key: cord-1030264-2rzohcxe authors: Noor, Nairah; Gani, Adil; Gani, Asir; Shah, Asima; Ashraf, Zanoor ul title: Exploitation of polyphenols and proteins using nanoencapsulation for anti-viral and brain boosting properties – Evoking a synergistic strategy to combat COVID-19 pandemic date: 2021-03-11 journal: Int J Biol Macromol DOI: 10.1016/j.ijbiomac.2021.03.028 sha: 4435e7cc374e570945f4fde8a7c9f340d8990cf5 doc_id: 1030264 cord_uid: 2rzohcxe The world is currently under the threat of COVID pandemic and has focused every dimension of research in finding a cure to this novel disease. In this current situation, people are facing mental stress, agony, fear, depression and other associated symptoms which are taking a toll on their overall mental health. Nanoencapsulation of certain brain boosting polyphenols including quercetin, caffeine, cocoa flavanols and proteins like lectins can become new area of interest in the present scenario. Besides the brain boosting benefits, we have also highlighted the anti- viral activities of these compounds which we assume can play a possible role in combating COVID-19 given to their previous history of action against certain viruses. This review outlines the nanoencapsulation approaches of such synergistic compounds as a novel strategy to take the ongoing research a step ahead and also provides a new insight in bringing the role of nanotechnology in addressing the issues related to COVID pandemic. The prospectus of anti-viral and brain boosting compounds derived from natural sources is more promising and some of these can grab a great deal of attention in coming years owing to their initial reports of anti-viral and brain stimulating effects. The domain of their health promoting factors is very wide which can have great scope amid this pandemic situation. The natural compounds including polyphenols and proteins have been studied over years to explore their anti-viral and brain stimulating effects. Summary of natural compounds with their anti-viral and brain boosting properties are given in Table 1 and 2. Some of these worth mentioning are: Table1. Summary of some polyphenols with anti-viral properties, their possible mode of action and target virus. Reported mechanism of action Effective against virus 1. Quercetin Inhibits viral entry and translation Ebola virus 12 Polio virus 13 Hepatitis C 14 Coronavirus 15 Mango virus 16 Pseudorabies virus 17 2 Resveratrol -Inhibits replication, protein synthesis, gene expression, and nucleic acid synthesis of virus -Inhibits viral attachment. HSV 18 Influenza 19 Rhinovirus 20 MERS-CoV 21 3 Fisetin, Rutin Induce inhibition of cytokine expression and synthesis 22 6 Kaempferol Inhibits secretion of many cytokines including IL-6 and IL-8. Human cytomegalovirus J o u r n a l P r e -p r o o f Coxsickie B virus 24,25 7 Myricetin Inhibits ATPase activity SARS-CoV 26 8 Theaflavin Inhibits RdRp activity SARS-CoV-2 26 9 Caffeine Promising inhibitors for 3-chymotrypsin-like protease of SARS-CoV-2 SARS-CoV-2 27 10 Tingenone Inhibits SARS-CoV 3CLpro SARS-CoV 26 11 Quercetin-3β-galactoside Competitively inhibits SARS-CoV 3CLpro SARS-CoV 26 12 Emodin Blocks the binding of S protein to ACE2 SARS-CoV 26 HSV-Herpes Simplex Virus, MERS-CoV-Middle East respiratory syndrome coronavirus, H1N1-Influenza A virus, RSV-Respiratory syncytial virus, CA-Coxsackievirus, CDV-Canine distemper virus, SARS -CoV severe acute respiratory syndrome coronavirus. Table 2 . Summary of the natural compounds with brain boosting activity. Category Reported mechanism of action 1 Epigallocatechin gallate (EGCG) Polyphenol Cross (BBB) model and protect neurons from oxidative-stressinduced cell death 28 2 Resveratrol Polyphenol -Modulate growth of dendrites and axons 29 -Decrease neuroinflammation 30 -Activates Protein kinase C gamma that help in neuroprotection 31 (2-(3,4- dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one) is the most widely available flavonoid compound present in green tea and has been reported to prevent neurons against apoptosis and oxidative stress [3] . Over the years, flavonoids have been recognized as agents that affect the central nervous system in a beneficial manner including the stimulation of neuronal regeneration, enhancement of neuron functionality, ability to prevent the susceptible neurons and inducing neurogenesis [34] [35] [36] [37] . Quercetin also has the ability to prevent cell apoptosis in hippocampus which is considered as the centre of processing the spatial memory and presents a clear view that it can be used as a novel agent to treat oxidative stress [3, 38] . It has anti-viral activity against RNA viruses due to its ability to inhibit reverse transcriptase of these viruses [39] . This feature can enable it to find great application in medicine as commonly