Pubitemid 43011518)
    • (2005) Langmuir , vol.21 , Issue.25 , pp. 11780-11787
    • Li, N.1    Bai, R.2    Liu, C.3
  • 273
    • 31644441917 scopus 로고    scopus 로고
    • Surface-initiated atom transfer radical polymerization (SI-ATRP) of styrene from chitosan particles
    • DOI 10.1016/j.matlet.2005.10.094, PII S0167577X05010803
    • P. Liu, and Z.X. Su Surface-initiated atom transfer radical polymerization (SI-ATRP) of styrene from chitosan particles Mater Lett 60 2006 1137 1139 (Pubitemid 43171837)
    • (2006) Materials Letters , vol.60 , Issue.9-10 , pp. 1137-1139
    • Liu, P.1    Su, Z.2
  • 274
    • 79955478547 scopus 로고    scopus 로고
    • Chitosan-A versatile semi-synthetic polymer in biomedical applications
    • M. Dash, F. Chiellini, R.M. Ottenbrite, and E. Chiellini Chitosan-A versatile semi-synthetic polymer in biomedical applications Prog Polym Sci 36 2011 981 1014
    • (2011) Prog Polym Sci , vol.36 , pp. 981-1014
    • Dash, M.1    Chiellini, F.2    Ottenbrite, R.M.3    Chiellini, E.4
  • 275
    • 33746314940 scopus 로고    scopus 로고
    • Versatile grafting of polysaccharides in homogeneous mild conditions by using atom transfer radical polymerization
    • DOI 10.1021/bm0601373
    • D. Bontempo, G. Masci, P. De Leonardis, L. Mannina, D. Capitani, and V. Crescenzi Versatile grafting of polysaccharides in homogeneous mild conditions by using atom transfer radical polymerization Biomacromolecules 7 2006 2154 2161 (Pubitemid 44103355)
    • (2006) Biomacromolecules , vol.7 , Issue.7 , pp. 2154-2161
    • Bontempo, D.1    Masci, G.2    De Leonardis, P.3    Mannina, L.4    Capitani, D.5    Crescenzi, V.6
  • 276
    • 0032476812 scopus 로고    scopus 로고
    • Polyvalent interactions in biological systems: Implications for design and use of multivalent ligands and inhibitors
    • M. Mammen, S.K. Choi, and G.M. Whitesides Polyvalent interactions in biological systems: implications for design and use of multivalent ligands and inhibitors Angew Chem Int Edit 37 1998 2755 2794
    • (1998) Angew Chem Int Edit , vol.37 , pp. 2755-2794
    • Mammen, M.1    Choi, S.K.2    Whitesides, G.M.3
  • 277
    • 0037151595 scopus 로고    scopus 로고
    • Hyperbranched molecular nanocapsules: Comparison of the hyperbranched architecture with the perfect linear analogue
    • S.E. Stiriba, H. Kautz, and H. Frey Hyperbranched molecular nanocapsules: comparison of the hyperbranched architecture with the perfect linear analogue J Am Chem Soc 124 2002 9698 9699
    • (2002) J Am Chem Soc , vol.124 , pp. 9698-9699
    • Stiriba, S.E.1    Kautz, H.2    Frey, H.3
  • 278
    • 0035874569 scopus 로고    scopus 로고
    • Polycationic graft copolymers as carriers for oligonucleotide delivery. Complexes of oligonucleotides with polycationic graft copolymers
    • DOI 10.1021/la001779t
    • H. Dautzenberg, A. Zintchenko, C. Konak, T. Reschel, V. Subr, and K. Ulbrich Polycationic graft copolymers as carriers for oligonucleotide delivery. Complexes of oligonucleotides with polycationic graft copolymers Langmuir 17 2001 3096 3102 (Pubitemid 35330495)
    • (2001) Langmuir , vol.17 , Issue.10 , pp. 3096-3102
    • Dautzenberg, H.1    Zintchenko, A.2    Konak, C.3    Reschel, T.4    Subr, V.5    Ulbrich, K.6
  • 280
    • 0032637389 scopus 로고    scopus 로고
    • Water-soluble dendrimer-poly(ethylene glycol) starlike conjugates as potential drug carriers
    • M.J. Liu, K. Kono, and J.M.J. Frechet Water-soluble dendrimer- poly(ethylene glycol) starlike conjugates as potential drug carriers J Polym Sci Part A: Polym Chem 37 1999 3492 3503
    • (1999) J Polym Sci Part A: Polym Chem , vol.37 , pp. 3492-3503
    • Liu, M.J.1    Kono, K.2    Frechet, J.M.J.3
  • 282
    • 0034026798 scopus 로고    scopus 로고
    • Poly(ethylene glycol) multiblock copolymer as a carrier of anti-cancer drug doxorubicin
    • DOI 10.1021/bc990092l
    • M. Pechar, K. Ulbrich, V. Subr, L.W. Seymour, and E.H. Schacht Poly(ethylene glycol) multiblock copolymer as a carrier of anti-cancer drug doxorubicin Bioconjug Chem 11 2000 131 139 (Pubitemid 30174478)
    • (2000) Bioconjugate Chemistry , vol.11 , Issue.2 , pp. 131-139
    • Pechar, M.1    Ulbrich, K.2    Subr, V.3    Seymour, L.W.4    Schacht, E.H.5
  • 284
    • 0034781645 scopus 로고    scopus 로고
    • Synthesis, isolation and characterization of Plasmodium falciparum antigenic tetrabranched peptide dendrimers obtained by thiazolidine linkages
    • DOI 10.1034/j.1399-3011.2001.00921.x
    • F. Chaves, J.C. Calvo, C. Carvajal, Z. Rivera, L. Ramirez, M. Pinto, M. Trujillo, F. Guzman, and M.E. Patarroyo Synthesis, isolation and characterization of Plasmodium falciparum antigenic tetrabranched peptide dendrimers obtained by thiazolidine linkages J Pept Res 58 2001 307 316 (Pubitemid 32989222)
    • (2001) Journal of Peptide Research , vol.58 , Issue.4 , pp. 307-316
    • Chaves, F.1    Calvo, J.C.2    Carvajal, C.3    Rivera, Z.4    Ramirez, L.5    Pinto, M.6    Trujillo, M.7    Guzman, F.8    Patarroyo, M.E.9
  • 285
    • 70450189516 scopus 로고    scopus 로고
    • Polymerization of enantiopure monomers using syndiospecific catalysts: A new approach to sequence control in polymer synthesis
    • C.M. Thomas, J.W. Kramer, D.S. Treitler, E.W. Dunn, P.M. Castro, T. Roisnel, and G.W. Coates Polymerization of enantiopure monomers using syndiospecific catalysts: a new approach to sequence control in polymer synthesis J Am Chem Soc 131 2009 16042 16044
    • (2009) J Am Chem Soc , vol.131 , pp. 16042-16044
    • Thomas, C.M.1    Kramer, J.W.2    Treitler, D.S.3    Dunn, E.W.4    Castro, P.M.5    Roisnel, T.6    Coates, G.W.7
  • 286
    • 79951998821 scopus 로고    scopus 로고
    • Controlled folding of synthetic polymer chains through the formation of positionable covalent bridges
    • B.V.K.J. Schmidt, N. Fechler, J. Falkenhagen, and J.F. Lutz Controlled folding of synthetic polymer chains through the formation of positionable covalent bridges Nat Chem 3 2011 234 238
    • (2011) Nat Chem , vol.3 , pp. 234-238
    • Schmidt, B.V.K.J.1    Fechler, N.2    Falkenhagen, J.3    Lutz, J.F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.