Gyurova Anna, Milkova Viktoria, Iliev Ivan, Lazarova-Zdravkova Nevena, Rashev Viktor, Simeonova Lora, Vilhelmova-Ilieva Neli
Institute of Physical Chemistry 'Acad. R. Kaischew', Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Institute of Experimental Morphology, Pathology and Anthropology with Museum, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Life (Basel). 2024 Sep 19;14(9):1180. doi: 10.3390/life14091180.
Disease's severity, mortality rates, and common failures to achieve clinical improvement during the unprecedented COVID-19 pandemic exposed the emergency need for new antiviral therapeutics with higher efficacy and fewer adverse effects. This study explores the potential to encapsulate multi-component plant extracts in liposomes as optimized delivery systems and to verify if they exert inhibitory effects against human seasonal betacoronavirus OC43 (HCoV-OC43) in vitro. The selection of , , , , and L. plant extracts was based on their established pharmacological and antiviral properties. The physicochemical characterization of extract-loaded liposomes was conducted by DLS and electrokinetics. Encapsulated amounts of the extract were evaluated based on the total flavonoid content (TFC) and total polyphenol content (TPC) by colorimetric methods. The BALB 3T3 neutral red uptake (NRU) phototoxicity/cytotoxicity assay was used to estimate compounds' safety. Photo irritation factors (PIFs) of the liposomes containing extracts were <2 which assigned them as non-phototoxic substances. The antiviral capacities of liposomes containing medicinal plant extracts against HCoV-OC43 were measured by the cytopathic effect inhibition test in susceptible HCT-8 cells. The antiviral activity increased by several times compared to "naked" extracts' activity reported previously. extract showed 16 times higher inhibitory properties reaching a selectivity index (SI) of 58.96. Virucidal and virus-adsorption effects were investigated using the endpoint dilution method and ∆lgs comparison with infected and untreated controls. The results confirmed that nanoparticles do not directly affect the viral surface or cell membrane, but only serve as carriers of the active substances and the observed protection is due solely to the intracellular action of the extracts.
在史无前例的新冠疫情期间,疾病的严重程度、死亡率以及临床改善方面常见的失败情况,凸显了对疗效更高、副作用更少的新型抗病毒疗法的迫切需求。本研究探索了将多成分植物提取物封装在脂质体中作为优化递送系统的潜力,并验证它们在体外是否对人类季节性β冠状病毒OC43(HCoV-OC43)具有抑制作用。选择[植物名称1]、[植物名称2]、[植物名称3]、[植物名称4]和[植物名称5]植物提取物是基于它们已确定的药理和抗病毒特性。通过动态光散射(DLS)和电动学对负载提取物的脂质体进行物理化学表征。通过比色法基于总黄酮含量(TFC)和总多酚含量(TPC)评估提取物的封装量。使用BALB 3T3中性红摄取(NRU)光毒性/细胞毒性试验来评估化合物的安全性。含有提取物的脂质体的光刺激因子(PIF)<2,这表明它们为非光毒性物质。通过在易感的HCT-8细胞中进行细胞病变效应抑制试验来测量含有药用植物提取物的脂质体对HCoV-OC43的抗病毒能力。与先前报道的“裸”提取物的活性相比,抗病毒活性提高了数倍。[提取物名称]提取物显示出高16倍的抑制特性,选择性指数(SI)达到58.96。使用终点稀释法和与感染及未处理对照的∆lgs比较来研究杀病毒和病毒吸附作用。结果证实,纳米颗粒不会直接影响病毒表面或细胞膜,而仅作为活性物质的载体,观察到的保护作用完全归因于提取物的细胞内作用。