used inhibitors including acyclovir and arabinosides have toxic nature and are not only lethal to viral cells but also damage the normal cells [39] . Apart from this, docking studies reveal that quercetin exhibits an inhibitory effect on Akt activity enabling cell survival, inhibits Cs2+-ATPase, ATPase of sarcoplasmic reticulum, protein disulfide isomerse and binds to CLUT1 thereby inhibiting glucose efflux [40] . Also quercetin (100µg) has been employed as the main ingredient in Gene-Eden-VIR/Novirin which is a patented herbal broad-spectrum antiviral treatment and was subsequently studied for its anti-viral activity against betacoronavairus [41] . The samples of COVID-19 patients depicted that COVID-19 strain is a betacoronavirus having close resemblance to human Severe Acute Respiratory Syndrome (SARS-CoV) accounting to 79 .5% sequence identity [42] , 96% identical 3-Chymotrypsine-Like protease (3CLpro) amino acid sequences [41] . In a 2012, a study carried out by Nguyen et al. reported that quercetin in combination with Epigallocatechin Gallate displayed inhibitory effect against 3CL pro the main protease of SARS exhibiting an IC50 of 73uM in vitro [43] . Quercetin has also shown its inhibitory action against 3CL pro and PL pro protease of SARS with IC50 value of 52.7uM and 8.6uM and 3CL pro protease of Middle Eastern Respiratory Syndrome virus (MERS) with IC50 value of 34.8uM in vitro [7] . Further quercetin can regulate the unfolded protein response (UPR) of cells and as coronaviruses use UPR for the completion of their life cycle so administration of quercetin can have inhibitory effects on their activity via modulation of the mentioned pathway [44] . A generalized mechanism of action of polyphenols on entry of viral particles is given in The most widely available sources of caffeine include coffee, tea, chocolate bars, cocoa beverages and soft drinks etc. Caffeine (1, 3, 7-trimethylxanthine) is the major psychostimulant that has been studied for its antagonist reaction towards adenosine receptors and for inhibition of phosphodiesterase 3 (PDE3) [45] . With the result, caffeine has been associated with numerous mechanisms that describe the pathology of depression [33] . Recent years saw a great work highlighting the role of caffeine in affecting the neuroinflammatory hypotheses of depression including tryptophan catabolism, oxidative stress and inflammation [33] . These pharmacological effects of caffeine have made it a potent source of increasing alertness, as a stimulator of CNS and relaxant of smooth muscles [46] . In vivo studies have also revealed the anti-depressant effects of caffeine and it has been reported that the chronic administration of 8mg/kg/day was able to reduce the symptoms of depression and the hippocampal secretion of serotonin and dopamine levels were comparable to that of the tricyclic deimipramine (10 mg/kg/day), which is J o u r n a l P r e -p r o o f the common anti-depressant [4] . Apart from these brain-boosting effects, caffeine has also displayed the anti-viral activity against Human immunodeficiency virus type I (HIV-1) [8] . An essential step of replication for this virus involves (HIV-1) DNA integration and this stage is usually accompanied with damage to cellular DNA and therefore needs certain cellular repair proteins for its completion which includes ATR (ataxia telangiectasia and Rad3 related), DNA-PK (DNA-dependent protein kinase) and in some cases, ATM (ataxia telangiectasia mutated). Caffeine has shown to inhibit ATR and ATM kinases which form a potent target site for anti-HIV therapeutics [8] .This tendency of caffeine can reduce the replication rate of HIV-1 lifecycle. This property of the caffeine can make it an attractive agent to be included in various COVID drug formulations. The immunomodulatory effect of caffeine has been attributed to antagonist activity of its adenosine receptors and cAMP-phosphodiesterase which work in a dose dependent manner [47] . Also caffeine treatment lowered the growth rate of tumors which was possibily due to the antagonist activity of adenosine A2A receptor. The activation of A2A receptors of T cells by adenosine results in reduction of CTL proliferation, cytokines (TNF-α and IFN-γ) production and expression of programmed cell death [48] . Caffeine has also been studied for anti-HCV drugs and reported replication of HCV by preventing its replication. The mechanism of action has not been ascertained yet. Also the expression of certain proteins such as heat shock protein 90 (HSP90), COX-2 and Ras-ERK also reduced in cells resulting in inhibition of HCV replication [49] . The long term consumption of caffeine has also been observed to elevate IFN-γ [50] . Thus it can be considered as potential candidate for further investigations in SARS-COV-2 