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Chemical and spectroscopic characterization of (Artemisinin/Quercetin/ Zinc) novel mixed ligand complex with assessment of its potent high antiviral activity against SARS-CoV-2 and antioxidant capacity against toxicity induced by acrylamide in male rats

El-Megharbel et al., PeerJ, doi:10.7717/peerj.15638
Jan 2024  
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Quercetin for COVID-19
24th treatment shown to reduce risk in July 2021, now with p = 0.0031 from 11 studies.
No treatment is 100% effective. Protocols combine treatments.
5,100+ studies for 109 treatments. c19early.org
In Vitro and animal study showing that a novel artemisinin/quercetin/zinc (Art/Q/Zn) complex exhibits potent anti-SARS-CoV-2 activity (IC50 = 10.14 μg/ml) without cytotoxicity (CC50 = 208.5 μg/ml). The complex alleviates acrylamide-induced oxidative stress, hepatic/pulmonary toxicity and inflammation in rats. Authors propose Art/Q/Zn inhibits SARS-CoV-2 by binding ACE2 and main protease receptors, preventing viral replication and infection. The antioxidant and organ-protective effects may also benefit COVID-19 patients.
Bioavailability. Quercetin has low bioavailability and studies typically use advanced formulations to improve bioavailability which may be required to reach therapeutic concentrations.
68 preclinical studies support the efficacy of quercetin for COVID-19:
In Silico studies predict inhibition of SARS-CoV-2, or minimization of side effects, with quercetin or metabolites via binding to the spikeA,6,7,19,21,22,27,35,36,38,39,59,60, MproB,4,6,8,10,12,14,15,17,20,21,27,31,33-35,39,40,42,60,61, RNA-dependent RNA polymeraseC,6,29, PLproD,34,42, ACE2E,19,20,25,34,38,60, TMPRSS2F,19, helicaseG,26,31, endoribonucleaseH,36, NSP16/10I,3, cathepsin LJ,23, Wnt-3K,19, FZDL,19, LRP6M,19, ezrinN,37, ADRPO,35, NRP1P,38, EP300Q,13, PTGS2R,20, HSP90AA1S,13,20, matrix metalloproteinase 9T,28, IL-6U,18,32, IL-10V,18, VEGFAW,32, and RELAX,32 proteins. In Vitro studies demonstrate inhibition of the MproB,12,43,48,56 protein, and inhibition of spike-ACE2 interactionY,44. In Vitro studies demonstrate efficacy in Calu-3Z,47, A549AA,18, HEK293-ACE2+AB,55, Huh-7AC,22, Caco-2AD,46, Vero E6AE,16,39,46, mTECAF,49, and RAW264.7AG,49 cells. Animal studies demonstrate efficacy in K18-hACE2 miceAH,52, db/db miceAI,49,58, BALB/c miceAJ,57, and rats62. Quercetin reduced proinflammatory cytokines and protected lung and kidney tissue against LPS-induced damage in mice57, inhibits LPS-induced cytokine storm by modulating key inflammatory and antioxidant pathways in macrophages2, and inhibits SARS-CoV-2 ORF3a ion channel activity, which contributes to viral pathogenicity and cytotoxicity51.
Study covers zinc and quercetin.
El-Megharbel et al., 2 Jan 2024, Egypt, peer-reviewed, 4 authors. Contact: dr_reham_z@yahoo.com, reham.z@tu.edu.sa.
