Hostname: page-component-76fb5796d-wq484 Total loading time: 0 Render date: 2024-04-25T14:14:41.608Z Has data issue: false hasContentIssue false

Alcohol-based hand sanitisers as first line of defence against SARS-CoV-2: a review of biology, chemistry and formulations

Published online by Cambridge University Press:  29 September 2020

D. Singh
Affiliation:
School of Health Sciences, University of Petroleum and Energy Studies, Energy Acres, Bidholi, Via Premnagar, Dehradun248007, Uttarakhand, India
K. Joshi
Affiliation:
Department of Biotechnology, BJM School of Biosciences, Indian Institute of Technology Madras, Chennai, 600036, India
A. Samuel
Affiliation:
Department of Morphology, Surgery and Experimental Medicine, Universita'Degli Studi di Ferrara, Via Savonarola, 9, 44121Ferrara, FE, Italy
J. Patra
Affiliation:
School of Health Sciences, University of Petroleum and Energy Studies, Energy Acres, Bidholi, Via Premnagar, Dehradun248007, Uttarakhand, India
N. Mahindroo*
Affiliation:
School of Health Sciences, University of Petroleum and Energy Studies, Energy Acres, Bidholi, Via Premnagar, Dehradun248007, Uttarakhand, India
*
Author for correspondence: N. Mahindroo, E-mail: nmahindroo@ddn.upes.ac.in; Neeraj.Mahindroo@yahoo.com
Rights & Permissions [Opens in a new window]

Abstract

The pandemic due to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has emerged as a serious global public health issue. Since the start of the outbreak, the importance of hand-hygiene and respiratory protection to prevent the spread of the virus has been the prime focus for infection control. Health regulatory organisations have produced guidelines for the formulation of hand sanitisers to the manufacturing industries. This review summarises the studies on alcohol-based hand sanitisers and their disinfectant activity against SARS-CoV-2 and related viruses. The literature shows that the type and concentration of alcohol, formulation and nature of product, presence of excipients, applied volume, contact time and viral contamination load are critical factors that determine the effectiveness of hand sanitisers.

Type
Review
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press

Background

The outbreak of respiratory infection with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) virus has emerged as a serious global public health threat [Reference Gorbalenya1]. It is the third time in the last two decades that an animal coronavirus has emerged to cause epidemic infection in humans. The disease was first reported in Wuhan province of China at the end of 2019 but rapidly spread to infect more than 23 million people as of 25 August 2020, and has been associated with > 800 000 deaths [2].

The World Health Organization (WHO) declared a pandemic on 11 March 2020 and the infection has spread across almost all countries and regions of the world. Most infections appear to be asymptomatic or with mild flu-like symptoms but severe and life-threatening presentations including pneumonia, fever, nausea and gastrointestinal upset have been associated with individuals with predisposing factors, particularly age, respiratory insufficiency, diabetes and obesity, among others [Reference Huang3]. The WHO, and national disease control agencies, have continuously emphasised the importance of hand hygiene to reduce spread of the virus. WHO guidelines recommend maintaining hand hygiene, by frequent washing using soap and water for at least 20 s especially after going to the bathroom, before eating and after coughing, sneezing or blowing one's nose. When soap and water are not available, the Food and Drug Administration (FDA) recommends sanitising of non-visibly soiled hands with an alcohol-based agent containing 80% v/v ethanol or 75% v/v isopropanol [4].

Enveloped viruses such as coronavirus and influenza A H1N1 are able to survive on inanimate surfaces for long periods [Reference Firquet5]. It has been reported that some COVID-19 patients discharged the virus in their stool for up to 73 days after symptom onset [Reference Leung6], and as diarrhoea is a common symptom, faecal to oral cross-transmission is likely [Reference Yu7], and hence maintaining effective hand hygiene is paramount.

Alcohol-based hand sanitisation is widely considered to be effective to reduce or eliminate bacterial/viral load, but with variable compliance rates [Reference Jing8]. The alcohols, ethanol, isopropanol and n-propanol as used for disinfection are commonly applied in the form of hand rub rinses, gels and foams.

Owing to the increasing demand for hand sanitisation to control the spread of SARS-CoV-2, some manufacturers have resorted to their own formulations, which are not validated and licensed for use. To combat this, the FDA, WHO, the United States Pharmacopeia (USP) and the Central Drugs Standard Control Organization (CDSCO), India, have produced guidelines for the formulation and manufacture of such preparations [4, 9, 10]. This review assesses available information on the composition, formulation and effectiveness of alcohol-based hand disinfection products with specific reference to their activity against SARS-CoV-2.

Structural features of SARS-CoV-2

SARS-CoV-2 is a new member of the family Coronaviridae, order Nidovirales, and comprise of two sub-families, Coronavirinae and Torovirinae [Reference Fehr11]; it is the seventh coronavirus known to infect humans [Reference Andersen12]. SARS-CoV-2 is relatively large in size (0.12 μm) and characterised by the presence of highly glycosylated spikes on the protein membrane in a crown-like arrangement, hence the name, Corona (Fig. 1). It has a single-stranded positive-sense RNA genome of 29 891 nucleotides. The glycosylated spike protein binds to the host angiotensin converting enzyme-2 (ACE-2) protein which serves as a functional receptor for entry into host respiratory cells. This receptor also binds the earlier SARS-CoV but with 10–20 times less affinity than for SARS-CoV-2 spike protein [Reference Daniel13, Reference Lu14].

