-
1
-
-
0037433470
-
Sulfonamide based pH-sensitive polymeric micelles: Physicochemical characteristics and pH-dependent aggregation
-
Han S.K., Na K., Bae Y.H. Sulfonamide based pH-sensitive polymeric micelles: physicochemical characteristics and pH-dependent aggregation. Colloids Surf., A. 214:2003;49-59.
-
(2003)
Colloids Surf., a
, vol.214
, pp. 49-59
-
-
Han, S.K.1
Na, K.2
Bae, Y.H.3
-
2
-
-
0033980297
-
Doxorubicin-loaded poly(ethylene glycol)-poly(β-benzyl-L-aspartate) copolymer micelles: Their pharmaceutical characteristics and biological significance
-
Kataoka K., Matsumoto T., Yokoyama M., Okano T., Sakurai Y., Fukushima S., Okamoto K., Kwon G.S. Doxorubicin-loaded poly(ethylene glycol)-poly(β- benzyl-L-aspartate) copolymer micelles: their pharmaceutical characteristics and biological significance. J. Control. Release. 64:2000;143-153.
-
(2000)
J. Control. Release
, vol.64
, 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
-
3
-
-
0032874430
-
Preparation and characterization of polymer micelles from poly(ethylene glycol)-poly(D,L-lactide) block copolymers as potential drug carrier
-
Yasugi K., Nagasaki Y., Kato M., Kataoka K. Preparation and characterization of polymer micelles from poly(ethylene glycol)-poly(D,L- lactide) block copolymers as potential drug carrier. J. Control. Release. 62:1999;89-100.
-
(1999)
J. Control. Release
, vol.62
, pp. 89-100
-
-
Yasugi, K.1
Nagasaki, Y.2
Kato, M.3
Kataoka, K.4
-
4
-
-
0031751919
-
Preparation and characterization of thermally responsive block copolymer micelles comprising poly(N-isopropylacrylamide-b-DL-lactide
-
Kohori F., Sakai K., Aoyagi T., Yokoyama M., Sakurai Y., Okano T. Preparation and characterization of thermally responsive block copolymer micelles comprising poly(N-isopropylacrylamide-b-DL-lactide. J. Control. Release. 55:1998;87-98.
-
(1998)
J. Control. Release
, vol.55
, pp. 87-98
-
-
Kohori, F.1
Sakai, K.2
Aoyagi, T.3
Yokoyama, M.4
Sakurai, Y.5
Okano, T.6
-
5
-
-
0027180686
-
Block copolymer micelles as vehicles for drug delivery
-
Kataoka K., Kwon G.S., Yokoyama M., Okano T., Sakurai Y. Block copolymer micelles as vehicles for drug delivery. J. Control. Release. 24:1993;119-132.
-
(1993)
J. Control. Release
, vol.24
, pp. 119-132
-
-
Kataoka, K.1
Kwon, G.S.2
Yokoyama, M.3
Okano, T.4
Sakurai, Y.5
-
6
-
-
0025015189
-
Polymer micelles as novel drug carrier: Adriamycin-conjugated poly(ethylene glycol)-poly(aspartic acid) block copolymer
-
Yokoyama M., Miyauchi M., Yamada N., Okano T., Sakurai Y., Kataoka K., Inoue S. Polymer micelles as novel drug carrier: adriamycin-conjugated poly(ethylene glycol)-poly(aspartic acid) block copolymer. J. Control. Release. 11:1990;269-278.
-
(1990)
J. Control. Release
, vol.11
, pp. 269-278
-
-
Yokoyama, M.1
Miyauchi, M.2
Yamada, N.3
Okano, T.4
Sakurai, Y.5
Kataoka, K.6
Inoue, S.7
-
7
-
-
0035937592
-
Block copolymer micelles for drug delivery: Design, characterization and biological significance
-
Kataoka K., Harada A., Nagasaki Y. Block copolymer micelles for drug delivery: design, characterization and biological significance. Adv. Drug Deliv. Rev. 47:2001;113-131.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.47
, pp. 113-131
-
-
Kataoka, K.1
Harada, A.2
Nagasaki, Y.3
-
8
-
-
0034907767
-
Amoxicillin-loaded polyethylcyanoacrylate nanoparticles: Influence of PEG coating on the particle size, drug release rate and phagocytic uptake
-
Fontana G., Licciardi M., Mansueto S., Schillaci D., Giammona G. Amoxicillin-loaded polyethylcyanoacrylate nanoparticles: influence of PEG coating on the particle size, drug release rate and phagocytic uptake. Biomaterials. 22:2001;2857-2865.
-
(2001)
Biomaterials
, vol.22
, pp. 2857-2865
-
-
Fontana, G.1
Licciardi, M.2
Mansueto, S.3
Schillaci, D.4
Giammona, G.5
-
9
-
-
0029091362
-
Non-stealth (poly(lactic acid/albumin)) and stealth (poly(lactic acid-polyethylene glycol)) nanoparticles as injectable drug carriers
-
Verrecchia 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. 36:1995;49-61.
-
(1995)
J. Control. Release
, vol.36
, pp. 49-61
-
-
Verrecchia, T.1
Spenlehauer, G.2
Bazile, D.V.3
Murry-Brelier, A.4
Archimbaud, Y.5
Veillard, M.6
-
10
-
-
0037133724
-
Biodistribution of long-circulating PEG-liposomes in a murine model of established subcutaneous abscesses
-
Stearne L.E.T., Schiffelers R.M., Smouter E., Bakker-Woudenberg I.A.J.M., Gyssens I.C. Biodistribution of long-circulating PEG-liposomes in a murine model of established subcutaneous abscesses. BBA, Biomembranes. 1561:2002;91-97.
-
(2002)
BBA, Biomembranes
, vol.1561
, pp. 91-97
-
-
Stearne, L.E.T.1
Schiffelers, R.M.2
Smouter, E.3
Bakker-Woudenberg, I.A.J.M.4
Gyssens, I.C.5
-
11
-
-
0034773527
-
Preparation of long-circulating immunoliposomes using PEG-cholesterol conjugates: Effect of the spacer arm between PEG and cholesterol on liposomal characteristics
-
Carrion C., Domingo J.C., de Madariaga M.A. Preparation of long-circulating immunoliposomes using PEG-cholesterol conjugates: effect of the spacer arm between PEG and cholesterol on liposomal characteristics. Chem. Phys. Lipids. 113:2001;97-110.
-
(2001)
Chem. Phys. Lipids
, vol.113
, pp. 97-110
-
-
Carrion, C.1
Domingo, J.C.2
De Madariaga, M.A.3
-
12
-
-
0032580445
-
Development of liposomal anthracyclines: From basics to clinical applications
-
Gabizon A., Goren D., Cohen R., Barenholz Y. Development of liposomal anthracyclines: from basics to clinical applications. J. Control. Release. 53:1998;275-279.
-
(1998)
J. Control. Release
, vol.53
, pp. 275-279
-
-
Gabizon, A.1
Goren, D.2
Cohen, R.3
Barenholz, Y.4
-
13
-
-
0342460488
-
Physical properties and tissue distribution of adriamycin encapsulated in polyethyleneglycol-coated liposomes
-
Sadzuka Y., Hirota S. Physical properties and tissue distribution of adriamycin encapsulated in polyethyleneglycol-coated liposomes. Adv. Drug Deliv. Rev. 24:1997;257-263.
-
(1997)
Adv. Drug Deliv. Rev.
, vol.24
, pp. 257-263
-
-
Sadzuka, Y.1
Hirota, S.2
-
14
-
-
0343923453
-
Long-circulating liposomes for drug delivery in cancer therapy: A review of biodistribution studies in tumor-bearing animals
-
Gabizon A., Goren D., Horowitz A.T., Tzemach D., Lossos A., Siegal T. Long-circulating liposomes for drug delivery in cancer therapy: a review of biodistribution studies in tumor-bearing animals. Adv. Drug Deliv. Rev. 24:1997;337-344.
-
(1997)
Adv. Drug Deliv. Rev.
, vol.24
, pp. 337-344
-
-
Gabizon, A.1
Goren, D.2
Horowitz, A.T.3
Tzemach, D.4
Lossos, A.5
Siegal, T.6
-
15
-
-
0035816143
-
Polymer-drug conjugates, PDEPT and 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, PDEPT and PELT: basic principles for design and transfer from the laboratory to clinic. J. Control. Release. 74:2001;135-146.
-
(2001)
J. Control. 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
-
16
-
-
0035964623
-
PDEPT: Polymer-directed enzyme prodrug therapy I. HPMA copolymer-cathepsin B and PK1 as a model combination
-
Satchi R., Connors T.A., Duncan R. PDEPT: polymer-directed enzyme prodrug therapy I. HPMA copolymer-cathepsin B and PK1 as a model combination. Br. J. Cancer. 85:2001;1070-1076.
-
(2001)
Br. J. Cancer
, vol.85
, pp. 1070-1076
-
-
Satchi, R.1
Connors, T.A.2
Duncan, R.3
-
17
-
-
0036318521
-
Synthesis and characterization of a catalytic antibody-HPMA copolymer-conjugate as a tool for tumor selective prodrug activation
-
Satchi-Fainaro R., Wrasidlo W., Lode H.N., Shabat D. Synthesis and characterization of a catalytic antibody-HPMA copolymer-conjugate as a tool for tumor selective prodrug activation. Bioorg. Med. Chem. 10:2002;3023-3029.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 3023-3029
-
-
Satchi-Fainaro, R.1
Wrasidlo, W.2
Lode, H.N.3
Shabat, D.4
-
18
-
-
0037072529
-
Poly(L-glutamic acid)-anticancer drug conjugates
-
Li C. Poly(L-glutamic acid)-anticancer drug conjugates. Adv. Drug Deliv. Rev. 54:2002;695-713.
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 695-713
-
-
Li, C.1
-
19
-
-
0037462994
-
Design strategies to improve soluble macromolecular delivery constructs
-
Christie R.J., Grainger D.W. Design strategies to improve soluble macromolecular delivery constructs. Adv. Drug Deliv. Rev. 55:2003;421-437.
-
(2003)
Adv. Drug Deliv. Rev.
, vol.55
, pp. 421-437
-
-
Christie, R.J.1
Grainger, D.W.2
-
20
-
-
0037122778
-
Design of novel bioconjugates for targeted drug delivery
-
Lu Z.R., Shiah J.G., Sakuma S., Kopečková P., Kopeček J. Design of novel bioconjugates for targeted drug delivery. J. Control. Release. 78:2002;165-173.
