Abstract
Quercetin is a phenolic flavonol compound with established antioxidant, anti-inflammatory, and immuno-stimulant properties. Recent studies demonstrate the potential of quercetin against COVID-19. This article highlighted the prophylactic/therapeutic potential of quercetin against COVID-19 in view of its clinical studies, inventions, and patents. The literature for the subject matter was collected utilizing different databases, including PubMed, Sci-Finder, Espacenet, Patentscope, and USPTO. Clinical studies expose the potential of quercetin monotherapy, and also its combination therapy with other compounds, including zinc, vitamin C, curcumin, vitamin D3, masitinib, hydroxychloroquine, azithromycin, and ivermectin. The patent literature also examines claims that quercetin containing nutraceuticals, pharmaceuticals, and dietary supplements, alone or in combination with other drugs/compounds, including favipiravir, remdesivir, molnupiravir, navitoclax, dasatinib, disulfiram, rucaparib, tamarixin, iota-carrageenan, and various herbal extracts (aloe, poria, rosemary, and sphagnum) has potential for use against COVID-19. The literature reveals that quercetin exhibits anti-COVID-19 activity because of its inhibitory effect on the expression of the human ACE2 receptors and the enzymes of SARS-CoV-2 (MPro, PLPro, and RdRp). The USFDA designated quercetin as a “Generally Recognized as Safe” substance for use in the food and beverage industries. It is also an inexpensive and readily available compound. These facts increase the possibility and foreseeability of making novel and economical drug combinations containing quercetin to prevent/treat COVID-19. Quercetin is an acidic compound and shows metabolic interaction with some antivirals, antibiotics, and anti-inflammatory agents. Therefore, the physicochemical and metabolic drug interactions between quercetin and the combined drugs/compounds must be better understood before developing new compositions.
1. Introduction
At present, the world population is aware of the COVID-19 pandemic and its causative virus (SARS-CoV-2). The first case of COVID-19 was identified in December 2019, and the World Health Organization (WHO) declared it a global pandemic in March 2020 [1]. As of 4 March 2022, the WHO’s website shows 440,807,756 confirmed COVID-19 cases, and 5,978,096 deaths due to COVID-19, and 10,585,766,316 vaccine dosages administered to people [2]. The mild symptoms of COVID-19 include cough, fever, diarrhea, myalgia, fatigue, and anosmia. If untreated, it may lead to acute respiratory distress syndrome (ARDS), lung injury, multiple organ failures due to cytokine storm, thromboembolic diseases, and death [3]. Elderly people suffering from chronic diseases (diabetes, hypertension, etc.) and the immunocompromised population are particularly susceptible to SARS-CoV-2 infection [4]. Since the start of this pandemic, some antiviral drugs were reported to be effective against COVID-19, including remdesivir [5], molnupiravir [6], favipiravir [7], and monoclonal antibodies such as bamlanivimab [8]. Many vaccines were developed and marketed by Pfizer, Moderna, Johnson & Johnson, and Astra Zeneca for the prevention of COVID-19 [9]. Apart from drugs and vaccines, many food supplements (vitamins, minerals, and immune boosters) [10] and herbal products were claimed to prevent/treat COVID-19 [11]. Quercetin is one of the natural compounds that demonstrates its efficacy to prevent/treat COVID-19 alone, or in combination with other adjuvants/drugs. This fact is also supported by some published reviews on quercetin [12,13,14,15,16,17]. The present review highlights the prophylactic/therapeutic potential of quercetin against COVID-19, in view of clinical studies and patented compositions.
2. Searching for Non-Patent Literature
The keyword/combination keyword search with the terms “quercetin”, “quercetin + COVID-19”, and “quercetin + SARS-CoV-2” was performed on the PubMed and Scifinder databases. The appropriate non-patent literature related to general aspects of quercetin (Section 3), biological effects of quercetin (Section 3), the potential of quercetin to prevent/treat COVID-19 (Section 4), and the clinical studies of quercetin against COVID-19 (Section 5) were reviewed and incorporated in this review.
