以生态友好的方式从柠檬皮和果汁中合成银纳米粒子及其对 HSV-1 和 SARS-CoV-2 的抗病毒功效

IF 2.5 4区 医学 Q3 VIROLOGY Virus research Pub Date : 2024-08-24 DOI:10.1016/j.virusres.2024.199455
Federica Dell'Annunziata , Ekaterine Mosidze , Veronica Folliero , Erwin P. Lamparelli , Valentina Lopardo , Pasquale Pagliano , Giovanna Della Porta , Massimiliano Galdiero , Aliosha Dzh Bakuridze , Gianluigi Franci
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引用次数: 0

摘要

病毒感染的威胁日益严重,需要创新的治疗方法来保障人类健康。纳米材料是克服传统疗法局限性的大有可为的解决方案。目前,银纳米粒子(AgNPs)的生态友好型合成是一种能保证抗菌效果、安全性和成本效益的方法。本研究探讨了从坎帕尼亚地区种植的柑橘柠檬 "Ovale di Sorrento "的果皮(Lp-AgNPs)和果汁(Lj-AgNPs)中提取的 AgNPs 的用途。针对冠状病毒科和疱疹病毒科病毒的抗病毒潜力进行了测试。使用硝酸银溶液与柠檬皮和果汁的水提取物混合,通过还原法合成了 AgNPs。使用紫外可见分光光度计评估了 Lp-AgNPs 和 Lj-AgNPs 的形成。通过动态光散射(DLS)、纳米颗粒跟踪分析(NTA)和场发射扫描电子显微镜(FE-SEM)评估了 AgNPs 的尺寸、ζ电位、浓度和形态。用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑试验(MTT)对 VERO-76 和 HaCaT 细胞进行了细胞毒性评估,浓度范围在 500 至 7.8 µg/mL 之间。抗病毒活性包括病毒预处理、联合处理、细胞预处理和感染后测试,以 0.01 的感染倍率(MOI)对 HSV-1 和 SARS-CoV-2 进行测试。斑块缩小试验和实时 PCR 提供了测试化合物抗病毒潜力的数据。Lp-AgNPs 和 Lj-AgNPs 呈球形,直径分别为 60 和 92 nm,浓度分别为 4.22 和 4.84 × 1010 粒子/毫升。MTT 数据显示细胞毒性极小,Lp-AgNPs 和 Lj-AgNPs 对 VERO 细胞的 50 % 细胞毒性浓度(CC50)分别为 754.6 和 486.7 µg/mL。同样,Lp-AgNPs 和 Lj-AgNPs 对 HaCaT 细胞的 CC50 值分别为 457.3 µg/mL 和 339.6 µg/mL。在病毒预处理试验中,Lp-AgNPs 和 Lj-AgNPs 对 HSV-1 和 SARS-CoV-2 的 90% 抑制浓度分别为 8.54-135.04 µg/mL 和 6.13-186.77 µg/mL。分子研究证实了这些抗病毒数据,在接触 AgNP 后,HSV-1 的 UL54 和 UL27 基因以及 SARS-CoV-2 的 Spike (S) 基因均有所减少。这项研究的结果表明,从 C. Limon 提取的 Lp-AgNPs 和 Lj-AgNPs 可以提供一种有效的生态、天然、本地和安全的抗病毒感染策略。
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Eco-friendly synthesis of silver nanoparticles from peel and juice C. limon and their antiviral efficacy against HSV-1 and SARS-CoV-2

The growing threat of viral infections requires innovative therapeutic approaches to safeguard human health. Nanomaterials emerge as a promising solution to overcome the limitations associated with conventional therapies. The eco-friendly synthesis of silver nanoparticles (AgNPs) currently represents a method that guarantees antimicrobial efficacy, safety, and cost-effectiveness. This study explores the use of AgNPs derived from the peel (Lp-AgNPs) and juice (Lj-AgNPs) Citrus limon “Ovale di Sorrento”, cultivars of the Campania region. The antiviral potential was tested against viruses belonging to the Coronaviridae and Herpesviridae. AgNPs were synthesized by reduction method using silver nitrate solution mixed with aqueous extract of C. limon peel and juice. The formation of Lp-AgNPs and Lj-AgNPs was assessed using a UV–Vis spectrophotometer. The size, ζ-potential, concentration, and morphology of AgNPs were evaluated by dynamic light scattering (DLS), nanoparticle tracking analysis (NTA), and field emission-scanning electron microscopy (FE-SEM). Cytotoxicity was evaluated in a concentration range between 500 and 7.8 µg/mL on VERO-76 and HaCaT cells, with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium test bromide (MTT). Antiviral activity consisted of virus pre-treatment, co-treatment, cellular pre-treatment, and post-infection tests versus HSV-1 and SARS-CoV-2 at a multiplicity of infections (MOI) of 0.01. Plaque reduction assays and real-time PCR provided data on the antiviral potential of tested compounds. Lp-AgNPs and Lj-AgNPs exhibited spherical morphology with respective diameters of 60 and 92 nm with concentrations of 4.22 and 4.84 × 1010 particles/mL, respectively. The MTT data demonstrated minimal cytotoxicity, with 50 % cytotoxic concentrations (CC50) of Lp-AgNPs and Lj-AgNPs against VERO cells of 754.6 and 486.7 µg/mL. Similarly, CC50 values against HaCaT were 457.3 µg/mL for Lp-AgNPs and 339.6 µg/mL for Lj-AgNPs, respectively. In the virus pre-treatment assay, 90 % inhibitory concentrations of HSV-1 and SARS-CoV-2 were 8.54–135.04 µg/mL for Lp-AgNPs and 6.13–186.77 µg/mL for Lj-AgNPs, respectively. The molecular investigation confirmed the antiviral data, recording a reduction in the UL54 and UL27 genes for HSV-1 and in the Spike (S) gene for SARS-CoV-2, following AgNP exposure. The results of this study suggest that Lp-AgNPs and Lj-AgNPs derived from C. Limon could offer a valid ecological, natural, local and safe strategy against viral infections.

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来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
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