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通过与蛋白质载体偶联来靶向抗病毒药物。

Targeting of antiviral drugs by coupling with protein carriers.

作者信息

Fiume L, Busi C, Mattioli A

出版信息

FEBS Lett. 1983 Mar 7;153(1):6-10. doi: 10.1016/0014-5793(83)80108-2.

Abstract

Side effects of antiviral drugs might be circumvented by their selective delivery into infected cells. This targeting can be obtained by conjugation of the drugs to macromolecules which are taken up specifically by the infected cells. The experiments reviewed, on this approach to antiviral chemotherapy, are mainly directed at improving the chemotherapeutic index of adenine arabinoside (ara-A) in the treatment of chronic hepatitis B by its coupling to galactosyl terminating glycoproteins.

摘要

抗病毒药物的副作用或许可以通过将它们选择性地递送至受感染细胞而得以规避。这种靶向作用可通过将药物与受感染细胞特异性摄取的大分子结合来实现。本文所综述的关于这种抗病毒化疗方法的实验,主要致力于通过将阿糖腺苷(ara - A)与末端带有半乳糖基的糖蛋白偶联,来提高其在治疗慢性乙型肝炎时的化疗指数。

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