메뉴 건너뛰기




Volumn 44, Issue 6, 2012, Pages 522-530

Boron neutron capture therapy assisted by boron-conjugated nanoparticles

Author keywords

biodistribution; boron neutron capture therapy; drug delivery systems; nanoparticle assisted BNCT; polymeric micelles

Indexed keywords

BIODISTRIBUTIONS; BORON NEUTRON CAPTURE THERAPY; DRUG DELIVERY SYSTEM; NANOPARTICLE-ASSISTED BNCT; POLYMERIC MICELLE;

EID: 84861920967     PISSN: 00323896     EISSN: 13490540     Source Type: Journal    
DOI: 10.1038/pj.2012.30     Document Type: Review
Times cited : (42)

References (62)
  • 1
    • 0026464493 scopus 로고
    • Boron neutron capture therapy of cancer: Realities and prospects
    • Barth, R. F., Soloway, A. H., Fairchild, R. G. & Brugger, R. M. Boron neutron capture therapy of cancer: Realities and prospects. Cancer 70, 2995-3007 (1992).
    • (1992) Cancer , vol.70 , pp. 2995-3007
    • Barth, R.F.1    Soloway, A.H.2    Fairchild, R.G.3    Brugger, R.M.4
  • 2
    • 20344394447 scopus 로고    scopus 로고
    • Boron neutron capture therapy of cancer: Current status and future prospects
    • DOI 10.1158/1078-0432.CCR-05-0035
    • Barth, R. F., Coderre, J. A., Vincente, G. H. & Blue, T. E. Boron neutron capture therapy of cancer: Current status and future property. Cli. Cancer Res. 11, 3987-4002 (2005). (Pubitemid 40791562)
    • (2005) Clinical Cancer Research , vol.11 , Issue.11 , pp. 3987-4002
    • Barth, R.F.1    Coderre, J.A.2    Vicente, M.G.H.3    Blue, T.E.4
  • 3
    • 0002046363 scopus 로고
    • Biological effects and therapeutic possibilities of neutrons
    • Locher, G. L. Biological effects and therapeutic possibilities of neutrons. Am. J. Roentgenol Radium Ther. 36, 1-13 (1936).
    • (1936) Am. J. Roentgenol Radium Ther. , vol.36 , pp. 1-13
    • Locher, G.L.1
  • 5
    • 84965188910 scopus 로고
    • Pathological study of eight patients with glioblastoma multiforme treated by neutroncapture therapy using boron-10
    • Godwin, J. T., Farr, L. E., Sweet, W. H. & Robertson, J. S. Pathological study of eight patients with glioblastoma multiforme treated by neutroncapture therapy using boron-10. Cancer 8, 601-615 (1955).
    • (1955) Cancer , vol.8 , pp. 601-615
    • Godwin, J.T.1    Farr, L.E.2    Sweet, W.H.3    Robertson, J.S.4
  • 6
    • 0015323909 scopus 로고
    • Neuropathological study of fourteen cases of malignant brain tumor treated by boron-10 slow neutron capture therapy
    • Asbury, A. K., Ojemann, Nielson, S. L. & Sweet, W. H. Neuropathological study of fourteen cases of malignant brain tumor treated by boron-10 slow neutron capture therapy. J. Neuropathol Exp. Neurol. 31, 278-303 (1972).
    • (1972) J. Neuropathol Exp. Neurol. , vol.31 , pp. 278-303
    • Asbury, A.K.1    Ojemann Nielson, S.L.2    Sweet, W.H.3
  • 8
    • 33947461630 scopus 로고
    • Synthesis of aromatic boronic acids. Aldehyde boronic acids and a boronic acid analog of tyrosine
    • Snyder, H. R., Reedy, A. J. & Lennarz, W. Synthesis of aromatic boronic acids. Aldehyde boronic acids and a boronic acid analog of tyrosine. J. Am. Chem. Soc. 80, 835-838 (1958).
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 835-838
    • Snyder, H.R.1    Reedy, A.J.2    Lennarz, W.3
  • 9
    • 0013063792 scopus 로고
    • Pluripotential amino acids. 1. (L)-p-dihydroxyborylphenylalanine (L-Bph) as a precursor of the L-Phe and L-Tyr containing peptides; Specific tritiation of L-Phe containing peptides as a final step in synthesis
    • Roberts, D. C., Suda, K., Samanen, J. & Kemp, D. S. Pluripotential amino acids. 1. (L)-p-dihydroxyborylphenylalanine (L-Bph) as a precursor of the L-Phe and L-Tyr containing peptides; specific tritiation of L-Phe containing peptides as a final step in synthesis. Tetrahedron Lett. 21, 3435-3438 (1989).
