| Literature DB >> 35039802 |
Ayesha Hashmi1, Vanya Nayak2,3, Kshitij Rb Singh1,2, Bhawana Jain1, Mitisha Baid1, Frank Alexis4, Ajaya Kumar Singh1.
Abstract
Graphene is a two-dimensional material with sp2 hybridization that has found its broad-spectrum potentialities in various domains like electronics, robotics, aeronautics, etc.; it has recently gained its utilities in the biomedical domain. The unique properties of graphene and its derivatives of graphene have helped them find their utilities in the biomedical domain. Additionally, the sudden outbreak of SARS-CoV-2 has immensely expanded the research field, which has also benefitted graphene and its derivatives. Currently, the world is facing a global pandemic due to the sudden outbreak of Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2), also known as COVID-19, from its major onset in Wuhan city, China, in December 2019. Presently, many new variants and mutants appear, which is more harmful than previous strains. However, researchers and scientists are focused on understanding the target structure of coronavirus, mechanism, causes and transmission mode, treatment, and alternatives to cure these diseases in this critical pandemic situation; many findings are achieved, but much more is unknown and pending to be explored. This review paper is dedicated to exploring the utilities of graphene and its derivatives in combating the SARS-CoV-2 by highlighting their mechanism and applications in the fabrication of biosensors, personal protection equipment (PPE) kits, 3-D printing, and antiviral coatings. Further, the paper also covers the cytotoxicity caused by graphene and its derivatives and highlights the graphene-based derivatives market aspects in biomedical domains. Thus, graphene and graphene-derived materials are our new hope in this pandemic time, and this review helps acquire broad knowledge about them.Entities:
Keywords: Applications; COVID-19 pandemic; Cytotoxicity; Graphene oxide (GO); Graphene-based derivatives; Nanotechnology; SARS-CoV-2
Year: 2022 PMID: 35039802 PMCID: PMC8755454 DOI: 10.1016/j.mtadv.2022.100208
Source DB: PubMed Journal: Mater Today Adv ISSN: 2590-0498
Fig. 1Systematic diagram of graphene and graphene-based derivatives.
Fig. 2A general diagrammatic illustration of highly sensitive and selective sandwich-type immunosensor [G@silver NPs@CS (G@Ag NPs@CS] for detecting the avian influenza virus H7.
Fig. 3The hypothetical mode of mechanism for the detection of the SARS-CoV-2/COVID-19 virus.
Illustration of graphene and graphene-based biosensors.
| Graphene and graphene derived materials | Varieties of bio-sensors | Biomarkers | Detection limit | Ref. |
|---|---|---|---|---|
| Gold/graphene nanocomposites | Amperometric | Monoclonal antibodies | 1.6 pg/mL | [ |
| GO | Electrochemical | Human immune-deficiency Virus Type 1 | 8.3 fM | [ |
| r-GO | Electrochemical | Plaque | 26 and 33 plaque-forming units | [ |
| r-GO | Field-effect transistor | Ebola virus glycoprotein | 2.4 pg/mL | [ |
| Graphene interlinked with gold electrode/piezoelectric sensors | Piezoelectric Quartz Crystal | Bacterial cell of Staphylococcus aureus | 41 cfu/mL | [ |
| Silver/graphene quantum dots (GQDs) | Electrochemical | Antibody | 3 fg/mL | [ |
Fig. 4Illustration of noteworthy properties of graphene and graphene-based materials in PPEs.
