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Volumn 49, Issue 25, 2006, Pages 7253-7269

Paclitaxel prodrugs: Toward smarter delivery of anticancer agents

Author keywords

[No Author keywords available]

Indexed keywords

2' [3 (N,N DIETHYLAMINO)PROPIONYL]PACLITAXEL; ANTIBODY CONJUGATE; CARBOXYL GROUP; CARBOXYMETHYLCYCLODEXTRAN; CREMOPHOR; DENDRIMER; DEXTRAN DERIVATIVE; HYALURONIC ACID; MACROGOL; METHYL GREEN; N (2 HYDROXYPROPYL)METHACRYLAMIDE; ORGANOPHOSPHATE; PACLITAXEL; POLYGLUTAMIC ACID; PRODRUG;

EID: 33845508580     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0602155     Document Type: Review
Times cited : (164)

References (178)
  • 1
    • 0015211527 scopus 로고
    • Plant antitumor agents. VI. Isolation and structure of Taxol, a novel antileukemic and antitumor agent from Taxus brevifolia
    • Wani, M. C.; Taylor, H.L.; Wall, M. E.; Coggon, P.; McPhail, A. T. Plant antitumor agents. VI. Isolation and structure of Taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. J. Am. Chem. Soc. 1971, 93, 2325-2327.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 2325-2327
    • Wani, M.C.1    Taylor, H.L.2    Wall, M.E.3    Coggon, P.4    McPhail, A.T.5
  • 5
    • 0018387446 scopus 로고
    • Promotion of microtubule assembly in vitro by Taxol
    • Schiff, P. B.; Fant, J.; Horwitz, S. B. Promotion of microtubule assembly in vitro by Taxol. Nature 1979, 277, 665-667.
    • (1979) Nature , vol.277 , pp. 665-667
    • Schiff, P.B.1    Fant, J.2    Horwitz, S.B.3
  • 6
    • 0037392444 scopus 로고    scopus 로고
    • Issues and progress with protein kinase inhibitors for cancer treatment
    • Dancey, J.; Sausville, E. A. Issues and progress with protein kinase inhibitors for cancer treatment. Nat. Rev. Drug Discovery 2003, 2, 296-313.
    • (2003) Nat. Rev. Drug Discovery , vol.2 , pp. 296-313
    • Dancey, J.1    Sausville, E.A.2
  • 7
    • 16844386676 scopus 로고    scopus 로고
    • Enhancement of the therapeutic efficacy of Taxol by the mitogen-activated protein kinase kinase inhibitor CI-1040 in nude mice bearing human heterotransplants
    • McDaid, H. M.; Lopez-Barcons, L.; Grossman, A.; Lia, M.; Keller. S.; Perez-Soler, R.; Horwitz, S. B. Enhancement of the therapeutic efficacy of Taxol by the mitogen-activated protein kinase kinase inhibitor CI-1040 in nude mice bearing human heterotransplants. Cancer Res. 2005, 65, 2854-2860.
    • (2005) Cancer Res. , vol.65 , pp. 2854-2860
    • McDaid, H.M.1    Lopez-Barcons, L.2    Grossman, A.3    Lia, M.4    Keller, S.5    Perez-Soler, R.6    Horwitz, S.B.7
  • 9
    • 0042014485 scopus 로고    scopus 로고
    • Transcriptional profiling of targets for combination therapy of lung carcinoma with paclitaxel and mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor
    • Taxman, D. J.; MacKeigan, J. P.; Clements, C.; Bergstralh, D. T.; Ting, J. P.-Y. Transcriptional profiling of targets for combination therapy of lung carcinoma with paclitaxel and mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor. Cancer Res. 2003, 63, 5095-5104.
    • (2003) Cancer Res. , vol.63 , pp. 5095-5104
    • Taxman, D.J.1    MacKeigan, J.P.2    Clements, C.3    Bergstralh, D.T.4    Ting, J.P.-Y.5
  • 10
    • 0037386774 scopus 로고    scopus 로고
    • Antitumor effects of ZD6474, a small molecule vascular endothelial growth factor receptor tyrosine kinase inhibitor, with additional activity against epidermal growth factor receptor tyrosine kinase
    • Ciardiello, F.; Caputo, R.; Damiano, V.; Caputo, R.; Troiani, T.; Vitagliano, D.; Carlomagno, F.; Veneziani, B. M.; Fontanini, G.; Bianco, A. R.; Tortora, G. Antitumor effects of ZD6474, a small molecule vascular endothelial growth factor receptor tyrosine kinase inhibitor, with additional activity against epidermal growth factor receptor tyrosine kinase. Clin. Cancer Rex. 2003, 9, 1546-1556.
    • (2003) Clin. Cancer Rex. , vol.9 , pp. 1546-1556
    • Ciardiello, F.1    Caputo, R.2    Damiano, V.3    Caputo, R.4    Troiani, T.5    Vitagliano, D.6    Carlomagno, F.7    Veneziani, B.M.8    Fontanini, G.9    Bianco, A.R.10    Tortora, G.11
  • 11
    • 0037341379 scopus 로고    scopus 로고
    • Blockade of epidermal growth factor receptor signaling in tumor cells and tumor-associated endothelial cells for therapy of androgen-independent human prostate cancer growing in the bone of nude mice
    • Kim, S. J.; Uehara, H.; Karashima, T.; Shepherd, D. L.; Killion, J. J.; Fidler, I. J. Blockade of epidermal growth factor receptor signaling in tumor cells and tumor-associated endothelial cells for therapy of androgen-independent human prostate cancer growing in the bone of nude mice. Clin. Cancer Res. 2003, 9, 1200-1210.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 1200-1210
    • Kim, S.J.1    Uehara, H.2    Karashima, T.3    Shepherd, D.L.4    Killion, J.J.5    Fidler, I.J.6
  • 12
    • 0037269505 scopus 로고    scopus 로고
    • Stabilization of the cyclin-dependent kinase 5 activator, p35, by paclitaxel decreases β-amyloid toxicity in cortical neurons
    • Li, G. Faibushevich, A.; Turunen, B. J.; Yoon, S. O.; Georg, G.; Michaelis, M. L.; Dobrowsky, R. T. Stabilization of the cyclin-dependent kinase 5 activator, p35, by paclitaxel decreases β-amyloid toxicity in cortical neurons. J. Neurochem. 2003, 84, 347-362.
    • (2003) J. Neurochem. , vol.84 , pp. 347-362
    • Li, G.1    Faibushevich, A.2    Turunen, B.J.3    Yoon, S.O.4    Georg, G.5    Michaelis, M.L.6    Dobrowsky, R.T.7
  • 15
    • 0041703019 scopus 로고    scopus 로고
    • Pharmacological effects of formulation vehicles: Implications for cancer chemotherapy
    • ten Tije, A. J.; Verweij, J.; Loos, W. J.; Sparreboom, A. Pharmacological cological effects of formulation vehicles: implications for cancer chemotherapy. Clin. Pharmacokinet. 2003, 42, 665-685.
    • (2003) Clin. Pharmacokinet. , vol.42 , pp. 665-685
    • Ten Tije, A.J.1    Verweij, J.2    Loos, W.J.3    Sparreboom, A.4
  • 16
    • 0842282637 scopus 로고    scopus 로고
    • Taxane-mediated antiangiogenesis in vitro: Influence of formulation vehicles and binding proteins
    • Ng, S. S. W.; Fig, 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    Fig, W.D.2    Sparreboom, A.3
  • 17
    • 2342481809 scopus 로고    scopus 로고
    • Lessons learned from marketed and investigational prodrugs
    • Ettmayer, P.; Amidon, G. L.; Clement, B.; Testa, B. Lessons learned from marketed and investigational prodrugs. J. Med. Chem. 2004, 47, 2393-2404.
    • (2004) J. Med. Chem. , vol.47 , pp. 2393-2404
    • Ettmayer, P.1    Amidon, G.L.2    Clement, B.3    Testa, B.4
  • 18
    • 7444253306 scopus 로고    scopus 로고
    • Prodrug research: Futile or fertile?
    • Testa, B. Prodrug research: futile or fertile? Biochem. Pharmacol. 2004, 68, 2097-2106.
    • (2004) Biochem. Pharmacol. , vol.68 , pp. 2097-2106
    • Testa, B.1
  • 19
    • 1642296611 scopus 로고    scopus 로고
    • Prodrug as therapeutics
    • Stella, V. J. Prodrug as therapeutics. Expert Opin. Ther. Pat. 2004, 14, 277-280.
    • (2004) Expert Opin. Ther. Pat. , vol.14 , pp. 277-280
    • Stella, V.J.1
  • 20
    • 0035736251 scopus 로고    scopus 로고
    • The role of prodrug therapy in the treatment of cancer
    • Ferguson M. J.; Ahmed, F. Y.; Cassidy, J. The role of prodrug therapy in the treatment of cancer. Drug Resist. Updates 2001, 4, 225-232.
    • (2001) Drug Resist. Updates , vol.4 , pp. 225-232
    • Ferguson, M.J.1    Ahmed, F.Y.2    Cassidy, J.3
  • 21
    • 0031953554 scopus 로고    scopus 로고
    • Taxanes and other microtubule stabilizing agents
    • Ter Haar, E. Taxanes and other microtubule stabilizing agents. Expert Opin. Ther. Pat. 1998, 8, 571-586.
