Keshavarz Fatemeh, Dorfaki Maryam, Bardania Hasan, Khosravani Fatemeh, Nazari Paria, Ghalamfarsa Ghasem
Department of Immunology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.
Iran J Med Sci. 2023 May;48(3):321-328. doi: 10.30476/IJMS.2022.95272.2658.
Quercetin is a flavonoid having anti-cancer properties; however, it has low stability, insufficient bioavailability, and poor solubility. This study aimed to load quercetin on nanoliposomes to enhance its efficiency against SW48 colorectal cancer cells. The cytotoxicity of free-quercetin and quercetin-loaded nanoliposomes on the expression of the epidermal growth factor receptor (EGER) gene was investigated.
This present study was conducted at Yasuj University of Medical Sciences (Yasuj, Iran) in 2021. In this study, the lipid thin-film hydration method was used to synthesize quercetin-loaded liposomes. Additionally, high-performance liquid chromatography (HPLC) analyses, dynamic light scattering (DLS), and transmission electron microscopy (TEM) investigations were used to characterize nanomaterials. Following that, MTT, flow cytometry, and real-time PCR were used to investigate the cytotoxicity of quercetin-loaded liposomes on the colorectal cancer cells SW48 cell line, the incidence of apoptosis, and the expression of the EGFR gene in these cells. Statistical analysis was performed using the SPSS (version 26.0), and the graphs were created with the GraphPad Prism version 8.4.3. P<0.05 was considered statistically significant.
The nanoparticles were spherical, homogenous, and 150±10 nm in size. According to HPLC, Quercetin had a 98% loading capacity. Although both free quercetin and quercetin-loaded liposomes indicated significant cytotoxicity against cancer cells (P˂0.001), the combined form was significantly more active (P=0.008). 50 µg/mL of this compound reduced the viability of SW48 cells by more than 80% (IC 10.65 µg/mL), while the viability of cells treated with free quercetin was only 66% (IC 18.74 µg/mL). The apoptosis was nearly doubled in the cells treated with quercetin-loaded nanoliposomes compared to free quercetin (54.8% versus 27.6%). EGFR gene expression, on the other hand, was significantly lower in cells treated with quercetin-loaded liposomes than the quercetin alone (P=0.006).
When combined with nanoliposomes, quercetin had greater anti-proliferative, apoptotic, and anti-EGFR expression than free quercetin.
槲皮素是一种具有抗癌特性的黄酮类化合物;然而,它稳定性低、生物利用度不足且溶解度差。本研究旨在将槲皮素负载于纳米脂质体上,以提高其对SW48结肠癌细胞的疗效。研究了游离槲皮素和负载槲皮素的纳米脂质体对表皮生长因子受体(EGER)基因表达的细胞毒性。
本研究于2021年在伊朗亚苏杰医科大学进行。在本研究中,采用脂质薄膜水化法合成负载槲皮素的脂质体。此外,还使用高效液相色谱(HPLC)分析、动态光散射(DLS)和透射电子显微镜(TEM)研究对纳米材料进行表征。随后,采用MTT法、流式细胞术和实时定量PCR法研究负载槲皮素的脂质体对结肠癌细胞SW48细胞系的细胞毒性、细胞凋亡发生率以及这些细胞中EGFR基因的表达。使用SPSS(版本26.0)进行统计分析,并用GraphPad Prism 8.4.3版本绘制图表。P<0.05被认为具有统计学意义。
纳米颗粒呈球形,均匀,大小为150±10 nm。根据HPLC分析,槲皮素的负载率为98%。虽然游离槲皮素和负载槲皮素的脂质体均对癌细胞显示出显著的细胞毒性(P˂0.001),但组合形式的活性明显更高(P=0.008)。50 µg/mL的该化合物使SW48细胞的活力降低了80%以上(IC 10.65 µg/mL),而用游离槲皮素处理的细胞活力仅为66%(IC 18.74 µg/mL)。与游离槲皮素相比,用负载槲皮素的纳米脂质体处理的细胞凋亡率几乎翻倍(54.8%对27.6%)。另一方面,用负载槲皮素的脂质体处理的细胞中EGFR基因表达明显低于单独使用槲皮素处理的细胞(P=0.006)。
与纳米脂质体结合时,槲皮素比游离槲皮素具有更强的抗增殖、促凋亡和抗EGFR表达能力。