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Volumn 219, Issue , 2015, Pages 383-395

One-component nanomedicine

Author keywords

Drug delivery; Nanomedicine

Indexed keywords

DISEASES; DRUG DELIVERY; FUNCTIONAL POLYMERS;

EID: 84947252300     PISSN: 01683659     EISSN: 18734995     Source Type: Journal    
DOI: 10.1016/j.jconrel.2015.09.056     Document Type: Article
Times cited : (127)

References (189)
  • 1
    • 77955175216 scopus 로고    scopus 로고
    • Strategies in the design of nanoparticles for therapeutic applications
    • R.A. Petros, and J.M. DeSimone Strategies in the design of nanoparticles for therapeutic applications Nat. Rev. Drug Discov. 9 2010 615 627
    • (2010) Nat. Rev. Drug Discov. , vol.9 , pp. 615-627
    • Petros, R.A.1    DeSimone, J.M.2
  • 2
    • 84880789806 scopus 로고    scopus 로고
    • Self-assembled Tat nanofibers as effective drug carrier and transporter
    • P.C. Zhang, A.G. Cheetham, Y.A. Lin, and H. Cui Self-assembled Tat nanofibers as effective drug carrier and transporter ACS Nano 7 2013 5965 5977
    • (2013) ACS Nano , vol.7 , pp. 5965-5977
    • Zhang, P.C.1    Cheetham, A.G.2    Lin, Y.A.3    Cui, H.4
  • 3
    • 14144250911 scopus 로고    scopus 로고
    • Recent advances with liposomes as pharmaceutical carriers
    • V.P. Torchilin Recent advances with liposomes as pharmaceutical carriers Nat. Rev. Drug Discov. 4 2005 145 160
    • (2005) Nat. Rev. Drug Discov. , vol.4 , pp. 145-160
    • Torchilin, V.P.1
  • 4
    • 0036096806 scopus 로고    scopus 로고
    • Liposome-based drug delivery in breast cancer treatment
    • J.W. Park Liposome-based drug delivery in breast cancer treatment Breast Cancer Res. 4 2002 93 97
    • (2002) Breast Cancer Res. , vol.4 , pp. 93-97
    • Park, J.W.1
  • 5
    • 0034734990 scopus 로고    scopus 로고
    • Virosomes: Evolution of the liposome as a targeted drug delivery system
    • Y. Kaneda Virosomes: evolution of the liposome as a targeted drug delivery system Adv. Drug Deliv. Rev. 43 2000 197 205
    • (2000) Adv. Drug Deliv. Rev. , vol.43 , pp. 197-205
    • Kaneda, Y.1
  • 6
    • 84870242534 scopus 로고    scopus 로고
    • Nanoparticle and targeted systems for cancer therapy
    • L. Brannon-Peppas, and J.O. Blanchette Nanoparticle and targeted systems for cancer therapy Adv. Drug Deliv. Rev. 64 2012 206 212
    • (2012) Adv. Drug Deliv. Rev. , vol.64 , pp. 206-212
    • Brannon-Peppas, L.1    Blanchette, J.O.2
  • 8
    • 0032580354 scopus 로고    scopus 로고
    • Drug delivery and targeting
    • R. Langer Drug delivery and targeting Nature 392 1998 5 10
    • (1998) Nature , vol.392 , pp. 5-10
    • Langer, R.1
  • 9
    • 37249093948 scopus 로고    scopus 로고
    • Biodegradable, polymeric nanoparticle delivery systems for cancer therapy
    • E.M. Pridgen, R. Langer, and O.C. Farokhzad Biodegradable, polymeric nanoparticle delivery systems for cancer therapy Nanomedicine (London) 2 2007 669 680
    • (2007) Nanomedicine (London) , vol.2 , pp. 669-680
    • Pridgen, E.M.1    Langer, R.2    Farokhzad, O.C.3
  • 12
    • 33644593095 scopus 로고    scopus 로고
    • PAMAM dendrimer-based multifunctional conjugate for cancer therapy: Synthesis, characterization, and functionality
    • I.J. Majoros, A. Myc, T. Thomas, C.B. Mehta, and J.R. Baker PAMAM dendrimer-based multifunctional conjugate for cancer therapy: synthesis, characterization, and functionality Biomacromolecules 7 2006 572 579
    • (2006) Biomacromolecules , vol.7 , pp. 572-579
    • Majoros, I.J.1    Myc, A.2    Thomas, T.3    Mehta, C.B.4    Baker, J.R.5
  • 14
    • 35948932622 scopus 로고    scopus 로고
    • Synthesis of dendrimers and drug-dendrimer conjugates for drug delivery
    • M. Najlah, and A. D'Emanuele Synthesis of dendrimers and drug-dendrimer conjugates for drug delivery Curr. Opin. Drug Discov. 10 2007 756 767
    • (2007) Curr. Opin. Drug Discov. , vol.10 , pp. 756-767
    • Najlah, M.1    D'Emanuele, A.2
  • 15
    • 84911888348 scopus 로고    scopus 로고
    • PH-responsive supramolecular hydrogels for codelivery of hydrophobic and hydrophilic anticancer drugs
    • J. Yu, W. Ha, J. Chen, and Y.P. Shi pH-responsive supramolecular hydrogels for codelivery of hydrophobic and hydrophilic anticancer drugs RSC Adv. 4 2014 58982 58989
    • (2014) RSC Adv. , vol.4 , pp. 58982-58989
    • Yu, J.1    Ha, W.2    Chen, J.3    Shi, Y.P.4
  • 17
    • 46749132642 scopus 로고    scopus 로고
    • Multifunctional magnetic nanoparticles for targeted imaging and therapy
    • J.R. McCarthy, and R. Weissleder Multifunctional magnetic nanoparticles for targeted imaging and therapy Adv. Drug Deliv. Rev. 60 2008 1241 1251
    • (2008) Adv. Drug Deliv. Rev. , vol.60 , pp. 1241-1251
    • McCarthy, J.R.1    Weissleder, R.2
  • 18
    • 40049086231 scopus 로고    scopus 로고
    • Recent advances in inorganic nanoparticle-based drug delivery systems
    • T. Murakami, and K. Tsuchida Recent advances in inorganic nanoparticle-based drug delivery systems Mini-Rev. Med. Chem. 8 2008 175 183
    • (2008) Mini-Rev. Med. Chem. , vol.8 , pp. 175-183
    • Murakami, T.1    Tsuchida, K.2
  • 19
    • 82455188744 scopus 로고    scopus 로고
    • Recombinant amphiphilic protein micelles for drug delivery
    • W.Y. Kim, J.T. Xiao, and E.L. Chaikof Recombinant amphiphilic protein micelles for drug delivery Langmuir 27 2011 14329 14334
    • (2011) Langmuir , vol.27 , pp. 14329-14334
    • Kim, W.Y.1    Xiao, J.T.2    Chaikof, E.L.3
  • 20
    • 84879389863 scopus 로고    scopus 로고
    • Peptide contour length determines equilibrium secondary structure in protein-analogous micelles
    • R. Marullo, M. Kastantin, L.B. Drews, and M. Tirrell Peptide contour length determines equilibrium secondary structure in protein-analogous micelles Biopolymers 99 2013 573 581
    • (2013) Biopolymers , vol.99 , pp. 573-581
    • Marullo, R.1    Kastantin, M.2    Drews, L.B.3    Tirrell, M.4
  • 21
    • 26944477029 scopus 로고    scopus 로고
    • Modular materials by self-assembly
    • M. Tirrell Modular materials by self-assembly AIChE J. 51 2005 2386 2390
    • (2005) AIChE J. , vol.51 , pp. 2386-2390
    • Tirrell, M.1
  • 22
    • 80053578944 scopus 로고    scopus 로고
    • Structural properties of soluble peptide amphiphile micelles
    • A. Trent, R. Marullo, B. Lin, M. Black, and M. Tirrell Structural properties of soluble peptide amphiphile micelles Soft Matter 7 2011 9572 9582
    • (2011) Soft Matter , vol.7 , pp. 9572-9582
    • Trent, A.1    Marullo, R.2    Lin, B.3    Black, M.4    Tirrell, M.5
  • 24
    • 70249106102 scopus 로고    scopus 로고
    • Nanodiamonds as vehicles for systemic and localized drug delivery
    • R. Lam, and D. Ho Nanodiamonds as vehicles for systemic and localized drug delivery Expert Opin. Drug Deliv. 6 2009 883 895
    • (2009) Expert Opin. Drug Deliv. , vol.6 , pp. 883-895
    • Lam, R.1    Ho, D.2
  • 26
    • 80054986446 scopus 로고    scopus 로고
    • Multimodal nanodiamond drug delivery carriers for selective targeting, imaging, and enhanced chemotherapeutic efficacy
    • X.Q. Zhang, R. Lam, X.Y. Xu, E.K. Chow, H.J. Kim, and D. Ho Multimodal nanodiamond drug delivery carriers for selective targeting, imaging, and enhanced chemotherapeutic efficacy Adv. Mater. 23 2011 4770 4775
    • (2011) Adv. Mater. , vol.23 , pp. 4770-4775
    • Zhang, X.Q.1    Lam, R.2    Xu, X.Y.3    Chow, E.K.4    Kim, H.J.5    Ho, D.6
  • 29
    • 32944466762 scopus 로고    scopus 로고
