메뉴 건너뛰기




Volumn 10, Issue 3, 2013, Pages 867-874

Well-defined degradable brush polymer-drug conjugates for sustained delivery of paclitaxel

Author keywords

brush polymer; click chemistry; drug delivery; paclitaxel; polylactide; polymer drug conjugate

Indexed keywords

DEGRADABLE BRUSH POLYMER; PACLITAXEL; POLYMER; UNCLASSIFIED DRUG;

EID: 84874606242     PISSN: 15438384     EISSN: 15438392     Source Type: Journal    
DOI: 10.1021/mp3004868     Document Type: Article
Times cited : (118)

References (43)
  • 1
    • 33747840618 scopus 로고    scopus 로고
    • Polymer conjugates as anticancer nanomedicines
    • Duncan, R. Polymer conjugates as anticancer nanomedicines Nat. Rev. Cancer 2006, 6, 688-701
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 688-701
    • Duncan, R.1
  • 2
    • 33845508580 scopus 로고    scopus 로고
    • Paclitaxel prodrugs: Toward smarter delivery of anticancer agents
    • Skwarczynski, M.; Hayashi, Y.; Kiso, Y. Paclitaxel prodrugs: toward smarter delivery of anticancer agents J. Med. Chem. 2006, 49, 7253-7269
    • (2006) J. Med. Chem. , vol.49 , pp. 7253-7269
    • Skwarczynski, M.1    Hayashi, Y.2    Kiso, Y.3
  • 4
    • 0842282637 scopus 로고    scopus 로고
    • Taxane-mediated antiangiogenesis in vitro: Influence of formulation vehicles and binding proteins
    • Ng, S. S. W.; Figg, W. D.; Sparreboom, A. Taxane-mediated antiangiogenesis in vitro: influence of formulation vehicles and binding proteins Cancer Res. 2004, 64, 821-824
    • (2004) Cancer Res. , vol.64 , pp. 821-824
    • Ng, S.S.W.1    Figg, W.D.2    Sparreboom, A.3
  • 5
    • 84858673601 scopus 로고    scopus 로고
    • Design of polymeric nanoparticles for biomedical delivery applications
    • Elsabahy, M.; Wooley, K. L. Design of polymeric nanoparticles for biomedical delivery applications Chem. Soc. Rev. 2012, 41, 2545-2561
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 2545-2561
    • Elsabahy, M.1    Wooley, K.L.2
  • 6
    • 34547797860 scopus 로고    scopus 로고
    • Anticancer polymeric nanomedicines
    • Tong, R.; Cheng, J. Anticancer polymeric nanomedicines Polym. Rev. 2007, 47, 345-381
    • (2007) Polym. Rev. , vol.47 , pp. 345-381
    • Tong, R.1    Cheng, J.2
  • 8
    • 42749091133 scopus 로고    scopus 로고
    • Polymer-drug conjugates: Recent development in clinical oncology
    • Li, C.; Wallace, S. Polymer-drug conjugates: Recent development in clinical oncology Adv. Drug Delivery Rev. 2008, 60, 886-898
    • (2008) Adv. Drug Delivery Rev. , vol.60 , pp. 886-898
    • Li, C.1    Wallace, S.2
  • 9
    • 34547585979 scopus 로고    scopus 로고
    • Biodegradable polymers as biomaterials
    • Nair, L. S.; Laurencin, C. T. Biodegradable polymers as biomaterials Prog. Polym. Sci. 2007, 32, 762-798
    • (2007) Prog. Polym. Sci. , vol.32 , pp. 762-798
    • Nair, L.S.1    Laurencin, C.T.2
  • 10
    • 37249093948 scopus 로고    scopus 로고
    • Biodegradable, polymeric nanoparticle delivery systems for cancer therapy
    • Pridgen, E. M.; Langer, R.; Farokhzad, O. C. Biodegradable, polymeric nanoparticle delivery systems for cancer therapy Nanomedicine 2007, 2, 669-680
    • (2007) Nanomedicine , vol.2 , pp. 669-680
    • Pridgen, E.M.1    Langer, R.2    Farokhzad, O.C.3
  • 11
    • 84862908762 scopus 로고    scopus 로고
    • Degradability of poly(lactic acid)-containing nanoparticles: Enzymatic access through a crosslinked shell barrier
    • Samarajeewa, S.; Shrestha, R.; Li, Y.; Wooley, K. L. Degradability of poly(lactic acid)-containing nanoparticles: enzymatic access through a crosslinked shell barrier J. Am. Chem. Soc. 2012, 134, 1235-1242
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 1235-1242
    • Samarajeewa, S.1    Shrestha, R.2    Li, Y.3    Wooley, K.L.4
