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Volumn 7, Issue 10, 2015, Pages 771-784

Degradable vinyl polymers for biomedical applications

Author keywords

[No Author keywords available]

Indexed keywords

BIOMATERIAL; POLYMER; VINYL DERIVATIVE;

EID: 84942103101     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/nchem.2343     Document Type: Article
Times cited : (297)

References (143)
  • 1
    • 84942178682 scopus 로고    scopus 로고
    • Plastics -the Facts 2014/2015 (PlasticsEurope, 2015)
    • Plastics -the Facts 2014/2015 (PlasticsEurope, 2015); http://www.plasticseurope.org/Document/plastics-the-facts-20142015.aspx
  • 2
    • 0038218178 scopus 로고    scopus 로고
    • Biodegradation of poly(vinyl alcohol) based materials
    • Chiellini, E., Corti, A., DAntone, S. & Solaro, R. Biodegradation of poly(vinyl alcohol) based materials. Prog. Polym. Sci. 28, 963-1014 (2003).
    • (2003) Prog. Polym. Sci. , vol.28 , pp. 963-1014
    • Chiellini, E.1    Corti, A.2    DAntone, S.3    Solaro, R.4
  • 3
    • 84873988655 scopus 로고    scopus 로고
    • Nitroxide-mediated polymerization
    • Nicolas, J., et al. Nitroxide-mediated polymerization. Prog. Polym. Sci. 38, 63-235 (2013).
    • (2013) Prog. Polym. Sci. , vol.38 , pp. 63-235
    • Nicolas, J.1
  • 4
    • 0035470133 scopus 로고    scopus 로고
    • Atom transfer radical polymerization
    • Matyjaszewski, K. & Xia, J. Atom transfer radical polymerization. Chem. Rev. 101, 2921-2990 (2001).
    • (2001) Chem. Rev. , vol.101 , pp. 2921-2990
    • Matyjaszewski, K.1    Xia, J.2
  • 5
    • 0035781198 scopus 로고    scopus 로고
    • Metal-catalyzed living radical polymerization
    • Kamigaito, M., Ando, T. & Sawamoto, M. Metal-catalyzed living radical polymerization. Chem. Rev. 101, 3689-3745 (2001).
    • (2001) Chem. Rev. , vol.101 , pp. 3689-3745
    • Kamigaito, M.1    Ando, T.2    Sawamoto, M.3
  • 6
    • 70749084818 scopus 로고    scopus 로고
    • Living radical polymerization by the RAFT process -A second update
    • Moad, G., Rizzardo, E. & Thang, S. H. Living radical polymerization by the RAFT process -a second update. Aust. J. Chem. 62, 1402-1472 (2009).
    • (2009) Aust. J. Chem. , vol.62 , pp. 1402-1472
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 7
    • 84856162916 scopus 로고    scopus 로고
    • Terminology for biorelated polymers and applications (IUPAC recommendations 2012)
    • Vert, M., et al. Terminology for biorelated polymers and applications (IUPAC recommendations 2012). Pure Appl. Chem. 84, 377-408 (2012).
    • (2012) Pure Appl. Chem. , vol.84 , pp. 377-408
    • Vert, M.1
  • 8
    • 34547607522 scopus 로고    scopus 로고
    • Polymer-drug conjugation, recent achievements and general strategies
    • Pasut, G. & Veronese, F. M. Polymer-drug conjugation, recent achievements and general strategies. Prog. Polym. Sci. 32, 933-961 (2007).
    • (2007) Prog. Polym. Sci. , vol.32 , pp. 933-961
    • Pasut, G.1    Veronese, F.M.2
  • 9
    • 79955471240 scopus 로고    scopus 로고
    • Polymers prepared using cleavable initiators: Syn
    • thesis, characterization and degradation
    • Rikkou, M. D. & Patrickios, C. S. Polymers prepared using cleavable initiators: synthesis, characterization and degradation. Prog. Polym. Sci. 36, 1079-1097 (2011).
    • (2011) Prog. Polym. Sci. , vol.36 , pp. 1079-1097
    • Rikkou, M.D.1    Patrickios, C.S.2
  • 10
    • 84880253134 scopus 로고    scopus 로고
    • Selenium-containing polymers: Promising biomaterials for controlled release and enzyme mimics
    • Xu, H., Cao, W. & Zhang, X. Selenium-containing polymers: promising biomaterials for controlled release and enzyme mimics. Acc. Chem. Res. 46, 1647-1658 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 1647-1658
    • Xu, H.1    Cao, W.2    Zhang, X.3
  • 11
    • 84904412134 scopus 로고    scopus 로고
    • Redox-sensitive materials for drug delivery: Targeting the correct intracellular environment, tuning release rates, and appropriate predictive systems
    • Phillips, D. J. & Gibson, M. I. Redox-sensitive materials for drug delivery: targeting the correct intracellular environment, tuning release rates, and appropriate predictive systems. Antioxid. Redox Sign. 21, 786-803 (2013).
    • (2013) Antioxid. Redox Sign. , vol.21 , pp. 786-803
    • Phillips, D.J.1    Gibson, M.I.2
  • 12
    • 0037137351 scopus 로고    scopus 로고
    • Reversible redox cleavage/coupling of polystyrene with disulfide or thiol groups prepared by atom transfer radical polymerization
    • Tsarevsky, N. V. & Matyjaszewski, K. Reversible redox cleavage/coupling of polystyrene with disulfide or thiol groups prepared by atom transfer radical polymerization. Macromolecules 35, 9009-9014 (2002).
    • (2002) Macromolecules , vol.35 , pp. 9009-9014
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 14
    • 82655171931 scopus 로고    scopus 로고
    • End-linked amphiphilic, degradable polymer conetworks: Synthesis by sequential atom transfer radical polymerization using a bifunctional, cleavable initiator
    • Rikkou-Kalourkoti, M., Loizou, E., Porcar, L., Matyjaszewski, K. & Patrickios, C. S. End-linked, amphiphilic, degradable polymer conetworks: synthesis by sequential atom transfer radical polymerization using a bifunctional, cleavable initiator. Polym. Chem. 3, 105-116 (2012).
    • (2012) Polym. Chem. , vol.3 , pp. 105-116
    • Rikkou-Kalourkoti, M.1    Loizou, E.2    Porcar, L.3    Matyjaszewski, K.4    Patrickios, C.S.5
  • 15
    • 34249693532 scopus 로고    scopus 로고
    • Synthesis of photocleavable linear macromonomers by ATRP and star macromonomers by a tandem ATRP?click reaction: Precursors to photodegradable model networks
    • Johnson, J. A., Finn, M. G., Koberstein, J. T. & Turro, N. J. Synthesis of photocleavable linear macromonomers by ATRP and star macromonomers by a tandem ATRP?click reaction: precursors to photodegradable model networks. Macromolecules 40, 3589-3598 (2007).
    • (2007) Macromolecules , vol.40 , pp. 3589-3598
    • Johnson, J.A.1    Finn, M.G.2    Koberstein, J.T.3    Turro, N.J.4
  • 16
    • 77957202358 scopus 로고    scopus 로고
    • A versatile strategy for the synthesis of block copolymers bearing a photocleavable junction
    • Schumers, J-M., Gohy, J-F. & Fustin, C-A. A versatile strategy for the synthesis of block copolymers bearing a photocleavable junction. Polym. Chem. 1, 161-163 (2010).
    • (2010) Polym. Chem. , vol.1 , pp. 161-163
    • Schumers, J.-M.1    Gohy, J.-F.2    Fustin, C.-A.3
  • 17
    • 84855591674 scopus 로고    scopus 로고
    • Photoresponsive polymersomes as smart, triggerable nanocarriers
    • Cabane, E., Malinova, V., Menon, S., Palivan, C. G. & Meier, W. Photoresponsive polymersomes as smart, triggerable nanocarriers. Soft Matter 7, 9167-9176 (2011).
    • (2011) Soft Matter , vol.7 , pp. 9167-9176
    • Cabane, E.1    Malinova, V.2    Menon, S.3    Palivan, C.G.4    Meier, W.5
  • 18
    • 34247330169 scopus 로고    scopus 로고
    • Facile synthesis of dumbbell-shaped dendritic-linear-dendritic triblock copolymer via reversible addition-fragmentation chain transfer polymerization
    • Ge, Z., et al. Facile synthesis of dumbbell-shaped dendritic-linear-dendritic triblock copolymer via reversible addition-fragmentation chain transfer polymerization. J. Polym. Sci. A 45, 1432-1445 (2007).
    • (2007) J. Polym. Sci. A , vol.45 , pp. 1432-1445
    • Ge, Z.1
  • 19
    • 67449122402 scopus 로고    scopus 로고
    • Temperature and redox responsive hydrogels from ABA triblock copolymers prepared by RAFT polymerization
    • Vogt, A. P. & Sumerlin, B. S. Temperature and redox responsive hydrogels from ABA triblock copolymers prepared by RAFT polymerization. Soft Matter 5, 2347-2351 (2009).