    • Nanoparticle albumin-bound paclitaxel for metastatic breast cancer
    • M. Harries, P. Ellis, and P. Harper Nanoparticle albumin-bound paclitaxel for metastatic breast cancer J. Clin. Oncol. 23 2005 7768 7771
    • (2005) J. Clin. Oncol. , vol.23 , pp. 7768-7771
    • Harries, M.1    Ellis, P.2    Harper, P.3
  • 30
    • 56949084877 scopus 로고    scopus 로고
    • Albumin as a drug carrier: Design of prodrugs, drug conjugates and nanoparticles
    • F. Kratz Albumin as a drug carrier: design of prodrugs, drug conjugates and nanoparticles J. Control. Release 132 2008 171 183
    • (2008) J. Control. Release , vol.132 , pp. 171-183
    • Kratz, F.1
  • 31
  • 33
    • 77949762340 scopus 로고    scopus 로고
    • Targeting of drugs and nanoparticles to tumors
    • E. Ruoslahti, S.N. Bhatia, and M.J. Sailor Targeting of drugs and nanoparticles to tumors J. Cell Biol. 188 2010 759 768
    • (2010) J. Cell Biol. , vol.188 , pp. 759-768
    • Ruoslahti, E.1    Bhatia, S.N.2    Sailor, M.J.3
  • 34
    • 14644439267 scopus 로고    scopus 로고
    • Cancer nanotechnology: Opportunities and challenges
    • M. Ferrari Cancer nanotechnology: opportunities and challenges Nat. Rev. Cancer 5 2005 161 171
    • (2005) Nat. Rev. Cancer , vol.5 , pp. 161-171
    • Ferrari, M.1
  • 35
    • 84907458579 scopus 로고    scopus 로고
    • Multifunctional nanocarriers for simultaneous encapsulation of hydrophobic and hydrophilic drugs in cancer treatment
    • C.W. Su, C.S. Chiang, W.M. Li, S.H. Hu, and S.Y. Chen Multifunctional nanocarriers for simultaneous encapsulation of hydrophobic and hydrophilic drugs in cancer treatment Nanomedicine (London) 9 2014 1499 1515
    • (2014) Nanomedicine (London) , vol.9 , pp. 1499-1515
    • Su, C.W.1    Chiang, C.S.2    Li, W.M.3    Hu, S.H.4    Chen, S.Y.5
  • 36
    • 81855170441 scopus 로고    scopus 로고
    • Nanomedicine(s) under the microscope
    • R. Duncan, and R. Gaspar Nanomedicine(s) under the microscope Mol. Pharm. 8 2011 2101 2141
    • (2011) Mol. Pharm. , vol.8 , pp. 2101-2141
    • Duncan, R.1    Gaspar, R.2
  • 37
    • 84896528555 scopus 로고    scopus 로고
    • Future opportunities in cancer nanotechnology-NCI strategic workshop report
    • P. Grodzinski, and D. Farrell Future opportunities in cancer nanotechnology-NCI strategic workshop report Cancer Res. 74 2014 1307 1310
    • (2014) Cancer Res. , vol.74 , pp. 1307-1310
    • Grodzinski, P.1    Farrell, D.2
  • 38
    • 84858652159 scopus 로고    scopus 로고
    • Targeted polymeric therapeutic nanoparticles: Design, development and clinical translation
    • N. Kamaly, Z.Y. Xiao, P.M. Valencia, A.F. Radovic-Moreno, and O.C. Farokhzad Targeted polymeric therapeutic nanoparticles: design, development and clinical translation Chem. Soc. Rev. 41 2012 2971 3010
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 2971-3010
    • Kamaly, N.1    Xiao, Z.Y.2    Valencia, P.M.3    Radovic-Moreno, A.F.4    Farokhzad, O.C.5
  • 40
    • 84873275186 scopus 로고    scopus 로고
    • Cancer nanomedicines: So many papers and so few drugs!
    • V.J. Venditto, and F.C. Szoka Cancer nanomedicines: so many papers and so few drugs! Adv. Drug Deliv. Rev. 65 2013 80 88
    • (2013) Adv. Drug Deliv. Rev. , vol.65 , pp. 80-88
    • Venditto, V.J.1    Szoka, F.C.2
  • 41
    • 84919742599 scopus 로고    scopus 로고
    • Supramolecular nanostructures as drug carriers
    • R. Lin, and H.G. Cui Supramolecular nanostructures as drug carriers Curr. Opin. Chem. Eng. 7 2015 75 83
    • (2015) Curr. Opin. Chem. Eng. , vol.7 , pp. 75-83
    • Lin, R.1    Cui, H.G.2
  • 42
    • 70549101139 scopus 로고    scopus 로고
    • Self-assembling chimeric polypeptide-doxorubicin conjugate nanoparticles that abolish tumours after a single injection
    • J.A. MacKay, M.N. Chen, J.R. McDaniel, W.G. Liu, A.J. Simnick, and A. Chilkoti Self-assembling chimeric polypeptide-doxorubicin conjugate nanoparticles that abolish tumours after a single injection Nat. Mater. 8 2009 993 999
    • (2009) Nat. Mater. , vol.8 , pp. 993-999
    • MacKay, J.A.1    Chen, M.N.2    McDaniel, J.R.3    Liu, W.G.4    Simnick, A.J.5    Chilkoti, A.6
  • 43
    • 84862676788 scopus 로고    scopus 로고
    • Squalenoylation: A generic platform for nanoparticular drug delivery
    • D. Desmaele, R. Gref, and P. Couvreur Squalenoylation: a generic platform for nanoparticular drug delivery J. Control. Release 161 2012 609 618
    • (2012) J. Control. Release , vol.161 , pp. 609-618
    • Desmaele, D.1    Gref, R.2    Couvreur, P.3
  • 44
    • 84870249426 scopus 로고    scopus 로고
    • Block copolymer micelles for drug delivery: Design, characterization and biological significance
    • K. Kataoka, A. Harada, and Y. Nagasaki Block copolymer micelles for drug delivery: design, characterization and biological significance Adv. Drug Deliv. Rev. 64 2012 37 48
    • (2012) Adv. Drug Deliv. Rev. , vol.64 , pp. 37-48
    • Kataoka, K.1    Harada, A.2    Nagasaki, Y.3
  • 46
    • 84893472129 scopus 로고    scopus 로고
    • Recent trends in the design of anticancer polymer prodrug nanocarriers
    • V. Delplace, P. Couvreur, and J. Nicolas Recent trends in the design of anticancer polymer prodrug nanocarriers Polym. Chem. (UK) 5 2014 1529 1544
    • (2014) Polym. Chem. (UK) , vol.5 , pp. 1529-1544
    • Delplace, V.1    Couvreur, P.2    Nicolas, J.3
  • 48
    • 84937064628 scopus 로고    scopus 로고
    • Engineering biomaterial-drug conjugates for local and sustained chemotherapeutic delivery
    • J.M. Coburn, and D.L. Kaplan Engineering biomaterial-drug conjugates for local and sustained chemotherapeutic delivery Bioconjug. Chem. 26 2015 1212 1223
    • (2015) Bioconjug. Chem. , vol.26 , pp. 1212-1223
    • Coburn, J.M.1    Kaplan, D.L.2
  • 50
    • 84908004705 scopus 로고    scopus 로고
    • Therapeutic protein-polymer conjugates: Advancing beyond PEGylation
    • E.M. Pelegri-O'Day, E.W. Lin, and H.D. Maynard Therapeutic protein-polymer conjugates: advancing beyond PEGylation J. Am. Chem. Soc. 136 2014 14323 14332
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 14323-14332
    • Pelegri-O'Day, E.M.1    Lin, E.W.2    Maynard, H.D.3
  • 52
    • 84870242380 scopus 로고    scopus 로고
    • Block copolymer micelles as long-circulating drug vehicles
    • G.S. Kwon, and K. Kataoka Block copolymer micelles as long-circulating drug vehicles Adv. Drug Deliv. Rev. 64 2012 237 245
    • (2012) Adv. Drug Deliv. Rev. , vol.64 , pp. 237-245
    • Kwon, G.S.1    Kataoka, K.2
  • 54
    • 84892923466 scopus 로고    scopus 로고
    • Elastin-based protein polymer nanoparticles carrying drug at both corona and core suppress tumor growth in vivo
    • P. Shi, S. Aluri, Y.A. Lin, M. Shah, M. Edman, J. Dhandhukia, H.G. Cui, and J.A. MacKay Elastin-based protein polymer nanoparticles carrying drug at both corona and core suppress tumor growth in vivo J. Control. Release 171 2013 330 338
    • (2013) J. Control. Release , vol.171 , pp. 330-338
    • Shi, P.1    Aluri, S.2    Lin, Y.A.3    Shah, M.4    Edman, M.5    Dhandhukia, J.6    Cui, H.G.7    MacKay, J.A.8
  • 58
    • 84881433502 scopus 로고    scopus 로고
    • Stimuli-responsive copolymer solution and surface assemblies for biomedical applications
    • E.G. Kelley, J.N.L. Albert, M.O. Sullivan, and T.H. Epps Stimuli-responsive copolymer solution and surface assemblies for biomedical applications Chem. Soc. Rev. 42 2013 7057 7071
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 7057-7071