Fig. 1. Binding of SARS-CoV-2 to ACE-2 receptor.

Chemistry of virucidal action of hand sanitisers

Several antimicrobial compounds have been utilised for hand disinfection and include, among others, alcohols, chlorhexidine, chloroxylenol, hexachlorophene, benzalkonium chloride, cetrimide, triclosan and povidone-iodine [15]. The alcohols, namely ethanol and isopropanol, are most commonly used for skin disinfection due to their broad activity against bacteria, viruses and fungi [Reference Kampf16]; their mode of action against enveloped viruses is shown in Figure 2.

Fig. 2. Antiviral mechanism of action of alcohol against enveloped viruses.

Lipid membrane dissolution and protein denaturation are key mechanisms of the antimicrobial action of ethanol, leading to the disruption of membrane and inhibition of metabolism [Reference Wanderlingh17, Reference Andrew18].

Alcohols are amphiphilic compounds, as they possess both hydrophilic and lipophilic (hydrophobic) properties that facilitate their entry through the viral envelope. The outermost membrane of SARS-CoV-2 comprises lipids bound together by an alkane chain of hydrophobic fatty acids. Contact of the virus with an alcohol leads to alteration in its membrane fluidity [Reference Ingram19]. The presence of polar oxygen atoms weaken the lipophilic interactions between the non-polar residues, and increase the internal affinity of the membrane for water, thus destabilising and denaturing the protein structure [Reference Wanderlingh17]. The antimicrobial mechanism of alcohol against enveloped viruses is similar to that for bacteria as both have a lipid-rich outer membrane. Non-enveloped viruses are relatively more resistant to this mechanism due to the lack of a lipid membrane.

Viruses similar to SARS-CoV-2

The family Coronaviridae is comprised of four groups (Table 1). SARS-CoV-2 is considered to be taxonomically related to group 2 coronaviruses [Reference Schoeman20, Reference Wang21]. Virus and bovine viral diarrhoea virus (BVDV) are used for testing the effectiveness of chemical disinfectants and antiseptics against enveloped viruses according to DVV/Robert Koch Institute (RKI) guidelines [22]. The Modified Vaccinia Ankara (MVA) virus can also be used as a surrogate model for this purpose as it exhibits high stability against alcohol-based inactivation. The latter virus does not replicate in humans, thus eliminating the risk of disease through unintentional inoculation [Reference Eggers23, Reference Rabenau24]. Bovine coronavirus (BCV) has been used as a surrogate virus for SARS-CoV [Reference Kramer25], and owing to its high (80%) relatedness to SARS-CoV-2, consequently may have potential value as a surrogate test agent for the latter.

Table 1. Classification of Coronaviruses

Guidelines for testing of hand-disinfecting agents

The two most widely used guidelines for testing and regulation of hand disinfectants are the European Committee for Standardization (CEN) and the Food and Drug Administration (FDA), according to standards set by the American Society for Testing and Materials (ASTM).

CEN standards

EN 1499 and EN 1500 are the standard methods related to hygienic hand wash and hygienic hand disinfection respectively [26, 27]. In EN 1499, agents are tested against a reference non-medicated soap and in EN 1500 against 60% v/v isopropanol, both applied for 1 min. In the latter standard, the test hand rub formulation should not be significantly inferior, in terms of log reduction of the challenge microbe, compared with the reference alcohol-based product.

EN 14476 is the standard method for evaluating the virucidal activity of disinfectants [28] and is based on an in-vitro quantitative suspension test in which agents should exhibit a minimum of 4-log reduction in viability of the microbe. Poliovirus, adenovirus and murine norovirus serve as the basis for efficacy evaluation of surface disinfectants.

prEN 16777 is also a quantitative virucidal test method and is recommended for nonporous surfaces (in-vivo carrier test); a 4-log reduction is specified and ready-to-use surface disinfectants should be tested undiluted using adenovirus and murine norovirus as test pathogens. This test method simulates practical conditions and together with EN 14476 forms the basis for biocidal product registration in Europe [29].

ASTM standards

ASTM E-1838

A finger pad test method designed to compare the virus-eliminating effectiveness of hand washing and hand rubbing sanitisers using at least three healthy participants. Exposure time should be 10–20 s for hand washing and 20–30 s for a hand sanitation. The recommended test viruses include adenovirus 5, feline calicivirus, rotavirus, rhinovirus and murine norovirus at a minimum of 104 infectious units with or without a soil load. A 4-log reduction in virus load must be demonstrated by the test product in the presence and absence of 5% foetal bovine serum [30].

ASTM E-2011

This method evaluates the virucidal activity of hand wash and hand rub agents against viruses and is claimed to better reflect actual working conditions as it incorporates mechanical friction during whole-hand decontamination. At least three healthy participants are required and following application of virus suspension, the specified product exposure times are 10–20 s for hand washing and 20–30 s for a sanitiser. Test viruses include adenovirus type 2 or 5, feline calicivirus, rotavirus, rhinovirus and murine norovirus in the presence and absence of 5% foetal bovine serum as an interfering substance to simulate dirty conditions [31, 32].

