Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Nanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
J Mater Sci Mater Med. 2021 Jun 30;32(7):78. doi: 10.1007/s10856-021-06538-2.
SN38 is the active metabolite of irinotecan with 1000-fold greater cytotoxicity compared to the parent drug. Despite the potential, its application as a drug is still seriously limited due to its stability concerns and low solubility in acceptable pharmaceutical solvents. To address these drawbacks here nanostructured lipid carrier (NLC) containing SN38 was prepared and its cytotoxicity against U87MG glioblastoma cell line was investigated. The formulations were prepared using hot ultrasonication and solvent evaporation/emulsification methods. NLCs with a mean size of 140 nm and particle size distribution (PDI) of 0.25 were obtained. The average loading efficiency was 9.5% and its entrapment efficiency was 81%. In order to obtain an accurate determination of released amount of SN38 a novel medium and extraction method was designed, which lead to an appropriate in vitro release profile of the drug from the prepared NLCs. The MTT test results revealed the significant higher cytotoxicity of NLCs on U87MG human glioblastoma cell line compared with the free drug. The confocal microscopy images confirmed the proper penetration of the nanostructures into the cells within the first 4 h. Consequently, the results indicated promising potentials of the prepared NLCs as a novel treatment for glioblastoma.
SN38 是伊立替康的活性代谢物,与母体药物相比,其细胞毒性要强 1000 倍。尽管有这种潜力,但由于其稳定性问题和在可接受的药物溶剂中的低溶解度,其作为药物的应用仍然受到严重限制。为了解决这些缺点,本文制备了含有 SN38 的纳米结构脂质载体(NLC),并研究了其对 U87MG 神经胶质瘤细胞系的细胞毒性。制剂采用热超声和溶剂蒸发/乳化法制备。获得了平均粒径为 140nm、粒径分布(PDI)为 0.25 的 NLC。平均载药效率为 9.5%,包封效率为 81%。为了准确测定 SN38 的释放量,设计了一种新的介质和提取方法,从而使药物从制备的 NLC 中呈现出适当的体外释放曲线。MTT 试验结果表明,与游离药物相比,NLC 对 U87MG 人神经胶质瘤细胞系具有更高的细胞毒性。共聚焦显微镜图像证实了这些纳米结构在最初的 4 小时内能够适当穿透细胞。因此,结果表明,所制备的 NLC 具有作为治疗神经胶质瘤的新型药物的潜力。