Is Nanotechnology Helping in the Fight Against COVID-19?

Introduction

For approximately two decades, the world has faced several outbreaks of viral diseases, including Ebola, Influenza A (H1N1), Severe Acute Respiratory Syndrome (SARS), Middle East Respiratory Syndrome (MERS), and Zika. All of these diseases had a significant impact on the global economy and public health (Boopathi et al., 2020). SARS was the first epidemic of the twenty-first century, reported in November 2002 in Guangdong, China, followed by MERS, in Jeddah, Saudi Arabia, a decade later in June 2012 (Lau and Chan, 2015; Zheng et al., 2019). In November 2019, the total number of confirmed cases of MERS-CoV infection reported by the World Health Organization (WHO) was 2,494, including 858 deaths, covering 27 countries. During the SARS-CoV outbreak, 26 countries were affected, with 8,096 confirmed cases and 744 deaths (Hassan et al., 2020; Hua et al., 2020; Wang et al., 2020a).

In December 2019, a new coronavirus (CoV), causing atypical pneumonia was reported in Wuhan, China (Du et al., 2020). The Chinese Center for Disease Control and Prevention identified the virus and classified it as Severe Acute Respiratory Syndrome CoV-2 (SARS-CoV-2) (Anastasopoulou and Athanasia, 2020; Lai et al., 2020; Wang et al., 2020). Since then, the infection from SARS-CoV-2 has increased exponentially, transforming an epidemic into a pandemic in a short time. The CoV disease 2019 (COVID-19) was declared a public health emergency of international concern by the WHO on March 11, 2020 (Adhikari et al., 2020; Hageman, 2020; Zhu N. et al., 2020).

SARS-CoV-2 has infected more than 21.8 million individuals, causing more than 772 thousand deaths in 216 countries: numbers that are still increasing (World Health Organization, 2020d). COVID-19 is considered to be one of the greatest humanitarian crises and, due to the severity of this situation, huge efforts have been made, aimed at fighting against the disease (Li et al., 2020; Liu et al., 2020; Walls et al., 2020). Among infected people, the common symptoms of COVID-19 are cough (68.7%), fever (85.6%), fatigue (39.4%) in addition to the loss of taste and smell. In more severe cases, other conditions have been reported such as pneumonia, difficulty in breathing, and ground-glass opacity in the lung. These symptoms have been used to screen suspected cases that are subsequently subjected to radiological exams of the chest, such as computed tomography and X-Ray (Huang C. et al., 2020; Rothan and Byrareddy, 2020; Weiss et al., 2020).

Studies show that the main route of transmission of SARS-CoV-2 is through contaminated droplets that are expelled by infected people, for example, by coughing or sneezing. Individuals can become infected by direct contact or indirectly via fomites. Direct contact transmission occurs through contact with saliva, respiratory secretions, or droplets, which are expelled by infected persons through cough, sneezes, or conversation. Indirect contact transmission involves contact of a susceptible host with a contaminated object or surface (fomite transmission) (Sharma et al., 2020; World Health Organization, 2020c; Yee et al., 2020). The infection is usually confirmed by the identification of the viral genetic material in the blood and secretion samples using the reverse transcription-polymerase chain reaction (RT-PCR) technique (Fehr and Perlman, 2015; Law et al., 2020). This diagnostic method is considered to be the gold standard for COVID-19 due to its high specificity and accuracy. However, the analyses require specialized professionals and expensive equipment, which need centralized laboratories. In the current situation, there is a high demand for these analyzes, which is overloading specialized centers and caused a critical delay in the final results of infected patients (Chhikara et al., 2020; Law et al., 2020).

There is currently no vaccine or clinically approved therapy for patients with COVID-19 (Aanouz et al., 2020; Astuti and Ysrafil, 2020). The standard treatment is based on repurposing antiviral drugs, an emerging strategy through which safe drugs are used to control emerging human diseases. However, it is important to highlight that several drugs have not generated clinical benefits and are recommended for restricted use, under supervision from the WHO (Senanayake, 2020). Therefore, these treatments are used to attenuate symptoms. Although some biomolecules are effective against CoV in vitro and in vivo, antiviral activity has not shown great results in humans (Srivastava and Saxena, 2020).

Nanotechnology-based therapeutic strategies represent a promising approach to overcome the limitations found in prevention, diagnosis, and therapies against COVID-19 (Weiss et al., 2020). To manage this disease, nanomaterials with antiviral properties can be used in personal protective equipment and in disinfection protocols to prevent SARS-CoV-2 contamination (Weiss et al., 2020) or as nanomaterials-based vaccines or immunomodulators (Chauhan et al., 2020; Weiss et al., 2020). In diagnosis, nanomaterials can also be used for the development of simple, fast, and low-cost methods to detect SARS-CoV-2. For treatment, the nanosystems are applied in the controlled delivery of antiviral and biomolecules to the pulmonary system, for example, to inhibit viral replication or to inactivate viral particles (Weiss et al., 2020).

This review introduces the main aspects of COVID-19, such as the structural characteristics of the virus, infection mechanisms, and treatments currently available. We also presented a discussion about how nanotechnology can be applied against this disease, detailing the most promising nanomaterials and the application possibilities, with properties and advantages over conventional strategies. Furthermore, we hope that the nanotechnology-based strategies addressed in this study can guide researchers in the development of new methods for the prevention, diagnosis, and treatment of COVID-19.

Structure of SARS-CoV-2

SARS-CoV-2 is an enveloped virus with positive-sense single-stranded RNA [(+)ssRNA] that has a spherical shape and a diameter range of 60–140 nm. This virus belongs to the Coronaviridae family, a group of viruses capable of infecting animals and humans. Based on the genomic structure, the family is organized into four genera, namely α-CoV, β-CoV, γ-CoV, and δ-CoV. There are several types of human CoV, among them MERS-CoV, SARS-CoV, and SARS-CoV-2, all belonging to β-CoV genera (Cao Y. et al., 2020; Ortiz-Prado et al., 2020).

Analyses of the SARS-CoV-2 genome revealed structural proteins similar to other types of CoV. The identification of spike (S), envelope (E), membrane (M), and nucleocapsid (N) proteins enable us to understand the activities and functions of the COVID-19 virus (Figure 1). For example, they have an attachment and entry mechanism are closely related to the binding of S protein to the host target cell angiotensin-converting enzyme 2 (ACE2) receptor, an integral membrane protein responsible for cleaving angiotensin I and II on the plasma membrane of human epithelial cells (Yan et al., 2020).

FIGURE 1

Figure 1. Schematic representation of the SARS-CoV-2 structure and spike-receptor binding mechanism (figure created with BioRender.com).

Localized in the endoplasmic reticulum-Golgi region, the N proteins interact with the (+)ssRNA (30 kb in length) and form a helical nucleocapsid to assist viral replication within the host cell. The M protein has a large structure with three transmembrane domains and is responsible for defining the shape, size, and assembly of the virus. The E protein is abundantly expressed inside the vesicle trafficking organelles of the infected cell and seems to be involved at multiple stages of the virus replication cycle, and fundamental in the pathogenesis processes of SARS-CoV-2. The envelope-anchored S protein is a trimeric class I fusion protein that is highly glycosylated (Graham et al., 2013), which gives crown-like morphology when seen in the electron microscopy. N and S proteins are especially important because they are responsible for the viral infectivity and mediate the entry of the virus into host cells (Astuti and Ysrafil, 2020; Cao Y. et al., 2020; Jiang et al., 2020; Li et al., 2020; Shereen et al., 2020).

S protein comprises two functional subunits (S1 and S2). The globular S1 subunit is responsible for recognition and binding to cell receptors and has a higher receptor-binding domain (RBD) in its structure. The S2 subunit is responsible for facilitating virus-cell fusion (Figure 1; Walls et al., 2020). The RBD region is crucial for virus interaction with host cells receptors and determines to some extent the host range (Li et al., 2005; Walls et al., 2020; Wu et al., 2020). SARS-CoV-2 uses the RBD region of S protein to interact with human cells via the ACE2 receptor followed by protease priming at the S1/S2 site, resulting in virus entry in the host cell and pathogenesis (Tariq et al., 2020).

S proteins have been studied in preventive and therapeutic strategies, with monoclonal antibodies (mAbs) targeting viral surface neutralizing SARS-CoV-2 (and SARS-CoV) activity. In vitro, this approach is recognized as a promising class of biomolecules against viral diseases (Wang et al., 2020b). Structural analysis from the RBD region of SARS-CoV-2 S protein can establish strong interactions with human ACE2 receptors with high affinity (Li et al., 2020; Wrapp et al., 2020).

Infection Mechanism of SARS-CoV-2

Viral entry into the host cell starts with the adsorption and interaction of the viral S protein (RBD domains) to host cell ACE2 receptors. Then, S protein undergoes proteolytic cleavage at the S1/S2 boundary, by transmembrane serine protease 2 (TMPRSS2), promoting the S1 dissociation and S2 structural change, required for membrane fusion and viral internalization via endocytosis (Astuti and Ysrafil, 2020; Yan et al., 2020).