    • (1998) Expert Opin. Ther. Pat. , vol.8 , pp. 571-586
    • Ter Haar, E.1
  • 22
    • 0034088338 scopus 로고    scopus 로고
    • Recent strategies in the development of taxane anticancer drugs
    • Lin, S.; Ojima, I. Recent strategies in the development of taxane anticancer drugs. Expert Opin. Ther. Pat. 2000, 10, 869-889.
    • (2000) Expert Opin. Ther. Pat. , vol.10 , pp. 869-889
    • Lin, S.1    Ojima, I.2
  • 24
    • 12344310295 scopus 로고    scopus 로고
    • Recent progress in structure activity relationship and mechanistic studies of taxol analogues
    • Fang, W. S.; Liang, X. T. Recent progress in structure activity relationship and mechanistic studies of taxol analogues. Mini-Rev. Med. Chem. 2005, 5, 1-12.
    • (2005) Mini-Rev. Med. Chem. , vol.5 , pp. 1-12
    • Fang, W.S.1    Liang, X.T.2
  • 26
    • 0142183622 scopus 로고    scopus 로고
    • Improved chemical strategies for the targeted therapy of cancer
    • Maison, W.; Frangioni, J. V. Improved chemical strategies for the targeted therapy of cancer. Angew. Chem., Int. Ed. 2003, 42, 4726-4728.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4726-4728
    • Maison, W.1    Frangioni, J.V.2
  • 27
    • 22844436226 scopus 로고    scopus 로고
    • Recent advances in tumor-targeting anticancer drug conjugates
    • Jaracz, S.; Chen, J.; Kuznetsova, L. V.; Ojima, I. Recent advances in tumor-targeting anticancer drug conjugates. Bioorg. Med. Chem. 2005, 13, 5043-5054.
    • (2005) Bioorg. Med. Chem. , vol.13 , pp. 5043-5054
    • Jaracz, S.1    Chen, J.2    Kuznetsova, L.V.3    Ojima, I.4
  • 28
    • 1542351340 scopus 로고    scopus 로고
    • Tumor specific novel taxoid-monoclonal antibody conjugates
    • Wu, X.; Ojima, I. Tumor specific novel taxoid-monoclonal antibody conjugates. Curr. Med. Chem. 2004, 11, 429-438.
    • (2004) Curr. Med. Chem. , vol.11 , pp. 429-438
    • Wu, X.1    Ojima, I.2
  • 29
    • 77957053118 scopus 로고
    • Paclitaxel (Taxol) Formulation and Prodrugs
    • Ed.; Farina, V., Ed.; Elsevier: Amsterdam, The Netherlands
    • Vyas, D. M. Paclitaxel (Taxol) Formulation and Prodrugs. In The Chemistry and Pharmacology of Taxol and Its Derivatives; Ed.; Farina, V., Ed.; Elsevier: Amsterdam, The Netherlands, 1995; pp 103-130.
    • (1995) The Chemistry and Pharmacology of Taxol and Its Derivatives , pp. 103-130
    • Vyas, D.M.1
  • 30
    • 0031463596 scopus 로고    scopus 로고
    • Comparative molecular field analysis of a series of paclitaxel analogs
    • Zhu, Q.; Guo, Z.; Huang, N.; Wang, M.; Chu, F. Comparative molecular field analysis of a series of paclitaxel analogs. J. Med. Chem. 1997, 40, 4319-4328.
    • (1997) J. Med. Chem. , vol.40 , pp. 4319-4328
    • Zhu, Q.1    Guo, Z.2    Huang, N.3    Wang, M.4    Chu, F.5
  • 31
    • 0034041275 scopus 로고    scopus 로고
    • Recent advances in the chemistry of Taxol
    • Kingston, D. G. I. Recent advances in the chemistry of Taxol. J. Nat. Prod. 2000, 63, 726-734.
    • (2000) J. Nat. Prod. , vol.63 , pp. 726-734
    • Kingston, D.G.I.1
  • 33
    • 0041919716 scopus 로고    scopus 로고
    • A novel approach of water-soluble paclitaxel prodrug with no auxiliary and no by product: Design and synthesis of isotaxel
    • Hayashi, Y.; Skwarczynsi, M.; Hamada, Y.; Sohma, Y.; Kimura, T.; Kiso, Y. A novel approach of water-soluble paclitaxel prodrug with no auxiliary and no by product: Design and synthesis of isotaxel. J. Med. Chem. 2003, 46, 3782-3784.
    • (2003) J. Med. Chem. , vol.46 , pp. 3782-3784
    • Hayashi, Y.1    Skwarczynsi, M.2    Hamada, Y.3    Sohma, Y.4    Kimura, T.5    Kiso, Y.6
  • 35
    • 0026317822 scopus 로고
    • Modified Taxols. 6. Preparation of water-soluble prodrugs of Taxol
    • Zhao, Z.; Kingston, D. G. I.; Crosswell, A. R. Modified Taxols. 6. Preparation of water-soluble prodrugs of Taxol. J. Nat. Prod. 1991, 54, 1607-1611.
    • (1991) J. Nat. Prod. , vol.54 , pp. 1607-1611
    • Zhao, Z.1    Kingston, D.G.I.2    Crosswell, A.R.3
  • 36
    • 0026567883 scopus 로고
    • Synthesis and evaluation of some water-soluble prodrugs and derivatives of taxol with antitumor activity
    • Mathew, A. E.; Mejillano, M. R.; Nath, J. P.; Himes, R. H.; Stella, V. J. Synthesis and evaluation of some water-soluble prodrugs and derivatives of taxol with antitumor activity. J. Med. Chem. 1992, 35, 145-151.
    • (1992) J. Med. Chem. , vol.35 , pp. 145-151
    • Mathew, A.E.1    Mejillano, M.R.2    Nath, J.P.3    Himes, R.H.4    Stella, V.J.5
  • 37
  • 38
    • 0141538127 scopus 로고    scopus 로고
    • Enzyme and proton-activated prodrugs for a selective cancer therapy
    • Tietze, L. F.; Feuerstein, T. Enzyme and proton-activated prodrugs for a selective cancer therapy. Curr. Pharm. Des. 2003, 9, 2155-2175.
    • (2003) Curr. Pharm. Des. , vol.9 , pp. 2155-2175
    • Tietze, L.F.1    Feuerstein, T.2
  • 41
    • 0035952221 scopus 로고    scopus 로고
    • Controlled drug release: New water-soluble prodrugs of an HIV protease inhibitor
    • and references cited therein
    • Matsumoto, H.; Sohma, Y.; Kimura, T.; Hayashi, Y.; Kiso, Y. Controlled drug release: new water-soluble prodrugs of an HIV protease inhibitor. Bioorg. Med. Chem. Lett. 2001, 11, 605-609 and references cited therein.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 605-609
    • Matsumoto, H.1    Sohma, Y.2    Kimura, T.3    Hayashi, Y.4    Kiso, Y.5
  • 43
    • 0028896858 scopus 로고
    • Novel, water-soluble phosphate derivatives of 2′- ethoxycarbonylpaclitaxel as potential prodrugs of paclitaxel: Synthesis and antitumor evaluation
    • Ueda, Y.; Matiskella, J. D.; Mikkilineni, A. B.; Farina, V.; Knipe, J. O.; Rose, W. C.; Casazza, A. M.; Vyas, D. M. Novel, water-soluble phosphate derivatives of 2′-ethoxycarbonylpaclitaxel as potential prodrugs of paclitaxel: synthesis and antitumor evaluation. Bioorg. Med. Chem. Lett. 1995, 5, 247-252.
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 247-252
    • Ueda, Y.1    Matiskella, J.D.2    Mikkilineni, A.B.3    Farina, V.4    Knipe, J.O.5    Rose, W.C.6    Casazza, A.M.7    Vyas, D.M.8
  • 45
    • 0029863926 scopus 로고    scopus 로고
    • The role of rat serum carboxylesterase in the activation of paclitaxel and camptothecin prodrugs
    • Senter, P. D.; Marquardt, H.; Thomas, B. A.; Hammock, B. D.; Frank, L. S.; Svensson, H. P. The role of rat serum carboxylesterase in the activation of paclitaxel and camptothecin prodrugs. Cancer Res. 1996, 56, 1471-1474.
    • (1996) Cancer Res. , vol.56 , pp. 1471-1474
    • Senter, P.D.1    Marquardt, H.2    Thomas, B.A.3    Hammock, B.D.4    Frank, L.S.5    Svensson, H.P.6
  • 48
    • 0031809859 scopus 로고    scopus 로고
    • New active paclitaxel amino acids derivatives with improved water solubility
    • Paradis, R.; Page, M. New active paclitaxel amino acids derivatives with improved water solubility. Anticancer Res. 1998, 18, 2711-2716.
    • (1998) Anticancer Res. , vol.18 , pp. 2711-2716
    • Paradis, R.1    Page, M.2
  • 49
    • 0036740121 scopus 로고    scopus 로고
    • A novel 2′-(N-methylpyridinium acetate) prodrug of paclitaxel induces superior antitumor responses in preclinical cancer models
    • Wrasidlo, W.; Gaedicke, G.; Guy, R. K.; Renaud, J.; Pitsinos, E.; Nicolaou, K. C.; Reisfeld, R. A.; Lode, H. N. A novel 2′-(N- methylpyridinium acetate) prodrug of paclitaxel induces superior antitumor responses in preclinical cancer models. Bioconjugate Chem. 2002, 13, 1093-1099.
