메뉴 건너뛰기




Volumn 28, Issue 30, 2012, Pages 11232-11240

Self-assembly of a diblock copolymer with pendant disulfide bonds and chromophore groups: A new platform for fast release

Author keywords

[No Author keywords available]

Indexed keywords

AMPHIPHILIC BLOCK COPOLYMERS; CHROMOPHORE GROUP; DISULFIDE BONDS; EXCIMERS; MICELLAR CORE; MOLECULAR COMPOUNDS; MONOMER PEAKS; POLYMERIC MICELLE; PYRENYL GROUP; RETENTION TIME; SELF-ASSEMBLE; THIOL GROUPS; TRANSMISSION ELECTRON MICROSCOPY TEM;

EID: 84864435960     PISSN: 07437463     EISSN: 15205827     Source Type: Journal    
DOI: 10.1021/la3020817     Document Type: Article
Times cited : (26)

References (41)
  • 1
    • 33751562849 scopus 로고    scopus 로고
    • Polymer genomics: An insight into pharmacology and toxicology of nanomedicines
    • Alexander V, K. Polymer genomics: An insight into pharmacology and toxicology of nanomedicines Adv. Drug Delivery Rev. 2006, 15, 1597-1621
    • (2006) Adv. Drug Delivery Rev. , vol.15 , pp. 1597-1621
    • Alexander, V.K.1
  • 2
    • 0038387390 scopus 로고    scopus 로고
    • The dawning era of polymer therapeutics
    • Duncan, R. The dawning era of polymer therapeutics Nat. Rev. Drug Discovery 2003, 5, 347-360
    • (2003) Nat. Rev. Drug Discovery , vol.5 , pp. 347-360
    • Duncan, R.1
  • 3
    • 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 Delivery Rev. 2001, 1, 113-131
    • (2001) Adv. Drug Delivery Rev. , vol.1 , pp. 113-131
    • Kataoka, K.1    Harada, A.2    Nagasaki, Y.3
  • 4
    • 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 Delivery Rev. 2004, 9, 1273-1289
    • (2004) Adv. Drug Delivery Rev. , vol.9 , pp. 1273-1289
    • Lukyanov, A.N.1    Torchilin, V.P.2
  • 5
    • 34447302274 scopus 로고    scopus 로고
    • Triggered destabilisation of polymeric micelles and vesicles by changing polymers polarity: An attractive tool for drug delivery
    • Rijcken, C. J. F.; Soga, O.; Hennink, W. E.; Nostrum, C. F. v. Triggered destabilisation of polymeric micelles and vesicles by changing polymers polarity: An attractive tool for drug delivery J. Controlled Release 2007, 3, 131-148
    • (2007) J. Controlled Release , vol.3 , pp. 131-148
    • Rijcken, C.J.F.1    Soga, O.2    Hennink, W.E.3    Nostrum, C.F.V.4
  • 6
    • 40549135373 scopus 로고    scopus 로고
    • A Biodegradable pH-sensitive micelle system for targeting acidic solid tumors
    • Sethuraman, V.; Lee, M.; Bae, Y. A Biodegradable pH-sensitive micelle system for targeting acidic solid tumors Pharm. Res. 2008, 3, 657-666
    • (2008) Pharm. Res. , vol.3 , pp. 657-666
    • Sethuraman, V.1    Lee, M.2    Bae, Y.3
  • 7
    • 67650459919 scopus 로고    scopus 로고
    • PH-responsive biodegradable micelles based on acid-labile polycarbonate hydrophobe: Synthesis and triggered drug release
    • Chen, W.; Meng, F.; Li, F.; Ji, S.-J.; Zhong, Z. pH-responsive biodegradable micelles based on acid-labile polycarbonate hydrophobe: synthesis and triggered drug release Biomacromolecules 2009, 7, 1727-1735
    • (2009) Biomacromolecules , vol.7 , pp. 1727-1735
    • Chen, W.1    Meng, F.2    Li, F.3    Ji, S.-J.4    Zhong, Z.5