interventions [51]. Lectins are the category of proteins that have the ability to bind carbohydrates that contain at least one non-catalytic domain which can attach itself reversibly to a particular saccharide [52] . The lectin isolated from banana binds particularly to glucose and mannose. These are proposed to possess antiviral properties due to the ability to bind to different types of glycans (having high densities of glycoproteins) which are present on the surfaces of viruses ( Fig 2) . Due to the presence of two key glycoproteins in influenza viruses namely, hemagglutinin (HA) and neuraminidase (NA), which play a major role in the replication cycle of influenza virus lectins have shown a potential anti-viral activity against influenza viruses. Furthermore, these viral glycoproteins serve the other functions such as binding the sialic acid-containing cell J o u r n a l P r e -p r o o f receptors and the viral membrane with the endosomal membrane, breaking the sialic acid entities resulting in release of virus and aggregation of the new virus particles [9] .The sensitivity of corona virus towards mannose specific lectins has been reported earlier in severe acute respiratory syndrome. The mechanism of their action towards corona virus has been attributed to their property to inhibit the viral attachment in early stages of replication and also decelerating the development of virus by binding towards the end of infection cycle [53] . But the use of lectins against the influenza viruses has limited applicability owing to their mutagenicity which results in inflammatory side effects [54] . In this context, an engineered banana lectin has been developed by inducing the mutation of single amino acid from histidine to threonine at position 84 called as (H84T BanLec, H84T) [9] . H84T when administered inernasally, is highly effective against avian influenza (in vitro), epidemic, pandemic, and fatal viral influenza infection (in vivo) [9] . However, the effects via other routes of administration and overall safety need an indepth research. EC50 values of rBanLec H84T for H1NI and H3N2 virus were reported to be ranging from 1-4 µg/mL and 0.06-0.1 µg/ml and for HCV genotypes ranging from 8.8-20.8 nM [55] . Also in vitro studies have revealed that lectin from bananas can modulate the immune cells [56, 56] . In a study carried in 2012 Dimitrijevic et al. reported that the oral administration of recombinant banana lectin in mice displayed a reaction with the mucosal membranes and triggered the formation of anti-bodies [58] . Also it has been reported that banana lectin through the medium of peripheral human cell cultures can produce IgG4 [59] . In a study carried in 2006, Allen et al. reported that a fructose binding lectin was isolated from Del Monte banana and it had the ability to induce cytokine interferon-gamma expression and inhibit the activity of HIV-1 reverse transcriptase and were subsequently suggested in anti-HIV formulation [60] . Since lectin has demonstrated a high anti-viral activity in the influenza type infections, focused and in depth study will provide more evidences in using these anti-viral compounds in drug formulations to combat COVID-19. In terms of brain boosting activity, lectins from marine alga Solieria filiformis lectin (SfL) reported anti-depressant effects in mice which were mostly due to its interaction with the dopaminergic system [61] . Another lectin ConBr obtained from Brazilian bean C. brasiliensis having affinity for mannose/glucose displayed an anti-depressant action by activating monoaminergic system in mice using forced swimming test [62] . Also it was shown that ConBr could prevent cell death, cause blocking of seizures, act as the inhibitor of N-methyl-D-aspartate (NMDA) receptor J o u r n a l P r e -p r o o f activation and can block the hippocampal neurotoxicity triggered by glutamate in vitro and quinolinic acid in vivo demonstrating the neuroprotective action via modulation of glutamatergic system [5, 62] . So with the proven brain boosting activity of lectins, lectins from banana can also be looked into for similar effects and projected as a novel compound to combat the depressive and viral conditions of COVID-19. The summary of some anti-viral Lectins with their EC50 values against SARS-CoV are given in Table 3 . Crandell Feline kidney cells. Lectins EC50 (µg/ml) CC50 (µg/ml) 1 GlcNAc-specific agglutinins  PallGlcNac  Nictaba Gal-specific agglutinins  Morniga G II 50±13 >100 5 Man/Glc-specific agglutinins  Cladistris 7.4±0.2 >100 GlcNac: N-acetyl glucosamine, Man: mannose, Gal: galactose. GalNAc: N-acetyl galactosamine. Adapted from the study of Keyaerts et al., (2007) [53] with permission from Elseiver. There is a high demand for cocoa and its derivatives worldwide given to their