    • (2002) Bioconjugate Chem. , vol.13 , pp. 1093-1099
    • Wrasidlo, W.1    Gaedicke, G.2    Guy, R.K.3    Renaud, J.4    Pitsinos, E.5    Nicolaou, K.C.6    Reisfeld, R.A.7    Lode, H.N.8
  • 50
    • 23144447156 scopus 로고    scopus 로고
    • Kinetics of paclitaxel 2′-N-methylpyridinium mesylate decomposition
    • Qasem, J. G.; Bummer, P. M.; Digenis, G. A. Kinetics of paclitaxel 2′-N-methylpyridinium mesylate decomposition. AAPS PharmSciTech 2003, 4, 164-171.
    • (2003) AAPS PharmSciTech , vol.4 , pp. 164-171
    • Qasem, J.G.1    Bummer, P.M.2    Digenis, G.A.3
  • 54
    • 0344824453 scopus 로고    scopus 로고
    • Arginine-based molecular transporters: The synthesis and chemical evaluation of releasable Taxol-transporter conjugates
    • Kirschberg, T. A.; VanDeusen, C. L.; Rothbard, J. B.; Yang, M.; Wender. P. A. Arginine-based molecular transporters: the synthesis and chemical evaluation of releasable Taxol-transporter conjugates. Org. Lett. 2003, 5, 3459-3462.
    • (2003) Org. Lett. , vol.5 , pp. 3459-3462
    • Kirschberg, T.A.1    VanDeusen, C.L.2    Rothbard, J.B.3    Yang, M.4    Wender, P.A.5
  • 55
    • 0037103242 scopus 로고    scopus 로고
    • Arginine-rich molecular transporters for drug delivery: Role of backbone spacing in cellular uptake
    • Rothbard, J. B.; Kreider, E.; VanDeusen, C. L.; Wright, L.; Wylie, B. L.; Wender, P. A. Arginine-rich molecular transporters for drug delivery: role of backbone spacing in cellular uptake. J. Med. Chem. 2002, 45, 3612-3618.
    • (2002) J. Med. Chem. , vol.45 , pp. 3612-3618
    • Rothbard, J.B.1    Kreider, E.2    Vandeusen, C.L.3    Wright, L.4    Wylie, B.L.5    Wender, P.A.6
  • 56
    • 0141942114 scopus 로고    scopus 로고
    • Membrane permeability commonly shared among arginine-rich peptides
    • Futaki, S.; Goto, S.; Sugiura, Y. Membrane permeability commonly shared among arginine-rich peptides. J. Mol. Recognit. 2003, 16, 260-264.
    • (2003) J. Mol. Recognit. , vol.16 , pp. 260-264
    • Futaki, S.1    Goto, S.2    Sugiura, Y.3
  • 57
    • 13844272403 scopus 로고    scopus 로고
    • Adaptive translocation: The role of hydrogen bonding and membrane potential in the uptake of guanidinium-rich transporters into cells
    • Rothbard, J. B.; Jessop, T. C.; Wender, P. A. Adaptive translocation: the role of hydrogen bonding and membrane potential in the uptake of guanidinium-rich transporters into cells. Adv. Drug Delivery-Rev. 2005, 57, 495-504.
    • (2005) Adv. Drug Delivery-Rev. , vol.57 , pp. 495-504
    • Rothbard, J.B.1    Jessop, T.C.2    Wender, P.A.3
  • 58
  • 59
    • 33645868648 scopus 로고    scopus 로고
    • Synthesis and biological activity of conjugates between paclitaxel and the cell delivery vector penetratin
    • Wang, S.; Zhelev, N. Z.; Duff, S.; Fischer, P. M. Synthesis and biological activity of conjugates between paclitaxel and the cell delivery vector penetratin. Bioorg. Med. Chem. Lett. 2006, 16, 2628-2631.
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 2628-2631
    • Wang, S.1    Zhelev, N.Z.2    Duff, S.3    Fischer, P.M.4
  • 61
    • 0034998446 scopus 로고    scopus 로고
    • Synthesis and preclinical characterization of a paclitaxel prodrug with improved antitumor activity and water solubility
    • Niethammer, A.; Gaedicke, G.; Lode, H. N.; Wrasidlo, W. Synthesis and preclinical characterization of a paclitaxel prodrug with improved antitumor activity and water solubility. Bioconjugate Chem. 2001, 12, 414-420.
    • (2001) Bioconjugate Chem. , vol.12 , pp. 414-420
    • Niethammer, A.1    Gaedicke, G.2    Lode, H.N.3    Wrasidlo, W.4
  • 64
    • 0036890172 scopus 로고    scopus 로고
    • Pivalate-generating prodrugs and carnitine homeostasis in man
    • Brass, E. P. Pivalate-generating prodrugs and carnitine homeostasis in man. Pharmacol. Rev. 2002, 54, 589-598.
    • (2002) Pharmacol. Rev. , vol.54 , pp. 589-598
    • Brass, E.P.1
  • 65
    • 0031952207 scopus 로고    scopus 로고
    • Fosphentoin
    • Luer, M. S. Fosphentoin. Neurol. Res. 1998, 20, 178-182.
    • (1998) Neurol. Res. , vol.20 , pp. 178-182
    • Luer, M.S.1
  • 66
    • 7944229908 scopus 로고    scopus 로고
    • Q-N intramolecular acyl migration reaction in the development of prodrugs and the synthesis of difficult sequence-containing bioactive peptides
    • Sohma, Y.; Hayashi, Y.; Skwarczynski, M.; Hamada, Y.; Sasaki, M.; Kimura, T.; Kiso, Y. Q-N intramolecular acyl migration reaction in the development of prodrugs and the synthesis of difficult sequence-containing bioactive peptides. Biopolymers 2004, 76, 344-356.
    • (2004) Biopolymers , vol.76 , pp. 344-356
    • Sohma, Y.1    Hayashi, Y.2    Skwarczynski, M.3    Hamada, Y.4    Sasaki, M.5    Kimura, T.6    Kiso, Y.7
  • 68
    • 17144381272 scopus 로고    scopus 로고
    • No auxiliary, no byproduct strategy for water-soluble prodrugs of taxoids: Scope and limitation of O-N intramolecular acyl and acyloxy migration reactions
    • Skwarczynski, M.; Sohma, Y.; Noguchi, M.; Kimura, M.; Hayashi, Y.; Hamada, Y.; Kimura, T.; Kiso, Y. No auxiliary, no byproduct strategy for water-soluble prodrugs of taxoids: scope and limitation of O-N intramolecular acyl and acyloxy migration reactions. J. Med. Chem. 2005, 48, 2655-2666.
    • (2005) J. Med. Chem. , vol.48 , pp. 2655-2666
    • Skwarczynski, M.1    Sohma, Y.2    Noguchi, M.3    Kimura, M.4    Hayashi, Y.5    Hamada, Y.6    Kimura, T.7    Kiso, Y.8
  • 69
    • 0035253404 scopus 로고    scopus 로고
    • Drug-targeting strategies in cancer therapy
    • Huang, P. S.; Oliff, A. Drug-targeting strategies in cancer therapy. Curr. Opin. Genet. Dev. 2001, 11, 104-110.
    • (2001) Curr. Opin. Genet. Dev. , vol.11 , pp. 104-110
    • Huang, P.S.1    Oliff, A.2
  • 70
    • 0036678137 scopus 로고    scopus 로고
    • Up-regulation of plasma membrane-associated ganglioside sialidase (Neu3) in human colon cancer and its involvement in apoptosis suppression
    • Kakugawa, Y.; Wada, T.; Yamaguchi, K.; Yamanami, H.; Ouchi, K.; Sato, I.; Miyagi, T. Up-regulation of plasma membrane-associated ganglioside sialidase (Neu3) in human colon cancer and its involvement in apoptosis suppression. Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 10718-10723.
    • (2002) Proc. Natl. Acad. Sci. U.S.A. , vol.99 , pp. 10718-10723
    • Kakugawa, Y.1    Wada, T.2    Yamaguchi, K.3    Yamanami, H.4    Ouchi, K.5    Sato, I.6    Miyagi, T.7
  • 71
    • 0032488645 scopus 로고    scopus 로고
    • Design and synthesis of a water-soluble Taxol analogue: Taxol-sialyl conjugate
    • Takahashi, T.; Tsukamoto, H.; Yamada, H. Design and synthesis of a water-soluble Taxol analogue: Taxol-sialyl conjugate. Bioorg. Med. Chem. Lett. 1998, 8, 113-116.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 113-116
    • Takahashi, T.1    Tsukamoto, H.2    Yamada, H.3
  • 72
    • 0034941481 scopus 로고    scopus 로고
    • Anticancer prodrugs for application in monotherapy: Targeting hypoxia, tumor-associated enzymes, and receptors
    • De Groot, F. M. H.; Darnen, E. W. P.; Scheeren, H. W. Anticancer prodrugs for application in monotherapy: targeting hypoxia, tumor-associated enzymes, and receptors. Curr. Med. Chem. 2001, 8, 1093-1122.
