Faculty of Pharmacy, Integral University, Lucknow, Uttar Pradesh, India.
Dr. D. Y. Patil Biotechnology and Bioinformatics Institute, Dr. D. Y. Patil Vidyapeeth, Pune, Pune, India.
Drug Res (Stuttg). 2022 Jun;72(5):284-293. doi: 10.1055/a-1800-5956. Epub 2022 May 3.
The current study focused on important bioactive compounds in plants that make them pharmacologically valuable. Therefore, this study was aimed to develop () seed extract loaded solid lipid nanoparticles and explore its cytotoxic effect on human liver cancer cells (HepG2 cells). The ethanolic extract of used to develop seed extract loaded solid lipid nanoparticles (SLNs) was analyzed by gas chromatography-mass spectrometry, thin-layer chromatography (TLC) and high-performance thin-layer chromatography (HPTLC) for phytochemical profiling. The seed extract loaded SLNs were efficaciously prepared by the nanoprecipitation method and screened on the basis of physicochemical properties. The seed extract loaded SLN-2 was characterized using various parameters like particle size (237.1±0.104), % entrapment efficiency (80±1.15), zeta potential (42.1±0.102) and % drug release (45% at the end 8 hours and release the entire amount in 12 h). The SLN-2 formulation was optimized based on the recipient factor, and SLN-2 was used to further evaluate the in vitro cytotoxicity of HepG2 cells in a dose-dependent manner by 3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide (MTT) assay. The IC50 value of SLN2 was 52.37 ug/ml and sub IC50 26.1 ug/ml at 24 h and 48 h, respectively. Thus, we concluded that extract loaded SLN-2 could act as an alternative therapy, possibly controlling therapeutic action by making a substantial reduction in side effects.
本研究关注植物中的重要生物活性化合物,这些化合物使它们具有药理学价值。因此,本研究旨在开发()种子提取物负载的固体脂质纳米粒,并探索其对人肝癌细胞(HepG2 细胞)的细胞毒性作用。采用气相色谱-质谱联用(GC-MS)、薄层色谱(TLC)和高效薄层色谱(HPTLC)对所用的进行了植物化学成分分析。采用纳米沉淀法有效地制备了负载的种子提取物固体脂质纳米粒(SLNs),并根据理化性质进行了筛选。采用各种参数对负载的 SLN-2 进行了表征,如粒径(237.1±0.104)、包封效率(80±1.15)、Zeta 电位(42.1±0.102)和药物释放(8 小时结束时释放 45%,12 小时内释放全部量)。基于受体因素对 SLN-2 进行了优化,并用 SLN-2 进一步评估 HepG2 细胞的体外细胞毒性,采用 3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法进行剂量依赖性评估。SLN2 的 IC50 值为 52.37 μg/ml,24 h 和 48 h 时的亚 IC50 值分别为 26.1 μg/ml。因此,我们得出结论,负载的 SLN-2 可以作为一种替代疗法,通过显著减少副作用来控制治疗作用。