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Volumn 470, Issue , 2015, Pages 60-69

RAFT preparation and the aqueous self-assembly of amphiphilic poly(octadecyl acrylate)-block-poly(polyethylene glycol methyl ether acrylate) copolymers

Author keywords

Amphiphilic brush copolymer; Diblock copolymer; PEGylated copolymer; RAFT end group; Self assembly

Indexed keywords

ALIPHATIC COMPOUNDS; BLOCK COPOLYMERS; DYNAMIC LIGHT SCATTERING; ETHERS; GEL PERMEATION CHROMATOGRAPHY; HIGH RESOLUTION TRANSMISSION ELECTRON MICROSCOPY; POLYETHYLENE GLYCOLS; POLYETHYLENES; SELF ASSEMBLY;

EID: 84922720243     PISSN: 09277757     EISSN: 18734359     Source Type: Journal    
DOI: 10.1016/j.colsurfa.2015.01.047     Document Type: Article
Times cited : (20)

References (99)
  • 1
    • 0242584817 scopus 로고    scopus 로고
    • Micellar nanocontainers distribute to defined cytoplasmic organelles
    • Savić R., et al. Micellar nanocontainers distribute to defined cytoplasmic organelles. Science 2003, 300(5619):615-618.
    • (2003) Science , vol.300 , Issue.5619 , pp. 615-618
    • Savić, R.1
  • 2
    • 0035937592 scopus 로고    scopus 로고
    • Block copolymer micelles for drug delivery: design, characterization and biological significance
    • Kataoka K., Harada A., Nagasaki Y. Block copolymer micelles for drug delivery: design, characterization and biological significance. Adv. Drug Deliv. Rev. 2001, 47(1):113-131.
    • (2001) Adv. Drug Deliv. Rev. , vol.47 , Issue.1 , pp. 113-131
    • Kataoka, K.1    Harada, A.2    Nagasaki, Y.3
  • 3
    • 0035803699 scopus 로고    scopus 로고
    • Advanced drug delivery devices via self-assembly of amphiphilic block copolymers
    • Rösler A., Vandermeulen G.W.M., Klok H.-A. Advanced drug delivery devices via self-assembly of amphiphilic block copolymers. Adv. Drug Deliv. Rev. 2001, 53(1):95-108.
    • (2001) Adv. Drug Deliv. Rev. , vol.53 , Issue.1 , pp. 95-108
    • Rösler, A.1    Vandermeulen, G.W.M.2    Klok, H.-A.3
  • 4
    • 28544450961 scopus 로고    scopus 로고
    • Block copolymer micelles: preparation, characterization and application in drug delivery
    • Gaucher G., et al. Block copolymer micelles: preparation, characterization and application in drug delivery. J. Control. Release 2005, 109(1-3):169-188.
    • (2005) J. Control. Release , vol.109 , Issue.1-3 , pp. 169-188
    • Gaucher, G.1
  • 5
    • 0032549746 scopus 로고    scopus 로고
    • Self-assembled aggregates of rod-coil block copolymers and their solubilization and encapsulation of fullerenes
    • Jenekhe S.A., Chen X.L. Self-assembled aggregates of rod-coil block copolymers and their solubilization and encapsulation of fullerenes. Science 1998, 279(5358):1903-1907.
    • (1998) Science , vol.279 , Issue.5358 , pp. 1903-1907
    • Jenekhe, S.A.1    Chen, X.L.2
  • 6
    • 0032874430 scopus 로고    scopus 로고
    • Preparation and characterization of polymer micelles from poly(ethylene glycol)-poly(d,l-lactide) block copolymers as potential drug carrier
    • Yasugi K., et al. Preparation and characterization of polymer micelles from poly(ethylene glycol)-poly(d,l-lactide) block copolymers as potential drug carrier. J. Control. Release 1999, 62(1-2):89-100.
    • (1999) J. Control. Release , vol.62 , Issue.1-2 , pp. 89-100
    • Yasugi, K.1
  • 7
    • 0346914086 scopus 로고    scopus 로고
    • Self-assembly of a novel organometallic-inorganic block copolymer in solution and the solid state: nonintrusive observation of novel wormlike poly(ferrocenyldimethylsilane)-b-poly(dimethylsiloxane) micelles
    • Massey J., et al. Self-assembly of a novel organometallic-inorganic block copolymer in solution and the solid state: nonintrusive observation of novel wormlike poly(ferrocenyldimethylsilane)-b-poly(dimethylsiloxane) micelles. J. Am. Chem. Soc. 1998, 120(37):9533-9540.
    • (1998) J. Am. Chem. Soc. , vol.120 , Issue.37 , pp. 9533-9540
    • Massey, J.1
  • 8
    • 1942486331 scopus 로고    scopus 로고
    • Micelles from lipid derivatives of water-soluble polymers as delivery systems for poorly soluble drugs
    • Lukyanov A.N., Torchilin V.P. Micelles from lipid derivatives of water-soluble polymers as delivery systems for poorly soluble drugs. Adv. Drug Deliv. Rev. 2004, 56(9):1273-1289.
    • (2004) Adv. Drug Deliv. Rev. , vol.56 , Issue.9 , pp. 1273-1289
    • Lukyanov, A.N.1    Torchilin, V.P.2
  • 9
    • 34547561267 scopus 로고    scopus 로고
    • Physical stimuli-responsive polymeric micelles for anti-cancer drug delivery
    • Rapoport N. Physical stimuli-responsive polymeric micelles for anti-cancer drug delivery. Prog. Polym. Sci. 2007, 32(8-9):962-990.
    • (2007) Prog. Polym. Sci. , vol.32 , Issue.8-9 , pp. 962-990
    • Rapoport, N.1
  • 10
    • 78649810957 scopus 로고    scopus 로고
    • Advances in polymeric micelles for drug delivery and tumor targeting
    • Kedar U., et al. Advances in polymeric micelles for drug delivery and tumor targeting. Nanomedicine: NBM 2010, 6(6):714-729.
    • (2010) Nanomedicine: NBM , vol.6 , Issue.6 , pp. 714-729
    • Kedar, U.1
  • 11
    • 0034000453 scopus 로고    scopus 로고
    • Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review
    • Maeda H., et al. Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J. Control. Release 2000, 65(1-2):271-284.
