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Volumn 161, Issue 1, 2012, Pages 124-131

Effect of molecular weight of PGG-paclitaxel conjugates on in vitro and in vivo efficacy

Author keywords

Drug delivery; Drug release; PGG copolymer; Physicochemical characteristics; Polymers; Subcellular trafficking

Indexed keywords

ANTICANCER ACTIVITIES; CELL UPTAKE; CHEMOTHERAPEUTIC AGENTS; DESIGN AND DEVELOPMENT; DRUG RELEASE; DRUG RESISTANCE; DRUG STABILITY; IN-VITRO; LINEAR POLYMERS; MAXIMUM TOLERATED DOSE; MODEL SYSTEM; PACLITAXEL; PARTICLE FORMATIONS; PHYSICOCHEMICAL CHARACTERISTICS; POLYMERIC PRODRUGS; PRODRUGS; SERUM STABILITY; SUB-CELLULAR; THERAPEUTIC INDEX;

EID: 84862618443     PISSN: 01683659     EISSN: 18734995     Source Type: Journal    
DOI: 10.1016/j.jconrel.2012.04.010     Document Type: Article
Times cited : (39)

References (34)
  • 1
    • 0022858683 scopus 로고
    • A new concept for macromolecular therapeutics in cancer chemotherapy: Mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs
    • Y. Matsumura, H. Maeda, A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent SMANCS, Cancer Res. 46 (1986) 6387-6392. (Pubitemid 17221789)
    • (1986) Cancer Research , vol.46 , Issue.12 I , pp. 6387-6392
    • Matsumura, Y.1    Maeda, H.2
  • 2
    • 52049105453 scopus 로고    scopus 로고
    • Recent trends in targeted anticancer prodrug and conjugate design
    • Y. Singh, M. Palombo, 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
  • 3
    • 51049090204 scopus 로고    scopus 로고
    • Nanoparticle therapeutics: An emerging treatment modality for cancer
    • M.E. Davis, Z.G. Chen, D.M. Shin, Nanoparticle therapeutics: an emerging treatment modality for cancer, Nat. Rev. Drug Discov. 7 (2008) 771-782.
    • (2008) Nat. Rev. Drug Discov. , vol.7 , pp. 771-782
    • Davis, M.E.1    Chen, Z.G.2    Shin, D.M.3
  • 4
    • 0032580444 scopus 로고    scopus 로고
    • Targetable HPMA copolymer-adriamycin conjugates. Recognition, internalization, and subcellular fate
    • DOI 10.1016/S0168-3659(97)00235-6, PII S0168365997002356
    • V. Omelyanenko, P. Kopečková, C. Gentry, J. Kopeček, Targetable HPMA copolymer-adriamycin conjugates. Recognition, internalization, and subcellular fate, J. Control. Release 53 (1998) 25-37. (Pubitemid 28218687)
    • (1998) Journal of Controlled Release , vol.53 , Issue.1-3 , pp. 25-37
    • Omelyanenko, V.1    Kopeckova, P.2    Gentry, C.3    Kopecek, J.4
  • 5
    • 0030111359 scopus 로고    scopus 로고
    • Hypersensitization of multidrug resistant human ovarian carcinoma cells by pluronic P85 block copolymer
    • V. Alakhov, E. Moskaleva, E.V. Batrakova, A.V. Kabanov, Hypersensitization of multidrug resistant human ovarian carcinoma cells by pluronic P85 block copolymer, Bioconjug. Chem. 7 (1996) 209-216.
