메뉴 건너뛰기




Volumn 15, Issue 4, 2005, Pages 295-299

The use of precursor polymers to prepare new excipients

Author keywords

Block copolymer; Excipient; Micelle; Polymer; Precursor polymer; Responsive polymer; Thiomer

Indexed keywords

COPOLYMER; EXCIPIENT; HOMOPOLYMER; POLYMER; THIOMER; UNCLASSIFIED DRUG;

EID: 24044485617     PISSN: 11571489     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1773-2247(05)50052-2     Document Type: Article
Times cited : (1)

References (30)
  • 1
    • 0041706170 scopus 로고    scopus 로고
    • Biotechnology partnerships-medicine for an ailing industry
    • DeLAMARTER J. - Biotechnology partnerships-medicine for an ailing industry. - Nature Biotech., 21 (8), 847-848, 2003.
    • (2003) Nature Biotech. , vol.21 , Issue.8 , pp. 847-848
    • Delamarter, J.1
  • 3
    • 0035803689 scopus 로고    scopus 로고
    • Combinatorial chemistry and biomedical polymer development
    • in press
    • BROCCHINI S. - Combinatorial chemistry and biomedical polymer development. - Adv. Drug Deliv. Rev., in press.
    • Adv. Drug Deliv. Rev.
    • Brocchini, S.1
  • 5
    • 0242407164 scopus 로고    scopus 로고
    • An information rich biomedical polymer library
    • PEDONE E., LI X., KOSEVA N., ALPAR O., BROCCHINIS. - An information rich biomedical polymer library. - J. Mat. Chem., 13 (11), 2825-2837, 2003.
    • (2003) J. Mat. Chem. , vol.13 , Issue.11 , pp. 2825-2837
    • Pedone, E.1    Li, X.2    Koseva, N.3    Alpar, O.4    Brocchini, S.5
  • 6
    • 9244249816 scopus 로고    scopus 로고
    • Well-defined polymer precursors synthesized by RAFT polymeriszation of N,N-dimethylacrylamide/N-acryloxysuccinimide: Random and block copolymer
    • RELOGIO P., CHARREYRE M.T., FARINHA J. P., MARTINHO J. M. G., PICHOT C. - Well-defined polymer precursors synthesized by RAFT polymeriszation of N,N-dimethylacrylamide/N-acryloxysuccinimide: random and block copolymer. - Polymer, 45, 8639-8648, 2004.
    • (2004) Polymer , vol.45 , pp. 8639-8648
    • Relogio, P.1    Charreyre, M.T.2    Farinha, J.P.3    Martinho, J.M.G.4    Pichot, C.5
  • 7
    • 0015446074 scopus 로고
    • Model reactions for synthesis of pharmacologically active polymers by way of monomeric and polymeric reactive esters
    • BATZ H., FRANZMANN G., RINGSDORF H. - Model reactions for synthesis of pharmacologically active polymers by way of monomeric and polymeric reactive esters. - Angew. Chem. Internat. Edit., 11 (12), 1103-1104, 1972.
    • (1972) Angew. Chem. Internat. Edit. , vol.11 , Issue.12 , pp. 1103-1104
    • Batz, H.1    Franzmann, G.2    Ringsdorf, H.3
  • 8
    • 0000166887 scopus 로고
    • High polymers of acrylic and methacrylic esters of N-hydroxysuccinimide as polyacrylamide and polymethacrylamide precursors
    • FERRUTI P., BETTELLI A., FERE A. - High polymers of acrylic and methacrylic esters of N-hydroxysuccinimide as polyacrylamide and polymethacrylamide precursors. - Polymer, 13, 462-464, 1972.
    • (1972) Polymer , vol.13 , pp. 462-464
    • Ferruti, P.1    Bettelli, A.2    Fere, A.3
  • 9
    • 0001123779 scopus 로고
    • Esterification and amidation of polymeric acyl chloides. A new route to polymethacrylates and polymethacrylamides with a variety of different side groups
    • STROHRIEGL P. - Esterification and amidation of polymeric acyl chloides. A new route to polymethacrylates and polymethacrylamides with a variety of different side groups. - Makromol. Chem., 194, 363-387, 1993.
    • (1993) Makromol. Chem. , vol.194 , pp. 363-387
    • Strohriegl, P.1
  • 10
    • 12044255240 scopus 로고
    • Polymer synthesis via activated esters: A new dimension of creativity in macromolecular chemistry
    • ARSHADY R. - Polymer synthesis via activated esters: a new dimension of creativity in macromolecular chemistry. - Adv. Polym. Sci., 111, 1-41, 1994.