    • Kelley, E.G.1    Albert, J.N.L.2    Sullivan, M.O.3    Epps, T.H.4
  • 59
    • 84891783043 scopus 로고    scopus 로고
    • Self-assembly of natural and synthetic drug amphiphiles into discrete supramolecular nanostructures
    • L.L. Lock, M. LaComb, K. Schwarz, A.G. Cheetham, Y.A. Lin, P.C. Zhang, and H.G. Cui Self-assembly of natural and synthetic drug amphiphiles into discrete supramolecular nanostructures Faraday Discuss. 166 2013 285 301
    • (2013) Faraday Discuss. , vol.166 , pp. 285-301
    • Lock, L.L.1    LaComb, M.2    Schwarz, K.3    Cheetham, A.G.4    Lin, Y.A.5    Zhang, P.C.6    Cui, H.G.7
  • 60
    • 77950342360 scopus 로고    scopus 로고
    • Self-assembly of peptide amphiphiles: From molecules to nanostructures to biomaterials
    • H.G. Cui, M.J. Webber, and S.I. Stupp Self-assembly of peptide amphiphiles: from molecules to nanostructures to biomaterials Biopolymers 94 2010 1 18
    • (2010) Biopolymers , vol.94 , pp. 1-18
    • Cui, H.G.1    Webber, M.J.2    Stupp, S.I.3
  • 61
    • 0035941074 scopus 로고    scopus 로고
    • Self-assembly and mineralization of peptide-amphiphile nanofibers
    • J.D. Hartgerink, E. Beniash, and S.I. Stupp Self-assembly and mineralization of peptide-amphiphile nanofibers Science 294 2001 1684 1688
    • (2001) Science , vol.294 , pp. 1684-1688
    • Hartgerink, J.D.1    Beniash, E.2    Stupp, S.I.3
  • 62
    • 84857319239 scopus 로고    scopus 로고
    • Functional supramolecular polymers
    • T. Aida, E.W. Meijer, and S.I. Stupp Functional supramolecular polymers Science 335 2012 813 817
    • (2012) Science , vol.335 , pp. 813-817
    • Aida, T.1    Meijer, E.W.2    Stupp, S.I.3
  • 64
  • 65
    • 0032901219 scopus 로고    scopus 로고
    • Encapsulation of hydrophilic and lipophilic drugs in PLGA nanoparticles by the nanoprecipitation method
    • J.M. Barichello, M. Morishita, K. Takayama, and T. Nagai Encapsulation of hydrophilic and lipophilic drugs in PLGA nanoparticles by the nanoprecipitation method Drug Dev. Ind. Pharm. 25 1999 471 476
    • (1999) Drug Dev. Ind. Pharm. , vol.25 , pp. 471-476
    • Barichello, J.M.1    Morishita, M.2    Takayama, K.3    Nagai, T.4
  • 66
    • 11144228000 scopus 로고    scopus 로고
    • Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles
    • U. Bilati, E. Allemann, and E. Doelker Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles Eur. J. Pharm. Sci. 24 2005 67 75
    • (2005) Eur. J. Pharm. Sci. , vol.24 , pp. 67-75
    • Bilati, U.1    Allemann, E.2    Doelker, E.3
  • 67
    • 0032952283 scopus 로고    scopus 로고
    • PLGA nanoparticles prepared by nanoprecipitation: Drug loading and release studies of a water soluble drug
    • T. Govender, S. Stolnik, M.C. Garnett, L. Illum, and S.S. Davis PLGA nanoparticles prepared by nanoprecipitation: drug loading and release studies of a water soluble drug J. Control. Release 57 1999 171 185
    • (1999) J. Control. Release , vol.57 , pp. 171-185
    • Govender, T.1    Stolnik, S.2    Garnett, M.C.3    Illum, L.4    Davis, S.S.5
  • 68
    • 37749004225 scopus 로고    scopus 로고
    • Protein therapeutics: A summary and pharmacological classification
    • B. Leader, Q.J. Baca, and D.E. Golan Protein therapeutics: a summary and pharmacological classification Nat. Rev. Drug Discov. 7 2008 21 39
    • (2008) Nat. Rev. Drug Discov. , vol.7 , pp. 21-39
    • Leader, B.1    Baca, Q.J.2    Golan, D.E.3
  • 69
    • 33747840618 scopus 로고    scopus 로고
    • Polymer conjugates as anticancer nanomedicines
    • R. Duncan Polymer conjugates as anticancer nanomedicines Nat. Rev. Cancer 6 2006 688 701
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 688-701
    • Duncan, R.1
  • 70
    • 34547797860 scopus 로고    scopus 로고
    • Anticancer polymeric nanomedicines
    • R. Tong, and J.J. Cheng Anticancer polymeric nanomedicines Polym. Rev. 47 2007 345 381
    • (2007) Polym. Rev. , vol.47 , pp. 345-381
    • Tong, R.1    Cheng, J.J.2
  • 71
    • 0038387390 scopus 로고    scopus 로고
    • The dawning era of polymer therapeutics
    • R. Duncan The dawning era of polymer therapeutics Nat. Rev. Drug Discov. 2 2003 347 360
    • (2003) Nat. Rev. Drug Discov. , vol.2 , pp. 347-360
    • Duncan, R.1
  • 72
    • 0017701219 scopus 로고
    • Alteration of immunological properties of bovine serum-albumin by covalent attachment of polyethylene-glycol
    • A. Abuchowski, T. Vanes, N.C. Palczuk, and F.F. Davis Alteration of immunological properties of bovine serum-albumin by covalent attachment of polyethylene-glycol J. Biol. Chem. 252 1977 3578 3581
    • (1977) J. Biol. Chem. , vol.252 , pp. 3578-3581
    • Abuchowski, A.1    Vanes, T.2    Palczuk, N.C.3    Davis, F.F.4
  • 73
    • 84858228160 scopus 로고    scopus 로고
    • Polymeric conjugates for drug delivery
    • N. Larson, and H. Ghandehari Polymeric conjugates for drug delivery Chem. Mater. 24 2012 840 853
    • (2012) Chem. Mater. , vol.24 , pp. 840-853
    • Larson, N.1    Ghandehari, H.2
  • 74
    • 80051753313 scopus 로고    scopus 로고
    • FDA-approved poly(ethylene glycol)-protein conjugate drugs
    • S.N.S. Alconcel, A.S. Baas, and H.D. Maynard FDA-approved poly(ethylene glycol)-protein conjugate drugs Polym. Chem. (UK) 2 2011 1442 1448
    • (2011) Polym. Chem. (UK) , vol.2 , pp. 1442-1448
    • Alconcel, S.N.S.1    Baas, A.S.2    Maynard, H.D.3
  • 77
    • 24344507278 scopus 로고    scopus 로고
    • Drug-conjugated monoclonal antibodies for the treatment of cancer
    • J.M. Lambert Drug-conjugated monoclonal antibodies for the treatment of cancer Curr. Opin. Pharmacol. 5 2005 543 549
    • (2005) Curr. Opin. Pharmacol. , vol.5 , pp. 543-549
    • Lambert, J.M.1
  • 78
    • 77951586447 scopus 로고    scopus 로고
    • Strategies and challenges for the next generation of therapeutic antibodies
    • A. Beck, T. Wurch, C. Bailly, and N. Corvaia Strategies and challenges for the next generation of therapeutic antibodies Nat. Rev. Immunol. 10 2010 345 352
    • (2010) Nat. Rev. Immunol. , vol.10 , pp. 345-352
    • Beck, A.1    Wurch, T.2    Bailly, C.3    Corvaia, N.4
  • 79
    • 84892615120 scopus 로고    scopus 로고
    • Site-specific antibody drug conjugates for cancer therapy
    • S. Panowski, S. Bhakta, H. Raab, P. Polakis, and J.R. Junutula Site-specific antibody drug conjugates for cancer therapy MAbs 6 2014 34 45
    • (2014) MAbs , vol.6 , pp. 34-45
    • Panowski, S.1    Bhakta, S.2    Raab, H.3    Polakis, P.4    Junutula, J.R.5
  • 80
    • 84923228905 scopus 로고    scopus 로고
    • Site-specific antibody-drug conjugates: The nexus of biciorthogonal chemistry, protein engineering, and drug development
    • P. Agarwal, and C.R. Bertozzi Site-specific antibody-drug conjugates: the nexus of biciorthogonal chemistry, protein engineering, and drug development Bioconjug. Chem. 26 2015 176 192
    • (2015) Bioconjug. Chem. , vol.26 , pp. 176-192
    • Agarwal, P.1    Bertozzi, C.R.2
  • 81
    • 79751479008 scopus 로고    scopus 로고
    • Emerging synthetic approaches for protein-polymer conjugations
    • R.M. Broyer, G.N. Grover, and H.D. Maynard Emerging synthetic approaches for protein-polymer conjugations Chem. Commun. 47 2011 2212 2226
    • (2011) Chem. Commun. , vol.47 , pp. 2212-2226
    • Broyer, R.M.1    Grover, G.N.2    Maynard, H.D.3
  • 82
    • 78649846541 scopus 로고    scopus 로고
    • Protein-polymer conjugates: Synthetic approaches by controlled radical polymerizations and interesting applications