ASTM E-2197

This method determines the efficacy of test disinfectants to inactivate viruses on disk carriers of brushed stainless steel, which act as a surrogate material for hard, non-porous environmental surfaces and medical devices [33, 34]

German standards

The German Society for Control of Viral Diseases (DVV) and Robert Koch-Institute (RKI) [Reference Blumel35] guidelines for quantitative virucidal tests on non-porous surfaces. Recommended test agents include the elstree vaccinia strain, poliovirus vaccination strain type I, LSc-2ab strain, adenovirus type 5 and polyomavirus (formerly, papovavirus) SV 40 strain 777.

DVV/RKI suspension test

This test is designed to determine activity against enveloped viruses, namely bovine diarrhoeal, and vaccinia viruses. The minimum test range for activity against all viruses is murine norovirus, adenovirus, poliovirus, polyomavirus and SV40 with a 4-log reduction in the presence and absence of 10% foetal calf serum [Reference Rabenau36].

DVV carrier test

This test is required to verify activity against vaccinia virus. The minimum test spectrum for all viruses is classified at two levels: (a) low level – vaccinia virus, murine norovirus and adenovirus and (b) high level – adenovirus, murine norovirus and murine parvovirus, with a minimum 4-log reduction in the presence and absence of 10% foetal calf serum [Reference Rabenau36].

Alcohol type and concentration

Most alcohols exhibit a broad spectrum of germicidal activity against vegetative bacteria, viruses and fungi. In general, isopropanol is considered to have better activity against bacteria, while ethanol is more potent against viruses. However, the degree of effect depends on the percentage concentrations of the alcohol and the physical properties of the target microorganism. Isopropanol is more lipophilic than ethanol and is consequently less active against hydrophilic viruses such as polioviruses. Being a lipophilic enveloped virus, SARS-CoV-2 exhibits greater susceptibility to isopropanol than ethanol [Reference Schoeman20, Reference Ionidis37, Reference Wu38].

The optimum bactericidal concentrations of alcohols range from 60% to 90% v/v solutions in water but are generally ineffective against most microorganisms below 50% v/v [Reference Morton39]. The effect of different concentrations of alcohol against enveloped viruses is shown in Table 2 [Reference Kramer25, Reference Ionidis37, Reference Larson40Reference Rabenau46]. A recent study has shown that >30% concentrations of ethanol or isopropanol were effective in inactivating SARS-CoV-2 within 30 s [Reference Kratzel47]. Propanol has a marginally higher boiling point than ethanol, hence, the drying time of isopropanol is slightly longer compared to ethanol [Reference Wilkinson48].

Table 2. Effect of alcohol type and concentration (% v/v)

WHO formulations for hand disinfection

The WHO has recommended two alcohol-based hand sanitiser formulations which differ only in their alcohol constituent, and is widely followed throughout the world.

Formulation 1: Ethanol 80% v/v, glycerol 1.45% v/v, hydrogen peroxide (H2O2) 0.125% v/v.

Formulation 2: Isopropyl alcohol 75% v/v, glycerol 1.45% v/v, hydrogen peroxide 0.125% v/v [49].

Due to the inherent variability of raw materials and the volatility of alcohol, and in response to the COVID-19 pandemic, the United States Pharmacopeia has issued a revision of WHO formulation 2 by increasing the concentration of isopropanol to 91% v/v [10]. An n-propanol-based formulation has not been proposed owing to the lack of safety data on human use [49]. In March 2020, the FDA recommended the industry to use either of the two WHO formulas but emphasised that ethanol should not be used at a concentration of <94.9% by volume. In a separate FDA guideline addressing the preparation and distribution of alcohol for incorporation in hand disinfectants, mention was made of the search for other active constituents including the use of denaturants such as acetone [50]. There was also comment that the recommended amount of glycerol in the WHO formulation might negatively impact the effectiveness of isopropanol [50]. Nevertheless, both WHO formulations have been shown to be effective against SARS-CoV-2 [Reference Kratzel47]. Indeed, with regards to the latter, CDC recommends the use of alcohol-based sanitisers containing >60% ethanol or 70% isopropanol for personnel working in healthcare settings [51]. This is supported by the finding that the WHO formulation containing isopropanol had higher activity against enveloped viruses [Reference Anindya52].

Factors influencing the effectiveness of sanitisers against SARS-CoV-2

The virucidal efficacy of hand sanitisers depends on several factors. As illustrated by the Ishikawa diagram (Fig. 3) showing the key factors which determine the efficacy of alcohol against SARS-CoV-2.

Fig. 3. Factors affecting the efficacy of alcohol-based hand sanitisers against SARS-CoV-2.

Formulation

The most commonly used formulations for hand sanitisers are rinse, foam, gel, wipes and spray. The 70% ethanol-based liquid products have proved highly effective against the non-enveloped viruses, poliovirus and adenovirus following exposure for 30 s [Reference Kampf53]. Alcohol-based hand rubs in the form of foam, rinse and gel did not differ significantly in trials of antimicrobial activity but the application volume and drying time had a profound effect on their efficacy [Reference Macinga54]. Another study, however, found that alcohol-based hand wipes were comparable in activity to foam and gel products against enveloped influenza (H1N1) virus. This was ascribed to better mechanical friction achieved with wipes, resulting in additional physical removal of virus that might survive the antimicrobial treatment [Reference Larson40]. Indeed, another comparative study concluded that hand gels are less effective for hand hygiene because of a shorter application time (<30 s) and therefore should not replace alcohol-based liquid hand disinfectants, or used as first choice agents [Reference Kramer55] despite the benefit of reducing skin irritation and dryness associated with liquid alcohol agents preparations. However, gel preparations containing 62% ethanol have been reported to be superior to 70% ethanol for the inactivation of surrogate coronaviruses MHV and TGEV on hard surfaces [Reference Hulkower41].