    • (1989) Tetrahedron Lett. , vol.21 , pp. 3435-3438
    • Roberts, D.C.1    Suda, K.2    Samanen, J.3    Kemp, D.S.4
  • 10
    • 0014106529 scopus 로고
    • Penetration of brain and brain tumor. VII. Tumor-binding sulfhydryl boron compounds
    • Soloway, A. H., Hatanaka, H. & Davis, M. A. Penetration of brain and brain tumor. VII. Tumor-binding sulfhydryl boron compounds. J. Med. Chem. 10, 714-717 (1967).
    • (1967) J. Med. Chem. , vol.10 , pp. 714-717
    • Soloway, A.H.1    Hatanaka, H.2    Davis, M.A.3
  • 11
    • 0016737844 scopus 로고
    • A revised boron-neutron capture therapy for malignant brain tumors: II. Interim clinical result with the patients excluding previous treatments
    • Hatanaka, H. A revised boron-neutron capture therapy for malignant brain tumors: II. Interim clinical result with the patients excluding previous treatments. J. Neurol. 209, 81-94 (1975).
    • (1975) J. Neurol. , vol.209 , pp. 81-94
    • Hatanaka, H.1
  • 12
    • 0028297726 scopus 로고
    • Clinical results of long-surviving brain tumor patients who underwent boron neutron capture therapy
    • Hatanaka, H. & Nakagawa, Y. Clinical results of long-surviving brain tumor patients who underwent boron neutron capture therapy. Int. J. Radiat. Oncol. Biol. Phys. 28, 1061-1066 (1994). (Pubitemid 24118041)
    • (1994) International Journal of Radiation Oncology Biology Physics , vol.28 , Issue.5 , pp. 1061-1066
    • Hatanaka, H.1    Nakagawa, Y.2
  • 13
    • 0024692381 scopus 로고
    • New thermal neutron capture therapy for malignant melanoma: Melanogenesis-seeking 10B molecule-melanoma cell interaction from in vitro to first clinical trial. Pigment
    • Mishima, Y., Ichihashi, M., Hatta, S., Honda, C., Yamaura, K. & Nakagawa, T. New thermal neutron capture therapy for malignant melanoma: melanogenesis-seeking 10B molecule-melanoma cell interaction from in vitro to first clinical trial. Pigment. Cell. Res. 2, 226-234 (1989).
    • (1989) Cell. Res. , vol.2 , pp. 226-234
    • Mishima, Y.1    Ichihashi, M.2    Hatta, S.3    Honda, C.4    Yamaura, K.5    Nakagawa, T.6
  • 14
    • 0037092870 scopus 로고    scopus 로고
    • Electrospray ionization mass spectrometry coupled to reversed-phase ion-pair high-performance liquid chromatography for quantitation of sodium borocaptate and application to pharmacokinetic analysis
    • DOI 10.1021/ac0112723
    • Gibson, C. R., Staubus, A. E., Barth, R. F., Yang, W., Kleinholz, N. M., Jones, R. B., Church, K. B. G., Tjarks, W. & Soloway, A. H. Electrospray ionization mass spectrometry coupled to reversed-phase ion-pair high-performance liquid chromatography for quantitation of sodium borocaptate and application to pharmacokinetic analysis. Anal. Chem. 74, 2394-2399 (2002). (Pubitemid 34526046)
    • (2002) Analytical Chemistry , vol.74 , Issue.10 , pp. 2394-2399
    • Gibson, C.R.1    Staubus, A.E.2    Barth, R.F.3    Yang, W.4    Kleinholz, N.M.5    Jones, R.B.6    Green-Church, K.B.7    Tjarks, W.8    Soloway, A.H.9
  • 15
    • 67649406025 scopus 로고    scopus 로고
    • Biodistribution of BPA and BSH after single, repeated and simultaneous administrations for neutron-capture therapy of cancer
    • Ichikawa, H., Taniguchi, E., Fujimoto, T. & Fukumori, Y. Biodistribution of BPA and BSH after single, repeated and simultaneous administrations for neutron-capture therapy of cancer. Appl. Radiat. Isot. 67, 111-114 (2009).