After internalization (+)ssRNA is released into the host cell cytosol and attached to the ribosomes, resulting in the translation of two large polyproteins (pp1a and pp1ab polyproteins), which will be subsequently cleaved into smaller components for the folding and packaging of new virions (Boopathi et al., 2020). The proteolytic cleavage, as well as the replication and new virions production, are mediated by enzymes, namely the papain-like proteases (PL-pro), 3C-like proteases (3CL-pro), and RNA-dependent RNA polymerase (RdRp). These enzymes are crucial for the survival and transmission of SARS-CoV-2 and are currently being considered as potential therapeutic targets (Naqvi et al., 2020). Novel viruses are formed (maturation process) and transported to the cellular surface in vesicles and, after being secreted (via exocytosis), start to infect other cells (Eastman et al., 2020; Hoffmann et al., 2020b; Wang et al., 2020). Figure 2 shows the mechanisms involved in the attachment, entry, and replication of SARS-CoV-2.

FIGURE 2

Figure 2. Infection mechanism and life cycle of SARS-CoV-2 in the host cells.

During infection by SARS-CoV-2, the viral S protein on the surface of the virus binds to the ACE2 receptor and enters target cells via endocytosis, after processing the S protein by the TMPRSS2 (1). After cell membrane fusion and release of the viral (+)ssRNA into the cell cytosol (2), the viral polymerase protein is translated (3), replicated, and there is a transcription of the RNA genome (- sense) (4). The replicated genomic RNA and subgenomic RNA transcripts lead to translation of the viral structural proteins (N, M, E, and S) (5) and, finally, the combination of S, E, M proteins with nucleocapsid (6), which allows the formation of new virions (7) that are then released from the host cells via exocytosis (8) (Figure created with BioRender.com).

Therapeutic Approaches Against COVID-19

There is currently no clinically approved treatment for COVID-19, and the therapeutic strategies that we do have are for managing symptoms. However, a few specific antiviral drugs, with several molecules, are undergoing clinical trials. These therapeutic interventions may extend to either direct-acting antiviral agents or immunomodulatory adjuvants, which have been investigated since the beginning of the COVID-19 outbreak (Nitulescu et al., 2020).

The treatments that are adopted for managing COVID-19 are based on the main physio-pathological characteristics of the disease. Drugs can be classified as virus-targeting antiviral (VTA) if they target essential viral proteins to promote virus internalization and replication. They are host-targeting antiviral (HTA) if they target proteins located in the host infected cell or immune system (Conteduca et al., 2014). Recently, strategies focusing on virus-host interactions (VHI) have been proposed. The main therapies that use these strategies, which are currently in the clinical trial phase, are described in Table 1.

TABLE 1

Table 1. Summary of current therapeutic strategies against COVID-19 in clinical trials.

As shown in Table 1, the limitations of antiviral therapies include a lack of specificity, which causes host cell cytotoxicity. Most of these potential drug treatments of COVID-19 are still under investigation in terms of safety and effectiveness, and current antiviral therapy has not yet achieved efficiency against COVID-19. For patient safety, the use of antivirals alone or in association with other treatments should be considered case-by-case to avoid adverse reactions. Moreover, as the development of drugs is a slow and expensive process, the COVID-19 situation requires new and more effective therapeutic alternatives. In this sense, nanotechnology can be a strong ally in the fight against COVID-19, as it brings novel potentials in terms of diagnosis, prevention, and treatment of the disease.

Nano Insights Into Diagnosis, Treatment, and Prevention of COVID-19

Nanotechnology can provide significant advantages in terms of its application in emergency viral diseases such as COVID-19 (Lembo et al., 2018). According to the Food and Drug Administration (FDA), nanoscale systems present different physicochemical and biological properties, compared to macro and micro materials. For example, drug encapsulation into nanocarriers makes it possible to control its release rate in the target sites, improve biocompatibility and decrease toxicity in healthy tissues (Singh and Lillard, 2009; Mora-Huertas et al., 2010).

Nanomaterials also avoid viral contamination by air and contact with infected surfaces and may be especially helpful in sterilizing protective equipment and in a hospital environment. Additionally, nanomaterials exhibit electrical and optical properties that have been widely explored in the development of diagnostic methods, for example, point-of-care (POC) biosensors. The sensitivity of detection could be improved by using nanoparticles, which enable us to identify the analysis at low concentrations. These strategies contribute to rapid diagnosis and isolation and may facilitate the treatment of people infected with SARS-CoV-2. The interactions between nanomaterials and biological interfaces are the basis for their potential (bio)medical applications (Mainardes and Diedrich, 2020).

Nanotechnology thus provides new opportunities in the fight against COVID-19 by enabling new and better forms of prevention, diagnosis, and treatment. Based on the properties and advantages of nanostructured systems, this review discusses nanomedicine strategies and possible applications that could facilitate management of the COVID-19 pandemic.

Nanotechnologies in the Diagnosis of COVID-19

Many nanomaterials have been employed in POC devices, as they have properties that are beneficial for sensing, which includes chemical stability, good electrical conductivity, and Localized Surface Plasmon Resonance (LSPR) effect (Syedmoradi et al., 2017; Kumar et al., 2019). The integrated use of nanomaterials in analytical devices could increase the sensitivity and specificity of detection systems (Zhang et al., 2020).

Gold NPs (AuNPs) are the one of the most attractive nanomaterials because they have optoelectronic properties which can be explored by different types of biosensors, in particular, those based on colorimetric, electrochemical, and plasmonic detection (Quesada-González et al., 2019; Huang Y. et al., 2020). In lateral flow assays (LFAs), for example, AuNPs have been extensively used to label the target molecule, providing a color change in the test zone, which can be read by the naked eye for qualitative results or analyzed by a smartphone that will determine the concentration of the target from a captured image (Brazaca et al., 2019). LFAs are commonly used in POC analyses to detect antibodies and proteins in complex samples such as urine, blood, and saliva. They are low-cost, provide rapid results (5–30 min), and can be stored at room temperature without compromising the function of biomolecules (Koczula and Gallotta, 2016). Although there are LFAs that use other labels, many studies have shown that AuNPs generate an increase in signal and sensitivity of the biosensor, which allows analyte detection at lower concentrations (Rodríguez et al., 2016; Quesada-González et al., 2019). This strategy has been employed in the diagnosis of several infectious diseases (Banerjee and Jaiswal, 2018), including hepatitis B (Kim et al., 2016), influenza (Le et al., 2017), and Zika (Lee et al., 2016).

Recently, LFAs biosensors were applied to the diagnosis of COVID-19 and are being distributed to healthcare systems to provide decentralized testing (Udugama et al., 2020). These LFAs detect only immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies that recognize the SARS-CoV-2 proteins, which indicates that the patient was infected (Morales-Narváez and Dincer, 2020; Sheridan, 2020). Although the sensitivity is lower than the RT-PCR tests, these devices represent an important tool for screening the population (Sheridan, 2020).

In addition to LFAs, other colorimetric detection systems explore the redshift in the LSPR band of AuNPs when they aggregate. The most common detection strategy is to functionalize these nanomaterials with biomolecules, meaning that when they bind to the target molecules, the AuNPs aggregate and cause a color change in the solution (Lin et al., 2009). Moitra et al. have reported a colorimetric assay based on this latter strategy for the detection of the SARS-CoV-2 (Moitra et al., 2020). Four antisense oligonucleotides (AOs) were designed to target the N protein gene of SARS-CoV-2 in two different regions. The AOs were modified with a thiol group at 3′ or 5′ end and conjugated to AuNPs. The hybridization between the target sequence and the AOs-capped AuNPs generated a redshift in the LSPR band of ca. 40 nm, and the solution color changed from violet to blue (Figure 3). The specificity of the detection system was confirmed using the sequences from MERS-CoV. Importantly, this colorimetric assay is based on the optical properties of the AuNPs can significantly contribute to COVID-19 management providing a fast and straightforward diagnosis.

FIGURE 3

Figure 3. Schematic representation of the colorimetric system using functionalized AuNPs for the detection of the SARS-CoV-2 virus (reprinted with permission from Moitra et al., 2020).

AuNPs are also employed in electrochemical biosensors to increase the electroactive area of the electrode and the electron transfer rate, amplifying the signal (Ye et al., 2018; Zarei et al., 2018). Recently, Layqah and Eissa developed an electrochemical immunosensor for the detection of MERS-CoV using carbon electrodes modified with AuNPs (Layqah and Eissa, 2019). The biosensor is based on a competitive method in which the nasal fluid sample is mixed with antibodies against the MERS-CoV S protein and then added to the electrode where S proteins were previously immobilized. After the incubation time, the electrode is washed, and a square wave voltammetry measurement is performed. When the free antibodies bind to the proteins immobilized on the electrodes, the electrical current decreases. However, when the antibodies were previously attached to MERS-CoV, the reduction in current was attenuated. The biosensor exhibited excellent analytical performance, and the low limit of detection was attributed to the deposition of AuNPs on the electrodes (Layqah and Eissa, 2019). This strategy also demonstrates the potential of AuNPs in the detection of COVID-19.