Foams have an advantage of better compliance by users due to ease of handling, non-spilling and non-stickiness. Bis-PEG12-dimethicone is commonly used as the foaming agent. It is recommended that an amount equivalent in size to a golf ball should be applied to hands [Reference Kampf56]; they also have the added benefit of the shortest drying times compared with rinses and gels [Reference Kampf57]. The approximate drying times of different alcohol-based formulations are given in Table 3.

Table 3. Effect of volume, type of alcohol-based formulation and drying time for hand disinfection

Volume and contact time

An increase in the volume of alcohol and contact time results in increased efficacy of alcohol-based hand sanitisers. One pump dispenser push releases approximately 1.5 ml of gel containing 70% alcohol has been found to be insufficient for complete coverage of both hands and hence, do not comply with ASTM efficacy standards [Reference Kampf57]. The use of 3 ml volume for foam, rinse and gel sanitisers containing 70%, 80% and 90% alcohol, respectively, is necessary to meet EN 1500 efficacy requirements, but the drying times of all preparations exceeded 30 s [Reference Macinga54]. The amount of sanitiser used also depends on the size of the subject's hands; females are relatively smaller (mean of eight volunteers 148.39 cm2, RSD = 5.17), and a lower volume of the agent could be sufficient when compared with men's hands (mean of eight volunteers 183.63 cm2, RSD = 7.5) [Reference Goroncy-Bermes58]. It is generally acknowledged that the ideal application volume is unknown, but US national guidelines suggest that a drying time of <15 s is insufficient [Reference Boyce59], while the WHO recommends use of a ‘palmful’ of product and that the hand-hygiene process should take at least 20 s [60]. Rotter et al. found that 3 ml of the EN 1500 reference product (isopropanol) takes more than 49 s to dry, despite a specified rub-time of 30 s [Reference Rotter61]. Similarly, a trial on disinfection of volunteer hands artificially contaminated with Escherichia coli K12 showed that WHO formulations containing either ethanol or isopropanol did not comply with the EN 1500 requirement as 60 s were taken to achieve the required log reduction. This led to the proposal that the ethanol concentration should be changed from 80% v/v to 80% w/w (equivalent to 85% v/v), and for isopropanol from 75% v/v to 75% w/w (equivalent to 80% v/v) [Reference Suchomel62]. The contact time of the agent is also relevant as a survey showed that the majority of nursing staff took only 6–24 s for hand cleansing [Reference Dharan63]. It has also been suggested that better compliance might be achievable in the hospital setting through listening to background music during the process [Reference Gautschi64].

Excipients

Glycerin is added in hand sanitisers as a humectant to reduce loss of skin moisture. WHO-recommended formulations contain glycerin but other nontoxic or allergenic emollients miscible in water and alcohol are not permitted for skin care [49].

Studies have shown that glycerol can reduce the efficacy of isopropanol-based sanitiser through agglomerates of flaking skin cells forming in the sticky glycerol [Reference Suchomel65]. A mixture of ethylhexylglycerin, dexpanthenol and a fatty alcohol serves as a suitable alternative with no effect on hand rub efficacy [Reference Suchomel66]. Indeed, the removal of glycerol from a formulation markedly increased the bactericidal activity of an isopropanol-based sanitiser [Reference Suchomel67]. This negative impact of glycerol has been noted in FDA guidelines regarding temporary compounding of alcohol-based hand sanitisers by industry during the COVID-19 pandemic [4]. Similarly, reducing the glycerol content from 1.45%, as per the WHO formulation, to 0.5% provided a better balance between antimicrobial efficacy and skin tolerance [Reference Menegueti68]. An extract of the Aloe vera plant has also been used as an emollient [Reference Berardi69].

pH

Human and canine corona viruses are reported to be more stable at a slightly acidic than alkaline pH [Reference Lamarre70, Reference Pratelli71] but mild alkaline (pH 8) conditions are sufficient to induce conformational changes in the spike protein of coronavirus mouse hepatitis virus [Reference Weismiller72]. Both high and low pH cause inactivation of SARS-CoV [Reference Darnell73]. The virucidal activity of ethanol against poliovirus and MS2 phage is significantly increased on the addition of sodium hydroxide [Reference Jones74] due to protein denaturation [Reference Alphin75]. Sodium hydroxide has also been shown to have cidal activity against surface dried lipid enveloped human immunodeficiency virus (HIV), bovine diarrhoeal virus and pseudorabies virus [Reference Terpstra76]. Other anti-viral agents include acetic acid and calcium hydroxide against influenza virus on hard and non-porous surfaces [Reference Alphin75]. Moreover, citric acid and urea (2%) have been reported to increase the effectiveness of alcohol-based sanitisers [Reference Ionidis37]; citric and malic acid, in combination with 70% alcohol have also been suggested to enhance killing of rhinovirus on hands [Reference Turner77].

