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The relative influences of product volume, delivery format and alcohol concentration on dry-time and efficacy of alcohol-based hand rubs
© Macinga et al.; licensee BioMed Central Ltd. 2014
Received: 17 January 2014
Accepted: 18 September 2014
Published: 20 September 2014
Alcohol-based hand rubs (ABHR) range in alcohol concentration from 60-95% and are available in a variety of delivery formats, such as rinses, gels, and foams. Recent studies suggest that some ABHR foams dry too slowly, thereby encouraging the use of inadequate volumes. This study investigates the influence of product volume, delivery format, and alcohol concentration on dry-time and antimicrobial efficacy of ABHR foams, gels and rinses.
ABHR dry-times were measured using volunteers to determine the influences of product volume, delivery format, and alcohol concentration. ABHR efficacies were evaluated according to the European Standard for Hygienic Hand Disinfection (EN 1500) using 3-mL application volumes rubbed for 30 s, and additionally, using volumes of the products determined to rub dry in 30 s.
Volumes of six ABHR determined to rub dry in 30 s ranged from 1.7 mL to 2.1 mL, and the rate of drying varied significantly between products. ABHR dry-times increased linearly with application volume and decreased linearly with increasing alcohol concentration, but were not significantly influenced by product format. An ABHR foam (70% EtOH), rinse (80% EtOH), and gel (90% EtOH) each met EN 1500 efficacy requirements when tested at a volume of 3 mL, but failed when tested at volumes that dried in 30 s.
Application volume is the primary driver of ABHR dry-time and efficacy, whereas delivery format does not significantly influence either. Although products with greater alcohol concentration dry more quickly, volumes required to meet EN 1500 can take longer than 30 s to dry, even when alcohol concentration is as high as 90%. Future studies are needed to better understand application volumes actually used by healthcare workers in practice, and to understand the clinical efficacy of ABHR at such volumes.
KeywordsAlcohol-based hand rub ABHR foam Application volume Dry-time In vivo efficacy EN 1500
Alcohol-based hand rubs (ABHRs) are recommended for routine hand disinfection in healthcare settings when hands are not visibly soiled [1, 2]. Their role and importance has been highlighted by numerous studies associating their use with clinical reductions in hospital-acquired infections (HAIs) [1, 2]. ABHR are available in a number of different delivery formats, such as rinses (i.e., thin liquids), gels, and foams. Each product format may offer a unique functional benefit, depending on the situation. For example, because gels and foams tend to drip from the hands less than rinses, the entire volume is delivered to the hands. And, beyond their functional attributes, there can be aesthetic preferences for specific ABHR formats .
Despite a large body of evidence supporting the use of ABHR for infection prevention, consensus is lacking as to the appropriate amount of a product that should be applied to the hands. The US Centers for Disease Control and Prevention (CDC) Guidelines for Hand Hygiene in Healthcare Settings acknowledges that the ideal volume of product to apply to the hands is unknown, but states that, if hands dry before 10 to 15 s, an insufficient amount was used . The World Health Organization (WHO) Guidelines on Hand Hygiene in Health Care recommends that a “palmful” of product be used and states that the hand-hygiene event should take 20-30 s . Despite lack of specific guidance on application volume, it has been clearly demonstrated by in-vivo microbiological studies and in clinical settings that antimicrobial efficacy of ABHR is directly proportional to application volume, and that ABHR will not meet global efficacy standards if insufficient volumes of product are applied [4–7]. It should be noted, further, that success criteria for current efficacy standards are arbitrary and not based on clinical outcomes [8, 9].
A recent study by Kampf et al. found that recommended use volumes for ABHR foams containing 62% ethanol exceeded the WHO recommended dry-time of 30 s, and that a volume that rubbed dry in 30 s (1.6 mL) was insufficient to meet the efficacy criterion of EN 1500 . The authors concluded that because the “…time required for dryness often exceeds the recommended 30 s … only a small volume of these foams (below that required to meet efficacy norms) is likely to be applied in clinical practice”. The study evaluated only ABHR foams, and all test products contained the same alcohol concentration; therefore, broad conclusions should not be drawn as to whether the observed drying rates are attributable to product format or to alcohol concentration. A study by Rotter et al. found that 3 mL of the EN 1500 Reference Product required, on average, more than 49 s to dry, despite the method specifying a rub-time of 30 s . These data suggest that dry-time versus volume of an ABHR, regardless of delivery format, is an important relationship for study.
The objectives of this study were 1) to determine the influence of product volume, delivery format, and alcohol concentration on ABHR dry-time and antimicrobial efficacy, and 2) to investigate the efficacy of ABHRs when applied at volumes drying in 30 s, as specified by WHO.
