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首页> 外文期刊>Food research international >Cytotoxic activity of poly-ε-caprolactone lipid-core nanocapsules loaded with lycopene-rich extract from red guava (Psidium guajava L.) on breast cancer cells
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Cytotoxic activity of poly-ε-caprolactone lipid-core nanocapsules loaded with lycopene-rich extract from red guava (Psidium guajava L.) on breast cancer cells

机译:多ε-己内酯脂质纳米胶囊的细胞毒性活性,富含红翅戊戊烯 - 富含番茄红素的提取物(Psidium Guajava L.)乳腺癌细胞

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The aims of this study were to produce poly-epsilon-caprolactone lipid-core nanocapsules containing lycopene-rich extract from red guava (LEG), to characterize those nanoparticles and to evaluate their cytotoxic effects on human breast cancer cells. Lipid-core nanocapsules containing the extract (nanoLEG) were produced by the method of interfacial deposition of the preformed polymer. The nanoparticles were characterized by Dynamic Light Scattering (DLS), Polydispersity Index, Zeta Potential, pH, Encapsulation Efficiency, Nanoparticle Tracking Analysis (NTA), Atomic Force Microscopy (AFM) and Transmission Electron Microscopy (TEM). Cell viability was evaluated by the MIT dye reduction method in the human breast cancer MCF-7 cell line and inhibition of ROS and NF-kappa B was assayed in living human microglial cell line (HMC3) by time-lapse images microscopy. A hemolytic activity assay was carried out with sheep blood. Data showed that nanoparticles average size was around 200 nm, nanoparticles concentration/mL was around 0.1 mu M, negative zeta potential, pH 5.0 and spherical shape, with low variation during a long storage period (7 months) at 5 degrees C, indicating stability of the system and protection against lycopene degradation. The percentage of encapsulation varied from 95% to 98%. The nanoLEG particles significantly reduced the viability of the MCF-7 cells after 24 h (61.47%) and 72 h (55.96%) of exposure, even at the lowest concentration tested (6.25-200 mu g/ml) and improved on the cytotoxicity of free LEG to MCF-7. NanoLEG inhibited LPS-induced NF-kappa B activation and ROS production in microglial cells. The particles did not affect the membrane integrity of sheep blood erythrocytes at the concentrations tested (6.25-200 mu g/mL). Thus, the formulation of lipid-core nanocapsules with a polysorbate 80-coated poly-epsilon-caprolactone wall was efficiently applied to stabilize the lycopene-rich extract from red guava, generating a product with satisfactory physico-chemical and biological properties for application as health-promoting nanotechnology-based nutraceutical, emphasizing its potential to be used as a cancer treatment.
机译:本研究的目的是生产含有富含番茄红素的提取物的聚ε-己内酯脂质纳米胶囊,来自红色番石榴(腿),以表征这些纳米颗粒并评估它们对人乳腺癌细胞的细胞毒性作用。含有提取物(纳米)的脂质核纳米胶囊通过预成型聚合物的界面沉积方法制备。通过动态光散射(DLS),多分散性指数,Zeta电位,pH,封装效率,纳米粒子跟踪分析(NTA),原子力显微镜(AFM)和透射电子显微镜(TEM)的特征在于,纳米颗粒。通过麻乳腺癌MIT染料还原方法评估细胞活力MCF-7细胞系,通过延时图像显微镜在活人的小胶质细胞系(HMC3)中测定ROS和NF-Kappa B的抑制。用绵羊血液进行溶血活性测定。数据显示,纳米颗粒的平均尺寸约为200nm,纳米颗粒浓度/ ml为约0.1μm,阴性ζ电位,pH <5.0和球形,在长储存期(7个月)处为5摄氏度,表明系统稳定性和番茄红素降解的保护。封装的百分比从95%变化到98%。即使在测试(6.25-200μmg/ ml)的最低浓度下,纳米颗粒明显降低了MCF-7细胞的活力(61.47%)和72小时(55.96%),即使在测试(6.25-200μmg/ ml)并改善细胞毒性自由腿到MCF-7。纳米抑制在微胶质细胞中抑制LPS诱导的NF-Kappa B活化和ROS产生。颗粒在测试的浓度(6.25-200μmg/ ml)上没有影响绵羊血液红细胞的膜完整性。因此,有效地施加具有聚山梨醇酯80涂层的聚ε-己内酯壁的脂核纳米胶囊的制剂,以稳定来自红色番石榴的富含番茄红素的提取物,产生具有令人满意的物理化学和生物学性质的产品作为健康 - 纳米技术的营养保健品,强调其潜力用作癌症治疗。

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