    • G.N. Grover, and H.D. Maynard Protein-polymer conjugates: synthetic approaches by controlled radical polymerizations and interesting applications Curr. Opin. Chem. Biol. 14 2010 818 827
    • (2010) Curr. Opin. Chem. Biol. , vol.14 , pp. 818-827
    • Grover, G.N.1    Maynard, H.D.2
  • 84
    • 65549152299 scopus 로고    scopus 로고
    • Viruses and virus-like protein assemblies-chemically programmable nanoscale building blocks
    • L.A. Lee, Z.W. Niu, and Q. Wang Viruses and virus-like protein assemblies-chemically programmable nanoscale building blocks Nano Res. 2 2009 349 364
    • (2009) Nano Res. , vol.2 , pp. 349-364
    • Lee, L.A.1    Niu, Z.W.2    Wang, Q.3
  • 86
    • 34250211933 scopus 로고    scopus 로고
    • Well-defined protein-polymer conjugates-synthesis and potential applications
    • P. Thordarson, B. Le Droumaguet, and K. Velonia Well-defined protein-polymer conjugates-synthesis and potential applications Appl. Microbiol. Biotechnol. 73 2006 243 254
    • (2006) Appl. Microbiol. Biotechnol. , vol.73 , pp. 243-254
    • Thordarson, P.1    Le Droumaguet, B.2    Velonia, K.3
  • 87
    • 84883308937 scopus 로고    scopus 로고
    • Polymer directed protein assemblies
    • P. van Rijn Polymer directed protein assemblies Polymers (Basel) 5 2013 576 599
    • (2013) Polymers (Basel) , vol.5 , pp. 576-599
    • Van Rijn, P.1
  • 90
    • 33847635554 scopus 로고    scopus 로고
    • Self-assembled architectures from biohybrid triblock copolymers
    • I.C. Reynhout, J.J.L.M. Cornelissen, and R.J.M. Nolte Self-assembled architectures from biohybrid triblock copolymers J. Am. Chem. Soc. 129 2007 2327 2332
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 2327-2332
    • Reynhout, I.C.1    Cornelissen, J.J.L.M.2    Nolte, R.J.M.3
  • 94
    • 78649707326 scopus 로고    scopus 로고
    • Protein-polymer amphiphilic chimeras: Recent advances and future challenges
    • K. Velonia Protein-polymer amphiphilic chimeras: recent advances and future challenges Polym. Chem. (UK) 1 2010 944 952
    • (2010) Polym. Chem. (UK) , vol.1 , pp. 944-952
    • Velonia, K.1
  • 95
    • 51649115626 scopus 로고    scopus 로고
    • In situ ATRP-mediated hierarchical formation of giant amphiphile bionanoreactors
    • B. Le Droumaguet, and K. Velonia In situ ATRP-mediated hierarchical formation of giant amphiphile bionanoreactors Angew. Chem. Int. Ed. 47 2008 6263 6266
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6263-6266
    • Le Droumaguet, B.1    Velonia, K.2
  • 98
    • 0031657330 scopus 로고    scopus 로고
    • Camptothecin delivery systems: Enhanced efficacy and tumor accumulation of camptothecin following its conjugation to polyethylene glycol via a glycine linker
    • C.D. Conover, R.B. Greenwald, A. Pendri, C.W. Gilbert, and K.L. Shum Camptothecin delivery systems: enhanced efficacy and tumor accumulation of camptothecin following its conjugation to polyethylene glycol via a glycine linker Cancer Chemother. Pharmacol. 42 1998 407 414
    • (1998) Cancer Chemother. Pharmacol. , vol.42 , pp. 407-414
    • Conover, C.D.1    Greenwald, R.B.2    Pendri, A.3    Gilbert, C.W.4    Shum, K.L.5
  • 99
    • 0041181628 scopus 로고    scopus 로고
    • HPMA copolymer-anticancer drug conjugates: Design, activity, and mechanism of action
    • J. Kopecek, P. Kopeckova, T. Minko, and Z.R. Lu HPMA copolymer-anticancer drug conjugates: design, activity, and mechanism of action Eur. J. Pharm. Biopharm. 50 2000 61 81
    • (2000) Eur. J. Pharm. Biopharm. , vol.50 , pp. 61-81
    • Kopecek, J.1    Kopeckova, P.2    Minko, T.3    Lu, Z.R.4
  • 100
    • 0035816202 scopus 로고    scopus 로고
    • Water-soluble poly-(L-glutamic acid)-Gly-camptothecin conjugates enhance camptothecin stability and efficacy in vivo
    • J.W. Singer, R. Bhatt, J. Tulinsky, K.R. Buhler, E. Heasley, P. Klein, and P. de Vries Water-soluble poly-(L-glutamic acid)-Gly-camptothecin conjugates enhance camptothecin stability and efficacy in vivo J. Control. Release 74 2001 243 247
    • (2001) J. Control. Release , vol.74 , pp. 243-247
    • Singer, J.W.1    Bhatt, R.2    Tulinsky, J.3    Buhler, K.R.4    Heasley, E.5    Klein, P.6    De Vries, P.7
  • 101
    • 84874606242 scopus 로고    scopus 로고
    • Well-defined degradable brush polymer-drug conjugates for sustained delivery of paclitaxel
    • Y. Yu, C.K. Chen, W.C. Law, J. Mok, J. Zou, P.N. Prasad, and C. Cheng Well-defined degradable brush polymer-drug conjugates for sustained delivery of paclitaxel Mol. Pharm. 10 2013 867 874
    • (2013) Mol. Pharm. , vol.10 , pp. 867-874
    • Yu, Y.1    Chen, C.K.2    Law, W.C.3    Mok, J.4    Zou, J.5    Prasad, P.N.6    Cheng, C.7
  • 102
    • 33646255225 scopus 로고    scopus 로고
    • Polymer-drug conjugates: Progress in polymeric prodrugs
    • J. Khandare, and T. Minko Polymer-drug conjugates: progress in polymeric prodrugs Prog. Polym. Sci. 31 2006 359 397
    • (2006) Prog. Polym. Sci. , vol.31 , pp. 359-397
    • Khandare, J.1    Minko, T.2
  • 104
    • 0025015189 scopus 로고
    • Polymer micelles as novel drug carrier - Adriamycin-conjugated poly(ethylene glycol) poly(aspartic acid) block copolymer
    • M. Yokoyama, M. Miyauchi, N. Yamada, T. Okano, Y. Sakurai, K. Kataoka, and S. Inoue Polymer micelles as novel drug carrier - Adriamycin-conjugated poly(ethylene glycol) poly(aspartic acid) block copolymer J. Control. Release 11 1990 269 278
    • (1990) J. Control. Release , vol.11 , pp. 269-278
    • Yokoyama, M.1    Miyauchi, M.2    Yamada, N.3    Okano, T.4    Sakurai, Y.5    Kataoka, K.6    Inoue, S.7
  • 105
    • 0025343062 scopus 로고
    • Characterization and anticancer activity of the micelle-forming polymeric anticancer drug Adriamycin-conjugated poly(ethylene glycol)-poly(aspartic acid) block copolymer
    • M. Yokoyama, M. Miyauchi, N. Yamada, T. Okano, Y. Sakurai, K. Kataoka, and S. Inoue Characterization and anticancer activity of the micelle-forming polymeric anticancer drug Adriamycin-conjugated poly(ethylene glycol)-poly(aspartic acid) block copolymer Cancer Res. 50 1990 1693 1700
    • (1990) Cancer Res. , vol.50 , pp. 1693-1700
    • Yokoyama, M.1    Miyauchi, M.2    Yamada, N.3    Okano, T.4    Sakurai, Y.5    Kataoka, K.6    Inoue, S.7
  • 106
    • 33750960634 scopus 로고    scopus 로고
    • Supramolecular assemblies of block copolymers in aqueous media as nanocontainers relevant to biological applications
    • A. Harada, and K. Kataoka Supramolecular assemblies of block copolymers in aqueous media as nanocontainers relevant to biological applications Prog. Polym. Sci. 31 2006 949 982
    • (2006) Prog. Polym. Sci. , vol.31 , pp. 949-982
    • Harada, A.1    Kataoka, K.2
  • 107
    • 12344269847 scopus 로고    scopus 로고
    • Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy
    • Y. Bae, N. Nishiyama, S. Fukushima, H. Koyama, M. Yasuhiro, and K. Kataoka Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy Bioconjug. Chem. 16 2005 122 130
    • (2005) Bioconjug. Chem. , vol.16 , pp. 122-130
    • Bae, Y.1    Nishiyama, N.2    Fukushima, S.3    Koyama, H.4    Yasuhiro, M.5    Kataoka, K.6
  • 108
    • 0032472352 scopus 로고    scopus 로고
    • Characterization of physical entrapment and chemical conjugation of Adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor
    • M. Yokoyama, S. Fukushima, R. Uehara, K. Okamoto, K. Kataoka, Y. Sakurai, and T. Okano Characterization of physical entrapment and chemical conjugation of Adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor J. Control. Release 50 1998 79 92