    • (2009) Appl. Radiat. Isot. , vol.67 , pp. 111-114
    • Ichikawa, H.1    Taniguchi, E.2    Fujimoto, T.3    Fukumori, Y.4
  • 18
    • 0022858683 scopus 로고
    • A new concept for macromolecular therapeutics in cancer chemotherapy: Mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs
    • Matsumura, Y. & Maeda, H. A new concept for macromolecular therapeutics in cancer chemotherapy: Mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. Cancer. Res. 46, 6387-6392 (1986). (Pubitemid 17221789)
    • (1986) Cancer Research , vol.46 , Issue.12 , pp. 6387-6392
    • Matsumura, Y.1    Maeda, H.2
  • 19
    • 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
    • DOI 10.1016/S0168-3659(01)00309-1, PII S0168365901003091
    • 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. Control Release. 74, 47-61 (2001). (Pubitemid 32727608)
    • (2001) Journal of Controlled Release , vol.74 , Issue.1-3 , pp. 47-61
    • Maeda, H.1    Sawa, T.2    Konno, T.3
  • 20
    • 0027950222 scopus 로고
    • Boronated starburst dendrimer-monoclonal antibody immunoconjugates: Evaluation as a potential delivery system for neutron capture therapy
    • Barth, R. F., Adams, D. M., Soloway, A. H., Alam, F. & Darby, M. V. Boronated starburst dendrimer-monoclonal antibody immunoconjugates: Evaluation as a potential delivery system for neutron capture therapy. Bioconjug Chem. 5, 58-66 (1994). (Pubitemid 2043885)
    • (1994) Bioconjugate Chemistry , vol.5 , Issue.1 , pp. 58-66
    • Barth, R.F.1    Adams, D.M.2    Soloway, A.H.3    Alam, F.4    Darby, M.V.5
  • 21
    • 0842285204 scopus 로고    scopus 로고
    • Site-Specific Conjugation of Boron-Containing Dendrimers to Anti-EGF Receptor Monoclonal Antibody Cetuximab (IMC-C225) and Its Evaluation as a Potential Delivery Agent for Neutron Capture Therapy
    • DOI 10.1021/bc0341674
    • Wu, G., Barth, R. F., Yang, W., Chatterjee, M., Tjarks, W., Ciesielski, M. J. & Fenstermaker, R. A. Site-specific conjugation of boron-containing dendrimers to anti-EGF receptor monoclonal antibody cetuximab (IMC-C225) and its evaluation as a potential delivery agent for neutron capture therapy. Bioconjug. Chem. 15, 185-194 (2004). (Pubitemid 38165994)
    • (2004) Bioconjugate Chemistry , vol.15 , Issue.1 , pp. 185-194
    • Wu, G.1    Barth, R.F.2    Yang, W.3    Chatterjee, M.4    Tjarks, W.5    Ciesielski, M.J.6    Fenstermaker, R.A.7
  • 22
    • 0030250865 scopus 로고    scopus 로고
    • Development and in vitro studies of epidermal growth factor-dextran conjugates for boron neutron capture therapy
    • DOI 10.1021/bc9600473
    • Gedda, L., Olsson, P., Ponten, J. & Carlsson, J. Development and in vitro studies of epidermal growth factor-dextran conjugates for boron neutron capture therapy. Bioconjug. Chem. 7, 584-591 (1996). (Pubitemid 26369623)
    • (1996) Bioconjugate Chemistry , vol.7 , Issue.5 , pp. 584-591
    • Gedda, L.1    Olsson, P.2    Ponten, J.3    Carlsson, J.4
  • 24
    • 0029874728 scopus 로고    scopus 로고
    • Liposomal formulations containing sodium mercaptoundecahydrododecaborate (BSH) for boron neutron capture therapy
    • Mehta, S. C., Lai, J. C. K. & Lu, D. R. Liposomal formulations containing sodium mercaptoundecahydrododecaborate (BSH) for boron neutron capture therapy J. Microencapsul. 13, 269-279 (1996). (Pubitemid 26150165)
    • (1996) Journal of Microencapsulation , vol.13 , Issue.3 , pp. 269-279
    • Mehta, S.C.1    Lai, J.C.K.2    Lu, D.R.3
  • 25
    • 0034866792 scopus 로고    scopus 로고
    • Liposomes bearing polyethyleneglycol-coupled transferrin with intracellular targeting property to the solid tumors in vivo
    • DOI 10.1023/A:1010960900254
    • Ishida, O., Maruyama, K., Tanahashi, H., Iwatsuru, M., Sasaki, K., Eriguchi, M. & Yanagie, H. Liposomes bearing polyethyleneglycol-coupled transferrin with intracellular targeting property to the solid tumors in vivo. Pharm. Res. 18, 1042-1048 (2001). (Pubitemid 32799953)
    • (2001) Pharmaceutical Research , vol.18 , Issue.7 , pp. 1042-1048
    • Ishida, O.1    Maruyama, K.2    Tanahashi, H.3    Iwatsuru, M.4    Sasaki, K.5    Eriguchi, M.6    Yanagie, H.7
  • 26
    • 3242679701 scopus 로고    scopus 로고
    • Intracellular targeting of sodium mercaptoundecahydrododecaborate (BSH) to solid tumors by transferrin-PEG liposomes, for boron neutron-capture therapy (BNCT)
    • DOI 10.1016/j.jconrel.2004.04.018, PII S0168365904002147
    • Maruyama, K., Ishida, O., Kasaoka, S., Takizawa, T., Utoguchi, N., Shinohara, M., Chiba, M., Kobayashi, H., Eriguchi, M. & Yanagie, H. Intracellular targeting of sodium mercaptoundecahydrododecaborate (BSH) to solid tumors by transferring-PEG liposomes, for boron neutron-capture therapy (BNCT). J. Control. Release. 98, 195-207 (2004). (Pubitemid 38950731)
    • (2004) Journal of Controlled Release , vol.98 , Issue.2 , pp. 195-207
    • Maruyama, K.1    Ishida, O.2    Kasaoka, S.3    Takizawa, T.4    Utoguchi, N.5    Shinohara, A.6    Chiba, M.7    Kobayashi, H.8    Eriguchi, M.9    Yanagie, H.10
  • 28
    • 0028416238 scopus 로고
    • Delivery of drugs, proteins and genes into cells using transferrin as a ligand for receptor-mediated endocytosis
    • DOI 10.1016/0169-409X(94)90008-6
    • Wagner, E., Curiel, D. & Cotton, M. Delivery of drugs, proteins and genes into cells using transferring as a ligand for receptor-mediated endocytosis. Adv. Drug. Deliv. Rev. 14, 113-135 (1994). (Pubitemid 24131676)
    • (1994) Advanced Drug Delivery Reviews , vol.14 , Issue.1 , pp. 113-135
    • Wagner, E.1    Curiel, D.2    Cotten, M.3
  • 29
    • 0028986615 scopus 로고
    • Selective boron delivery to murine tumors by lipophilic species incorporated in the membranes of unilamellar liposomes
    • Feakes, D. A., Shelly, K. & Hawthorne, M. F. Selective boron delivery to murine tumors by lipophilic species incorporated in the membranes of unilamellar liposomes. Proc. Natl. Acad. Sci. USA 92, 1367-1370 (1995).