    • (2009) Soft Matter , vol.5 , pp. 2347-2351
    • Vogt, A.P.1    Sumerlin, B.S.2
  • 20
    • 52649147539 scopus 로고    scopus 로고
    • Biocompatible wound dressings based on chemically degradable triblock copolymer hydrogels
    • Madsen, J., et al. Biocompatible wound dressings based on chemically degradable triblock copolymer hydrogels. Biomacromolecules 9, 2265-2275 (2008).
    • (2008) Biomacromolecules , vol.9 , pp. 2265-2275
    • Madsen, J.1
  • 21
    • 33746217408 scopus 로고    scopus 로고
    • A new class of biochemically degradable, stimulus-responsive triblock copolymer gelators
    • Li, C., Madsen, J., Armes, S. P. & Lewis, A. L. A new class of biochemically degradable, stimulus-responsive triblock copolymer gelators. Angew. Chem. Int. Ed. 118, 3510-3513 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.118 , pp. 3510-3513
    • Li, C.1    Madsen, J.2    Armes, S.P.3    Lewis, A.L.4
  • 22
    • 77956397868 scopus 로고    scopus 로고
    • Stepwise cleavable star polymers and polymeric gels thereof
    • Jiang, X., Chen, Y. & Xi, F. Stepwise cleavable star polymers and polymeric gels thereof. Macromolecules 43, 7056-7061 (2010).
    • (2010) Macromolecules , vol.43 , pp. 7056-7061
    • Jiang, X.1    Chen, Y.2    Xi, F.3
  • 23
    • 79954995181 scopus 로고    scopus 로고
    • Synthesis and properties of star-comb polymers and their doxorubicin conjugates
    • Chen, B., et al. Synthesis and properties of star-comb polymers and their doxorubicin conjugates. Bioconjugate Chem. 22, 617-624 (2011).
    • (2011) Bioconjugate Chem. , vol.22 , pp. 617-624
    • Chen, B.1
  • 24
    • 84879725842 scopus 로고    scopus 로고
    • Development of degradable, pH-sensitive star vectors for enhancing the cytoplasmic delivery of nucleic acids
    • Durmaz, Y. Y., Lin, Y-L. & ElSayed, M. E. H. Development of degradable, pH-sensitive star vectors for enhancing the cytoplasmic delivery of nucleic acids. Adv. Funct. Mater. 23, 3885-3895 (2013).
    • (2013) Adv. Funct. Mater. , vol.23 , pp. 3885-3895
    • Durmaz, Y.Y.1    Lin, Y.-L.2    ElSayed, M.E.H.3
  • 26
    • 47249126318 scopus 로고    scopus 로고
    • One-pot aynthesis of ABC type triblock copolymers via a combination of click chemistry and atom transfer nitroxide radical coupling chemistry
    • Lin, W., Fu, Q., Zhang, Y. & Huang, J. One-pot aynthesis of ABC type triblock copolymers via a combination of click chemistry and atom transfer nitroxide radical coupling chemistry. Macromolecules 41, 4127-4135 (2008).
    • (2008) Macromolecules , vol.41 , pp. 4127-4135
    • Lin, W.1    Fu, Q.2    Zhang, Y.3    Huang, J.4
  • 27
    • 70449380746 scopus 로고    scopus 로고
    • Rapid, selective, and reversible nitroxide radical coupling (NRC) reactions at ambient temperature
    • Kulis, J., Bell, C. A., Micallef, A. S., Jia, Z. & Monteiro, M. J. Rapid, selective, and reversible nitroxide radical coupling (NRC) reactions at ambient temperature. Macromolecules 42, 8218-8227 (2009).
    • (2009) Macromolecules , vol.42 , pp. 8218-8227
    • Kulis, J.1    Bell, C.A.2    Micallef, A.S.3    Jia, Z.4    Monteiro, M.J.5
  • 28
    • 36949006962 scopus 로고    scopus 로고
    • A facile method for the synthesis of cleavable block copolymers from ATRP-based homopolymers
    • Klaikherd, A., Ghosh, S. & Thayumanavan, S. A facile method for the synthesis of cleavable block copolymers from ATRP-based homopolymers. Macromolecules 40, 8518-8520 (2007).
    • (2007) Macromolecules , vol.40 , pp. 8518-8520
    • Klaikherd, A.1    Ghosh, S.2    Thayumanavan, S.3
  • 29
    • 67749137431 scopus 로고    scopus 로고
    • Multi-stimuli sensitive amphiphilic block copolymer assemblies
    • Klaikherd, A., Nagamani, C. & Thayumanavan, S. Multi-stimuli sensitive amphiphilic block copolymer assemblies. J. Am. Chem. Soc. 131, 4830-4838 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4830-4838
    • Klaikherd, A.1    Nagamani, C.2    Thayumanavan, S.3
  • 30
    • 78650377304 scopus 로고    scopus 로고
    • Main-chain supramolecular block copolymers
    • Yang, S. K., Ambade, A. V. & Weck, M. Main-chain supramolecular block copolymers. Chem. Soc. Rev. 40, 129-137 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 129-137
    • Yang, S.K.1    Ambade, A.V.2    Weck, M.3
  • 31
    • 84891403315 scopus 로고    scopus 로고
    • Multi-stimuli responsive supramolecular diblock copolymers
    • Sambe, L., et al. Multi-stimuli responsive supramolecular diblock copolymers. Polym. Chem. 5, 1031-1036 (2014).
    • (2014) Polym. Chem. , vol.5 , pp. 1031-1036
    • Sambe, L.1
  • 32
    • 84862926288 scopus 로고    scopus 로고
    • Triply triggered doxorubicin release from supramolecular nanocontainers
    • Loh, X. J., et al. Triply triggered doxorubicin release from supramolecular nanocontainers. Biomacromolecules 13, 84-91 (2011).
    • (2011) Biomacromolecules , vol.13 , pp. 84-91
    • Loh, X.J.1
  • 33
    • 67649945491 scopus 로고    scopus 로고
    • Non-covalently connected micelles (NCCMs): The origins and development of a new concept
    • Guo, M. & Jiang, M. Non-covalently connected micelles (NCCMs): the origins and development of a new concept. Soft Matter 5, 495-500 (2009).
    • (2009) Soft Matter , vol.5 , pp. 495-500
    • Guo, M.1    Jiang, M.2
  • 34
    • 46949084260 scopus 로고    scopus 로고
    • Noncovalently connected micelles, nanoparticles, and metal-functionalized nanocages using supramolecular self-assembly
    • Moughton, A. O. & OReilly, R. K. Noncovalently connected micelles, nanoparticles, and metal-functionalized nanocages using supramolecular self-assembly. J. Am. Chem. Soc. 130, 8714-8725 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 8714-8725
    • Moughton, A.O.1    OReilly, R.K.2
  • 35
    • 76149098835 scopus 로고    scopus 로고
    • Supramolecular ABC triblock copolymers via one-pot, orthogonal self-assembly
    • Yang, S. K., Ambade, A. V. & Weck, M. Supramolecular ABC triblock copolymers via one-pot, orthogonal self-assembly. J. Am. Chem. Soc. 132, 1637-1645 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1637-1645
    • Yang, S.K.1    Ambade, A.V.2    Weck, M.3
  • 36
    • 84886292840 scopus 로고    scopus 로고
    • Stimuli-responsive nanocarriers for drug delivery systems
    • Mura, S., Nicolas, J. & Couvreur, P. Stimuli-responsive nanocarriers for drug delivery systems. Nature Mater. 12, 991-1003 (2013).
    • (2013) Nature Mater. , vol.12 , pp. 991-1003
    • Mura, S.1    Nicolas, J.2    Couvreur, P.3
  • 37
    • 77955835980 scopus 로고    scopus 로고
    • Voltage-responsive vesicles based on orthogonal assembly of two homopolymers
    • Yan, Q., et al. Voltage-responsive vesicles based on orthogonal assembly of two homopolymers. J. Am. Chem. Soc. 132, 9268-9270 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 9268-9270
    • Yan, Q.1
  • 38
    • 38349150863 scopus 로고    scopus 로고
    • Synthesis of multisegmented degradable polymers by atom transfer radical cross-coupling
    • Nicolaÿ, R., Marx, L., Hémery, P. & Matyjaszewski, K. Synthesis of multisegmented degradable polymers by atom transfer radical cross-coupling. Macromolecules 40, 9217-9223 (2007).
    • (2007) Macromolecules , vol.40 , pp. 9217-9223
    • Nicolaÿ, R.1    Marx, L.2    Hémery, P.3    Matyjaszewski, K.4
  • 39
    • 79953684291 scopus 로고    scopus 로고
    • Embedding multiple site-specific functionalities into polymer chains via nitrone-mediated radical coupling reactions
    • Wong, E. H. H., Stenzel, M. H., Junkers, T. & Barner-Kowollik, C. Embedding multiple site-specific functionalities into polymer chains via nitrone-mediated radical coupling reactions. J. Polym. Sci. A 49, 2118-2126 (2011).