-
(2002)
J. Control. Release
, vol.78
, pp. 165-173
-
-
Lu, Z.R.1
Shiah, J.G.2
Sakuma, S.3
Kopečková, P.4
Kopeček, J.5
-
21
-
-
0342316475
-
Polymeric drugs based on conjugates of synthetic and natural macromolecules: I. Synthesis and physico-chemical characterisation
-
Ulbrich K., Šubr V., Strohalm J., Plocová D., Jelínková M., Říhová B. Polymeric drugs based on conjugates of synthetic and natural macromolecules: I. Synthesis and physico-chemical characterisation. J. Control. Release. 64:2000;63-79.
-
(2000)
J. Control. Release
, vol.64
, pp. 63-79
-
-
Ulbrich, K.1
Šubr, V.2
Strohalm, J.3
Plocová, D.4
Jelínková, M.5
Říhová, B.6
-
22
-
-
0041962221
-
Polymeric drugs based on conjugates of synthetic and natural macromolecules: II. Anti-cancer activity of antibody or (Fab')2-targeted conjugates and combined therapy with immunomodulators
-
Říhová B., Jelínková M., Strohalm J., Šubr V., Plocová D., Hovorka O., Novák M., Plundrová D., Germano Y., Ulbrich K. Polymeric drugs based on conjugates of synthetic and natural macromolecules: II. Anti-cancer activity of antibody or (Fab')2-targeted conjugates and combined therapy with immunomodulators. J. Control. Release. 64:2000;241-261.
-
(2000)
J. Control. Release
, vol.64
, pp. 241-261
-
-
Říhová, B.1
Jelínková, M.2
Strohalm, J.3
Šubr, V.4
Plocová, D.5
Hovorka, O.6
Novák, M.7
Plundrová, D.8
Germano, Y.9
Ulbrich, K.10
-
23
-
-
0346551010
-
Polymer conjugates with anticancer activity
-
Putnam D., Kopeček J. Polymer conjugates with anticancer activity. Adv. Polym. Sci. 122:1995;55-123.
-
(1995)
Adv. Polym. Sci.
, vol.122
, pp. 55-123
-
-
Putnam, D.1
Kopeček, J.2
-
24
-
-
0035904966
-
Targeted drug conjugates: Principles and progress
-
Garnett M.C. Targeted drug conjugates: principles and progress. Adv. Drug Deliv. Rev. 53:2001;171-216.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.53
, pp. 171-216
-
-
Garnett, M.C.1
-
25
-
-
0033180164
-
Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs
-
Dubowchik G.M., Walker M.A. Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs. Pharmacol. Ther. 83:1999;67-123.
-
(1999)
Pharmacol. Ther.
, vol.83
, pp. 67-123
-
-
Dubowchik, G.M.1
Walker, M.A.2
-
26
-
-
0042787657
-
Progress in immunoconjugate cancer therapeutics
-
Payne G. Progress in immunoconjugate cancer therapeutics. Cancer Cell. 3:2003;207-212.
-
(2003)
Cancer Cell
, vol.3
, pp. 207-212
-
-
Payne, G.1
-
27
-
-
0032872567
-
Monoclonal antibody drug conjugates in the treatment of cancer
-
Trail P.A., Bianchi A.B. Monoclonal antibody drug conjugates in the treatment of cancer. Curr. Opin. Immunol. 11:1999;584-588.
-
(1999)
Curr. Opin. Immunol.
, vol.11
, pp. 584-588
-
-
Trail, P.A.1
Bianchi, A.B.2
-
28
-
-
0036781811
-
Ligand-targeted therapeutics in anticancer therapy
-
Allen T.M. Ligand-targeted therapeutics in anticancer therapy. Nat. Rev. Cancer. 2:2002;750-763.
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 750-763
-
-
Allen, T.M.1
-
29
-
-
0038387390
-
The dawning era of polymer therapeutics
-
Duncan R. The dawning era of polymer therapeutics. Nat. Rev. Drug Discov. 2:2003;347-360.
-
(2003)
Nat. Rev. Drug Discov.
, vol.2
, pp. 347-360
-
-
Duncan, R.1
-
31
-
-
0030576517
-
Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis
-
Hanahan D., Folkman J. Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis. Cell. 86:1996;353-364.
-
(1996)
Cell
, vol.86
, pp. 353-364
-
-
Hanahan, D.1
Folkman, J.2
-
32
-
-
0034993240
-
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. 41:2001;189-207.
-
(2001)
Adv. Enzyme Regul.
, vol.41
, pp. 189-207
-
-
Maeda, H.1
-
33
-
-
0029039418
-
Influence of molecular weight on passive tumour accumulation of a soluble macromolecular drug carrier
-
Seymour L.W., Miyamoto Y., Maeda H., Brereton M., Strohalm J., Ulbrich K., Duncan R. Influence of molecular weight on passive tumour accumulation of a soluble macromolecular drug carrier. Eur. J. Cancer. 31:1995;766-770.
-
(1995)
Eur. J. Cancer
, vol.31
, pp. 766-770
-
-
Seymour, L.W.1
Miyamoto, Y.2
Maeda, H.3
Brereton, M.4
Strohalm, J.5
Ulbrich, K.6
Duncan, R.7
-
34
-
-
0037334516
-
Vascular permeability enhancement in solid tumor: Various factors, mechanisms involved and its implications
-
Maeda H., Fang J., Inutsuka T., Kitamoto Y. Vascular permeability enhancement in solid tumor: various factors, mechanisms involved and its implications. Int. Immunopharmacol. 3:2003;319-328.
-
(2003)
Int. Immunopharmacol.
, vol.3
, pp. 319-328
-
-
Maeda, H.1
Fang, J.2
Inutsuka, T.3
Kitamoto, Y.4
-
35
-
-
0034000453
-
Tumor vascular permeability and the EPR effect in macromolecular therapeutics: A review
-
Maeda H., Wu J., Sawa T., Matsumura Y., Hori K. Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J. Control. Release. 65:2000;271-284.
-
(2000)
J. Control. Release
, vol.65
, pp. 271-284
-
-
Maeda, H.1
Wu, J.2
Sawa, T.3
Matsumura, Y.4
Hori, K.5
-
36
-
-
0026926609
-
Conjugates of anticancer agents and polymers: Advantages of macromolecular therapeutics in vivo
-
Maeda H., Seymour L.W., Miyamoto Y. Conjugates of anticancer agents and polymers: advantages of macromolecular therapeutics in vivo. Bioconjug. Chem. 3:1992;351-362.
-
(1992)
Bioconjug. Chem.
, vol.3
, pp. 351-362
-
-
Maeda, H.1
Seymour, L.W.2
Miyamoto, Y.3
-
37
-
-
0035816204
-
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. Control. Release. 74:2001;47-61.
-
(2001)
J. Control. Release
, vol.74
, pp. 47-61
-
-
Maeda, H.1
Sawa, T.2
Konno, T.3
-
38
-
-
0028833556
-
Macromolecular drug carrier systems in cancer-chemotherapy- macromolecular prodrugs
-
Takakura Y., Hashida M. Macromolecular drug carrier systems in cancer-chemotherapy-macromolecular prodrugs. Crit. Rev. Oncol. Hematol. 18:1995;207-231.
-
(1995)
Crit. Rev. Oncol. Hematol.
, vol.18
, pp. 207-231
-
-
Takakura, Y.1
Hashida, M.2
-
39
-
-
0346434985
-
Molecular Biology of the Cell
-
London: Taylor & Francis Group
-
Alberts B., Johnson A., Lewis J., Raff M., Roberts K., Walter P. Molecular Biology of the Cell. 4th ed. 2002;Taylor & Francis Group, London.
-
(2002)
4th Ed.
-
-
Alberts, B.1
Johnson, A.2
Lewis, J.3
Raff, M.4
Roberts, K.5
Walter, P.6
-
40
-
-
0036009640
-
Star structure of antibody-targeted HPMA copolymer-bound doxoribicin: A novel type of polymeric conjugate for targeted drug delivery with potent anti-tumor effect
-
Kovář M., Strohalm J., Etrych T., Ulbrich K., Říhová B. Star structure of antibody-targeted HPMA copolymer-bound doxoribicin: a novel type of polymeric conjugate for targeted drug delivery with potent anti-tumor effect. Bioconjug. Chem. 13:2002;206-215.
-
(2002)
Bioconjug. Chem.
, vol.13
, pp. 206-215
-
-
Kovář, M.1
Strohalm, J.2
Etrych, T.3
Ulbrich, K.4
Říhová, B.5
-
41
-
-
0000859980
-
Polymers containing enzymatically degradable bonds 8. Degradation of oligopeptide sequences in N-(2-hydroxypropyl)methacrylamide copolymers by bovine spleen cathepsin B
-
Rejmanová P., Kopeček J., Pohl J., Baudyš M., Kostka V. Polymers containing enzymatically degradable bonds 8. Degradation of oligopeptide sequences in N-(2-hydroxypropyl)methacrylamide copolymers by bovine spleen cathepsin B. Makromol. Chem. 184:1983;2009-2020.
-
(1983)
Makromol. Chem.
, vol.184
, pp. 2009-2020
-
-
Rejmanová, P.1
Kopeček, J.2
Pohl, J.3
Baudyš, M.4
Kostka, V.5
-
42
-
-
0037334066
-
Binding and cytotoxicity of HPMA copolymer conjugates to lymphocytes mediated by receptor-binding epitopes
-
Tang A.J., Kopečková P., Kopeček J. Binding and cytotoxicity of HPMA copolymer conjugates to lymphocytes mediated by receptor-binding epitopes. Pharm. Res. 20:2003;360-367.
-
(2003)
Pharm. Res.
, vol.20
, pp. 360-367
-
-
Tang, A.J.1
Kopečková, P.2
Kopeček, J.3
-
43
-
-
0034682892
-
Genes expressed in human tumor endothelium
-
St Croix B., Rago C., Velculescu V., Traverso G., Romans K.E., Montgomery E., Lal A., Riggins G.J., Lengauer C., Vogelstein B., Kinzler K.W. Genes expressed in human tumor endothelium. Science. 289:2000;1197-1202.