    • (2001) Curr. Med. Chem. , vol.8 , pp. 1093-1122
    • De Groot, F.M.H.1    Darnen, E.W.P.2    Scheeren, H.W.3
  • 73
    • 0034632849 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2′-carbamate-linked and 2′-carbonate-linked prodrugs of paclitaxel. Selective activation by the tumor-associated protease plasmin
    • de Groot, F. M. H.; van Berkom, L. W. A.; Scheeren, H. W. Synthesis and biological evaluation of 2′-carbamate-linked and 2′-carbonate-linked prodrugs of paclitaxel. Selective activation by the tumor-associated protease plasmin. J. Med. Chem. 2000, 43, 3093-3102.
    • (2000) J. Med. Chem. , vol.43 , pp. 3093-3102
    • De Groot, F.M.H.1    Van Berkom, L.W.A.2    Scheeren, H.W.3
  • 75
    • 0035904930 scopus 로고    scopus 로고
    • Bioreductive and gene therapy approaches to hypoxic diseases
    • Jaffar, M.; Williams, K. J.; Stratford, I J. Bioreductive and gene therapy approaches to hypoxic diseases. Adv. Drug Delivery Rev. 2001, 55, 217-228.
    • (2001) Adv. Drug Delivery Rev. , vol.55 , pp. 217-228
    • Jaffar, M.1    Williams, K.J.2    Stratford, I.J.3
  • 76
    • 2942590732 scopus 로고    scopus 로고
    • Exploiting tumor hypoxia in cancer treatment
    • Brown, J. M.; Wilson, W. R. Exploiting tumor hypoxia in cancer treatment. Nat. Rev. Cancer 2004, 4, 437-447.
    • (2004) Nat. Rev. Cancer , vol.4 , pp. 437-447
    • Brown, J.M.1    Wilson, W.R.2
  • 78
    • 21244461192 scopus 로고    scopus 로고
    • Hypoxia-activated anticancer drugs
    • Denny, W. A. Hypoxia-activated anticancer drugs. Expert Opin. Ther. Pat. 2005, 15, 635-646.
    • (2005) Expert Opin. Ther. Pat. , vol.15 , pp. 635-646
    • Denny, W.A.1
  • 82
    • 8744295088 scopus 로고    scopus 로고
    • Antibody-directed enzyme prodrua therapy (ADEPT) for cancer
    • Bagshawe, K. D.; Sharma, S. K.; Begent, R. H. J. Antibody-directed enzyme prodrua therapy (ADEPT) for cancer. Expert Opin. Biol. Ther. 2004, 4, 1777-1789.
    • (2004) Expert Opin. Biol. Ther. , vol.4 , pp. 1777-1789
    • Bagshawe, K.D.1    Sharma, S.K.2    Begent, R.H.J.3
  • 83
    • 0035181464 scopus 로고    scopus 로고
    • Strategies for enzyme/prodrug cancer therapy
    • Xu, G.; McLeod, H. L. Strategies for enzyme/prodrug cancer therapy. Clin. Cancer Res. 2001, 7, 3314-3324.
    • (2001) Clin. Cancer Res. , vol.7 , pp. 3314-3324
    • Xu, G.1    McLeod, H.L.2
  • 84
    • 0029279040 scopus 로고
    • Synthesis and β-lactamase-mediated activation of a cephalosporin-Taxol prodrug
    • Rodrigues, M. L.; Carter, P.; Wirth, C.; Mullins, S.; Lee, A.; Blackburn, B. K. Synthesis and β-lactamase-mediated activation of a cephalosporin-Taxol prodrug. Chem. Biol. 1995, 2, 223-227.
    • (1995) Chem. Biol. , vol.2 , pp. 223-227
    • Rodrigues, M.L.1    Carter, P.2    Wirth, C.3    Mullins, S.4    Lee, A.5    Blackburn, B.K.6
  • 85
    • 0037328509 scopus 로고    scopus 로고
    • Cephalosporin prodrugs of paclitaxel for immunologically specific activation by L-49-sFv-β-lactamase fusion protein
    • Vrudhula, V. M.; Kerr, D. E.; Siemers, N. O.; Dubowchik, G. M.; Senter, P. D. Cephalosporin prodrugs of paclitaxel for immunologically specific activation by L-49-sFv-β-lactamase fusion protein. Bioorg. Med. Chem. Lett. 2003, 13, 539-542.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 539-542
    • Vrudhula, V.M.1    Kerr, D.E.2    Siemers, N.O.3    Dubowchik, G.M.4    Senter, P.D.5
  • 87
    • 0031081690 scopus 로고    scopus 로고
    • Synthesis and biological activity of β-glucuronyl carbamate-based prodrugs of paclitaxel as potential candidates for ADEPT
    • De Bont, D. B. A.; Leenders, R. G. G.; Haisma, H. J.; Van der Meulen-Muileman, L; Scheeren, H. W. Synthesis and biological activity of β-glucuronyl carbamate-based prodrugs of paclitaxel as potential candidates for ADEPT. Bioorg. Med. Chem. 1997, 5, 405-414.
    • (1997) Bioorg. Med. Chem. , vol.5 , pp. 405-414
    • De Bont, D.B.A.1    Leenders, R.G.G.2    Haisma, H.J.3    Van Der Meulen-Muileman, L.4    Scheeren, H.W.5
  • 88
    • 0034988631 scopus 로고    scopus 로고
    • Cancer chemotherapy: A paclitaxel prodrug for ADEPT (antibody-directed enzyme prodrug therapy)
    • Schmidt, F.; Ungureanu, I.; Duval, R.; Pompon, A.; Monneret, C. Cancer chemotherapy: A paclitaxel prodrug for ADEPT (antibody-directed enzyme prodrug therapy). Eur. J. Org. Chem. 2001, 11, 2129-2134.
    • (2001) Eur. J. Org. Chem. , vol.11 , pp. 2129-2134
    • Schmidt, F.1    Ungureanu, I.2    Duval, R.3    Pompon, A.4    Monneret, C.5
  • 90
    • 33646763486 scopus 로고    scopus 로고
    • New Taxol (paclitaxel) prodrugs designed for ADEPT and PMT strategies in cancer chemotherapy
    • El, Alaoui, A.; Saha, N.; Schmidt, F.; Monneret, C.; Florent, J. C. New Taxol (paclitaxel) prodrugs designed for ADEPT and PMT strategies in cancer chemotherapy. Bioorg. Med. Chem. 2006, 14, 5012-5019.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 5012-5019
    • El Alaoui, A.1    Saha, N.2    Schmidt, F.3    Monneret, C.4    Florent, J.C.5
  • 91
    • 2942612987 scopus 로고    scopus 로고
    • Membrane transporter/receptor-targeted prodrug design: Strategies for human and veterinary drug development
    • Majumdar, S.; Duvvuri, S.; Mitra, A. K. Membrane transporter/receptor- targeted prodrug design: strategies for human and veterinary drug development. Adv. Drug Delivery Rev. 2004, 56, 1437-1452.
    • (2004) Adv. Drug Delivery Rev. , vol.56 , pp. 1437-1452
    • Majumdar, S.1    Duvvuri, S.2    Mitra, A.K.3
  • 92
    • 0032727981 scopus 로고    scopus 로고
    • Paclitaxel derivatives for targeted therapy of cancer: Toward the development of smart taxanes
    • Safavy, A.; Raisch, K. P.; Khazaeli, M. B.; Buchsbaum, D. J.; Bonner, J. A. Paclitaxel derivatives for targeted therapy of cancer: toward the development of smart taxanes. J. Med. Chem. 1999, 42, 4919-4924.
    • (1999) J. Med. Chem. , vol.42 , pp. 4919-4924
    • Safavy, A.1    Raisch, K.P.2    Khazaeli, M.B.3    Buchsbaum, D.J.4    Bonner, J.A.5
  • 93
    • 0032797051 scopus 로고    scopus 로고
    • Cancer chemotherapy based on targeting of cytotoxic peptide conjugates to their receptors on tumors
    • Schally, A. V.; Nagy, A. Cancer chemotherapy based on targeting of cytotoxic peptide conjugates to their receptors on tumors. Eur. J. Endocrinol. 1999, 141, 1-14.
    • (1999) Eur. J. Endocrinol. , vol.141 , pp. 1-14
    • Schally, A.V.1    Nagy, A.2
  • 94
    • 15544371477 scopus 로고    scopus 로고
    • Targeting cytotoxic conjugates of somatostatin, luteinizing hormone-releasing hormone and bombesin to cancers expressing their receptors: A "smarter" chemotherapy
    • Nagy, A.; Schally, A. V. Targeting cytotoxic conjugates of somatostatin, luteinizing hormone-releasing hormone and bombesin to cancers expressing their receptors: a "smarter" chemotherapy. Curr. Pharm. Des. 2005, 11, 1167-1180.
    • (2005) Curr. Pharm. Des. , vol.11 , pp. 1167-1180
    • Nagy, A.1    Schally, A.V.2
  • 95
    • 33646909900 scopus 로고    scopus 로고
    • Single-drug multiligand conjugates: Synthesis and preliminary cytotoxicity evaluation of a paclitaxel-dipeptide "scorpion" molecule
    • Safavy, A.; Raisch, K. P.; Matusiak, D.; Bhatnagar, S.; Helson, L. Single-drug multiligand conjugates: synthesis and preliminary cytotoxicity evaluation of a paclitaxel-dipeptide "scorpion" molecule. Bioconjugate Chem. 2006, 17, 565-570.