    • (1998) J. Control. Release , vol.50 , pp. 79-92
    • Yokoyama, M.1    Fukushima, S.2    Uehara, R.3    Okamoto, K.4    Kataoka, K.5    Sakurai, Y.6    Okano, T.7
  • 109
    • 0028135121 scopus 로고
    • Improved synthesis of Adriamycin-conjugated poly(ethylene oxide) poly(aspartic acid) block-copolymer and formation of unimodal micellar structure with controlled amount of physically entrapped Adriamycin
    • M. Yokoyama, T. Okano, Y. Sakurai, and K. Kataoka Improved synthesis of Adriamycin-conjugated poly(ethylene oxide) poly(aspartic acid) block-copolymer and formation of unimodal micellar structure with controlled amount of physically entrapped Adriamycin J. Control. Release 32 1994 269 277
    • (1994) J. Control. Release , vol.32 , pp. 269-277
    • Yokoyama, M.1    Okano, T.2    Sakurai, Y.3    Kataoka, K.4
  • 110
    • 77952208384 scopus 로고    scopus 로고
    • Poly(ethylene glycol)-b-poly(epsilon-caprolactone) micelles containing chemically conjugated and physically entrapped docetaxel: Synthesis, characterization, and the influence of the drug on micelle morphology
    • A.S. Mikhail, and C. Allen Poly(ethylene glycol)-b-poly(epsilon-caprolactone) micelles containing chemically conjugated and physically entrapped docetaxel: synthesis, characterization, and the influence of the drug on micelle morphology Biomacromolecules 11 2010 1273 1280
    • (2010) Biomacromolecules , vol.11 , pp. 1273-1280
    • Mikhail, A.S.1    Allen, C.2
  • 111
    • 84867760514 scopus 로고    scopus 로고
    • Synthesis and in vivo pharmacokinetic evaluation of degradable shell cross-linked polymer nanoparticles with poly(carboxybetaine) versus poly(ethylene glycol) surface-grafted coatings
    • A. Li, H.P. Luehmann, G.R. Sun, S. Samarajeewa, J. Zou, S.Y. Zhang, F.W. Zhang, M.J. Welch, Y.J. Liu, and K.L. Wooley Synthesis and in vivo pharmacokinetic evaluation of degradable shell cross-linked polymer nanoparticles with poly(carboxybetaine) versus poly(ethylene glycol) surface-grafted coatings ACS Nano 6 2012 8970 8982
    • (2012) ACS Nano , vol.6 , pp. 8970-8982
    • Li, A.1    Luehmann, H.P.2    Sun, G.R.3    Samarajeewa, S.4    Zou, J.5    Zhang, S.Y.6    Zhang, F.W.7    Welch, M.J.8    Liu, Y.J.9    Wooley, K.L.10
  • 112
    • 84874625977 scopus 로고    scopus 로고
    • In vitro efficacy of paclitaxel-loaded dual-responsive shell cross-linked polymer nanoparticles having orthogonally degradable disulfide cross-linked corona and polyester core domains
    • S. Samarajeewa, R. Shrestha, M. Elsabahy, A. Karwa, A. Li, R.P. Zentay, J.G. Kostelc, R.B. Dorshow, and K.L. Wooley In vitro efficacy of paclitaxel-loaded dual-responsive shell cross-linked polymer nanoparticles having orthogonally degradable disulfide cross-linked corona and polyester core domains Mol. Pharm. 10 2013 1092 1099
    • (2013) Mol. Pharm. , vol.10 , pp. 1092-1099
    • Samarajeewa, S.1    Shrestha, R.2    Elsabahy, M.3    Karwa, A.4    Li, A.5    Zentay, R.P.6    Kostelc, J.G.7    Dorshow, R.B.8    Wooley, K.L.9
  • 113
    • 84880888396 scopus 로고    scopus 로고
    • Shell crosslinked knedel-like nanoparticles for delivery of cisplatin: Effects of crosslinking
    • F.W. Zhang, M. Elsabahy, S.Y. Zhang, L.Y. Lin, J. Zou, and K.L. Wooley Shell crosslinked knedel-like nanoparticles for delivery of cisplatin: effects of crosslinking Nanoscale 5 2013 3220 3225
    • (2013) Nanoscale , vol.5 , pp. 3220-3225
    • Zhang, F.W.1    Elsabahy, M.2    Zhang, S.Y.3    Lin, L.Y.4    Zou, J.5    Wooley, K.L.6
  • 114
    • 84858673601 scopus 로고    scopus 로고
    • Design of polymeric nanoparticles for biomedical delivery applications
    • M. Elsabahy, and K.L. Wooley Design of polymeric nanoparticles for biomedical delivery applications Chem. Soc. Rev. 41 2012 2545 2561
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 2545-2561
    • Elsabahy, M.1    Wooley, K.L.2
  • 115
    • 84875799880 scopus 로고    scopus 로고
    • Poly(ethylene oxide)-block-polyphosphester-based paclitaxel conjugates as a platform for ultra-high paclitaxel-loaded multifunctional nanoparticles
    • S.Y. Zhang, J. Zou, M. Elsabahy, A. Karwa, A. Li, D.A. Moore, R.B. Dorshow, and K.L. Wooley Poly(ethylene oxide)-block-polyphosphester-based paclitaxel conjugates as a platform for ultra-high paclitaxel-loaded multifunctional nanoparticles Chem. Sci. 4 2013 2122 2126
    • (2013) Chem. Sci. , vol.4 , pp. 2122-2126
    • Zhang, S.Y.1    Zou, J.2    Elsabahy, M.3    Karwa, A.4    Li, A.5    Moore, D.A.6    Dorshow, R.B.7    Wooley, K.L.8
  • 116
    • 84895459227 scopus 로고    scopus 로고
    • Poly(ethylene oxide)-block-polyphosphoester-graft-paclitaxel conjugates with acid-labile linkages as a pH-sensitive and functional nanoscopic platform for paclitaxel delivery
    • J. Zou, F.W. Zhang, S.Y. Zhang, S.F. Pollack, M. Elsabahy, J.W. Fan, and K.L. Wooley Poly(ethylene oxide)-block-polyphosphoester-graft-paclitaxel conjugates with acid-labile linkages as a pH-sensitive and functional nanoscopic platform for paclitaxel delivery Adv. Healthc. Mater. 3 2014 441 448
    • (2014) Adv. Healthc. Mater. , vol.3 , pp. 441-448
    • Zou, J.1    Zhang, F.W.2    Zhang, S.Y.3    Pollack, S.F.4    Elsabahy, M.5    Fan, J.W.6    Wooley, K.L.7
  • 118
    • 84876740969 scopus 로고    scopus 로고
    • Giant Gemini surfactants based on polystyrene-hydrophilic polyhedral oligomeric silsesquioxane shape amphiphiles: Sequential "click" chemistry and solution self-assembly
    • Z. Wang, Y.W. Li, X.H. Dong, X.F. Yu, K. Guo, H. Su, K. Yue, C. Wesdemiotis, S.Z.D. Cheng, and W.B. Zhang Giant Gemini surfactants based on polystyrene-hydrophilic polyhedral oligomeric silsesquioxane shape amphiphiles: sequential "click" chemistry and solution self-assembly Chem. Sci. 4 2013 1345 1352
    • (2013) Chem. Sci. , vol.4 , pp. 1345-1352
    • Wang, Z.1    Li, Y.W.2    Dong, X.H.3    Yu, X.F.4    Guo, K.5    Su, H.6    Yue, K.7    Wesdemiotis, C.8    Cheng, S.Z.D.9    Zhang, W.B.10
  • 119
    • 0029311154 scopus 로고
    • Multiple morphologies of crew-cut aggregates of polystyrene-B-poly(acrylic acid) block-copolymers
    • L.F. Zhang, and A. Eisenberg Multiple morphologies of crew-cut aggregates of polystyrene-B-poly(acrylic acid) block-copolymers Science 268 1995 1728 1731
    • (1995) Science , vol.268 , pp. 1728-1731
    • Zhang, L.F.1    Eisenberg, A.2
  • 121
    • 12944257416 scopus 로고    scopus 로고
    • Atom transfer polymerization: Use of uridine and adenosine derivatized monomers and initiators
    • A. Marsh, A. Khan, D.M. Haddleton, and M.J. Hannon Atom transfer polymerization: use of uridine and adenosine derivatized monomers and initiators Macromolecules 32 1999 8725 8731
    • (1999) Macromolecules , vol.32 , pp. 8725-8731
    • Marsh, A.1    Khan, A.2    Haddleton, D.M.3    Hannon, M.J.4
  • 122
    • 72449201610 scopus 로고    scopus 로고
    • Polymeric phosphorylcholine-camptothecin conjugates prepared by controlled free radical polymerization and click chemistry
    • X.J. Chen, S. McRae, S. Parelkar, and T. Emrick Polymeric phosphorylcholine-camptothecin conjugates prepared by controlled free radical polymerization and click chemistry Bioconjug. Chem. 20 2009 2331 2341
    • (2009) Bioconjug. Chem. , vol.20 , pp. 2331-2341
    • Chen, X.J.1    McRae, S.2    Parelkar, S.3    Emrick, T.4
  • 123
    • 84873390333 scopus 로고    scopus 로고
