Inserm, UMR-S 646, Angers, France.
J Control Release. 2011 Apr 10;151(1):74-82. doi: 10.1016/j.jconrel.2010.11.032. Epub 2010 Dec 5.
Taking advantage from the development of SV30, a new analogue of the pro-apoptotic molecule HA14-1, the aim of this study was to functionally evaluate SV30 and to develop safe nanocarriers for its administration. By using an inversion phase process, 57nm organic solvent-free lipid nanocapsules loaded with SV30 (SV30-LNCs) were formulated. Biological performance of SV30 and SV30-LNCs were evaluated on F98 cells that express Bax and Bcl-2, through survival assays, HPLC, flow cytometry, confocal microscopy and spectral imaging. We observed that SV30 alone or in combination with paclitaxel, etoposide or beam radiation could trigger cell death in a similar fashion to HA14-1. Although partially blocked by Z-VAD-fmk, this effect was coincident to caspase-3 activation. Hence, we established that SV30-LNCs improved SV30 biological activity together with a potentiation of the mitochondrial membrane potential decrease. Interestingly, flow cytometry and confocal analysis indicated that SV30 itself conferred to LNCs improved mitochondrial targeting skills that may present a great interest toward the development of mitochondria targeted nanomedicines.
利用 SV30 的发展,一种新的促凋亡分子 HA14-1 的类似物,本研究旨在评估 SV30 的功能,并开发用于其给药的安全纳米载体。通过使用反相过程,制备了负载 SV30 的 57nm 无有机溶剂的脂质纳米胶囊(SV30-LNCs)。通过生存测定、HPLC、流式细胞术、共聚焦显微镜和光谱成像,在表达 Bax 和 Bcl-2 的 F98 细胞上评估了 SV30 和 SV30-LNCs 的生物学性能。我们观察到 SV30 单独或与紫杉醇、依托泊苷或射线联合使用,能够以类似于 HA14-1 的方式触发细胞死亡。尽管被 Z-VAD-fmk 部分阻断,但这种效应与 caspase-3 激活一致。因此,我们确定 SV30-LNCs 提高了 SV30 的生物学活性,并增强了线粒体膜电位的降低。有趣的是,流式细胞术和共聚焦分析表明,SV30 本身赋予 LNCs 提高了线粒体靶向的技能,这可能对开发线粒体靶向纳米药物具有重要意义。