Graphene and graphene-based modified fabrics with efficient properties for fabricating smart and personal protective cloths.
| Materials | Methods | Enhanced properties of materials | Applications | Ref. |
|---|---|---|---|---|
| PET/Graphene | Melt compounding (Brabender mixer) and compression molding | Enhanced Electrical conductivity | Smart PPE | [ |
| Cotton/GO/TiO2 (Fe, N-doped) | Dispersed, hydrothermal method, by immersion and coating method TiO2/Fe/N/GO dried smeared over to the textiles | Self-compatible, great antimicrobial Activity and biologically compatible | Medical apron, Sporting garments, fighting uniform tc. | [ |
| Silk/r-GO | Using the dip and dry method, silk material was bound by GO; treated fabrics were then chemically reduced by sodium hydrosulfite. | Excellent electrical conductivity, water repulsive and show antiultraviolet nature | Medical cloth and E-textile | [ |
| Silk/r-GO/bovine serum albumin (BSA) or remodeling and spacing factor 1 (RSF) Protein | By using the dipping method, Silk fabric was wrapped with GO suspension. BSA and RSF protein was used as a bonding agent. It is very much condensed by thermal treatment. | Shows great Electrical conductivity | Smart fabrics | [ |
| Wool/r-GO/TiO2 | GO/TiO2 turned into immersed with wool, where hydrolysis of titanium isopropoxide and chemical conversion with the aid of sodium hydrosulfite occurred to form graphene/TiO2 nanocomposite. Then the composite dried out and condensed by chemically route. | Great antimicrobial activity and self-cleaning competence | Medical care cloths and smart Fabric. | [ |
| PET/r-GO/polypyrrole | Polypyrrole was coated on PET/r-GO fabric via in-situ synthesis. By using the chemical reduction method, PET turned into covered on GO by dip and dry method. The organized composite was hot pressed to make a film. | Surface chemistry and show a best soaking ability | Shielding Clothing | [ |
| Polyester/r-GO | With the aid of plasma treatment and bovine serum albumin as a bonding agent | Boost Conductivity | Smart fabrics | [ |
| Nylon-12/GO | Soften compounding and compression molding techniques | Tensile strength, improved bearing strength, elongation at the wreck, and durability defensive | Protective Wear | [ |
| Para aramid/graphene/Polyurethane | By way of immersion and drying approach, Para-aramid fiber was enfolded by graphene/waterborne polyurethane. Then prepared composites were hot pressed under distinct temperatures. | Cleaning durability | Protective Wear | [ |
Commercially available graphene and graphene-based face mask.
| Product name | Developed by | Antibacterial agents | Efficiency of the products | Observations | Ref. |
|---|---|---|---|---|---|
| Guardian G-Volt | LIGC Applications (US) | Graphene and electrical Charge | – | Deposited particles were repelled by electric charge. 99% effective towards 0.3 mm particles. | [ |
| Graphene-enhanced face mask | Planar TECH & IDEATI's | Graphene and other carbon-based derivatives | 99.95% effective against S. aureus within 24 h | Reusable up to 10 cycles, Repels the PM 2.5 dust, pack of three masks available at costs at 24.95 USD | [ |
| Leaf | Redcliffe Medical Devices Inc. (US) | Ultraviolet C (UVC) | Discount of influenza A Virus approx 99.99% | FDA cleared UVC N99 to face mask, HEPA and vigorous carbon filters, 99.9997% filtration ability of 0.3 mm size | [ |
| Maya sticker | National Emergency crew of Israel and Israel Institute of Technology | Nanofibres glazed with Disinfectants | Blocks and diminish the effect of viral Debris. | This label can be involved in ordinary surgical face guises for utilization. | [ |
| Nsafe+ | Nanoscale solutions and Indian Institute of Technology Delhi (India) | – | – | Antimicrobial layer on the mask with Triple-layer filtration, best filtration efficiency around 99.2%, as much as 50 times recyclable affinity. | [ |
Fig. 5Expressive representation of graphene-based three-layered mask to protect against coronavirus.