Dirt and soil contamination

It is quite likely that the effect of hand sanitisers is reduced in the presence of dirt or soil on hands. A number of interfering substances have been used to simulate dirty conditions including foetal calf serum, bovine serum albumin and sheep erythrocytes according to DVV, RKI, ASTM and CEN standard guidelines [Reference Ionidis37, Reference Sickbert-Bennett78]. Soap hand wash coupled with an alcohol gel sanitiser was shown to be more effective than either agent used alone, and activity persisted for longer [Reference Paulson79]. These findings are corroborated by other studies showing increased reduction of murine norovirus with a wash-sanitiser regimen compared to washing with 70% ethanol alone in the presence of a high level of organic loads [Reference Edmonds80]. However, it is worth noting that hand washing with soap and water alone was found to be more effective than alcohol-based rubs for hands soiled with meat [Reference Charbonneau81].

Conclusion

Hand hygiene by washing hands with soap and water or with alcohol-based hand sanitisers are primary preventive measures against the spread of SARS-CoV-2. This review of the literature shows that several factors are pertinent to the antiviral activity of sanitising agents. Alcohol-based agents cause dissolution of the lipid membrane and denature proteins, thereby disrupting the virus membrane and inhibiting metabolism. The concentration of alcohol in hand-cleansing products, the volume used, contact time, degree of soiling, product formulation and use of excipients are some of the critical factors that affect the efficacy of alcohol against viruses.

Due to its relatively greater lipophilicity, isopropanol is considered more effective than ethanol against SARS-CoV-2. To ensure a greater than 3-log reduction of SARS-CoV-2, a hand sanitiser should ideally contain >80% v/v ethanol or >75% v/v isopropanol. However, recent study which suggests that ethanol and isopropanol used above 30% v/v is effective against SARS-CoV-2 [Reference Kratzel47] requires confirmation by other investigators. Gel-based hand sanitisers are reported to have more efficacy against enveloped viruses while foam-based preparations have the most rapid drying time. It is recommended that at least 3 ml of product should be used with a total contact time of around 45–50 s. Soiled hands can limit the efficacy of alcohol-based products as well as the presence of excipients; for isopropanol-based formulations, the replacement of glycerol with other emollients is recommended. Similarly, the addition of sodium hydroxide potentiates the antiviral activity of alcohols. Further studies are clearly needed on the optimum design and delivery form of agents for efficient hand decontamination of SARS-CoV-2. Such knowledge will prove of benefit for preparedness against other highly infectious viruses.

Acknowledgements

The Doctoral Research Fellowship from the University of Petroleum and Energy Studies to Jeevan Patra is gratefully acknowledged.

Conflict of interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Data availability statement

The datasets supporting the conclusions of this review article are included within the article and in references listed in the paper.