    • (2006) Bioconjugate Chem. , vol.17 , pp. 565-570
    • Safavy, A.1    Raisch, K.P.2    Matusiak, D.3    Bhatnagar, S.4    Helson, L.5
  • 96
    • 0033927859 scopus 로고    scopus 로고
    • Targeting delivery of paclitaxel into tumor cells via somatostatin receptor endocytosis
    • Huang, C. M.; Wu, Y. T.; Chen, S. T. Targeting delivery of paclitaxel into tumor cells via somatostatin receptor endocytosis. Chem. Biol. 2000, 7, 453-461.
    • (2000) Chem. Biol. , vol.7 , pp. 453-461
    • Huang, C.M.1    Wu, Y.T.2    Chen, S.T.3
  • 97
    • 13944278751 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of dimeric RGD peptide-paclitaxel conjugate as a model for integrin-targeted drug delivery
    • Chen, X.; Plasencia, C.; Hou, Y.; Neamati, N. Synthesis and biological evaluation of dimeric RGD peptide-paclitaxel conjugate as a model for integrin-targeted drug delivery. J. Med. Chem. 2005, 48, 1098-1106.
    • (2005) J. Med. Chem. , vol.48 , pp. 1098-1106
    • Chen, X.1    Plasencia, C.2    Hou, Y.3    Neamati, N.4
  • 98
    • 0032580526 scopus 로고    scopus 로고
    • Folate-mediated targeting of antineoplastic drugs, imaging agents, and nucleic acids to cancer cells
    • Wang, S.; Low, P. S. Folate-mediated targeting of antineoplastic drugs, imaging agents, and nucleic acids to cancer cells. J. Controlled Release 1998, 53, 39-48.
    • (1998) J. Controlled Release , vol.53 , pp. 39-48
    • Wang, S.1    Low, P.S.2
  • 99
    • 1942503277 scopus 로고    scopus 로고
    • Folate receptor-targeted immunotherapy of cancer: Mechanism and therapeutic potential
    • Lu, Y.; Sega, E.; Leamon, C. P.; Low, P. S. Folate receptor-targeted immunotherapy of cancer: mechanism and therapeutic potential. Adv. Drug Delivery Rev. 2004, 56, 1161-1176.
    • (2004) Adv. Drug Delivery Rev. , vol.56 , pp. 1161-1176
    • Lu, Y.1    Sega, E.2    Leamon, C.P.3    Low, P.S.4
  • 100
    • 0036242840 scopus 로고    scopus 로고
    • Synthesis and evaluation of Taxol-folic acid conjugates as targeted antineoplastics
    • Lee, J. W.; Lu, J. Y.; Low, P. S.; Fuchs, P. L. Synthesis and evaluation of Taxol-folic acid conjugates as targeted antineoplastics. Bioorg. Med. Chem. 2002, 10, 2397-2414.
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 2397-2414
    • Lee, J.W.1    Lu, J.Y.2    Low, P.S.3    Fuchs, P.L.4
  • 101
    • 1442285546 scopus 로고    scopus 로고
    • Design, synthesis, and bioactivities of steroid-linked Taxol analogues as potential targeted drugs for prostate and breast cancer
    • Liu, C.; Strobl, J. S.; Bane, S.; Schilling, J. K.; McCracken, M.; Chatterjee, S. K.; Rahim-Bata, R.; Kingston, D. G. I. Design, synthesis, and bioactivities of steroid-linked Taxol analogues as potential targeted drugs for prostate and breast cancer. J. Nat. Prod. 2004, 67, 152-159.
    • (2004) J. Nat. Prod. , vol.67 , pp. 152-159
    • Liu, C.1    Strobl, J.S.2    Bane, S.3    Schilling, J.K.4    McCracken, M.5    Chatterjee, S.K.6    Rahim-Bata, R.7    Kingston, D.G.I.8
  • 103
    • 0842333184 scopus 로고    scopus 로고
    • A folate receptor-targeted emulsion formulation for paclitaxel
    • Stevens, P. J.; Lee, R. J. A folate receptor-targeted emulsion formulation for paclitaxel. Anticancer Res. 2003, 23, 4927-4932.
    • (2003) Anticancer Res. , vol.23 , pp. 4927-4932
    • Stevens, P.J.1    Lee, R.J.2
  • 104
    • 17644366858 scopus 로고    scopus 로고
    • A folate receptor-targeted lipid nanoparticle formulation for a lipophilic paclitaxel prodrug
    • Stevens, P. J.; Sekido, M.; Lee, R. J. A folate receptor-targeted lipid nanoparticle formulation for a lipophilic paclitaxel prodrug. Pharm. Res. 2004, 21, 2153-2157.
    • (2004) Pharm. Res. , vol.21 , pp. 2153-2157
    • Stevens, P.J.1    Sekido, M.2    Lee, R.J.3
  • 105
    • 24744446010 scopus 로고    scopus 로고
    • A fullerene-paclitaxel chemotherapeutic: Synthesis, characterization, and study of biological activity in tissue culture
    • Zakharian, T. Y.; Seryshev, A.; Sitharaman, B.; Gilbert, B. E.; Knight, V.; Wilson, L. J. A fullerene-paclitaxel chemotherapeutic: synthesis, characterization, and study of biological activity in tissue culture. J. Am. Chem. Soc. 2005, 127, 12508-12509.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 12508-12509
    • Zakharian, T.Y.1    Seryshev, A.2    Sitharaman, B.3    Gilbert, B.E.4    Knight, V.5    Wilson, L.J.6
  • 106
    • 0033253860 scopus 로고    scopus 로고
    • Growth inhibition of a human ovarian tumor by a novel paclitaxel derivative in SCID mice
    • Ahmad, I.; Masters, G. R.; Schupsky, J. J.; Nguyen, J.; Ali. S.; Janoff, A. S.; Mayhew, E. Growth inhibition of a human ovarian tumor by a novel paclitaxel derivative in SCID mice. Oncol. Res. 1999, 11, 273-280.
    • (1999) Oncol. Res. , vol.11 , pp. 273-280
    • Ahmad, I.1    Masters, G.R.2    Schupsky, J.J.3    Nguyen, J.4    Ali, S.5    Janoff, A.S.6    Mayhew, E.7
  • 107
    • 0034036028 scopus 로고    scopus 로고
    • A differential scanning calorimetry study of phosphocholines mixed with paclitaxel and its bromoacylated taxanes
    • Ali, S.; Minchey, S.; Janoff, A.; Mayhew. E. A differential scanning calorimetry study of phosphocholines mixed with paclitaxel and its bromoacylated taxanes. Biophys. J. 2000, 78, 246-256.
    • (2000) Biophys. J. , vol.78 , pp. 246-256
    • Ali, S.1    Minchey, S.2    Janoff, A.3    Mayhew, E.4
  • 109
    • 0037426690 scopus 로고    scopus 로고
    • A lipophilic paclitaxel derivative incorporated in a lipid emulsion for parenteral administration
    • Lundberg, B. B.; Risovic, V.; Ramaswamy, M.; Wasan, K. M. A lipophilic paclitaxel derivative incorporated in a lipid emulsion for parenteral administration. J. Controlled Release 2003, 86, 93-100.
    • (2003) J. Controlled Release , vol.86 , pp. 93-100
    • Lundberg, B.B.1    Risovic, V.2    Ramaswamy, M.3    Wasan, K.M.4
  • 110
    • 18744406323 scopus 로고    scopus 로고
    • Improvement of paclitaxel therapeutic index by derivatization and association to a cholesterol-rich microemulsion: In vitro and in vivo studies
    • Rodrigues, D. G.; Maria, D. A.; Fernandes, D. C.; Valduga, C. J.; Couto, R. D.; Ibanez, O. C. M.; Maranhao, R. C. Improvement of paclitaxel therapeutic index by derivatization and association to a cholesterol-rich microemulsion: in vitro and in vivo studies. Cancer Chemother. Pharmacol. 2005, 55, 565-576.
    • (2005) Cancer Chemother. Pharmacol. , vol.55 , pp. 565-576
    • Rodrigues, D.G.1    Maria, D.A.2    Fernandes, D.C.3    Valduga, C.J.4    Couto, R.D.5    Ibanez, O.C.M.6    Maranhao, R.C.7
  • 115
    • 9144249673 scopus 로고    scopus 로고
    • Phase I/II study of DHA-paclitaxel in combination with carboplatin in patients with advanced malignant solid tumours
    • Harries, M.; O'Donnell, A.; Scurr, M.; Reade, S.; Cole, C.; Judson, I.; Greystoke, A.; Twelves, C.; Kaye, S. Phase I/II study of DHA-paclitaxel in combination with carboplatin in patients with advanced malignant solid tumours. Br. J. Cancer 2004, 91, 1651-1655.