-
(2000)
Science
, vol.289
, pp. 1197-1202
-
-
St Croix, B.1
Rago, C.2
Velculescu, V.3
Traverso, G.4
Romans, K.E.5
Montgomery, E.6
Lal, A.7
Riggins, G.J.8
Lengauer, C.9
Vogelstein, B.10
Kinzler, K.W.11
-
44
-
-
0037112310
-
Drug targeting to specific vascular sites
-
Ruoslahti E. Drug targeting to specific vascular sites. Drug Discov. Today. 7:2002;1138-1143.
-
(2002)
Drug Discov. Today
, vol.7
, pp. 1138-1143
-
-
Ruoslahti, E.1
-
45
-
-
0038162536
-
Integrin-mediated targeting of drug delivery to irradiated tumor blood vessels
-
Hallahan D., Geng L., Qu S.M., Scarfone C., Giorgio T., Donnelly E., Gao X., Clanton J. Integrin-mediated targeting of drug delivery to irradiated tumor blood vessels. Cancer Cell. 3:2003;63-74.
-
(2003)
Cancer Cell
, vol.3
, pp. 63-74
-
-
Hallahan, D.1
Geng, L.2
Qu, S.M.3
Scarfone, C.4
Giorgio, T.5
Donnelly, E.6
Gao, X.7
Clanton, J.8
-
46
-
-
0035816144
-
Targeting drug delivery to radiation-induced neoantigens in tumor microvasculature
-
Hallahan D.E., Geng L., Cmelak A.J., Chakravarthy A.B., Martin W., Scarfone C., Gonzalez A. Targeting drug delivery to radiation-induced neoantigens in tumor microvasculature. J. Control. Release. 74:2001;183-191.
-
(2001)
J. Control. Release
, vol.74
, pp. 183-191
-
-
Hallahan, D.E.1
Geng, L.2
Cmelak, A.J.3
Chakravarthy, A.B.4
Martin, W.5
Scarfone, C.6
Gonzalez, A.7
-
47
-
-
0037022366
-
Targeting the prostate for destruction through a vascular address
-
Arap W., Haedicke W., Bernasconi M., Kain R., Rajotte D., Krajewski S., Ellerby H.M., Bredesen D.E., Pasqualini R., Ruoslahti E. Targeting the prostate for destruction through a vascular address. Proc. Natl. Acad. Sci. USA. 99:2002;1527-1531.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 1527-1531
-
-
Arap, W.1
Haedicke, W.2
Bernasconi, M.3
Kain, R.4
Rajotte, D.5
Krajewski, S.6
Ellerby, H.M.7
Bredesen, D.E.8
Pasqualini, R.9
Ruoslahti, E.10
-
48
-
-
0033950895
-
Aminopeptidase N is a receptor for tumor-homing peptides and a target for inhibiting angiogenesis
-
Pasqualini R., Koivunen E., Kain R., Lahdenranta J., Sakamoto M., Stryhn A., Ashmun R.A., Shapiro L.H., Arap W., Ruoslahti E. Aminopeptidase N is a receptor for tumor-homing peptides and a target for inhibiting angiogenesis. Cancer Res. 60:2000;722-727.
-
(2000)
Cancer Res.
, vol.60
, pp. 722-727
-
-
Pasqualini, R.1
Koivunen, E.2
Kain, R.3
Lahdenranta, J.4
Sakamoto, M.5
Stryhn, A.6
Ashmun, R.A.7
Shapiro, L.H.8
Arap, W.9
Ruoslahti, E.10
-
49
-
-
4143122876
-
Identification of novel carrier peptides for the specific delivery of therapeutics into cancer cells
-
Shadidi M., Sioud M. Identification of novel carrier peptides for the specific delivery of therapeutics into cancer cells. FASEB J. 16:2002;U478-U494.
-
(2002)
FASEB J.
, vol.16
-
-
Shadidi, M.1
Sioud, M.2
-
50
-
-
0016622773
-
Structure and properties of pharmacologically active polymers
-
Ringsdorf H. Structure and properties of pharmacologically active polymers. J. Polym. Sci., Polym. Symp. 51:1975;135-153.
-
(1975)
J. Polym. Sci., Polym. Symp.
, vol.51
, pp. 135-153
-
-
Ringsdorf, H.1
-
51
-
-
0020515183
-
Regeneration characteristics of mitomycin C-dextran conjugate in relation to its activity
-
Hashida M., Takakura Y., Matsumoto S., Sasaki H., Kato A., Kojima T., Muranishi S., Sezaki H. Regeneration characteristics of mitomycin C-dextran conjugate in relation to its activity. Chem. Pharm. Bull. 31:1983;2055-2063.
-
(1983)
Chem. Pharm. Bull.
, vol.31
, pp. 2055-2063
-
-
Hashida, M.1
Takakura, Y.2
Matsumoto, S.3
Sasaki, H.4
Kato, A.5
Kojima, T.6
Muranishi, S.7
Sezaki, H.8
-
52
-
-
0027987791
-
Polymer conjugates - Pharmacokinetic considerations for design and development
-
Duncan R., Spreafico F. Polymer conjugates - pharmacokinetic considerations for design and development. Clin. Phamacokinet. 27:1994;290-306.
-
(1994)
Clin. Phamacokinet.
, vol.27
, pp. 290-306
-
-
Duncan, R.1
Spreafico, F.2
-
53
-
-
0033971326
-
New derivatives of polyglutamic acid as drug carrier systems
-
Hoste K., Schacht E.H., Seymour L.W. New derivatives of polyglutamic acid as drug carrier systems. J. Control. Release. 64:2000;53-61.
-
(2000)
J. Control. Release
, vol.64
, pp. 53-61
-
-
Hoste, K.1
Schacht, E.H.2
Seymour, L.W.3
-
54
-
-
0036763519
-
N-(2-hydroxypropyl)-methacrylamide copolymer-9-aminocamptothecin conjugate: Colon-specific drug delivery in rats
-
Sakuma S., Lu Z.R., Pecharová B., Kopečková P., Kopeček J. N-(2-hydroxypropyl)-methacrylamide copolymer-9- aminocamptothecin conjugate: colon-specific drug delivery in rats. J. Bioact. Compat. Polym. 17:2002;305-319.
-
(2002)
J. Bioact. Compat. Polym.
, vol.17
, pp. 305-319
-
-
Sakuma, S.1
Lu, Z.R.2
Pecharová, B.3
Kopečková, P.4
Kopeček, J.5
-
55
-
-
0034814014
-
N-(2-hydroxypropyl)methacrylamide copolymer-6-(3-aminopropyl) -ellipticine conjugates. Synthesis, in vitro, and preliminary in vivo evaluation
-
Searle F., Gac-Breton S., Keane R., Dimitrijevic S., Brocchini S., Sausville E.A., Duncan R. N-(2-hydroxypropyl)methacrylamide copolymer-6-(3- aminopropyl)-ellipticine conjugates. Synthesis, in vitro, and preliminary in vivo evaluation. Bioconjug. Chem. 12:2001;711-718.
-
(2001)
Bioconjug. Chem.
, vol.12
, pp. 711-718
-
-
Searle, F.1
Gac-Breton, S.2
Keane, R.3
Dimitrijevic, S.4
Brocchini, S.5
Sausville, E.A.6
Duncan, R.7
-
57
-
-
0032959549
-
Phase I clinical and pharmacokinetic study of PK1 [N-(2-hydroxypropyl) methacrylamide copolymer doxorubicin]: First member of a new class of chemotherapeutic agents - Drug-polymer conjugates
-
Vasey P.A., Kaye S.B., Morrison R., Twelves C., Wilson P., Duncan R., Thomson A.H., Murray L.S., Hilditch T.E., Murray T., Burtles S., Fraier D., Frigerio E., Cassidy J. Phase I clinical and pharmacokinetic study of PK1 [N-(2-hydroxypropyl)methacrylamide copolymer doxorubicin]: first member of a new class of chemotherapeutic agents - drug-polymer conjugates. Clin. Cancer Res. 5:1999;83-94.
-
(1999)
Clin. Cancer Res.
, vol.5
, pp. 83-94
-
-
Vasey, P.A.1
Kaye, S.B.2
Morrison, R.3
Twelves, C.4
Wilson, P.5
Duncan, R.6
Thomson, A.H.7
Murray, L.S.8
Hilditch, T.E.9
Murray, T.10
Burtles, S.11
Fraier, D.12
Frigerio, E.13
Cassidy, J.14
-
58
-
-
0033013012
-
Preliminary clinical study of the distribution of HPMA copolymers bearing doxorubicin and galactosamine
-
Julyan P.J., Seymour L.W., Ferry D.R., Daryani S., Boivin C.M., Doran J., David M., Anderson D., Christodoulou C., Young A.M. Preliminary clinical study of the distribution of HPMA copolymers bearing doxorubicin and galactosamine. J. Control. Release. 57:1999;281-290.
-
(1999)
J. Control. Release
, vol.57
, pp. 281-290
-
-
Julyan, P.J.1
Seymour, L.W.2
Ferry, D.R.3
Daryani, S.4
Boivin, C.M.5
Doran, J.6
David, M.7
Anderson, D.8
Christodoulou, C.9
Young, A.M.10
-
59
-
-
0035667083
-
Preclinical evaluation of the cardiotoxicity of PK2: A novel HPMA copolymer-doxorubicin-galactosamine conjugate antitumour agent
-
Hopewell J.W., Duncan R., Wilding D., Chakrabarti K. Preclinical evaluation of the cardiotoxicity of PK2: a novel HPMA copolymer-doxorubicin- galactosamine conjugate antitumour agent. Hum. Exp. Toxicol. 20:2001;461-470.
-
(2001)
Hum. Exp. Toxicol.
, vol.20
, pp. 461-470
-
-
Hopewell, J.W.1
Duncan, R.2
Wilding, D.3
Chakrabarti, K.4
-
60
-
-
17144464252
-
Drug-HPMA-HuIg conjugates effective against human solid cancer
-
Říhová B., Strohalm J., Kubáč ková K., Jelínková M., Rozprimová L., Šírová M., Plocová D., Mrkvan T., Kovář M., Pokorná J., Etrych T., Ulbrich K. Drug-HPMA-HuIg conjugates effective against human solid cancer. Adv. Exp. Med. Biol. 519:2003;125-143.
-
(2003)
Adv. Exp. Med. Biol.
, vol.519
, pp. 125-143
-
-
Říhová, B.1
Strohalm, J.2
Kubáčková, K.3
Jelínková, M.4
Rozprimová, L.5
Šírová, M.6
Plocová, D.7
Mrkvan, T.8
Kovář, M.9
Pokorná, J.10
Etrych, T.11
Ulbrich, K.12
-
61
-
-
0021354226
-
Novel mode of cytotoxicity obtained by coupling inactive anthracycline to a polymer
-
Rogers K.E., Tokes Z.A. Novel mode of cytotoxicity obtained by coupling inactive anthracycline to a polymer. Biochem. Pharmacol. 33:1984;605-608.