    • (2000) J. Control. Release , vol.65 , Issue.1-2 , pp. 271-284
    • Maeda, H.1
  • 12
    • 33747762229 scopus 로고    scopus 로고
    • Exploiting the enhanced permeability and retention effect for tumor targeting
    • Iyer A.K., et al. Exploiting the enhanced permeability and retention effect for tumor targeting. Drug Discov. Today 2006, 11(17-18):812-818.
    • (2006) Drug Discov. Today , vol.11 , Issue.17-18 , pp. 812-818
    • Iyer, A.K.1
  • 13
    • 0343191443 scopus 로고    scopus 로고
    • 'Stealth' corona-core nanoparticles surface modified by polyethylene glycol (PEG): influences of the corona (PEG chain length and surface density) and of the core composition on phagocytic uptake and plasma protein adsorption
    • Gref R., et al. 'Stealth' corona-core nanoparticles surface modified by polyethylene glycol (PEG): influences of the corona (PEG chain length and surface density) and of the core composition on phagocytic uptake and plasma protein adsorption. Colloids Surf. B 2000, 18(3-4):301-313.
    • (2000) Colloids Surf. B , vol.18 , Issue.3-4 , pp. 301-313
    • Gref, R.1
  • 14
    • 0036164232 scopus 로고    scopus 로고
    • MMA/MPEOMA/VSA copolymer as a novel blood-compatible material: effect of PEO and negatively charged side chains on protein adsorption and platelet adhesion
    • Lee J.H., Oh S.H. MMA/MPEOMA/VSA copolymer as a novel blood-compatible material: effect of PEO and negatively charged side chains on protein adsorption and platelet adhesion. J. Biomed. Mater. Res. 2002, 60(1):44-52.
    • (2002) J. Biomed. Mater. Res. , vol.60 , Issue.1 , pp. 44-52
    • Lee, J.H.1    Oh, S.H.2
  • 15
    • 0032486501 scopus 로고    scopus 로고
    • Comparison of tethered star and linear poly(ethylene oxide) for control of biomaterials surface properties
    • Irvine D.J., et al. Comparison of tethered star and linear poly(ethylene oxide) for control of biomaterials surface properties. J. Biomed. Mater. Res. 1998, 40(3):498-509.
    • (1998) J. Biomed. Mater. Res. , vol.40 , Issue.3 , pp. 498-509
    • Irvine, D.J.1
  • 16
    • 0030213765 scopus 로고    scopus 로고
    • Self-consistent field analysis of grafted star polymers
    • Irvine D.J., Mayes A.M., Griffith-Cima L. Self-consistent field analysis of grafted star polymers. Macromolecules 1996, 29(18):6037-6043.
    • (1996) Macromolecules , vol.29 , Issue.18 , pp. 6037-6043
    • Irvine, D.J.1    Mayes, A.M.2    Griffith-Cima, L.3
  • 17
    • 16344387672 scopus 로고    scopus 로고
    • Comparison of coatings from reactive star shaped PEG-stat-PPG prepolymers and grafted linear PEG for biological and medical applications
    • Groll J., et al. Comparison of coatings from reactive star shaped PEG-stat-PPG prepolymers and grafted linear PEG for biological and medical applications. Biomacromolecules 2005, 6(2):956-962.
    • (2005) Biomacromolecules , vol.6 , Issue.2 , pp. 956-962
    • Groll, J.1
  • 18
    • 81255185800 scopus 로고    scopus 로고
    • Effect of polymer brush architecture on antibiofouling properties
    • Gunkel G., et al. Effect of polymer brush architecture on antibiofouling properties. Biomacromolecules 2011, 12(11):4169-4172.
    • (2011) Biomacromolecules , vol.12 , Issue.11 , pp. 4169-4172
    • Gunkel, G.1
  • 19
    • 47349088100 scopus 로고    scopus 로고
    • Imparting antifouling properties of poly(2-hydroxyethyl methacrylate) hydrogels by grafting poly(oligoethylene glycol methyl ether acrylate)
    • Bozukova D., et al. Imparting antifouling properties of poly(2-hydroxyethyl methacrylate) hydrogels by grafting poly(oligoethylene glycol methyl ether acrylate). Langmuir 2008, 24(13):6649-6658.
    • (2008) Langmuir , vol.24 , Issue.13 , pp. 6649-6658
    • Bozukova, D.1
  • 20
    • 5044233605 scopus 로고    scopus 로고
    • Enhanced stability of core-surface cross-linked micelles fabricated from amphiphilic brush copolymers
    • Xu P., et al. Enhanced stability of core-surface cross-linked micelles fabricated from amphiphilic brush copolymers. Biomacromolecules 2004, 5(5):1736-1744.
    • (2004) Biomacromolecules , vol.5 , Issue.5 , pp. 1736-1744
    • Xu, P.1
  • 21
    • 79955648510 scopus 로고    scopus 로고
    • Steric stabilisation of self-assembled cubic lyotropic liquid crystalline nanoparticles: high throughput evaluation of triblock polyethylene oxide-polypropylene oxide-polyethylene oxide copolymers
    • Chong J.Y.T., et al. Steric stabilisation of self-assembled cubic lyotropic liquid crystalline nanoparticles: high throughput evaluation of triblock polyethylene oxide-polypropylene oxide-polyethylene oxide copolymers. Soft Matter 2011, 7(10):4768-4777.
    • (2011) Soft Matter , vol.7 , Issue.10 , pp. 4768-4777
    • Chong, J.Y.T.1
  • 22
    • 84862852662 scopus 로고    scopus 로고
    • High-throughput discovery of novel steric stabilizers for cubic lyotropic liquid crystal nanoparticle dispersions
    • Chong J.Y.T., et al. High-throughput discovery of novel steric stabilizers for cubic lyotropic liquid crystal nanoparticle dispersions. Langmuir 2012, 28(25):9223-9232.