    • Nanoparticles with in vivo anticancer activity from polymer prodrug amphiphiles prepared by living radical polymerization
    • S. Harrisson, J. Nicolas, A. Maksimenko, D.T. Bui, J. Mougin, and P. Couvreur Nanoparticles with in vivo anticancer activity from polymer prodrug amphiphiles prepared by living radical polymerization Angew. Chem. Int. Ed. 52 2013 1678 1682
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 1678-1682
    • Harrisson, S.1    Nicolas, J.2    Maksimenko, A.3    Bui, D.T.4    Mougin, J.5    Couvreur, P.6
  • 124
    • 84903289431 scopus 로고    scopus 로고
    • Significant tumor growth inhibition from naturally occurring lipid-containing polymer prodrug nanoparticles obtained by the drug-initiated method
    • A. Maksimenko, D.T. Bui, D. Desmaele, P. Couvreur, and J. Nicolas Significant tumor growth inhibition from naturally occurring lipid-containing polymer prodrug nanoparticles obtained by the drug-initiated method Chem. Mater. 26 2014 3606 3609
    • (2014) Chem. Mater. , vol.26 , pp. 3606-3609
    • Maksimenko, A.1    Bui, D.T.2    Desmaele, D.3    Couvreur, P.4    Nicolas, J.5
  • 127
    • 48849091040 scopus 로고    scopus 로고
    • Paclitaxel-initiated, controlled polymerization of lactide for the formulation of polymeric nanoparticulate delivery vehicles
    • R. Tong, and J.J. Cheng Paclitaxel-initiated, controlled polymerization of lactide for the formulation of polymeric nanoparticulate delivery vehicles Angew. Chem. Int. Ed. 47 2008 4830 4834
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4830-4834
    • Tong, R.1    Cheng, J.J.2
  • 128
    • 67749111695 scopus 로고    scopus 로고
    • Ring-opening polymerization-mediated controlled formulation of polylactide-drug nanoparticles
    • R. Tong, and J.J. Cheng Ring-opening polymerization-mediated controlled formulation of polylactide-drug nanoparticles J. Am. Chem. Soc. 131 2009 4744 4754
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4744-4754
    • Tong, R.1    Cheng, J.J.2
  • 129
    • 77950354591 scopus 로고    scopus 로고
    • Elastin-like polypeptides: Biomedical applications of tunable biopolymers
    • S.R. MacEwan, and A. Chilkoti Elastin-like polypeptides: biomedical applications of tunable biopolymers Biopolymers 94 2010 60 77
    • (2010) Biopolymers , vol.94 , pp. 60-77
    • MacEwan, S.R.1    Chilkoti, A.2
  • 130
    • 0037130974 scopus 로고    scopus 로고
    • Design of thermally responsive, recombinant polypeptide carriers for targeted drug delivery
    • A. Chilkoti, M.R. Dreher, and D.E. Meyer Design of thermally responsive, recombinant polypeptide carriers for targeted drug delivery Adv. Drug Deliv. Rev. 54 2002 1093 1111
    • (2002) Adv. Drug Deliv. Rev. , vol.54 , pp. 1093-1111
    • Chilkoti, A.1    Dreher, M.R.2    Meyer, D.E.3
  • 132
    • 0035866357 scopus 로고    scopus 로고
    • Targeting a genetically engineered elastin-like polypeptide to solid tumors by local hyperthermia
    • D.E. Meyer, G.A. Kong, M.W. Dewhirst, M.R. Zalutsky, and A. Chilkoti Targeting a genetically engineered elastin-like polypeptide to solid tumors by local hyperthermia Cancer Res. 61 2001 1548 1554
    • (2001) Cancer Res. , vol.61 , pp. 1548-1554
    • Meyer, D.E.1    Kong, G.A.2    Dewhirst, M.W.3    Zalutsky, M.R.4    Chilkoti, A.5
  • 134
    • 29244462519 scopus 로고    scopus 로고
    • Structural optimization of a "smart" doxorubicin-polypeptide conjugate for thermally targeted delivery to solid tumors
    • D.Y. Furgeson, M.R. Dreher, and A. Chilkoti Structural optimization of a "smart" doxorubicin-polypeptide conjugate for thermally targeted delivery to solid tumors J. Control. Release 110 2006 362 369
    • (2006) J. Control. Release , vol.110 , pp. 362-369
    • Furgeson, D.Y.1    Dreher, M.R.2    Chilkoti, A.3
  • 135
    • 33751434981 scopus 로고    scopus 로고
    • Stimulus responsive elastin biopolymers: Applications in medicine and biotechnology
    • A. Chilkoti, T. Christensen, and J.A. MacKay Stimulus responsive elastin biopolymers: applications in medicine and biotechnology Curr. Opin. Chem. Biol. 10 2006 652 657
    • (2006) Curr. Opin. Chem. Biol. , vol.10 , pp. 652-657
    • Chilkoti, A.1    Christensen, T.2    MacKay, J.A.3
  • 136
    • 84873325849 scopus 로고    scopus 로고
    • Self-assembly of thermally responsive nanoparticles of a genetically encoded peptide polymer by drug conjugation
    • J.R. McDaniel, J. Bhattacharyya, K.B. Vargo, W. Hassouneh, D.A. Hammer, and A. Chilkoti Self-assembly of thermally responsive nanoparticles of a genetically encoded peptide polymer by drug conjugation Angew. Chem. Int. Ed. 52 2013 1683 1687
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 1683-1687
    • McDaniel, J.R.1    Bhattacharyya, J.2    Vargo, K.B.3    Hassouneh, W.4    Hammer, D.A.5    Chilkoti, A.6
  • 137
    • 84900466456 scopus 로고    scopus 로고
    • Rational design of "heat seeking" drug loaded polypeptide nanoparticles that thermally target solid tumors
    • J.R. McDaniel, S.R. MacEwan, X.H. Li, D.C. Radford, C.D. Landon, M. Dewhirst, and A. Chilkoti Rational design of "heat seeking" drug loaded polypeptide nanoparticles that thermally target solid tumors Nano Lett. 14 2014 2890 2895
    • (2014) Nano Lett. , vol.14 , pp. 2890-2895
    • McDaniel, J.R.1    MacEwan, S.R.2    Li, X.H.3    Radford, D.C.4    Landon, C.D.5    Dewhirst, M.6    Chilkoti, A.7
  • 140
    • 0342316475 scopus 로고    scopus 로고
    • Polymeric drugs based on conjugates of synthetic and natural macromolecules I. Synthesis and physico-chemical characterisation
    • K. Ulbrich, V. Subr, J. Strohalm, D. Plocova, M. Jelinkova, and B. Rihova Polymeric drugs based on conjugates of synthetic and natural macromolecules I. Synthesis and physico-chemical characterisation J. Control. Release 64 2000 63 79
    • (2000) J. Control. Release , vol.64 , pp. 63-79
    • Ulbrich, K.1    Subr, V.2    Strohalm, J.3    Plocova, D.4    Jelinkova, M.5    Rihova, B.6
  • 141
    • 1942438684 scopus 로고    scopus 로고
    • Polymeric anticancer drugs with pH-controlled activation
    • K. Ulbrich, and V. Subr Polymeric anticancer drugs with pH-controlled activation Adv. Drug Deliv. Rev. 56 2004 1023 1050
    • (2004) Adv. Drug Deliv. Rev. , vol.56 , pp. 1023-1050
    • Ulbrich, K.1    Subr, V.2
  • 143
    • 84874887528 scopus 로고    scopus 로고
    • Biodegradable ferulic acid-containing poly(anhydride-ester): Degradation products with controlled release and sustained antioxidant activity
    • M.A. Ouimet, J. Griffin, A.L. Carbone-Howell, W.H. Wu, N.D. Stebbins, R. Di, and K.E. Uhrich Biodegradable ferulic acid-containing poly(anhydride-ester): degradation products with controlled release and sustained antioxidant activity Biomacromolecules 14 2013 854 861
    • (2013) Biomacromolecules , vol.14 , pp. 854-861
    • Ouimet, M.A.1    Griffin, J.2    Carbone-Howell, A.L.3    Wu, W.H.4    Stebbins, N.D.5    Di, R.6    Uhrich, K.E.7
  • 144
    • 84885622596 scopus 로고    scopus 로고
    • Biodegradable polyesters containing ibuprofen and naproxen as pendant groups
    • R. Rosario-Melendez, W.L. Yu, and K.E. Uhrich Biodegradable polyesters containing ibuprofen and naproxen as pendant groups Biomacromolecules 14 2013 3542 3548
    • (2013) Biomacromolecules , vol.14 , pp. 3542-3548
    • Rosario-Melendez, R.1    Yu, W.L.2    Uhrich, K.E.3
  • 145
    • 23644442075 scopus 로고    scopus 로고
    • Controllable selective synthesis of a polymerizable prodrug of cytarabine by enzymatic and chemical methods