-
(1984)
Biochem. Pharmacol.
, vol.33
, pp. 605-608
-
-
Rogers, K.E.1
Tokes, Z.A.2
-
62
-
-
0020584967
-
Cell surface-mediated cyto-toxicity of polymer-bound adriamycin against drug-resistant hepatocytes
-
Rogers K.E., Carr B.I., Tokes Z.A. Cell surface-mediated cyto-toxicity of polymer-bound adriamycin against drug-resistant hepatocytes. Cancer Res. 43:1983;2741-2748.
-
(1983)
Cancer Res.
, vol.43
, pp. 2741-2748
-
-
Rogers, K.E.1
Carr, B.I.2
Tokes, Z.A.3
-
63
-
-
0021354472
-
Controlled biodegradability of polymers - A key to drug delivery systems
-
Kopeček J. Controlled biodegradability of polymers - a key to drug delivery systems. Biomaterials. 5:1984;19-25.
-
(1984)
Biomaterials
, vol.5
, pp. 19-25
-
-
Kopeček, J.1
-
64
-
-
0030590499
-
The crucial role of spacer groups in macromolecular prodrug design
-
Soyez H., Schacht E., Vanderkerken S. The crucial role of spacer groups in macromolecular prodrug design. Adv. Drug Deliv. Rev. 21:1996;81-106.
-
(1996)
Adv. Drug Deliv. Rev.
, vol.21
, pp. 81-106
-
-
Soyez, H.1
Schacht, E.2
Vanderkerken, S.3
-
65
-
-
0024461551
-
Physicochemical properties and antitumor activities of polymeric prodrugs of mitomycin C with different regeneration rates
-
Takakura Y., Matsumoto S., Hashida M., Sezaki H. Physicochemical properties and antitumor activities of polymeric prodrugs of mitomycin C with different regeneration rates. J. Control. Release. 10:1989;97-105.
-
(1989)
J. Control. Release
, vol.10
, pp. 97-105
-
-
Takakura, Y.1
Matsumoto, S.2
Hashida, M.3
Sezaki, H.4
-
66
-
-
0029971428
-
Cellular pH gradient in tumor versus normal tissue: Potential exploitation for the treatment of cancer
-
Gerweck L.E., Seetharaman K. Cellular pH gradient in tumor versus normal tissue: potential exploitation for the treatment of cancer. Cancer Res. 56:1996;1194-1198.
-
(1996)
Cancer Res.
, vol.56
, pp. 1194-1198
-
-
Gerweck, L.E.1
Seetharaman, K.2
-
67
-
-
0027323489
-
PH in human tumor xenografts - Effect of intravenous administration of glucose
-
Volk T., Jahde E., Fortmeyer H.P., Glusenkamp K.H., Rajewsky M.F. pH in human tumor xenografts - effect of intravenous administration of glucose. Br. J. Cancer. 68:1993;492-500.
-
(1993)
Br. J. Cancer
, vol.68
, pp. 492-500
-
-
Volk, T.1
Jahde, E.2
Fortmeyer, H.P.3
Glusenkamp, K.H.4
Rajewsky, M.F.5
-
69
-
-
1942494462
-
In vitro and in vivo antitumor efficacy of acid sensitive albumin and poly(ethylene) glycol conjugates of doxorubicin
-
Roth T., Kratz F., Steidle C., Unger C., Fiebig H.H. In vitro and in vivo antitumor efficacy of acid sensitive albumin and poly(ethylene) glycol conjugates of doxorubicin. Ann. Oncol. 9:1998;102.
-
(1998)
Ann. Oncol.
, vol.9
, pp. 102
-
-
Roth, T.1
Kratz, F.2
Steidle, C.3
Unger, C.4
Fiebig, H.H.5
-
70
-
-
0037204252
-
Synthesis of HPMA copolymers containing doxorubicin bound via a hydrazone linkage. Effect of spacer on drug release and in vitro cytotoxicity
-
Etrych T., Chytil P., Jelínková M., Ríhová B., Ulbrich K. Synthesis of HPMA copolymers containing doxorubicin bound via a hydrazone linkage. Effect of spacer on drug release and in vitro cytotoxicity. Macromol. Biosci. 2:2002;43-52.
-
(2002)
Macromol. Biosci.
, vol.2
, pp. 43-52
-
-
Etrych, T.1
Chytil, P.2
Jelínková, M.3
Ríhová, B.4
Ulbrich, K.5
-
71
-
-
0035907178
-
New HPMA copolymers containing doxorubicin bound via pH-sensitive linkage: Synthesis and preliminary in vitro and in vivo biological properties
-
Etrych T., Jelínková M., Říhová B., Ulbrich K. New HPMA copolymers containing doxorubicin bound via pH-sensitive linkage: synthesis and preliminary in vitro and in vivo biological properties. J. Control. Release. 73:2001;89-102.
-
(2001)
J. Control. Release
, vol.73
, pp. 89-102
-
-
Etrych, T.1
Jelínková, M.2
Říhová, B.3
Ulbrich, K.4
-
72
-
-
0035816157
-
Doxorubicin bound to a HPMA copolymer carrier through hydrazone bond is effective also in a cancer cell line with a limited content of lysosomes
-
Říhová B., Etrych T., Pechar M., Jelínková M., Št'astný M., Hovorka O., Kovář M., Ulbrich K. Doxorubicin bound to a HPMA copolymer carrier through hydrazone bond is effective also in a cancer cell line with a limited content of lysosomes. J. Control. Release. 74:2001;225-232.
-
(2001)
J. Control. Release
, vol.74
, pp. 225-232
-
-
Říhová, B.1
Etrych, T.2
Pechar, M.3
Jelí nková, M.4
Št'Astný, M.5
Hovorka, O.6
Kovář, M.7
Ulbrich, K.8
-
73
-
-
0037458920
-
HPMA copolymers with pH-controlled release of doxorubicin. In vitro cytotoxicity and in vivo antitumor activity
-
Ulbrich K., Etrych T., Chytil P., Jelínková M., Říhová B. HPMA copolymers with pH-controlled release of doxorubicin. In vitro cytotoxicity and in vivo antitumor activity. J. Control. Release. 87:2003;33-47.
-
(2003)
J. Control. Release
, vol.87
, pp. 33-47
-
-
Ulbrich, K.1
Etrych, T.2
Chytil, P.3
Jelínková, M.4
Říhová, B.5
-
74
-
-
0026437916
-
Synthesis, conformation, biodistribution, and in vitro cytotoxicity of daunomycin branched polypeptide conjugates
-
Hudecz F., Clegg J.A., Kajtar J., Embleton M.J., Szekerke M., Baldwin R.W. Synthesis, conformation, biodistribution, and in vitro cytotoxicity of daunomycin branched polypeptide conjugates. Bioconjug. Chem. 3:1992;49-57.
-
(1992)
Bioconjug. Chem.
, vol.3
, pp. 49-57
-
-
Hudecz, F.1
Clegg, J.A.2
Kajtar, J.3
Embleton, M.J.4
Szekerke, M.5
Baldwin, R.W.6
-
75
-
-
0344129078
-
Synthesis of HPMA copolymer containing adriamycin bound via an acid-labile spacer and its activity toward human ovarian carcinoma cells
-
Choi W.M., Kopečková P., Minko T., Kopeček J. Synthesis of HPMA copolymer containing adriamycin bound via an acid-labile spacer and its activity toward human ovarian carcinoma cells. J. Bioact. Compat. Polym. 14:1999;447-456.
-
(1999)
J. Bioact. Compat. Polym.
, vol.14
, pp. 447-456
-
-
Choi, W.M.1
Kopečková, P.2
Minko, T.3
Kopeček, J.4
-
76
-
-
0019786031
-
Cis-Aconityl spacer between daunomycin and macromolecular carriers - A model of pH-sensitive linkage releasing drug from a lysosomotropic conjugate
-
Shen W.C., Ryser H.J.P. cis-Aconityl spacer between daunomycin and macromolecular carriers - a model of pH-sensitive linkage releasing drug from a lysosomotropic conjugate. Biochem. Biophys. Res. Commun. 102:1981;1048-1054.
-
(1981)
Biochem. Biophys. Res. Commun.
, vol.102
, pp. 1048-1054
-
-
Shen, W.C.1
Ryser, H.J.P.2
-
77
-
-
0019170967
-
Soluble macromolecules as carriers for daunorubicin
-
Hurwitz E., Wilchek M., Pitha J. Soluble macromolecules as carriers for daunorubicin. J. Appl. Biochem. 2:1980;25-35.
-
(1980)
J. Appl. Biochem.
, vol.2
, pp. 25-35
-
-
Hurwitz, E.1
Wilchek, M.2
Pitha, J.3
-
78
-
-
0342460614
-
Synthesis and stability of four maleimide derivatives of the anticancer drug doxorubicin for the preparation of chemoimmunoconjugates
-
Kruger M., Beyer U., Schumacher P., Unger C., Zahn H., Kratz F. Synthesis and stability of four maleimide derivatives of the anticancer drug doxorubicin for the preparation of chemoimmunoconjugates. Chem. Pharm. Bull. 45:1997;399-401.
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 399-401
-
-
Kruger, M.1
Beyer, U.2
Schumacher, P.3
Unger, C.4
Zahn, H.5
Kratz, F.6
-
79
-
-
0031886252
-
Preparation, characterization and in vitro efficacy of albumin conjugates of doxorubicin
-
Kratz F., Beyer U., Collery P., Lechenault F., Cazabat A., Schumacher P., Falken U., Unger C. Preparation, characterization and in vitro efficacy of albumin conjugates of doxorubicin. Biol. Pharm. Bull. 21:1998;56-61.
-
(1998)
Biol. Pharm. Bull.