References

Gorbalenya, AE, et al. (2020) The species severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2. Nature Microbiology 5, 536–44.Google Scholar
John Hopkins Coronavirus Resource Center. Available at https://coronavirus.jhu.edu/map.html (Accessed August 25, 2020).Google Scholar
Huang, C et al. (2020) Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet (London, England) 395, 497506.CrossRefGoogle ScholarPubMed
Policy for temporary compounding of certain alcohol-based hand sanitizer products during the public health emergency immediately in effect guidance for industry. U.S. Department of Health and Human Services. Food and Drug Administration, Center for Drug Evaluation and Research (CDER), March 2020. Available at https://www.fda.gov/media/136118/download (Accessed on April 6, 2020).Google Scholar
Firquet, S et al. (2015) Survival of enveloped and non-enveloped viruses on inanimate surfaces. Microbes and Environments 30, 140–44.CrossRefGoogle ScholarPubMed
Leung, WK et al. (2003) Enteric involvement of severe acute respiratory syndrome-associated coronavirus infection. Gastroenterology 125, 1011–7.CrossRefGoogle ScholarPubMed
Yu, H et al. (2020) Public health might be endangered by possible prolonged discharge of SARS-CoV-2 in stool. Journal of Infection 80, e18–e9.Google Scholar
Jing, J et al. (2020) Hand sanitizers: a review on formulation aspects, adverse effects, and regulations. International Journal of Environmental Research and Public Health 17, 3326.CrossRefGoogle ScholarPubMed
Notification on: Monitoring of quality standards of hand sanitizers as per drugs and cosmetics act 1940, and rules made thereunder and expediting the licensing of manufacturers of such products (2020) Government of India, Directorate General of Health Services, Central Drugs Standard Control Organization, New Delhi, India: FDA Bhawan, Available at https://cdsco.gov.in/opencms/opencms/system/modules/CDSCO.WEB/elements/download_file_division.jsp?num_id=NTc4Nw== (Accessed on April 12, 2020).Google Scholar
Compounding Alcohol-Based Hand Sanitizer during COVID-19 Pandemic, March 25, 2020. Available at https://www.usp.org/sites/default/files/usp/document/about/public-policy/usp-covid19-handrub.pdf. (Accessed on April 12, 2020).Google Scholar
Fehr, AR et al. (2015) Coronaviruses: an overview of their replication and pathogenesis. Methods in Molecular Biology 1282, 123.CrossRefGoogle ScholarPubMed
Andersen, K et al. (2020) The proximal origin of SARS-CoV-2. Nature Medicine 26, 450–2.CrossRefGoogle ScholarPubMed
Daniel, W et al. (2020) Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation. Science (New York, N.Y.) 367, 1260–63.Google Scholar
Lu, R et al. (2020) Genomic characterization and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet (London, England) 395, 565–74.Google Scholar
WHO Guidelines on Hand Hygiene in Health Care (Advanced Draft) Global Patient Safety Challenge 2005–2006. (2009). Clean Care is Safer Care, 2009. Geneva, Switzerland: WHO Press. Available at https://www.who.int/patientsafety/information_centre/Last_April_versionHH_Guidelines%5B3%5D.pdf (Accessed on April 4, 2020).Google Scholar
Kampf, G et al. (2002) Spectrum of antimicrobial activity and user acceptability of the hand disinfectant agent sterillium gel. Journal of Hospital Infection 52, 141–7.CrossRefGoogle ScholarPubMed
Wanderlingh, U et al. (2010) Interaction of alcohol with phospholipid membrane: NMR and XRD investigations on DPPC–hexanol system. Spectroscopy 24, 375–80.CrossRefGoogle Scholar
Andrew, P et al. (2020) Hand sanitizers: a review of ingredients, mechanisms of action, modes of delivery, and efficacy against coronaviruses. American Journal of Infection Control 48, 1062–7.Google Scholar
Ingram, LO (1976) Adaptation of membrane lipids to alcohols. Journal of Bacteriology 125, 670–8.CrossRefGoogle ScholarPubMed
Schoeman, D et al. (2019) Coronavirus envelope protein: current knowledge. Virology Journal 16, 6990.CrossRefGoogle ScholarPubMed
Wang, L et al. (2020) A review of the 2019 Novel Coronavirus (COVID-19) based on current evidence. International Journal of Antimicrobial Agents 55, 105948.CrossRefGoogle ScholarPubMed
Guidelines of the DVV. Bode Science Center. Available at https://www.bode-science-center.com/center/glossary/guidelines-of-the-dvv.html (Accessed April 4, 2020).Google Scholar
Eggers, M et al. (2015) Povidone-iodine hand wash and hand rub products demonstrated excellent in vitro virucidal efficacy against Ebola virus and modified vaccinia virus Ankara, the new European test virus for enveloped viruses. BMC Infectious Diseases 15, 375–83.CrossRefGoogle ScholarPubMed
Rabenau, HF et al. (2010) Can vaccinia virus be replaced by MVA virus for testing virucidal activity of chemical disinfectants? BMC Infectious Diseases 10, 185–93.CrossRefGoogle ScholarPubMed
Kramer, A et al. (2006) Virucidal activity of a new hand disinfectant with reduced ethanol content: comparison with other alcohol-based formulations. Journal of Hospital Infection 62, 98106.CrossRefGoogle ScholarPubMed
European Standard EN 1499 (1997) Chemical Disinfectants and Antiseptics. Hygienic Hand Wash. Test Method and Requirements. Brussels: European Committee for Standardization.Google Scholar
European Standard EN 1500 (1997) Chemical Disinfectants and Antiseptics. Hygienic Handrub. Test Method and Requirements. Brussels: European Committee for Standardization.Google Scholar
European Committee for Standardization (2013) Chemical disinfectants and antiseptics – quantitative suspension test for the evaluation of virucidal activity in the medical area – test method and requirements (phase 2/step 1). Brussels, Belgium: EN 14476:2013 European Committee for Standardization.Google Scholar