great sensory attributes. It is a rich source of polyphenols especially the flavonoids like (+)catechin, (−) -epicatechin, and their dimmers like B1 (PB1) and procyanidins B2 (PB2) [63] . The daily intake of the cocoa flavanols have been reported to enhance sensitivity of insulin, decrease the blood pressure and fat oxidation and most importantly improve the brain function by increasing the flow of blood in the brain via spiked vasodilation [64] [65] [66] . The proper functioning of brain and the neuroprotection in mammals has been linked to the neurotrophic factors which play a key role in such regulation [67] . Also there are growing evidences that suggest the association between the neurotropic factors, brain and the polyphenolic compounds. Polyphenols are classified flavonoids, stilbenes, phenolic acids, and lignans. Their neuroprotective activities have been investigated in animal model studies indicating their ability to affect various pathological states of the nervous system including the modulation and protection against building up of ROS and oxidative stress, inflammation, dysfunctioning of mitochondria, accumulation of metals and all those processes that lead to the neurodegenerative diseases [6] . Furthermore, polyphenol and flavonoid rich diets have also been linked to alleviate the risks associated with neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, Huntington's disease, stroke and multiple sclerosis [6, 68] . The mechanism of their neuroprotective action and cognition activity is due to their modulatory effects on gene expression and cell death process via neuronal pathways. For instance, flavonoids inhibit MAP kinase cascades like p38 or signaling of ERK1/2 which affects the cytokine production and transcription factors like TNF-α, NF-κB and interleukines in iNOS that are the key determinants of the neuro-inflammatory response in the CNS [69] [70] [71] . The recent study on human Alzheimer's disease using an in vitro model, revealed that the polyphenolic extract of cocoa spiked the BDNF/ TrkB signaling pathway thereby increasing neuroprotection [72] . Also its regular consumption has been linked to improved cognition and decrease in the risks associated with Alzheimer disease (AD) [73] [46] . The principle flavanol present in cocoa is epi-catechin and plays the great role in regulating the vascular function such as regulation of blood pressure and vascular tone due to increase in the bioavailability of nitric oxide [74] . Also cocoa flavonols can accumulate in hippocampus which aids in improving the memory and learning [75] . There has been a growing research which provides great evidence that intake of the cocoa -derived products and chocolate consumption can aid in improving memory and attention in people with decrease in cognition thereby J o u r n a l P r e -p r o o f improving the neurocognitive and neuroprotective functions [74] . In terms of the anti-viral activities, flavonoids can influence the IgM and IgG in blood circulation and many such polyphenolic extracts have been associated with the anti-viral activities against poxviruses, influenza, HIV-1 and herpes [76] . Although no in depth study has been made with respect to the anti-viral activity of polyphenols extracted from cocoa, but in general polyphenols, particularly flavonoids has been reported to inhibit the fusion of viral membrane with that of the lysosome [10] . The underlying mechanism of this anti-viral activity of the flavnoids is still unknown but it is assumed that flavonoids inhibit PG's that help in fusion of cell membranes [77] . Also, flavonoids have been reported to inhibit the proton pump which acidifies and activates lysosomes [78] . Another anti-viral property of flavanoids is the production of IFNs. These compounds exhibit their anti-viral effects through modifying the process of phosphorylation behavior of protein translation eIFs (Eukaryotic initiation factors) resulting in stoppage of biosynthesis of all proteins including that of viral proteins, production of nucleases that attack the genome of virus and fortifying the membranes [79] . In vitro studies have shown that flavonoids also exhibit the anti-viral activity against human immune deficiency virus (HIV) [80] . Nanotechnology has been widely used to carry out the target delivery of nutraceuticals and other therapeutics. The engineered nanoparticles possess high surface to volume ratio, good J o u r n a l P r e -p r o o f absorption properties and many bioactive components including resveratrol, curcumin, polyphenols, genistein, lycopene, anthocyanins and quercetin have been subjected to nanoencapsulation to combat the poor water solubility, low oral bioavailability and low taste profiles. Various techniques of encapsulating these target compounds have been