3. Quercetin
Quercetin (yellowish crystals; insoluble in water; soluble in acetic acid/alkali solutions; slightly soluble in alcohol; CAS registry number: 117-39-5; molecular weight: 302.24; melting point: 316.5 °C; chemical name: 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one) is a flavonol, which is found in many fruits (grape, apple, strawberry, cloudberry, and raspberry), and vegetables (onion, tomato, lettuce, and green bean) [18]. The chemical structure of quercetin is depicted in Figure 1. Quercetin contains four phenolic groups, which make it a strong scavenger of the reactive oxygen species (ROS), antioxidant, immune booster, and anti-inflammatory substance [18]. Quercetin is also an excellent metal ionophore (antioxidative, anti-inflammatory, and immunomodulatory zinc ionophore) [19], and also increases the glutathione (antioxidant) level in the body [20]. These properties make quercetin an important therapeutic agent to prevent/treat many diseases caused by oxidative stress and the release of pro-inflammatory substances in the body (Figure 1) [18,21,22].
Figure 1.
Chemical structure and biological effects of quercetin [18,21,22].
Quercetin is obtained from the hydrolysis of rutin (a quercetin glycoside) [18]. The United States Food and Drug Administration (USFDA) designated quercetin as a GRAS (generally recognized as safe) substance, up to a level of 500 mg/day [23]. The releasable information (parts 1, 2, and 3) of the GRAS notice number 341 of the USFDA discusses the chemistry, manufacturing process, stability/photostability, impurities, metabolism, toxicology, clinical studies, and reason for granting the GRAS status to quercetin. In short, this states that the shelf life of pure quercetin is about 5 years; quercetin is absorbed from the stomach with 24–53% bioavailability; quercetin forms a albumin–quercetin complex that may be toxic in chronic use, but the limited bioavailability of quercetin prevents this event from happening; quercetin does not produce systemic toxicity up to 2.231 g/kg/day, or carcinogenicity; quercetin does not adversely impact the CYP450 enzymes and does not deplete the glutathione enzyme; quercetin is metabolized to two non-carcinogenic compounds, namely, 3′-O-methylquercetin and 4′-O-methylquercetin, and is excreted via urine as well as feces. Being a GRAS product, quercetin is used in nutraceuticals, the food/beverage industry, and as a diet supplement (Figure 2) [24].
Figure 2.
Application segments of quercetin according to end use [24].
4. Mechanism of Action of Quercetin against SARS-CoV-2
The SARS-CoV-2 virus is an RNA virus. It enters the human cell through the angiotensin-converting enzyme 2 receptors (hACE-2) [5,6,9]. The virus’s entry into the human cell causes the release of pro-inflammatory substances, oxidative stress, and acute respiratory distress syndrome [25,26]. The virus needs 3CLPro (main protease enzyme) and RNA-dependent RNA polymerase (RdRp) for its replication [5,6,9]. Quercetin demonstrates anti-COVID-19/anti-SARS-CoV-2 activity by lowering/inhibiting the expression of the hACE-2, the release of pro-inflammatory substances, 3CLPro, and RdRp [12,27,28,29] (Figure 3).
Figure 3.
Life cycle of SARS-CoV-2 and mechanism of action of quercetin [5,6,9,12,25,26,27,28,29].
The molecular docking studies displayed the anti-SARS-CoV-2 activities of quercetin [12,27,28]. In silico studies using SARS-CoV-2 protease protein (PDB ID: 6LU7) demonstrate that quercetin inhibits SARS-CoV-2 protease by making hydrogen bonds with some residues (His164, Glu166, Asp187, Gln192, and Thr190) of 6LU7 [12,27]. Quercetin also reduces the expression of many human genes that encode SARS-CoV-2 proteins, and reduces the severity of SARS-CoV-2 infection [27]. It is known that the first phase of COVID-19 relates to immunodeficiency and the second phase is connected to a cytokine storm due to the overexpression of pro-inflammatory substances, including inflammasomes, cytokines, interleukin 1β, and interleukin 18 [27,28]. Therefore, immune boosters and anti-inflammatory therapies are recommended during the first and second phases of COVID-19, respectively [27]. Quercetin is a recognized antioxidant possessing immunomodulatory activity, anti-inflammatory activity, and anti-SARS-CoV-2 activity (Figure 1). Therefore, quercetin is believed to possess all the attributes required for COVID-19 therapy [12,18,21,22,27,28,29].