  • 12
    • 79951599543 scopus 로고    scopus 로고
    • Organocatalytic synthesis of astaxanthin-containing poly(lactide)s
    • Middleton, H.; Tempelaar, S.; Haddleton, D. M.; Dove, A. P. Organocatalytic synthesis of astaxanthin-containing poly(lactide)s Polym. Chem. 2011, 2, 595-600
    • (2011) Polym. Chem. , vol.2 , pp. 595-600
    • Middleton, H.1    Tempelaar, S.2    Haddleton, D.M.3    Dove, A.P.4
  • 14
    • 80054697015 scopus 로고    scopus 로고
    • Clicking well-defined biodegradable nanoparticles and nanocapsules by UV-Induced thiol-ene cross-linking in transparent miniemulsions
    • Zou, J.; Hew, C. C.; Themistou, E.; Li, Y.; Chen, C.-K.; Alexandridis, P.; Cheng, C. Clicking well-defined biodegradable nanoparticles and nanocapsules by UV-Induced thiol-ene cross-linking in transparent miniemulsions Adv. Mater. 2011, 23, 4274-4277
    • (2011) Adv. Mater. , vol.23 , pp. 4274-4277
    • Zou, J.1    Hew, C.C.2    Themistou, E.3    Li, Y.4    Chen, C.-K.5    Alexandridis, P.6    Cheng, C.7
  • 16
    • 55049115208 scopus 로고    scopus 로고
    • Functionalized amphiphilic hyperbranched polymers for targeted drug delivery
    • Chen, S.; Zhang, X.-Z.; Cheng, S.-X.; Zhuo, R.-X.; Gu, Z.-W. Functionalized amphiphilic hyperbranched polymers for targeted drug delivery Biomacromolecules 2008, 9, 2578-2585
    • (2008) Biomacromolecules , vol.9 , pp. 2578-2585
    • Chen, S.1    Zhang, X.-Z.2    Cheng, S.-X.3    Zhuo, R.-X.4    Gu, Z.-W.5
  • 17
    • 23944513297 scopus 로고    scopus 로고
    • Dendrimeric micelles for controlled drug release and targeted delivery
    • Ambade, A. V.; Savariar, E. N.; Thayumanavan, S. Dendrimeric micelles for controlled drug release and targeted delivery Mol. Pharmaceutics 2005, 2, 264-272
    • (2005) Mol. Pharmaceutics , vol.2 , pp. 264-272
    • Ambade, A.V.1    Savariar, E.N.2    Thayumanavan, S.3
  • 18
    • 28944442206 scopus 로고    scopus 로고
    • Methoxy poly(ethylene glycol)- block -poly(δ-valerolactone) copolymer micelles for formulation of hydrophobic drugs
    • Lee, H.; Zeng, F.; Dunne, M.; Allen, C. Methoxy poly(ethylene glycol)- block -poly(δ-valerolactone) copolymer micelles for formulation of hydrophobic drugs Biomacromolecules 2005, 6, 3119-3128
    • (2005) Biomacromolecules , vol.6 , pp. 3119-3128
    • Lee, H.1    Zeng, F.2    Dunne, M.3    Allen, C.4
  • 19
    • 79960210899 scopus 로고    scopus 로고
    • Synthesis of amphiphilic alternating polyesters with oligo(ethylene glycol) side chains and potential use for sustained release drug delivery
    • Wang, W.; Ding, J. X.; Xiao, C. S.; Tang, Z. H.; Li, D.; Chen, J.; Zhuang, X. L.; Chen, X. S. Synthesis of amphiphilic alternating polyesters with oligo(ethylene glycol) side chains and potential use for sustained release drug delivery Biomacromolecules 2011, 12, 2466-2474
    • (2011) Biomacromolecules , vol.12 , pp. 2466-2474
    • Wang, W.1    Ding, J.X.2    Xiao, C.S.3    Tang, Z.H.4    Li, D.5    Chen, J.6    Zhuang, X.L.7    Chen, X.S.8
  • 20
    • 0037202148 scopus 로고    scopus 로고
    • Lipophilic drug loaded nanospheres prepared by nanoprecipitation: Effect of formulation variables on size, drug recovery and release kinetics
    • Chorny, M.; Fishbein, I.; Danenberg, H. D.; Golomb, G. Lipophilic drug loaded nanospheres prepared by nanoprecipitation: effect of formulation variables on size, drug recovery and release kinetics J. Controlled Release 2002, 83, 389-400
    • (2002) J. Controlled Release , vol.83 , pp. 389-400
    • Chorny, M.1    Fishbein, I.2    Danenberg, H.D.3    Golomb, G.4
  • 21
    • 84863419906 scopus 로고    scopus 로고
    • Drug-initiated, controlled ring-opening polymerization for the synthesis of polymer-drug conjugates