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 1367-1370
    • Feakes, D.A.1    Shelly, K.2    Hawthorne, M.F.3
  • 30
    • 33749005130 scopus 로고    scopus 로고
    • Transferrin-loaded nido-carborane liposomes: Tumor-targeting boron delivery system for neutron capture therapy
    • DOI 10.1021/bc060064k
    • Miyajima, Y., Nakamura, H., Kuwata, Y., Lee, J. D., Masunaga, S., Ono, K. & Maruyama, K. Transferrin-loaded nido-carborane liposomes: tumor-targeting boron delivery system for neutron capture therapy. Bioconjug. Chem. 17, 1314-1320 (2006). (Pubitemid 44455341)
    • (2006) Bioconjugate Chemistry , vol.17 , Issue.5 , pp. 1314-1320
    • Miyajima, Y.1    Nakamura, H.2    Kuwata, Y.3    Lee, J.-D.4    Masunaga, S.5    Ono, K.6    Maruyama, K.7
  • 31
    • 31544434568 scopus 로고    scopus 로고
    • Unilamellar liposomes with enhanced boron content
    • DOI 10.1021/bc0501350
    • Li, T., Hamdi, J. & Hawthorne, M. F. Unilamellar liposomes with enhanced boron content. Bioconjug. Chem. 17, 15-20 (2006). (Pubitemid 43157580)
    • (2006) Bioconjugate Chemistry , vol.17 , Issue.1 , pp. 15-20
    • Li, T.1    Hamdi, J.2    Hawthorne, M.F.3
  • 32
    • 33846646040 scopus 로고    scopus 로고
    • Synthesis of boron cluster lipids: Closo-dodecaborate as an alternative hydrophilic function of boronated liposomes for neutron capture therapy
    • Lee, J. D., Ueno, M., Miyajima, Y. & Nakamura, H. Synthesis of boron cluster lipids: closo-dodecaborate as an alternative hydrophilic function of boronated liposomes for neutron capture therapy. Org. Lett. 9, 323-326 (2007).
    • (2007) Org. Lett. , vol.9 , pp. 323-326
    • Lee, J.D.1    Ueno, M.2    Miyajima, Y.3    Nakamura, H.4
  • 33
    • 77951206163 scopus 로고    scopus 로고
    • Dodecaborate lipid liposomes as new vehicles for boron delivery system of neutron capture therapy
    • Ueno, M., Ban, H. S., Nakai, K., Inomata, R., Kaneda, Y., Matsumura, A. & Nakamura, H. Dodecaborate lipid liposomes as new vehicles for boron delivery system of neutron capture therapy. Bioorg. Med. Chem. 18, 3059-3065 (2010).
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 3059-3065
    • Ueno, M.1    Ban, H.S.2    Nakai, K.3    Inomata, R.4    Kaneda, Y.5    Matsumura, A.6    Nakamura, H.7
  • 34
    • 0035937592 scopus 로고    scopus 로고
    • Block copolymer micelles for drug delivery: Design, characterization and biological significance
    • DOI 10.1016/S0169-409X(00)00124-1, PII S0169409X00001241
    • Kataoka, K., Harada, A. & Nagasaki, Y. Block copolymer micelles for drug delivery: design characterization and biological significance. Adv. Drug. Dliv. Rev. 47, 113-131 (2001). (Pubitemid 32209236)
    • (2001) Advanced Drug Delivery Reviews , vol.47 , Issue.1 , pp. 113-131
    • Kataoka, K.1    Harada, A.2    Nagasaki, Y.3
  • 35
    • 28544450961 scopus 로고    scopus 로고
    • Block copolymer micelles: Preparation, characterization and application in drug delivery
    • Gaucher, G., Dufresne, M. H., Sant, V. P., Kang, N., Maysinger, D. & Leroux, J. C. Block copolymer micelles: preparation, characterization and application in drug delivery. J. Control Release 109, 169-199 (2005).
