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冷物理等离子体介导的维甲酸前药激活赋予上皮细胞额外的细胞毒性。

Cold Physical Plasma-Mediated Fenretinide Prodrug Activation Confers Additive Cytotoxicity in Epithelial Cells.

作者信息

Ahmadi Mohsen, Singer Debora, Potlitz Felix, Nasri Zahra, von Woedtke Thomas, Link Andreas, Bekeschus Sander, Wende Kristian

机构信息

ZIK plasmatis, Leibniz Institute for Plasma Science and Technology (INP), Felix Hausdorff-Str. 2, 17489 Greifswald, Germany.

Clinic and Policlinic for Dermatology and Venereology, Rostock University Medical Center, Strempelstr. 13, 18057 Rostock, Germany.

出版信息

Antioxidants (Basel). 2023 Jun 14;12(6):1271. doi: 10.3390/antiox12061271.

Abstract

Cold physical plasma is a partially ionized gas operated at body temperature and utilized for heat-sensitive technical and medical purposes. Physical plasma is a multi-component system consisting of, e.g., reactive species, ions and electrons, electric fields, and UV light. Therefore, cold plasma technology is an interesting tool for introducing biomolecule oxidative modifications. This concept can be extended to anticancer drugs, including prodrugs, which could be activated in situ to enhance local anticancer effects. To this end, we performed a proof-of-concept study on the oxidative prodrug activation of a tailor-made boronic pinacol ester fenretinide treated with the atmospheric pressure argon plasma jet kINPen operated with either argon, argon-hydrogen, or argon-oxygen feed gas. Fenretinide release from the prodrug was triggered via Baeyer-Villiger-type oxidation of the boron-carbon bond based on hydrogen peroxide and peroxynitrite, which were generated by plasma processes and chemical addition using mass spectrometry. Fenretinide activation led to additive cytotoxic effects in three epithelial cell lines in vitro compared to the effects of cold plasma treatment alone regarding metabolic activity reduction and an increase in terminal cell death, suggesting that cold physical plasma-mediated prodrug activation is a new direction for combination cancer treatment studies.

摘要

冷物理等离子体是一种在体温下运行的部分电离气体,用于热敏技术和医学目的。物理等离子体是一个多组分系统,例如由反应性物种、离子和电子、电场以及紫外线组成。因此,冷等离子体技术是引入生物分子氧化修饰的一种有趣工具。这一概念可以扩展到抗癌药物,包括前药,它们可以在原位被激活以增强局部抗癌效果。为此,我们对用大气压氩等离子体射流kINPen处理的定制硼酸频哪醇酯非诺贝特的氧化前药激活进行了概念验证研究,该射流使用氩气、氩 - 氢气或氩 - 氧气作为进料气体运行。基于过氧化氢和过氧亚硝酸盐的硼 - 碳键的拜耳 - 维利格型氧化触发了前药中非诺贝特的释放,过氧化氢和过氧亚硝酸盐是通过等离子体过程和使用质谱的化学添加产生的。与单独冷等离子体处理相比,非诺贝特激活在体外对三种上皮细胞系产生了相加的细胞毒性作用,表现为代谢活性降低和终末细胞死亡增加,这表明冷物理等离子体介导的前药激活是联合癌症治疗研究的一个新方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87c5/10295284/7867c3adcfca/antioxidants-12-01271-g0A1.jpg

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