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出 处:《Chinese Journal of Cancer Research》1991年第3期37-41,共5页中国癌症研究(英文版)
摘 要:Sheep anti-human ferritin IgG (AHFI) and nonspecific normal sheep IgG (NSIgG) were conjugated with Daunomycin (Dau) separately via a mediator Dextran T40. The conjugates (AHFI-Dex-Dau and NSIgG-Dex-Dau) were labelled with 125I and given 1. v. into Balb/c nude mice bearingan hepatocellular carcinoma ( HCC ) . The blodistribution of the two conjugates in different organs or tissues 3 days after injection of radiolabels were measured. Selective tumor accumulation of AHFI-Dex-Dau was observed. The specific localization index was at least fourteen times higher in case of the specific AHFI-Dex-Dau when compared to another control conjugate (NSIgG-Dex-Dau ) in liver tissues. In vivo treatment experiment the results demonstrated that conjugation of Dau to IgG could greatly reduce its nonspecific chemical toxicity and significantly increase its ability to inhibit the engrafted tumor growth.Sheep anti-human ferritin IgG (AHFI) and nonspecific normal sheep IgG (NSIgG) were conjugated with Daunomycin (Dau) separately via a mediator Dextran T40. The conjugates (AHFI-Dex-Dau and NSIgG-Dex-Dau) were labelled with 125I and given 1. v. into Balb/c nude mice bearingan hepatocellular carcinoma ( HCC ) . The blodistribution of the two conjugates in different organs or tissues 3 days after injection of radiolabels were measured. Selective tumor accumulation of AHFI-Dex-Dau was observed. The specific localization index was at least fourteen times higher in case of the specific AHFI-Dex-Dau when compared to another control conjugate (NSIgG-Dex-Dau ) in liver tissues. In vivo treatment experiment the results demonstrated that conjugation of Dau to IgG could greatly reduce its nonspecific chemical toxicity and significantly increase its ability to inhibit the engrafted tumor growth.
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