首页> 美国卫生研究院文献>Journal of Enzyme Inhibition and Medicinal Chemistry >Acridine Orange/exosomes increase the delivery and the effectiveness of Acridine Orange in human melanoma cells: A new prototype for theranostics of tumors
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Acridine Orange/exosomes increase the delivery and the effectiveness of Acridine Orange in human melanoma cells: A new prototype for theranostics of tumors

机译:cr啶橙/外泌体增加了cr啶橙在人黑素瘤细胞中的递送和效力:肿瘤治疗学的新原型

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摘要

Specifically targeted drug delivery systems with low immunogenicity and toxicity are deemed to increase efficacy of cancer chemotherapy. Acridine Orange (AO) is an acidophilic dye with a strong tumoricidal action following excitation with a light source at 466 nm. However, to date the clinical use of AO is limited by the potential side effects elicited by systemic administration. The endogenous nanocarrier exosomes have been recently introduced as a natural delivery system for therapeutic molecules. In this article, we show the outcome of the administration to human melanoma cells of AO charged Exosomes (Exo-AO), in both monolayer and spheroid models. The results showed an extended drug delivery time of Exo-AO to melanoma cells as compared to the free AO, improving the cytotoxicity of AO. This study shows that Exo-AO have a great potential for a real exploitation as a new theranostic approach against tumors based on AO delivered through the exosomes.
机译:具有低免疫原性和毒性的特异性靶向药物递送系统被认为增加了癌症化学疗法的功效。 cr啶橙(AO)是一种嗜酸性染料,在466nm的光源激发后具有很强的杀伤作用。然而,迄今为止,AO的临床应用受到全身给药引起的潜在副作用的限制。最近已经引入内源性纳米载体外来体作为用于治疗分子的天然递送系统。在本文中,我们显示了在单层模型和球体模型中对带人AO的外泌体(Exo-AO)进行人黑素瘤细胞给药的结果。结果表明,与游离AO相比,Exo-AO向黑素瘤细胞的药物递送时间延长,从而改善了AO的细胞毒性。这项研究表明,Exo-AO具有巨大的潜力,可以作为一种通过通过外泌体传递的AO来治疗肿瘤的新治疗方法,成为一种真正的开发手段。

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