    • (2011) J. Polym. Sci. A , vol.49 , pp. 2118-2126
    • Wong, E.H.H.1    Stenzel, M.H.2    Junkers, T.3    Barner-Kowollik, C.4
  • 40
    • 34347344017 scopus 로고    scopus 로고
    • A Versatile approach to reducible vinyl polymers via oxidation of telechelic polymers prepared by reversible addition fragmentation chain transfer polymerization
    • You, Y-Z., Manickam, D. S., Zhou, Q-H. & Oupický, D. A Versatile approach to reducible vinyl polymers via oxidation of telechelic polymers prepared by reversible addition fragmentation chain transfer polymerization. Biomacromolecules 8, 2038-2044 (2007).
    • (2007) Biomacromolecules , vol.8 , pp. 2038-2044
    • You, Y.-Z.1    Manickam, D.S.2    Zhou, Q.-H.3    Oupický, D.4
  • 41
    • 36949005845 scopus 로고    scopus 로고
    • Dually responsive multiblock copolymers via reversible addition?fragmentation chain transfer polymerization: Synthesis of temperature-and redox-responsive copolymers of poly(N-isopropylacrylamide) and poly(2-(dimethylamino)ethyl methacrylate)
    • You, Y-Z., et al. Dually responsive multiblock copolymers via reversible addition?fragmentation chain transfer polymerization: synthesis of temperature-and redox-responsive copolymers of poly(N-isopropylacrylamide) and poly(2-(dimethylamino)ethyl methacrylate). Macromolecules 40, 8617-8624 (2007).
    • (2007) Macromolecules , vol.40 , pp. 8617-8624
    • You, Y.-Z.1
  • 42
    • 84867483398 scopus 로고    scopus 로고
    • Biodegradable poly(disulfide)s derived from raft polymerization: Monomer scope, glutathione degradation, and tunable thermal responses
    • Phillips, D. J. & Gibson, M. I. Biodegradable poly(disulfide)s derived from raft polymerization: monomer scope, glutathione degradation, and tunable thermal responses. Biomacromolecules 13, 3200-3208 (2012).
    • (2012) Biomacromolecules , vol.13 , pp. 3200-3208
    • Phillips, D.J.1    Gibson, M.I.2
  • 43
    • 84869059099 scopus 로고    scopus 로고
    • Degradable thermoresponsive polyesters by atom transfer radical polyaddition and click chemistry
    • Zhang, L-J., Dong, B-T., Du, F-S. & Li, Z-C. Degradable thermoresponsive polyesters by atom transfer radical polyaddition and click chemistry. Macromolecules 45, 8580-8587 (2012).
    • (2012) Macromolecules , vol.45 , pp. 8580-8587
    • Zhang, L.-J.1    Dong, B.-T.2    Du, F.-S.3    Li, Z.-C.4
  • 44
    • 75749149269 scopus 로고    scopus 로고
    • HPMA copolymers: Origins, early developments, present, and future
    • Kopeček, J. & Kopečková, P. HPMA copolymers: origins, early developments, present, and future. Adv. Drug Deliver. Rev. 62, 122-149 (2010).
    • (2010) Adv. Drug Deliver. Rev. , vol.62 , pp. 122-149
    • Kopeček, J.1    Kopečková, P.2
  • 46
    • 79955017504 scopus 로고    scopus 로고
    • Biodegradable multiblock poly[N-(2-hydroxypropyl)methacrylamide] via reversible addition?fragmentation chain transfer polymerization and click chemistry
    • Luo, K., Yang, J., Kopečková, P. & Kopeček, J. Biodegradable multiblock poly[N-(2-hydroxypropyl)methacrylamide] via reversible addition?fragmentation chain transfer polymerization and click chemistry. Macromolecules 44, 2481-2488 (2011).
    • (2011) Macromolecules , vol.44 , pp. 2481-2488
    • Luo, K.1    Yang, J.2    Kopečková, P.3    Kopeček, J.4
  • 47
    • 84879102342 scopus 로고    scopus 로고
    • Efficiency of high molecular weight backbone degradable HPMA copolymer-Prostaglandin E1 conjugate in promotion of bone formation in ovariectomized rats
    • Pan, H., et al. Efficiency of high molecular weight backbone degradable HPMA copolymer-Prostaglandin E1 conjugate in promotion of bone formation in ovariectomized rats. Biomaterials 34, 6528-6538 (2013).
    • (2013) Biomaterials , vol.34 , pp. 6528-6538
    • Pan, H.1
  • 48
    • 84873332319 scopus 로고    scopus 로고
    • Synthesis and evaluation of a backbone biodegradable multiblock HPMA copolymer nanocarrier for the systemic delivery of paclitaxel
    • Zhang, R., et al. Synthesis and evaluation of a backbone biodegradable multiblock HPMA copolymer nanocarrier for the systemic delivery of paclitaxel. J. Control. Rel. 166, 66-74 (2013).
    • (2013) J. Control. Rel. , vol.166 , pp. 66-74
    • Zhang, R.1
  • 49
    • 78651333306 scopus 로고    scopus 로고
    • Backbone degradable multiblock N-(2-hydroxypropyl)methacrylamide copolymer conjugates via reversible addition?fragmentation chain transfer polymerization and thiol?ene coupling reaction
    • Pan, H., Yang, J., Kopečková, P. & Kopeček, J. Backbone degradable multiblock N-(2-hydroxypropyl)methacrylamide copolymer conjugates via reversible addition?fragmentation chain transfer polymerization and thiol?ene coupling reaction. Biomacromolecules 12, 247-252 (2010).
    • (2010) Biomacromolecules , vol.12 , pp. 247-252
    • Pan, H.1    Yang, J.2    Kopečková, P.3    Kopeček, J.4
  • 50
    • 84901617707 scopus 로고    scopus 로고
    • Combination cytotoxicity of backbone degradable HPMA copolymer gemcitabine and platinum conjugates toward human ovarian carcinoma cells
    • Duangjai, A., Luo, K., Zhou, Y., Yang, J. & Kopeček, J. Combination cytotoxicity of backbone degradable HPMA copolymer gemcitabine and platinum conjugates toward human ovarian carcinoma cells. Eur. J. Pharm. Biopharm. 87, 187-196 (2014).
    • (2014) Eur. J. Pharm. Biopharm. , vol.87 , pp. 187-196
    • Duangjai, A.1    Luo, K.2    Zhou, Y.3    Yang, J.4    Kopeček, J.5
  • 51
    • 84884132243 scopus 로고    scopus 로고
    • Biodegradable multiblock poly(N-2-hydroxypropyl)methacrylamide gemcitabine and paclitaxel conjugates for ovarian cancer cell combination treatment
    • Larson, N., et al. Biodegradable multiblock poly(N-2-hydroxypropyl)methacrylamide gemcitabine and paclitaxel conjugates for ovarian cancer cell combination treatment. Int. J. Pharm. 454, 435-443 (2013).
    • (2013) Int. J. Pharm. , vol.454 , pp. 435-443
    • Larson, N.1
  • 52
    • 84874034404 scopus 로고    scopus 로고
    • Synthesis of long-circulating, backbone degradable HPMA copolymer-doxorubicin conjugates and evaluation of molecular-weight-dependent antitumor efficacy
    • Pan, H., Sima, M., Yang, J. & Kopeček, J. Synthesis of long-circulating, backbone degradable HPMA copolymer-doxorubicin conjugates and evaluation of molecular-weight-dependent antitumor efficacy. Macromol. Biosci. 13, 155-160 (2013).
    • (2013) Macromol. Biosci. , vol.13 , pp. 155-160
    • Pan, H.1    Sima, M.2    Yang, J.3    Kopeček, J.4
  • 53
    • 80052517546 scopus 로고    scopus 로고
    • Biodegradable star HPMA polymer-drug conjugates: Biodegradability, distribution and anti-tumor efficacy
    • Etrych, T., et al. Biodegradable star HPMA polymer-drug conjugates: biodegradability, distribution and anti-tumor efficacy. J. Control. Rel. 154, 241-248 (2011).
    • (2011) J. Control. Rel. , vol.154 , pp. 241-248
    • Etrych, T.1
  • 54
    • 77952856580 scopus 로고    scopus 로고
    • Metal-catalyzed simultaneous chain-and step-growth radical polymerization: Marriage of vinyl polymers and polyesters
    • Mizutani, M., Satoh, K. & Kamigaito, M. Metal-catalyzed simultaneous chain-and step-growth radical polymerization: marriage of vinyl polymers and polyesters. J. Am. Chem. Soc. 132, 7498-7507 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 7498-7507
    • Mizutani, M.1    Satoh, K.2    Kamigaito, M.3
  • 55
    • 61549124029 scopus 로고    scopus 로고
    • Metal-catalyzed radical polyaddition for aliphatic polyesters via evolution of atom transfer radical addition into step-growth polymerization
    • Mizutani, M., Satoh, K. & Kamigaito, M. Metal-catalyzed radical polyaddition for aliphatic polyesters via evolution of atom transfer radical addition into step-growth polymerization. Macromolecules 42, 472-480 (2008).