    • N. Wang, Z.C. Chen, D. Lu, and M.F. Lin Controllable selective synthesis of a polymerizable prodrug of cytarabine by enzymatic and chemical methods Bioorg. Med. Chem. Lett. 15 2005 4064 4067
    • (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 4064-4067
    • Wang, N.1    Chen, Z.C.2    Lu, D.3    Lin, M.F.4
  • 146
    • 33645857400 scopus 로고    scopus 로고
    • Controllable synthesis of polymerizable ester and amide prodrugs of acyclovir by enzyme in organic solvent
    • X. Li, Q. Wu, D.S. Lv, and X.F. Lin Controllable synthesis of polymerizable ester and amide prodrugs of acyclovir by enzyme in organic solvent Bioorg. Med. Chem. 14 2006 3377 3382
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 3377-3382
    • Li, X.1    Wu, Q.2    Lv, D.S.3    Lin, X.F.4
  • 147
    • 84907564348 scopus 로고    scopus 로고
    • Polymerizable disulfide paclitaxel prodrug for controlled drug delivery
    • Y. Ding, W.L. Chen, J.H. Hu, M. Du, and D. Yang Polymerizable disulfide paclitaxel prodrug for controlled drug delivery Mater. Sci. Eng. C Mater. 44 2014 386 390
    • (2014) Mater. Sci. Eng. C Mater. , vol.44 , pp. 386-390
    • Ding, Y.1    Chen, W.L.2    Hu, J.H.3    Du, M.4    Yang, D.5
  • 148
    • 84888355194 scopus 로고    scopus 로고
    • Polyprodrug amphiphiles: Hierarchical assemblies for shape-regulated cellular internalization, trafficking, and drug delivery
    • X.L. Hu, J.M. Hu, J. Tian, Z.S. Ge, G.Y. Zhang, K.F. Luo, and S.Y. Liu Polyprodrug amphiphiles: hierarchical assemblies for shape-regulated cellular internalization, trafficking, and drug delivery J. Am. Chem. Soc. 135 2013 17617 17629
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 17617-17629
    • Hu, X.L.1    Hu, J.M.2    Tian, J.3    Ge, Z.S.4    Zhang, G.Y.5    Luo, K.F.6    Liu, S.Y.7
  • 150
    • 84899506759 scopus 로고    scopus 로고
    • A convergent synthetic platform for single-nanoparticle combination cancer therapy: Ratiometric loading and controlled release of cisplatin, doxorubicin, and camptothecin
    • L.Y. Liao, J. Liu, E.C. Dreaden, S.W. Morton, K.E. Shopsowitz, P.T. Hammond, and J.A. Johnson A convergent synthetic platform for single-nanoparticle combination cancer therapy: ratiometric loading and controlled release of cisplatin, doxorubicin, and camptothecin J. Am. Chem. Soc. 136 2014 5896 5899
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 5896-5899
    • Liao, L.Y.1    Liu, J.2    Dreaden, E.C.3    Morton, S.W.4    Shopsowitz, K.E.5    Hammond, P.T.6    Johnson, J.A.7
  • 151
    • 84915753675 scopus 로고    scopus 로고
    • Synthesis of acid-labile PEG and PEG-doxorubicin-conjugate nanoparticles via brush-first ROMP
    • A.X. Gao, L.Y. Liao, and J.A. Johnson Synthesis of acid-labile PEG and PEG-doxorubicin-conjugate nanoparticles via brush-first ROMP ACS Macro Lett. 3 2014 854 857
    • (2014) ACS Macro Lett. , vol.3 , pp. 854-857
    • Gao, A.X.1    Liao, L.Y.2    Johnson, J.A.3
  • 152
    • 79959972712 scopus 로고    scopus 로고
    • Prodrugs for improving tumor targetability and efficiency
    • R. Mahato, W.Y. Tai, and K. Cheng Prodrugs for improving tumor targetability and efficiency Adv. Drug Deliv. Rev. 63 2011 659 670
    • (2011) Adv. Drug Deliv. Rev. , vol.63 , pp. 659-670
    • Mahato, R.1    Tai, W.Y.2    Cheng, K.3
  • 153
    • 79960671231 scopus 로고    scopus 로고
    • Prodrugs-from serendipity to rational design
    • K.M. Huttunen, H. Raunio, and J. Rautio Prodrugs-from serendipity to rational design Pharmacol. Rev. 63 2011 750 771
    • (2011) Pharmacol. Rev. , vol.63 , pp. 750-771
    • Huttunen, K.M.1    Raunio, H.2    Rautio, J.3
  • 154
    • 52049105453 scopus 로고    scopus 로고
    • Recent trends in targeted anticancer prodrug and conjugate design
    • Y. Singh, M. Palombo, and P.J. Sinko Recent trends in targeted anticancer prodrug and conjugate design Curr. Med. Chem. 15 2008 1802 1826
    • (2008) Curr. Med. Chem. , vol.15 , pp. 1802-1826
    • Singh, Y.1    Palombo, M.2    Sinko, P.J.3
  • 155
    • 84889031691 scopus 로고    scopus 로고
    • Self-assembly of squalene-based nucleolipids: Relating the chemical structure of the bioconjugates to the architecture of the nanoparticles
    • E. Lepeltier, C. Bourgaux, V. Rosilio, J.H. Poupaert, F. Meneau, F. Zouhiri, S. Lepetre-Mouelhi, D. Desmaele, and P. Couvreur Self-assembly of squalene-based nucleolipids: relating the chemical structure of the bioconjugates to the architecture of the nanoparticles Langmuir 29 2013 14795 14803
    • (2013) Langmuir , vol.29 , pp. 14795-14803
    • Lepeltier, E.1    Bourgaux, C.2    Rosilio, V.3    Poupaert, J.H.4    Meneau, F.5    Zouhiri, F.6    Lepetre-Mouelhi, S.7    Desmaele, D.8    Couvreur, P.9
  • 157
    • 77954871375 scopus 로고    scopus 로고
    • Novel nanoassemblies composed of squalenoyl-paclitaxel derivatives: Synthesis, characterization, and biological evaluation
    • F. Dosio, L.H. Reddy, A. Ferrero, B. Stella, L. Cattel, and P. Couvreur Novel nanoassemblies composed of squalenoyl-paclitaxel derivatives: synthesis, characterization, and biological evaluation Bioconjug. Chem. 21 2010 1349 1361
    • (2010) Bioconjug. Chem. , vol.21 , pp. 1349-1361
    • Dosio, F.1    Reddy, L.H.2    Ferrero, A.3    Stella, B.4    Cattel, L.5    Couvreur, P.6
  • 159
  • 163
    • 84906351138 scopus 로고    scopus 로고
    • Combination of small molecule prodrug and nanodrug delivery: Amphiphilic drug-Drug conjugate for cancer Therapy
    • P. Huang, D.L. Wang, Y. Su, W. Huang, Y.F. Zhou, D.X. Cui, X.Y. Zhu, and D.Y. Yan Combination of small molecule prodrug and nanodrug delivery: amphiphilic drug-Drug conjugate for cancer Therapy J. Am. Chem. Soc. 136 2014 11748 11756
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 11748-11756
    • Huang, P.1    Wang, D.L.2    Su, Y.3    Huang, W.4    Zhou, Y.F.5    Cui, D.X.6    Zhu, X.Y.7    Yan, D.Y.8
  • 164
    • 60649096673 scopus 로고    scopus 로고
    • Self-assembling materials for therapeutic delivery
    • M.C. Branco, and J.P. Schneider Self-assembling materials for therapeutic delivery Acta Biomater. 5 2009 817 831
    • (2009) Acta Biomater. , vol.5 , pp. 817-831
    • Branco, M.C.1    Schneider, J.P.2
  • 165
    • 4444292034 scopus 로고    scopus 로고
    • Bottom-up design of biomimetic assemblies
    • R.S. Tu, and M. Tirrell Bottom-up design of biomimetic assemblies Adv. Drug Deliv. Rev. 56 2004 1537 1563
    • (2004) Adv. Drug Deliv. Rev. , vol.56 , pp. 1537-1563
    • Tu, R.S.1    Tirrell, M.2
  • 166
    • 84870940796 scopus 로고    scopus 로고
    • Controlling peptide-based hydrogelation
    • H.M. Wang, Z.M. Yang, and D.J. Adams Controlling peptide-based hydrogelation Mater. Today 15 2012 500 507
    • (2012) Mater. Today , vol.15 , pp. 500-507
    • Wang, H.M.1    Yang, Z.M.2    Adams, D.J.3
  • 167
    • 1842454609 scopus 로고    scopus 로고
    • Water gelation by small organic molecules
    • L.A. Estroff, and A.D. Hamilton Water gelation by small organic molecules Chem. Rev. 104 2004 1201 1217
    • (2004) Chem. Rev. , vol.104 , pp. 1201-1217
    • Estroff, L.A.1    Hamilton, A.D.2
  • 169
    • 84901194883 scopus 로고    scopus 로고
    • Supramolecular hydrogels made of basic biological building blocks
    • X.W. Du, J. Zhou, and B. Xu Supramolecular hydrogels made of basic biological building blocks Chem. Asian. J. 9 2014 1446 1472
    • (2014) Chem. Asian. J. , vol.9 , pp. 1446-1472
    • Du, X.W.1    Zhou, J.2    Xu, B.3