Various graphene and graphene-based derivatives for antiviral surfaces and coatings.
| Graphene and graphene-based derivatives | Mechanism | Targeted virus | Remarks | Ref. |
|---|---|---|---|---|
| GO | The GO-Infection physiochemical associations cause infection catching and RNA spillage from the infection. | EV71 (RNA capsid Infection, Capsid Infection, extremely normal among kids) H9N2 (RNA wrapped infection, liable for human flu alongside bird influenza). | GO altogether upholds outright destruction, rejection, and sterilization, coming about in somewhere around a 6-log decrease in infectivity. The GO nanoparticles are a progressive method for anticipating infection transmission in the climate and bringing down the danger of disease through diminished ecological defilement, handling time, and cost. | [ |
| Curcumin-decorated with β –CD functionalized sulfonated graphene (GSCC) | Through a competitive inhibitory mechanism | RSV (wrapped RNA infection can taint the respiratory lobes and regularly causes respiratory sickness in recently conceived newborn youngsters, youths, mature individuals, and immune-compromised people groups). | The powerful grouping of GSCC is discovered to be non-harmful to the host cells. The viral titer showed four sets of decreases utilizing GSCC. | [ |
| GO, r-GO, Graphite, Graphite oxide, GO-PVP, | The antiviral component is ascribed to the negative charge of GO and its nanosheet structure. | PRV (DNA infection, contaminate the greater part of the vertebrates, cause injuries fundamentally in CNS, respiratory framework and regenerative framework) PEDV (RNA infection, having a place with emphatically charged alpha Covid, liable for high death rate in Pigs). | PRV and PEDV by underlying obliteration before the viral passage into the cell. GO, GO-PDDA and GO-PVP show the best antiviral effect even at a low concentration. | [ |
| GO and r-GO/SO3 | Competitive Inhibition Mechanism | Herpes simplex virus type-1 (HSV-1) (DNA infection, contaminating 70–90% mortal populace) | GO and r-GO/SO3 show good inhibition of the viral infection at low concentration and reduce plaque development. Both graphene and SO3 based reduced graphene shows non-toxic behavior to the Vero cell culture. | [ |
| GO/AgNPs | The inhibitory work represents an obstacle to the infection entering the host cell and by advancing ISGs and IFN-a. | Procine reproductive and respiratory syndrome virus (PRRSV) typically contaminate the young pigs) | GO-AgNPs nanocomposites inhibit the PRRSV towards the inside in the host cell and its replication. | [ |
Graphene and its compounds cause cytotoxicity in vitro and in vivo
| Materials | In vitro/in vivo | Different Cell tissue | Dosage variation | Cytotoxic/biological effect | References |
|---|---|---|---|---|---|
| GO | The outermost cell of Skin (Keratinocyte) | 0.4, 1.2, 3.7, 11.1, 33.3, and 100 g/mL at 3–72 h | Reactive oxygen species generation is dose and time dependant. | [ | |
| GO-PEG | Mouse osteoblast progenitor cells (Saos-2; | For 24 h, 75 μg/mL | GO-PEG accumulates on F-actin, resulting in the construction of reactive oxygen species (ROS). | [ | |
| GO-NH2 | Mice | 250 μg/kg | There was no pulmonary embolism. | [ | |
| r-GO; | Human lung cell (A549) | 1–200 μg/mL | Toxicity that is dose dependant. | [ | |
| r-GO-PEG | Albino mice | 10 mg/kg | The liver, kidneys, bone marrow, spleen, and brain all contain r-GO/PEG. | [ | |
| GO | Human | For 3 h at different concentration such as, 3.12, 6.25, 12.5, 25, 50, 100, and 200 μg/mL | Size and dose dependent | [ | |
| GO | Rabbits | 100–300 | There was no alteration found in the appearance of the eyeball or the intraocular pressure. | [ | |
| hGO; GO | B6 mice | 2 mg/kg | In alveolar macrophages, hydrated GOs caused more significant lung irritation and lipid peroxidation than GOs individually. | [ | |
| Green r-GO | Human | 50, 100 and 250 μg/mL | At >100 μg/mL, lysosomal integrity is lost. | [ | |
| TRG | Vero cell of monkey | 10, 50, 100 and 300 μg/mL for 24 h | Apoptosis at >100 μg/mL | [ | |
| GO | Swine | 1–4 h at 0.5, 1, 5, 10, and 50 μg/mL | Toxicity that is dose dependant. At a concentration of >10 μg/mL, cells die. | [ |