    • (2008) Macromolecules , vol.42 , pp. 472-480
    • Mizutani, M.1    Satoh, K.2    Kamigaito, M.3
  • 56
    • 84880305872 scopus 로고    scopus 로고
    • Sequence-regulated vinyl copolymers by metal-catalysed step-growth radical polymerization
    • Satoh, K., Ozawa, S., Mizutani, M., Nagai, K. & Kamigaito, M. Sequence-regulated vinyl copolymers by metal-catalysed step-growth radical polymerization. Nature Commun. 1, 6 (2010).
    • (2010) Nature Commun. , vol.1 , pp. 6
    • Satoh, K.1    Ozawa, S.2    Mizutani, M.3    Nagai, K.4    Kamigaito, M.5
  • 57
    • 84861162086 scopus 로고    scopus 로고
    • Design and synthesis of self-degradable antibacterial polymers by simultaneous chain-and step-growth radical copolymerization
    • Mizutani, M., et al. Design and synthesis of self-degradable antibacterial polymers by simultaneous chain-and step-growth radical copolymerization. Biomacromolecules 13, 1554-1563 (2012).
    • (2012) Biomacromolecules , vol.13 , pp. 1554-1563
    • Mizutani, M.1
  • 58
    • 0033879611 scopus 로고    scopus 로고
    • Convenient synthesis of polymers containing labile bonds in the main chain by radical alternating copolymerization of alkyl sorbates with oxygen
    • Matsumoto, A. & Higashi, H. convenient synthesis of polymers containing labile bonds in the main chain by radical alternating copolymerization of alkyl sorbates with oxygen. Macromolecules 33, 1651-1655 (2000).
    • (2000) Macromolecules , vol.33 , pp. 1651-1655
    • Matsumoto, A.1    Higashi, H.2
  • 59
    • 84860346847 scopus 로고    scopus 로고
    • Facile synthesis of main-chain degradable block copolymers for performance enhanced dismantlable adhesion
    • Sato, E., Hagihara, T. & Matsumoto, A. Facile synthesis of main-chain degradable block copolymers for performance enhanced dismantlable adhesion. ACS Appl. Mater. Interfaces 4, 2057-2064 (2012).
    • (2012) ACS Appl. Mater. Interfaces , vol.4 , pp. 2057-2064
    • Sato, E.1    Hagihara, T.2    Matsumoto, A.3
  • 60
    • 82655184936 scopus 로고    scopus 로고
    • Synthesis and characterization of a biodegradable polymer prepared viaradical copolymerization of 2-(acetoacetoxy)ethyl methacrylate and molecular oxygen
    • Pal, S., Das, A., Maiti, S. & De, P. Synthesis and characterization of a biodegradable polymer prepared viaradical copolymerization of 2-(acetoacetoxy)ethyl methacrylate and molecular oxygen. Polym. Chem. 3, 182-189 (2012).
    • (2012) Polym. Chem. , vol.3 , pp. 182-189
    • Pal, S.1    Das, A.2    Maiti, S.3    De, P.4
  • 61
    • 0036434072 scopus 로고    scopus 로고
    • A novel strategy for synthesis of multiblock copolymers
    • You, Y-Z., Hong, C-Y. & Pan, C-Y. A novel strategy for synthesis of multiblock copolymers. Chem. Commun. 2800-2801 (2002).
    • (2002) Chem. Commun. , pp. 2800-2801
    • You, Y.-Z.1    Hong, C.-Y.2    Pan, C.-Y.3
  • 62
    • 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
    • Bailey, W. J., Ni, Z. & Wu, S. R. 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, 711-714 (1982).
    • (1982) Macromolecules , vol.15 , pp. 711-714
    • Bailey, W.J.1    Ni, Z.2    Wu, S.R.3
  • 63
    • 78649698417 scopus 로고    scopus 로고
    • Chemistry chances and limitations of the radical ring-opening polymerization of cyclic ketene acetals for the synthesis of degradable polyesters
    • Agarwal, S. Chemistry, chances and limitations of the radical ring-opening polymerization of cyclic ketene acetals for the synthesis of degradable polyesters. Polym. Chem. 1, 953-964 (2010).
    • (2010) Polym. Chem. , vol.1 , pp. 953-964
    • Agarwal, S.1
  • 64
    • 36949017070 scopus 로고    scopus 로고
    • Biocompatible, thermoresponsive, and biodegradable: A simple preparation of all-in-one biorelevant polymers
    • Lutz, J-F., Andrieu, J., Üzgün, S., Rudolph, C. & Agarwal, S. Biocompatible, thermoresponsive, and biodegradable: a simple preparation of all-in-one biorelevant polymers. Macromolecules 40, 8540-8543 (2007).
    • (2007) Macromolecules , vol.40 , pp. 8540-8543
    • Lutz, J.-F.1    Andrieu, J.2    Üzgün, S.3    Rudolph, C.4    Agarwal, S.5
  • 65
    • 84885640131 scopus 로고    scopus 로고
    • Degradable and comblike PEG-based copolymers by nitroxide-mediated radical ring-opening polymerization
    • Delplace, V., et al. Degradable and comblike PEG-based copolymers by nitroxide-mediated radical ring-opening polymerization. Biomacromolecules 14, 2837-2847 (2013).
    • (2013) Biomacromolecules , vol.14 , pp. 2837-2847
    • Delplace, V.1
  • 66
    • 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
    • Siegwart, D. J., Bencherif, S. A., Srinivasan, A., Hollinger, J. O. & Matyjaszewski, K. 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. A 87, 345-358 (2008).
    • (2008) J. Biomed. Mater. Res. A , vol.87 , pp. 345-358
    • Siegwart, D.J.1    Bencherif, S.A.2    Srinivasan, A.3    Hollinger, J.O.4    Matyjaszewski, K.5
  • 67
    • 66549100888 scopus 로고    scopus 로고
    • Polycaprolactone-based novel degradable ionomers by radical ring-opening polymerization of 2-methylene-1,3-dioxepane
    • Agarwal, S. & Ren, L. Polycaprolactone-based novel degradable ionomers by radical ring-opening polymerization of 2-methylene-1,3-dioxepane. Macromolecules 42, 1574-1579 (2009).
    • (2009) Macromolecules , vol.42 , pp. 1574-1579
    • Agarwal, S.1    Ren, L.2
  • 68
    • 70449379571 scopus 로고    scopus 로고
    • Degradable polymer brushes prepared via surface-initiated controlled radical polymerization
    • Riachi, C., Schu?wer, N. & Klok, H-A. Degradable polymer brushes prepared via surface-initiated controlled radical polymerization. Macromolecules 42, 8076-8081 (2009).
    • (2009) Macromolecules , vol.42 , pp. 8076-8081
    • Riachi, C.1    Schuwer, N.2    Klok, H.-A.3
  • 69
    • 84878886126 scopus 로고    scopus 로고
    • Copolymerization of 2-methylene-1,3-dioxepane and glycidyl methacrylate, a well-defined and efficient process for achieving functionalized polyesters for covalent binding of bioactive molecules
    • Undin, J., Finne-Wistrand, A. & Albertsson, A-C. Copolymerization of 2-methylene-1,3-dioxepane and glycidyl methacrylate, a well-defined and efficient process for achieving functionalized polyesters for covalent binding of bioactive molecules. Biomacromolecules 14, 2095-2102 (2013).
    • (2013) Biomacromolecules , vol.14 , pp. 2095-2102
    • Undin, J.1    Finne-Wistrand, A.2    Albertsson, A.-C.3
  • 70
    • 80053477592 scopus 로고    scopus 로고
    • Synthesis of photo-scissible poly(p-hydroxystyrene) derivatives by radical copolymerization of p-hydroxystyrene derivatives and methyl vinyl ketone
    • Ishikawa, T., Morino, K., Sudo, A. & Endo, T. Synthesis of photo-scissible poly(p-hydroxystyrene) derivatives by radical copolymerization of p-hydroxystyrene derivatives and methyl vinyl ketone. J. Polym. Sci. A 49, 4714-4720 (2011).
    • (2011) J. Polym. Sci. A , vol.49 , pp. 4714-4720
    • Ishikawa, T.1    Morino, K.2    Sudo, A.3    Endo, T.4
  • 71
    • 0030260984 scopus 로고    scopus 로고
    • Free-radical ring-opening polymerization of cyclic allylic sulfides
    • Evans, R. A. & Rizzardo, E. Free-radical ring-opening polymerization of cyclic allylic sulfides. Macromolecules 29, 6983-6989 (1996).