    • (2005) J. Control Release , vol.109 , pp. 169-199
    • Gaucher, G.1    Dufresne, M.H.2    Sant, V.P.3    Kang, N.4    Maysinger, D.5    Leroux, J.C.6
  • 36
    • 0029091362 scopus 로고
    • Non-stealth (poly(lactic acid/albumin)) and stealth (poly(lactic acid-polyethylene glycol)) nanoparticles as injectable drug carriers
    • Verrechia, T., Spenlehauer, G., Bazile, D. V., Murry-Brelier, A., Archimbaud, Y. & Veillard, M. Non-stealth (poly(lactic acid/albumin)) and stealth (poly(lactic acid-polyethylene glycol)) nanoparticles as injectable drug carriers. J. Control. Release 36, 49-61 (1995).
    • (1995) J. Control. Release , vol.36 , pp. 49-61
    • Verrechia, T.1    Spenlehauer, G.2    Bazile, D.V.3    Murry-Brelier, A.4    Archimbaud, Y.5    Veillard, M.6
  • 37
    • 0000952093 scopus 로고    scopus 로고
    • Polylactide-poly(ethylene glycol) copolymers as drug delivery systems. 1. Characterization of water dispersible micelle-forming systems
    • Hagan, S. A., Coombes, A. G. A., Garnett, M. C., Dunn, S. E., Davies, M. C., Illum, L., Davis, S. S., Harding, S. E., Purkiss, S. & Gellert, P. R. Polylactide-poly(ethylene glycol) copolymers as drug delivery systems. 1. characterization of water dispersible micelle-forming systems. Langmuir. 12, 2153-2161 (1996). (Pubitemid 126564672)
    • (1996) Langmuir , vol.12 , Issue.9 , pp. 2153-2161
    • Hagan, S.A.1    Coombes, A.G.A.2    Garnett, M.C.3    Dunn, S.E.4    Davies, M.C.5    Illum, L.6    Davis, S.S.7    Harding, S.E.8    Purkiss, S.9    Gellert, P.R.10
  • 38
    • 0035834269 scopus 로고    scopus 로고
    • Long-circulating poly(ethylene glycol)-poly(D,L-lactide) block copolymer micelles with modulated surface charge
    • DOI 10.1016/S0168-3659(01)00451-5, PII S0168365901004515
    • Yamamoto, Y., Nagasaki, Y., Kato, Y., Sugiyama, Y. & Kataoka, K. Long-circulating poly(ethylene glycol)-poly(D, L-lactide) block copolymer micelles with modulated surface charge. J. Control. Release. 77, 27-38 (2001). (Pubitemid 33022613)
    • (2001) Journal of Controlled Release , vol.77 , Issue.1-2 , pp. 27-38
    • Yamamoto, Y.1    Nagasaki, Y.2    Kato, Y.3    Sugiyama, Y.4    Kataoka, K.5
  • 39
    • 33748307713 scopus 로고    scopus 로고
    • In vitro ageing and degradation of PEG-PLA diblock copolymer-based nanoparticles
    • DOI 10.1016/j.polymdegradstab.2006.05.009, PII S0141391006001820
    • Stefani, M., Coudane, J. & Vert, M. In vitro ageing and degradation of PEG-PLA diblock copolymer-based nanoparticles. Polym. Degrad. Stab. 91, 2554-2559 (2006). (Pubitemid 44331408)
    • (2006) Polymer Degradation and Stability , vol.91 , Issue.11 , pp. 2554-2559
    • Stefani, M.1    Coudane, J.2    Vert, M.3
  • 40
    • 77957674431 scopus 로고    scopus 로고
    • In vitro degradation behavior of Poly(lactide)-Poly(ethylene glycol) block copolymer micelles in aqueous solution
    • Yang, L., Ghzaoui, A. E. & Li, S. In vitro degradation behavior of Poly(lactide)-Poly(ethylene glycol) block copolymer micelles in aqueous solution. Int. J. Pharm. 400, 96-103 (2010).
    • (2010) Int. J. Pharm. , vol.400 , pp. 96-103
    • Yang, L.1    Ghzaoui, A.E.2    Li, S.3
  • 41
    • 73649133678 scopus 로고    scopus 로고
    • Overcoming the barriers in micellar drug delivery: Loading efficiency, in vivo stability, and micelle-cell interaction
    • Kim, S., Shi, Y., Kim, J. Y., Park, K. & Cheng, J. X. Overcoming the barriers in micellar drug delivery: loading efficiency, in vivo stability, and micelle-cell interaction. Expert Opin. Drug. Deliv. 7, 49-62 (2010).