Products tested in this study
Test product name
PURELL® Instant Hand Sanitizer Foam
62% ethanol (v/v)
PURELL® Advanced Instant Hand Sanitizer Foam
70% ethanol (v/v)
PURELL® Advanced Instant Hand Sanitizer
70% ethanol (v/v)
70% ethanol (v/v)
WHO-recommended hand rub formulation with ethanol
80% ethanol (v/v)
Sterillium® Comfort Gel™
90% ethanol (v/v)a
[85% ethanol (w/w)]
Determination of ABHR dry-times
ABHR gels, rinses, and ethanol-in-water solutions were applied using adjustable pipettes set to a desired volume. For gels, positive-displacement pipettes were used. ABHR foams were dispensed from pumps delivering a known constant quantity (0.4 mL), and total volumes were controlled by the number of pump activations. A specified quantity of an ABHR was placed in a subject’s cupped palms, and the subject rubbed the product onto all surfaces of the hands up to the wrists “until the hands felt dry” to them. No instructions were given regarding rub-in technique. A calibrated digital timer was used to record the time interval from when a subject began rubbing to when they indicated their hands felt dry. After using each test product, subjects washed their hands with a bland soap and waited at least 30 minutes before a subsequent evaluation. Ethical approval was not considered necessary for this part of the study.
Comparison of ABHR drying rates among multiple products
Statistical comparison of drying rates and volumes of six ABHR test products as a function of volume
Volume in mL drying in 30 sa
Drying rate in s/mL (95%CI)b
Drying rate Significance groupsc
62% ethanol (v/v)
70% ethanol (v/v)
70% ethanol (v/v)
15.5 (12.9- 18.0)
70% ethanol (v/v)
80% ethanol (v/v)
90% ethanol (v/v)d
Relationship between ABHR dry-time and product delivery format
To evaluate the specific influence of delivery format (gel, rinse, or foam) on dry-time, a panel of nurses evaluated each of three closely related test products (i.e., having identical ethanol concentrations and nearly identical excipient ingredient composition) delivered at two specific volumes, 0.8 mL and 1.6 mL, estimated to dry in approximately 15 s and 30 s, respectively, based on data for application volume versus dry-time. The sample size (n = 30) was calculated specifically to enable detection of a difference in dry-times as small as 5 s at 95% power. The calculation was based on data from the testing of dry-times versus application volume using thirteen subjects (Table 2). Rinse D represented the base formulation, with Foam B differing only by addition of a foaming agent (<2% w/w), and Gel C by addition of a gelling agent (<0.3% w/w). Each formulation comprised more than 97% alcohol and water w/w, with non-volatile ingredients contributing less than 3% w/w. In addition to recording dry-times, occurrence of product dripping from a subject’s hands during application and rubbing was noted. These data were analyzed using an ANOVA (and fit in R) that accounted for the repeated measures from each subject by including a random effect for subject and fixed effects, including the two-way interaction, for product format and dripping events. From this ANOVA, three Bonferroni simultaneous 90% confidence intervals (CIs) were generated to compare the mean dry-times amongst the three product formats, with statistical equivalence at 95% confidence concluded if all three Cls were contained in the interval (-5, 5) . In other words, mean differences as large as 5 seconds were assumed negligible and not of practical importance.
Relationship between ABHR dry-time and ethanol concentration
In a separate, but related experiment a panel of eleven subjects was used to determine dry-times for 1.7-mL volumes of five ethanol-in-water rinse solutions ranging in concentration from 50% to 90% w/w in 10% increments. The 1.7-mL volume was selected based on data from the testing of dry-times versus application volume, viz., the volume of the two in-test ABHR foams that rubbed dry in 30 s (Table 2). A repeated-measures regression analysis with a random intercept and rate for subject was applied to determine the linear relationship between ethanol concentration and ABHR dry-time (in R). A repeated-measures ANOVA (Minitab 16) was used to compare the mean dry-times amongst the five ethanol concentrations used in the study, with a random effect for subject.