    • (1996) Macromolecules , vol.29 , pp. 6983-6989
    • Evans, R.A.1    Rizzardo, E.2
  • 72
    • 67650477200 scopus 로고    scopus 로고
    • Free radical polymers with tunable and selective bio-and chemical degradability
    • Paulusse, J. M. J., Amir, R. J., Evans, R. A. & Hawker, C. J. Free radical polymers with tunable and selective bio-and chemical degradability. J. Am. Chem. Soc. 131, 9805-9812 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 9805-9812
    • Paulusse, J.M.J.1    Amir, R.J.2    Evans, R.A.3    Hawker, C.J.4
  • 73
    • 84861362971 scopus 로고    scopus 로고
    • New degradable alternating copolymers from naturally occurring aldehydes: Well-controlled cationic copolymerization and complete degradation
    • Ishido, Y., Kanazawa, A., Kanaoka, S. & Aoshima, S. New degradable alternating copolymers from naturally occurring aldehydes: well-controlled cationic copolymerization and complete degradation. Macromolecules 45, 4060-4068 (2012).
    • (2012) Macromolecules , vol.45 , pp. 4060-4068
    • Ishido, Y.1    Kanazawa, A.2    Kanaoka, S.3    Aoshima, S.4
  • 74
    • 84892771625 scopus 로고    scopus 로고
    • Efficient design for stimuli-responsive polymers with quantitative acid-degradability: Specifically designed alternating controlled cationic copolymerization and facile complete degradation
    • Aoshima, S., et al. Efficient design for stimuli-responsive polymers with quantitative acid-degradability: specifically designed alternating controlled cationic copolymerization and facile complete degradation. ACS Macro Lett. 3, 80-85 (2013).
    • (2013) ACS Macro Lett. , vol.3 , pp. 80-85
    • Aoshima, S.1
  • 75
    • 80054002869 scopus 로고    scopus 로고
    • Selective enzymatic degradation of self-assembled particles from amphiphilic block copolymers obtained by the combination of N-carboxyanhydride and nitroxide-mediated polymerization
    • Habraken, G. J. M., Peeters, M., Thornton, P. D., Koning, C. E. & Heise, A. Selective enzymatic degradation of self-assembled particles from amphiphilic block copolymers obtained by the combination of N-carboxyanhydride and nitroxide-mediated polymerization. Biomacromolecules 12, 3761-3769 (2011).
    • (2011) Biomacromolecules , vol.12 , pp. 3761-3769
    • Habraken, G.J.M.1    Peeters, M.2    Thornton, P.D.3    Koning, C.E.4    Heise, A.5
  • 76
    • 84875872476 scopus 로고    scopus 로고
    • Synthesis and thiol-responsive degradation of polylactide-based block copolymers having disulfide junctions using ATRP and ROP
    • Ko, N. R., Yao, K., Tang, C. & Oh, J. K. Synthesis and thiol-responsive degradation of polylactide-based block copolymers having disulfide junctions using ATRP and ROP. J. Polym. Sci. A 51, 3071-3080 (2013).
    • (2013) J. Polym. Sci. A , vol.51 , pp. 3071-3080
    • Ko, N.R.1    Yao, K.2    Tang, C.3    Oh, J.K.4
  • 77
    • 55049116157 scopus 로고    scopus 로고
    • Stimuli-responsive zwitterionic block copolypeptides: Poly(N-isopropylacrylamide)-block-poly(lysine-co-glutamic acid)
    • Li, J., et al. Stimuli-responsive zwitterionic block copolypeptides: poly(N-isopropylacrylamide)-block-poly(lysine-co-glutamic acid). Biomacromolecules 9, 2670-2676 (2008).
    • (2008) Biomacromolecules , vol.9 , pp. 2670-2676
    • Li, J.1
  • 78
    • 84882605866 scopus 로고    scopus 로고
    • Synthesis of polypeptide block copolymer hybrids by the combination of N-carboxyanhydride polymerization and RAFT
    • Jacobs, J., Gathergood, N. & Heise, A. Synthesis of polypeptide block copolymer hybrids by the combination of N-carboxyanhydride polymerization and RAFT. Macromol. Rapid Commun. 34, 1325-1329 (2013).
    • (2013) Macromol. Rapid Commun. , vol.34 , pp. 1325-1329
    • Jacobs, J.1    Gathergood, N.2    Heise, A.3
  • 79
    • 0032543065 scopus 로고    scopus 로고
    • Simultaneous dual living polymerizations: A novel one-step approach to block and graft copolymers
    • Mecerreyes, D., et al. Simultaneous dual living polymerizations: a novel one-step approach to block and graft copolymers. Angew. Chem. Int. Ed. 37, 1274-1276 (1998).
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1274-1276
    • Mecerreyes, D.1
  • 80
    • 58149170600 scopus 로고    scopus 로고
    • Degradable poly(2-hydroxyethyl methacrylate)-co-polycaprolactone hydrogels for tissue engineering scaffolds
    • Atzet, S., Curtin, S., Trinh, P., Bryant, S. & Ratner, B. Degradable poly(2-hydroxyethyl methacrylate)-co-polycaprolactone hydrogels for tissue engineering scaffolds. Biomacromolecules 9, 3370-3377 (2008).
    • (2008) Biomacromolecules , vol.9 , pp. 3370-3377
    • Atzet, S.1    Curtin, S.2    Trinh, P.3    Bryant, S.4    Ratner, B.5
  • 81
    • 38849096378 scopus 로고    scopus 로고
    • Thermo-responsive porous membranes of controllable porous morphology from triblock copolymers of polycaprolactone and poly(N-isopropylacrylamide) prepared by atom transfer radical polymerization
    • Xu, F. J., et al. Thermo-responsive porous membranes of controllable porous morphology from triblock copolymers of polycaprolactone and poly(N-isopropylacrylamide) prepared by atom transfer radical polymerization. Biomacromolecules 9, 331-339 (2007).
    • (2007) Biomacromolecules , vol.9 , pp. 331-339
    • Xu, F.J.1
  • 82
    • 77953814044 scopus 로고    scopus 로고
    • Synthesis characterization, and molecular recognition of sugar-functionalized nanoparticles prepared by a combination of ROP, ATRP, and click chemistry
    • Jubeli, E., Moine, L. & Barratt, G. Synthesis, characterization, and molecular recognition of sugar-functionalized nanoparticles prepared by a combination of ROP, ATRP, and click chemistry. J. Polym. Sci. A 48, 3178-3187 (2010).
    • (2010) J. Polym. Sci. A , vol.48 , pp. 3178-3187
    • Jubeli, E.1    Moine, L.2    Barratt, G.3
  • 83
    • 84866736510 scopus 로고    scopus 로고
    • P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellular localization and drug efficiency
    • Barz, M., et al. P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellular localization and drug efficiency. J. Control. Rel. 163, 63-74 (2012).
    • (2012) J. Control. Rel. , vol.163 , pp. 63-74
    • Barz, M.1
  • 84
    • 0034685469 scopus 로고    scopus 로고
    • Shell cross-linked nanoparticles containing hydrolytically degradable, crystalline core domains
    • Zhang, Q., Remsen, E. E. & Wooley, K. L. Shell cross-linked nanoparticles containing hydrolytically degradable, crystalline core domains. J. Am. Chem. Soc. 122, 3642-3651 (2000).
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 3642-3651
    • Zhang, Q.1    Remsen, E.E.2    Wooley, K.L.3
  • 85
    • 33846199887 scopus 로고    scopus 로고
    • Selectively degradable core cross-linked
    • star polymers
    • Wiltshire, J. T. & Qiao, G. G. Selectively degradable core cross-linked star polymers. Macromolecules 39, 9018-9027 (2006).
    • (2006) Macromolecules , vol.39 , pp. 9018-9027
    • Wiltshire, J.T.1    Qiao, G.G.2
  • 86
    • 39749127107 scopus 로고    scopus 로고
    • Synthesis of core cross-linked star polymers with adjustable coronal properties
    • Wiltshire, J. T. & Qiao, G. G. Synthesis of core cross-linked star polymers with adjustable coronal properties. Macromolecules 41, 623-631 (2007).
    • (2007) Macromolecules , vol.41 , pp. 623-631
    • Wiltshire, J.T.1    Qiao, G.G.2
  • 87
    • 84863124640 scopus 로고    scopus 로고
    • Molecular bottlebrushes with polypeptide backbone prepared via ring-opening polymerization of NCA and ATRP
    • Liu, Y., Chen, P. & Li, Z. Molecular bottlebrushes with polypeptide backbone prepared via ring-opening polymerization of NCA and ATRP. Macromol. Rapid Commun. 33, 287-295 (2012).