    • (2012) Langmuir , vol.28 , Issue.25 , pp. 9223-9232
    • Chong, J.Y.T.1
  • 23
    • 84924366598 scopus 로고    scopus 로고
    • Novel steric stabilizers for lyotropic liquid crystalline nanoparticles: PEGylated-phytanyl copolymers
    • Chong J.Y.T., et al. Novel steric stabilizers for lyotropic liquid crystalline nanoparticles: PEGylated-phytanyl copolymers. Langmuir 2014, 10.1021/la501471z.
    • (2014) Langmuir
    • Chong, J.Y.T.1
  • 24
    • 84900400508 scopus 로고    scopus 로고
    • Accelerated Stability Assay (ASA) for colloidal systems
    • Chong J.Y.T., et al. Accelerated Stability Assay (ASA) for colloidal systems. ACS Comb. Sci. 2014, 16(5):205-210.
    • (2014) ACS Comb. Sci. , vol.16 , Issue.5 , pp. 205-210
    • Chong, J.Y.T.1
  • 25
    • 34548045025 scopus 로고    scopus 로고
    • In vivo biological evaluation of high molecular weight hyperbranched polyglycerols
    • Kainthan R.K., Brooks D.E. In vivo biological evaluation of high molecular weight hyperbranched polyglycerols. Biomaterials 2007, 28(32):4779-4787.
    • (2007) Biomaterials , vol.28 , Issue.32 , pp. 4779-4787
    • Kainthan, R.K.1    Brooks, D.E.2
  • 26
    • 77956036859 scopus 로고    scopus 로고
    • Poly(ethylene glycol) in drug delivery: pros and cons as well as potential alternatives
    • Knop K., et al. Poly(ethylene glycol) in drug delivery: pros and cons as well as potential alternatives. Angew. Chem. Int. Ed. 2010, 49(36):6288-6308.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , Issue.36 , pp. 6288-6308
    • Knop, K.1
  • 27
    • 75749110533 scopus 로고    scopus 로고
    • Dendritic polyglycerols for biomedical applications
    • Calderón M., et al. Dendritic polyglycerols for biomedical applications. Adv. Mater. 2010, 22(2):190-218.
    • (2010) Adv. Mater. , vol.22 , Issue.2 , pp. 190-218
    • Calderón, M.1
  • 28
    • 79952768405 scopus 로고    scopus 로고
    • Functionalization of inorganic nanoparticles with polymers for stealth biomedical applications
    • Neoh K.G., Kang E.T. Functionalization of inorganic nanoparticles with polymers for stealth biomedical applications. Polym. Chem. 2011, 2(4):747-759.
    • (2011) Polym. Chem. , vol.2 , Issue.4 , pp. 747-759
    • Neoh, K.G.1    Kang, E.T.2
  • 29
    • 84857119766 scopus 로고    scopus 로고
    • Recent advances in stealth coating of nanoparticle drug delivery systems
    • Amoozgar Z., Yeo Y. Recent advances in stealth coating of nanoparticle drug delivery systems. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2012, 4(2):219-233.
    • (2012) Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. , vol.4 , Issue.2 , pp. 219-233
    • Amoozgar, Z.1    Yeo, Y.2
  • 30
    • 25444497533 scopus 로고    scopus 로고
    • Cylindrical polymer brushes
    • Zhang M., Müller A.H.E. Cylindrical polymer brushes. J. Polym. Sci. A 2005, 43(16):3461-3481.
    • (2005) J. Polym. Sci. A , vol.43 , Issue.16 , pp. 3461-3481
    • Zhang, M.1    Müller, A.H.E.2
  • 31
    • 0000626776 scopus 로고    scopus 로고
    • Molecular bottlebrushes
    • Wintermantel M., et al. Molecular bottlebrushes. Macromolecules 1996, 29(3):978-983.
    • (1996) Macromolecules , vol.29 , Issue.3 , pp. 978-983
    • Wintermantel, M.1
  • 32
    • 85021584376 scopus 로고
    • Study on the radical polymerization behavior of macromonomers
    • Tsukahara Y., et al. Study on the radical polymerization behavior of macromonomers. Macromolecules 1989, 22(4):1546-1552.
    • (1989) Macromolecules , vol.22 , Issue.4 , pp. 1546-1552
    • Tsukahara, Y.1
  • 33
    • 0025590934 scopus 로고
    • Radical polymerization behavior of macromonomers. 2. Comparison of styrene macromonomers having a methacryloyl end group and a vinylbenzyl end group
    • Tsukahara Y., et al. Radical polymerization behavior of macromonomers. 2. Comparison of styrene macromonomers having a methacryloyl end group and a vinylbenzyl end group. Macromolecules 1990, 23(25):5201-5208.
    • (1990) Macromolecules , vol.23 , Issue.25 , pp. 5201-5208
    • Tsukahara, Y.1
  • 35
    • 0032320184 scopus 로고    scopus 로고
    • The synthesis of densely grafted copolymers by atom transfer radical polymerization
    • Beers K.L., et al. The synthesis of densely grafted copolymers by atom transfer radical polymerization. Macromolecules 1998, 31(26):9413-9415.
    • (1998) Macromolecules , vol.31 , Issue.26 , pp. 9413-9415
    • Beers, K.L.1
  • 36
    • 0035949906 scopus 로고    scopus 로고
    • Amphiphilic cylindrical core-shell brushes via a "grafting from" process using ATRP
    • Cheng G., et al. Amphiphilic cylindrical core-shell brushes via a "grafting from" process using ATRP. Macromolecules 2001, 34(20):6883-6888.
    • (2001) Macromolecules , vol.34 , Issue.20 , pp. 6883-6888
    • Cheng, G.1
  • 37
    • 0035913015 scopus 로고    scopus 로고
    • Synthesis of molecular brushes with block copolymer side chains using atom transfer radical polymerization
    • Börner H.G., et al. Synthesis of molecular brushes with block copolymer side chains using atom transfer radical polymerization. Macromolecules 2001, 34(13):4375-4383.
    • (2001) Macromolecules , vol.34 , Issue.13 , pp. 4375-4383
    • Börner, H.G.1
  • 38
    • 0345772124 scopus 로고    scopus 로고
    • Amphiphilic cylindrical brushes with poly(acrylic acid) core and poly(n-butyl acrylate) shell and narrow length distribution
    • Zhang M., et al. Amphiphilic cylindrical brushes with poly(acrylic acid) core and poly(n-butyl acrylate) shell and narrow length distribution. Polymer 2003, 44(5):1449-1458.