, vol.21
, pp. 56-61
-
-
Kratz, F.1
Beyer, U.2
Collery, P.3
Lechenault, F.4
Cazabat, A.5
Schumacher, P.6
Falken, U.7
Unger, C.8
-
80
-
-
0031552150
-
Synthesis of new maleimide derivatives of daunorubicin and biological activity of acid labile transferrin conjugates
-
Kratz F., Beyer U., Schumacher P., Kruger M., Zahn H., Roth T., Fiebig H.H., Unger C. Synthesis of new maleimide derivatives of daunorubicin and biological activity of acid labile transferrin conjugates. Bioorg. Med. Chem. Lett. 7:1997;617-622.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 617-622
-
-
Kratz, F.1
Beyer, U.2
Schumacher, P.3
Kruger, M.4
Zahn, H.5
Roth, T.6
Fiebig, H.H.7
Unger, C.8
-
81
-
-
0009211348
-
Antitumour activity of acid labile transferrin and albumin doxorubicin conjugates in in vitro and in vivo human tumour xenograft models
-
Kratz F., Fichtner I., Beyer U., Schumacher P., Roth T., Fiebig H.H., Unger C. Antitumour activity of acid labile transferrin and albumin doxorubicin conjugates in in vitro and in vivo human tumour xenograft models. Eur. J. Cancer. 33:1997;784.
-
(1997)
Eur. J. Cancer
, vol.33
, pp. 784
-
-
Kratz, F.1
Fichtner, I.2
Beyer, U.3
Schumacher, P.4
Roth, T.5
Fiebig, H.H.6
Unger, C.7
-
82
-
-
0344236832
-
In vitro antitumor efficacy of acid-labile transferrin conjugates of doxorubicin in ten human xenografts
-
Roth, T., Fiebig, H.H., Eckert, C., Spitzmüller, B., Beyer, U., Schumacher, P., Unger, C., Kratz, F., In vitro antitumor efficacy of acid-labile transferrin conjugates of doxorubicin in ten human xenografts, Proc. Am. Assoc. Cancer Res. 38 1997, S433, 2898.
-
(1997)
Proc. Am. Assoc. Cancer Res.
, vol.38
-
-
Roth, T.1
Fiebig, H.H.2
Eckert, C.3
Spitzmüller, B.4
Beyer, U.5
Schumacher, P.6
Unger, C.7
Kratz, F.8
-
83
-
-
0033067973
-
In vivo and in vitro efficacy of an acid-sensitive albumin conjugate of adriamycin compared to the parent compound in murine renal-cell carcinoma
-
Drevs J., Hofmann I., Marme D., Unger C., Kratz F. In vivo and in vitro efficacy of an acid-sensitive albumin conjugate of adriamycin compared to the parent compound in murine renal-cell carcinoma. Drug Deliv. 6:1999;89-95.
-
(1999)
Drug Deliv.
, vol.6
, pp. 89-95
-
-
Drevs, J.1
Hofmann, I.2
Marme, D.3
Unger, C.4
Kratz, F.5
-
84
-
-
0344236830
-
Structure-activity relationships of novel polyethylene glycol conjugates (MW 20,000 and 70,000) of the antitumor drug daunomycin
-
Rodrigues P.C.A., Schumacher P., Roth T., Fiebig H.H., Unger C., Mülhaupt R., Kratz F. Structure-activity relationships of novel polyethylene glycol conjugates (MW 20,000 and 70,000) of the antitumor drug daunomycin. 3rd International Symposium on Polymer Therapeutics, London:1998.
-
(1998)
3rd International Symposium on Polymer Therapeutics, London
-
-
Rodrigues, P.C.A.1
Schumacher, P.2
Roth, T.3
Fiebig, H.H.4
Unger, C.5
Mülhaupt, R.6
Kratz, F.7
-
85
-
-
0345530569
-
Efficacy of acid labile transferrin and albumin doxorubicin conjugates in in vitro and in vivo breast carcinoma systems
-
Fichtner I., Beyer U., Falken U., Meyer G., Schumacher P., Unger C., Kratz F. Efficacy of acid labile transferrin and albumin doxorubicin conjugates in in vitro and in vivo breast carcinoma systems. 2nd International Symposium on Polymer Therapeutics, Kumamoto, Japan:1997.
-
(1997)
2nd International Symposium on Polymer Therapeutics, Kumamoto, Japan
-
-
Fichtner, I.1
Beyer, U.2
Falken, U.3
Meyer, G.4
Schumacher, P.5
Unger, C.6
Kratz, F.7
-
86
-
-
0035053943
-
Differences in the intracellular distribution of acid-sensitive doxorubicin-protein conjugates in comparison to free and liposomal formulated doxorubicin as shown by confocal microscopy
-
Beyer U., Rothen-Rutishauser B., Unger C., Wunderli-Allenspach H., Kratz F. Differences in the intracellular distribution of acid-sensitive doxorubicin-protein conjugates in comparison to free and liposomal formulated doxorubicin as shown by confocal microscopy. Pharm. Res. 18:2001;29-38.
-
(2001)
Pharm. Res.
, vol.18
, pp. 29-38
-
-
Beyer, U.1
Rothen-Rutishauser, B.2
Unger, C.3
Wunderli-Allenspach, H.4
Kratz, F.5
-
87
-
-
0031855765
-
Synthesis and in vitro efficacy of transferrin conjugates of the anticancer drug chlorambucil
-
Beyer U., Roth T., Schumacher P., Maier G., Unold A., Frahm A.W., Fiebig H.H., Unger C., Kratz F. Synthesis and in vitro efficacy of transferrin conjugates of the anticancer drug chlorambucil. J. Med. Chem. 41:1998;2701-2708.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2701-2708
-
-
Beyer, U.1
Roth, T.2
Schumacher, P.3
Maier, G.4
Unold, A.5
Frahm, A.W.6
Fiebig, H.H.7
Unger, C.8
Kratz, F.9
-
88
-
-
0031981046
-
Albumin conjugates of the anticancer drug chlorambucil: Synthesis, characterization, and in vitro efficacy
-
Kratz F., Beyer U., Roth T., Schutte M.T., Unold A., Fiebig H.H., Unger C. Albumin conjugates of the anticancer drug chlorambucil: synthesis, characterization, and in vitro efficacy. Arch. Pharm. 331:1998;47-53.
-
(1998)
Arch. Pharm.
, vol.331
, pp. 47-53
-
-
Kratz, F.1
Beyer, U.2
Roth, T.3
Schutte, M.T.4
Unold, A.5
Fiebig, H.H.6
Unger, C.7
-
89
-
-
0029981640
-
Synthesis of polyglutamine and dextran conjugates of streptomycin with an acid-sensitive drug-carrier linkage
-
Coessens V., Schacht E., Domurado D. Synthesis of polyglutamine and dextran conjugates of streptomycin with an acid-sensitive drug-carrier linkage. J. Control. Release. 38:1996;141-150.
-
(1996)
J. Control. Release
, vol.38
, pp. 141-150
-
-
Coessens, V.1
Schacht, E.2
Domurado, D.3
-
90
-
-
0028997161
-
Synthesis, controlled-release properties and antitumor-activity of alginate-cis-aconityl-daunomycin conjugates
-
Alshamkhani A., Duncan R. Synthesis, controlled-release properties and antitumor-activity of alginate-cis-aconityl-daunomycin conjugates. Int. J. Pharm. 122:1995;107-119.
-
(1995)
Int. J. Pharm.
, vol.122
, pp. 107-119
-
-
Alshamkhani, A.1
Duncan, R.2
-
91
-
-
0024438996
-
Poly(carboxylic acid) polymers as carriers for anthracyclines
-
Zunino F., Pratesi G., Micheloni A. Poly(carboxylic acid) polymers as carriers for anthracyclines. J. Control. Release. 10:1989;65-73.
-
(1989)
J. Control. Release
, vol.10
, pp. 65-73
-
-
Zunino, F.1
Pratesi, G.2
Micheloni, A.3
-
92
-
-
0028023917
-
Evaluation of the hydrolytic and enzymatic stability of macromolecular mitomycin C derivatives
-
De Marre A., Seymour L.W., Schacht E. Evaluation of the hydrolytic and enzymatic stability of macromolecular mitomycin C derivatives. J. Control. Release. 31:1994;89-97.
-
(1994)
J. Control. Release
, vol.31
, pp. 89-97
-
-
De Marre, A.1
Seymour, L.W.2
Schacht, E.3
-
93
-
-
0035581125
-
Synthesis and pharmacological activity of a novel water-soluble hepatocyte-specific polymeric prodrug of prostaglandin E1 using lactosylated poly(L-glutamic hydrazide) as a carrier
-
Akamatsu K., Yamasaki Y., Nishikawa M., Takakura Y., Hashida M. Synthesis and pharmacological activity of a novel water-soluble hepatocyte-specific polymeric prodrug of prostaglandin E1 using lactosylated poly(L-glutamic hydrazide) as a carrier. Biochem. Pharmacol. 62:2001;1531-1536.
-
(2001)
Biochem. Pharmacol.
, vol.62
, pp. 1531-1536
-
-
Akamatsu, K.1
Yamasaki, Y.2
Nishikawa, M.3
Takakura, Y.4
Hashida, M.5
-
94
-
-
0032845612
-
Design of polymeric prodrugs of prostaglandin E-1 having galactose residue for hepatocyte targeting
-
Hashida M., Akamatsu K., Nishikawa M., Yamashita F., Takakura Y. Design of polymeric prodrugs of prostaglandin E-1 having galactose residue for hepatocyte targeting. J. Control. Release. 62:1999;253-262.
-
(1999)
J. Control. Release
, vol.62
, pp. 253-262
-
-
Hashida, M.1
Akamatsu, K.2
Nishikawa, M.3
Yamashita, F.4
Takakura, Y.5
-
95
-
-
0032794161
-
Development of a hepatocyte-specific prostaglandin E-1 polymeric prodrug and its potential for preventing carbon tetrachloride-induced fulminant hepatitis in mice
-
Akamatsu K., Yamasaki Y., Nishikawa M., Takakura Y., Hashida M. Development of a hepatocyte-specific prostaglandin E-1 polymeric prodrug and its potential for preventing carbon tetrachloride-induced fulminant hepatitis in mice. J. Pharmacol. Exp. Ther. 290:1999;1242-1249.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, pp. 1242-1249
-
-
Akamatsu, K.1
Yamasaki, Y.2
Nishikawa, M.3
Takakura, Y.4
Hashida, M.5
-
96
-
-
0031890623
-
Low toxicity and high antitumour activity of daunomycin by conjugation to an immunopotential amphoteric branched polypeptide
-
Gaál D., Hudecz F. Low toxicity and high antitumour activity of daunomycin by conjugation to an immunopotential amphoteric branched polypeptide. Eur. J. Cancer. 34:1998;155-161.