explored including the designing of various nanocarrier systems including liposomes, nanosuspensions, nanoemulsions, nanodimensionsal lipid transporters, host matrices or micelles made up of polysaccharides, nanometer phytosomes proteins or their conjugates or complexes and solid lipid nanoparticles (SLNs) [81] . In addition to these, many inclusion complexes made up of amylose and cyclodextrins, nanotransporters like yeast cells, nanogels, nanofibres and nanosponges fabricated from polysaccharides and lipids have been employed for nanoencapsulation [82] . With the massive research going in the field of nanoscience, different carrier systems have been employed to carry forth the bioactive compounds. A novel approach for designing the nanodelivery system may be the structuring of colloidal delivery system [83] . A number of such delivery systems including starch nanocomposites and chitosan-coated liposomes have been used to encapsulate curcumin [84, 85] . Similarly for encapsulating resveratrol soy protein isolates have been used as wall materials [86] . For quercetin delivery a novel strategy was employed by encapsulating the bioactive in nanostructures like nanotubes and conjugates [87] [88] [89] [90] . Also, superparamagnetic iron oxide nanoparticles (SPION) have been used as the carriers of quercetin owing to superparamagnetic nature, high ratio of spin polarization and elevated conductivity [91] . The use of this delivery system has added features like sensitivity to diagnostic tests, target delivery to amyloid beta (Aβ) in the brain arteries, inhibition of microglial cells, detection of DNA and magnetic resonance imaging (MRI) [92] [93] [94] [95] . Still the toxicity of SPION is a major issue in its rapid commercialization. For caffeine, which is an amphiphilic drug having considerable lipolytic activity, many host compounds have been used as wall materials including liposomes, concentrated protein hydrogels, poly-(epsilon-caprolactone) polymer, cyclodextrins, niosomes, PLGA-mPEG copolymers and silica [96] . Encapsulation controls the release of caffeine and ensures its stability from rapid degradation, enables its target delivery and masks the bitter taste of caffeine [46] . In 2014, Bagheri et al. prepared the nano-particles of caffeine (300 nm) loaded in bioactive peptides (whey proteins) which were further encapsulated in alginate microparticles resulting in a more stable system and accounted for the slow release of caffeine in the gastric fluid [97] . A J o u r n a l P r e -p r o o f copolymerized temperature and pH-sensitive nanogel termed as poly (NIPAM-co-AAc) comprising of poly (N-isopropylacrylamide) (polyNIPAM) and 5% acrylic acid (AAc) was used as a drug carrier system for delivery of caffeine [98] . It was shown that in vitro diffusion of caffeine loaded in poly (NIPAM-co-AAc) at 2-4 •C enhanced the delivery of caffeine by the magnitude of 3.5 as compared to the saturated solution of caffeine. Since the nanogels were stimuli-reponsive, so the release of encapsulant (caffeine) was directed by the changes in its temperature which was the major stimuli for release of caffeine. Nanostructures like electrospun nanofibres have also been a recent area of interest in drug delivery systems and many polymers have been investigated for their applicability to form nano fibres like fibrinogen, collagen, poly (lactic acid), chitosan and poly (d,l-lactide-co-glycolide) [99] . Electrospun poly (lactic-coglycolic acid) fibre meshes have been employed as the carrier system to release retinoic acid [100] , electrospun poly (dl-lactide) nanofibres have been used for controlled release of paracetamol [101] and electrospun nanofibers made from poly-caprolactone have been used for the drug metronidazole benzoate for treatment of periodontal diseases [102] . A similar attempt with respect to these electrospun nanofibres as medium to act delivery systems have been put forth [99] . The workers employed electrospun polyvinyl-alcohol nanofibers as oral fastdissolving delivery system and the results displayed that caffeine was released in a burst about 100 % within 60 s from such nanofibres. The latest nano carrier system has been produced using the Gold nanoparticles (Au NPs), which serve as the affinity probes for the trapping lectins like BanLec [103] Con A [104] [105] [106] , and ricin B [107] [108] [109] . In a study carried out by Selvaprakash & Chen al. functionalized gold nanoparticles (AuNPs) were generated from chicken egg white (cew) proteins. The obtained Au@cew nanoparticles were then encapsulated within ovalbumin, whose surface was enriched with hybrid mannose and Galβ (1→4) GlcNAc terminated glycan ligands. Thus the complex generated from such fabrication i.e. Au@cew NPs encapsulating hybrid mannose and Galβ (1→4) GlcNAc