    • (1996) Bioconjug. Chem. , vol.7 , pp. 209-216
    • Alakhov, V.1    Moskaleva, E.2    Batrakova, E.V.3    Kabanov, A.V.4
  • 6
    • 21744444124 scopus 로고    scopus 로고
    • Pluronic block copolymers alter apoptotic signal transduction of doxorubicin in drug-resistant cancer cells
    • DOI 10.1016/j.jconrel.2005.03.019, PII S0168365905001628
    • T. Minko, E.V. Batrakova, S. Li, Y. Li, R.I. Pakunlu, V.Y. Alakhov, A.V. Kabanov, Pluronic block copolymers alter apoptotic signal transduction of doxorubicin in drug-resistant cancer cells, J. Control. Release 105 (2005) 269-278. (Pubitemid 40941992)
    • (2005) Journal of Controlled Release , vol.105 , Issue.3 , pp. 269-278
    • Minko, T.1    Batrakova, E.V.2    Li, S.3    Li, Y.4    Pakunlu, R.I.5    Alakhov, V.Yu.6    Kabanov, A.V.7
  • 7
    • 17744382615 scopus 로고    scopus 로고
    • Effect of pluronic P85 on ATPase activity of drug efflux transporters
    • DOI 10.1007/s11095-004-7675-5
    • E.V. Batrakova, S. Li, Y. Li, V.Y. Alakhov, A.V. Kabanov, Effect of pluronic P85 on ATPase activity of drug efflux transporters, Pharm. Res. 21 (2004) 2226-2233. (Pubitemid 40575635)
    • (2004) Pharmaceutical Research , vol.21 , Issue.12 , pp. 2226-2233
    • Batrakova, E.V.1    Li, S.2    Li, Y.3    Alakhov, V.Yu.4    Kabanov, A.V.5
  • 8
  • 9
    • 0346551010 scopus 로고
    • Polymer conjugates with anticancer activity
    • D. Putnam, J. Kopecek, Polymer conjugates with anticancer activity, Adv. Polym. Sci. 122 (1995) 55-123.
    • (1995) Adv. Polym. Sci. , vol.122 , pp. 55-123
    • Putnam, D.1    Kopecek, J.2
  • 10
    • 0025913143 scopus 로고
    • Prodrugs of peptides. 11. Chemical and enzymatic hydrolysis kinetics of N-acyloxymethyl derivatives of a peptide-like bond
    • H. Bundgaard, G.J. Rasmussen, Prodrugs of peptides. 11. Chemical and enzymatic hydrolysis kinetics of N-acyloxymethyl derivatives of a peptide-like bond, Pharm. Res. 8 (1991) 1238-1242.
    • (1991) Pharm. Res. , vol.8 , pp. 1238-1242
    • Bundgaard, H.1    Rasmussen, G.J.2
  • 11
    • 0025922579 scopus 로고
    • Prodrugs of peptides. 9. Bioreversible N-alpha-hydroxyalkylation of the peptide bond to effect protection against carboxypeptidase or other proteolytic enzymes
    • H. Bundgaard, G.J. Rasmussen, Prodrugs of peptides. 9. Bioreversible N-alpha-hydroxyalkylation of the peptide bond to effect protection against carboxypeptidase or other proteolytic enzymes, Pharm. Res. 8 (1991) 313-322.
    • (1991) Pharm. Res. , vol.8 , pp. 313-322
    • Bundgaard, H.1    Rasmussen, G.J.2
  • 12
    • 0024367481 scopus 로고
    • A novel solution-stable, water-soluble prodrug type for drugs containing a hydroxyl or an NH-acidic group
    • DOI 10.1021/jm00132a001
    • H. Bundgaard, E. Falch, E. Jensen, A novel solution-stable, water-soluble prodrug type for drugs containing a hydroxyl or an NH-acidic group, J. Med. Chem. 32 (1989) 2503-2507. (Pubitemid 20002796)
    • (1989) Journal of Medicinal Chemistry , vol.32 , Issue.12 , pp. 2503-2507
    • Bundgaard, H.1    Falch, E.2    Jensen, E.3
  • 13
    • 33845508580 scopus 로고    scopus 로고
    • Paclitaxel prodrugs: Toward smarter delivery of anticancer agents
    • DOI 10.1021/jm0602155
    • M. Skwarczynski, Y. Hayashi, Y. Kiso, Paclitaxel prodrugs: toward smarter delivery of anticancer agents, J. Med. Chem. 49 (2006) 7253-7269. (Pubitemid 44913386)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.25 , pp. 7253-7269
    • Skwarczynski, M.1    Hayashi, Y.2    Kiso, Y.3
  • 14
    • 0035145742 scopus 로고    scopus 로고
    • Biodistribution and antitumour efficacy of long-circulating N-(2-hydroxypropyl) methacrylamide copolymer-doxorubicin conjugates in nude mice
    • J.G. Shiah, M. Dvořák, P. Kopečková, Y. Sun, C.M. Peterson, J. Kopeček, Biodistribution and antitumour efficacy of long-circulating N-(2-hydroxypropyl) methacrylamide copolymer-doxorubicin conjugates in nude mice, Eur. J. Cancer 37 (2001) 131-139.