European Committee for Standardization (2014) Chemical disinfectants and antiseptics. Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area. Test method and requirements (phase 2/step 2). prEN 16777:2014. Brussels, Belgium: European Committee for Standardization.Google Scholar
ASTM E1838 Determining the virus-eliminating effectiveness of hygienic handwash and handrub agents using the fingerpads of adults. Eurofins CRL. Available at https://vivotesting.com/information/astm-e1838-virucidal-fingerpad-testing (Accessed on April 4, 2020).Google Scholar
ASTM E2011-13 (2013) Standard Test Method for Evaluation of Hygienic Handwash and Handrub Formulations for Virus-Eliminating Activity Using the Entire Hand. West Conshohocken, PA, ASTM International.Google Scholar
ASTM E2197-17e1 – Standard Quantitative Disk Carrier Test Method for Determining Bactericidal, Virucidal, Fungicidal, Mycobactericidal, and Sporicidal Activities of Chemicals, ASTM International, West Conshohocken, PA, 2017.Google Scholar
Blumel, J et al. (2009) Guideline of deutsche vereinigung zur bekampfungder viruskrankheiten e.V. (DVV; German Association for the Control of Virus Diseases) and Robert Koch Institute (RKI; German Federal Health Authority) for testing the virucidal efficacy of chemical disinfectants in the human medical area. Hygiene Medicine 34, 293–9.Google Scholar
Rabenau, HF et al. (2012) Leitline der deutschen vereinigung zur bekämpfung der viruskrankheiten (DVV) e.V. zur quantitativen prüfung der viruziden wirksamkeit chemischer desinfektionsmittel auf nicht-porösen oberflächen. Anwendung im bereich humanmedizin. Hygiene Medicine 37, 459–66.Google Scholar
Ionidis, G et al. (2016) Development and virucidal activity of a novel alcohol-based hand disinfectant supplemented with urea and citric acid. BMC Infectious Diseases 16, 7787.CrossRefGoogle ScholarPubMed
Wu, Q et al. (2003) The E protein is a multifunctional membrane protein of SARS-CoV. Genomics, Proteomics and Bioinformatics 1, 131–44.CrossRefGoogle Scholar
Morton, HE (1950) The relationship of concentration and germicidal efficiency of ethyl alcohol. Annals of the New York Academy of Sciences 53, 191–96.CrossRefGoogle ScholarPubMed
Larson, EL et al. (2012) Analysis of alcohol-based hand sanitizer delivery systems: efficacy of foam, gel, and wipes against influenza A (H1N1) virus on hands. American Journal of Infection Control 40, 806–9.CrossRefGoogle ScholarPubMed
Hulkower, RL et al. (2011) Inactivation of surrogate coronaviruses on hard surfaces by health care germicides. American Journal of Infection Control 39, 401–7.CrossRefGoogle ScholarPubMed
Sattar, SA et al. (1989) Chemical disinfection of non-porous inanimate surfaces experimentally contaminated with four human pathogenic viruses. Epidemiology and Infection 102, 493505.CrossRefGoogle ScholarPubMed
Krilov, LR et al. (1993) Inactivation of respiratory syncytial virus by detergents and disinfectants. The Pediatric Infectious Disease Journal 12, 582–3.CrossRefGoogle ScholarPubMed
Kariwa, H et al. (2006) Inactivation of SARS coronavirus by means of povidone-iodine, physical conditions and chemical reagents. Dermatology (Basel, Switzerland) 212, 119–23.CrossRefGoogle ScholarPubMed
Rabenau, HF et al. (2004) Stability and inactivation of SARS coronavirus. Medical Microbiology and Immunology 194, 16.CrossRefGoogle Scholar
Rabenau, HF et al. (2005) Efficacy of various disinfectants against SARS coronavirus. Journal of Hospital Infection 61, 107–11.CrossRefGoogle ScholarPubMed
Kratzel, A et al. (2020) Inactivation of severe acute respiratory syndrome coronavirus 2 by WHO-recommended hand rub formulations and alcohols. Emerging Infectious Diseases 26, 1592–5.CrossRefGoogle ScholarPubMed
Wilkinson, MAC et al. (2018) Comparison of the efficacy and drying times of liquid, gel and foam formats of alcohol-based hand rubs. Journal of Hospital Infection 98, 359–64.CrossRefGoogle ScholarPubMed
Guide to local Production(2009) WHO Recommended Hand-rub Formulations. Geneva, Switzerland: WHO Press. Available at https://www.who.int/gpsc/5may/Guide_to_Local_Production.pdf. (Accessed on April 4, 2020).Google Scholar
Temporary policy for manufacture of alcohol for incorporation into alcohol based hand sanitizer products during the Public Health Emergency (COVID-19); Guidance for industry U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), 2020. Available at https://www.fda.gov/media/136390/download (Accessed April 4, 2020).Google Scholar
CDC Statement for Healthcare Personnel on Hand Hygiene during the Response to the International Emergence of COVID-19. Coronavirus Disease 2019, Centers for Disease Control and Prevention. Available at https://www.cdc.gov/coronavirus/2019-ncov/infection-control/hcp-hand-sanitizer.html (Accessed on April 4, 2020).Google Scholar
Anindya, S et al. (2017) Virucidal activity of World Health Organization-recommended formulations against enveloped viruses, including Zika, Ebola, and emerging coronaviruses. Journal of Infectious Diseases 215, 902–6.Google Scholar
Kampf, G et al. (2013) Efficacy of hand rubs with a low alcohol concentration listed as effective by a national hospital hygiene society in Europe. Antimicrobial Resistance and Infection Control 2, 1926.CrossRefGoogle ScholarPubMed
Macinga, DR et al. (2014) The relative influences of product volume, delivery format and alcohol concentration on dry-time and efficacy of alcohol-based hand rubs. BMC Infectious Diseases 14, 511–19.CrossRefGoogle ScholarPubMed
Kramer, A et al. (2002) Limited efficacy of alcohol-based hand gels. Lancet (London, England) 359, 1489–90.CrossRefGoogle ScholarPubMed
Kampf, G et al. (2010) Efficacy of ethanol-based hand foams using clinically relevant amounts: a cross-over controlled study among healthy volunteers. BMC Infectious Diseases 10, 7883.CrossRefGoogle ScholarPubMed