    • (2012) Macromol. Rapid Commun. , vol.33 , pp. 287-295
    • Liu, Y.1    Chen, P.2    Li, Z.3
  • 88
    • 51549085471 scopus 로고    scopus 로고
    • Hetero-grafted block brushes with PCL and PBA side chains
    • Lee, H-i., Matyjaszewski, K., Yu-Su, S. & Sheiko, S. S. Hetero-grafted block brushes with PCL and PBA side chains. Macromolecules 41, 6073-6080 (2008).
    • (2008) Macromolecules , vol.41 , pp. 6073-6080
    • Lee, H.-I.1    Matyjaszewski, K.2    Yu-Su, S.3    Sheiko, S.S.4
  • 89
    • 0000307127 scopus 로고    scopus 로고
    • Living free radical polymerization of macromonomers: Preparation of well defined graft copolymers
    • Hawker, C. J., et al. Living free radical polymerization of macromonomers: preparation of well defined graft copolymers. Macromol. Chem. Phys. 198, 155-166 (1997).
    • (1997) Macromol. Chem. Phys. , vol.198 , pp. 155-166
    • Hawker, C.J.1
  • 90
    • 33746913474 scopus 로고    scopus 로고
    • Cylindrical core?shell brushes prepared by a combination of ROP and ATRP
    • Lee, H-i., Jakubowski, W., Matyjaszewski, K., Yu, S. & Sheiko, S. S. Cylindrical core?shell brushes prepared by a combination of ROP and ATRP. Macromolecules 39, 4983-4989 (2006).
    • (2006) Macromolecules , vol.39 , pp. 4983-4989
    • Lee, H.-I.1    Jakubowski, W.2    Matyjaszewski, K.3    Yu, S.4    Sheiko, S.S.5
  • 91
    • 84868707532 scopus 로고    scopus 로고
    • Rapidly thiol-responsive degradable block copolymer nanocarriers with facile bioconjugation
    • Aleksanian, S., Khorsand, B., Schmidt, R. & Oh, J. K. Rapidly thiol-responsive degradable block copolymer nanocarriers with facile bioconjugation. Polym. Chem. 3, 2138-2147 (2012).
    • (2012) Polym. Chem. , vol.3 , pp. 2138-2147
    • Aleksanian, S.1    Khorsand, B.2    Schmidt, R.3    Oh, J.K.4
  • 93
    • 0021356699 scopus 로고
    • Degradation of poly(isobutyl cyanoacrylate) nanoparticles
    • Lenaerts, V., et al. Degradation of poly(isobutyl cyanoacrylate) nanoparticles. Biomaterials 5, 65-68 (1984).
    • (1984) Biomaterials , vol.5 , pp. 65-68
    • Lenaerts, V.1
  • 95
    • 77950351203 scopus 로고    scopus 로고
    • Design of fluorescently tagged poly(alkyl cyanoacrylate) nanoparticles for human brain endothelial cell imaging
    • Brambilla, D., et al. Design of fluorescently tagged poly(alkyl cyanoacrylate) nanoparticles for human brain endothelial cell imaging. Chem. Commun. 46, 2602-2604 (2010).
    • (2010) Chem. Commun. , vol.46 , pp. 2602-2604
    • Brambilla, D.1
  • 96
    • 84864273268 scopus 로고    scopus 로고
    • PEGylated nanoparticles bind to and alter amyloid-beta peptide conformation: Toward engineering of functional nanomedicines for Alzheimers disease
    • Brambilla, D., et al. PEGylated nanoparticles bind to and alter amyloid-beta peptide conformation: toward engineering of functional nanomedicines for Alzheimers disease. ACS Nano 6, 5897-5908 (2012).
    • (2012) ACS Nano , vol.6 , pp. 5897-5908
    • Brambilla, D.1
  • 97
    • 84864210191 scopus 로고    scopus 로고
    • Versatile and efficient targeting from a single nanoparticulate platform: Application to cancer and Alzheimers disease
    • Le Droumaguet, B., et al. Versatile and efficient targeting from a single nanoparticulate platform: application to cancer and Alzheimers disease. ACS Nano 6, 5866-5879 (2012).
    • (2012) ACS Nano , vol.6 , pp. 5866-5879
    • Le Droumaguet, B.1
  • 98
    • 84878835759 scopus 로고    scopus 로고
    • Intracellular drug delivery nanocarriers of glutathione-responsive degradable block copolymers having pendant disulfide linkages
    • Khorsand, B., Lapointe, G., Brett, C. & Oh, J. K. Intracellular drug delivery nanocarriers of glutathione-responsive degradable block copolymers having pendant disulfide linkages. Biomacromolecules 14, 2103-2111 (2013).
    • (2013) Biomacromolecules , vol.14 , pp. 2103-2111
    • Khorsand, B.1    Lapointe, G.2    Brett, C.3    Oh, J.K.4
  • 99
    • 36849070485 scopus 로고    scopus 로고
    • Degradable-brushed pHEMA-pDMAEMA synthesized via ATRP and click chemistry for gene delivery
    • Jiang, X., Lok, M. C. & Hennink, W. E. Degradable-brushed pHEMA-pDMAEMA synthesized via ATRP and click chemistry for gene delivery. Bioconjugate Chem. 18, 2077-2084 (2007).
    • (2007) Bioconjugate Chem. , vol.18 , pp. 2077-2084
    • Jiang, X.1    Lok, M.C.2    Hennink, W.E.3
  • 100
    • 84891712440 scopus 로고    scopus 로고
    • Reduction biodegradable brushed PDMAEMA derivatives synthesized by atom transfer radical polymerization and click chemistry for gene delivery
    • Liu, J., et al. Reduction biodegradable brushed PDMAEMA derivatives synthesized by atom transfer radical polymerization and click chemistry for gene delivery. Acta Biomater. 9, 7758-7766 (2013).
    • (2013) Acta Biomater , vol.9 , pp. 7758-7766
    • Liu, J.1
  • 101
    • 22944482156 scopus 로고    scopus 로고
    • Synthesis of degradable miktoarm star copolymers via atom transfer radical polymerization
    • Gao, H., Tsarevsky, N. V. & Matyjaszewski, K. Synthesis of degradable miktoarm star copolymers via atom transfer radical polymerization. Macromolecules 38, 5995-6004 (2005).
    • (2005) Macromolecules , vol.38 , pp. 5995-6004
    • Gao, H.1    Tsarevsky, N.V.2    Matyjaszewski, K.3
  • 102
    • 80053994498 scopus 로고    scopus 로고
    • Synthesis of biocompatible PEG-based
    • star polymers with cationic and degradable core for siRNA delivery
    • Cho, H. Y., et al. Synthesis of biocompatible PEG-based star polymers with cationic and degradable core for siRNA delivery. Biomacromolecules 12, 3478-3486 (2011).
    • (2011) Biomacromolecules , vol.12 , pp. 3478-3486
    • Cho, H.Y.1
  • 103
    • 26944465370 scopus 로고    scopus 로고
    • Synthesis and chemical degradation of branched vinyl polymers prepared via ATRP: Use of a cleavable disulfide-based branching agent
    • Li, Y. & Armes, S. P. Synthesis and chemical degradation of branched vinyl polymers prepared via ATRP: use of a cleavable disulfide-based branching agent. Macromolecules 38, 8155-8162 (2005).
    • (2005) Macromolecules , vol.38 , pp. 8155-8162
    • Li, Y.1    Armes, S.P.2
  • 104
    • 68949171912 scopus 로고    scopus 로고
    • Synthesis of highly branched methacrylic copolymers: Observation of near-ideal behavior using RAFT polymerization
    • Rosselgong, J., Armes, S. P., Barton, W. & Price, D. Synthesis of highly branched methacrylic copolymers: observation of near-ideal behavior using RAFT polymerization. Macromolecules 42, 5919-5924 (2009).
    • (2009) Macromolecules , vol.42 , pp. 5919-5924
    • Rosselgong, J.1    Armes, S.P.2    Barton, W.3    Price, D.4
  • 105
    • 33745548631 scopus 로고    scopus 로고
    • Synthesis and peptide-induced degradation of biocompatible fibers based on highly branched poly(2-hydroxyethyl methacrylate)
    • Wang, L., Li, C., Ryan, A. J. & Armes, S. P. Synthesis and peptide-induced degradation of biocompatible fibers based on highly branched poly(2-hydroxyethyl methacrylate). Adv. Mater. 18, 1566-1570 (2006).
    • (2006) Adv. Mater. , vol.18 , pp. 1566-1570
    • Wang, L.1    Li, C.2    Ryan, A.J.3    Armes, S.P.4
  • 106
    • 1942486827 scopus 로고    scopus 로고
    • Biodegradability of poly(2-hydroxyethyl methacrylate) in the presence of the J774.2 macrophage cell line
    • Mabilleau, G., Moreau, M. F., Filmon, R., Baslé, M. F. & Chappard, D. Biodegradability of poly(2-hydroxyethyl methacrylate) in the presence of the J774.2 macrophage cell line. Biomaterials 25, 5155-5162 (2004).