    • (2010) Expert Opin. Drug. Deliv. , vol.7 , pp. 49-62
    • Kim, S.1    Shi, Y.2    Kim, J.Y.3    Park, K.4    Cheng, J.X.5
  • 42
    • 44649136172 scopus 로고    scopus 로고
    • Fast release of lipophilic agents from circulation PEG-PDLLA micelles revealed by in vivo förster resonance energy transfer imaging
    • Chen, H., Kim, S., He, W., Wang, H., Low, P. S., Park, K. & Cheng, J. X. Fast release of lipophilic agents from circulation PEG-PDLLA micelles revealed by in vivo förster resonance energy transfer imaging. Langmuir. 24, 5213-5217 (2008).
    • (2008) Langmuir , vol.24 , pp. 5213-5217
    • Chen, H.1    Kim, S.2    He, W.3    Wang, H.4    Low, P.S.5    Park, K.6    Cheng, J.X.7
  • 43
    • 0032828963 scopus 로고    scopus 로고
    • Development of copolymers of poly(D,L-lactide) and methoxypolyethylene glycol as micellar carriers of paclitaxel
    • DOI 10.1016/S0927-7765(99)00067-3, PII S0927776599000673
    • Burt, H. M., Zhang, X., Toleikis, P., Embree, L. & Hunter, W. L. Development of copolymers of poly(D, L-lactide) and methoxypolyethylene glycol as micellar carriers of paclitaxel. Colloids Surf. B. Biointerfaces 16, 161-171 (1999). (Pubitemid 29486803)
    • (1999) Colloids and Surfaces B: Biointerfaces , vol.16 , Issue.1-4 , pp. 161-171
    • Burt, H.M.1    Zhang, X.2    Toleikis, P.3    Embree, L.4    Hunter, W.L.5
  • 44
    • 77955251550 scopus 로고    scopus 로고
    • Enhanced Stability of PEG-block-poly(N-hexyl stearate L-aspartamide) micelles in the presence of serum proteins
    • Diezi, T. A., Bae, Y. & Kwon, G. S. Enhanced Stability of PEG-block-poly(N-hexyl stearate L-aspartamide) micelles in the presence of serum proteins. Mol. Pharm. 7, 1355-1360 (2010).
    • (2010) Mol. Pharm. , vol.7 , pp. 1355-1360
    • Diezi, T.A.1    Bae, Y.2    Kwon, G.S.3
  • 45
    • 0035803699 scopus 로고    scopus 로고
    • Advanced drug delivery devices via self-assembly of amphiphilic block copolymers
    • DOI 10.1016/S0169-409X(01)00222-8, PII S0169409X01002228
    • Rösler, A., Vandermeulen, G. W. & Klok, H. A. Advanced drug delivery devices via selfassembly of amphiphilic block copolymers. Adv. Drug. Deliv. Rev. 53, 95-108 (2001). (Pubitemid 33152835)
    • (2001) Advanced Drug Delivery Reviews , vol.53 , Issue.1 , pp. 95-108
    • Rosler, A.1    Vandermeulen, G.W.M.2    Klok, H.-A.3
  • 46
    • 33750281612 scopus 로고    scopus 로고
    • Cross-linked block copolymer micelles: Functional nanostructures of great potential and versatility
    • DOI 10.1039/b514858h
    • O'Reilly, R. K., Hawker, C. J. & Wooley, K. L. Cross-linked block copolymer micelles: functional nanostructures of great potential and versatility. Chem. Soc. Rev. 35, 1068-1083 (2006). (Pubitemid 44611720)
    • (2006) Chemical Society Reviews , vol.35 , Issue.11 , pp. 1068-1083
    • O'Reilly, R.K.1    Hawker, C.J.2    Wooley, K.L.3
  • 47
    • 2442640615 scopus 로고    scopus 로고
    • Core-cross-linked polymeric micelles as paclitaxel carriers
    • DOI 10.1021/bc034113u
    • Shuai, X., Merdan, T., Schaper, A. K., Xi, F. & Kissel, T. Core-cross-linked polymeric micelles as paclitaxel carriers. Bioconjug. Chem. 15, 441-448 (2004). (Pubitemid 38657848)
    • (2004) Bioconjugate Chemistry , vol.15 , Issue.3 , pp. 441-448
    • Shuai, X.1    Merdan, T.2    Schaper, A.K.3    Xi, F.4    Kissel, T.5
  • 48
    • 35349022545 scopus 로고    scopus 로고
    • Hydrolysable core-crosslinked thermosensitive polymeric micelles: Synthesis, characterisation and in vivo studies
    • DOI 10.1016/j.biomaterials.2007.08.047, PII S0142961207007028
    • Rijcken, C. J., Snel, C. J., Schiffelers, R. M., Nostrum, C. F. & Hennink, W. E. Hydrolysable core-crosslinked thermosensitive polymeric micelles: synthesis, characterization and in vivo studies. Biomaterials 28, 5581-5593 (2007). (Pubitemid 47599643)
    • (2007) Biomaterials , vol.28 , Issue.36 , pp. 5581-5593
    • Rijcken, C.J.1    Snel, C.J.2    Schiffelers, R.M.3    Van Nostrum, C.F.4    Hennink, W.E.5
  • 49
    • 0033076145 scopus 로고    scopus 로고
    • Core-polymerized reactive micelles from heterotelechelic amphiphilic block copolymers
    • Iijima, M., Nagasaki, Y., Okada, T., Kato, M. & Kataoka, K. Core-polymerized reactive micelles from heterotelechelic amphiphilic block copolymers. Macromolecules 32, 1140-1146 (1999).