    • (2004) Br. J. Cancer , vol.91 , pp. 1651-1655
    • Harries, M.1    O'Donnell, A.2    Scurr, M.3    Reade, S.4    Cole, C.5    Judson, I.6    Greystoke, A.7    Twelves, C.8    Kaye, S.9
  • 116
    • 13944258970 scopus 로고    scopus 로고
    • Intracellular targeting of polymer-bound drugs for cancer chemotherapy
    • Nori, A.; Kopecek, J. Intracellular targeting of polymer-bound drugs for cancer chemotherapy. Adv. Drug Delivery Rev. 2005, 57, 609-636.
    • (2005) Adv. Drug Delivery Rev. , vol.57 , pp. 609-636
    • Nori, A.1    Kopecek, J.2
  • 117
    • 0034993240 scopus 로고    scopus 로고
    • The enhanced permeability and retention (EPR) effect in tumor vasculature: The key role of tumor-selective macromolecular drug targeting
    • Maeda, H. The enhanced permeability and retention (EPR) effect in tumor vasculature: The key role of tumor-selective macromolecular drug targeting. Adv. Enzyme Regul. 2001, 41, 189-207.
    • (2001) Adv. Enzyme Regul. , vol.41 , pp. 189-207
    • Maeda, H.1
  • 118
    • 0035816204 scopus 로고    scopus 로고
    • Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS
    • Maeda, H.; Sawa, T.; Konno, T. Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS. J. Controlled Release 2001, 74, 47-61.
    • (2001) J. Controlled Release , vol.74 , pp. 47-61
    • Maeda, H.1    Sawa, T.2    Konno, T.3
  • 120
    • 0028062072 scopus 로고
    • Highly water soluble taxol derivatives: 2′-polyethylene glycol esters as potential prodrugs
    • Greenwald, R. B.; Pendri, A.; Bolikal, D.; Gilbert, C. W. Highly water soluble taxol derivatives: 2′-polyethylene glycol esters as potential prodrugs. Bioorg. Med. Chem. Lett. 1994, 4, 2465-2470.
    • (1994) Bioorg. Med. Chem. Lett. , vol.4 , pp. 2465-2470
    • Greenwald, R.B.1    Pendri, A.2    Bolikal, D.3    Gilbert, C.W.4
  • 121
    • 0030071043 scopus 로고    scopus 로고
    • Drug delivery systems: Water soluble Taxol 2′-poly(ethylene glycol) ester prodrugs. Design and in vivo effectiveness
    • Greenwald, R. B.; Gilbert, C. W.; Pendri, A.; Conover, C. D.; Xia, J.; Martinez, A. Drug delivery systems: water soluble Taxol 2′-poly(ethylene glycol) ester prodrugs. Design and in vivo effectiveness. J. Med. Chem. 1996, 39, 424-431.
    • (1996) J. Med. Chem. , vol.39 , pp. 424-431
    • Greenwald, R.B.1    Gilbert, C.W.2    Pendri, A.3    Conover, C.D.4    Xia, J.5    Martinez, A.6
  • 122
    • 0031857631 scopus 로고    scopus 로고
    • Antitumor activity of paclitaxel-2′-glycinate conjugated to poly(ethylene glycol): A water-soluble prodrug
    • Pendri, A.; Conover, C. D.; Greenwald, R. B. Antitumor activity of paclitaxel-2′-glycinate conjugated to poly(ethylene glycol): a water-soluble prodrug. Anti-Cancer Drug Des. 1998, 13, 387-395.
    • (1998) Anti-Cancer Drug Des. , vol.13 , pp. 387-395
    • Pendri, A.1    Conover, C.D.2    Greenwald, R.B.3
  • 123
    • 0029981113 scopus 로고    scopus 로고
    • Synthesis and evaluation of water-soluble polyethylene glycol-paclitaxel conjugate as a paclitaxel prodrug
    • Li, C.; Yu, D.; Inoue, T.; Yang, D. J.; Milas, L.; Hunter, N. R.; Kim, E. E.; Wallace, S. Synthesis and evaluation of water-soluble polyethylene glycol-paclitaxel conjugate as a paclitaxel prodrug. Anti-Cancer Drugs 1996, 7, 642-648.
    • (1996) Anti-Cancer Drugs , vol.7 , pp. 642-648
    • Li, C.1    Yu, D.2    Inoue, T.3    Yang, D.J.4    Milas, L.5    Hunter, N.R.6    Kim, E.E.7    Wallace, S.8
  • 124
    • 0033978316 scopus 로고    scopus 로고
    • Preparation, characterization, cytotoxicity and pharmacokinetics of liposomes containing water-soluble prodrugs of paclitaxel
    • Ceruti, M.; Crosasso, P.; Brusa, P.; Arpicco, S.; Dosio, F.; Cattel, L. Preparation, characterization, cytotoxicity and pharmacokinetics of liposomes containing water-soluble prodrugs of paclitaxel. J. Controlled Release 2000, 63, 141-153.
    • (2000) J. Controlled Release , vol.63 , pp. 141-153
    • Ceruti, M.1    Crosasso, P.2    Brusa, P.3    Arpicco, S.4    Dosio, F.5    Cattel, L.6
  • 125
    • 0037131724 scopus 로고    scopus 로고
    • Synthesis and evaluation of water-soluble paclitaxel prodrugs
    • Feng, X.; Yuan, Y.-J.; Wu, J.-C. Synthesis and evaluation of water-soluble paclitaxel prodrugs. Bioorg. Med. Chem. Lett. 2002, 12, 3301-3303.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 3301-3303
    • Feng, X.1    Yuan, Y.-J.2    Wu, J.-C.3
  • 127
    • 1942438684 scopus 로고    scopus 로고
    • Polymeric anticancer drugs with pH-controlled activation
    • Ulbrich, K.; Subr, V. Polymeric anticancer drugs with pH-controlled activation. Adv. Drug Delivery Rev. 2004, 56, 123-1050.
    • (2004) Adv. Drug Delivery Rev. , vol.56 , pp. 123-1050
    • Ulbrich, K.1    Subr, V.2
  • 129
    • 9644266802 scopus 로고    scopus 로고
    • Synthesis and characterization of the paclitaxel/MPEG-PLA block copolymer conjugate
    • Zhang, X.; Li, Y.; Chen, X.; Wang, X.; Xu, X.; Liang, Q.; Hu, J.; Jing, X. Synthesis and characterization of the paclitaxel/MPEG-PLA block copolymer conjugate. Biomaterials 2005, 26, 2121-2128.
    • (2005) Biomaterials , vol.26 , pp. 2121-2128
    • Zhang, X.1    Li, Y.2    Chen, X.3    Wang, X.4    Xu, X.5    Liang, Q.6    Hu, J.7    Jing, X.8
  • 130
    • 3242736466 scopus 로고    scopus 로고
    • Enhanced paclitaxel bioavailability after oral administration of PEGylated paclitaxel prodrug for oral delivery in rats
    • Choi, J.-S.; Jo, B. W. Enhanced paclitaxel bioavailability after oral administration of PEGylated paclitaxel prodrug for oral delivery in rats. Int. J. Pharm. 2004, 280, 221-227.
    • (2004) Int. J. Pharm. , vol.280 , pp. 221-227
    • Choi, J.-S.1    Jo, B.W.2
  • 131
    • 1442359716 scopus 로고    scopus 로고
    • Enhanced paclitaxel bioavailability after oral administration of paclitaxel or prodrug to rats pretreated with quercetin
    • Choi, J. S.; Jo, B. W.; Kim, Y. C. Enhanced paclitaxel bioavailability after oral administration of paclitaxel or prodrug to rats pretreated with quercetin. Eur. J. Pharm, Biopharm. 2004, 57, 313-318.
    • (2004) Eur. J. Pharm, Biopharm. , vol.57 , pp. 313-318
    • Choi, J.S.1    Jo, B.W.2    Kim, Y.C.3
  • 132
    • 13844256394 scopus 로고    scopus 로고
    • Enhanced paclitaxel bioavailability after oral coadministration of paclitaxel prodrug with naringin to rats
    • Choi, J. S.; Shin, S. C. Enhanced paclitaxel bioavailability after oral coadministration of paclitaxel prodrug with naringin to rats. Int. J. Pharm. 2005, 292, 149-156.
    • (2005) Int. J. Pharm. , vol.292 , pp. 149-156
    • Choi, J.S.1    Shin, S.C.2
  • 133
    • 0033200301 scopus 로고    scopus 로고
    • Synthesis and selective cytotoxicity of a hyaluronic acid-antitumor bioconjugate
    • Luo, Y.; Prestwich, G. D. Synthesis and selective cytotoxicity of a hyaluronic acid-antitumor bioconjugate. Bioconjugate Chem. 1999, 10, 755-763.
    • (1999) Bioconjugate Chem. , vol.10 , pp. 755-763
    • Luo, Y.1    Prestwich, G.D.2
  • 134
    • 0034208501 scopus 로고    scopus 로고
    • A hyaluronic acid - Taxol antitumor bioconjugate targeted to cancer cells
    • Luo, Y.; Ziebell, M. R.; Prestwich, G. D. A hyaluronic acid-Taxol antitumor bioconjugate targeted to cancer cells. Biomacromolecules 2000, 1, 208-218.
