Abstract
Adriamycin linked to oxidized dextran (ADM-OXD) via Schiff's base formation was compared with free adriamycin with regard to antitumor activity, acute toxicity and plasma pharmacokinetics in rats following i.v. administration. ADM-OXD showed higher activity against Walker carcinosarcoma 256 than free adriamycin. On the other hand, the acute toxicity of ADM-OXD was adout three times less than that of free adriamycin. In contrast to free adriamycin, a very high plasma level of adriamycin was found after i.v. administration of ADM-OXD. The area under the plasma concentration curve with ADM-OXD was about 160-fold higher than with free adriamycin. Thus, the improvement of the therapeutic index in the case of ADM-OXD might be due to the difference in the disposition of ADM-OXD and free adriamycin in rats. © 1989, The Pharmaceutical Society of Japan. All rights reserved.
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Ueda, Y., Munechika, K., Kikukawa, A., Kanoh, Y., Yamanouchi, K., & Yokoyama, K. (1989). Comparison of Efficacy, Toxicity and Pharmacokinetics of Free Adriamycin and Adriamycin Linked to Oxidized Dextran in Rats. Chemical and Pharmaceutical Bulletin, 37(6), 1639–1641. https://doi.org/10.1248/cpb.37.1639
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