Magnetic NPs (MNPs) have also been used in biosensing devices, especially for signal amplification (Dau et al., 2019), analyte pre-concentration (Tran et al., 2018), and magnetic separation (Glynn et al., 2014). The detection of analytes directly from complex samples such as blood and urine presents some limitations, such as the low concentration of the analyte or the signal interference due to other biomolecules in the sample, which can significantly decrease the accuracy of the analysis (Zhu et al., 2020). Several studies have employed MNPs, functionalized with bioreceptors to overcome these limitations and to improve the performance of biosensors. Luo et al. have reported an electrochemiluminescence biosensor for the selective detection of the H9N2 avian influenza virus (H9N2 AIV) using MNPs modified with mAbs to capture the virus (Luo F. et al., 2020). The authors highlighted that through magnetic separation, the interference of the complex samples was decreased, and ultrasensitive detection of the virus was possible, achieving the limit of detection (LOD) of 14 fg/mL (Luo F. et al., 2020). Lu et al. employed functionalized magnetic NPs to develop a digital microfluidic chip for H1N1 virus detection (Lu et al., 2020) in which the NPs capture the virus, and electromagnetically-driven to the channels, passing through spots where they are labeled with fluorescent probes and detected. Biosensors based on magnetic NPs represent promising alternatives for the diagnosis of COVID-19.

Graphene and its derivatives, including graphene oxide (GO) and reduced graphene oxide (RGO), represent another class of nanomaterials with interesting properties for applications in biosensing. The sp2-hybridized carbon atoms arranged in a two-dimensional monolayer confer to graphene high electrical and thermal conductivity, increased surface area, and excellent chemical stability (Dau et al., 2019). These physicochemical properties can be exploited to improve the performance of biosensors, for example, by increasing the sensitivity of the system so that even lower concentrations of the analyte can be detected (Justino et al., 2017). The carboxylic groups on the surface of the oxidized graphene allow for the immobilization of biomolecules such as DNA and antibodies through covalent bonding without requiring additional functionalization steps (Hammond et al., 2016).

Graphene-based nanomaterials have been used in electrochemical and field-effect transistors (FET) biosensors. Singh et al. reported an electrochemical immunosensor integrated with a microfluidic device to detect the H1N1 virus (Singh R. et al., 2017). RGO-modified electrodes were employed to increase the sensitivity of the biosensor. The specific antibodies used to capture the virus were immobilized through a covalent bond on the RGO sheets. Using this strategy, a low detection limit of 0.5 PFU/mL was achieved. Recently, Seo et al. used graphene sheets modified with antibodies against the S protein of SARS-CoV-2 to develop a FET-based biosensor for COVID-19 diagnosis (Seo et al., 2020). The performance of the biosensor was evaluated using a virus in culture medium and clinical samples, obtaining a detection limit of 1.6 × 10¹ PFU/mL and 2.42 × 10² copies/L, respectively.

These examples show how nanomaterials can contribute to the development of more accurate, sensitive, and easy-to-handle POC biosensors, in particular, for the diagnosis of viral diseases. Together with biosensing technologies, nanomaterials represent promising tools for the decentralization of COVID-19 diagnostic tests and for obtaining rapid results, which are crucial to quickly isolate infected patients.

Nanotechnologies in the Treatment of COVID-19

In COVID-19 therapy, nanotechnology has broad applications and can act in different stages of the disease, with the potential to inhibit virus-cell interaction, membrane fusion, cell internalization, transcription, translation, and viral replication, in addition to activating intracellular mechanisms that cause irreversible damage to viruses (Mainardes and Diedrich, 2020).

Nanoparticles (NPs) (organic and inorganic) have attracted considerable attention due to their properties. In the case of inorganic NPs (INPs), such features include luminescence, tunable size, shape, composition, large surface-volume ratio, and the ability to expose multiple interaction sites on the surface. The most commons types of inorganics NPs are mesoporous silica NPs, iron oxide NPs, and metallic NPs (gold, silver). Organic NPs are also advantageous due to the possibility of site-specific targeting of drugs, control drug release, biodegradability, biocompatibility, and non-toxicity. The most used organic NPs include polymeric and lipid-based NPs, dendrimers, extracellular vesicles (or exosomes), liposomes, and nanomicelles (Kerry et al., 2019).

Here, we highlight the potential application of nanostructured systems for the delivery of approved and repurposing antiviral drugs, which can increase treatment effectiveness through controlled release and decreased toxicity. A brief classification of the main types and an overview of the properties, synthesis, and toxicity of nanomaterials is discussed in the next section. Figure 4 summarizes possible nanostructures to be used in the therapy against SARS-CoV-2.

FIGURE 4

Figure 4. Types of nanoparticles to application in COVID-19 therapy (figure created with BioRender.com).

Inorganic Nanoparticles

INPs outstand from the others due to their optical properties. In medicine, these materials have been used as contrast agents and in photothermal therapy. The major attributes which have to lead to biomedical applications of INPs include controlled stability, enhanced permeability, high functionalization capability, and triggered controlled release (Anselmo and Mitragotri, 2019). Other properties such as luminescence, the possibility of size adjustments, shape, composition, and high surface-volume ratio show versatility for several therapeutic applications. The ability of these INPs to expose multiple surface binding sites are widely explored (Kerry et al., 2019).

In terms of clinical use, the cytotoxic properties of inorganic NPs remain an open issue. In healthy tissues, metallic NPs may induce reactive oxygen species, genotoxicity, change in cellular morphology, and cytoskeleton defects (Soenen et al., 2011). Although the conjugation of NPs with polymers or biological components aids in reducing these problems, concentration and intracellular localization could generate some side effects. For example, the acid pH of phagolysosomes (pH 4–5) produces free ions into the cytoplasm after degrading the iron surface (Mulens-Arias et al., 2020). Besides, this reduced nanostructure dimension facilitates entry into the cell nucleus and attachment to the decondensed nucleic acid streams (Soenen et al., 2011). In contrast, large particles are deposited in high vascularized organs and easily captured by macrophages. In blood, the enzymatic degradation allows it to use NPs residues (like iron and gold) in physiological metabolism, but in the lung, tissues microparticles are retained in the bronchi and nanocomposites may cluster in the alveoli, making it difficult to eliminate them from the organism before healthy cells endocytose (De Matteis, 2017).

In this section, we assess the use of AuNPs, silver NPs (AgNPs), iron oxide NPs (IONPs), and mesoporous silica (MSNPs) for viral infection therapies. Since the interaction of nanocomposites and the capsid structure from the virus can prevent its binding to the cells, surface functionalization of NPs exhibit an excellent potential for developing novel treatment agents against COVID-19 (Cagno et al., 2018).

Gold Nanoparticles

AuNPs have attracted interest in several fields of science due to features (previously described in section Nanotechnologies in the Diagnosis of COVID-19) that allow them to be applied in diagnostics and therapy. A relevant attribute is the ease of functionalization using the strong bond between gold and thiol ligands (Yang et al., 2015).

Sulfonate ligands are the most used molecules to functionalize metallic NPs because they mimic the heparan sulfate proteoglycans (HSPG) site on the cell surface. Accordingly, the virus binds to the NPs surface, blocking the infection in cells (Baram-Pinto et al., 2010). A recent study showed that AuNPs with long links of sulfonate mercaptoethanesulfonate (MES) and undecanesulfonic acid (MUS) caused irreversible deformation in several virus types, including respiratory syncytial virus, in vitro and in vivo studies. The mechanistic understanding of this interaction revealed that AuNPs functionalized with MUS present a multivalent binding to the virus, which collapses the capsid structure. Therefore, this multivalent binding could be a particularly interesting strategy for therapy in COVID-19 (Cagno et al., 2018).

In another work, Zacheo et al. showed that AuNPs functionalized with sugars with multiple sulfonate groups, especially glucose, and lactose-based ligands, showed a low effective concentration for Dengue virus. Docking experiments demonstrated that the length of the molecule that presented the best results was the one that fitted better in the β-OG pocket (Zacheo et al., 2020), suggesting that for the functionalization of AuNPs against viral infections, the length of the molecule is a crucial parameter (Cagno et al., 2018). Porous AuNPs showed a greater ability to inhibit the influenza virus compared to non-porous AuNPs and AgNPs, mainly due to the large surface area. The proposed mechanism suggests that the porous ability of AuNPs blocks the disulfide bonds in hemagglutinin, preventing the attachment in the cells (Kim et al., 2020).