    • (2000) Biomacromolecules , vol.1 , pp. 208-218
    • Luo, Y.1    Ziebell, M.R.2    Prestwich, G.D.3
  • 135
    • 13644257605 scopus 로고    scopus 로고
    • Delivery platform for hydrophobic drugs: Prodrug approach combined with self-assembled multilayers
    • Thierry, B.; Kujawa, P.; Tkaczyk, C.; Winnik, F. M.; Bilodeau, L.; Tabrizian, M. Delivery platform for hydrophobic drugs: prodrug approach combined with self-assembled multilayers. J. Am. Chem. Soc. 2005, 127, 1626-1627.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 1626-1627
    • Thierry, B.1    Kujawa, P.2    Tkaczyk, C.3    Winnik, F.M.4    Bilodeau, L.5    Tabrizian, M.6
  • 136
    • 0141615972 scopus 로고    scopus 로고
    • Clinical implications of N-(2-hydroxypropyl)methacrylamide copolymers
    • Rihova, B.; Kubackova, K. Clinical implications of N-(2-hydroxypropyl) methacrylamide copolymers. Curr. Pharm. Biotechnol 2003, 4, 311-322.
    • (2003) Curr. Pharm. Biotechnol. , vol.4 , pp. 311-322
    • Rihova, B.1    Kubackova, K.2
  • 137
    • 0035816143 scopus 로고    scopus 로고
    • Polymer-drug conjugates, polymer-directed enzyme prodrug therapy (PDEPT) and (polymer-enzyme liposome therapy) PELT: Basic principles for design and transfer from the laboratory to clinic
    • Duncan, R.; Gac-Breton, S.; Keane, R.; Musila, R.; Sat, Y. N.; Satchi, R.; Searle, F. Polymer-drug conjugates, polymer-directed enzyme prodrug therapy (PDEPT) and (polymer-enzyme liposome therapy) PELT: basic principles for design and transfer from the laboratory to clinic. J. Controlled Release 2001, 74, 135-146.
    • (2001) J. Controlled Release , vol.74 , pp. 135-146
    • Duncan, R.1    Gac-Breton, S.2    Keane, R.3    Musila, R.4    Sat, Y.N.5    Satchi, R.6    Searle, F.7
  • 139
    • 0036579776 scopus 로고    scopus 로고
    • Paclitaxel delivery systems: The use of amino acid linkers in the conjugation of paclitaxel with carboxymethyldextran to create prodrugs
    • Sugahara, S.; Kajiki, M.; Kuriyama, H.; Kobayashi, T. Paclitaxel delivery systems: the use of amino acid linkers in the conjugation of paclitaxel with carboxymethyldextran to create prodrugs. Biol. Pharm. Bull. 2002, 25, 632-641.
    • (2002) Biol. Pharm. Bull. , vol.25 , pp. 632-641
    • Sugahara, S.1    Kajiki, M.2    Kuriyama, H.3    Kobayashi, T.4
  • 140
    • 2942685195 scopus 로고    scopus 로고
    • Synthesis, physico-chemical and biological characterization of a paclitaxel macromolecular prodrug
    • Cavallaro, G.; Licciardi, M.; Caliceti, P.; Salmaso, S.; Giammona, G. Synthesis, physico-chemical and biological characterization of a paclitaxel macromolecular prodrug. Eur. J. Pharm. Biopharm. 2004. 58, 151-159.
    • (2004) Eur. J. Pharm. Biopharm. , vol.58 , pp. 151-159
    • Cavallaro, G.1    Licciardi, M.2    Caliceti, P.3    Salmaso, S.4    Giammona, G.5
  • 141
    • 17844397724 scopus 로고    scopus 로고
    • Preparation and characterization of water-soluble prodrug, liposomes and micelles of paclitaxel
    • Dhanikula, A. B.; Panchagnula, R. Preparation and characterization of water-soluble prodrug, liposomes and micelles of paclitaxel. Curr. Drug Delivery 2005, 2. 75-91.
    • (2005) Curr. Drug Delivery , vol.2 , pp. 75-91
    • Dhanikula, A.B.1    Panchagnula, R.2
  • 142
    • 17844400324 scopus 로고    scopus 로고
    • In vivo pharmacokinetic and tissue distribution studies in mice of alternative formulations for local and systemic delivery of paclitaxel: Gel, film, prodrug, liposomes and micelles
    • Dhanikula, A. B.; Singh, D. R.; Panchagnula, R. In vivo pharmacokinetic and tissue distribution studies in mice of alternative formulations for local and systemic delivery of paclitaxel: Gel, film, prodrug, liposomes and micelles. Curr. Drug Delivery 2005, 2, 35-44.
    • (2005) Curr. Drug Delivery , vol.2 , pp. 35-44
    • Dhanikula, A.B.1    Singh, D.R.2    Panchagnula, R.3
  • 143
    • 0037072529 scopus 로고    scopus 로고
    • Poly(L-glutamic acid)-anticancer drug conjugates
    • Li, C. Poly(L-glutamic acid)-anticancer drug conjugates. Adv. Drug Delivery Rev. 2002, 54, 695-713.
    • (2002) Adv. Drug Delivery Rev. , vol.54 , pp. 695-713
    • Li, C.1
  • 144
    • 0032101105 scopus 로고    scopus 로고
    • Complete regression of well-established tumors using a novel water-soluble poly(L-glutamic acid)-paclitaxel conjugate
    • Li, C.; Yu, D. F.; Newman, R. A.; Cabral, F.; Stephens, L. C.; Hunter, N.; Milas, L.; Wallace, S. Complete regression of well-established tumors using a novel water-soluble poly(L-glutamic acid)-paclitaxel conjugate. Cancer Res. 1998, 58, 2404-2409.
    • (1998) Cancer Res. , vol.58 , pp. 2404-2409
    • Li, C.1    Yu, D.F.2    Newman, R.A.3    Cabral, F.4    Stephens, L.C.5    Hunter, N.6    Milas, L.7    Wallace, S.8
  • 146
    • 0033629139 scopus 로고    scopus 로고
    • Comparison of action of paclitaxel and poly(L-glutamic acid)-paclitaxel conjugate in human breast cancer cells
    • Oldham, E. A.; Li, C.; Ke, S.; Wallace, S.; Huang, P. Comparison of action of paclitaxel and poly(L-glutamic acid)-paclitaxel conjugate in human breast cancer cells. Int. J. Oncol, 2000, 16, 125-132.
    • (2000) Int. J. Oncol , vol.16 , pp. 125-132
    • Oldham, E.A.1    Li, C.2    Ke, S.3    Wallace, S.4    Huang, P.5
  • 148
    • 0037619168 scopus 로고    scopus 로고
    • Poly-(L)-glutamic acid-paclitaxel (CT-2103) [XYOTAX], a biodegradable polymeric drug conjugate: Characterization, preclinical pharmacology, and preliminary clinical data
    • Singer, J. W.; Baker, B.; De Vries, P.; Kumar, A.; Shaffer, S.; Vawter, E.; Bolton, M.; Garzone, P. Poly-(L)-glutamic acid-paclitaxel (CT-2103) [XYOTAX], a biodegradable polymeric drug conjugate: characterization, preclinical pharmacology, and preliminary clinical data. Adv. Exp. Med. Biol. 2003, 519, 81-99.
    • (2003) Adv. Exp. Med. Biol. , vol.519 , pp. 81-99
    • Singer, J.W.1    Baker, B.2    De Vries, P.3    Kumar, A.4    Shaffer, S.5    Vawter, E.6    Bolton, M.7    Garzone, P.8
  • 149
    • 0036187909 scopus 로고    scopus 로고
    • Superior therapeutic profile of poly-L-glutamic acid-paclitaxel copolymer compared with Taxol in xenogeneic compartmental models of human ovarian carcinoma
    • Auzenne, E.; Donato, N. J.; Li, C.; Leroux, E.; Price, R. E.; Farquhar, D.; Klostergaard, J. Superior therapeutic profile of poly-L-glutamic acid-paclitaxel copolymer compared with Taxol in xenogeneic compartmental models of human ovarian carcinoma. Clin. Cancer Res. 2002, 8, 573-581.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 573-581
    • Auzenne, E.1    Donato, N.J.2    Li, C.3    Leroux, E.4    Price, R.E.5    Farquhar, D.6    Klostergaard, J.7
  • 150
    • 8444230023 scopus 로고    scopus 로고
    • Antitumor activity of hydrophilic paclitaxel copolymer prodrug using locoregional delivery in human orthotopic non-small cell lung cancer xenograft models
    • Zou, Y.; Fu, H.; Ghosh, S.; Farquhar, D.; Klostergaard, J. Antitumor activity of hydrophilic paclitaxel copolymer prodrug using locoregional delivery in human orthotopic non-small cell lung cancer xenograft models. Clin. Cancer Res. 2004, 10, 7382-7391.
    • (2004) Clin. Cancer Res. , vol.10 , pp. 7382-7391
    • Zou, Y.1    Fu, H.2    Ghosh, S.3    Farquhar, D.4    Klostergaard, J.5
  • 151
    • 3543011323 scopus 로고    scopus 로고
    • Dilemmas in management: The controversial role of chemotherapy in PS 2 advanced NSCLC and the potential role of CT-2103 (Xyotax)
    • Langer, C. J. Dilemmas in management: the controversial role of chemotherapy in PS 2 advanced NSCLC and the potential role of CT-2103 (Xyotax). Oncologist 2004, 9, 398-405.
