Bioactive Compounds from Vicia sativa L. and Vicia monantha Retz. with Unveiling Antiviral Potentials in Newly Green Synthesized CdO Nanoparticles.

IF 2.2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Alyaa Nasr, Ezzat H Elshazly, Dalia F Slima, Mohamed E Elnosary, Ahmed M Sadek, Mona Khamis, Yu Gong, Qian Tian, Gamal A Gouda, Guo-Ping Zhu
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引用次数: 0

Abstract

Background: in the current study, a comparative phytochemical analysis was carried out to explore the phenolic and flavonoid contents in the aerial parts of Vicia sativa L and Vicia monantha Retz growing in cultivated, reclaimed, and desert habitats.

Methods: High-performance liquid chromatography (HPLC) was used to detect Vicia methanolic extracts' individual phenolic and flavonoid constituents. The first-time synthesis of cadmium oxide nanoparticles (CdO NPs) using the aqueous extract of V. monantha has been developed using a green approach. Also, the cytotoxicity of V. monantha extract and CdO NPs was examined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay for unveiling them as anti-HAV and anti-AdV.

Results: Our results indicated that in the case of desert habitat, the contents of total phenolics (76.37 mg/g) and total flavonoids (65.23 mg/g) of V. monantha were higher than those of V. sativa (67.35 mg/g and 47.34 mg/g, respectively) and the contents of these secondary metabolites were even increased in V. monantha collected from reclaimed land (phenolics: 119.77 mg/g, flavonoids: 88.61 mg/g). Also, V. monantha surpassed V. sativa in the contents of some individual HPLC constituents, and hence, V. monantha was used to synthesize the green CdO NPs and subsequent antiviral tests. The average size of CdO NPs was determined to be 24.28 nm, and the transmission electron microscopy (TEM) images of CdO NPs clearly showed their spherical form and varying particle sizes, with different diameters in the range of 19-29 nm. MTT assay was positive to the exposure of CdO NPs in the normal cell line, proposing that CdO NPs can reduce cell viability. V. monantha extract showed promising antiviral activity against Hepatitis A virus (HAV) and Adenovirus (AdV) with SI of 16.40 and 10.54. On the other hand, CdONPs had poor antiviral activity against HAV with an SI of 4.74 and moderate antiviral activity against AdV with an SI of 10.54.

Conclusion: V. monantha is now considered a new, valuable natural resource for phenolics and flavonoids, especially when grown in reclaimed soil. The green CdO NPs based on V. monantha extract showed a promising antiviral effect against HAV and AdV.

新近绿色合成的氧化镉纳米粒子中的生物活性化合物与抗病毒潜力的揭示
背景:本研究采用高效液相色谱法(HPLC)对生长在栽培地、开垦地和沙漠中的紫花地丁(Vicia sativa L)和紫花地丁(Vicia monantha Retz)的气生部分的酚类和黄酮类成分进行了植物化学比较分析。方法:采用高效液相色谱法(HPLC)检测了紫云英甲醇提取物中的单个酚类和黄酮类成分;首次采用绿色方法利用紫云英甲醇提取物合成了氧化镉纳米粒子(CdO NPs)。此外,还利用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)试验检测了 V. monantha 提取物和 CdO NPs 的细胞毒性,以揭示它们具有抗 HAV 和抗 AdV 的作用:结果表明,在沙漠生境中,V. monantha 的总酚含量(76.37 毫克/克)和总黄酮含量(65.23 毫克/克)高于 V. sativa(分别为 67.35 毫克/克和 47.34 毫克/克),在开垦地采集的 V. monantha 中,这些次生代谢物的含量甚至有所增加(酚类:119.77 毫克/克,黄酮类:88.61 毫克/克)。此外,V. monantha 的某些 HPLC 成分含量超过了 V. sativa,因此 V. monantha 被用于合成绿色 CdO NPs 和随后的抗病毒测试。经测定,CdO NPs 的平均粒径为 24.28 nm,CdO NPs 的透射电子显微镜(TEM)图像清楚地显示了其球形和不同的粒径,不同粒径的 CdO NPs 的粒径范围为 19-29 nm。在正常细胞系中暴露 CdO NPs 后,MTT 检测结果呈阳性,表明 CdO NPs 能降低细胞活力。V. monantha 提取物对甲型肝炎病毒(HAV)和腺病毒(AdV)具有良好的抗病毒活性,其 SI 值分别为 16.40 和 10.54。另一方面,CdONPs 对 HAV 的抗病毒活性较差,SI 值为 4.74,对 AdV 的抗病毒活性一般,SI 值为 10.54:目前,V. monantha 被认为是一种新的、有价值的酚类和黄酮类天然资源,尤其是在再生土壤中生长时。基于 V. monantha 提取物的绿色 CdO NPs 对 HAV 和 AdV 具有良好的抗病毒效果。
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来源期刊
Current pharmaceutical biotechnology
Current pharmaceutical biotechnology 医学-生化与分子生物学
CiteScore
5.60
自引率
3.60%
发文量
203
审稿时长
6 months
期刊介绍: Current Pharmaceutical Biotechnology aims to cover all the latest and outstanding developments in Pharmaceutical Biotechnology. Each issue of the journal includes timely in-depth reviews, original research articles and letters written by leaders in the field, covering a range of current topics in scientific areas of Pharmaceutical Biotechnology. Invited and unsolicited review articles are welcome. The journal encourages contributions describing research at the interface of drug discovery and pharmacological applications, involving in vitro investigations and pre-clinical or clinical studies. Scientific areas within the scope of the journal include pharmaceutical chemistry, biochemistry and genetics, molecular and cellular biology, and polymer and materials sciences as they relate to pharmaceutical science and biotechnology. In addition, the journal also considers comprehensive studies and research advances pertaining food chemistry with pharmaceutical implication. Areas of interest include: DNA/protein engineering and processing Synthetic biotechnology Omics (genomics, proteomics, metabolomics and systems biology) Therapeutic biotechnology (gene therapy, peptide inhibitors, enzymes) Drug delivery and targeting Nanobiotechnology Molecular pharmaceutics and molecular pharmacology Analytical biotechnology (biosensing, advanced technology for detection of bioanalytes) Pharmacokinetics and pharmacodynamics Applied Microbiology Bioinformatics (computational biopharmaceutics and modeling) Environmental biotechnology Regenerative medicine (stem cells, tissue engineering and biomaterials) Translational immunology (cell therapies, antibody engineering, xenotransplantation) Industrial bioprocesses for drug production and development Biosafety Biotech ethics Special Issues devoted to crucial topics, providing the latest comprehensive information on cutting-edge areas of research and technological advances, are welcome. Current Pharmaceutical Biotechnology is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the latest and most important developments.
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