Alhakamy Nabil A, Badr-Eldin Shaimaa M, A Fahmy Usama, Alruwaili Nabil K, Awan Zuhier A, Caruso Giuseppe, Alfaleh Mohamed A, Alaofi Ahmed L, Arif Faris O, Ahmed Osama A A, Alghaith Adel F
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. 2020 Aug 12;12(8):761. doi: 10.3390/pharmaceutics12080761.
Thymoquinone (TQ), a natural polyphenol, has been associated with various pharmacological responses; however, low bioavailability of TQ limits its clinical application. Thus, a novel phytosomal delivery system of TQ-Phospholipon 90H complex (TQ-phytosome) was developed by refluxing combined with anti-solvent precipitation. This TQ delivery system was optimized by a three-factor, three-level Box-Behnken design. The optimized TQ-phytosome size was (45.59 ± 1.82 nm) and the vesicle size was confirmed by transmission electron microscopy. The in vitro release pattern of the formulation indicated a biphasic release pattern, where an initial burst release was observed within 2 h, followed by a prolonged release. A remarkable increase in dose-dependent cytotoxicity was evident from the significant decrease in IC value of TQ-phytosomes (4.31 ± 2.21 µM) against the A549 cell line. The differential effect of TQ-phytosomes in cell cycle analysis was observed, where cancer cells were accumulated on G2-M and pre-G1 phases. Furthermore, increased apoptotic induction and cell necrosis of TQ-phytosomes were revealed with the annexin V staining technique via activation of caspase-3. In reactive oxygen species (ROS) analysis, TQ-phytosomes acted to significantly increase ROS generation in A549 cells. In conclusion, the sustained release profile with significantly-improved anticancer potential could be obtained with TQ by this phytosomal nanocarrier platform.
百里醌(TQ)是一种天然多酚,与多种药理反应相关;然而,TQ的低生物利用度限制了其临床应用。因此,通过回流结合反溶剂沉淀法开发了一种新型的TQ-磷脂酰胆碱90H复合物(TQ-脂质体)植物药递送系统。该TQ递送系统通过三因素、三水平的Box-Behnken设计进行优化。优化后的TQ-脂质体大小为(45.59±1.82nm),其囊泡大小通过透射电子显微镜得以确认。该制剂的体外释放模式显示为双相释放模式,即在2小时内观察到初始的突释,随后是缓释。TQ-脂质体对A549细胞系的半数抑制浓度(IC值)显著降低(4.31±2.21μM),这表明其剂量依赖性细胞毒性显著增加。在细胞周期分析中观察到了TQ-脂质体的不同作用效果,癌细胞在G2-M期和G1期之前积累。此外,通过膜联蛋白V染色技术,经半胱天冬酶-3激活,揭示了TQ-脂质体诱导凋亡和细胞坏死增加。在活性氧(ROS)分析中,TQ-脂质体可显著增加A549细胞中ROS的生成。总之,通过这种脂质体纳米载体平台,TQ可实现具有显著改善的抗癌潜力的缓释特性。