  • 8
    • 71949095056 scopus 로고    scopus 로고
    • Degradable thermoresponsive core cross-linked micelles: Fabrication, surface functionalization, and biorecognition
    • Jiang, X.; Liu, S.; Narain, R. Degradable thermoresponsive core cross-linked micelles: fabrication, surface functionalization, and biorecognition Langmuir 2009, 23, 13344-13350
    • (2009) Langmuir , vol.23 , pp. 13344-13350
    • Jiang, X.1    Liu, S.2    Narain, R.3
  • 10
    • 77956317952 scopus 로고    scopus 로고
    • Thermo- and light responsive micellation of azobenzene containing block copolymers
    • Jochum, F. D.; Theato, P. Thermo- and light responsive micellation of azobenzene containing block copolymers Chem. Commun. 2010, 36, 6717-6719
    • (2010) Chem. Commun. , vol.36 , pp. 6717-6719
    • Jochum, F.D.1    Theato, P.2
  • 11
    • 83055196964 scopus 로고    scopus 로고
    • Near-infrared light-triggered dissociation of block copolymer micelles using upconverting nanoparticles
    • Yan, B.; Boyer, J.-C.; Branda, N. R.; Zhao, Y. Near-infrared light-triggered dissociation of block copolymer micelles using upconverting nanoparticles J. Am. Chem. Soc. 2011, 49, 19714-19717
    • (2011) J. Am. Chem. Soc. , vol.49 , pp. 19714-19717
    • Yan, B.1    Boyer, J.-C.2    Branda, N.R.3    Zhao, Y.4
  • 12
    • 77954387049 scopus 로고    scopus 로고
    • Disassemblable micelles based on reduction-degradable amphiphilic graft copolymers for intracellular delivery of doxorubicin
    • Sun, Y.; Yan, X.; Yuan, T.; Liang, J.; Fan, Y.; Gu, Z.; Zhang, X. Disassemblable micelles based on reduction-degradable amphiphilic graft copolymers for intracellular delivery of doxorubicin Biomaterials 2010, 27, 7124-7131
    • (2010) Biomaterials , vol.27 , pp. 7124-7131
    • Sun, Y.1    Yan, X.2    Yuan, T.3    Liang, J.4    Fan, Y.5    Gu, Z.6    Zhang, X.7
  • 13
    • 57049181954 scopus 로고    scopus 로고
    • Degradable disulfide core-cross-linked micelles as a drug delivery system prepared from vinyl functionalized nucleosides via the RAFT process
    • Zhang, L.; Liu, W.; Lin, L.; Chen, D.; Stenzel, M. H. Degradable disulfide core-cross-linked micelles as a drug delivery system prepared from vinyl functionalized nucleosides via the RAFT process Biomacromolecules 2008, 11, 3321-3331
    • (2008) Biomacromolecules , vol.11 , pp. 3321-3331
    • Zhang, L.1    Liu, W.2    Lin, L.3    Chen, D.4    Stenzel, M.H.5
  • 15
    • 84862908762 scopus 로고    scopus 로고
    • Degradability of poly(lactic acid)-containing nanoparticles: Enzymatic access through a cross-linked shell barrier
    • Samarajeewa, S.; Shrestha, R.; Li, Y.; Wooley, K. L. Degradability of poly(lactic acid)-containing nanoparticles: enzymatic access through a cross-linked shell barrier J. Am. Chem. Soc. 2011, 2, 1235-1242
    • (2011) J. Am. Chem. Soc. , vol.2 , pp. 1235-1242
    • Samarajeewa, S.1    Shrestha, R.2    Li, Y.3    Wooley, K.L.4
  • 16
    • 80053969259 scopus 로고    scopus 로고
    • Biodegradable block copolymer micelles with thiol-responsive sheddable coronas
