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Preparation, characterization, and anti-tumor property of podophyllotoxin-loaded solid lipid nanoparticles

机译:鬼臼毒素固体脂质纳米粒的制备,表征及抗肿瘤性能

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In an effort to develop an alternative formulation of podophyllotoxin suitable for drug release and delivery, podophyllotoxin-loaded solid lipid nanoparticles (PPT-SLNs) were constructed, characterized and examined for in vitro cytotoxicity and tumor inhibition. The SLNs were prepared by using a solvent emulsification-evaporation method, and their size was around 50 nm. TEM detection showed that the SLNs were homogeneous and spherical in shape, and differential scanning calorimetry (DSC) measurement revealed a new conformation of PPT-SLNs. An in vitro drug release study showed that PPT was released from the SLNs in a slow but time-dependent manner. Furthermore, the treatment of 293T and HeLa cells with PPT-SLNs demonstrated that PPT-SLNs were less toxic to normal cells and more effective in anti-tumor potency compared with unconjugated PPT. A colony forming efficiency assay showed an effective long-term cancer growth suppression of PPT-SLNs; in addition, they can also enhance the apoptotic and cellular uptake processes on tumor cells compared with PPT. These results collectively demonstrated that this SLN formulation has a potential application as an alternative delivery system for anti-tumor drugs.
机译:为了开发适合药物释放和递送的鬼臼毒素的替代制剂,构建了装载鬼臼毒素的固体脂质纳米颗粒(PPT-SLNs),对其进行了表征并检查了其体外细胞毒性和肿瘤抑制作用。通过使用溶剂乳化-蒸发方法制备SLN,它们的尺寸为约50nm。 TEM检测显示SLN是均匀的球形,而差示扫描量热法(DSC)测量揭示了新的PPT-SLN构象。一项体外药物释放研究表明,PPT以缓慢但时间依赖的方式从SLNs中释放出来。此外,用PPT-SLNs处理293T和HeLa细胞表明,与未结合的PPT相比,PPT-SLNs对正常细胞毒性较小,在抗肿瘤效力方面更有效。菌落形成效率分析表明,PPT-SLNs长期有效地抑制了癌症的生长。此外,与PPT相比,它们还可以增强肿瘤细胞的凋亡和细胞摄取过程。这些结果共同证明,这种SLN制剂作为抗肿瘤药物的替代递送系统具有潜在的应用前景。

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