In-vivoevaluation of antimicrobial efficacy
The influence of application volume on ABHR efficacy was evaluated in two studies conducted according to the CEN phase 2/step 2 standard EN 1500 rev:2009 (Hygienic Handrub) methodology, as described previously [8, 15]. Studies were conducted in Germany and were performed in compliance with the Declaration of Helsinki (DoH): Ethical Principles for Medical Research Involving Human Subjects (October 2013). Ethics board approval was not required based on the classification of Escherichia coli K12 (NCTC 10538) as a Risk Group 1 non-pathogenic organism by the German Safety Ordinance on Gene Technology. The laboratory was accredited in accordance with EN ISO 17025 (EN 45000) and recognized by ZLG, German Central Authority of the federal states for Health Protection of Pharmaceuticals and Medical Products. All areas of testing were approved and reported to the Ministry of Labour, Gender and Social Affairs of the Federal State of Mecklenburg - Western Pomerania, Germany. Written informed consent was obtained from each subject prior to their participation in the study. A Latin-square design was used in each study to test three test products and a reference product (60% isopropyl alcohol), with 20 subjects per study for a total of 40 subjects. The reference product was evaluated as specified in the standard: 3 mL rubbed for 30 s, followed by an additional 3 mL rubbed for 30 s. Test products were evaluated by each subject using a single application of each product. In the first study, test products were evaluated at an application volume of 3 mL and rubbed for a timed 30 s, in accordance with EN 1500 rev:2009 procedure, after which the fingertips were rinsed for 5 s under running tap water, excess water shaken off, and hands immediately sampled. In the second study, the procedure was modified such that test products were rubbed until completely dry and then, without rinsing, sampled immediately thereafter. Neutraliser (3.0% polysorbate 80 + 3.0% saponine + 0.1% histidine + 0.1% cysteine) validated prior to testing was used as the sampling fluid and diluent for all products tested. Application volumes were 1.6 mL of Foam B, 2.0 mL of Rinse E, and 2.1 mL of Gel F, volumes of each indicated to rub dry in 30 s based on testing described above (Table 2). Because the volume of Foam B indicated to dry in 30 s (1.7 mL) could not be achieved with the available pump device, the smaller, conservative volume was used. A log10 reduction factor (RF) produced by each product per subject was calculated, and the Hodges-Lehman test was applied for comparison of the mean log10 RF to the mean log10 RF for the reference procedure, as recommended by EN 1500 rev:2009. In addition, mean log10 RFs were compared between the test products using a repeated-measures ANOVA with a random effect for Day (Minitab 16). Follow-up Tukey 95% CIs of the mean log10 RF difference between each test product and reference were generated. Test products that demonstrated inferiority (i.e., mean log10 RF significantly less than that observed from the reference solution) were classified as not meeting the norm. Non-inferiority of each test product compared to the reference was analyzed as specified by EN 1500 rev:2009; that is, non-inferiority was concluded if all of the Tukey 95% CIs were contained in the interval (-∞, 0.6].
In all statistical tests of differences, a level of 5% (i.e., P ≤ 0.05) was used to determine statistical significance. The tests for equivalence amongst product formats were also performed at a significance level of 5%, as explained above. However, to be consistent with EN 1500 rev:2009, the non-inferiority analyses were conducted at a significance level of 2.5%.
Influence of ABHR application volume on dry-time
Influence of product delivery format on ABHR dry-time
Mean dry-times of three ABHR test products evaluated at two application volumes
0.8 mL application volume
1.6 mL application volume
Mean dry-time in sa
Range in s
# of Subjects dripping product
Mean dry-time in sa
Range in s
# of Subjects dripping product
Relationship between ABHR dry-time and ethanol concentration
Influence of ABHR application volume on antimicrobial efficacy
Efficacy of three ABHRs evaluated according to procedures of EN 1500
Efficacy at 3-mL application volume
Efficacy at volume drying in 30 s
mean log RF ± SD
mean log RF ± SD
EN 1500 reference
2 × 3 mLc
4.63 ± 0.60
2 × 3 mL
4.83 ± 0.79
4.56 ± 0.68
3.81 ± 0.61
4.50 ± 0.90
4.03 ± 0.55
4.61 ± 0.94
4.02 ± 0.60
In this study, we evaluated the influence of several variables on ABHR dry-time, including product format, application volume, and alcohol concentration. Consistent with previous studies, ABHR dry-times increased proportionally to product application volume (Figure 1) [10, 11], and the rates at which different ABHR products dried varied significantly (Table 2). The volume of the two foams evaluated in this study drying in 30 s was 1.7 mL (1.5 g), which is similar to that reported by Kampf et al. for ABHR foams (1.6 g) . Furthermore, the drying rates calculated in Table 2 revealed that the two foams were the slowest drying products tested. However, careful examination of Table 2 in the context of alcohol concentration of each test product indicates that rate of drying was faster for products with higher alcohol concentration, regardless of format. Noting the inverse relationship between ABHR dry-time and alcohol concentration clearly demonstrated in Figure 2, the observed differences in test product drying rates likely result from differences in alcohol concentration. That is, as the alcohol concentration of ABHR is increased, the volume of product that will rub dry in 30 s also increases. Note that 2.1 mL of Gel F (90% v/v) dried in 30 s, as did 1.7 mL of Gel A (62% ethanol v/v), a difference of 0.4 mL (Table 2).