    • Khorsand Sourkohi, B.; Cunningham, A.; Zhang, Q.; Oh, J. K. Biodegradable block copolymer micelles with thiol-responsive sheddable coronas Biomacromolecules 2011, 10, 3819-3825
    • (2011) Biomacromolecules , vol.10 , pp. 3819-3825
    • Khorsand Sourkohi, B.1    Cunningham, A.2    Zhang, Q.3    Oh, J.K.4
  • 17
    • 79955805690 scopus 로고    scopus 로고
    • Bioreducible micelles self-assembled from amphiphilic hyperbranched multiarm copolymer for glutathione-mediated intracellular drug delivery
    • Liu, J.; Pang, Y.; Huang, W.; Huang, X.; Meng, L.; Zhu, X.; Zhou, Y.; Yan, D. Bioreducible micelles self-assembled from amphiphilic hyperbranched multiarm copolymer for glutathione-mediated intracellular drug delivery Biomacromolecules 2011, 5, 1567-1577
    • (2011) Biomacromolecules , vol.5 , pp. 1567-1577
    • Liu, J.1    Pang, Y.2    Huang, W.3    Huang, X.4    Meng, L.5    Zhu, X.6    Zhou, Y.7    Yan, D.8
  • 18
    • 77950826451 scopus 로고    scopus 로고
    • Shell-sheddable micelles based on dextran-SS-poly (ε-caprolactone) diblock copolymer for efficient intracellular release of doxorubicin
    • Sun, H.; Guo, B.; Li, X.; Cheng, R.; Meng, F.; Liu, H.; Zhong, Z. Shell-sheddable micelles based on dextran-SS-poly (ε-caprolactone) diblock copolymer for efficient intracellular release of doxorubicin Biomacromolecules 2010, 4, 848-854
    • (2010) Biomacromolecules , vol.4 , pp. 848-854
    • Sun, H.1    Guo, B.2    Li, X.3    Cheng, R.4    Meng, F.5    Liu, H.6    Zhong, Z.7
  • 19
    • 80054808953 scopus 로고    scopus 로고
    • Bioreducible block copolymers based on poly(ethylene glycol) and poly(γ-benzyl l -glutamate) for intracellular delivery of camptothecin
    • Thambi, T.; Yoon, H. Y.; Kim, K.; Kwon, I. C.; Yoo, C. K.; Park, J. H. Bioreducible block copolymers based on poly(ethylene glycol) and poly(γ-benzyl l -glutamate) for intracellular delivery of camptothecin Bioconjugate Chem. 2011, 10, 1924-1931
    • (2011) Bioconjugate Chem. , vol.10 , pp. 1924-1931
    • Thambi, T.1    Yoon, H.Y.2    Kim, K.3    Kwon, I.C.4    Yoo, C.K.5    Park, J.H.6
  • 20
    • 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. 2010, 2, 161-163
    • (2010) Polym. Chem. , vol.2 , pp. 161-163
    • Schumers, J.-M.1    Gohy, J.-F.2    Fustin, C.-A.3
  • 21
    • 33746362871 scopus 로고    scopus 로고
    • Toward Photocontrolled release using light-dissociable block copolymer micelles
    • Jiang, J.; Tong, X.; Morris, D.; Zhao, Y. Toward Photocontrolled release using light-dissociable block copolymer micelles Macromolecules 2006, 13, 4633-4640
    • (2006) Macromolecules , vol.13 , pp. 4633-4640
    • Jiang, J.1    Tong, X.2    Morris, D.3    Zhao, Y.4
  • 22
    • 84255162601 scopus 로고    scopus 로고
    • Synthesis and self-assembly of diblock copolymers bearing 2-nitrobenzyl photocleavable side groups
    • Schumers, J. M.; Bertrand, O.; Fustin, C. A.; Gohy, J. F. Synthesis and self-assembly of diblock copolymers bearing 2-nitrobenzyl photocleavable side groups J. Polym. Sci., Part A: Polym. Chem. 2012, 3, 599-608
    • (2012) J. Polym. Sci., Part A: Polym. Chem. , vol.3 , pp. 599-608