were used to bind the specific lectins. The workers used various model lectins including Banna lectin, concanavalin A and ricin B that posses certain binding moieties towards particular sugars like mannose, glucose, and β-lactose. The results revealed that Au@cew nanoparticles can bind lectins and selectively release them using specific sugar moieties like glucose, mannose and β-lactose as the releasing agents from Au@cew NP-lectin conjugates [110] . For flavanols, which belongs to the category of polyphenols, low water solubility due to high molecular weight may be a constraint for their bioavailability [111] . Also their stability in the gastro intestinal tract is very poor and degrades easily in acidic medium. In a study carried out by McGhie and Walton, at a pH of intestinal tract, anthocyanins displayed poor stability [112] . Similarly, for polyphenol like EGCG, pH below 1.5 resulted in poor stability whereas nanoencapsulation resulted in the doubling of stability at pH 1.2 [113] . In general encapsulation of polyphenols in generated nanoparticles increases their water solubility as shown by encapsulation of curcumin in the chitosan or (poly-lactic-co-glycolic acid) nanoparticles [114] [115] [116] [117] [118] [119] . Since the site of absorption of polyphenols is the small intestine and because the epithelia of small intestine have no specific receptors, so the polyphenols are transported via passive diffusion [120, 121] . Nanoparticles encapsulating polyphenols can improve the transportation by inducing paracellular or transcellular mechanism [122] . Also nanoparticles can disrupt the tight junctions of the epithelial cells which favours the entry of these polyphenols. Overall nanoencapsulation of these synergistic compounds may become a good area of research in the coming times due to role of these bioactives as an anti viral and brain boosting system. The delivery of anti-viral drugs into the upper respiratory tract is often exposed to a number of hurdles including lower flow of blood, small surface area, presence of a mucus layer trapping the inhaled entities and filtration of foreign bodies [123] . The ideal environment for the effective drug delivery might be the presence of large surface area and ciliated cells which are present in the lower respiratory tract but even these pose certain challenges including branched alveolar macrophages and presence of phospholipids, proteins and mucins which acts as surfactants and decrease drug efficiency [124] . To address these issues, nano delivery system can be employed due to their enhanced features. A novel strategy of applying nanotechnology has been demonstrated recently in which Novochizol, a potential COVID-19 drug has been formulated using an advanced delivery system. The drug delivery system is comprised of a nanoparticlebased aerosol in which chitosan nanoparticles (forming the polysaccharide delivery system) adheres to the wall of lung epithelia and provides for sustained release [125] . Talking about plant based therapeutics, the herbal metal nanoparticles obtained by green technology presents a novel strategy for combating the chronic respiratory disorders due to the minimal toxicity, physiological compatibility, scalability and cost effectiveness [128] . The metal nanoparticles derived from plant source offers an ability to block the entry of viral particles inside the healthy cells which prevents the propagation of these viral particles [129] . Apart from these benefits, the unique magnetic, physicochemical and optical properties of the metal nanoparticles enable them to be modified into a sensor to detect the presence of virus or evaluate the buildup of metabolites generated by the virus infection. Quantum dots have also been proposed to act as antiviral agents. "Quantum dots (QDs)," also called as "semiconductor nanomaterials," are based on longterm fluorescence imaging of cellular processes. Their size ranges from 1 to 10 nm with tunable optical wavelength. As such these can be used as a novel probes for molecular imaging [131] . The use of QDs in combating SARS-CoV-2 infections can become a great area of research owing to its ability to be traceable under specific wavelength of light, to be tunable to desired range of sizes (1-10nm) and shape. Owing to their nano size and shape, QDs can easily penetrate SARS-CoV-2 with size ranging from 60 and 140 nm [132] . QDs can also not only sequester the S protein of SARS-CoV-2 due to their positive surface charge but their cationic surface charge can also intereact with negative RNA strand of the virus, creating reactive oxygen species within SARS-CoV-2. [133] . In a study reported by Du et al., reported the antiviral activity of carbon dots (CDs) against respiratory syndrome virus, pseudorabies virus and porcine