Department of Drug and Food Control, Kerman University of Medical Sciences, Kerman, Iran.
Herbal and Traditional Medicines Research Center, Kerman University of Medical Sciences, Kerman, Iran.
J Biomater Sci Polym Ed. 2024 Oct;35(15):2363-2379. doi: 10.1080/09205063.2024.2381372. Epub 2024 Jul 26.
The objective of this work was to design a new drug nanoparticle (NP) composed of chitosan/β-cyclodextrin/sodium tripolyphosphate/alginate (CS/βCD/TPP/AL) loaded with a clove extract (CE) for potential anticancer effects. The extract was prepared by two extraction methods: hydroalcoholic maceration (MAC) with 80% MeOH and supercritical fluid (SCF). The MACCE and SCFCE CE NPs had particle sizes of 71 nm and 20 nm, respectively with irregular spherical shapes. The nanocarriers achieved entrapment efficiencies of over 90%. MACCE-NPs and SCFCE-NPs released 18.35% and 10.12% of the extract after 6 h, respectively. Cell viability decreased to 54%, 7%, and 12% in HeLa, U87, and KB cell lines, respectively, after a 48-hour treatment with SCFCE-NPs and 75%, 8%, and 17% after treatment with MACCE-NPs, significantly reduced compared to the control. It is concluded that NPs containing CE exhibit a higher degree of toxicity due to better penetration into cells.
本工作旨在设计一种新型药物纳米粒子(NP),由壳聚糖/β-环糊精/三聚磷酸钠/海藻酸钠(CS/βCD/TPP/AL)负载丁香油提取物(CE),以发挥潜在的抗癌作用。提取物通过两种提取方法制备:80%甲醇的水醇浸提(MAC)和超临界流体(SCF)。MACCE 和 SCFCE 的 CE NPs 的粒径分别为 71nm 和 20nm,呈不规则的球形。纳米载体的包封效率超过 90%。MACCE-NPs 和 SCFCE-NPs 在 6 小时后分别释放出 18.35%和 10.12%的提取物。SCFCE-NPs 处理 HeLa、U87 和 KB 细胞系 48 小时后,细胞活力分别降至 54%、7%和 12%,而 MACCE-NPs 处理后分别降至 75%、8%和 17%,与对照组相比显著降低。结果表明,由于更好地渗透到细胞中,载有 CE 的 NPs 表现出更高的毒性。