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靶向与蛋白质载体结合的抗病毒药物。

Targeting of antiviral drugs bound to protein carriers.

作者信息

Fiume L, Busi C, Mattioli A, Spinosa G

机构信息

Dipartimento di Patologia Sperimentale, University of Bologna, Italy.

出版信息

Crit Rev Ther Drug Carrier Syst. 1988;4(4):265-84.

PMID:3289759
Abstract

The value of antiviral drugs would be improved by their selective delivery into infected cells. This goal can be achieved by conjugating the drug to a protein which is taken up specifically by the cells where the virus grows. Conjugates will be pharmacologically effective in these cells if the bond linking the drug to the carrier does not suppress the activity of the drug or if the bond is broken down with consequent intracellular release of the drug. Experiments on this approach to antiviral chemotherapy have been directed mainly at selectively delivering antiviral agents into hepatocytes in order to increase their chemotherapeutic index in the treatment of chronic hepatitis B.

摘要

通过将抗病毒药物选择性地递送至受感染细胞中,其价值将得到提升。这一目标可通过将药物与一种蛋白质偶联来实现,该蛋白质会被病毒生长所在的细胞特异性摄取。如果连接药物与载体的化学键不抑制药物活性,或者该化学键断裂从而使药物在细胞内释放,那么偶联物在这些细胞中将具有药理活性。关于这种抗病毒化疗方法的实验主要致力于将抗病毒药物选择性地递送至肝细胞,以提高其在治疗慢性乙型肝炎中的化疗指数。

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