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Nanoparticles for the delivery of zoledronic acid to prostate cancer cells: A comparative analysis through time lapse video-microscopy technique

机译:用于将唑来膦酸递送至前列腺癌细胞的纳米颗粒:通过延时视频显微镜技术进行的比较分析

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摘要

Time-lapse live cell imaging is a powerful tool for studying the responses of cells to drugs. Zoledronic acid (ZOL) is the most potent aminobiphosphonate able to induce cell growth inhibition at very low concentrations. The lack of clear evidence of ZOL-induced anti-cancer effects is likely due to its unfavorable pharmacokinetic profile. The use of nanotechnology-based formulations allows overcoming these limitations in ZOL pharmaco-distribution. Recently, stealth liposomes (LIPOs) and new self-assembly PEGylated nanoparticles (NPs) encapsulating ZOL were developed. Both the delivery systems showed promising anticancer activity in vitro and in vivo.In this work, we investigated the cytostatic effect of these novel formulations (LIPOs and NPs) compared with free ZOL on 2 different prostate cancer cell lines, PC 3 and DU 145 and on prostate epithelial primary cells EPN using time lapse video-microscopy (TLVM). In PC3 cells, free ZOL showed a significant anti-proliferative effect but this effect was lower than that induced by LIPOs and NPs encapsulating ZOL; moreover, LIPO-ZOL was more potent in inducing growth inhibition than NP-ZOL. On the other hand, LIPO-ZOL slightly enhanced the free ZOL activity on growth inhibition of DU 145, while the anti-proliferative effect of NP-ZOL was not statistically relevant. These novel formulations did not induce anti-proliferative effects on EPN cells. Finally, we evaluated cytotoxic effects on DU145 where, LIPO-ZOL induced the highest cytotoxicity compared with NP-ZOL and free ZOL. In conclusion, ZOL can be transformed in a powerful anticancer agent, if administered with nanotechnology-based formulations without damaging the healthy tissues.
机译:延时活细胞成像是研究细胞对药物反应的强大工具。唑来膦酸(ZOL)是最有效的氨基双膦酸盐,能够以非常低的浓度诱导细胞生长抑制。 ZOL诱导的抗癌作用缺乏明确证据,可能是由于其不利的药代动力学特性。基于纳米技术的制剂的使用可以克服ZOL药物分布中的这些限制。最近,开发了隐性脂质体(LIPO)和新的自组装ZOL封装的聚乙二醇化纳米颗粒(NPs)。两种递送系统均显示出有希望的体内外抗癌活性。在这项工作中,我们研究了与游离ZOL相比,这些新型制剂(LIPOs和NPs)对2种不同的前列腺癌细胞系PC 3和DU 145和使用延时视频显微镜(TLVM)对前列腺上皮原代细胞EPN进行检测。在PC3细胞中,游离ZOL表现出显着的抗增殖作用,但这种作用要低于LIPO和NP包裹ZOL所诱导的作用。此外,与NP-ZOL相比,LIPO-ZOL在诱导生长抑制方面更有效。另一方面,LIPO-ZOL对DU 145生长抑制的游离ZOL活性稍有增强,而NP-ZOL的抗增殖作用在统计学上不相关。这些新颖的制剂没有诱导对EPN细胞的抗增殖作用。最后,我们评估了对DU145的细胞毒性作用,与NP-ZOL和游离ZOL相比,LIPO-ZOL诱导的细胞毒性最高。总而言之,如果将ZOL与基于纳米技术的制剂一起使用,而不会损害健康组织,则可以将其转化为强大的抗癌剂。

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