    • (2003) Polymer , vol.44 , Issue.5 , pp. 1449-1458
    • Zhang, M.1
  • 39
    • 0001197174 scopus 로고    scopus 로고
    • Synthesis, dimensions and solution properties of linear and macrocyclic poly(chloroethyl vinyl ether)-g-polystyrene comblike polymers
    • Schappacher M., et al. Synthesis, dimensions and solution properties of linear and macrocyclic poly(chloroethyl vinyl ether)-g-polystyrene comblike polymers. Macromol. Chem. Phys. 1999, 200(10):2377-2386.
    • (1999) Macromol. Chem. Phys. , vol.200 , Issue.10 , pp. 2377-2386
    • Schappacher, M.1
  • 40
    • 0038335037 scopus 로고    scopus 로고
    • Functional polystyrene combs and dendrigrafts, 1
    • Schappacher M., Bernard J., Deffieux A. Functional polystyrene combs and dendrigrafts, 1. Macromol. Chem. Phys. 2003, 204(5-6):762-769.
    • (2003) Macromol. Chem. Phys. , vol.204 , Issue.5-6 , pp. 762-769
    • Schappacher, M.1    Bernard, J.2    Deffieux, A.3
  • 41
    • 0032647784 scopus 로고    scopus 로고
    • Synthesis and characterization of star and comb polystyrenes using isometric poly(chloroethyl vinyl ether) oligomers as reactive backbone
    • Deffieux A., Schappacher M. Synthesis and characterization of star and comb polystyrenes using isometric poly(chloroethyl vinyl ether) oligomers as reactive backbone. Macromolecules 1999, 32(6):1797-1802.
    • (1999) Macromolecules , vol.32 , Issue.6 , pp. 1797-1802
    • Deffieux, A.1    Schappacher, M.2
  • 42
    • 0034206994 scopus 로고    scopus 로고
    • Anionic synthesis of well-defined poly(m-halomethylstyrene)s and branched polymers via graft-onto methodology
    • Ryu S.W., Hirao A. Anionic synthesis of well-defined poly(m-halomethylstyrene)s and branched polymers via graft-onto methodology. Macromolecules 2000, 33(13):4765-4771.
    • (2000) Macromolecules , vol.33 , Issue.13 , pp. 4765-4771
    • Ryu, S.W.1    Hirao, A.2
  • 43
    • 80955140308 scopus 로고    scopus 로고
    • Amphiphilic silicone architectures via anaerobic thiol-ene chemistry
    • Keddie D.J., et al. Amphiphilic silicone architectures via anaerobic thiol-ene chemistry. Org. Lett. 2011, 13(22):6006-6009.
    • (2011) Org. Lett. , vol.13 , Issue.22 , pp. 6006-6009
    • Keddie, D.J.1
  • 44
    • 84861572381 scopus 로고    scopus 로고
    • An investigation into the effect of amphiphilic siloxane oligomers on dermal fibroblasts
    • Farrugia B.L., et al. An investigation into the effect of amphiphilic siloxane oligomers on dermal fibroblasts. J. Biomed. Mater. Res. A 2012, 100A(7):1919-1927.
    • (2012) J. Biomed. Mater. Res. A , vol.100 A , Issue.7 , pp. 1919-1927
    • Farrugia, B.L.1
  • 45
    • 0037161412 scopus 로고    scopus 로고
    • Synthesis of molecular brushes with gradient in grafting density by atom transfer polymerization
    • Börner H.G., et al. Synthesis of molecular brushes with gradient in grafting density by atom transfer polymerization. Macromolecules 2002, 35(9):3387-3394.
    • (2002) Macromolecules , vol.35 , Issue.9 , pp. 3387-3394
    • Börner, H.G.1
  • 46
    • 64549145345 scopus 로고    scopus 로고
    • Well-defined brush copolymers with high grafting density of amphiphilic side chains by combination of ROP, ROMP, and ATRP
    • Xie M., et al. Well-defined brush copolymers with high grafting density of amphiphilic side chains by combination of ROP, ROMP, and ATRP. Macromolecules 2008, 41(23):9004-9010.
    • (2008) Macromolecules , vol.41 , Issue.23 , pp. 9004-9010
    • Xie, M.1
  • 47
    • 0347356734 scopus 로고    scopus 로고
    • Synthesis of polymer brushes using atom transfer radical polymerization
    • Pyun J., Kowalewski T., Matyjaszewski K. Synthesis of polymer brushes using atom transfer radical polymerization. Macromol. Rapid Commun. 2003, 24(18):1043-1059.
    • (2003) Macromol. Rapid Commun. , vol.24 , Issue.18 , pp. 1043-1059
    • Pyun, J.1    Kowalewski, T.2    Matyjaszewski, K.3
  • 49
    • 33747199349 scopus 로고    scopus 로고
    • Synthesis of well-defined, brush-type, amphiphilic [poly(styrene-co-2-hydroxyethyl methacrylate)-graft-poly(e{open}-caprolactone)]-b-poly(ethylene oxide)-b-[poly(styrene-co-2-hydroxyethyl methacrylate)-graft-poly(e{open}-caprolactone)] and its aggregation behavior inaqueous media
    • Xu X., et al. Synthesis of well-defined, brush-type, amphiphilic [poly(styrene-co-2-hydroxyethyl methacrylate)-graft-poly(e{open}-caprolactone)]-b-poly(ethylene oxide)-b-[poly(styrene-co-2-hydroxyethyl methacrylate)-graft-poly(e{open}-caprolactone)] and its aggregation behavior inaqueous media. J. Polym. Sci. A 2006, 44(15):4396-4408.
    • (2006) J. Polym. Sci. A , vol.44 , Issue.15 , pp. 4396-4408
    • Xu, X.1
  • 50
    • 27144538616 scopus 로고    scopus 로고
    • Preparation of end-grafted polymer brushes by nitroxide-mediated free radical polymerization of vaporized vinyl monomers
    • Li J., Chen X., Chang Y.-C. Preparation of end-grafted polymer brushes by nitroxide-mediated free radical polymerization of vaporized vinyl monomers. Langmuir 2005, 21(21):9562-9567.