5. Clinical Studies of Quercetin against COVID-19
The clinical studies of quercetin were searched on the clinical trial database [30] on 8 March 2022, using the term “quercetin”. This search revealed 101 clinical studies related to the use of quercetin to prevent/treat various diseases, including oxidative stress, inflammation, viral infections (COVID-19), COPD, asthma, cardiovascular diseases (coronary artery disease/progression, atherosclerosis, endothelial dysfunction, etc.), carcinoma, aging, Fanconi anemia, and Alzheimer’s disease. This search also provided 15 clinical studies related to the use of quercetin, or its compositions, against COVID-19, which are summarized in Table 1. Among the 15 clinical studies, 11 were related to the treatment of COVID-19, 3 were for the prevention of COVID-19, and 1 was an observational study. Four studies have been conducted in Pakistan, two in Tunisia, and one each in Turkey, Saudi Arabia, the United States, Belgium, Italy, France, and Indonesia. Two studies did not provide the location of their studies. The clinical trials of Table 1 are related to the monotherapy of quercetin and isoquercetin, and their compositions including one or more substances selected from the group of zinc, vitamin C, curcumin, vitamin D3, masitinib, hydroxychloroquine, azithromycin, and ivermectin.
Table 1.
Clinical studies on quercetin and its compositions against COVID-19.
It is interesting to note that many clinical studies mentioned in Table 1 are not publicized as per the information provided in the database. Moreover, our search revealed more clinical studies relate to the efficacy of quercetin compositions against COVID-19.
In one study, the combination of quercetin (1 g of quercetin daily for 7 days) with remdesivir and favipiravir is evaluated among hospitalized 60 COVID-19 patients. The intervention group patients (quercetin + remdesivir/favipiravir) have a better recovery rate than the control group patients (remdesivir/favipiravir). The quercetin-treated patients also show an improvement in hemoglobin level, respiratory rate, and ALP/LDH levels. The authors of this study recommend further investigations of the tested combination among ICU patients [31].
In another study, the administration of 1 dose/day oral composition comprising quercetin (400 mg), zinc (25 mg), quina (10 drops), vitamin C (1 g), vitamin D3 (25 mg), vitamin E (400 IU), and l-lysine (500 mg) among >100 individuals confirms the efficacy of the tested combination for the prophylaxis of COVID-19 [32].
One group of investigators disclose quercetin phytosome (a bioavailable phospholipid delivery form of quercetin) as possessing anti-SARS-CoV-2 activity [33]. They conducted a 2 week trial utilizing 21 outpatients availing standard care, and 21 outpatients availing standard care, in the combination of quercetin phytosome tablets (200 mg, 3 times/day). The results show that the incorporation of quercetin phytosome into standard care shortened the recovery time and severity of COVID-19. The quercetin phytosome-treated outpatients also show an improvement in the blood parameters (LDH, Ferritin, CRP, and D-dimer). As per the disclosure of this article, NCT04861298 (Table 1) is the registered clinical trial number of this study.
As per the literature, the study related to NCT04578158 (Table 1) has also been published [34]. This study also relates to the quercetin phytosome. The quercetin phytosome (1 g/day) was given to 153 COVID-19 outpatients. The results are promising and demonstrate a decrease in the recovery time, oxygen demand, and hospitalization need. The investigators also state quercetin phytosome is an anti-fatigue and pro-appetite composition with a good safety profile.
The published result of NCT05037240 (Table 1) [35] relates to quercetin phytosome (250 mg 2 times/day) among 120 subjects and indicates that the co-administration of quercetin phytosome with standard care provides more protective effects against COVID-19 than a placebo. In addition, further studies are recommended to use quercetin as a general prophylactic of SARS-CoV-2 infection.
The results of NCT04377789 (Table 1) have also been publicized [35]. This study was conducted on 429 patients utilizing a composition comprising quercetin, vitamin C, and bromelain in combination with standard care. The administered composition improves the recovery rate and the blood parameters also. Moreover, the article recommends further studies to assess the dose/response relationship and the bioavailability of the quercetin composition.
