Alhakamy Nabil A, Caruso Giuseppe, Al-Rabia Mohammed W, Badr-Eldin Shaimaa M, Aldawsari Hibah M, Asfour Hani Z, Alshehri Samah, Alzaharani Sami H, Alhamdan Meshari M, Rizg Waleed Y, Allam Ahmed N
Department of Pharmaceutics, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Advanced Drug Delivery Research Group, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Pharmaceutics. 2021 Apr 29;13(5):638. doi: 10.3390/pharmaceutics13050638.
Piceatannol (PIC) is a naturally occurring polyphenolic stilbene, and it has pleiotropic pharmacological properties. Moreover, PIC has cytotoxic actions among various cancer cells. In this work, preparations of PIC-loaded bilosome-zein (PIC-BZ) were designed, formulated, and characterized, and the optimized PIC-BZ cytotoxic activities, measured as half maximal inhibitory concentration (IC), against lung cancer cell line was investigated. Box-Behnken design was utilized in order to examine the effect of preparation factors on drug entrapment and particle size. PIC-BZ showed a spherical shape after optimization, and its particle size was determined as 157.45 ± 1.62 nm. Moreover, the efficiency of drug entrapment was found as 93.14 ± 2.15%. The cytotoxic activity evaluation revealed that the adjusted formulation, which is PIC-BZ formula, showed a substantially smaller IC versus A549 cells. Cell cycle analysis showed accumulation of cells in the G2-M phase. Moreover, it showed in the sub-G1 phase, a rise of cell fraction suggestion apoptotic improving activity. Increased early and late phases of apoptosis were demonstrated by staining of cells with annexin V. Furthermore, the cellular caspase-3 protein expression was significantly raised by PIC-BZ. In addition, the wound healing experiment confirmed the results. To conclude, compared to pure PIC, PIC-BZ demonstrated a higher cell death-inducing activity against A549 cells.
白皮杉醇(PIC)是一种天然存在的多酚芪类化合物,具有多种药理特性。此外,PIC对多种癌细胞具有细胞毒性作用。在本研究中,设计、制备并表征了负载PIC的双分子层-玉米醇溶蛋白制剂(PIC-BZ),并研究了优化后的PIC-BZ对肺癌细胞系的细胞毒性活性,以半数最大抑制浓度(IC)来衡量。采用Box-Behnken设计来考察制备因素对药物包封率和粒径的影响。优化后的PIC-BZ呈球形,其粒径测定为157.45±1.62nm。此外,药物包封率为93.14±2.15%。细胞毒性活性评估显示,调整后的制剂即PIC-BZ配方对A549细胞的IC值明显更小。细胞周期分析显示细胞在G2-M期积累。此外,在亚G1期,细胞分数增加表明其具有促进凋亡的活性。用膜联蛋白V对细胞进行染色显示凋亡的早期和晚期均增加。此外,PIC-BZ显著提高了细胞半胱天冬酶-3蛋白的表达。另外,伤口愈合实验证实了该结果。总之,与纯PIC相比,PIC-BZ对A549细胞表现出更高的诱导细胞死亡的活性。