    • (1994) Adv. Polym. Sci. , vol.111 , pp. 1-41
    • Arshady, R.1
  • 11
    • 0028805760 scopus 로고
    • Effective inhibitors of hemagglutination by influenza virus synthesised from polymers having active ester groups. Insight in mechanism of inhibition
    • MAMMEN M., DAHMANN G., WHITESIDES G. - Effective inhibitors of hemagglutination by influenza virus synthesised from polymers having active ester groups. Insight in mechanism of inhibition. - J. Med. Chem., 38, 4179-4190, 1995.
    • (1995) J. Med. Chem. , vol.38 , pp. 4179-4190
    • Mammen, M.1    Dahmann, G.2    Whitesides, G.3
  • 12
    • 0000596050 scopus 로고
    • Phosphatase catalysis developed via combinatorial organic chemistry
    • MENGER F., ELISEEV A., MIGULIN V. - Phosphatase catalysis developed via combinatorial organic chemistry. - J. Org. Chem., 60, 6666-6667, 1995.
    • (1995) J. Org. Chem. , vol.60 , pp. 6666-6667
    • Menger, F.1    Eliseev, A.2    Migulin, V.3
  • 13
    • 0031002854 scopus 로고    scopus 로고
    • Generation and in situ evaluation of libraries of poly(acrylic acid) presenting sialosides as side chains as polyvalent inhibitors of influenza-mediated hemagglutination
    • CHOI S., MAMMEN M., WHITESIDES G. - Generation and in situ evaluation of libraries of poly(acrylic acid) presenting sialosides as side chains as polyvalent inhibitors of influenza-mediated hemagglutination. - J. Am. Chem. Soc., 119, 4103-4111, 1997.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4103-4111
    • Choi, S.1    Mammen, M.2    Whitesides, G.3
  • 14
    • 0032476812 scopus 로고    scopus 로고
    • Polyvalent interactions in biological systems: Implications for design and use of multivalent ligands and inhibitors
    • MAMMEN M., CHOI S., WHITESIDES G. - Polyvalent interactions in biological systems: Implications for design and use of multivalent ligands and inhibitors. - Angew. Chem. Int. Ed., 37, 2754-2794, 1998.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2754-2794
    • Mammen, M.1    Choi, S.2    Whitesides, G.3
  • 15
    • 0001057603 scopus 로고    scopus 로고
    • Combinatorial catalysis of an elimination reaction
    • MENGER F., DING J., BARRAGAN V. - Combinatorial catalysis of an elimination reaction. - J. Org. Chem., 63, 7578-7579, 1998.
    • (1998) J. Org. Chem. , vol.63 , pp. 7578-7579
    • Menger, F.1    Ding, J.2    Barragan, V.3
  • 16
    • 0023450012 scopus 로고
    • Effect of molecular weight (Mw) of N-(2-hydroxypropyl)methacrylamide copolymers on body distributions and rate of excretion after subcutaneous, intraperitoneal and intravenous administration to rats
    • SEYMOUR L., DUNCAN R., STROHALM J., KOPECEK J. - Effect of molecular weight (Mw) of N-(2-hydroxypropyl)methacrylamide copolymers on body distributions and rate of excretion after subcutaneous, intraperitoneal and intravenous administration to rats. - J. Biomed. Mater. Res., 21, 1341-1358, 1987.
    • (1987) J. Biomed. Mater. Res. , vol.21 , pp. 1341-1358
    • Seymour, L.1    Duncan, R.2    Strohalm, J.3    Kopecek, J.4
  • 17
    • 0347985281 scopus 로고    scopus 로고
    • Synthesis of precursors of poly(acryl amides) by copper mediated living radical polymerization in DMSO
    • MONGE S., HADDLETON D. - Synthesis of precursors of poly(acryl amides) by copper mediated living radical polymerization in DMSO. - Eur. Polym. J., 40 (1), 37-45, 2004.
    • (2004) Eur. Polym. J. , vol.40 , Issue.1 , pp. 37-45
    • Monge, S.1    Haddleton, D.2
  • 18
    • 0033020555 scopus 로고    scopus 로고
    • Polymers with thiol groups: A new generation of mucoadhesive polymers?
    • BERNKOP-SCHNURCH A., SCHWARZ V., STEININGER S. - Polymers with thiol groups: a new generation of mucoadhesive polymers? - Pharm. Res., 16 (6), 876-881, 1999.
    • (1999) Pharm. Res. , vol.16 , Issue.6 , pp. 876-881