    • Tong, R.; Cheng, J. Drug-initiated, controlled ring-opening polymerization for the synthesis of polymer-drug conjugates Macromolecules 2012, 45, 2225-2232
    • (2012) Macromolecules , vol.45 , pp. 2225-2232
    • Tong, R.1    Cheng, J.2
  • 22
    • 48849091040 scopus 로고    scopus 로고
    • Paclitaxel-initiated, controlled polymerization of lactide for the formulation of polymeric nanoparticulate delivery vehicles
    • Tong, R.; Cheng, J. Paclitaxel-initiated, controlled polymerization of lactide for the formulation of polymeric nanoparticulate delivery vehicles Angew. Chem., Int. Ed. 2008, 47, 4830-4834
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4830-4834
    • Tong, R.1    Cheng, J.2
  • 23
    • 33846439358 scopus 로고    scopus 로고
    • Soluble camptothecin derivatives prepared by click cycloaddition chemistry on functional aliphatic polyesters
    • Parrish, B.; Emrick, T. Soluble camptothecin derivatives prepared by click cycloaddition chemistry on functional aliphatic polyesters Bioconjugate Chem. 2007, 18, 263-267
    • (2007) Bioconjugate Chem. , vol.18 , pp. 263-267
    • Parrish, B.1    Emrick, T.2
  • 25
    • 79959460542 scopus 로고    scopus 로고
    • Functional polylactide- g -paclitaxel-poly(ethylene glycol) by azide-alkyne click chemistry
    • Yu, Y.; Zou, J.; Yu, L.; Ji, W.; Li, Y.; Law, W.-C.; Cheng, C. Functional polylactide- g -paclitaxel-poly(ethylene glycol) by azide-alkyne click chemistry Macromolecules 2011, 44, 4793-4800
    • (2011) Macromolecules , vol.44 , pp. 4793-4800
    • Yu, Y.1    Zou, J.2    Yu, L.3    Ji, W.4    Li, Y.5    Law, W.-C.6    Cheng, C.7
  • 26
    • 82255164023 scopus 로고    scopus 로고
    • Well-defined drug-conjugated biodegradable nanoparticles by azide-alkyne click crosslinking in miniemulsion
    • Zou, J.; Yu, Y.; Yu, L.; Li, Y.; Chen, C.-K.; Cheng, C. Well-defined drug-conjugated biodegradable nanoparticles by azide-alkyne click crosslinking in miniemulsion J. Polym. Sci., Part A: Polym. Chem. 2012, 50, 142-148
    • (2012) J. Polym. Sci., Part A: Polym. Chem. , vol.50 , pp. 142-148
    • Zou, J.1    Yu, Y.2    Yu, L.3    Li, Y.4    Chen, C.-K.5    Cheng, C.6
  • 27
    • 84864998581 scopus 로고    scopus 로고
    • Molecular nanoworm with PCL core and PEO shell as a non-spherical carrier for drug delivery
    • Zhao, P.; Liu, L.; Feng, X.; Wang, C.; Shuai, X.; Chen, Y. Molecular nanoworm with PCL core and PEO shell as a non-spherical carrier for drug delivery Macromol. Rapid Commun. 2012, 33, 1351-1355
    • (2012) Macromol. Rapid Commun. , vol.33 , pp. 1351-1355
    • Zhao, P.1    Liu, L.2    Feng, X.3    Wang, C.4    Shuai, X.5    Chen, Y.6
  • 28
    • 68849123688 scopus 로고    scopus 로고
    • Evaluation of polymeric micelles from brush polymer with poly(ε-caprolactone)- b -poly(ethylene glycol) side chains as drug carrier
    • Du, J.-Z.; Tang, L.-Y.; Song, W.-J.; Shi, Y.; Wang, J. Evaluation of polymeric micelles from brush polymer with poly(ε-caprolactone)- b -poly(ethylene glycol) side chains as drug carrier Biomacromolecules 2009, 10, 2169-2174
    • (2009) Biomacromolecules , vol.10 , pp. 2169-2174
    • Du, J.-Z.1    Tang, L.-Y.2    Song, W.-J.3    Shi, Y.4    Wang, J.5
  • 32
    • 76949103845 scopus 로고    scopus 로고
    • PEGylated polymers for medicine: From conjugation to self-assembled systems
    • Joralemon, M. J.; McRae, S.; Emrick, T. PEGylated polymers for medicine: from conjugation to self-assembled systems Chem. Commun. 2010, 46, 1377-1393
    • (2010) Chem. Commun. , vol.46 , pp. 1377-1393
    • Joralemon, M.J.1    McRae, S.2    Emrick, T.3
  • 33
    • 73249130570 scopus 로고    scopus 로고
    • Applications of orthogonal "click" chemistries in the synthesis of functional soft materials