Ahmed et al. reported a study using AuNPs against RNA virus. The nanosystems were used to increase the antiviral activity of ribavirin (repurposed agents for COVID-19, as seen in Table 1) loaded in AuNPs against the measles virus on the Vero cell line. The results showed a reduction of 78.1% for Vero cells treated with ribavirin-loaded AuNPs (99.5 μg/ml). In comparison, a reduction of only 25.4% was obtained for the cells treated with isolated ribavirin (500 μg/ml). The results demonstrated the ability of AuNPs to increase the antiviral activity of the drug, which represents a potential platform against SARS-CoV-2 (Ahmed et al., 2020).

The shape of a nanoparticle affects how they interact with host cells and the virus. Nanorods have attracted considerable attention due to their optical and physicochemical properties. In a recent study, a series of heptad repeat peptide 1 (HR1) inhibitors were developed to inhibit HR1/HR2-mediated membrane fusion between MERS-CoV and host cells. The results revealed that the inhibitory effects of the peptides were increased after complexing with nanorods, showing higher metabolic stability and biocompatibility in vitro and in vivo. The authors concluded that the systems effectively prevented the membrane fusion associated with MERS-CoV, demonstrating the enormous potential of the systems for the treatment of MERS in the clinic (Huang C. et al., 2020) with the possibility of COVID-19 treatment.

Silver Nanoparticles

The increased attention to the use of AgNPs has focused on antimicrobial activity, as well as optical, electrical, and thermal properties. These singular characteristics have been used widely in nanotechnology-based products (Chapman et al., 2012; Anselmo and Mitragotri, 2015). The main advantage of AgNPs is the possibility that they could be used as antiviral agents without surface modifications. A study showed that naked AgNPs (with a diameter of 55 nm) have demonstrated inhibitory actions against the Monkeypox Virus (MPV), preventing virus internalization (Rogers et al., 2008). This antiviral property relies on three possible mechanisms: AgNPs might attach to glycoproteins on the virus surface, be internalized by the cells, and block genome replication, attaching to the cell membrane surface and preventing virus fusion (Rai et al., 2016). However, the application of naked AgNPs has limitations regarding the intrinsic cytotoxicity they exhibit. To overcome these limitations, polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP) can be used as coating materials (Elbaz et al., 2016). Lara et al. showed that PVP coated AgNPs (30–50 nm) had antiviral activity on human immunodeficiency virus (HIV-1) strains. This early-stage effect occurs due to the binding of NPs in GP120 (glycoprotein exposed on the surface of the HIV envelope) on the virus, preventing fusion in the CD4 cell receptors (Lara et al., 2010).

Curcumin functionalized AgNPs also showed high antiviral properties for Respiratory Syncytial Virus (RSV), and no cytotoxicity was observed after incubation with cells. The proposed mechanism is the inactivation of the virus before the interaction with cells (Yang et al., 2016). Morris et al. demonstrated the PVP AgNPs antiviral activity for RSV, using 10 nm particles at a concentration that exhibited a robust antiviral behavior but no cytotoxicity for epithelial cells (Morris et al., 2019).

Iron Oxide Nanoparticles

IONPs are widely used for biomedical applications, mainly as contrast agents for magnetic resonance imaging. Due to their biocompatibility, there are several IONPs-based products approved by the FDA (Anselmo and Mitragotri, 2019). The magnetic characteristics of IONPs are related to the superparamagnetic behavior of small NPs that appear in response to an external magnetic field (Williams and Corr, 2013).

This antiviral activity relies on surface modification with sulfonates or other molecules. Bromberg et al. (2012) synthesized core-shell silica-magnetic NPs functionalized with poly(hexamethylene biguanide) (PHMBG). The authors reported that NPs exhibited a notable virucidal effect on several virus strains, which occurred via amino alkylation of their genomic materials, blocking genome replication and leading to viral inactivation (Bromberg et al., 2012).

Mannose-loaded IONPs were developed for delivery in dendritic cells (DC). A significant increase in the expression of IL-6, TNF-α, and IFN-γ was observed in the DCs compared to IONPs without mannose in vitro studies. In vivo studies also showed higher levels of TNF-α, IL-2, IL-4, IL-12, and INF-γ using mannose-loaded IONPs (Rezaei et al., 2019).

More attention must be given to IONPs, considering the iron dysregulation in COVID-19. Recent studies have suggested that interactions between SARS-CoV-2 and hemoglobin (and other receptors) occur in the erythrocyte or red blood cell precursors, resulting in the hemoglobin denaturation and iron metabolism dysregulation. Iron overload in tissues is a major concern (Cavezzi et al., 2020). Some papers have shown higher levels of ferritin and lower hemoglobin levels in patients that did not survive (Liu and Li, 2020; Zhou et al., 2020). These iron level changes can reduce the use of these NPs in clinical applications since they might lead to side effects (Bisso and Leroux, 2020).

Mesoporous Silica Nanoparticles

Mesoporous silica NPs (MSNPs) have tunable size pores that allow accommodating molecules inside and outside for co-delivery. These dual characteristics could provide an excellent platform to treat COVID-19 if they can be functionalized with several ligands to inactivate the entry of the virus in the host cell and to the site-specific release of these ligands, preventing viral replication. Lee et al. have reported on the dual delivery features of MSNPs for antiviral applications. Acyclovir-loaded MSNPs (coated with glycosaminoglycan) were used to inhibit the entry of HSV-1 and HSV-2 (herpes simplex virus types). The results showed that NPs act in the early stages of viral internalization and DNA replication simultaneously (Lee E. C. et al., 2018).

Lipid-coated MSNPs containing the antiviral (E)-2-(1,4-Dimethylpiperazin-2-ylidene)amino)-5-nitro-N-phenyl benzamide (ML336) were developed as a strategy to improve antiviral circulation time and biocompatibility. Although nanosystems have shown a virucidal effect in the Venezuelan equine encephalitis virus, low stability and solubility mean that they have limited clinical uses. In vitro results have revealed a dose-dependent virus inhibition and an additional ML336 release after cell endocytosis, while the in vivo results showed that the NPs demonstrated significate antiviral activity and no toxicity (LaBauve et al., 2018).

Organic Nanoparticles

Carbon Nanotubes and Graphene Nanoparticles

Carbon-based nanomaterials such as carbon nanotubes (CNTs), graphenes, and fullerenes NPs present interesting physicochemical properties for innovative scientific and technological applications (Comparetti et al., 2018). CNTs have covalent bonds (sp²+sp³ hybrid phases) and excellent electric conductivity, enabling their use in different research fields. Single wall carbon nanotubes (SWCNT) and multi-wall carbon nanotubes (MWCNT) are folded graphene sheets with a diameter of 5–20 nm, and a length ranging from 50 to 1,000 nm (Rashid and Ralph, 2017).

As a perspective for COVID-19 treatment, CNTs exhibit limitations in terms of toxicity (Alidori et al., 2016). When exposed to the lungs they activate macrophages in the lower respiratory tract, inducing fibrosis, and the formation of collagen in the lesions (Mangum et al., 2006). Moreover, it was already demonstrated that CNTs are spontaneously internalized by lung cells via binding with the epidermal growth factor (EGF) receptor (Luanpitpong et al., 2014). In vitro studies also demonstrated an enhancement of influenza H1N1 virus infectivity in lung epithelial cells after intranasal administration of CNTs (Sanpui et al., 2014). The functionalization of CNTs may be a promising strategy to overcome these disadvantages. Hussain et al. demonstrated that the inflammatory processes significantly reduce when biomolecules (proteins and polymers) were conjugated on the CNTs surface, decreasing cytotoxicity in the respiratory system (Hussain et al., 2016).

The functionalization of CNTs with hyaluronic acid increases the interaction of nanosystems with bronchial cells and prevents the inflammatory process in the pulmonary tissues since they are not captured by alveolar macrophages (Hussain et al., 2016). These results corroborate the fact that CNTs modification with cellular ligands increases NPs uptake and drug release at targeted tissues by endocytic absorption without plasmatic membrane damages (Maruyama et al., 2015; Hussain et al., 2016). Wang et al. also succeeded in increasing single-wall carbon nanotubes (SWCNTs) specificity to lung cell receptors after conjugation with anti-CTLA-4 antibodies. Besides, CNTs and graphene quantum dots functionalized with antiretroviral drugs (CHI360, CHI415, CHI499, and CDF119) were able to inhibit reverse transcriptase enzyme activity in lymphocytes of HIV-positive patients (Iannazzo et al., 2015, 2018). These strategies may be interesting for future treatments against COVID-19 because NPs could improve the effectiveness of therapeutic agents, speeding-up the delivery of drugs to diseased cells. Although it is possible to reduce immune cell activation and the inflammation processes using carbon NPs, the application of them in therapy is not recommended.

