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The Influence of Electroporation on in Vitro Photodynamic Therapy of Human Breast Carcinoma Cells

机译:电穿孔对人乳腺癌细胞体外光动力治疗的影响

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Phototoxicity of drugs used in cancer photodynamic therapy could be augmented by increasedaccumulation of a photosensitizer in target cells. Theintracellular delivery mode that enhances drugtransportation could facilitate therapy by reducingthe exposure time. Doses of the administered drugand related side effects could be lowered, whilstmaintaining the same therapeutic efficiency. Electroporation supports transport of many drugs by creating electric field-induced transient nanopores in theplasma membrane. In this study, the electroporation-assisted transport of a photosensitizer was tested in vitro in human breast carcinoma cell lines:wild-type (MCF-7/WT) and doxorubicin-resistant(MCF-7/DOX). The efficacy of photodynamic therapy alone and in combination with electroporationwas evaluated by cell viability with MTT test, usinga haematoporphyrin derivative as a model. The datapresented show up to 10-fold greater efficacy of thecombined method, with very significantly reduceddrug exposure times.
机译:通过增加靶细胞中光敏剂的积累,可以增强用于癌症光动力疗法的药物的光毒性。增强药物运输的细胞内递送模式可通过减少暴露时间来促进治疗。可以降低所给药药物的剂量和相关的副作用,同时保持相同的治疗效率。电穿孔通过在质膜上产生电场诱导的瞬态纳米孔来支持许多药物的运输。在这项研究中,在人乳腺癌细胞系:野生型(MCF-7 / WT)和抗阿霉素(MCF-7 / DOX)的体外,测试了光敏剂的电穿孔辅助转运。使用血卟啉衍生物作为模型,通过MTT测试通过细胞生存力评估单独的光动力疗法和与电穿孔结合的功效。所提供的数据显示,该联合方法的功效提高了10倍,而且药物暴露时间大大缩短。

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