    • (2005) Langmuir , vol.21 , Issue.21 , pp. 9562-9567
    • Li, J.1    Chen, X.2    Chang, Y.-C.3
  • 51
    • 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. 1997, 198(1):155-166.
    • (1997) Macromol. Chem. Phys. , vol.198 , Issue.1 , pp. 155-166
    • Hawker, C.J.1
  • 52
    • 0041473866 scopus 로고    scopus 로고
    • Acrylamide-based amphiphilic block copolymers via nitroxide-mediated radical polymerization
    • Schierholz K., et al. Acrylamide-based amphiphilic block copolymers via nitroxide-mediated radical polymerization. Macromolecules 2003, 36(16):5995-5999.
    • (2003) Macromolecules , vol.36 , Issue.16 , pp. 5995-5999
    • Schierholz, K.1
  • 53
    • 0035800302 scopus 로고    scopus 로고
    • Synthesis of poly(macromonomer)s by repeating ring-opening metathesis polymerization (ROMP) with Mo(CHCMe2Ph)(NAr)(OR)2 initiators
    • Nomura K., Takahashi S., Imanishi Y. Synthesis of poly(macromonomer)s by repeating ring-opening metathesis polymerization (ROMP) with Mo(CHCMe2Ph)(NAr)(OR)2 initiators. Macromolecules 2001, 34(14):4712-4723.
    • (2001) Macromolecules , vol.34 , Issue.14 , pp. 4712-4723
    • Nomura, K.1    Takahashi, S.2    Imanishi, Y.3
  • 54
    • 0037066215 scopus 로고    scopus 로고
    • Well-defined diblock copolymers via termination of living ROMP with anionically polymerized macromolecular aldehydes
    • Notestein J.M., Lee L.-B.W., Register R.A. Well-defined diblock copolymers via termination of living ROMP with anionically polymerized macromolecular aldehydes. Macromolecules 2002, 35(6):1985-1987.
    • (2002) Macromolecules , vol.35 , Issue.6 , pp. 1985-1987
    • Notestein, J.M.1    Lee, L.-B.W.2    Register, R.A.3
  • 55
    • 23844439250 scopus 로고    scopus 로고
    • Dual-brush-type amphiphilic triblock copolymer with intact epoxide functional groups from consecutive RAFT polymerizations and ATRP
    • Cheng Z., et al. Dual-brush-type amphiphilic triblock copolymer with intact epoxide functional groups from consecutive RAFT polymerizations and ATRP. Macromolecules 2005, 38(16):7187-7192.
    • (2005) Macromolecules , vol.38 , Issue.16 , pp. 7187-7192
    • Cheng, Z.1
  • 56
    • 23844519389 scopus 로고    scopus 로고
    • Brush-type amphiphilic diblock copolymers from "living"/controlled radical polymerizations and their aggregation behavior
    • Cheng Z., et al. Brush-type amphiphilic diblock copolymers from "living"/controlled radical polymerizations and their aggregation behavior. Langmuir 2005, 21(16):7180-7185.
    • (2005) Langmuir , vol.21 , Issue.16 , pp. 7180-7185
    • Cheng, Z.1
  • 57
    • 78651267711 scopus 로고    scopus 로고
    • Synthesis and self-assembly of amphiphilic asymmetric macromolecular brushes
    • Lian X., et al. Synthesis and self-assembly of amphiphilic asymmetric macromolecular brushes. Macromolecules 2010, 43(18):7434-7445.
    • (2010) Macromolecules , vol.43 , Issue.18 , pp. 7434-7445
    • Lian, X.1
  • 58
    • 84890842717 scopus 로고    scopus 로고
    • A guide to the synthesis of block copolymers using reversible-addition fragmentation chain transfer (RAFT) polymerization
    • Keddie D.J. A guide to the synthesis of block copolymers using reversible-addition fragmentation chain transfer (RAFT) polymerization. Chem. Soc. Rev. 2014, 43(2):496-505.
    • (2014) Chem. Soc. Rev. , vol.43 , Issue.2 , pp. 496-505
    • Keddie, D.J.1
  • 59
    • 30644477371 scopus 로고    scopus 로고
    • Macromolecular design via reversible addition-fragmentation chain transfer (RAFT)/xanthates (MADIX) polymerization
    • Perrier S., Takolpuckdee P. Macromolecular design via reversible addition-fragmentation chain transfer (RAFT)/xanthates (MADIX) polymerization. J. Polym. Sci. A 2005, 43(22):5347-5393.
    • (2005) J. Polym. Sci. A , vol.43 , Issue.22 , pp. 5347-5393
    • Perrier, S.1    Takolpuckdee, P.2
  • 60
    • 84871600434 scopus 로고    scopus 로고
    • Surface-adhered composite poly(vinyl alcohol) physical hydrogels: polymersome-aided delivery of therapeutic small molecules
    • Hosta-Rigau L., et al. Surface-adhered composite poly(vinyl alcohol) physical hydrogels: polymersome-aided delivery of therapeutic small molecules. Adv. Healthc. Mater. 2012, 1(6):791-795.
    • (2012) Adv. Healthc. Mater. , vol.1 , Issue.6 , pp. 791-795
    • Hosta-Rigau, L.1
  • 61
    • 78650150375 scopus 로고    scopus 로고
    • Synthesis and self-assembly of amphiphilic semi-brush and dual brush block copolymers in solution and on surfaces
    • Zehm D., et al. Synthesis and self-assembly of amphiphilic semi-brush and dual brush block copolymers in solution and on surfaces. Polym. Chem. 2011, 2(1):137-147.
    • (2011) Polym. Chem. , vol.2 , Issue.1 , pp. 137-147
    • Zehm, D.1
  • 62
    • 84905388190 scopus 로고    scopus 로고
    • Controlled synthesis of multifunctional polymers by RAFT for personal care applications
    • American Chemical Society
    • Haeussler M., et al. Controlled synthesis of multifunctional polymers by RAFT for personal care applications. Polymers for Personal Care and Cosmetics 2013, 157-172. American Chemical Society.