    • (2001) Eur. J. Cancer , vol.37 , pp. 131-139
    • Shiah, J.G.1    Dvořák, M.2    Kopečková, P.3    Sun, Y.4    Peterson, C.M.5    Kopeček, J.6
  • 15
    • 0038387390 scopus 로고    scopus 로고
    • The dawning era of polymer therapeutics
    • DOI 10.1038/nrd1088
    • R. Duncan, The dawning era of polymer therapeutics, Nat. Rev. Drug Discov. 2 (2003) 347-360. (Pubitemid 37361705)
    • (2003) Nature Reviews Drug Discovery , vol.2 , Issue.5 , pp. 347-360
    • Duncan, R.1
  • 17
    • 79251478025 scopus 로고    scopus 로고
    • Novel free paclitaxel-loaded poly(L-gamma-glutamylglutamine)-paclitaxel nanoparticles
    • D. Yang, S. Van, X. Jiang, L. Yu, Novel free paclitaxel-loaded poly(L-gamma-glutamylglutamine)-paclitaxel nanoparticles, Int. J. Nanomedicine 6 (2011) 85-91.
    • (2011) Int. J. Nanomedicine , vol.6 , pp. 85-91
    • Yang, D.1    Van, S.2    Jiang, X.3    Yu, L.4
  • 18
    • 77649190943 scopus 로고    scopus 로고
    • Preclinical efficacy studies of a novel nanoparticle-based formulation of paclitaxel that out-performs Abraxane
    • Z. Feng, G. Zhao, L. Yu, D. Gough, S.B. Howell, Preclinical efficacy studies of a novel nanoparticle-based formulation of paclitaxel that out-performs Abraxane, Cancer Chemother. Pharmacol. 65 (2010) 923-930.
    • (2010) Cancer Chemother. Pharmacol. , vol.65 , pp. 923-930
    • Feng, Z.1    Zhao, G.2    Yu, L.3    Gough, D.4    Howell, S.B.5
  • 19
    • 75549085440 scopus 로고    scopus 로고
    • Pharmacokinetics and tissue distribution of PGG-paclitaxel, a novel macromolecular formulation of paclitaxel, in nu/nu mice bearing NCI-460 lung cancer xenografts
    • X. Wang, G. Zhao, S. Van, N. Jiang, L. Yu, D. Vera, S.B. Howell, Pharmacokinetics and tissue distribution of PGG-paclitaxel, a novel macromolecular formulation of paclitaxel, in nu/nu mice bearing NCI-460 lung cancer xenografts, Cancer Chemother. Pharmacol. 65 (2010) 515-526.
    • (2010) Cancer Chemother. Pharmacol. , vol.65 , pp. 515-526
    • Wang, X.1    Zhao, G.2    Van, S.3    Jiang, N.4    Yu, L.5    Vera, D.6    Howell, S.B.7
  • 20
    • 84862611592 scopus 로고    scopus 로고
    • Controlled Synthesis of Polyglutamic Acid
    • United States Patent, US2011/0144315A1, June 16
    • Wang, H. and Taylor, W.D. Controlled Synthesis of Polyglutamic Acid. United States Patent, US2011/0144315A1, June 16, 2011.