This PaperQuercetinAll
Chemical and spectroscopic characterization of (Artemisinin/Querctin/ Zinc) novel mixed ligand complex with assessment of its potent high antiviral activity against SARS-CoV-2 and antioxidant capacity against toxicity induced by acrylamide in male rats
Samy M El-Megharbel, Safa H Qahl, Bander Albogami, Reham Z Hamza
PeerJ, doi:10.7717/peerj.15638
A novel Artemisinin/Quercetin/Zinc (Art/Q/Zn) mixed ligand complex was synthesized, tested for its antiviral activity against coronavirus (SARS-CoV-2), and investigated for its effect against toxicity and oxidative stress induced by acrylamide (Acy), which develops upon cooking starchy foods at high temperatures. The synthesized complex was chemically characterized by performing elemental analysis, conductance measurements, FT-IR, UV, magnetic measurements, and XRD. The morphological surface of the complex Art/Q/Zn was investigated using scanning and transmission electron microscopy (SEM and TEM) and energy dispersive X-ray analysis (XRD). The in vitro antiviral activity of the complex Art/Q/Zn against SARS-CoV-2 and its in vivo activity against Acy-induced toxicity in hepatic and pulmonary tissues were analyzed. An experimental model was used to evaluate the beneficial effects of the novel Art/Q/Zn novel complex on lung and liver toxicities of Acy. Forty male rats were randomly divided into four groups: control, Acy (500 mg/Kg), Art/Q/Zn (30 mg/kg), and a combination of Acy and Art/Q/Zn. The complex was orally administered for 30 days. Hepatic function and inflammation marker (CRP), tumor necrosis factor, interleukin-6 (IL-6), antioxidant enzyme (CAT, SOD, and GPx), marker of oxidative stress (MDA), and blood pressure levels were investigated. Histological and ultrastructure alterations and caspase-3 variations (immunological marker) were also investigated. FT-IR spectra revealed that Zn (II) is able to chelate through C=O and C-OH (Ring II) which are the carbonyl oxygen atoms of the quercetin ligand and carbonyl oxygen atom C=O of the Art ligand, forming Art/Q/Zn complex with the chemical formula The novel complex exhibited a potent anti-SARS-CoV-2 activity even at a low concentration (IC 50 = 10.14 µg/ml) and was not cytotoxic to the cellular host (CC 50 = 208.5 µg/ml). Art/Q/Zn may inhibit the viral replication and binding to the angiotensin-converting enzyme-2 (ACE2) receptor and the main How to cite this article El-Megharbel SM, Qahl SH, Albogami B, Hamza RZ. 2024. Chemical and spectroscopic characterization of (Artemisinin/Querctin/ Zinc) novel mixed ligand complex with assessment of its potent high antiviral activity against SARS-CoV-2 and antioxidant capacity against toxicity induced by acrylamide in male rats. PeerJ 12:e15638 http://doi.org/10.7717/peerj.15638 protease inhibitor (M Pro ), thereby inhibiting the activity of SARS-CoV-2 and this proved by the molecular dynamics simulation. It alleviated Acy hepatic and pulmonary toxicity by improving all biochemical markers. Therefore, it can be concluded that the novel formula Art/Q/Zn complex is an effective antioxidant agent against the oxidative stress series, and it has high inhibitory effect against SARS-CoV-2.
ADDITIONAL INFORMATION AND DECLARATIONS Funding The researchers were funded by the Deanship of Scientific Research, Taif University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Grant Disclosures The following grant information was disclosed by the authors: The Deanship of Scientific Research, Taif University. Competing Interests The authors declare there are no competing interests. Author Contributions • Samy M. El-Megharbel conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft. • Safa H. Qahl conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft. • Bander Albogami conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft. • Reham Z. Hamza conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft. Animal Ethics The following information was supplied relating to ethical approvals (i.e., approving body and any reference numbers): The Zagazig University ethical..