    • (2013) Polymers for Personal Care and Cosmetics , pp. 157-172
    • Haeussler, M.1
  • 63
    • 34547157027 scopus 로고    scopus 로고
    • Thiocarbonylthio end group removal from RAFT-synthesized polymers by radical-induced reduction
    • Chong Y.K., et al. Thiocarbonylthio end group removal from RAFT-synthesized polymers by radical-induced reduction. Macromolecules 2007, 40(13):4446-4455.
    • (2007) Macromolecules , vol.40 , Issue.13 , pp. 4446-4455
    • Chong, Y.K.1
  • 64
    • 2542433779 scopus 로고    scopus 로고
    • Amphiphilic block copolymers based on poly(2-acryloyloxyethyl phosphorylcholine) prepared via RAFT polymerisation as biocompatible nanocontainers
    • Stenzel M.H., et al. Amphiphilic block copolymers based on poly(2-acryloyloxyethyl phosphorylcholine) prepared via RAFT polymerisation as biocompatible nanocontainers. Macromol. Biosci. 2004, 4(4):445-453.
    • (2004) Macromol. Biosci. , vol.4 , Issue.4 , pp. 445-453
    • Stenzel, M.H.1
  • 65
    • 34948848666 scopus 로고    scopus 로고
    • Shell-cross-linked micelles containing cationic polymers synthesized via the RAFT process: toward a more biocompatible gene delivery system
    • Zhang L., et al. Shell-cross-linked micelles containing cationic polymers synthesized via the RAFT process: toward a more biocompatible gene delivery system. Biomacromolecules 2007, 8(9):2890-2901.
    • (2007) Biomacromolecules , vol.8 , Issue.9 , pp. 2890-2901
    • Zhang, L.1
  • 66
    • 73249137928 scopus 로고    scopus 로고
    • Bioapplications of RAFT polymerization
    • Boyer C., et al. Bioapplications of RAFT polymerization. Chem. Rev. 2009, 109(11):5402-5436.
    • (2009) Chem. Rev. , vol.109 , Issue.11 , pp. 5402-5436
    • Boyer, C.1
  • 67
    • 76249126590 scopus 로고    scopus 로고
    • In vitro cytotoxicity of RAFT polymers
    • Pissuwan D., et al. In vitro cytotoxicity of RAFT polymers. Biomacromolecules 2010, 11(2):412-420.
    • (2010) Biomacromolecules , vol.11 , Issue.2 , pp. 412-420
    • Pissuwan, D.1
  • 68
    • 34547697294 scopus 로고    scopus 로고
    • Core-shell microspheres with surface grafted poly(vinyl alcohol) as drug carriers for the treatment of hepatocellular carcinoma
    • Nguyen T.L.U., et al. Core-shell microspheres with surface grafted poly(vinyl alcohol) as drug carriers for the treatment of hepatocellular carcinoma. J. Polym. Sci. A 2007, 45(15):3256-3272.
    • (2007) J. Polym. Sci. A , vol.45 , Issue.15 , pp. 3256-3272
    • Nguyen, T.L.U.1
  • 69
    • 72449148216 scopus 로고    scopus 로고
    • Thiocarbonylthio end group removal from RAFT-synthesized polymers by a radical-induced process
    • Chen M., Moad G., Rizzardo E. Thiocarbonylthio end group removal from RAFT-synthesized polymers by a radical-induced process. J. Polym. Sci. A: Polym. Chem. 2009, 47(23):6704-6714.
    • (2009) J. Polym. Sci. A: Polym. Chem. , vol.47 , Issue.23 , pp. 6704-6714
    • Chen, M.1    Moad, G.2    Rizzardo, E.3
  • 70
    • 78650474535 scopus 로고    scopus 로고
    • End-functional polymers, thiocarbonylthio group removal/transformation and reversible addition-fragmentation-chain transfer (RAFT) polymerization
    • Moad G., Rizzardo E., Thang S.H. End-functional polymers, thiocarbonylthio group removal/transformation and reversible addition-fragmentation-chain transfer (RAFT) polymerization. Polym. Int. 2011, 60(1):9-25.
    • (2011) Polym. Int. , vol.60 , Issue.1 , pp. 9-25
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 71
    • 77955254389 scopus 로고    scopus 로고
    • End group removal and modification of RAFT polymers
    • Willcock H., O'Reilly R.K. End group removal and modification of RAFT polymers. Polym. Chem. 2010, 1(2):149-157.
    • (2010) Polym. Chem. , vol.1 , Issue.2 , pp. 149-157
    • Willcock, H.1    O'Reilly, R.K.2
  • 72
    • 0037136162 scopus 로고    scopus 로고
    • Radical deoxygenation of alcohols and vicinal diols with N-ethylpiperidine hypophosphite in water
    • Jang D.O., Cho D.H. Radical deoxygenation of alcohols and vicinal diols with N-ethylpiperidine hypophosphite in water. Tetrahedron Lett. 2002, 43(34):5921-5924.
    • (2002) Tetrahedron Lett. , vol.43 , Issue.34 , pp. 5921-5924
    • Jang, D.O.1    Cho, D.H.2
  • 73
    • 0343114482 scopus 로고    scopus 로고
    • Preparation and characterization of pH-responsive polymeric micelles for the delivery of photosensitizing anticancer drugs
    • Taillefer J., et al. Preparation and characterization of pH-responsive polymeric micelles for the delivery of photosensitizing anticancer drugs. J. Pharm. Sci. 2000, 89(1):52-62.
    • (2000) J. Pharm. Sci. , vol.89 , Issue.1 , pp. 52-62
    • Taillefer, J.1
  • 74
    • 14644437731 scopus 로고    scopus 로고
    • Optimization of the synthesis of poly(octadecyl acrylate) by atom transfer radical polymerization and the preparation of all comblike amphiphilic diblock copolymers
    • Street G., Illsley D., Holder S.J. Optimization of the synthesis of poly(octadecyl acrylate) by atom transfer radical polymerization and the preparation of all comblike amphiphilic diblock copolymers. J. Polym. Sci. A: Polym. Chem. 2005, 43(5):1129-1143.