    • (2004) Oncologist , vol.9 , pp. 398-405
    • Langer, C.J.1
  • 156
    • 28444450450 scopus 로고    scopus 로고
    • Paclitaxel poliglumex (XYOTAX, CT-2103): A macromolecular taxane
    • Singer, J. W. Paclitaxel poliglumex (XYOTAX, CT-2103): A macromolecular taxane. J. Controlled Release 2005, 109, 120-126.
    • (2005) J. Controlled Release , vol.109 , pp. 120-126
    • Singer, J.W.1
  • 158
    • 0033927015 scopus 로고    scopus 로고
    • Tumor irradiation enhances the tumor-specific distribution of poly(L-glutamic acid)-conjugated paclitaxel and its antitumor efficacy
    • Li, C.; Ke, S.; Wu, Q. P.; Tansey, W.; Hunter, N.; Buchmiller, L. M.; Milas, L.; Charnsangavej, C.; Wallace, S. Tumor irradiation enhances the tumor-specific distribution of poly(L-glutamic acid)-conjugated paclitaxel and its antitumor efficacy. Clin. Cancer Res. 2000, 6, 2824-2834.
    • (2000) Clin. Cancer Res. , vol.6 , pp. 2824-2834
    • Li, C.1    Ke, S.2    Wu, Q.P.3    Tansey, W.4    Hunter, N.5    Buchmiller, L.M.6    Milas, L.7    Charnsangavej, C.8    Wallace, S.9
  • 159
    • 0037358299 scopus 로고    scopus 로고
    • Poly(L-glutamic acid)-paclitaxel conjugate is a potent enhancer of tumor radiocurability
    • Milas, L.; Mason, K. A.; Hunter, N.; Li, C.; Wallace, S. Poly(L-glutamic acid)-paclitaxel conjugate is a potent enhancer of tumor radiocurability. Int. J. Radiat. Oncol., Biol. Phys. 2003, 55, 707-712.
    • (2003) Int. J. Radiat. Oncol., Biol. Phys. , vol.55 , pp. 707-712
    • Milas, L.1    Mason, K.A.2    Hunter, N.3    Li, C.4    Wallace, S.5
  • 160
    • 0037360766 scopus 로고    scopus 로고
    • Polymer-conjugated paclitaxel as a radiosensitizing agent. A big step forward for combined modality therapy
    • Tishler, Roy B. Polymer-conjugated paclitaxel as a radiosensitizing agent. A big step forward for combined modality therapy. Int. J. Radiat. Oncol., Biol., Phys. 2003, 55, 563-564.
    • (2003) Int. J. Radiat. Oncol., Biol., Phys. , vol.55 , pp. 563-564
    • Tishler, R.B.1
  • 161
    • 0032421248 scopus 로고    scopus 로고
    • Serum proteins as drug carriers of anticancer agents: A review
    • Kratz, F.; Beyer, U. Serum proteins as drug carriers of anticancer agents: a review. Drug Delivery 1998, 5, 281-299.
    • (1998) Drug Delivery , vol.5 , pp. 281-299
    • Kratz, F.1    Beyer, U.2
  • 162
    • 2442691304 scopus 로고    scopus 로고
    • Tumor targeting based on the effect of enhanced permeability and retention (EPR) and the mechanism of receptor-mediated endocytosis (RME)
    • Tanaka, T.; Shiramoto, S.; Miyashita, M.; Fujishima, Y.; Kaneo, Y. Tumor targeting based on the effect of enhanced permeability and retention (EPR) and the mechanism of receptor-mediated endocytosis (RME). Int. J. Pharm. 2004, 277, 39-61.
    • (2004) Int. J. Pharm. , vol.277 , pp. 39-61
    • Tanaka, T.1    Shiramoto, S.2    Miyashita, M.3    Fujishima, Y.4    Kaneo, Y.5
  • 163
    • 0031715649 scopus 로고    scopus 로고
    • In vitro cytotoxicity of paclitaxel-transferrin conjugate on H69 cells
    • Bicamumpaka, C.; Page, M. In vitro cytotoxicity of paclitaxel-transferrin conjugate on H69 cells. Oncol. Rep. 1998, 5, 1381-1383.
    • (1998) Oncol. Rep. , vol.5 , pp. 1381-1383
    • Bicamumpaka, C.1    Page, M.2
  • 164
    • 0030947239 scopus 로고    scopus 로고
    • Preparation, characterization and properties in vitro and in vivo of a paclitaxel-albumin conjugate
    • Dosio, F.; Brusa, P.; Crosasso, P.; Arpicco, S.; Cattel, L. Preparation, characterization and properties in vitro and in vivo of a paclitaxel-albumin conjugate. J. Controlled Release 1997, 47, 293-304.
    • (1997) J. Controlled Release , vol.47 , pp. 293-304
    • Dosio, F.1    Brusa, P.2    Crosasso, P.3    Arpicco, S.4    Cattel, L.5
  • 165
    • 0035845748 scopus 로고    scopus 로고
    • Poly(ethylene glycol)-human serum albumin-paclitaxel conjugates: Preparation, characterization and pharmacokinetics
    • Dosio, F.; Arpicco, S.; Brusa, P.; Stella, B.; Cattel, L. Poly(ethylene glycol)-human serum albumin-paclitaxel conjugates: preparation, characterization and pharmacokinetics. J. Controlled Release 2001, 76, 107-117.
    • (2001) J. Controlled Release , vol.76 , pp. 107-117
    • Dosio, F.1    Arpicco, S.2    Brusa, P.3    Stella, B.4    Cattel, L.5
  • 166
  • 167
    • 0141670339 scopus 로고    scopus 로고
    • "Cascade-release dendrimers" liberate all end groups upon a single triggering event in the dendritic core
    • De Groot, F. M. H.; Albrecht, C.; Koekkoek, R.; Beusker, P. H.; Scheeren, H. W. "Cascade-release dendrimers" liberate all end groups upon a single triggering event in the dendritic core. Angew. Chem., Int. Ed. 2003, 42, 4490-4494.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4490-4494
    • De Groot, F.M.H.1    Albrecht, C.2    Koekkoek, R.3    Beusker, P.H.4    Scheeren, H.W.5
  • 168
    • 0029953670 scopus 로고    scopus 로고
    • Cathepsin B: Multiple enzyme forms from a single gene and their relation to cancer
    • Keppler, D.; Sloane, B. F. Cathepsin B: multiple enzyme forms from a single gene and their relation to cancer. Enzyme Protein 1996, 49, 94-105.
    • (1996) Enzyme Protein , vol.49 , pp. 94-105
    • Keppler, D.1    Sloane, B.F.2
  • 169
    • 0030792535 scopus 로고    scopus 로고
    • Monomethoxytrityl (MMT) as a versatile amino protecting group for complex prodrugs of anticancer compounds sensitive to strong acids, bases and nucleophiles
    • Dubowchik, G. M.; Radia, S. Monomethoxytrityl (MMT) as a versatile amino protecting group for complex prodrugs of anticancer compounds sensitive to strong acids, bases and nucleophiles. Tetrahedron Lett. 1997, 38, 5257-5260.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5257-5260
    • Dubowchik, G.M.1    Radia, S.2
  • 170
    • 0032402572 scopus 로고    scopus 로고
    • Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mitomycin C and doxorubicin
    • Dubowchik, G. M.; Mesure, K.; Knipe, J. O.; Firestone, R. A. Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mitomycin C and doxorubicin. Bioorg. Med. Chem. Lett. 1998, 8, 3347-3352.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3347-3352
    • Dubowchik, G.M.1    Mesure, K.2    Knipe, J.O.3    Firestone, R.A.4
  • 171
    • 0035862692 scopus 로고    scopus 로고
    • Taxane-antibody conjugates afford potent cytotoxicity, enhanced solubility, and tumor target selectivity
    • Guillemard, V.; Saragovi, H. U. Taxane-antibody conjugates afford potent cytotoxicity, enhanced solubility, and tumor target selectivity. Cancer Res. 2001, 61, 694-699.
    • (2001) Cancer Res. , vol.61 , pp. 694-699
    • Guillemard, V.1    Saragovi, H.U.2
  • 172
    • 0034161454 scopus 로고    scopus 로고
    • Development of pharmacological agents for targeting neurotrophins and their receptors
    • Saragovi, H. U.; Gehring, K. Development of pharmacological agents for targeting neurotrophins and their receptors. Trends Pharmacol. Sci. 2000, 2, 93-98.
    • (2000) Trends Pharmacol. Sci. , vol.2 , pp. 93-98
    • Saragovi, H.U.1    Gehring, K.2
  • 176
    • 0344582568 scopus 로고    scopus 로고
    • Synthesis and evaluation of paclitaxel immunoconjugate with antitumor activity in vitro
    • Correa, J. J.; Page, M. Synthesis and evaluation of paclitaxel immunoconjugate with antitumor activity in vitro. Tumor Targeting Cancer Ther. 2002, 165-178.
    • (2002) Tumor Targeting Cancer Ther. , pp. 165-178
    • Correa, J.J.1    Page, M.2
  • 178
    • 1642362625 scopus 로고    scopus 로고
    • Drug delivery system: Entering the main stream
    • Allen, T. M.; Cullis, P. R. Drug delivery system: entering the main stream. Science 2004, 303, 1818-1822.
    • (2004) Science , vol.303 , pp. 1818-1822
    • Allen, T.M.1    Cullis, P.R.2


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