Laboratory for Molecular and Functional Imaging: from Physiology to Therapy, UMR5231 CNRS/University Victor Segalen Bordeaux, 146 rue Leo Saignat, Case 117, 33076, Bordeaux, France.
Mol Imaging Biol. 2011 Apr;13(2):239-49. doi: 10.1007/s11307-010-0346-5.
Ultrasound-induced cavitation facilitates cellular uptake of drugs via increased membrane permeability. Here, the purpose was to evaluate the duration of enhanced membrane permeability following ultrasound treatment in cell culture.
Optical chromophores with fluorescence intensity increasing 100-1,000-fold upon intercalation with nucleic acids served as smart agents for reporting cellular uptake. Opticell chambers with a monolayer of C6 cells were subjected to ultrasound in the presence of microbubbles followed by varying delays between 0 and 24 h before addition of Sytox Green optical contrast agent. Micro- and macroscopic fluorescence were used for qualitative and quantitative analysis.
Up to 25% of viable cells showed uptake of contrast agent with a half time of 8 h, with cellular uptake persisting even at 24 h. Only cells exposed to ultrasound showed the effect.
The temporal window of increased membrane permeability is much longer in these studies than previously suggested. This may have important repercussions for in vivo studies in which membrane permeability may be temporally separated from drug delivery.
超声致空化通过增加细胞膜通透性促进药物的细胞摄取。本研究旨在评估细胞培养中超声处理后增强的细胞膜通透性的持续时间。
光学显色剂与核酸插入后荧光强度增加 100-1000 倍,可用作报告细胞摄取的智能试剂。Opticell 室单层 C6 细胞在微泡存在下接受超声处理,然后在添加 Sytox Green 光学对比剂之前,延迟 0 至 24 小时。采用微观和宏观荧光进行定性和定量分析。
多达 25%的存活细胞显示出对造影剂的摄取,半衰期为 8 小时,即使在 24 小时后仍持续存在细胞摄取。只有暴露于超声的细胞显示出这种效果。
与先前的研究相比,这些研究中增加的细胞膜通透性的时间窗口要长得多。这对于体内研究可能具有重要影响,因为在体内研究中,膜通透性可能与药物递送在时间上分开。