Polymeric Nanoparticles

Currently, there are several products based on biodegradable polymers approved by the FDA and European Medicines Agency (EMA), used in the development of NPs for delivery of new antiviral molecules. Polymeric NPs are promising materials to be used against viral diseases since they can be engineered to reach specific targets (extracellular or intracellular) and block virus attachment to host cell receptors. These characteristics are essential to control viral diseases, as well as to reduce adverse effects (Singh L. et al., 2017), improving the safety of the antiviral drugs and overcoming the cellular drug resistance (Lembo et al., 2018).

The delivery of active molecules using NPs has been proven efficient in inhibiting virus replication (Lee E. C. et al., 2018). For example, nanocarriers based on a β-cyclodextrin-poly(4-acryloylmorpholine) mono-conjugate (βCD-PACM) polymer functionalized with guanine analogs (acyclovir) were capable of reducing extracellular virus uptake (Cavalli et al., 2009). Studies already demonstrate the effectiveness of acyclovir delivery using NPs, enhancing the blockage of DNA replication at herpes virus-infected cells (Lee E. C. et al., 2018). Also, poly(ethylene glycol)- poly(lactic-co-glycolic acid) (PEG)-PLGA) diblock copolymers have been studied to coupling two ATPase inhibitors (dyphylline and bafilomycin) for antiviral activity. The intravenous administration of PLGA nanocarriers improved the anti-influenza applicability of dyphylline in H1N1 infection, exhibiting controlled drug release in the lungs and providing significant protection against lethal doses of the virus in vitro and in vivo models (Hu et al., 2018).

Ge et al. used polyethyleneimine (PEI) NPs loaded with siRNA and demonstrated the ability of the NPs to inhibit influenza virus replication from a conserved genetic locus linked to virus susceptibility. PEI complexes are efficient siRNA carriers into the lungs, able to reduce 1,000-fold virus infection than other oligonucleotides encoding vectors (Ge et al., 2004; Beyerle et al., 2011). Although the high concentration of PEI for drug delivery is not indicated, PEG modification improves particle hydrophobicity with less pro-inflammatory responses and no cytotoxic side effects in healthy tissues (Beyerle et al., 2011). To optimize safe formulations, NPs PEGylation prevents classical macrophages activation and the elimination from the lungs for at least 1 month (Shen et al., 2015).

Other strategies for polymeric NPs have been proposed, which suggest replacing molecules and mAbs to block virus uptake in host cells. As a perspective, these NPs could be used to inhibit the interaction between SARS-CoV-2 and ACE2, preventing the infection of the virus in human tissues. Henning et al. reported the use of polymeric structures (branched-PEG molecules and polyamidoamine (PAMAM)-dendrimers NPs) to bind angiotensin receptors and act as antagonist agents along with viral infection (Hennig et al., 2015). Similarly, angiotensin ligands-loaded copolymer structures bind to angiotensin enzymes, ensuring treatment specificity in ACE2⁺ cells for future drug delivery studies (Figueroa et al., 2019). Therefore, the ability of NPs to prevent viral binding at ACE2 appears to be promising against CoVs infection.

To treat respiratory diseases, therapeutic strategies in nanomedicines have taken into account the promising results coming from administration by inhalation. Mouth and nasal routes require nanostructures with diverse functionalities to cross biological barriers in highly vascularized tissues for depositing drugs into targeted sites. Polymeric structures or polymer-based NPs are indicated to pulmonary systemic absorption, exhibiting lower cytotoxic effects to healthy cells than inorganic NPs (Ajdary et al., 2018).

The main administration methods responsible for delivering particles on the respiratory tract are jet nebulizers, pressurized metered-dose inhalers, dry powder inhalers, and soft-mist inhalers. These strategies deposit structures with a size between 10 and 5,000 nm in pulmonary tissues by Gravitational Sedimentation (0.5–5 μm), Brownian Diffusion (<0.5 μm), Electrostatic Precipitation, and Interception (Kaur et al., 2012; Muralidharan et al., 2015). The biocompatibility and low toxicity of polymeric NPs make them highly promising for treating respiratory diseases through inhalation. Moreover, the properties of mucoadhesives allow for the crossing of biological barriers in pulmonary systemic absorption (Ajdary et al., 2018). In vivo, microparticles loaded with bronchodilators have low efficiency than conventional methods (Lai et al., 1993). However, corticosteroids-loaded polymeric NPs used to treat asthma, and chronic obstructive pulmonary illness exhibited deep penetration in the lung by aerosol administering (Singh et al., 2019).

Nanocomposites have limitations in inhalation therapy because they decompose in the respiratory system, have drug resistance, and involve a periodic structural mutation in infectious organisms. Polymeric NPs are promising materials for such applications, due to their improved biocompatibility. The nanocarriers have been widely studied to induce higher antiviral activity against respiratory infectious than the administration of anti-virus alone. For example, as a novel vaccine strategy, NPs were used to deliver influenza virus antigens intended to re-educate the cellular inflammatory profile. The intranasal delivery of chitosan NPs induces a controlled release of H1N1 proteins for macrophages activation, followed by an adaptative immune response to the virus infection (Liu et al., 2015).

In the COVID-19 patients, the infection leads to severe expression of inflammatory cytokines by activated immune cells (Hirano and Murakami, 2020). Due to the intense phagocytosis performed by white blood cells, nebulization of PLGA NPs coated with chitosan were able to cease the migration of eosinophils and neutrophils in the lungs, preventing severe biological dysfunctions (Aragao-Santiago et al., 2016). Nanostructures loaded with anti-inflammatory drugs reduce the generation of intracellular reactive oxygen species (ROS) in the pulmonary epithelium and avoid the expression of IL-6 and chemokine MIP-2 by alveolar macrophages (Yoo et al., 2013; Shen et al., 2015). Another strategy to neutralize pro-inflammatory cytokines uses anti-IL-6 antibodies immobilized on chitosan NPs to remove such molecules from diseased tissues. To avoid organ failure, this approach prolongs mAbs activity (in comparison to the free isoform), trapping cytokines in the inflammatory region (Lima et al., 2018), which addresses the cytokine release syndrome (CRS) caused by SARS-CoV-2.

Polymeric NPs can also be used as adjuvant therapies, collecting and eliminating cytotoxic molecules from the human body. Like antiviral agents, NPs can be designed to attach viral proteins, decreasing disease infectivity. Recently, Bawa et al. showed that polymer-coated NPs can be used to trap and destroy viral particles (Bawa et al., 2016). Nanoviricides (NanoViricides Inc.) binds to multiple virus receptors and neutralize organism replication after avoiding cell internalization. NPs functionalized with targeting proteins increase the affinity and specificity to the desired virus and, upon simple modifications, may provide a fast therapeutic platform to treat new diseases. Their conjugation with undecanesulfonic acid (MUS) aids them to recognize and induce an irreversible structural deformation in respiratory viruses, inhibiting binding to the extracellular matrix of eukaryotic cells (Cagno et al., 2018).

Currently, therapies with methotrexate (MTX)-loaded NPs had been approved in Brazil for phase I and II clinical trials (NCT04352465). This study aims to evaluate the effectiveness and safety of the MTX-loaded NPs in severe inflammatory reactions, which could result in acute lung injury during the treatment of COVID-19 patients. Multi-functional polymeric nanocarriers had been approved as novel nanoplatforms for clinical application and could be immediately updated for safe use in the current SARS-CoV-2 pandemic (U.S. National Library of Medicine, 2020).

Dendrimers

Dendrimers represent a revolution in nanotechnology as novel nanocarriers able to improve the efficiency of drugs and bioactive compounds. Structurally, the dendrimers are radially symmetric macromolecules with homogenous, well-defined, and highly branched three-dimensional structures that present compact globular structures. Unique physicochemical properties, such as solubility, low polydispersity, effective drug-encapsulation capacity (Lembo et al., 2018), biodegradability, and biocompatibility mean that they are useful in encapsulating hydrophobic therapeutic agents (Li and De Clercq, 2020). The ability of dendrimers to establish strong interactions with viruses may increase antiviral activity, making them promising systems against viral infections (Kim et al., 2018; Lembo et al., 2018; Itani et al., 2020).

Dendrimers have been widely studied for applications against HIV infection. The systems are engineered with specific functional end groups able to interact preferentially with the E protein of HIV and host cell receptors and, consequently, to suppress viral replication (Mhlwatika and Aderibigbe, 2018). One example of a dendrimer that is commercially available is SPL7013 Gel (VivaGel^®), a type of microbicide dendrimer comprising a divalent benzhydryl amine (BHA) core, four generations of lysine branches with the outermost branches capped with a total of 32 naphthalene di-sulfonic acid groups, developed for the prevention of HIV and HSV infections. The clinical effectiveness of SPL7013 Gel as a topical vaginal microbicide has already been demonstrated (Price et al., 2011; Kim et al., 2018).