    • (2005) J. Polym. Sci. A: Polym. Chem. , vol.43 , Issue.5 , pp. 1129-1143
    • Street, G.1    Illsley, D.2    Holder, S.J.3
  • 75
    • 84872101971 scopus 로고    scopus 로고
    • The ends of the story
    • Lavine M.S. The ends of the story. Science 2011, 333(6041):386.
    • (2011) Science , vol.333 , Issue.6041 , pp. 386
    • Lavine, M.S.1
  • 76
    • 79960367214 scopus 로고    scopus 로고
    • Self-assembly of hydrophilic homopolymers: a matter of RAFT end groups
    • Du J., et al. Self-assembly of hydrophilic homopolymers: a matter of RAFT end groups. Small 2011, 7(14):2070-2080.
    • (2011) Small , vol.7 , Issue.14 , pp. 2070-2080
    • Du, J.1
  • 77
    • 84872111272 scopus 로고    scopus 로고
    • Probing into homopolymer self-assembly: how does hydrogen bonding influence morphology?
    • Zhu Y., Liu L., Du J. Probing into homopolymer self-assembly: how does hydrogen bonding influence morphology?. Macromolecules 2012, 46(1):194-203.
    • (2012) Macromolecules , vol.46 , Issue.1 , pp. 194-203
    • Zhu, Y.1    Liu, L.2    Du, J.3
  • 78
    • 84906226140 scopus 로고    scopus 로고
    • Novel RAFT amphiphilic brush copolymer steric stabilisers for cubosomes: poly(octadecyl acrylate)-block-poly(polyethylene glycol methyl ether acrylate)
    • Chong J.Y.T., et al. Novel RAFT amphiphilic brush copolymer steric stabilisers for cubosomes: poly(octadecyl acrylate)-block-poly(polyethylene glycol methyl ether acrylate). Soft Matter 2014, 10(35):6666-6676.
    • (2014) Soft Matter , vol.10 , Issue.35 , pp. 6666-6676
    • Chong, J.Y.T.1
  • 79
    • 0027876078 scopus 로고
    • Critical micellization phenomena in block polyelectrolyte solutions
    • Astafieva I., Zhong X.F., Eisenberg A. Critical micellization phenomena in block polyelectrolyte solutions. Macromolecules 1993, 26(26):7339-7352.
    • (1993) Macromolecules , vol.26 , Issue.26 , pp. 7339-7352
    • Astafieva, I.1    Zhong, X.F.2    Eisenberg, A.3
  • 80
    • 0028413537 scopus 로고
    • Micellization of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymers in aqueous solutions: thermodynamics of copolymer association
    • Alexandridis P., Holzwarth J.F., Hatton T.A. Micellization of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymers in aqueous solutions: thermodynamics of copolymer association. Macromolecules 1994, 27(9):2414-2425.
    • (1994) Macromolecules , vol.27 , Issue.9 , pp. 2414-2425
    • Alexandridis, P.1    Holzwarth, J.F.2    Hatton, T.A.3
  • 81
    • 52949101332 scopus 로고    scopus 로고
    • Synthesis and characterization of perfluorocyclobutyl aryl ether-based amphiphilic diblock copolymer
    • Tong L., et al. Synthesis and characterization of perfluorocyclobutyl aryl ether-based amphiphilic diblock copolymer. Polymer 2008, 49(21):4534-4540.
    • (2008) Polymer , vol.49 , Issue.21 , pp. 4534-4540
    • Tong, L.1
  • 82
    • 65549132877 scopus 로고    scopus 로고
    • PTPFCBBMA-b-PEG-b-PTPFCBBMA amphiphilic triblock copolymer: synthesis and self-assembly behavior
    • Tong L., et al. PTPFCBBMA-b-PEG-b-PTPFCBBMA amphiphilic triblock copolymer: synthesis and self-assembly behavior. Polymer 2009, 50(11):2341-2348.
    • (2009) Polymer , vol.50 , Issue.11 , pp. 2341-2348
    • Tong, L.1
  • 83
    • 84880920672 scopus 로고    scopus 로고
    • Effects of end groups on the thermal response of poly(N-isopropylacrylamide) microgels
    • Chen S., Jiang X., Sun L. Effects of end groups on the thermal response of poly(N-isopropylacrylamide) microgels. J. Appl. Polym. Sci. 2013, 130(2):1164-1171.
    • (2013) J. Appl. Polym. Sci. , vol.130 , Issue.2 , pp. 1164-1171
    • Chen, S.1    Jiang, X.2    Sun, L.3
  • 84
    • 84856302957 scopus 로고    scopus 로고
    • Engineering a sharp physiological transition state for poly(n-isopropylacrylamide) through structural control
    • Chang K., Dicke Z.T., Taite L.J. Engineering a sharp physiological transition state for poly(n-isopropylacrylamide) through structural control. J. Polym. Sci. A: Polym. Chem. 2012, 50(5):976-985.
    • (2012) J. Polym. Sci. A: Polym. Chem. , vol.50 , Issue.5 , pp. 976-985
    • Chang, K.1    Dicke, Z.T.2    Taite, L.J.3
  • 85
    • 55649090812 scopus 로고    scopus 로고
    • Tuning the temperature response of branched poly(N-isopropylacrylamide) prepared by RAFT polymerization
    • Vogt A.P., Sumerlin B.S. Tuning the temperature response of branched poly(N-isopropylacrylamide) prepared by RAFT polymerization. Macromolecules 2008, 41(20):7368-7373.
    • (2008) Macromolecules , vol.41 , Issue.20 , pp. 7368-7373
    • Vogt, A.P.1    Sumerlin, B.S.2
  • 86
    • 33846398136 scopus 로고    scopus 로고
    • Design, synthesis, and aqueous aggregation behavior of nonionic single and multiple thermoresponsive polymers
    • Skrabania K., et al. Design, synthesis, and aqueous aggregation behavior of nonionic single and multiple thermoresponsive polymers. Langmuir 2006, 23(1):84-93.