-
(1998)
Eur. J. Cancer
, vol.34
, pp. 155-161
-
-
Gaál, D.1
Hudecz, F.2
-
97
-
-
0030995513
-
Synthesis and in vitro stability of macromolecular prodrugs of norfloxacin
-
Coessens V., Schacht E.H., Domurado D. Synthesis and in vitro stability of macromolecular prodrugs of norfloxacin. J. Control. Release. 47:1997;283-291.
-
(1997)
J. Control. Release
, vol.47
, pp. 283-291
-
-
Coessens, V.1
Schacht, E.H.2
Domurado, D.3
-
98
-
-
0033997597
-
Polymer-bound camptothecin: Initial biodistribution and antitumour activity studies
-
Caiolfa V.R., Zamai M., Fiorino A., Frigerio E., Pellizzoni C., d'Argy R., Ghiglieri A., Castelli M.G., Farao M., Pesenti E. Polymer-bound camptothecin: initial biodistribution and antitumour activity studies. J. Control. Release. 65:2000;105-119.
-
(2000)
J. Control. Release
, vol.65
, pp. 105-119
-
-
Caiolfa, V.R.1
Zamai, M.2
Fiorino, A.3
Frigerio, E.4
Pellizzoni, C.5
D'Argy, R.6
Ghiglieri, A.7
Castelli, M.G.8
Farao, M.9
Pesenti, E.10
-
99
-
-
0031933130
-
Preclinical toxicology of a novel polymeric antitumour agent: HPMA copolymer-doxorubicin (PK1)
-
Duncan R., Coatsworth J.K., Burtles S. Preclinical toxicology of a novel polymeric antitumour agent: HPMA copolymer-doxorubicin (PK1). Hum. Exp. Toxicol. 17:1998;93-105.
-
(1998)
Hum. Exp. Toxicol.
, vol.17
, pp. 93-105
-
-
Duncan, R.1
Coatsworth, J.K.2
Burtles, S.3
-
100
-
-
0032867961
-
Population pharmacokinetics in phase I drug development: A phase I study of PK1 in patients with solid tumours
-
Thomson A.H., Vasey P.A., Murray L.S., Cassidy J., Fraier D., Frigerio E., Twelves C. Population pharmacokinetics in phase I drug development: a phase I study of PK1 in patients with solid tumours. Br. J. Cancer. 81:1999;99-108.
-
(1999)
Br. J. Cancer
, vol.81
, pp. 99-108
-
-
Thomson, A.H.1
Vasey, P.A.2
Murray, L.S.3
Cassidy, J.4
Fraier, D.5
Frigerio, E.6
Twelves, C.7
-
101
-
-
0028969911
-
Synthesis and cytotoxic activity of conjugates of monomethoxy poly(ethylene-glycol) end-capped with doxorubicin via ester, amide, or Schiff-base bond
-
Ohya Y., Kuroda H., Hirai K., Ouchi T. Synthesis and cytotoxic activity of conjugates of monomethoxy poly(ethylene-glycol) end-capped with doxorubicin via ester, amide, or Schiff-base bond. J. Bioact. Compat. Polym. 10:1995;51-66.
-
(1995)
J. Bioact. Compat. Polym.
, vol.10
, pp. 51-66
-
-
Ohya, Y.1
Kuroda, H.2
Hirai, K.3
Ouchi, T.4
-
102
-
-
0346540566
-
Design of antitumor agent-terminated poly(ethylene glycol) conjugate as macromolecular prodrug
-
Ouchi T., Kuroda H., Ohya Y. Design of antitumor agent-terminated poly(ethylene glycol) conjugate as macromolecular prodrug. Acs. Ser. Symp. 680:1997;284-296.
-
(1997)
Acs. Ser. Symp.
, vol.680
, pp. 284-296
-
-
Ouchi, T.1
Kuroda, H.2
Ohya, Y.3
-
103
-
-
17744403100
-
Acid-sensitive polyethylene glycol conjugates of doxorubicin: Preparation, in vitro efficacy and intracellular distribution
-
Rodrigues P.C.A., Beyer U., Schumacher P., Roth T., Fiebig H.H., Unger C., Messori L., Orioli P., Paper D.H., Mulhaupt R., Kratz F. Acid-sensitive polyethylene glycol conjugates of doxorubicin: preparation, in vitro efficacy and intracellular distribution. Bioorg. Med. Chem. 7:1999;2517-2524.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 2517-2524
-
-
Rodrigues, P.C.A.1
Beyer, U.2
Schumacher, P.3
Roth, T.4
Fiebig, H.H.5
Unger, C.6
Messori, L.7
Orioli, P.8
Paper, D.H.9
Mulhaupt, R.10
Kratz, F.11
-
104
-
-
0037325515
-
Synthesis and in vitro efficacy of acid-sensitive poly(ethylene glycol) paclitaxel conjugates
-
Rodrigues P.C.A., Scheuermann K., Stockmar C., Maier G., Fiebig H.H., Unger C., Mulhaupt R., Kratz F. Synthesis and in vitro efficacy of acid-sensitive poly(ethylene glycol) paclitaxel conjugates. Bioorg. Med. Chem. Lett. 13:2003;355-360.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 355-360
-
-
Rodrigues, P.C.A.1
Scheuermann, K.2
Stockmar, C.3
Maier, G.4
Fiebig, H.H.5
Unger, C.6
Mulhaupt, R.7
Kratz, F.8
-
105
-
-
0028467797
-
Strategies for covalent attachment of doxorubicin to poly(Peg-Lys), a new water-soluble poly(ether urethane)
-
Nathan A., Zalipsky S., Kohn J. Strategies for covalent attachment of doxorubicin to poly(Peg-Lys), a new water-soluble poly(ether urethane). J. Bioact. Compat. Polym. 9:1994;239-251.
-
(1994)
J. Bioact. Compat. Polym.
, vol.9
, pp. 239-251
-
-
Nathan, A.1
Zalipsky, S.2
Kohn, J.3
-
106
-
-
1942462087
-
Enzymatically degradable PEG multiblock copolymers with hydrazone-attached doxorubicin in cancer therapy
-
Abstract
-
Pechar M., Ulbrich K., Jelínková M., Ří hová B. Enzymatically degradable PEG multiblock copolymers with hydrazone-attached doxorubicin in cancer therapy. 6th European Symposium on Controlled Drug Delivery, Noordwijkaan Zee (Neederlands). 2000;155-156. Abstract.
-
(2000)
6th European Symposium on Controlled Drug Delivery, Noordwijkaan Zee (Neederlands)
, pp. 155-156
-
-
Pechar, M.1
Ulbrich, K.2
Jelínková, M.3
Ří hová, B.4
-
107
-
-
1942462077
-
Enzymatically degradable PEG multiblock copolymers with hydrazone-attached doxorubicin in cancer therapy
-
Pechar M., Ulbrich K., Jelínková M., Ří hová B. Enzymatically degradable PEG multiblock copolymers with hydrazone-attached doxorubicin in cancer therapy. J. Control. Release. 72:2001;253-254.
-
(2001)
J. Control. Release
, vol.72
, pp. 253-254
-
-
Pechar, M.1
Ulbrich, K.2
Jelínková, M.3
Ří hová, B.4
-
108
-
-
1942494467
-
Polymeric anticancer drugs with pH-controlled activation
-
Proceedings
-
Ulbrich K., Etrych T., Chytil P., Jelínková M., Říhová B. Polymeric anticancer drugs with pH-controlled activation. 11th International Pharmaceutical Technology Symposium "Intelligent Drug Delivery Systems", Istanbul, Turkey. 2002;9-10. Proceedings.
-
(2002)
11th International Pharmaceutical Technology Symposium "intelligent Drug Delivery Systems", Istanbul, Turkey
, pp. 9-10
-
-
Ulbrich, K.1
Etrych, T.2
Chytil, P.3
Jelínková, M.4
Říhová, B.5
-
109
-
-
1942462081
-
Novel generation of polymer-drug-carrier systems for site-specific therapy
-
Abstract
-
Ulbrich K., Etrych T., Pechar M., Jelínková M., Říhová B. Novel generation of polymer-drug-carrier systems for site-specific therapy. 7th European Symposium on Controlled Drug Delivery Systems, Noordwijk aan Zee (Netherlands). 2002;13-15. Abstract.
-
(2002)
7th European Symposium on Controlled Drug Delivery Systems, Noordwijk Aan Zee (Netherlands)
, pp. 13-15
-
-
Ulbrich, K.1
Etrych, T.2
Pechar, M.3
Jelínková, M.4
Říhová, B.5
-
110
-
-
0037080616
-
Pendent chain functionalized polyacetals that display pH-dependent degradation: A platform for the development of novel polymer therapeutics
-
Tomlinson R., Klee M., Garrett S., Heller J., Duncan R., Brocchini S. Pendent chain functionalized polyacetals that display pH-dependent degradation: a platform for the development of novel polymer therapeutics. Macromolecules. 35:2002;473-480.
-
(2002)
Macromolecules
, vol.35
, pp. 473-480
-
-
Tomlinson, R.1
Klee, M.2
Garrett, S.3
Heller, J.4
Duncan, R.5
Brocchini, S.6
-
111
-
-
0023710359
-
Para-benzylthiocarbamoyl-aspartyl-daunorubicin-substituted polytrisacryl - A new drug acid-labile arm-carrier conjugate
-
Daussin F., Boschetti E., Delmotte F., Monsigny M. Para- benzylthiocarbamoyl-aspartyl-daunorubicin-substituted polytrisacryl - a new drug acid-labile arm-carrier conjugate. Eur. J. Biochem. 176:1988;625-628.
-
(1988)
Eur. J. Biochem.
, vol.176
, pp. 625-628
-
-
Daussin, F.1
Boschetti, E.2
Delmotte, F.3
Monsigny, M.4
-
112
-
-
0035731866
-
Conjugate of doxorubicin with a thermosensitive polymer drug carrier
-
Chytrý V., Ulbrich K. Conjugate of doxorubicin with a thermosensitive polymer drug carrier. J. Bioact. Compat. Polym. 16:2001;427-440.
-
(2001)
J. Bioact. Compat. Polym.
, vol.16
, pp. 427-440
-
-
Chytrý, V.1
Ulbrich, K.2
-
113
-
-
0033886221
-
Quaternized poly(propylene imine) dendrimers as novel pH-sensitive controlled-release systems
-
Sideratou Z., Tsiourvas D., Paleos C.M. Quaternized poly(propylene imine) dendrimers as novel pH-sensitive controlled-release systems. Langmuir. 16:2000;1766-1769.