The first pilot study employed polycationic dendrimers (generations 2–5) based on primary amine to assess in vitro antiviral activity against the MERS-CoV. It was evaluated the effect of dendrimer size and terminal charge on the ability of MERS-CoV to produce viral plaques in infected Vero cells. The results demonstrated that polyanionic dendrimers can be successfully used in drug delivery, improving antiviral activity (Kandeel and Al-Nazawi, 2020). To date, no studies have used dendrimers against SARS-CoV-2, however, the potential of dendrimers for application in the treatment of viral infections has been demonstrated (Mhlwatika and Aderibigbe, 2018), suggesting it as an interesting potential approach in the fight against COVID-19.

Lipid-Based Nanoparticles

Lipid-based NPs have great potential to translate into clinical contexts of COVID-19 because they biodegrade and have promising biocompatibility (Puri et al., 2009). Several lipid-based formulations have already been successfully adapted into a marketed drug product (e.g., Doxil, AmBisome). Different types of lipid raw materials can be employed in the development of nanocarriers such as phospholipids, fatty acids, mono-, di- and triglycerides, waxes, and oils, which assemble in water in different structured systems due to their hydrophobic and amphiphilic nature. The resulting particles share some similarities with biological components such as cell membranes and the pulmonary surfactant biomembrane system (Kulkarni, 2012). For this reason, the toxicity of lipid nanoparticles is lower compared with other types of nanomaterials. Lipid-based NPs have already been explored for the treatment of HIV, herpes, and hepatitis B (HBV) and C (HCV) viruses because they can encapsulate different classes of antiviral drugs, mediating the delivery from the administration site to the target and modulating specific biological responses (Pollock et al., 2010; Jain et al., 2011; Shah et al., 2017).

Liposomes are bilayered structures extensively investigated as nanomedicine platforms for drug delivery. They are mainly composed of synthetic or natural phospholipids (e.g., phosphatidylcholine, phosphatidylserine), cholesterol, and sphingolipids (Akbarzadeh et al., 2013). The existence of hydrophobic layers and aqueous compartments in the vesicular assembly makes these nanocarriers suitable for the encapsulation of lipophilic and hydrophilic molecules. Liposome-based carriers have also been used for encapsulation of antiviral to be used in the treatment of infected cells, due to their ability to promote intracellular delivery of different types of drugs (Clayton et al., 2009; Pollock et al., 2010; Croci et al., 2016). Furthermore, the lipid composition affects the infectivity of cells. Kolyvushku et al. reported that cationic and anionic liposomes interact with equine herpesvirus type 1 (EHV-1) inhibiting infection. The authors of this study attributed this response to the charged phospholipids 1,2-dioleoyloxy-3-(trimethylammonium)propane (DOTAP) and phosphatidylserine, once the neutral phosphatidylcholine was not able to modulate the virus entry in cells to inhibit infection (Kolyvushko et al., 2020). In another study, Pollock et al. showed that polyunsaturated liposomes had high antiviral inhibition against three viral types: HBV, HCV, and HIV. The study demonstrated that a reduced infection was dependent on the cellular and virus associated-cholesterol levels (Pollock et al., 2010).

Surface-modified liposomes increase the potential of the nanocarriers toward a more precise nanomedicine platform. Hydrophilic polymers, proteins, and mAbs are commonly used in liposome functionalization. For example, the use of hydrophilic PEG minimizes unspecific cellular uptake. PEGylated liposomes have increased stability and longer circulation times and also improved targeting immunological attributes (Mohamed et al., 2019). Recently, it was demonstrated that the PEGylation of liposomes resulted in macrophage uptake independent of protein corona formation (Weber et al., 2019). This strategy is particularly interesting in the context of COVID-19 therapy because alveolar macrophages remove particles in the respiratory surface, which could hinder the therapeutic effects on pneumocytes. Regarding protein or mAb functionalization, it was reported that this strategy could add specificity to the nanocarriers toward viral proteins (Eloy et al., 2017). Furthermore, these targeted liposomes have improved cellular uptake, which can be explored for modulating antiviral responses in infected cells. Following this research line, Clayton et al. reported that liposomes that were carrying the PI1 protease inhibitor, functionalized with PEG and an HIV-directed mAb fragment, promoted a sustained and specific inhibition of HIV-1 replication (Clayton et al., 2009).

Liquid crystalline NPs (LCNPs) are non-lamellar self-assembled systems formed by polar lipids such as Phytantriol (PHYT) and Glyceryl Monooleate (GMO) (Azmi et al., 2015). This class of nanocarriers has received attention as they can accommodate small and large molecules and imaging agents in their nano compartments (Zhai et al., 2019). LCNPs have a diverse phase behavior ranging from cubic (cubosomes) to inverted hexagonal nanostructures (hexosomes) (Rodrigues et al., 2016; Barriga et al., 2019). The lipid supramolecular arrangement of LCNP with water channels interpenetrated networks in the structure that make them a suitable host for hydrophilic and hydrophobic drugs (Azmi et al., 2015). The non-lamellar morphology confers distinct biological interactions to the LCNPs. For example, it has been demonstrated that cellular uptake of hexosomes is independent of endocytosis, the most common mechanism for liposome uptake. Additionally, the internalization of hexosomes seems to be dependent on the degree of cell membrane tension: lower tension leads to higher internalization. This feature makes this class of lipid-based nanocarriers interesting for infectious diseases in which the biophysical properties of cellular membranes are somewhat altered (Rodrigues et al., 2019).

It has been reported that LCNPs could be potential drug delivery carriers due to their sustained release capacity in comparison with other nanocarriers (Karami and Hamidi, 2016). Cubosomes favor the absorption of poorly soluble drugs in the intestines due to their sustained action. However, this effect was dependent on the internal structure of the LCNPs: GMO-based cubosomes did not sustain the absorption of the drug at the same level as PHYT-based ones. The differences in the behavior of the main polar lipid that generates the liquid crystalline phase and the addition of saturated fatty acids (e.g., lauric, myristic, stearic, etc.) affect the drug release behavior (Thapa et al., 2013). Furthermore, the addition of fatty acids into the formulation confers to the particles a pH-triggering response (Tran et al., 2015; Mertins et al., 2020). The latter can be exploited in the inflammatory conditions present in SARS-CoV-2 infection due to alterations in the alveolar pH microenvironment. Therefore, it is crucial to optimize composition factors toward the control of the lipid supramolecular arrangement in LCNPs to achieve the desired action (Huang and Gui, 2018).

Microemulsions (ME) and nanoemulsions (NE) are two similar systems composed primarily of water (W), oil (O), and surfactant (S) assembled in nanodroplets. Unconventionally, the main difference between these two lipid-based systems is not related to the range of particle sizes but their physicochemical stability. While ME are formed spontaneously by mixing the components and present thermodynamic stability, NE are fabricated using an energy input, and they are thermodynamic unstable, though they exhibit kinetic stability (McClements, 2012). These physicochemical characteristics make ME susceptible to dilution procedures, which can be interesting for fabricating systems with stimuli-responsive properties triggered by contacting biological fluids. The dynamic nature of ME self-assembly is explored by self-microemulsifying drug delivery systems (SMEDDS) aiming at improving the bioavailability of poorly soluble drugs by the oral route (Gursoy and Benita, 2004; Deshmukh et al., 2019).

On the other hand, NE droplets are stable during dilution, which is interesting for parenteral applications. ME and NE can accommodate both lipo- and hydrophilic substances as the components can self-organize in oil-in-water (O/W) or water-in-oil (W/O) structures. Both systems have already been explored as vehicles for vaccines and antiviral therapies (Bernstein et al., 2019).

Solid lipid NPs (SLNs) and nanostructured lipid carriers (NLCs) are relatively new nanosystems based on solid lipids or a combination of solid and liquid lipids, respectively. The hybrid nature of NLCs brings some advantages over the SLNs, such as the control of crystallinity degree, an essential factor to be considered for drug loading (Ganesan and Narayanasamy, 2017). Despite this physicochemical difference, both systems have been used for the delivery of poorly soluble drugs by different routes of administration (Khosa et al., 2018). It has been reported that SLNs can be used to achieve the alveolar macrophages, a type of cell involved in pulmonary infectious diseases such as COVID-19 (Chuan et al., 2013). Repeated inhalation of SLNs was demonstrated to be safe in a murine model (Nassimi et al., 2010), and their clearance was shown to be similar to conventional liposomes (Haque et al., 2018).

Nanotechnologies in the Prevention of COVID-19

Environment and Surface Cleaning and Health Care Antiseptics

Several products use nanomaterials with antimicrobial activity for disinfection. One of these, CAC-717, is a product containing mesostructured NPs with effectiveness at inactivating enveloped (Nakashima et al., 2017) and non-enveloped viruses (Sakudo et al., 2020). Tungsten carbide NPs are also promising methods of disinfection due to their broad virucidal activity (Pfaff et al., 2019).

