Laboratoire IMRCP, UMR CNRS 5623, Université Paul Sabatier, 31062 Toulouse Cedex 9, France.
Int J Pharm. 2011 Jan 17;403(1-2):230-6. doi: 10.1016/j.ijpharm.2010.10.024. Epub 2010 Oct 23.
Among drug delivery systems, catanionic vesicles now appear as powerful candidates for pharmaceutical applications because they are relatively cheap and easy to use, thus well corresponding to industrial requirements. Using labelled vesicles made of a tricatenar catanionic surfactant, the work reported here aims at exploring the mechanisms by which internalisation into a cell occurs. The study was performed on various cell types such as phagocytic as well as non-phagocytic cells using confocal laser scanning microscopy and flow cytometry. Using various inhibitors, endocytosis and also a passive process, as probably fusion, were highlighted as interaction phenomena between catanionic vesicles and cell membranes. Finally, the interaction modelled with giant liposomes as membrane models confirmed the hypothesis of the occurrence of a fusion phenomenon between the nanovectors and cell membranes. This process highlights the potential of catanionic vesicles for a future pharmaceutical application as a universal drug delivery system.
在药物传递系统中,双离子囊泡因其相对廉价且易于使用,因此非常符合工业要求,现在似乎成为了药物应用的有力候选者。本工作使用标记的由三嵌段双离子表面活性剂组成的囊泡,旨在探索内吞作用进入细胞的机制。使用共聚焦激光扫描显微镜和流式细胞术,对各种细胞类型(包括吞噬细胞和非吞噬细胞)进行了研究。使用各种抑制剂,强调了内吞作用以及可能的融合等被动过程,作为双离子囊泡与细胞膜之间的相互作用现象。最后,用巨脂质体作为膜模型进行相互作用模拟,证实了纳米载体与细胞膜之间发生融合现象的假设。该过程突出了双离子囊泡作为通用药物传递系统在未来药物应用中的潜力。