The Shufeng Jiedu capsules comprising polydatin, wogonin, and quercetin as its main components were evaluated on 43 patients as a possible treatment of COVID-19 [36]. The addition of the capsule with the standard antiviral therapy significantly decreases the recovery time and the symptoms (fatigue and cough) of COVID-19 patients. The investigators also suggest a large-scale clinical trial related to the subject matter.
A clinical trial on 97 patients was reported for Yindan Jiedu granules [37]. The main components of these granules are luteolin, quercetin, and kaempferol. The results demonstrate the promising anti-inflammatory effects of Yindan Jiedu granules on COVID-19 patients.
6. Patent Searching
The patent search was performed on 8 March 2022, employing different patent databases described in the literature [38,39,40,41,42], using the combination terms “Quercetin + COVID-19” and “Quercetin + SARS-CoV-2”. The patent database, Espacenet (quercetin + COVID-19 = 45 hits and quercetin + SARS-CoV-2 = 47 hits), Sci-Finder (quercetin + COVID-19 = 47 hits and quercetin + SARS-CoV-2 = 18 hits), USPTO (quercetin + COVID-19 = 31 hits and quercetin + SARS-CoV-2 = 29 hits), and Patentscope (quercetin + COVID-19 = 44 hits and quercetin + SARS-CoV-2 = 45 hits) revealed many patents and patent applications (Table 2). The duplicate patent family members were removed. The patents/patent applications of a single patent family that specifically mentioned quercetin, or its compositions, in the claim section for the prevention and treatment of COVID-19 were included for further analysis. The patent applications claiming the use of novel non-clinical (clinical studies have never been performed) compounds in combination with quercetin were excluded. The patent/patent applications containing a broad dependent claim concerning quercetin without any experimental support were also excluded. The information about the international patent classification (IPC), priority countries, publication date, and the status of the cited patents/patent applications were obtained from the Espacenet and USPTO databases.
Table 2.
The data and the summary of the claimed invention in patent/patent applications.
It is evident from the data of Table 2 that only a few patent applications provide examples related to the use of quercetin, or its compositions, to prevent/treat COVID-19. Other patent applications claim the use of quercetin as an optional ingredient of the claimed composition. Accordingly, an analysis of the patent applications that contain examples of using quercetin or its compositions to prevent/treat COVID-19 is provided below.
US2021315857A1 covers a pharmaceutical micronutrient composition comprising ascorbate (10 mg to 200,000 mg), N-acetylcysteine (2 mg to 30,000 mg), theaflavin (5 mg to 3000 mg), resveratrol (10 mg to 5000 mg), cruciferous plant extracts (5 mg to 5000 mg), curcumin (5 mg to 10,000 mg), quercetin (5 mg to 2000 mg), naringenin (5 mg to 3000 mg), polyphenol extract from green tea (1 mg to 10,000 mg), brazilin (1 mg to 5000 mg), and baicalin (5 mg to 3000 mg) [43]. The claimed composition inhibits the SARS-CoV-2 entry into the body by decreasing the expression of hACE-2 receptors. The in vitro study reveals that the composition D (resveratrol, cruciferous plant extract, curcumin, quercetin, naringenin, baicalin, theaflavin, vitamin C, and N-acetylcysteine) provides the best inhibition of receptor binding of SARS-CoV-2 to hACE-2. However, the patent application is silent about the rationale of quercetin in the claimed composition.
WO2021259441A1 provides a composition containing quercetin and tamarixin [44]. The patent application states that quercetin and tamarixin bind with ACE2, and prevent the binding of SARS-CoV-2 with the ACE2; they also inhibit the formation of ACE2 from ACE1, which results in several beneficial events (vasodilatation, vascular protection, antifibrosis, antiproliferation, antiinflammation, and increase nitric oxide release), and act as a metal ionophore for zinc, which has antiviral effects. The clinical trial studies provided in the specification of this patent application reveal that the claimed composition has a prophylactic effect against COVID-19; improves rhinitis, pharyngitis, and general symptoms of fatigue; decreases the need for the antibiotic duration; prevents acute respiratory distress syndrome (ARDS); protects lungs from infection/complications of COVID-19; can be used as an add on treatment for moderate cases infected with coronaviruses; and can be used as an antifibrotic drug for the treatment of interstitial pulmonary fibrosis.