  • 172
    • 63049113732 scopus 로고    scopus 로고
    • Molecular hydrogels of therapeutic agents
    • F. Zhao, M.L. Ma, and B. Xu Molecular hydrogels of therapeutic agents Chem. Soc. Rev. 38 2009 883 891
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 883-891
    • Zhao, F.1    Ma, M.L.2    Xu, B.3
  • 174
    • 33745938073 scopus 로고    scopus 로고
    • Enzyme catalysis: Tool to make and break amygdalin hydrogelators from renewable resources: A delivery model for hydrophobic drugs
    • P.K. Vemula, J. Li, and G. John Enzyme catalysis: tool to make and break amygdalin hydrogelators from renewable resources: a delivery model for hydrophobic drugs J. Am. Chem. Soc. 128 2006 8932 8938
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 8932-8938
    • Vemula, P.K.1    Li, J.2    John, G.3
  • 175
    • 55249104281 scopus 로고    scopus 로고
    • Self-assembled prodrugs: An enzymatically triggered drug-delivery platform
    • P.K. Vemula, G.A. Cruikshank, J.M. Karp, and G. John Self-assembled prodrugs: an enzymatically triggered drug-delivery platform Biomaterials 30 2009 383 393
    • (2009) Biomaterials , vol.30 , pp. 383-393
    • Vemula, P.K.1    Cruikshank, G.A.2    Karp, J.M.3    John, G.4
  • 176
    • 0037132667 scopus 로고    scopus 로고
    • Hydrophobic interaction and hydrogen bonding cooperatively confer a vancomycin hydrogel: A potential candidate for biomaterials
    • B.G. Xing, C.W. Yu, K.H. Chow, P.L. Ho, D.G. Fu, and B. Xu Hydrophobic interaction and hydrogen bonding cooperatively confer a vancomycin hydrogel: a potential candidate for biomaterials J. Am. Chem. Soc. 124 2002 14846 14847
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 14846-14847
    • Xing, B.G.1    Yu, C.W.2    Chow, K.H.3    Ho, P.L.4    Fu, D.G.5    Xu, B.6
  • 177
    • 70349756884 scopus 로고    scopus 로고
    • Enzyme-instructed molecular self-assembly confers nanofibers and a supramolecular hydrogel of taxol derivative
    • Y. Gao, Y. Kuang, Z.F. Guo, Z.H. Guo, I.J. Krauss, and B. Xu Enzyme-instructed molecular self-assembly confers nanofibers and a supramolecular hydrogel of taxol derivative J. Am. Chem. Soc. 131 2009 13576 13577
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 13576-13577
    • Gao, Y.1    Kuang, Y.2    Guo, Z.F.3    Guo, Z.H.4    Krauss, I.J.5    Xu, B.6
  • 178
    • 78650257262 scopus 로고    scopus 로고
    • Molecular nanofibers of olsalazine form supramolecular hydrogels for reductive release of an anti-inflammatory agent
    • X.M. Li, J.Y. Li, Y.A. Gao, Y. Kuang, J.F. Shi, and B. Xu Molecular nanofibers of olsalazine form supramolecular hydrogels for reductive release of an anti-inflammatory agent J. Am. Chem. Soc. 132 2010 17707 17709
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 17707-17709
    • Li, X.M.1    Li, J.Y.2    Gao, Y.A.3    Kuang, Y.4    Shi, J.F.5    Xu, B.6
  • 179
    • 84872586525 scopus 로고    scopus 로고
    • D-amino acids boost the selectivity and confer supramolecular hydrogels of a nonsteroidal anti-inflammatory drug (NSAID)
    • J.Y. Li, Y. Kuang, Y. Gao, X.W. Du, J.F. Shi, and B. Xu D-amino acids boost the selectivity and confer supramolecular hydrogels of a nonsteroidal anti-inflammatory drug (NSAID) J. Am. Chem. Soc. 135 2013 542 545
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 542-545
    • Li, J.Y.1    Kuang, Y.2    Gao, Y.3    Du, X.W.4    Shi, J.F.5    Xu, B.6
  • 180
    • 84897554101 scopus 로고    scopus 로고
    • A polymer additive boosts the anti-cancer efficacy of supramolecular nanofibers of taxol
    • C.B. Yang, M.J. Bian, and Z.M. Yang A polymer additive boosts the anti-cancer efficacy of supramolecular nanofibers of taxol Biomater. Sci. (UK) 2 2014 651 654
    • (2014) Biomater. Sci. (UK) , vol.2 , pp. 651-654
    • Yang, C.B.1    Bian, M.J.2    Yang, Z.M.3
  • 181
    • 84881608235 scopus 로고    scopus 로고
    • Beta-amino acid and amino-alcohol conjugation of a nonsteroidal anti-Inflammatory drug (NSAID) imparts hydrogelation displaying remarkable biostability, biocompatibility, and anti-inflammatory properties
    • J. Majumder, M.R. Das, J. Deb, S.S. Jana, and P. Dastidar Beta-amino acid and amino-alcohol conjugation of a nonsteroidal anti-Inflammatory drug (NSAID) imparts hydrogelation displaying remarkable biostability, biocompatibility, and anti-inflammatory properties Langmuir 29 2013 10254 10263
    • (2013) Langmuir , vol.29 , pp. 10254-10263
    • Majumder, J.1    Das, M.R.2    Deb, J.3    Jana, S.S.4    Dastidar, P.5
  • 182
    • 84867314001 scopus 로고    scopus 로고
    • Folic acid as a versatile motif to construct molecular hydrogelators through conjugations with hydrophobic therapeutic agents
    • X.Y. Li, C.B. Yang, Z.L. Zhang, Z.D. Wu, Y. Deng, G.L. Liang, Z.M. Yang, and H. Chen Folic acid as a versatile motif to construct molecular hydrogelators through conjugations with hydrophobic therapeutic agents J. Mater. Chem. 22 2012 21838 21840
    • (2012) J. Mater. Chem. , vol.22 , pp. 21838-21840
    • Li, X.Y.1    Yang, C.B.2    Zhang, Z.L.3    Wu, Z.D.4    Deng, Y.5    Liang, G.L.6    Yang, Z.M.7    Chen, H.8
  • 184
    • 84929603273 scopus 로고    scopus 로고
    • Enzyme-specific doxorubicin drug beacon as drug-resistant theranostic molecular probes
    • L.L. Lock, Z. Tang, D. Keith, C. Reyes, and H.G. Cui Enzyme-specific doxorubicin drug beacon as drug-resistant theranostic molecular probes ACS Macro Lett. 4 2015 552 555
    • (2015) ACS Macro Lett. , vol.4 , pp. 552-555
    • Lock, L.L.1    Tang, Z.2    Keith, D.3    Reyes, C.4    Cui, H.G.5
  • 185
    • 84901743395 scopus 로고    scopus 로고
    • Enhanced cellular entry and efficacy of Tat conjugates by rational design of the auxiliary segment
    • P.C. Zhang, L.L. Lock, A.G. Cheetham, and H.G. Cui Enhanced cellular entry and efficacy of Tat conjugates by rational design of the auxiliary segment Mol. Pharm. 11 2014 964 973
    • (2014) Mol. Pharm. , vol.11 , pp. 964-973
    • Zhang, P.C.1    Lock, L.L.2    Cheetham, A.G.3    Cui, H.G.4
  • 186
    • 84877686279 scopus 로고    scopus 로고
    • Supramolecular filaments containing a fixed 41% paclitaxel loading
    • R. Lin, A.G. Cheetham, P.C. Zhang, Y.A. Lin, and H.G. Cui Supramolecular filaments containing a fixed 41% paclitaxel loading Chem. Commun. 49 2013 4968 4970
    • (2013) Chem. Commun. , vol.49 , pp. 4968-4970
    • Lin, R.1    Cheetham, A.G.2    Zhang, P.C.3    Lin, Y.A.4    Cui, H.G.5
  • 187
    • 84907902834 scopus 로고    scopus 로고
    • Synthesis and self-assembly of a mikto-arm star dual drug amphiphile containing both paclitaxel and camptothecin
    • A.G. Cheetham, P. Zhang, Y.A. Lin, R. Lin, and H. Cui Synthesis and self-assembly of a mikto-arm star dual drug amphiphile containing both paclitaxel and camptothecin J. Mater. Chem. B 2 2014 7316 7326
    • (2014) J. Mater. Chem. B , vol.2 , pp. 7316-7326
    • Cheetham, A.G.1    Zhang, P.2    Lin, Y.A.3    Lin, R.4    Cui, H.5
  • 189
    • 84899923752 scopus 로고    scopus 로고
    • Linker-determined drug release mechanism of free camptothecin from self-assembling drug amphiphiles
    • A.G. Cheetham, Y.C. Ou, P.C. Zhang, and H.G. Cui Linker-determined drug release mechanism of free camptothecin from self-assembling drug amphiphiles Chem. Commun. 50 2014 6039 6042
    • (2014) Chem. Commun. , vol.50 , pp. 6039-6042
    • Cheetham, A.G.1    Ou, Y.C.2    Zhang, P.C.3    Cui, H.G.4


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