-
(2000)
Langmuir
, vol.16
, pp. 1766-1769
-
-
Sideratou, Z.1
Tsiourvas, D.2
Paleos, C.M.3
-
114
-
-
0036000121
-
Polyester dendritic systems for drug delivery applications: Design, synthesis, and characterization
-
Ihre H.R., De Jesus O.L.P., Szoka F.C., Frechet J.M.J. Polyester dendritic systems for drug delivery applications: design, synthesis, and characterization. Bioconjug. Chem. 13:2002;443-452.
-
(2002)
Bioconjug. Chem.
, vol.13
, pp. 443-452
-
-
Ihre, H.R.1
De Jesus, O.L.P.2
Szoka, F.C.3
Frechet, J.M.J.4
-
115
-
-
0037130252
-
Doxorubicin-conjugated biodegradable polymeric micelles having acid-cleavable linkages
-
Yoo H.S., Lee E.A., Park T.G. Doxorubicin-conjugated biodegradable polymeric micelles having acid-cleavable linkages. J. Control. Release. 82:2002;17-27.
-
(2002)
J. Control. Release
, vol.82
, pp. 17-27
-
-
Yoo, H.S.1
Lee, E.A.2
Park, T.G.3
-
116
-
-
0024561482
-
New antitumor monoclonal-antibody Vinca conjugates Ly203725 and related-compounds-design, preparation, and representative in vivo activity
-
Laguzza B.C., Nichols C.L., Briggs S.L., Cullinan G.J., Johnson D.A., Starling J.J., Baker A.L., Bumol T.F., Corvalan J.R.F. New antitumor monoclonal-antibody Vinca conjugates Ly203725 and related-compounds-design, preparation, and representative in vivo activity. J. Med. Chem. 32:1989;548-555.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 548-555
-
-
Laguzza, B.C.1
Nichols, C.L.2
Briggs, S.L.3
Cullinan, G.J.4
Johnson, D.A.5
Starling, J.J.6
Baker, A.L.7
Bumol, T.F.8
Corvalan, J.R.F.9
-
117
-
-
0030909534
-
In vitro and in vivo antitumor activity of immunoconjugates prepared by linking 5-fluorouridine to antiadenocarcinoma monoclonal antibody
-
Brusa P., Dosio F., Coppo S., Pacchioni D., Arpicco S., Crosasso P., Cattel L. In vitro and in vivo antitumor activity of immunoconjugates prepared by linking 5-fluorouridine to antiadenocarcinoma monoclonal antibody. Farmaco. 52:1997;71-81.
-
(1997)
Farmaco
, vol.52
, pp. 71-81
-
-
Brusa, P.1
Dosio, F.2
Coppo, S.3
Pacchioni, D.4
Arpicco, S.5
Crosasso, P.6
Cattel, L.7
-
118
-
-
0026164319
-
New hydrazone derivatives of adriamycin and their immunoconjugates - A correlation between acid stability and cytotoxicity
-
Kaneko T., Willner D., Monkovic I., Knipe J.O., Braslawsky G.R., Greenfield R.S., Vyas D.M. New hydrazone derivatives of adriamycin and their immunoconjugates - a correlation between acid stability and cytotoxicity. Bioconjug. Chem. 2:1991;133-141.
-
(1991)
Bioconjug. Chem.
, vol.2
, pp. 133-141
-
-
Kaneko, T.1
Willner, D.2
Monkovic, I.3
Knipe, J.O.4
Braslawsky, G.R.5
Greenfield, R.S.6
Vyas, D.M.7
-
119
-
-
0027134326
-
(6-Maleimidocaproyl)hydrazone of doxorubicin - A new derivative for the preparation of immunoconjugates of doxorubicin
-
Willner D., Trail P.A., Hofstead S.J., King H.D., Lasch S.J., Braslawsky G.R., Greenfield R.S., Kaneko T., Firestone R.A. (6-Maleimidocaproyl)hydrazone of doxorubicin - a new derivative for the preparation of immunoconjugates of doxorubicin. Bioconjug. Chem. 4:1993;521-527.
-
(1993)
Bioconjug. Chem.
, vol.4
, pp. 521-527
-
-
Willner, D.1
Trail, P.A.2
Hofstead, S.J.3
King, H.D.4
Lasch, S.J.5
Braslawsky, G.R.6
Greenfield, R.S.7
Kaneko, T.8
Firestone, R.A.9
-
120
-
-
0025185802
-
Evaluation in vitro of adriamycin immunoconjugates synthesized using an acid-sensitive hydrazone linker
-
Greenfield R.S., Kaneko T., Daues A., Edson M.A., Fitzgerald K.A., Olech L.J., Grattan J.A., Spitalny G.L., Braslawsky G.R. Evaluation in vitro of adriamycin immunoconjugates synthesized using an acid-sensitive hydrazone linker. Cancer Res. 50:1990;6600-6607.
-
(1990)
Cancer Res.
, vol.50
, pp. 6600-6607
-
-
Greenfield, R.S.1
Kaneko, T.2
Daues, A.3
Edson, M.A.4
Fitzgerald, K.A.5
Olech, L.J.6
Grattan, J.A.7
Spitalny, G.L.8
Braslawsky, G.R.9
-
121
-
-
0025027766
-
Antitumor-activity of adriamycin (hydrazone-linked) immunoconjugates compared with free adriamycin and specificity of tumor-cell killing
-
Braslawsky G.R., Edson M.A., Pearce W., Kaneko T., Greenfield R.S. Antitumor-activity of adriamycin (hydrazone-linked) immunoconjugates compared with free adriamycin and specificity of tumor-cell killing. Cancer Res. 50:1990;6608-6614.
-
(1990)
Cancer Res.
, vol.50
, pp. 6608-6614
-
-
Braslawsky, G.R.1
Edson, M.A.2
Pearce, W.3
Kaneko, T.4
Greenfield, R.S.5
-
122
-
-
0025773754
-
Adriamycin(hydrazone)-antibody conjugates require internalization and intracellular acid-hydrolysis for antitumor-activity
-
Braslawsky G.R., Kadow K.F., Knipe J., Mcgoff K., Edson M., Kaneko T., Greenfield R.S. Adriamycin(hydrazone)-antibody conjugates require internalization and intracellular acid-hydrolysis for antitumor-activity. Cancer Immunol. Immunother. 33:1991;367-374.
-
(1991)
Cancer Immunol. Immunother.
, vol.33
, pp. 367-374
-
-
Braslawsky, G.R.1
Kadow, K.F.2
Knipe, J.3
Mcgoff, K.4
Edson, M.5
Kaneko, T.6
Greenfield, R.S.7
-
123
-
-
0031031895
-
Effect of linker variation on the stability, potency, and efficacy of carcinoma-reactive BR64-doxorubicin immunoconjugates
-
Trail P.A., Willner D., Knipe J., Henderson A.J., Lasch S.J., Zoeckler M.E., TrailSmith M.D., Doyle T.W., King H.D., Casazza A.M., Braslawsky G.R., Brown J., Hofstead S.J., Greenfield R.S., Firestone R.A., Mosure K., Kadow K.F., Yang M.B., Hellström K.E., Hellström I. Effect of linker variation on the stability, potency, and efficacy of carcinoma-reactive BR64-doxorubicin immunoconjugates. Cancer Res. 57:1997;100-105.
-
(1997)
Cancer Res.
, vol.57
, pp. 100-105
-
-
Trail, P.A.1
Willner, D.2
Knipe, J.3
Henderson, A.J.4
Lasch, S.J.5
Zoeckler, M.E.6
Trailsmith, M.D.7
Doyle, T.W.8
King, H.D.9
Casazza, A.M.10
Braslawsky, G.R.11
Brown, J.12
Hofstead, S.J.13
Greenfield, R.S.14
Firestone, R.A.15
Mosure, K.16
Kadow, K.F.17
Yang, M.B.18
Hellström, K.E.19
Hellström, I.20
more..
-
124
-
-
0027218284
-
Cure of xenografted human carcinomas by Br96-doxorubicin immunoconjugates
-
Trail P.A., Willner D., Lasch S.J., Henderson A.J., Hofstead S., Casazza A.M., Firestone R.A., Hellström I., Hellström K.E. Cure of xenografted human carcinomas by Br96-doxorubicin immunoconjugates. Science. 261:1993;212-215.
-
(1993)
Science
, vol.261
, pp. 212-215
-
-
Trail, P.A.1
Willner, D.2
Lasch, S.J.3
Henderson, A.J.4
Hofstead, S.5
Casazza, A.M.6
Firestone, R.A.7
Hellström, I.8
Hellström, K.E.9
-
125
-
-
0029997822
-
Synthesis and antitumor activity of the immunoconjugate BR96-Dox
-
Firestone R.A., Willner D., Hofstead S.J., King H.D., Kaneko T., Braslawsky G.R., Greenfield R.S., Trail P.A., Lasch S.J., Henderson A.J., Casazza A.M., Hellström I. Synthesis and antitumor activity of the immunoconjugate BR96-Dox. J. Control. Release. 39:1996;251-259.
-
(1996)
J. Control. Release
, vol.39
, pp. 251-259
-
-
Firestone, R.A.1
Willner, D.2
Hofstead, S.J.3
King, H.D.4
Kaneko, T.5
Braslawsky, G.R.6
Greenfield, R.S.7
Trail, P.A.8
Lasch, S.J.9
Henderson, A.J.10
Casazza, A.M.11
Hellström, I.12
-
126
-
-
0025491169
-
Antibody conjugates with morpholinodoxorubicin and acid-cleavable linkers
-
Mueller B.M., Wrasidlo W.A., Reisfeld R.A. Antibody conjugates with morpholinodoxorubicin and acid-cleavable linkers. Bioconjug. Chem. 1:1990;325-330.
-
(1990)
Bioconjug. Chem.
, vol.1
, pp. 325-330
-
-
Mueller, B.M.1
Wrasidlo, W.A.2
Reisfeld, R.A.3
-
127
-
-
0025433983
-
Immunoconjugate design: A predictive approach for coupling of daunomycin to monoclonal antibodies
-
Hudecz F., Ross H., Price M.R., Baldwin R.W. Immunoconjugate design: a predictive approach for coupling of daunomycin to monoclonal antibodies. Bioconjug. Chem. 1:1990;197-204.
-
(1990)
Bioconjug. Chem.
