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化学修饰酶用于癌症治疗。I. 聚乙二醇 - 天冬酰胺酶偶联物的抗肿瘤特性。

Cancer therapy with chemically modified enzymes. I. Antitumor properties of polyethylene glycol-asparaginase conjugates.

作者信息

Abuchowski A, Kazo G M, Verhoest C R, Van Es T, Kafkewitz D, Nucci M L, Viau A T, Davis F F

出版信息

Cancer Biochem Biophys. 1984 Jun;7(2):175-86.

PMID:6467175
Abstract

The covalent attachment of monomethoxypolyethylene glycol (PEG) to asparaginases from Escherichia coli and Vibrio succinogenes by new coupling methodology produced conjugates that are active, stable, without significant immune response, and with greatly extended plasma half-lives in mice. Therapeutic efficacies were greater for the PEG-asparaginases than for the unmodified asparaginases in mice infected with the L5178Y lymphosarcoma or the 6C3HED tumor. Large single doses of native or modified enzymes were more effective against tumors than the same amount of enzyme given in smaller doses over several days.

摘要

通过新的偶联方法将单甲氧基聚乙二醇(PEG)共价连接到来自大肠杆菌和产琥珀酸弧菌的天冬酰胺酶上,产生的缀合物具有活性、稳定性好、无明显免疫反应,并且在小鼠体内的血浆半衰期大大延长。在感染L5178Y淋巴肉瘤或6C3HED肿瘤的小鼠中,聚乙二醇化天冬酰胺酶的治疗效果优于未修饰的天冬酰胺酶。大剂量单次给予天然或修饰酶比在几天内分小剂量给予相同量的酶对肿瘤更有效。

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