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Induction of oxidative stress by Taxol® vehicle Cremophor-EL triggers production of interleukin-8 by peripheral blood mononuclear cells through the mechanism not requiring de novo synthesis of mRNA

机译:Taxol®载体Cremophor-EL诱导的氧化应激通过不需要从头合成mRNA的机制触发外周血单核细胞产生白介素8

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摘要

Understanding the ability of cytotoxic oncology drugs, and their carriers and formulation excipients, to induce pro-inflammatory responses is important for establishing safe and efficacious formulations. Literature data about cytokine response induction by the traditional formulation of paclitaxel, Taxol®, is controversial, and no data is available about the pro-inflammatory profile of the nano-albumin formulation of this drug, Abraxane®. Herein, we demonstrate and explain the difference in the cytokine induction profile between Taxol® and Abraxane®, and describe a novel mechanism of cytokine induction by a nanosized excipient, Cremophor EL, which is not unique to Taxol® and is commonly used in the pharmaceutical industry for delivery of a wide variety of small molecular drugs.
机译:了解细胞毒性肿瘤药物及其载体和制剂赋形剂诱导促炎反应的能力对于建立安全有效的制剂很重要。关于通过紫杉醇的传统制剂Taxol®诱导细胞因子应答的文献资料是有争议的,尚无有关该药物纳米白蛋白制剂Abraxane®的促炎特性的数据。在本文中,我们证明和解释了Taxol®和Abraxane®之间的细胞因子诱导特性的差异,并描述了纳米赋形剂Cremophor EL诱导细胞因子的新机制,这不是Taxol®独有的,在药物中通常使用工业上提供各种小分子药物。

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