    • (2004) Biomaterials , vol.25 , pp. 5155-5162
    • Mabilleau, G.1    Moreau, M.F.2    Filmon, R.3    Baslé, M.F.4    Chappard, D.5
  • 107
    • 53849140413 scopus 로고    scopus 로고
    • Novel biodegradable adaptive hydrogels: Controlled synthesis and full characterization of the amphiphilic co-networks
    • Mespouille, L., et al. Novel biodegradable adaptive hydrogels: controlled synthesis and full characterization of the amphiphilic co-networks. Chem. Eur. J. 14, 6369-6378 (2008).
    • (2008) Chem. Eur. J. , vol.14 , pp. 6369-6378
    • Mespouille, L.1
  • 108
    • 80055007412 scopus 로고    scopus 로고
    • Evaluation of redox-responsive disulfide cross-linked poly(hydroxyethyl methacrylate) hydrogels
    • Ejaz, M., et al. Evaluation of redox-responsive disulfide cross-linked poly(hydroxyethyl methacrylate) hydrogels. Polymer 52, 5262-5270 (2011).
    • (2011) Polymer , vol.52 , pp. 5262-5270
    • Ejaz, M.1
  • 109
    • 0037164040 scopus 로고    scopus 로고
    • A novel strategy for encapsulation and release of proteins: Hydrogels and microgels with acid-labile acetal cross-linkers
    • Murthy, N., Thng, Y. X., Schuck, S., Xu, M. C. & Fréchet, J. M. J. A novel strategy for encapsulation and release of proteins: hydrogels and microgels with acid-labile acetal cross-linkers. J. Am. Chem. Soc. 124, 12398-12399 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12398-12399
    • Murthy, N.1    Thng, Y.X.2    Schuck, S.3    Xu, M.C.4    Fréchet, J.M.J.5
  • 110
    • 17444413755 scopus 로고    scopus 로고
    • Combining atom transfer radical polymerization and disulfide/thiol redox chemistry: A route to well-defined (bio)degradable polymeric materials
    • Tsarevsky, N. V. & Matyjaszewski, K. Combining atom transfer radical polymerization and disulfide/thiol redox chemistry: a route to well-defined (bio)degradable polymeric materials. Macromolecules 38, 3087-3092 (2005).
    • (2005) Macromolecules , vol.38 , pp. 3087-3092
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 112
    • 84876173876 scopus 로고    scopus 로고
    • Synthesis and fabrication of a degradable poly(N-isopropyl acrylamide) scaffold for tissue engineering applications
    • Galperin, A., Long, T. J., Garty, S. & Ratner, B. D. Synthesis and fabrication of a degradable poly(N-isopropyl acrylamide) scaffold for tissue engineering applications. J. Biomed. Mater. Res. A 101, 775-786 (2013).
    • (2013) J. Biomed. Mater. Res. A , vol.101 , pp. 775-786
    • Galperin, A.1    Long, T.J.2    Garty, S.3    Ratner, B.D.4
  • 113
    • 68549090562 scopus 로고    scopus 로고
    • Nanostructured hybrid hydrogels prepared by a combination of atom transfer radical polymerization and free radical polymerization
    • Bencherif, S. A., et al. Nanostructured hybrid hydrogels prepared by a combination of atom transfer radical polymerization and free radical polymerization. Biomaterials 30, 5270-5278 (2009).
    • (2009) Biomaterials , vol.30 , pp. 5270-5278
    • Bencherif, S.A.1
  • 114
    • 16344383659 scopus 로고    scopus 로고
    • Chymotrypsin responsive hydrogel: Application of a disulfide exchange protocol for the preparation of methacrylamide containing peptides
    • Plunkett, K. N., Berkowski, K. L. & Moore, J. S. Chymotrypsin responsive hydrogel: application of a disulfide exchange protocol for the preparation of methacrylamide containing peptides. Biomacromolecules 6, 632-637 (2005).
    • (2005) Biomacromolecules , vol.6 , pp. 632-637
    • Plunkett, K.N.1    Berkowski, K.L.2    Moore, J.S.3
  • 115
    • 0038071856 scopus 로고    scopus 로고
    • Tailoring the degradation of hydrogels formed from multivinyl poly(ethylene glycol) and poly(vinyl alcohol) macromers for cartilage tissue engineering
    • Martens, P. J., Bryant, S. J. & Anseth, K. S. Tailoring the degradation of hydrogels formed from multivinyl poly(ethylene glycol) and poly(vinyl alcohol) macromers for cartilage tissue engineering. Biomacromolecules 4, 283-292 (2003).
    • (2003) Biomacromolecules , vol.4 , pp. 283-292
    • Martens, P.J.1    Bryant, S.J.2    Anseth, K.S.3
  • 116
    • 84858137138 scopus 로고    scopus 로고
    • Development of a biostable replacement for PEGDA hydrogels
    • Browning, M. B. & Cosgriff-Hernandez, E. Development of a biostable replacement for PEGDA hydrogels. Biomacromolecules 13, 779-786 (2012).
    • (2012) Biomacromolecules , vol.13 , pp. 779-786
    • Browning, M.B.1    Cosgriff-Hernandez, E.2
  • 117
    • 0037967001 scopus 로고    scopus 로고
    • A macromolecular delivery vehicle for protein-based vaccines: Acid-degradable protein-loaded microgels
    • Murthy, N., et al. A macromolecular delivery vehicle for protein-based vaccines: acid-degradable protein-loaded microgels. Proc. Natl Acad. Sci. USA 100, 4995-5000 (2003).
    • (2003) Proc. Natl Acad. Sci. USA , vol.100 , pp. 4995-5000
    • Murthy, N.1
  • 118
    • 9244220169 scopus 로고    scopus 로고
    • Acid-degradable particles for protein-based vaccines: Enhanced survival rate for tumor-challenged mice using ovalbumin model
    • Standley, S. M., et al. Acid-degradable particles for protein-based vaccines: enhanced survival rate for tumor-challenged mice using ovalbumin model. Bioconjugate Chem. 15, 1281-1288 (2004).
    • (2004) Bioconjugate Chem. , vol.15 , pp. 1281-1288
    • Standley, S.M.1
  • 119
    • 14644426549 scopus 로고    scopus 로고
    • Directed antigen presentation using polymeric microparticulate carriers degradable at lysosomal pH for controlled immune responses
    • Kwon, Y. J., Standley, S. M., Goodwin, A. P., Gillies, E. R. & Fréchet, J. M. J. Directed antigen presentation using polymeric microparticulate carriers degradable at lysosomal pH for controlled immune responses. Mol. Pharm. 2, 83-91 (2005).
    • (2005) Mol. Pharm. , vol.2 , pp. 83-91
    • Kwon, Y.J.1    Standley, S.M.2    Goodwin, A.P.3    Gillies, E.R.4    Fréchet, J.M.J.5
  • 120
    • 2442669391 scopus 로고    scopus 로고
    • Cross-linked microparticles as carriers for the delivery of plasmid DNA for vaccine development
    • Goh, S. L., Murthy, N., Xu, M. & Fréchet, J. M. J. Cross-linked microparticles as carriers for the delivery of plasmid DNA for vaccine development. Bioconjugate Chem. 15, 467-474 (2004).
    • (2004) Bioconjugate Chem. , vol.15 , pp. 467-474
    • Goh, S.L.1    Murthy, N.2    Xu, M.3    Fréchet, J.M.J.4
  • 121
    • 33846405268 scopus 로고    scopus 로고
    • Incorporation of CpG oligonucleotide ligand into protein-loaded particle vaccines promotes antigen-specific CD8 T-cell immunity
    • Standley, S. M., et al. Incorporation of CpG oligonucleotide ligand into protein-loaded particle vaccines promotes antigen-specific CD8 T-cell immunity. Bioconjugate Chem. 18, 77-83 (2006).
    • (2006) Bioconjugate Chem. , vol.18 , pp. 77-83
    • Standley, S.M.1
  • 122
    • 68249106468 scopus 로고    scopus 로고
    • In vivo studies on the effect of co-encapsulation of CpG DNA and antigen in acid-degradable microparticle vaccines
    • Beaudette, T. T., et al. In vivo studies on the effect of co-encapsulation of CpG DNA and antigen in acid-degradable microparticle vaccines. Mol. Pharm. 6, 1160-1169 (2009).
    • (2009) Mol. Pharm. , vol.6 , pp. 1160-1169
    • Beaudette, T.T.1
  • 123
    • 42949116303 scopus 로고    scopus 로고
    • Enhanced cell penetration of acid-degradable particles functionalized with cell-penetrating peptides
    • Cohen, J. L., et al. Enhanced cell penetration of acid-degradable particles functionalized with cell-penetrating peptides. Bioconjugate Chem. 19, 876-881 (2008).