WO2021257252A1 claims a composition encompassing luteolin (80 mg to 220 mg), quercetin (90 mg to 310 mg), kaempferol (80 mg to 220), vitamin C (475 mg to 525 mg), and a pharmaceutically acceptable carrier [45]. The claimed composition utilized quercetin as an inhibitor of the expression of the hACE-2 receptors, and luteolin as a furin inhibitor. It is claimed that both of these components reduce the pathogenicity of the SARS-CoV-2 virus. The presence of kaempferol and vitamin C in the composition enhances the bioavailability of luteolin and quercetin. The clinical studies data of the claimed invention reveal improvement in COVID-19 symptoms among patients after 1 day of the treatment, and the symptoms disappeared completely after 3 days.
WO2021255464A1 claims a nutraceutical composition comprising curcumin (1 to 8%), vitamin C (40 to 90%), chlorella (5 to 20%), spirulina, and Boswellia resin (1.0 to 15) that may optionally contain quercetin (0.5 to 5%) [46]. The clinical data provided in the patent application suggests that the claimed composition improves the COVID-19 symptoms among the patient. The composition utilizes quercetin as an antioxidant, antiviral, and anti-inflammatory compound. However, the clinical data are silent about the exact role of quercetin.
WO2021240481A2 claims an oral composition comprising hesperidin (10% to 25%), curcumin (15% to 35%), epigallocatechin (15% to 30%), rutin (10% to 25%), quercetin (0.5% to 8%), luteolin (1% to 10%), baicalin (1% to 15%), piperine (0.03% to 3%), and one or more excipients [47]. The claimed composition exhibits functional synergy among its ingredients; prevents virus replication and/or virus entry into human cells; modulates the immune response of the patient, and protects organs/cells. However, this patent application is silent about the functional role/rationale of using quercetin in the composition.
WO2021205083A2 relates to the composition containing 2,6-di-tert-butyl-4-methyl-phenol (BHT, 0.01 mg to 1 g) alone, or in combination with another antioxidant (quercetin, 100 to 200 mg) and/or an anti-inflammatory agent (N-acetylcysteine, 100 mg) possessing antiviral activity against SARS-CoV-2 [48]. The patent application provides in vitro data and clinical protocols related to the use of BHT and its compositions against SARS-CoV-2 infected cells. However, the patent application is published in French. The English translation of the text on Espacenet is not well defined. Therefore, the authors avoid discussing the experimental results due to a lack of clarity.
WO2021168173A1 claims a nasal composition of quercetin (0.5% to 25% w/w) and iota-carrageenan (0.05 to 5.0% w/w), along with other ingredients, including ethyl lactate [49]. It demonstrates that ethyl lactate increases the solubility of quercetin 10-fold. The examples demonstrate that the DMSO solution of quercetin (140 uM) inhibits the main protease (Mpro) of SARS-CoV-2 by about 95%, in comparison to disulfiram (a known protease inhibitor). Another example shows that iota-carrageenan treatment reduces the proportion of SARS-CoV-2 infected Vero cells in a dose-dependent manner. The third example verifies that the combination of quercetin and iota-carrageenan in different concentrations also reduces the number and the ratio of SARS-CoV-2 infected A549 cells. The composition is supposed to inhibit the viral entry into the cells by lowering the expression of hACE-2 receptors.
US2022040227A1 claims a composition comprised of copper chelator (tetra-thiomolybdate salt), a 5-lipoxygenase inhibitor (diethylcarbamazine or Zileuton), and quercetin [50]. This invention recognizes that the COVID-19 can become lethal because of its inflammatory damage to the lung/heart. The claimed invention treats COVID-19 because of its anti-inflammatory effects. This patent application is silent about the experimental data of the claimed invention against COVID-19.