Another strategy in the prevention of the spread of COVID-19 could involve creating self-disinfecting surfaces that are coated with nanomaterials such as silver, zinc oxide, and copper NPs, which oxidize and release ions with antimicrobial properties (Murphy et al., 2020; Weiss et al., 2020). For example, AgNPs are already widely used as a disinfectant with biomedical, environmental, and industrial applications (Deshmukh et al., 2019). They have antiviral activity against several types of viruses such as respiratory syncytial, HBV, and HIV (Galdiero et al., 2011), and can also be used in air filter materials (Deshmukh et al., 2019) and clothing fabrics (Noor et al., 2019).

Disinfection can also be performed by UV light-activated photosensitizers, which use nanosized titanium dioxide (TiO₂) to disinfect indoor environments, such as hospitals and clinics (Nakano et al., 2012; Boyce, 2016; Murphy et al., 2020). The effect of TiO₂ NPs on the influenza virus was evaluated by Mazurkova et al. (2010) and the results revealed that virus inactivation was dependent on the NPs concentration and the incubation period.

In addition to procedures for cleaning surfaces, the adoption of adequate personal and interpersonal hygiene practices, such as hand washing and care when sneezing and coughing, are essential to reduce the spread rate of COVID-19. An excellent option for hand hygiene is the AgNPs gel recently described for Ahmed et al. (2019). Researchers from Shri Shiv Chhatrapati College have also used a nanometal compound and an aromatic medicinal herb in a handwash formulation (eco-friendly and non-toxic for humans) with antiviral and antibacterial properties that can also be used for washing clothes (Joshi, 2020).

Graphene is another important nanomaterial with significant antimicrobial and antiviral activity. The ability to promote the steric impediment of bacterial, viruses, and other molecular agents, allows graphene to be used as a photoactivated agent or as a heat generator to sterilize fabrics and filters (Palmieri and Papi, 2020). Since coronavirus survives for up to about 3 h suspended in the environment, nanocomposites can also be used in air purifier devices to trap floating particles, preventing the spread of the virus in public and private spaces. Currently, carbon NPs-based membrane filters remove and destroy pathogens in the air and the water (Table 2). It was already demonstrated that CNTs and graphene sheets attach viral membrane by hydrogen bonds and electrostatic forces, entrapping infection agents and inactivating them by compression in carbon-based fibers (Brady-Estévez et al., 2010; Song et al., 2015; Rashid and Ralph, 2017).

TABLE 2

Table 2. Some types of carbon nanofillers used to remove viruses of air and water.

New elements have been tested to fabricate multifunctional devices that can remove contaminants from the air, including silicone, glass, alumina ceramics, and cellulose substrates. These have been superficially modified with nanostructures to capture pathogens by direct interception, Brownian diffusion, inertia impact, sedimentation, and electrostatic forces (Viswanathan et al., 2004; Zhao et al., 2005; Park and Hwang, 2014; Rashid and Ralph, 2017). In controlled conditions, Yeh et al. incorporated CNTs on a silicon surface to increase flu virus retention. Negatively charged MWCNTs (with length ranging from 10 to 1,000 nm) interact with bacteria and viruses by covalent bond, resulting in a filtration efficiency of 92% (Park and Hwang, 2014; Yeh et al., 2016). Although alumina ceramics membrane containing MWCNTs retain particles with diameters above 300 nm, polyethylene terephthalate (PET) conjugated with SWCNTs retained particle with a diameter between 11 and 650 nm (Nasibulin et al., 2011; Zhao et al., 2015). A single sheet of carbon nanotubes increases the filter thickness by 40 nm, but air purification efficiency is increased to 99.9% (Nasibulin et al., 2011).

Personal Protective Equipment (PPEs)

The use of protectives clothes, face masks, and respirators are essential for self-protection in vulnerable populations, who include infected patients, the elderly, immunocompromised individuals, and health professionals (Srivastava and Saxena, 2020). Several types of nanomaterials can be used in the development of more efficient filtration face masks and respirators, or to apply antimicrobial properties in personal protective equipment (PPEs). N95 respirators are well-known and, typically, used for high-risk situations (Chughtai et al., 2013). With a pore size of around 300 nm, N95 shows 85% efficiency for filtration of sub-300 nm particles, which is favorable to avoid contamination by SARS-CoV-2 (Bar-On et al., 2020). The use of disposable flexible nanoporous silicon-based membranes may improve the efficiency of N95 respirators since a filtering efficiency enhancement is obtained (pores down to 5 nm). Moreover, the reusability of the N95 face masks could be a strategy to minimize the problems related to the shortages of single-use face masks (El-Atab et al., 2020).

In a recent study, Si et al. developed green bioprotective nanofiber membranes with refillable antibacterial and antiviral activities, which were capable of producing biocidal reactive oxygen species when exposed to daylight. The membranes showed a high capacity to block fine particles (>99%), in addition to having high bactericidal (>99.999%), and virucidal (>99.999%) activities (Si et al., 2018). These results show that the use of nanostructured membranes could prevent the high spread of SARS-CoV-2. Nanofibers are also promising as filter materials for face masks and clothing (Ramakrishna et al., 2006; Akduman and Akcakoca Kumbasar, 2018). Some examples are TiO₂-coated nanofibers for the capture and destruction of viruses by UV radiation or natural sunlight (Weiss et al., 2020); electrospun nanofibers with the ability to retain aerosol particles with sizes from 20 to 200 nm (filtration efficiency over 99% for the thicker layer) (Faccini et al., 2012), and nylon-silver composite nanofibers (Francis et al., 2010; Montazer and Malekzadeh, 2012). Recently, the development of new reusable nano-filtered face masks containing nanofibers (diameter ranging from 100 to 500 nm) was announced by the research team at the Korea Advanced Institute of Science and Technology (KAIST). These face masks can be washed more than 20 times, without causing deformation in the nanomembrane structure (Kim, 2020).

Other attractive nanomaterials for filters, face masks, and protective clothing, are copper iodide NPs (Fujimori et al., 2012) and AgNPs (Galdiero et al., 2011). Zhong et al. have developed reusable graphene oxide face masks with super-hydrophobic properties able to improve protection performance. The products can be submitted to sunlight sterilization and recycled for desalination (Zhong et al., 2020). Additionally, after the COVID-19 outbreak, a silver nanocluster/silica composite coating was tested and showed a virucidal effect, reducing the SARS-CoV-2 titer to zero, under test conditions. This coating can be deposited on filtering media and ceramic, metallic, glass, and polymeric surfaces (Balagna et al., 2020). All these nanosystems show high potential for application against SARS-CoV-2.

Vaccines

Prophylactic vaccination is one of the most important, cheapest, and effective forms of health intervention. It is responsible for the control or the near eradication of many diseases, such as smallpox, polio, and measles (Nasrollahzadeh et al., 2020). According to the WHO, immunization prevents 2–3 million deaths per year in all age groups (World Health Organization, 2020b). Since the genetic sequence of SARS-CoV-2 was identified, a global race for a vaccine has started (Le et al., 2020), and 156 clinical vaccine development trials were registered when this review was written. Among them are RNA vaccines (NCT04368728), artificial antigen-presenting cell vaccine (NCT04299724), synthetic mini-gene vaccine (NCT04276896), recombinant novel CoV vaccine—Adenovirus type 5 vector (NCT04313127), and autologous dendritic cells loaded with antigens from SARS CoV-2 (NCT04386252) (U.S. National Library of Medicine, 2020).

Nanotechnology represents an excellent tool for vaccine development. It can be beneficial for antigen protection from premature degradation to enhance immunity response, control release kinetics, reduce adverse effects, deliver site-specific antigens, and facilitate intracellular uptakes (Zaman et al., 2013; Chen et al., 2017; Nasrollahzadeh et al., 2020; Poon and Patel, 2020). There are currently many commercially available nanotechnology-based vaccines, such as Gardasil^TM, Cervarix^TM, Inflexal^® V, and Epaxal^® (Chen et al., 2017).

Organic NPs gained traction concerning vaccine formulations due to the promising properties. Organic NPs have been used successfully in vaccine development, such as liposomes, lipid-based NPs, and polymeric NPs. Liposomes are the most used nanoparticles with clinically approved products for hepatitis A, and influenza A and B (Poon and Patel, 2020). Lipid-based NPs were previously used for the intradermal administration of mRNA for MERS-CoV S proteins, demonstrating significant humoral immune responses (Liu et al., 2020). Among the polymeric NPs, we can cite chitosan NPs for nasal SARS-CoV DNA immunization against SARS-CoV (Raghuwanshi et al., 2012) and PEI NPs, which are used for SARS-CoV plasmid DNA nasal vaccination (Shim et al., 2010).

Biopolymer-based NPs, such as protein-based NPs, are also attractive due to their low toxicity and biodegradability (Lohcharoenkal et al., 2014). SARS-CoV S protein NPs were used as a vaccine and induced antibody production in mice, especially when combined with Matrix M1 adjuvant. The NPs, with diameters of ca. 25 nm, were formed by the S trimers during protein purification (Coleman et al., 2014).