    • (2011)
    • Wang, H.1    Taylor, W.D.2
  • 21
    • 33748289523 scopus 로고    scopus 로고
    • NK105, a paclitaxel-incorporating micellar nanoparticle, is a more potent radiosensitising agent compared to free paclitaxel
    • DOI 10.1038/sj.bjc.6603311, PII 6603311
    • T. Negishi, F. Koizumi, H. Uchino, J. Kuroda, T. Kawaguchi, S. Naito, Y. Matsumura, NK105, a paclitaxel-incorporating micellar nanoparticle, is a more potent radiosensitising agent compared to free paclitaxel, Br. J. Cancer 95 (2006) 601-606. (Pubitemid 44325900)
    • (2006) British Journal of Cancer , vol.95 , Issue.5 , pp. 601-606
    • Negishi, T.1    Koizumi, F.2    Uchino, H.3    Kuroda, J.4    Kawaguchi, T.5    Naito, S.6    Matsumura, Y.7
  • 22
    • 0028337034 scopus 로고
    • Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice
    • DOI 10.1002/jps.2600830432
    • T. Yamaoka, Y. Tabata, Y. Ikada, Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice, J. Pharm. Sci. 83 (1994) 601-606. (Pubitemid 24222392)
    • (1994) Journal of Pharmaceutical Sciences , vol.83 , Issue.4 , pp. 601-606
    • Yamaoka, T.1    Tabata, Y.2    Ikada, Y.3
  • 23
    • 0025099302 scopus 로고
    • The potential of water-soluble polymeric carriers in targeted and site-specific drug delivery
    • J. Kopecek, The potential of water-soluble polymeric carriers in targeted and site-specific drug delivery, J. Control. Release 11 (1990) 279-290. (Pubitemid 20070105)
    • (1990) Journal of Controlled Release , vol.11 , Issue.1-3 , pp. 279-290
    • Kopecek, J.1
  • 24
    • 77950518001 scopus 로고    scopus 로고
    • Endocytic uptake of a large array of HPMA copolymers: Elucidation into the dependence on the physicochemical characteristics
    • J. Liu, H. Bauer, J. Callahan, P. Kopeckova, H. Pan, J. Kopecek, Endocytic uptake of a large array of HPMA copolymers: elucidation into the dependence on the physicochemical characteristics, J. Control. Release 143 (2010) 71-79.
    • (2010) J. Control. Release , vol.143 , pp. 71-79
    • Liu, J.1    Bauer, H.2    Callahan, J.3    Kopeckova, P.4    Pan, H.5    Kopecek, J.6
  • 25
    • 1242314681 scopus 로고    scopus 로고
    • Uptake and Cytotoxicity of Chitosan Molecules and Nanoparticles: Effects of Molecular Weight and Degree of Deacetylation
    • DOI 10.1023/B:PHAM.0000016249.52831.a5
    • M. Huang, E. Khor, L.Y. Lim, Uptake and cytotoxicity of chitosan molecules and nanoparticles: effects of molecular weight and degree of deacetylation, Pharm. Res. 21 (2004) 344-353. (Pubitemid 38221982)
    • (2004) Pharmaceutical Research , vol.21 , Issue.2 , pp. 344-353
    • Huang, M.1    Khor, E.2    Lim, L.-Y.3
  • 27
    • 33847671358 scopus 로고    scopus 로고
    • TAT peptide-based micelle system for potential active targeting of anti-cancer agents to acidic solid tumors
    • DOI 10.1016/j.jconrel.2006.12.008, PII S016836590600705X
    • V.A. Sethuraman, Y.H. Bae, TAT peptide-based micelle system for potential active targeting of anti-cancer agents to acidic solid tumors, J. Control. Release 118 (2007) 216-224. (Pubitemid 46350711)
    • (2007) Journal of Controlled Release , vol.118 , Issue.2 , pp. 216-224
    • Sethuraman, V.A.1    Bae, Y.H.2
  • 28
    • 39049105552 scopus 로고    scopus 로고
    • Physicochemical characteristics of pH-sensitive poly(L-histidine)-b- poly(ethylene glycol)/poly(L-lactide)- B-poly(ethylene glycol) mixedmicelles
    • H. Yin, E.S. Lee, D. Kim, K.H. Lee, K.T. Oh, Y.H. Bae, Physicochemical characteristics of pH-sensitive poly(L-histidine)-b-poly(ethylene glycol)/poly(L-lactide)- b-poly(ethylene glycol) mixedmicelles, J. Control. Release 126 (2008) 130-138.