    • Schumers, J.M.1    Bertrand, O.2    Fustin, C.A.3    Gohy, J.F.4
  • 23
    • 20444460701 scopus 로고    scopus 로고
    • A new design for light-breakable polymer micelles
    • Jiang, J.; Tong, X.; Zhao, Y. A new design for light-breakable polymer micelles J. Am. Chem. Soc. 2005, 23, 8290-8291
    • (2005) J. Am. Chem. Soc. , vol.23 , pp. 8290-8291
    • Jiang, J.1    Tong, X.2    Zhao, Y.3
  • 25
    • 0033537026 scopus 로고    scopus 로고
    • Environment-sensitive stabilization of core-shell structured polyion complex micelle by reversible cross-linking of the core through disulfide bond
    • Kakizawa, Y.; Harada, A.; Kataoka, K. Environment-sensitive stabilization of core-shell structured polyion complex micelle by reversible cross-linking of the core through disulfide bond J. Am. Chem. Soc. 1999, 48, 11247-11248
    • (1999) J. Am. Chem. Soc. , vol.48 , pp. 11247-11248
    • Kakizawa, Y.1    Harada, A.2    Kataoka, K.3
  • 28
    • 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.; Siegwart, D. J.; Lee, H.; Sherwood, G.; Peteanu, L.; Hollinger, J. O.; Kataoka, K.; Matyjaszewski, K. Biodegradable nanogels prepared by atom transfer radical polymerization as potential drug delivery carriers: synthesis, biodegradation, in vitro release, and bioconjugation J. Am. Chem. Soc. 2007, 18, 5939-5945
    • (2007) J. Am. Chem. Soc. , vol.18 , pp. 5939-5945
    • Oh, J.K.1    Siegwart, D.J.2    Lee, H.3    Sherwood, G.4    Peteanu, L.5    Hollinger, J.O.6    Kataoka, K.7    Matyjaszewski, K.8
  • 29
    • 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 2005, 8, 3087-3092
    • (2005) Macromolecules , vol.8 , pp. 3087-3092
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 30
    • 79959843144 scopus 로고    scopus 로고
    • Disulfide core cross-linked PEGylated polypeptide nanogel prepared by a one-step ring opening copolymerization of N-carboxyanhydrides for drug delivery
    • Xing, T.; Lai, B.; Ye, X.; Yan, L. Disulfide core cross-linked PEGylated polypeptide nanogel prepared by a one-step ring opening copolymerization of N-carboxyanhydrides for drug delivery Macromol. Biosci. 2011, 7, 962-969
    • (2011) Macromol. Biosci. , vol.7 , pp. 962-969
    • Xing, T.1    Lai, B.2    Ye, X.3    Yan, L.4
  • 31
    • 70749125578 scopus 로고    scopus 로고
    • Facile one-pot preparation of reversible, disulfide-containing shell cross-linked micelles from a RAFT-synthesized, pH-responsive triblock copolymer in water at room temperature
    • Xu, X.; Smith, A. E.; McCormick, C. L. Facile one-pot preparation of reversible, disulfide-containing shell cross-linked micelles from a RAFT-synthesized, pH-responsive triblock copolymer in water at room temperature Aust. J. Chem. 2009, 11, 1520-1527
    • (2009) Aust. J. Chem. , vol.11 , pp. 1520-1527
    • Xu, X.1    Smith, A.E.2    McCormick, C.L.3
  • 33
    • 77953633752 scopus 로고    scopus 로고
    • Surface-functionalizable polymer nanogels with facile hydrophobic guest encapsulation capabilities
    • Ryu, J.-H.; Jiwpanich, S.; Chacko, R.; Bickerton, S.; Thayumanavan, S. Surface-functionalizable polymer nanogels with facile hydrophobic guest encapsulation capabilities J. Am. Chem. Soc. 2010, 24, 8246-8247