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{ 'indexed': {'date-parts': [[2024, 1, 3]], 'date-time': '2024-01-03T00:57:38Z', 'timestamp': 1704243458534}, 'reference-count': 82, 'publisher': 'PeerJ', 'license': [ { 'start': { 'date-parts': [[2024, 1, 2]], 'date-time': '2024-01-02T00:00:00Z', 'timestamp': 1704153600000}, 'content-version': 'unspecified', 'delay-in-days': 0, 'URL': 'https://creativecommons.org/licenses/by/4.0/'}], 'funder': [{'name': 'The Deanship of Scientific Research, Taif University'}], 'content-domain': {'domain': [], 'crossmark-restriction': False}, 'abstract': '<jats:p>A novel Artemisinin/Quercetin/Zinc (Art/Q/Zn) mixed ligand complex was synthesized, ' 'tested for its antiviral activity against coronavirus (SARS-CoV-2), and investigated for its ' 'effect against toxicity and oxidative stress induced by acrylamide (Acy), which develops upon ' 'cooking starchy foods at high temperatures. The synthesized complex was chemically ' 'characterized by performing elemental analysis, conductance measurements, FT-IR, UV, magnetic ' 'measurements, and XRD. The morphological surface of the complex Art/Q/Zn was investigated ' 'using scanning and transmission electron microscopy (SEM and TEM) and energy dispersive X-ray ' 'analysis (XRD). The <jats:italic>in vitro</jats:italic> antiviral activity of the complex ' 'Art/Q/Zn against SARS-CoV-2 and its <jats:italic>in vivo</jats:italic> activity against ' 'Acy-induced toxicity in hepatic and pulmonary tissues were analyzed. An experimental model ' 'was used to evaluate the beneficial effects of the novel Art/Q/Zn novel complex on lung and ' 'liver toxicities of Acy. Forty male rats were randomly divided into four groups: control, Acy ' '(500 mg/Kg), Art/Q/Zn (30 mg/kg), and a combination of Acy and Art/Q/Zn. The complex was ' 'orally administered for 30 days. Hepatic function and inflammation marker (CRP), tumor ' 'necrosis factor, interleukin-6 (IL-6), antioxidant enzyme (CAT, SOD, and GPx), marker of ' 'oxidative stress (MDA), and blood pressure levels were investigated. Histological and ' 'ultrastructure alterations and caspase-3 variations (immunological marker) were also ' 'investigated. FT-IR spectra revealed that Zn (II) is able to chelate through C=O and C-OH ' '(Ring II) which are the carbonyl oxygen atoms of the quercetin ligand and carbonyl oxygen ' 'atom C=O of the Art ligand, forming Art/Q/Zn complex with the chemical formula ' '[Zn(Q)(Art)(Cl)(H<jats:sub>2</jats:sub>O)<jats:sub>2</jats:sub>]⋅3H<jats:sub>2</jats:sub>O. ' 'The novel complex exhibited a potent anti-SARS-CoV-2 activity even at a low concentration ' '(IC<jats:sub>50</jats:sub> = 10.14 µg/ml) and was not cytotoxic to the cellular host ' '(CC<jats:sub>50</jats:sub> = 208.5 µg/ml). Art/Q/Zn may inhibit the viral replication and ' 'binding to the angiotensin-converting enzyme-2 (ACE2) receptor and the main protease ' 'inhibitor (M<jats:sup>Pro</jats:sup>), thereby inhibiting the activity of SARS-CoV-2 and this ' 'proved by the molecular dynamics simulation. It alleviated Acy hepatic and pulmonary toxicity ' 'by improving all biochemical markers. Therefore, it can be concluded that the novel formula ' 'Art/Q/Zn complex is an effective antioxidant agent against the oxidative stress series, and ' 'it has high inhibitory effect against SARS-CoV-2.</jats:p>', 'DOI': '10.7717/peerj.15638', 'type': 'journal-article', 'created': {'date-parts': [[2024, 1, 2]], 'date-time': '2024-01-02T12:29:50Z', 'timestamp': 1704198590000}, 'page': 'e15638', 'source': 'Crossref', 'is-referenced-by-count': 0, 'title': 'Chemical and spectroscopic characterization of (Artemisinin/Querctin/ Zinc) novel mixed ligand ' 'complex with assessment of its potent high antiviral activity against SARS-CoV-2 and antioxidant ' 'capacity against toxicity induced by acrylamide in male rats', 'prefix': '10.7717', 'volume': '12', 'author': [ { 'given': 'Samy M.', 'family': 'El-Megharbel', 'sequence': 'first', 'affiliation': [ { 'name': 'Department of Chemistry, College of Sciences, Taif University, ' 'Taif, Saudi Arabia'}]}, { 'given': 'Safa H.', 'family': 'Qahl', 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