    • (1999) Macromolecules , vol.32 , pp. 1140-1146
    • Iijima, M.1    Nagasaki, Y.2    Okada, T.3    Kato, M.4    Kataoka, K.5
  • 50
    • 0033344176 scopus 로고    scopus 로고
    • Core-stabilized polymeric micelle as potential drug carrier: Increased solubilization of taxol
    • DOI 10.1002/(SICI)1099-1581(199911)10:11<647::AID-PAT918>3.0.CO;2-Y
    • Kim, J. H., Emoto, K., Iijima, M., Nagasaki, Y., Aoyagi, T., Okano, T., Sakurai, Y. & Kataoka, K. Core-stabilized polymeric micelle as potential drug carrier: increased solubilization of taxol. Polym. Adv. Technol. 10, 647-654 (1999). (Pubitemid 30509479)
    • (1999) Polymers for Advanced Technologies , vol.10 , Issue.11 , pp. 647-654
    • Kim, J.-H.1    Emoto, K.2    Iijima, M.3    Nagasaki, Y.4    Aoyagi, T.5    Okano, T.6    Sakurai, Y.7    Kataoka, K.8
  • 51
    • 58149091269 scopus 로고    scopus 로고
    • 19F-and fluorescently labeled micelles as nanoscopic assemblies for chemotherapeutic delivery
    • Du, W., Nyström, A. M., Zhang, K., Leonard, J. R. & Wooley, K. L. 19F-and fluorescently labeled micelles as nanoscopic assemblies for chemotherapeutic delivery. Bioconjug. Chem. 19, 2492-2498 (2008).
    • (2008) Bioconjug. Chem. , vol.19 , pp. 2492-2498
    • Du, W.1    Nyström, A.M.2    Zhang, K.3    Leonard, J.R.4    Wooley, K.L.5
  • 52
    • 0025874282 scopus 로고
    • Toxicity and antitumor activity against solid tumors of micelle-forming polymeric anticancer drug and its extremely long circulation in blood
    • Yokoyama, M., Okano, T., Sakurai, Y., Ekimoto, H., Shibazaki, C. & Kataoka, K. Toxicity and antitumor activity against solid tumors of micelle-forming polymeric anticancer drug and its extremely long circulation in blood. Cancer Res. 51, 3229-3236 (1991).
    • (1991) Cancer Res. , vol.51 , pp. 3229-3236
    • Yokoyama, M.1    Okano, T.2    Sakurai, Y.3    Ekimoto, H.4    Shibazaki, C.5    Kataoka, K.6
  • 53
    • 0037130252 scopus 로고    scopus 로고
    • Doxorubicin-conjugated biodegradable polymeric micelles having acid-cleavable linkages
    • DOI 10.1016/S0168-3659(02)00088-3, PII S0168365902000883
    • Yoo, H. S., Lee, E. A. & Park, T. G. Doxorubicin-conjugated biodegradable polymeric micelles having acid-cleavable linkage. J. Control Release 82, 17-27 (2002). (Pubitemid 34775044)
    • (2002) Journal of Controlled Release , vol.82 , Issue.1 , pp. 17-27
    • Yoo, H.S.1    Lee, E.A.2    Park, T.G.3
  • 54
    • 0142119372 scopus 로고    scopus 로고
    • Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change
    • DOI 10.1002/anie.200250653
    • Bae, Y., Fukushima, S., Harada, A. & Kataoka, K. Design of environment-sensitive supramolecular assemblies for intercellular drug delivery: polymeric micelles that are responsive to intracellular pH change. Angew. Chem. Int. Ed. Engl. 42, 4640-4643 (2003). (Pubitemid 37271305)
    • (2003) Angewandte Chemie - International Edition , vol.42 , Issue.38 , pp. 4640-4643
    • Bae, Y.1    Fukushima, S.2    Harada, A.3    Kataoka, K.4
  • 55
    • 0033980297 scopus 로고    scopus 로고
    • Doxorubicin-loaded poly(ethylene glycol)-poly(β-benzyl-L-aspartate) copolymer micelles: Their pharmaceutical characteristics and biological significance
    • DOI 10.1016/S0168-3659(99)00133-9, PII S0168365999001339
    • Kataoka, K., Matsumoto, T., Yokoyama, M., Okano, T., Sakurai, Y., Fukushima, S., Okamoto, K. & Kwon, G. S. Doxorubicin-loaded poly(ethylene glycol)-poly(b-benzyl-Laspartate) copolymer micelles: Their pharmaceutical characteristics and biological significance. J. Control Release 64, 143-153 (2000). (Pubitemid 30035315)
    • (2000) Journal of Controlled Release , vol.64 , Issue.1-3 , pp. 143-153
    • Kataoka, K.1    Matsumoto, T.2    Yokoyama, M.3    Okano, T.4    Sakurai, Y.5    Fukushima, S.6    Okamoto, K.7    Kwon, G.S.8