US2021393579A1 claims a composition (sugar syrup) comprising anthocyanins (extracted from a food plant) and quercetin [51]. The composition uses a sugar-based agent (sucrose) to obtain the quercetin into a solution and to facilitate the absorption of quercetin in the body. The composition claims to improve the respiratory/joint health of the patient by reducing the inflammation of the lung cells/joints with the help of prophetic examples.
US2021386779A1 claims a composition containing a zinc ionophore (quercetin, 50 mg to 1500 mg) and a bio-assimilable form of zinc (Zn+2) (5 mg to 100 mg) to enhance the immune system function [52]. This dietary supplement may optionally contain l-lysine, vitamin C, vitamin D, and vitamin E. The clinical study data (5 weeks and 20 weeks) strongly suggests that zinc supplementation (25 mg daily) together with zinc ionophores (Quina tree bark extract and quercetin), along with vitamins C/D3/E, and l-lysine provides a strong protective prophylactic effect against COVID-19.
US2021361700A1 claims a composition encompassing at least two components selected from the group consisting of zinc (10–75 mg/day), quercetin (100–1500 mg/day), vitamin E (50–800 mg/day), and epigallocatechin gallate (EGCG, 300–600 mg/day) [53]. All four components of the composition were selected based on their antiviral effects against COVID-19. The patent application provides a prophetic clinical protocol to study the effect of the composition against COVID-19. The invention claims to reduce the hospitalization time, intubation time, disease duration, limit the clinical progression, and reduce the symptom severity of COVID-19. The composition also inhibits viral entry into cells and viral reproduction in the cell; increases T cell function; reduces inflammation, cytokine levels, reactive oxygen species, and tissue damage in the subject.
US2021290718A1 claims a composition (oral aerosolized spray) comprising quercetin, vitamin C (250 mg to 10,000 mg), vitamin D (1000 mg to 100,000 mg), zinc (5 mg to 100 mg), and artemisia to prevent/treat COVID-19 [54]. This is interesting to note that this patent application provides clinical studies related to the compositions of hydroxychloroquine, azithromycin, vitamin C, vitamin D, and zinc. However, it is silent about the rationale of quercetin and its concentration in the claimed composition.
CN112457281A provides quercetin disulfonated derivatives that block the binding of COVID-19 spike protein to the human angiotensin-converting enzyme 2 (hACE-2) [55]. One of the quercetin disulfonated derivatives, at a concentration of 7.6 μM, demonstrates 51.8% inhibition of the COVID-19 spike protein receptor-binding domain and Hela cells expressing hACE-2. The higher concentration (>250μM) also demonstrates more than 75% inhibition.
CN112263598A covers the aqueous ethanol extract of Tianjihuang [56]. The in vitro antiviral activity against SARS-CoV-2 infected VeroE6 cells demonstrate better antiviral activity of the Tianjihuang extract (IC50 = 12.70 µg·mL−1) than quercetin (IC50 = 52.24 µg·mL−1) and proleucoside B (IC50 = 32.84 µg·mL−1). However, no mechanism of action is postulated for the antiviral effect of the extract. The higher antiviral activity of the extract is attributed to its chemical constituents (quercetin, isoquercetin, quercetin B, quercetin, etc.).
CN112022845A claims the use of quercetin (dose 12.5 to 100 μg/mL) to treat COVID-19 [57]. The experiments reveal a reduction in the SARS-CoV-2 viral load in virus-infected Vero cells after 48 h of the administration of the DMSO solution of quercetin (2.86, 4.07, 23.31, and 1290 times reduction after the 12.5, 25, 50, and 100 μg/mL dose of quercetin), in comparison to non-treated virus-infected cells. The inventors identify that the dose of quercetin (>100 μg/mL) is cytotoxic for Vero cells. Accordingly, they suggest a dose of quercetin < 100 μg/mL to treat COVID-19. However, this document is silent about the mechanism of action of quercetin.
WO2021262749A1 claims a pharmaceutical composition comprising quercetin (0.1 g to 2.5 g), and hydrogen peroxide (1–3 mL) [58]. The claimed composition shows a surprising and unexpected antiviral effect against SARS-CoV-2. The composition further demonstrates improved results among cancer patients suffering from COVID-19, by inhibiting the PI3K gene. The clinical data provided in the specifications of this patent application supports the efficacy of the claimed invention against COVID-19, as well as among cancer patients sufferings from COVID-19.