    • (2006) Langmuir , vol.23 , Issue.1 , pp. 84-93
    • Skrabania, K.1
  • 87
    • 33846156518 scopus 로고    scopus 로고
    • Solution properties of star and linear poly(N-isopropylacrylamide)
    • Plummer R., Hill D.J.T., Whittaker A.K. Solution properties of star and linear poly(N-isopropylacrylamide). Macromolecules 2006, 39(24):8379-8388.
    • (2006) Macromolecules , vol.39 , Issue.24 , pp. 8379-8388
    • Plummer, R.1    Hill, D.J.T.2    Whittaker, A.K.3
  • 88
    • 34547218477 scopus 로고    scopus 로고
    • Highly branched poly-(N-isopropylacrylamide)s with arginine-glycine-aspartic acid (RGD)- or COOH-chain ends that form sub-micron stimulus-responsive particles above the critical solution temperature
    • Rimmer S., et al. Highly branched poly-(N-isopropylacrylamide)s with arginine-glycine-aspartic acid (RGD)- or COOH-chain ends that form sub-micron stimulus-responsive particles above the critical solution temperature. Soft Matter 2007, 3(8):971-973.
    • (2007) Soft Matter , vol.3 , Issue.8 , pp. 971-973
    • Rimmer, S.1
  • 89
    • 62649095349 scopus 로고    scopus 로고
    • Self-assembly of brush-like poly[poly(ethylene glycol) methyl ether methacrylate] synthesized via aqueous atom transfer radical polymerization
    • Hussain H., Mya K.Y., He C. Self-assembly of brush-like poly[poly(ethylene glycol) methyl ether methacrylate] synthesized via aqueous atom transfer radical polymerization. Langmuir 2008, 24(23):13279-13286.
    • (2008) Langmuir , vol.24 , Issue.23 , pp. 13279-13286
    • Hussain, H.1    Mya, K.Y.2    He, C.3
  • 90
    • 0242408160 scopus 로고    scopus 로고
    • ABA triblock copolymers: from controlled synthesis to controlled function
    • Holder S.J., et al. ABA triblock copolymers: from controlled synthesis to controlled function. J. Mater. Chem. 2003, 13(11):2771-2778.
    • (2003) J. Mater. Chem. , vol.13 , Issue.11 , pp. 2771-2778
    • Holder, S.J.1
  • 91
    • 3042517573 scopus 로고    scopus 로고
    • Electroformed giant vesicles from thiophene-containing rod-coil diblock copolymers
    • Vriezema D.M., et al. Electroformed giant vesicles from thiophene-containing rod-coil diblock copolymers. Macromolecules 2004, 37(12):4736-4739.
    • (2004) Macromolecules , vol.37 , Issue.12 , pp. 4736-4739
    • Vriezema, D.M.1
  • 92
    • 76149089224 scopus 로고    scopus 로고
    • Synthesis of hetero-grafted amphiphilic diblock molecular brushes and their self-assembly in aqueous medium
    • Li Z., et al. Synthesis of hetero-grafted amphiphilic diblock molecular brushes and their self-assembly in aqueous medium. Macromolecules 2010, 43(3):1182-1184.
    • (2010) Macromolecules , vol.43 , Issue.3 , pp. 1182-1184
    • Li, Z.1
  • 93
    • 34547876486 scopus 로고    scopus 로고
    • Effect of polymer architecture of amphiphilic poly(2-oxazoline) copolymers on the aggregation and aggregate structure
    • Bonné T.B., et al. Effect of polymer architecture of amphiphilic poly(2-oxazoline) copolymers on the aggregation and aggregate structure. Macromol. Chem. Phys. 2007, 208(13):1402-1408.
    • (2007) Macromol. Chem. Phys. , vol.208 , Issue.13 , pp. 1402-1408
    • Bonné, T.B.1
  • 94
    • 25844470934 scopus 로고    scopus 로고
    • Synthesis and characterization of mPEG-PLA prodrug micelles
    • Hans M., et al. Synthesis and characterization of mPEG-PLA prodrug micelles. Biomacromolecules 2005, 6(5):2708-2717.
    • (2005) Biomacromolecules , vol.6 , Issue.5 , pp. 2708-2717
    • Hans, M.1
  • 95
    • 0038379544 scopus 로고    scopus 로고
    • From vesicle size distributions to bilayer elasticity via cryo-transmission and freeze-fracture electron microscopy
    • Coldren B., et al. From vesicle size distributions to bilayer elasticity via cryo-transmission and freeze-fracture electron microscopy. Langmuir 2003, 19(14):5632-5639.
    • (2003) Langmuir , vol.19 , Issue.14 , pp. 5632-5639
    • Coldren, B.1
  • 96
    • 78651347060 scopus 로고    scopus 로고
    • Controlling the micellar morphology of binary PEO-PCL block copolymers in water-THF through controlled blending
    • Schuetz P., et al. Controlling the micellar morphology of binary PEO-PCL block copolymers in water-THF through controlled blending. Soft Matter 2011, 7(2):749-759.
    • (2011) Soft Matter , vol.7 , Issue.2 , pp. 749-759
    • Schuetz, P.1
  • 97
    • 84879088542 scopus 로고    scopus 로고
    • Functionalized nanoscale micelles improve drug delivery for cancer therapy in vitro and in vivo
    • Wei T., et al. Functionalized nanoscale micelles improve drug delivery for cancer therapy in vitro and in vivo. Nano Lett. 2013, 13(6):2528-2534.
    • (2013) Nano Lett. , vol.13 , Issue.6 , pp. 2528-2534
    • Wei, T.1
  • 98
    • 34249023676 scopus 로고    scopus 로고
    • Functionalized micellar systems for cancer targeted drug delivery
    • Sutton D., et al. Functionalized micellar systems for cancer targeted drug delivery. Pharm. Res. 2007, 24(6):1029-1046.
    • (2007) Pharm. Res. , vol.24 , Issue.6 , pp. 1029-1046
    • Sutton, D.1
  • 99
    • 0001205413 scopus 로고
    • Calculation of HLB values of non-ionic surfactants
    • Griffin W.C. Calculation of HLB values of non-ionic surfactants. J. Soc. Cosmet. Chem. 1954, 5:249.
    • (1954) J. Soc. Cosmet. Chem. , vol.5 , pp. 249
    • Griffin, W.C.1


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