    • Iha, R. K.; Wooley, K. L.; Nystrom, A. M.; Burke, D. J.; Kade, M. J.; Hawker, C. J. Applications of orthogonal "click" chemistries in the synthesis of functional soft materials Chem. Rev. 2009, 109, 5620-5686
    • (2009) Chem. Rev. , vol.109 , pp. 5620-5686
    • Iha, R.K.1    Wooley, K.L.2    Nystrom, A.M.3    Burke, D.J.4    Kade, M.J.5    Hawker, C.J.6
  • 34
    • 0035898494 scopus 로고    scopus 로고
    • New paradigms for organic catalysts: The first organocatalytic living polymerization
    • Nederberg, F.; Connor, E. F.; Moeller, M.; Glauser, T.; Hedrick, J. L. New paradigms for organic catalysts: the first organocatalytic living polymerization Angew. Chem., Int. Ed. 2001, 40, 2712-2715
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2712-2715
    • Nederberg, F.1    Connor, E.F.2    Moeller, M.3    Glauser, T.4    Hedrick, J.L.5
  • 35
    • 36849030401 scopus 로고    scopus 로고
    • A facile synthesis of azido-terminated heterobifunctional poly(ethylene glycol)s for "click" conjugation
    • Hiki, S.; Kataoka, K. A facile synthesis of azido-terminated heterobifunctional poly(ethylene glycol)s for "click" conjugation Bioconjugate Chem. 2007, 18, 2191-2196
    • (2007) Bioconjugate Chem. , vol.18 , pp. 2191-2196
    • Hiki, S.1    Kataoka, K.2
  • 37
    • 66149129222 scopus 로고    scopus 로고
    • Albumin-bound formulation of paclitaxel (Abraxane ABI-007) in the treatment of breast cancer
    • Miele, E.; Spinelli, G. P.; Miele, E.; Tomao, F.; Tomao, S. Albumin-bound formulation of paclitaxel (Abraxane ABI-007) in the treatment of breast cancer Int. J. Nanomed. 2009, 4, 99-105
    • (2009) Int. J. Nanomed. , vol.4 , pp. 99-105
    • Miele, E.1    Spinelli, G.P.2    Miele, E.3    Tomao, F.4    Tomao, S.5
  • 38
    • 24944469502 scopus 로고    scopus 로고
    • Synthesis of a novel polyfunctional anionic macroinitiator from a polyfunctional 1,1-diphenylethylene agent
    • Cheng, C.; Yang, N.-L. Synthesis of a novel polyfunctional anionic macroinitiator from a polyfunctional 1,1-diphenylethylene agent Macromol. Rapid Commun. 2005, 26, 1395-1399
    • (2005) Macromol. Rapid Commun. , vol.26 , pp. 1395-1399
    • Cheng, C.1    Yang, N.-L.2
  • 39
    • 77955175216 scopus 로고    scopus 로고
    • Strategies in the design of nanoparticles for therapeutic applications
    • Petros, R. A.; DeSimone, J. M. Strategies in the design of nanoparticles for therapeutic applications Nat. Rev. Drug Discovery 2010, 9, 615-627
    • (2010) Nat. Rev. Drug Discovery , vol.9 , pp. 615-627
    • Petros, R.A.1    Desimone, J.M.2
  • 40
    • 84859510563 scopus 로고    scopus 로고
    • The journey of a drug-carrier in the body: An anatomo-physiological perspective
    • Bertrand, N.; Leroux, J.-C. The journey of a drug-carrier in the body: an anatomo-physiological perspective J. Controlled Release 2012, 161, 152-163
    • (2012) J. Controlled Release , vol.161 , pp. 152-163
    • Bertrand, N.1    Leroux, J.-C.2
  • 42
    • 0001728046 scopus 로고
    • The influence of hydrogen and hydrophobic bonds on the stability of the carboxylic acid dimers in aqueous solution
    • Schrier, E. E.; Pottle, M.; Scheraga, H. A. The influence of hydrogen and hydrophobic bonds on the stability of the carboxylic acid dimers in aqueous solution J. Am. Chem. Soc. 1964, 86, 3444-3449
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 3444-3449
    • Schrier, E.E.1    Pottle, M.2    Scheraga, H.A.3
  • 43
    • 0021816546 scopus 로고
    • Spectrofluorometric studies of the lipid probe, nile red
    • Greenspan, P.; Fowler, S. D. Spectrofluorometric studies of the lipid probe, nile red J. Lipid Res. 1985, 26, 781-789
    • (1985) J. Lipid Res. , vol.26 , pp. 781-789
    • Greenspan, P.1    Fowler, S.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.