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阿霉素偶联聚戊二醛微球的合成及其细胞生长抑制活性评估。

Synthesis of adriamycin-coupled polyglutaraldehyde microspheres and evaluation of their cytostatic activity.

作者信息

Tokes Z A, Rogers K E, Rembaum A

出版信息

Proc Natl Acad Sci U S A. 1982 Mar;79(6):2026-30. doi: 10.1073/pnas.79.6.2026.

Abstract

Adriamycin was coupled to polyglutaraldehyde microspheres having an average diameter of 4500 A. The coupled microspheres remained stable during incubation with cells. Full cytostatic activity was observed when the coupled adriamycin was tested with murine or human leukemia and murine sarcoma cell lines. A 10-fold increase in sensitivity was obtained with drug-resistant human leukemia cell lines. Repeated use of the coupled microspheres in the cytostatic assays did not increase their activity, indicating that these complexes can be recycled. The results suggest that coupled adriamycin sufficiently perturbs the plasma membrane to lead to cytostatic activity. It is proposed that this mode of drug delivery provides multiple and repetitious sites for drug-cell interactions. In addition, the drug-polymer complexes may overcome those forms of resistance that are the result of decreased drug binding at the cell surface.

摘要

阿霉素与平均直径为4500埃的聚戊二醛微球偶联。偶联后的微球在与细胞孵育期间保持稳定。当用偶联的阿霉素对小鼠或人白血病细胞系以及小鼠肉瘤细胞系进行测试时,观察到了完全的细胞抑制活性。对于耐药的人白血病细胞系,敏感性提高了10倍。在细胞抑制试验中重复使用偶联的微球并没有增加其活性,这表明这些复合物可以循环使用。结果表明,偶联的阿霉素足以扰乱质膜,从而导致细胞抑制活性。有人提出,这种药物递送方式为药物与细胞的相互作用提供了多个重复的位点。此外,药物-聚合物复合物可能克服那些因细胞表面药物结合减少而产生的耐药形式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf90/346115/89da51567a75/pnas00445-0354-a.jpg

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