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分子量对超声穿孔介导的人细胞摄取的影响。

Effect of Molecular Weight on Sonoporation-Mediated Uptake in Human Cells.

作者信息

Bhutto Danyal F, Murphy Emily M, Priddy Mariah C, Centner Connor C, Moore Iv Joseph B, Bolli Roberto, Kopechek Jonathan A

机构信息

Department of Bioengineering, University of Louisville, Louisville, Kentucky, USA.

Institute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, Kentucky, USA.

出版信息

Ultrasound Med Biol. 2018 Dec;44(12):2662-2672. doi: 10.1016/j.ultrasmedbio.2018.08.008. Epub 2018 Sep 29.

Abstract

Ultrasound-induced microbubble destruction can enhance drug delivery to cells. The molecular weight of therapeutic compounds varies significantly (from <1 kDa for small molecule drugs, to 7-15 kDa for siRNAs/miRNAs, to >1000 kDa for DNA plasmids). Therefore, the objective of this study was to determine the relationship between uptake efficiency and molecular weight using equal molar concentrations. Uptake efficiency of fluorescent compounds with different molecular weights (0.3, 10 and 2000 kDa) was explored in vitro using human cardiac mesenchymal cells and breast cancer cells exposed to microbubbles and 2.5-MHz ultrasound pulses. Uptake by viable cells was quantified using flow cytometry. After correction for the fluorescence yield of each compound, there was a significant size-dependent difference in fluorescence intensity, indicating an inverse relationship between size and uptake efficiency. These results suggest that diffusion of therapeutic compounds across permeabilized cell membranes may be an important mechanism for ultrasound-mediated drug delivery.

摘要

超声诱导的微泡破坏可增强药物向细胞的递送。治疗性化合物的分子量差异很大(小分子药物小于1 kDa,小干扰RNA/微小RNA为7 - 15 kDa,DNA质粒大于1000 kDa)。因此,本研究的目的是使用等摩尔浓度来确定摄取效率与分子量之间的关系。在体外,使用人心脏间充质细胞和乳腺癌细胞,使其暴露于微泡和2.5兆赫的超声脉冲下,探讨不同分子量(0.3、10和2000 kDa)的荧光化合物的摄取效率。使用流式细胞术对活细胞的摄取进行定量。在对每种化合物的荧光产率进行校正后,荧光强度存在显著的尺寸依赖性差异,表明尺寸与摄取效率之间呈反比关系。这些结果表明,治疗性化合物跨透化细胞膜的扩散可能是超声介导药物递送的重要机制。

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