    • (2008) J. Control. Release , vol.126 , pp. 130-138
    • Yin, H.1    Lee, E.S.2    Kim, D.3    Lee, K.H.4    Oh, K.T.5    Bae, Y.H.6
  • 30
    • 67651149709 scopus 로고    scopus 로고
    • Poly(amidoamine) conjugates containing doxorubicin bound via an acid-sensitive linker
    • N. Lavignac, J.L. Nicholls, P. Ferruti, R. Duncan, Poly(amidoamine) conjugates containing doxorubicin bound via an acid-sensitive linker, Macromol. Biosci. 9 (2009) 480-487.
    • (2009) Macromol. Biosci. , vol.9 , pp. 480-487
    • Lavignac, N.1    Nicholls, J.L.2    Ferruti, P.3    Duncan, R.4
  • 31
    • 33751520245 scopus 로고    scopus 로고
    • Thermo- and pH-responsive polymers in drug delivery
    • DOI 10.1016/j.addr.2006.09.020, PII S0169409X06001839
    • D. Schmaljohann, Thermo- and pH-responsive polymers in drug delivery, Adv. Drug Deliv. Rev. 58 (2006) 1655-1670. (Pubitemid 44830149)
    • (2006) Advanced Drug Delivery Reviews , vol.58 , Issue.15 , pp. 1655-1670
    • Schmaljohann, D.1
  • 32
    • 3843138529 scopus 로고    scopus 로고
    • Release from polymeric prodrugs: Linkages and their degradation
    • DOI 10.1002/jps.20096
    • A.J. D'Souza, E.M. Topp, Release from polymeric prodrugs: linkages and their degradation, J. Pharm. Sci. 93 (2004) 1962-1979. (Pubitemid 39045479)
    • (2004) Journal of Pharmaceutical Sciences , vol.93 , Issue.8 , pp. 1962-1979
    • D'Souza, A.J.M.1    Topp, E.M.2
  • 33
    • 0032827680 scopus 로고    scopus 로고
    • New biodegradable polymers for injectable drug delivery systems
    • DOI 10.1016/S0168-3659(99)00061-9, PII S0168365999000619
    • B. Jeong, Y.K. Choi, Y.H. Bae, G. Zentner, S.W. Kim, New biodegradable polymers for injectable drug delivery systems, J. Control. Release 62 (1999) 109-114. (Pubitemid 29486489)
    • (1999) Journal of Controlled Release , vol.62 , Issue.1-2 , pp. 109-114
    • Jeong, B.1    Choi, Y.K.2    Bae, Y.H.3    Zentner, G.4    Kim, S.W.5
  • 34
    • 0031845277 scopus 로고    scopus 로고
    • Different molecular weight chitosan microspheres: Influence on drug loading and drug release
    • I. Genta, P. Perugini, F. Pavanetto, Different molecular weight chitosan microspheres: influence on drug loading and drug release, Drug Dev. Ind. Pharm. 24 (1998) 779-784. (Pubitemid 28346453)
    • (1998) Drug Development and Industrial Pharmacy , vol.24 , Issue.8 , pp. 779-784
    • Genta, I.1    Perugini, P.2    Pavanetto, F.3


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