reproductive virus [134] . CDs can activate interferonstimulated genes in particular interferon-α which can suppress viral replication. In a recent study by Loczechin et al, CDs were prepared by hydrothermal conjugation and carbonization with boronic acid (carbon quantum dots-3) and were observed to show anti-viral activity against pathogenic human coronavirus in a dose-dependent manner [135] . Overall nanoparticles can deliver range of anti-viral moieties and target both the adaptive as well as innate immune system. The nanodimensions and the flexibility are the key features for developing a vaccine in future. Nanoparticles can not only be administered orally but intranasal, subcutaneous and intramuscular routes are also an option. The potential of nanotechnology in fighting this deadly disease has not only been realized in context of developing a nano-vaccine but by delivering the nano-based anti-viral agents. In case of former, scientists have proposed the designing of the virus-like nanoparticles i.e. NANOparticles (1c-SApNPs) a self assembling protein bearing SARSCoV-like 2 protein spikes (StatNano.com.). As reported the system can J o u r n a l P r e -p r o o f Journal Pre-proof stimulate the immune system to generate anti-bodies which can be detrimental to coronavirus and ultimately offer the first hand protection against real SARS-CoV-2 virus [136] . The system exploits the characteristic properties of high surface area to volume ratio of nanoparticles in association of the virus surface proteins to evoke an immune response. The system has certain shortcomings as well, particularly in terms of manufacturing and cost effectiveness of the process. To overcome these short comings, novel vaccines based on messenger RNA (mRNA) have been suggested. These produce viral proteins through the action of host body on synthetic mRNA of the virus. The development of such nanovaccines using nanotechnology has a tremendous potential of bringing forth the possibilities of eliminating this deadly virus. For instance, angiotensin-converting enzyme 2 (ACE2) receptor is a known receptor for SARS-CoV and related human respiratory coronavirus NL63 present in the lung parenchyma and epithelium of air passage [137] . So a strategy of developing the SARS-CoV nanovaccine will lie in the delivery of the oral synthetic mRNA which will target the interaction sites between SARS-CoV and ACE2 and thus uplift the immunostimulatory effect of vaccine. Apart from these nanovaccines, which seems to the reliable possibility, other immune boosting anti-viral agents can also be targeted for inhibiting the either the replication or entry of virus. For this purpose nano based vehicles have already entered in line for instance, nanoparticles attached to ligands have shown the ability to act as a barrier on the cell wall to prevent the entry of virus. Another preventive strategy has shown that polyphenols have intrinsic anti-viral properties which can enhance the synthesis of pro-inflammatory cytokines and interferon-stimulating genes (ISGs) by the host cells and these can retard the production of negative-strand RNA of the virus and prevent the entry of viral particles inside the cell membrane [138, 139] . Since the virus are structurally different and phylogentically apart, so the vaccines which will be developed in future will be virus specific. In such a situation, a promising strategy will be to develop broad spectrum anti-viral nanoparticles which will help in prevention and treatment of COVID-19. So reviewing the novel anti-viral agents and their nano based delivery systems might generate an approach of devising the treatment to combat COVID-19. The overall scenario created by this pandemic has put a tremendous pressure on the workers to look into every possibility to come with the anti-virals and associated compounds that can alleviate the COVID symptoms. The mental agony and trauma inflicted upon the COVID J o u r n a l P r e -p r o o f patients and general masses has surpassed like never before. So it becomes the need of the hour to focus the research towards those naturally occurring substances which can help to reduce these complications as no chemical therapeutic is available till date. In order to provide comprehensive information of such compounds we have reviewed some naturally occurring compounds including quercitin, lectin, caffeine and cocoa flavonoids for their brain stimulating and anti-viral activities. Further we have summed up few nano-carrier systems for such synergistic compounds. Nanoencapsulation of these target compounds may provide a new area of research to derive the benefits and modify the pharmacologically active part of these compounds. There are no conflicts to declare. 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