, vol.1
, pp. 197-204
-
-
Hudecz, F.1
Ross, H.2
Price, M.R.3
Baldwin, R.W.4
-
128
-
-
0023781775
-
Superiority of an acid-labile daunorubicin monoclonal antibody immunoconjugate compared to free drug
-
Dillman R.O., Johnson D.E., Shawler D.L., Koziol J.A. Superiority of an acid-labile daunorubicin monoclonal antibody immunoconjugate compared to free drug. Cancer Res. 48:1988;6097-6102.
-
(1988)
Cancer Res.
, vol.48
, pp. 6097-6102
-
-
Dillman, R.O.1
Johnson, D.E.2
Shawler, D.L.3
Koziol, J.A.4
-
129
-
-
0001577078
-
Doxorubicin conjugated with a monoclonal-antibody directed to a human melanoma-associated proteoglycan suppresses the growth of established tumor xenografts in nude-mice
-
Yang H.M., Reisfeld R.A. Doxorubicin conjugated with a monoclonal-antibody directed to a human melanoma-associated proteoglycan suppresses the growth of established tumor xenografts in nude-mice. Proc. Natl. Acad. Sci. USA. 85:1988;1189-1193.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 1189-1193
-
-
Yang, H.M.1
Reisfeld, R.A.2
-
130
-
-
0025342216
-
Application of target-specific drug immunoconjugates to experimental bone-marrow replacement therapy in mice
-
Ding L., Yu L.Z., Xie S.S., Gong D.G., Vergidis R., Diener E. Application of target-specific drug immunoconjugates to experimental bone-marrow replacement therapy in mice. Cancer Res. 50:1990;1538-1543.
-
(1990)
Cancer Res.
, vol.50
, pp. 1538-1543
-
-
Ding, L.1
Yu, L.Z.2
Xie, S.S.3
Gong, D.G.4
Vergidis, R.5
Diener, E.6
-
131
-
-
0031848767
-
Lectin-mediated drug targeting: Preparation, binding characteristics, and antiproliferative activity of wheat germ agglutinin conjugated doxorubicin on Caco-2 cells
-
Wirth M., Fuchs A., Wolf M., Ertl B., Gabor F. Lectin-mediated drug targeting: preparation, binding characteristics, and antiproliferative activity of wheat germ agglutinin conjugated doxorubicin on Caco-2 cells. Pharm. Res. 15:1998;1031-1037.
-
(1998)
Pharm. Res.
, vol.15
, pp. 1031-1037
-
-
Wirth, M.1
Fuchs, A.2
Wolf, M.3
Ertl, B.4
Gabor, F.5
-
132
-
-
0036709119
-
Lectin-mediated drug delivery: Discrimination between cytoadhesion and cytoinvasion and evidence for lysosomal accumulation of wheat germ agglutinin in the Caco-2 model
-
Wirth M., Kneuer C., Lehr C.M., Gabor F. Lectin-mediated drug delivery: discrimination between cytoadhesion and cytoinvasion and evidence for lysosomal accumulation of wheat germ agglutinin in the Caco-2 model. J. Drug Target. 10:2002;439-448.
-
(2002)
J. Drug Target.
, vol.10
, pp. 439-448
-
-
Wirth, M.1
Kneuer, C.2
Lehr, C.M.3
Gabor, F.4
-
133
-
-
0037177459
-
Lectin-mediated drug delivery: Binding and uptake of BSA-WGA conjugates using the Caco-2 model
-
Gabor F., Schwarzbauer A., Wirth M. Lectin-mediated drug delivery: binding and uptake of BSA-WGA conjugates using the Caco-2 model. Int. J. Pharm. 237:2002;227-239.
-
(2002)
Int. J. Pharm.
, vol.237
, pp. 227-239
-
-
Gabor, F.1
Schwarzbauer, A.2
Wirth, M.3
-
134
-
-
0037133115
-
Lectin-mediated drug delivery: Influence of mucin on cytoadhesion of plant lectins in vitro
-
Wirth M., Gerhardt K., Warm C., Gabor F. Lectin-mediated drug delivery: influence of mucin on cytoadhesion of plant lectins in vitro. J. Control. Release. 79:2002;183-191.
-
(2002)
J. Control. Release
, vol.79
, pp. 183-191
-
-
Wirth, M.1
Gerhardt, K.2
Warm, C.3
Gabor, F.4
-
135
-
-
0037227180
-
Lectin-mediated drug delivery: Fundamentals and perspectives
-
Gabor F., Wirth M. Lectin-mediated drug delivery: fundamentals and perspectives. Stp Pharma Sci. 13:2003;3-16.
-
(2003)
Stp Pharma Sci.
, vol.13
, pp. 3-16
-
-
Gabor, F.1
Wirth, M.2
-
136
-
-
0036119355
-
Targeting of doxorubicin to the urinary bladder of the rat shows increased cytotoxicity in the bladder urine combined with an absence of renal toxicity
-
Haas M., Moolenaar F., Elsinga A., Van der Wouden E.A., De Jong P.E., Meijer D.K.F., De Zeeuw D. Targeting of doxorubicin to the urinary bladder of the rat shows increased cytotoxicity in the bladder urine combined with an absence of renal toxicity. J. Drug Target. 10:2002;81-89.
-
(2002)
J. Drug Target.
, vol.10
, pp. 81-89
-
-
Haas, M.1
Moolenaar, F.2
Elsinga, A.3
Van Der Wouden, E.A.4
De Jong, P.E.5
Meijer, D.K.F.6
De Zeeuw, D.7
-
137
-
-
0030198183
-
Novel acid labile COL1 trityl-linked difluoronucleoside immunoconjugates: Synthesis, characterization, and biological activity
-
Patel V.F., Hardin J.N., Mastro J.M., Law K.L., Zimmermann J.L., Ehlhardt W.J., Woodland J.M., Starling J.J. Novel acid labile COL1 trityl-linked difluoronucleoside immunoconjugates: synthesis, characterization, and biological activity. Bioconjug. Chem. 7:1996;497-510.
-
(1996)
Bioconjug. Chem.
, vol.7
, pp. 497-510
-
-
Patel, V.F.1
Hardin, J.N.2
Mastro, J.M.3
Law, K.L.4
Zimmermann, J.L.5
Ehlhardt, W.J.6
Woodland, J.M.7
Starling, J.J.8
-
140
-
-
0024502871
-
New protein cross-linking reagents that are cleaved by mild acid
-
Srinivasachar K., Neville D.M. New protein cross-linking reagents that are cleaved by mild acid. Biochemistry. 28:1989;2501-2509.
-
(1989)
Biochemistry
, vol.28
, pp. 2501-2509
-
-
Srinivasachar, K.1
Neville, D.M.2
-
141
-
-
0024414652
-
Enhancement of immunotoxin efficacy by acid-cleavable cross-linking agents utilizing diphtheria-toxin and toxin mutants
-
Neville D.M., Srinivasachar K., Stone R., Scharff J. Enhancement of immunotoxin efficacy by acid-cleavable cross-linking agents utilizing diphtheria-toxin and toxin mutants. J. Biol. Chem. 264:1989;14653-14661.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 14653-14661
-
-
Neville, D.M.1
Srinivasachar, K.2
Stone, R.3
Scharff, J.4
-
142
-
-
0024323595
-
Inhibition of human-tumor growth in nude-mice by a conjugate of doxorubicin with monoclonal-antibodies to epidermal growth-factor receptor
-
Aboud-Pirak E., Hurwitz E., Bellot F., Schlessinger J., Sela M. Inhibition of human-tumor growth in nude-mice by a conjugate of doxorubicin with monoclonal-antibodies to epidermal growth-factor receptor. Proc. Natl. Acad. Sci. USA. 86:1989;3778-3781.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 3778-3781
-
-
Aboud-Pirak, E.1
Hurwitz, E.2
Bellot, F.3
Schlessinger, J.4
Sela, M.5
-
143
-
-
0026529567
-
Preparation and characterization of a water soluble dextran immunoconjugate of doxorubicin and the monoclonal antibody (ABL 364)
-
Brich Z., Ravel S., Kissel T., Fritsch J., Schoffmann A. Preparation and characterization of a water soluble dextran immunoconjugate of doxorubicin and the monoclonal antibody (ABL 364). J. Control. Release. 19:1992;245-257.
-
(1992)
J. Control. Release
, vol.19
, pp. 245-257
-
-
Brich, Z.1
Ravel, S.2
Kissel, T.3
Fritsch, J.4
Schoffmann, A.5
-
144
-
-
0028930439
-
Inhibition of Epstein-Barr-virus-transformed human chronic lymphocytic leukemic B-cells with monoclonal-antibody adriamycin (doxorubicin) conjugates
-
Zhu Z.P., Kralovec J., Ghose T., Mammen M. Inhibition of Epstein-Barr-virus-transformed human chronic lymphocytic leukemic B-cells with monoclonal-antibody adriamycin (doxorubicin) conjugates. Cancer Immunol. Immunother. 40:1995;257-267.
-
(1995)
Cancer Immunol. Immunother.
, vol.40
, pp. 257-267
-
-
Zhu, Z.P.1
Kralovec, J.2
Ghose, T.3
Mammen, M.4
-
145
-
-
0026830298
-
Preparation and properties of the immunoconjugate composed of anti-human colon cancer monoclonal-antibody and mitomycin C-dextran conjugate
-
Noguchi A., Takahashi T., Yamaguchi T., Kitamura K., Takakura Y., Hashida M., Sezaki H. Preparation and properties of the immunoconjugate composed of anti-human colon cancer monoclonal-antibody and mitomycin C-dextran conjugate. Bioconjug. Chem. 3:1992;132-137.
-
(1992)
Bioconjug. Chem.
, vol.3
, pp. 132-137
-
-
Noguchi, A.1
Takahashi, T.2
Yamaguchi, T.3
Kitamura, K.4
Takakura, Y.5
Hashida, M.6
Sezaki, H.7
-
146
-
-
0037161313
-
Differences in the intracellular fate of free and polymer-bound doxorubicin
-
Hovorka O., Štastný M., Etrych T., Šubr V., Strohalm J., Ulbrich K., Říhová B. Differences in the intracellular fate of free and polymer-bound doxorubicin. J. Control. Release. 80:2002;101-117.
-
(2002)
J. Control. Release
, vol.80
, pp. 101-117
-
-
Hovorka, O.1
Štastný, M.2
Etrych, T.3
Šubr, V.4
Strohalm, J.5
Ulbrich, K.6
Říhová, B.7
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