    • (2008) Bioconjugate Chem. , vol.19 , pp. 876-881
    • Cohen, J.L.1
  • 124
    • 33646462613 scopus 로고    scopus 로고
    • Inverse miniemulsion ATRP: A new method for synthesis and functionalization of well-defined water-soluble/cross-linked polymeric particles
    • Oh, J. K., Tang, C., Gao, H., Tsarevsky, N. V. & Matyjaszewski, K. Inverse miniemulsion ATRP: a new method for synthesis and functionalization of well-defined water-soluble/cross-linked polymeric particles. J. Am. Chem. Soc. 128, 5578-5584 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 5578-5584
    • Oh, J.K.1    Tang, C.2    Gao, H.3    Tsarevsky, N.V.4    Matyjaszewski, K.5
  • 125
    • 36649034654 scopus 로고    scopus 로고
    • Synthesis and biodegradation of nanogels as delivery carriers for carbohydrate drugs
    • Oh, J. K., Siegwart, D. J. & Matyjaszewski, K. Synthesis and biodegradation of nanogels as delivery carriers for carbohydrate drugs. Biomacromolecules 8, 3326-3331 (2007).
    • (2007) Biomacromolecules , vol.8 , pp. 3326-3331
    • Oh, J.K.1    Siegwart, D.J.2    Matyjaszewski, K.3
  • 126
    • 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
    • Oh, J. K., et al. 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, 5939-5945 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5939-5945
    • Oh, J.K.1
  • 127
    • 80055023654 scopus 로고    scopus 로고
    • Acid degradable and biocompatible polymeric nanoparticles for the potential codelivery of therapeutic agents
    • Duong, H. T. T., Marquis, C. P., Whittaker, M., Davis, T. P. & Boyer, C. Acid degradable and biocompatible polymeric nanoparticles for the potential codelivery of therapeutic agents. Macromolecules 44, 8008-8019 (2011).
    • (2011) Macromolecules , vol.44 , pp. 8008-8019
    • Duong, H.T.T.1    Marquis, C.P.2    Whittaker, M.3    Davis, T.P.4    Boyer, C.5
  • 128
    • 72449181386 scopus 로고    scopus 로고
    • Synthesis of hyperbranched degradable polymers by atom transfer radical (co)polymerization of inimers with ester or disulfide groups
    • Tsarevsky, N. V., Huang, J. & Matyjaszewski, K. Synthesis of hyperbranched degradable polymers by atom transfer radical (co)polymerization of inimers with ester or disulfide groups. J. Polym. Sci. A 47, 6839-6851 (2009).
    • (2009) J. Polym. Sci. A , vol.47 , pp. 6839-6851
    • Tsarevsky, N.V.1    Huang, J.2    Matyjaszewski, K.3
  • 129
    • 12944288303 scopus 로고    scopus 로고
    • ABC BCD polymerization: A self-condensing vinyl and cyclic ester polymerization by combination free-radical and ring-opening techniques
    • Mecerreyes, D., Trollss, M. & Hedrick, J. L. ABC BCD polymerization: a self-condensing vinyl and cyclic ester polymerization by combination free-radical and ring-opening techniques. Macromolecules 32, 8753-8759 (1999).
    • (1999) Macromolecules , vol.32 , pp. 8753-8759
    • Mecerreyes, D.1    Trollss, M.2    Hedrick, J.L.3
  • 130
    • 77956621320 scopus 로고    scopus 로고
    • Layer-by-layer-assembled capsules and films for therapeutic delivery
    • Becker, A. L., Johnston, A. P. R. & Caruso, F. Layer-by-layer-assembled capsules and films for therapeutic delivery. Small 6, 1836-1852 (2010).
    • (2010) Small , vol.6 , pp. 1836-1852
    • Becker, A.L.1    Johnston, A.P.R.2    Caruso, F.3
  • 131
    • 70350046443 scopus 로고    scopus 로고
    • Low-fouling poly(N-vinyl pyrrolidone) capsules with engineered degradable properties
    • Kinnane, C. R., et al. Low-fouling poly(N-vinyl pyrrolidone) capsules with engineered degradable properties. Biomacromolecules 10, 2839-2846 (2009).
    • (2009) Biomacromolecules , vol.10 , pp. 2839-2846
    • Kinnane, C.R.1
  • 132
    • 77954665290 scopus 로고    scopus 로고
    • Subcompartmentalized polymer hydrogel capsules with selectively degradable carriers and subunits
    • Kulygin, O., et al. Subcompartmentalized polymer hydrogel capsules with selectively degradable carriers and subunits. Small 6, 1558-1564 (2010).
    • (2010) Small , vol.6 , pp. 1558-1564
    • Kulygin, O.1
  • 133
    • 0038387390 scopus 로고    scopus 로고
    • The dawning era of polymer therapeutics
    • Duncan, R. The dawning era of polymer therapeutics. Nature Rev. Drug Discov. 2, 347-360 (2003).
    • (2003) Nature Rev. Drug Discov. , vol.2 , pp. 347-360
    • Duncan, R.1
  • 134
    • 36549050782 scopus 로고    scopus 로고
    • Releasable PEGylation of proteins with customized linkers
    • Filpula, D. & Zhao, H. Releasable PEGylation of proteins with customized linkers. Adv. Drug Deliver. Rev. 60, 29-49 (2008).
    • (2008) Adv. Drug Deliver. Rev. , vol.60 , pp. 29-49
    • Filpula, D.1    Zhao, H.2
  • 135
    • 77955574264 scopus 로고    scopus 로고
    • Recent advances in the design of bioconjugates from controlled/living radical polymerization
    • Le Droumaguet, B. & Nicolas, J. Recent advances in the design of bioconjugates from controlled/living radical polymerization. Polym. Chem. 1, 563-598 (2010).
    • (2010) Polym. Chem. , vol.1 , pp. 563-598
    • Le Droumaguet, B.1    Nicolas, J.2
  • 136
    • 50249149604 scopus 로고    scopus 로고
    • Direct synthesis of well-defined heterotelechelic polymers for bioconjugations
    • Boyer, C., et al. Direct synthesis of well-defined heterotelechelic polymers for bioconjugations. Macromolecules 41, 5641-5650 (2008).
    • (2008) Macromolecules , vol.41 , pp. 5641-5650
    • Boyer, C.1
  • 137
    • 9644254051 scopus 로고    scopus 로고
    • Cysteine-reactive polymers synthesized by atom transfer radical polymerization for conjugation to proteins
    • Bontempo, D., Heredia, K. L., Fish, B. A. & Maynard, H. D. Cysteine-reactive polymers synthesized by atom transfer radical polymerization for conjugation to proteins. J. Am. Chem. Soc. 126, 15372-15373 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 15372-15373
    • Bontempo, D.1    Heredia, K.L.2    Fish, B.A.3    Maynard, H.D.4
  • 138
    • 47249085509 scopus 로고    scopus 로고
    • Reversible siRNA-polymer conjugates by RAFT polymerization
    • Heredia, K. L., et al. Reversible siRNA-polymer conjugates by RAFT polymerization. Chem. Commun. 3245-3247 (2008).
    • (2008) Chem. Commun. , pp. 3245-3247
    • Heredia, K.L.1
  • 139
    • 70350065902 scopus 로고    scopus 로고
    • Branched polymer-protein conjugates made from mid-chain-functional P(HPMA)
    • Tao, L., Liu, J. & Davis, T. P. Branched polymer-protein conjugates made from mid-chain-functional P(HPMA). Biomacromolecules 10, 2847-2851 (2009).
    • (2009) Biomacromolecules , vol.10 , pp. 2847-2851
    • Tao, L.1    Liu, J.2    Davis, T.P.3
  • 141
    • 84925671760 scopus 로고    scopus 로고
    • Degradable PEGylated protein conjugates utilizing RAFT polymerization
    • Decker, C. G. & Maynard, H. D. Degradable PEGylated protein conjugates utilizing RAFT polymerization. Eur. Polym. J. 65, 305-312 (2015).
    • (2015) Eur. Polym. J. , vol.65 , pp. 305-312
    • Decker, C.G.1    Maynard, H.D.2
  • 142
    • 28844444181 scopus 로고    scopus 로고
    • In situ preparation of protein-"smart" polymer conjugates with retention of bioactivity
    • Heredia, K. L., et al. In situ preparation of protein-"smart" polymer conjugates with retention of bioactivity. J. Am. Chem. Soc. 127, 16955-16960 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 16955-16960
    • Heredia, K.L.1
  • 143
    • 34250158892 scopus 로고    scopus 로고
    • In situ formation of protein-polymer conjugates through reversible addition fragmentation chain transfer polymerization
    • Liu, J., et al. In situ formation of protein-polymer conjugates through reversible addition fragmentation chain transfer polymerization. Angew. Chem. Int. Ed. 46, 3099-3103 (2007).
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 3099-3103
    • Liu, J.1


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