Virus-like proteins (VLPs) also have advantageous properties. They are formed by viral proteins displaying a high density of epitopes. Besides their high thermal stability, they lack any viral DNA/RNA, which makes them non-infectious. Furthermore, they can have non-protein antigens coupled to the surface and can induce cross-protection against different viruses. FDA vaccines have already approved some VLPs for the prevention of human papillomavirus, and hepatitis (Gregory et al., 2013; Poon and Patel, 2020). Moreover, a patent application was requested by Novavax for a MERS-CoV VLPs vaccine in 2015. The same company announced that their vaccine candidates for COVID-19 were developed using a recombinant NPs vaccine technology (Liu et al., 2020).

Several other nanotechnology-based systems have been used as carriers or adjuvants in the development of vaccines, among them AuNPs, which have been investigated against more than 45 pathogens, at different sizes, shapes, and functionalization (Dykman, 2020). Two important reviews summarize the conjugation of these metallic NPs with several viral antigens. We highlight a study that demonstrated the production of high levels of specific antibodies to M2e, a highly preserved peptide among serotypes, 15 months after immunization against influenza (Bimler et al., 2019). Aluminum NPs are another metallic structure that could be used in vaccines for respiratory pathogens, such as MERS-CoV and SARS-CoV, delivering antigens and inducing both humoral and cellular immune responses (Wang N. et al., 2020).

Recently, a significant result for COVID-19 was demonstrated by Sekimukai et al. AuNPs functionalized with S protein of SARS-CoV induced an antigen-specific response, however, they did not induce protective antibodies as nano vaccines and limited eosinophilic infiltration. This insufficient immunization against SARS-CoV indicates that more studies are needed for the development of better adjuvants to assist not only in SARS but also in MERS and COVID-19 situations (Sekimukai et al., 2020).

MSNPs present high surface area and large pore volume, which enable vaccine antigen incorporation by co-condensation or post-synthesis grafting (Poon and Patel, 2020). Guo et al. have demonstrated that MSNPs provide a slow release of proteins, resulting in an extended last immune response in mice (Guo et al., 2012).

Although they are widely applied to cancer treatment, cell-membrane-based nanostructures are also promising for antibacterial or antiviral vaccines (Rao et al., 2020). They can include membrane-coated NPs and vesicular structures, such as outer membrane vesicles (OMVs) and exosomes (Fang et al., 2017). Bacteria release OMVs as spherical structures (50–200 nm), which can be highly immunogenic. A dual vaccine for Influenza A H1N1 and MERS-CoV viruses based on OMVs had been recently proposed by Shehata et al. (2019). Currently, OMVs are being applied for COVID-19 vaccines (World Health Organization, 2020a) and there are four ongoing pre-clinical trials for protein subunit delivery from Intravacc/Epivax (in two trials), Quadram Institute Biosciences, and BiOMViS Srl/University of Trento (World Health Organization, 2020a).

In addition to antigen and genetic material delivery, NPs can be used as a substitute for aluminum-containing adjuvants. The mechanism is not clear, but it is suggested that these nanomaterials increase antigen uptake and promote the immunostimulation of antigen-presenting cells (Zaman et al., 2013). Graphene, nanodiamonds, and polystyrene particles can induce immune system activation, as well as CNTs, depending on their functionalization (Weiss et al., 2020). IONPs (Poon and Patel, 2020), AgNPs (Sanchez-Guzman et al., 2019), cobalt oxide NPs (Cho et al., 2012), aluminum NPs (Wang N. et al., 2020), AuNPs (Teng et al., 2018; Dykman, 2020), Au nanorods (Xu et al., 2012), and MSNPs (Carvalho et al., 2010) have also been evaluated as adjuvants in the immunization process. For instance, aluminum NPs were used as vaccine adjuvant-delivery systems (VADS) for pulmonary immunization using ovalbumin as a model antigen, improving the drainage of VADS to lymph nodes. This strategy represents a promising tool for targeting the vaccines to the respiratory tract, against pathogen microorganisms such as SARS-CoV and MERS-CoV (Wang N. et al., 2020).

Some studies using nanotechnology-based delivery and adjuvant for viral diseases are listed in Table 3. Nasrollahzadeh et al. and Nikaeen et al. have reported examples of NPs as virus vaccine delivery systems. Among them are AuNPs, chitosan NPs, VLPs, alginate-coated chitosan NPs, PLA and PLGA NPs, and di-lauroyl phosphatidylcholine liposomes. They highlight gold, ferritin, and S protein polymeric NPs as CoV vaccine candidates (Nasrollahzadeh et al., 2020; Nikaeen et al., 2020).

TABLE 3

Table 3. Nanomaterials used as adjuvants or delivery systems for viral diseases.

In the current situation, one of the main concerns is the development of a specific vaccine that provides safe and efficient prophylactic measures against SARS-CoV-2. All the studies described here have demonstrated the potential of nanotechnology to design effective immunization strategies. In pre-clinical COVID-19 studies among 139 candidates, several are based on nanomaterials such as a VLP developed by Geovax/BravoVax, an S protein subunit liposomal formulation for nasal delivery proposed by the University of Virginia, a lipid-based NPs for peptide delivery from IMV Inc., and recombinant protein NPs studied by the Saint-Petersburg research Institute (World Health Organization, 2020a).

One of the first clinical studies to evaluate the safety and immunogenicity of an NPs vaccine based on SARS-CoV-2 recombinant S protein with the MATRIX-M^TM Adjuvant I is being conducted by Novavax (NCT04368988). Other studies have used lipid-based NPs for RNA delivery (NCT04283461, ISRCTN 17072692, and NCT04368728) and plant-derived VLP (NCT04450004). Great expectations have been generated around vaccines, since the Moderna company, responsible for one of the RNA vaccines, announced that the product is potentially protective, eliciting antibody levels above the titers obtained for convalescent people in some initial participants (Weiss et al., 2020). Several other clinical trials are also underway to obtain a vaccine to SARS-CoV-2 (U.S. National Library of Medicine, 2020; World Health Organization, 2020a), and in Figure 5 we summarize the nanomaterials that can be used in the prevention against SARS-CoV-2.

FIGURE 5

Figure 5. Schematic representation of the nanomaterials used in COVID-19 prevention (figure created with BioRender.com).

Conclusions

Since December 2019, the SARS-CoV-2 outbreak has taken many lives and put countries all over the world on high alert. The severe nature of this COVID-19 pandemic situation highlights the importance of new technological proposals as a means of containing and stopping the spread of disease. The lack of approved antiviral drugs or vaccines, as well as the low efficacy and occurrence of adverse reactions, requires the use of novel therapeutic strategies against COVID-19. Currently, standard therapeutic approaches are based on antiviral drugs and adjuvant molecules that are already used in other viral diseases, and which can inhibit the virus uptake in tissues and block proteases activity in the infected cells. However, this strategy only decreases virus replication and symptoms.

Nanomedicine is a significant resource in the fight against novel coronavirus, but its use in clinical practice still presents great challenges, mainly concerning in vivo behavior, nanocarriers toxicity, and production on an industrial scale. Other important issues are a lack of a higher understanding of the particular characteristics and aspects of disease physiopathology, the processes involved in the nano-biointerface, as well as biocompatibility, safety, and regulatory issues. COVID-19 specific features and the physicochemical properties of the nanosystems can be explored and used to design personalized nanostructures for specific therapeutic purposes, seeking to neutralize the current threat to global public health and create more sustainable approaches based on nanotechnology. Although these factors have not yet been fully explored, they are essential for the safe and effective implementation of nanotechnologies against SARS-CoV-2 infection.

This review has discussed how nanotechnology could be used to prevent viral dissemination, improving the efficiency of protective equipment, increasing personal and social safety, and increasing the accuracy of COVID-19 diagnosis through fast and precise detection of infectious pathogens that involve a tiny volume of biological fluids. Moreover, nanosystems improve conventional therapies and aid in overcoming their therapeutic barrier since these nanocarriers can be modified to deliver antiviral molecules direct to diseased cells and, simultaneously, activate a host immune response against the virus. Therefore, nanomedicine has significant benefits for the prevention, diagnosis, and treatment of COVID-19, but it needs to be further explored and understood. The absence of antiviral therapies against COVID-19 in many ways presents an opportunity to boost the use of nanotechnological tools in virology.

Author Contributions

VC: supervision, conceptualization, investigation, writing, review, and editing. BM, EC, IS, LF, and PL: conceptualization, investigation, writing, and review. VZ: supervision, conceptualization, project administration, and funding acquisition. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors are thankful for the financial support of the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (Grant No. 2014/50947-7), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (Grant No. 440496/2016-0), and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Brasil (CAPES) (Grants No. 88881.130763/2016-01 and 23038.013951/2020-79).

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