    • Bernkop-Schnurch, A.1    Schwarz, V.2    Steininger, S.3
  • 19
    • 0035157888 scopus 로고    scopus 로고
    • Thiolation of polycarbophil enhances its inhibition of intestinal brush border membrane bound aminopeptidase N
    • BERNKOP-SCHNURCH A., ZARTI H., WALKER G.F. - Thiolation of polycarbophil enhances its inhibition of intestinal brush border membrane bound aminopeptidase N. - J. Pharm. Sci., 90 (11), 1907-1914, 2001.
    • (2001) J. Pharm. Sci. , vol.90 , Issue.11 , pp. 1907-1914
    • Bernkop-Schnurch, A.1    Zarti, H.2    Walker, G.F.3
  • 20
    • 0035845737 scopus 로고    scopus 로고
    • Thiolated polymers: Synthesis and in vitro evaluation of polymer-cysteamine conjugates
    • BERNKOP-SCHNURCH A., CLAUSEN A.E., HNATYSZYN M. - Thiolated polymers: synthesis and in vitro evaluation of polymer-cysteamine conjugates. - Int. J. Pharm., 226 (1-2), 185-194, 2001.
    • (2001) Int. J. Pharm. , vol.226 , Issue.1-2 , pp. 185-194
    • Bernkop-Schnurch, A.1    Clausen, A.E.2    Hnatyszyn, M.3
  • 21
    • 0037241111 scopus 로고    scopus 로고
    • Mucoadhesive and cohesive properties of poly(acrylic acid)-cysteine conjugates with regard to their molecular mass
    • 20003
    • LEITNER V.M., MARSCHUTZ M.K., BERNKOP-SCHNURCH A. - Mucoadhesive and cohesive properties of poly(acrylic acid)-cysteine conjugates with regard to their molecular mass. - Eur. J. Pharm. Sci., 18 (1), 89-96, 20003.
    • Eur. J. Pharm. Sci. , vol.18 , Issue.1 , pp. 89-96
    • Leitner, V.M.1    Marschutz, M.K.2    Bernkop-Schnurch, A.3
  • 25
    • 12044255356 scopus 로고
    • Disulfide bond formation in peptides by dimethyl-sulfoxide - Socop and applications
    • TAM J., WU C., LIU L., ZHANG J. - Disulfide bond formation in peptides by dimethyl-sulfoxide - socop and applications. - J. Am. Chem. Soc., 113 (17), 6657-6662, 1991.
    • (1991) J. Am. Chem. Soc. , vol.113 , Issue.17 , pp. 6657-6662
    • Tam, J.1    Wu, C.2    Liu, L.3    Zhang, J.4
  • 27
    • 0025343062 scopus 로고
    • Characterization and anticancer activity of the micelle-forming polymeric anticancer drug adriamycin-conjugated poly(ethyleneglycol)-poly(aspartic acid) block copolymer
    • YOKOYAMA M., MIYAUCHI M., YAMADA N., OKANO T., SAKURAI Y., KATAOKA K., INOUE S. - Characterization and anticancer activity of the micelle-forming polymeric anticancer drug adriamycin-conjugated poly(ethyleneglycol)- poly(aspartic acid) block copolymer. - Cancer Res., 50, 1693-1700, 1990.
    • (1990) Cancer Res. , vol.50 , pp. 1693-1700
    • Yokoyama, M.1    Miyauchi, M.2    Yamada, N.3    Okano, T.4    Sakurai, Y.5    Kataoka, K.6    Inoue, S.7
  • 28
    • 0032472352 scopus 로고    scopus 로고
    • Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor
    • YOKOYAMA M., FUKUSHIMA S., UEHARA R., OKAMOTO K., KATAOKA K., SAKURAI Y., OKANO T. - Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor. - J. Contr. Rel., 50, 79-92, 1998.
    • (1998) J. Contr. Rel. , vol.50 , pp. 79-92
    • Yokoyama, M.1    Fukushima, S.2    Uehara, R.3    Okamoto, K.4    Kataoka, K.5    Sakurai, Y.6    Okano, T.7
  • 29
    • 0037148675 scopus 로고    scopus 로고
    • Block copolymer micelles for delivery of gene and related compounds
    • KAKIZAWA Y., KATAOKA K. - Block copolymer micelles for delivery of gene and related compounds. - Adv. Drug Del. Rev., 54, 202-222, 2002.
    • (2002) Adv. Drug Del. Rev. , vol.54 , pp. 202-222
    • Kakizawa, Y.1    Kataoka, K.2
  • 30
    • 0024379967 scopus 로고
    • Acid pH in tumours and its potential for therapeutic exploitation
    • TANNOCK I., ROTIN D. - Acid pH in tumours and its potential for therapeutic exploitation. - Cancer Res., 49, 4373-4384, 1989.
    • (1989) Cancer Res. , vol.49 , pp. 4373-4384
    • Tannock, I.1    Rotin, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.