7. Conclusions
The clinical trials, inventive compositions, and the patent literature on quercetin demonstrate its potential as a prophylactic/therapeutic agent against COVID-19, because of its inhibitory effect on the expression of the human ACE2 receptors, enzymes of SARS-CoV-2 (MPro, PLPro, and RdRp), antioxidant activity, anti-inflammatory activity, and immunomodulatory activity. Quercetin is a GRAS substance, as per the USFDA. Accordingly, it may be used in combination with clinically used antivirals, and drugs that control the symptoms of COVID-19. Therefore, the authors imagine the development of many more quercetin-based inventive/patentable compositions as monotherapy or combination therapy for the prevention/treatment of COVID-19. However, the potential interactions between the combined drugs must be understood before developing a new composition.
8. Discussion
Quercetin is an established antioxidant and anti-inflammatory compound [18]. It demonstrates its anti-COVID-19 activity by inhibiting the expression of ACE2 receptor, and enzymes of SARS-CoV-2 (3CLPro and RdRp) (Figure 1). These facts were confirmed based on in silico, in vitro, in vivo, and clinical studies (Table 1 and Table 2) [12,14]. The infection of SARS-CoV-2 can also cause cytokine storms. If untreated, the cytokine storm leads to blood clotting, multiple organ failure, and ultimately death (Figure 1) [3]. Quercetin can prevent the trigger of a cytokine storm, and blood clotting, due to its antioxidant, anti-inflammatory, and anti-thrombin activity [12]. The clinical studies on quercetin-based monotherapy and combination therapy with zinc, vitamin C, curcumin, vitamin D3, masitinib, hydroxychloroquine, azithromycin, and ivermectin were promising against COVID-19 (Table 1) [31,32,33]. These clinical studies demonstrate faster recovery and a decrease in the hospitalization time of the COVID-19 patients. Quercetin is also in a clinical trial for diseases such as oxidative stress, inflammation, cardiovascular diseases, and carcinoma [30]. Therefore, the compositions containing quercetin may be useful to treat COVID-19 among the high-risk population (hypertensive, diabetics, cancer, etc.). The initial SARS-CoV-2 infection does not need advanced treatment. Quercetin is present in many fruits, vegetables, and health supplements. The studies also advocate a regular intake of quercetin-containing food (onion, etc.) and quercetin supplements during the pandemic [14]. However, it is still questionable if quercetin-rich food/supplements can be used prophylactically for COVID-19 among the high-risk population. Quercetin is lipophilic and its low water solubility limits its absorption [16]. This led to the discovery of a phospholipid-based delivery system of quercetin with improved bioavailability, which displays promising outcomes to treat/prevent COVID-19 [33]. This discovery opens the doors to developing more anti-COVID-19 quercetin conjugates, prodrugs, liposomes, nano-formulations, and nano-particle systems possessing a better pharmacokinetic profile.
The authors searched the patent literature on quercetin and COVID-19. Most of the patent applications were filed in the United States (Figure 4). The majority of these patent applications were published in 2021, which is expected. Many of these patent applications provide evidence (in silico, in vitro, in vivo, and clinical studies) for the prophylactic/therapeutic potential of quercetin and its nutraceutical/pharmaceutical compositions (oral and inhale formulations) against COVID-19 (Table 2).
Figure 4.
The patent application filing countries related to the quercetin-based anti-COVID-19 compositions.
