New conjugates of antitumor antibiotic doxorubicin with water-soluble galactomannan: Synthesis and biological activity
New water-soluble conjugates in the form of Schiff bases (DGM-1 and DGM-2) were prepared by the interaction of water-soluble periodate-oxidized galactomannan with doxorubicin or @@iN@-(@@iL@-lysyl)doxorubicin, respectively. The water-soluble galactomannan (DAVANAT^+, a commercial product of Pro-Phar...
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Veröffentlicht in: | Russian journal of bioorganic chemistry 2007-02, Vol.33 (1), p.139-145 |
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container_title | Russian journal of bioorganic chemistry |
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creator | Tevyashova, A. N. Olsufyeva, E. N. Preobrazhenskaya, M. N. Klyosov, A. A. Zomer, E. Platt, D. |
description | New water-soluble conjugates in the form of Schiff bases (DGM-1 and DGM-2) were prepared by the interaction of water-soluble periodate-oxidized galactomannan with doxorubicin or @@iN@-(@@iL@-lysyl)doxorubicin, respectively. The water-soluble galactomannan (DAVANAT^+, a commercial product of Pro-Pharmaceuticals company) was obtained by partial acidic hydrolysis of high-molecular-mass galactomannan from @@iCyamopsis tetragonoloba@ (guar gum) seeds. The conjugate stability was studied in aqueous solutions. The DGM-1 anti-proliferative activity was comparable with that of doxorubicin on three models: cell lines of murine melanoma B16-F1 and human breast cancer MCF-7 (HTB-22) and human colon cancer HT-29 (HTB-38). DGM-2 was poorly active in all the three tests. DGM-1 can thus be regarded as a high-molecular-mass depot form of doxorubicin. |
doi_str_mv | 10.1134/S1068162007010153 |
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The DGM-1 anti-proliferative activity was comparable with that of doxorubicin on three models: cell lines of murine melanoma B16-F1 and human breast cancer MCF-7 (HTB-22) and human colon cancer HT-29 (HTB-38). DGM-2 was poorly active in all the three tests. 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The conjugate stability was studied in aqueous solutions. The DGM-1 anti-proliferative activity was comparable with that of doxorubicin on three models: cell lines of murine melanoma B16-F1 and human breast cancer MCF-7 (HTB-22) and human colon cancer HT-29 (HTB-38). DGM-2 was poorly active in all the three tests. DGM-1 can thus be regarded as a high-molecular-mass depot form of doxorubicin.</abstract><doi>10.1134/S1068162007010153</doi><tpages>7</tpages></addata></record> |
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subjects | Cyamopsis tetragonoloba |
title | New conjugates of antitumor antibiotic doxorubicin with water-soluble galactomannan: Synthesis and biological activity |
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