Kampf, G et al. (2013) Less and less-influence of volume on hand coverage and bactericidal efficacy in hand disinfection. BMC Infectious Diseases 13, 472–79.CrossRefGoogle ScholarPubMed
Goroncy-Bermes, P et al. (2010) Impact of the amount of hand rub applied in hygienic hand disinfection on the reduction of microbial counts on hands. Journal of Hospital Infection 74, 212–8.CrossRefGoogle ScholarPubMed
Boyce, JM et al. (2002) Healthcare infection control practices advisory committee; HICPAC/SHEA/APIC/IDSA hand hygiene task force. Guideline for hand hygiene in health-care settings. Recommendations of the healthcare infection control practices advisory committee and the HIPAC/SHEA/APIC/IDSA hygiene task force. American Journal of Infection Control 30, S146.CrossRefGoogle ScholarPubMed
World Health Organization (2009) WHO Guidelines on Hand Hygiene in Health Care, 2009. Geneva [Switzerland]: WHO Press. Available at https://apps.who.int/iris/bitstream/handle/10665/44102/9789241597906_eng.pdf;jsessionid=83179514CB5F49214E3F10DBBE827651?sequence=1 (Accessed on April 4, 2020).Google Scholar
Rotter, M et al. (2009) Impact of shortening the duration of application and the standardized rubbing sequence as well as the reduction of the disinfectant volume used for the hygienic hand rub with 2-propanol (60% v/v). Hygiene Medicine 34, 1923.Google Scholar
Suchomel, M et al. (2012) Testing of the World Health Organization recommended formulations in their application as hygienic hand rubs and proposals for increased efficacy. American Journal of Infection Control 40, 328–31.CrossRefGoogle ScholarPubMed
Dharan, S et al. (2003) Comparison of waterless hand antisepsis agents at short application times: raising the flag of concern. Infection Control and Hospital Epidemiology 24, 160–4.CrossRefGoogle ScholarPubMed
Gautschi, N et al. (2017) Effect of music on surgical hand disinfection: a video-based intervention study. Journal of Hospital Infection 95, 352–4.CrossRefGoogle ScholarPubMed
Suchomel, M et al. (2017) Influence of glycerol and an alternative humectant on the immediate and 3-hours bactericidal efficacies of two isopropanol-based antiseptics in laboratory experiments in vivo according to EN 12791. Antimicrobial Resistance and Infection Control 6, 72–7.CrossRefGoogle Scholar
Suchomel, M et al. (2013) Glycerol significantly decreases the 3-hours efficacy of alcohol-based surgical hand rubs. Journal of Hospital Infection 83, 284–7.CrossRefGoogle Scholar
Suchomel, M et al. (2013) Modified world health organization hand rub formulations comply with european efficacy requirements for preoperative surgical hand preparations. Infection Control and Hospital Epidemiology 34, 245–50.CrossRefGoogle ScholarPubMed
Menegueti, MG et al. (2019) Glycerol content within the WHO ethanol-based handrub formulation: balancing tolerability with antimicrobial efficacy. Antimicrobial Resistance and Infection Control 8, 109–17.Google ScholarPubMed
Berardi, A et al. (2020) Hand sanitisers amid CoVID-19: a critical review of alcohol-based products on the market and formulation approaches to respond to increasing demand. International Journal of Pharmaceutics 584, 119431.CrossRefGoogle ScholarPubMed
Lamarre, A et al. (1989) Effect of pH and temperature on the infectivity of human coronavirus 229E. Canadian Journal of Microbiology 35, 972–4.CrossRefGoogle ScholarPubMed
Pratelli, A (2008) Canine coronavirus inactivation with physical and chemical agents. The Veterinary Journal 177, 71–9.CrossRefGoogle ScholarPubMed
Weismiller, DJ et al. (1990) Monoclonal antibodies to the peplomer glycoprotein of coronavirus mouse hepatitis virus identify two subunits and detect a conformational change in the subunit released under mild alkaline conditions. Journal of Virology 64, 3051–5.CrossRefGoogle ScholarPubMed
Darnell, MER et al. (2004) Inactivation of the coronavirus that induces severe acute respiratory syndrome, SARS-CoV. Journal of Virological Methods 121, 8591.CrossRefGoogle ScholarPubMed
Jones, MV et al. (1991) The use of bacteriophage MS2 as a model system to evaluate virucidal hand disinfectants. Journal of Hospital Infection 17, 279–85.CrossRefGoogle ScholarPubMed
Alphin, RL et al. (2009) Inactivation of avian influenza virus using four common chemicals and one detergent. Poultry Science 88, 1181–5.CrossRefGoogle ScholarPubMed
Terpstra, AG et al. (2007) Resistance of surface-dried virus to common disinfection procedures. Journal of Hospital Infection 66, 332–8.CrossRefGoogle ScholarPubMed
Turner, RB et al. (2010) Effectiveness of hand sanitizers with and without organic acids for removal of rhinovirus from hands. Antimicrobial Agents and Chemotherapy 54, 1363–4.CrossRefGoogle ScholarPubMed
Sickbert-Bennett, EE et al. (2004) The effects of test variables on the efficacy of hand hygiene agents. American Journal of Infection Control 32, 6983.CrossRefGoogle ScholarPubMed
Paulson, DS et al. (1999) A close look at alcohol gel as an antimicrobial sanitizing agent. American Journal of Infection Control 27, 332–8.CrossRefGoogle Scholar
Edmonds, SL et al. (2012) Hand hygiene regimens for the reduction of risk in food service environments. Journal of Food Protection 75, 1303–9.CrossRefGoogle ScholarPubMed
Charbonneau, DL, et al. (2000) A method of assessing the efficacy of hand sanitizers: use of real soil encountered in the food service industry. Journal of Food Protection 63, 495501.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. Binding of SARS-CoV-2 to ACE-2 receptor.

Figure 1

Fig. 2. Antiviral mechanism of action of alcohol against enveloped viruses.

Figure 2

Table 1. Classification of Coronaviruses

Figure 3

Table 2. Effect of alcohol type and concentration (% v/v)

Figure 4

Fig. 3. Factors affecting the efficacy of alcohol-based hand sanitisers against SARS-CoV-2.

Figure 5

Table 3. Effect of volume, type of alcohol-based formulation and drying time for hand disinfection