    • (2010) J. Am. Chem. Soc. , vol.24 , pp. 8246-8247
    • Ryu, J.-H.1    Jiwpanich, S.2    Chacko, R.3    Bickerton, S.4    Thayumanavan, S.5
  • 34
    • 0035781198 scopus 로고    scopus 로고
    • Metal-catalyzed living radical polymerization
    • Kamigaito, M.; Ando, T.; Sawamoto, M. Metal-catalyzed living radical polymerization Chem. Rev. 2001, 12, 3689-3746
    • (2001) Chem. Rev. , vol.12 , pp. 3689-3746
    • Kamigaito, M.1    Ando, T.2    Sawamoto, M.3
  • 35
    • 0035470133 scopus 로고    scopus 로고
    • Atom transfer radical polymerization
    • Matyjaszewski, K.; Xia, J. Atom transfer radical polymerization Chem. Rev. 2001, 9, 2921-2990
    • (2001) Chem. Rev. , vol.9 , pp. 2921-2990
    • Matyjaszewski, K.1    Xia, J.2
  • 36
    • 60849114425 scopus 로고    scopus 로고
    • Bioconjugation of biotin to the interfaces of polymeric micelles via in situ click chemistry
    • Wang, X.; Liu, L.; Luo, Y.; Zhao, H. Bioconjugation of biotin to the interfaces of polymeric micelles via in situ click chemistry Langmuir 2008, 2, 744-750
    • (2008) Langmuir , vol.2 , pp. 744-750
    • Wang, X.1    Liu, L.2    Luo, Y.3    Zhao, H.4
  • 37
    • 56549116405 scopus 로고    scopus 로고
    • Synthesis of comb copolymers with pendant chromophore groups based on RAFT polymerization and click chemistry and formation of electron donor-acceptor supramolecules
    • Zhang, X.; Lian, X.; Liu, L.; Zhang, J.; Zhao, H. Synthesis of comb copolymers with pendant chromophore groups based on RAFT polymerization and click chemistry and formation of electron donor-acceptor supramolecules Macromolecules 2008, 21, 7863-7869
    • (2008) Macromolecules , vol.21 , pp. 7863-7869
    • Zhang, X.1    Lian, X.2    Liu, L.3    Zhang, J.4    Zhao, H.5
  • 38
    • 78651267711 scopus 로고    scopus 로고
    • Synthesis and self-assembly of amphiphilic asymmetric macromolecular brushes
    • Lian, X.; Wu, D.; Song, X.; Zhao, H. Synthesis and self-assembly of amphiphilic asymmetric macromolecular brushes Macromolecules 2010, 18, 7434-7445
    • (2010) Macromolecules , vol.18 , pp. 7434-7445
    • Lian, X.1    Wu, D.2    Song, X.3    Zhao, H.4
  • 39
    • 33947488208 scopus 로고
    • Reduction of disulfides with tributylphosphine
    • Humphrey, R. E.; Potter, J. L. Reduction of disulfides with tributylphosphine Anal. Chem. 1965, 1, 164-165
    • (1965) Anal. Chem. , vol.1 , pp. 164-165
    • Humphrey, R.E.1    Potter, J.L.2
  • 40
    • 0024311671 scopus 로고
    • The synthesis and properties of block-copoly (amino acid)s with folded structures: A primitive enzyme model
    • Suda, Y.; Ohe, Y.; Okazaki, Y.; Tanimura, K.; Tetsumi, T.; Nishi, M.; Sumi, M. The synthesis and properties of block-copoly (amino acid)s with folded structures: a primitive enzyme model J. Bioact. Compat. Polym. 1989, 2, 137-150
    • (1989) J. Bioact. Compat. Polym. , vol.2 , pp. 137-150
    • Suda, Y.1    Ohe, Y.2    Okazaki, Y.3    Tanimura, K.4    Tetsumi, T.5    Nishi, M.6    Sumi, M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.