  • 56
    • 1642441855 scopus 로고    scopus 로고
    • Incorporation and release behavior of hydrophobic drug in functionalized poly(D,L-lactide)-block-poly(ethylene oxide) micelles
    • DOI 10.1016/j.jconrel.2003.10.012
    • Lee, J., Cho, E. C. & Cho, K. Incorporation and release behavior of hydrophobic drug in functionalized poly(D, L-lactide)-block-poly(ethylene oxide) micelles. J. Control Release 94, 323-335 (2004). (Pubitemid 38117144)
    • (2004) Journal of Controlled Release , vol.94 , Issue.2-3 , pp. 323-335
    • Lee, J.1    Cho, E.C.2    Cho, K.3
  • 57
    • 74449091264 scopus 로고    scopus 로고
    • Self-assembling Methoxypoly(ethylene glycol)-b-poly(carbonate-co-L- lactide) block copolymer for drug delivery
    • Danquah, M., Fujiwara, T. & Mahato, R. I. Self-assembling Methoxypoly(ethylene glycol)-b-poly(carbonate-co-L-lactide) block copolymer for drug delivery. Biomaterials 31, 2358-2370 (2010).
    • (2010) Biomaterials , vol.31 , pp. 2358-2370
    • Danquah, M.1    Fujiwara, T.2    Mahato, R.I.3
  • 58
    • 34548011255 scopus 로고    scopus 로고
    • Synthesis and properties of carborane-containing dendronized polymers
    • DOI 10.1021/ma0702039
    • Benhabbour, S. R., Parott, M. C., Gratton, E. A. & Adronov, A. Synthesis and properties of carborane-containing dendronized polymers. Macromolecules 40, 5678-5688 (2007). (Pubitemid 47280840)
    • (2007) Macromolecules , vol.40 , Issue.16 , pp. 5678-5688
    • Benhabbour, S.R.1    Parrott, M.C.2    Gratton, S.E.A.3    Adronov, A.4
  • 59
    • 79957501894 scopus 로고    scopus 로고
    • Carborane confined nanoparticles for boron neutron capture therapy: Improved stability, blood circulation time and tumor accumulation
    • Sumitani, S., Oishi, M. & Nagasaki, Y. Carborane confined nanoparticles for boron neutron capture therapy: improved stability, blood circulation time and tumor accumulation. React Funct. Polym. 71, 684-693 (2011).
    • (2011) React Funct. Polym. , vol.71 , pp. 684-693
    • Sumitani, S.1    Oishi, M.2    Nagasaki, Y.3
  • 60
    • 0000795639 scopus 로고    scopus 로고
    • Definitive crystal structures of ortho-, meta- And para-carboranes: Supramolecular structures directed solely by C-HyO hydrogen bonding to hmpa (hmpa = hexamethylphosphoramide)
    • Davidson, M. G., Hibbert, T. G., Howard, J. A. K., Mackinnon, A. & Wade, K. Definitive crystal structures of ortho-, meta-and para-carboranes: supramolecular structures directed solely by C-HyO hydrogen bonding to hmpa (hmpa1/4 hexamethylphosphoramide). Chem. Commun. 19, 2285-2286 (1996). (Pubitemid 126679248)
    • (1996) Chemical Communications , Issue.19 , pp. 2285-2286
    • Davidson, M.G.1    Hibbert, T.G.2    Howard, J.A.K.3    Mackinnon, A.4    Wade, K.5
  • 61
    • 84862776877 scopus 로고    scopus 로고
    • Pharmacokinetics of core-polymerized, boron-conjugated micelles designed for boron neutron capture therapy for cancer
    • Sumitani, S., Oishi, M., Yaguchi, T., Murotani, H., Horiguchi, Y., Suzuki, M., Ono, K., Yanagie, H. & Nagasaki, Y. Pharmacokinetics of core-polymerized, boron-conjugated micelles designed for boron neutron capture therapy for cancer. Biomaterials 33, 3568-3577 (2012).
    • (2012) Biomaterials , vol.33 , pp. 3568-3577
    • Sumitani, S.1    Oishi, M.2    Yaguchi, T.3    Murotani, H.4    Horiguchi, Y.5    Suzuki, M.6    Ono, K.7    Yanagie, H.8    Nagasaki, Y.9
  • 62
    • 38849111818 scopus 로고    scopus 로고
    • Cytotoxicity of nanoparticles
    • Lewinski, N., Colvin, V. & Drezek, R. Cytotoxicity of nanoparticles. Small 4, 26-49 (2008).
    • (2008) Small , vol.4 , pp. 26-49
    • Lewinski, N.1    Colvin, V.2    Drezek, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.