The anti-SARS-CoV-2 effect of quercetin in specific doses (12.5 to 100 μg/mL) is claimed in a Chinese patent application [57]. This patent application filing also strengthens the concept of utilizing quercetin as an anti-COVID-19 agent. The combinations of quercetin with favipiravir, remdesivir, molnupiravir, navitoclax, dasatinib, disulfiram, rucaparib, tamarixin, iota-carrageenan, and various herbal extracts (aloe, poria, rosemary, and sphagnum) are also claimed in patent applications (Table 2 and Figure 5) [43,44,45,46,47,48,49,50,51,52,53,58]. Most of these combinations were developed as an oral dosage form (tablet, solution, capsule, oral inhaler, etc.), and reveal synergistic/additive anti-SARS-CoV-2 effects. It is quite interesting to note that the patent applications claim combinations of quercetin with a large number of antioxidants, antivirals, immunomodulators, and anti-inflammatory agents. However, these patent applications exemplify the anti-SARS-CoV-2 effect of only a few combinations (Table 2). This indicates that there are a large number of experimentally unexplored quercetin combinations. Therefore, there is a high possibility that some of the experimentally unexplored quercetin combinations may provide unexpected/surprising results against COVID-19.
Figure 5.
Important anti-COVID-19 combinations of quercetin [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96], Table 2.
It is important to note that quercetin is an acidic compound [18], due to the presence of phenolic groups in its structure (Figure 1). Therefore, it shows the acid–base interaction with basic drugs/compounds (Figure 6). This interaction affects the biological response of quercetin. Quercetin is also a GRAS substance, according to the USFDA., but it can alter the metabolism of some drugs [18]. The literature has highlighted interactions of quercetin with many drugs, including ivermectin, antibiotics (azithromycin, ciprofloxacin, ofloxacin, itraconazole, and posaconazole), antivirals (indinavir, nelfinavir, ritonavir, and saquinavir), and steroidal anti-inflammatory drugs (cortisone and dexamethasone). It is known that the treatment of COVID-19 encompasses antivirals, antibiotics, and anti-inflammatory agents. Accordingly, the authors trust that the physicochemical and metabolic drug interactions of quercetin must be understood before making a combination of quercetin with other drugs/compounds. Further, quercetin is also an established metal ionophore [19]. It binds with beneficial metals like zinc, which provides a synergistic effect. However, the binding of quercetin with non-beneficial metals should also be considered while making combinations.
Figure 6.
Factor that may affect the quercetin-based drug combinations.
To date, many variants of COVID-19 (α, β, γ, δ, Omicron, etc.) with a high transmission rate were identified [2]. The appearance of these variants is posing challenges to the existing vaccines and drugs (molnupiravir and remdesivir) used against COVID-19 [2,43]. A multicomponent composition comprising quercetin that is effective against coronavirus mutants is reported [44]. However, the specific use/effect of quercetin against coronavirus mutants is not clarified in this report [43]. The emergence of many variants of COVID-19 makes it essential to develop safe and inexpensive treatments for COVID-19. Quercetin is a GRAS substance, inexpensive, and demonstrates beneficial effects among the high-risk population. The authors foresee quercetin as a potential candidate to develop an anti-COVID-19 therapy. Therefore, quercetin, and its drug combinations, must be explored clinically on a large scale to identify a potential quercetin-based COVID-19 treatment. The clinical efficacy of quercetin against emerging variants of COVID-19 (α, β, γ, δ, Omicron, etc.) also needs further investigation.
Author Contributions
Conceptualization, M.I., A.A., H.K.T. and S.M.B.A.; methodology, M.I. and A.A.; software, S.I.A.; validation, S.A. and M.K.; formal analysis, A.D. and M.K.; investigation, M.K.A. and A.R.A.; resources, S.A.; data curation, S.I.A.; writing—original draft preparation, A.A., M.K.A., H.K.T., S.I.A. and A.R.A.; writing—review and editing, M.I., M.K.A. and S.M.B.A.; visualization, A.D. and A.R.A.; supervision, M.I.; project administration, S.A.; funding acquisition, S.A. and H.K.T. All authors have read and agreed to the published version of the manuscript.
Funding
This work was funded by the Deputyship for Research and Innovation, Ministry of Education, Saudi Arabia, via grant number “IF-2020-NBU-217”. The APC was also funded by the Deputyship for Research and Innovation, Ministry of Education, Saudi Arabia.
Acknowledgments
The authors extend their appreciation to the Deputyship for Research and Innovation, Ministry of Education, Saudi Arabia, for funding this work through the project number IF-2020-NBU-217.
Conflicts of Interest
The authors declare no conflict of interest.
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