By evaluating products of equivalent alcohol concentration, differing only by the presence of thickening or foaming agents, delivery format was found to have no influence on ABHR dry-time (Table 3). This result is not surprising, considering that ABHR formulations consist predominantly of alcohol and water. Despite differences in physical characteristics, Foam B, Gel C, and Rinse D each comprise greater than 97% alcohol and water by weight and differ in composition by less than 3%. This similarity is further evidenced by the identical densities of the 3 products (Table 1). Based on demonstrated influence of alcohol concentration on dry-time (Figure 2) and lack of influence of delivery format on dry-time, we would attribute the differences in drying rates to alcohol concentration.
In agreement with previous studies, product application volume was found to be a critical determinant of ABHR efficacy [4, 7]. Each of the three products evaluated (Foam B, Rinse E, and Gel F) met the performance criteria of EN 1500 when tested at 3-mL application volumes, but failed when tested at volumes drying in 30 s (Table 4). Statistical equivalence of the mean log10 RFs was established amongst the three products when applied in volumes that dried in 30 s, despite the fact that Gel F, the test product with the highest alcohol concentration, was also tested at the largest application volume. Taken together, these data suggest that time that product remains wet on the hands may be the most important determinant of ABHR efficacy when evaluated under actual use conditions (i.e., rubbed until dry), irrespective of other variables.
By expanding the studies of Kampf et al. to include gels and rinses we can expand upon their conclusions. Regardless of delivery format or alcohol concentration, the volume ABHR drying in 30 s is considerably less than 3 mL. Furthermore, when 3 mL of product are used, dry-times are considerably greater than 30 s. Importantly, when used at volumes drying in 30 s, gel, foam, and rinse products did not meet the efficacy criteria of EN 1500. Therefore, the assertion that the use of ABHR foams would encourage users to apply volumes too low to meet EN 1500 standards  should be expanded to include gels and rinses. The data presented herein suggest that it may be more appropriate to make ABHR application recommendations based on formulation specific efficacy data.
Indeed, there is currently limited understanding of the actual ABHR application volumes used by healthcare workers in practice, despite recommendations [1, 2]. A recent survey of ABHR dispensers in U.S. hospitals found that outputs ranged from 0.6 mL to 1.3 mL, and that product dry-times ranged from 12 s to 26 s . Whether healthcare workers use more than one dispenser actuation is unknown; anecdotally, it is expected they most frequently do not. An often-cited publication by Voss and Widmer argued that the use of ABHR saves significant time and can promote hand hygiene compliance . Note, however, that the time estimated for application of an ABHR was 20 s; considerably shorter than the dry-time for the 3-mL volume required to meet EN 1500 efficacy requirements.
To better understand ABHR efficacy under clinical use conditions, “in particular, short application times and volumes”, experts have called for the development of improved in-vivo protocols that more closely simulate real-world conditions [2, 18]. EN 1500 specifies that test subjects rub 3 mL of test product onto the hands for 30 s and then to neutralize the remaining alcohol . However, as Table 2 indicates, typical volumes of ABHRs drying in 30 s range from 1.7 to 2.1 mL, and Figure 1 illustrates that 3 mL can take as long as 90 s to dry on the hands. This uncoupling of dry-time from application volume does not represent real use conditions. The modification to EN 1500 used in this study, where the test product is rubbed until dry, with no subsequent rinse, more closely simulates product usage in clinical settings and results in more accurate recommendations for application volume.
Our study has several limitations. For product dry-time experiments, that subjects did not use a standardized rub-in technique may have had a minor impact on dry-times. However, adherence of healthcare workers to the standardized technique is unknown, but unlikely, and this technique has been previously shown to have minimal impact on ABHR efficacy . Efficacy studies were performed using a limited number of subjects and a laboratory-based method with success criteria not linked to clinical outcome, and they should be understood in that way. Lastly, this study evaluated efficacy of only a single representative of each product delivery type (rinse, gel, and foam). Because product formulation also impacts efficacy , broad conclusions regarding the efficacy of other products should be made with caution.
In conclusion, application volume was found to be the primary driver of ABHR dry-time and, therefore, of efficacy. Our data suggest that ABHR application volumes consistent with WHO recommendations may fail to meet EN 1500 efficacy requirements, irrespective of delivery format or alcohol concentration. The implications of this are unknown, but should be of considerable concern. Further research is needed to better understand ABHR application volumes actually used by healthcare workers in clinical practice and how these relate to product effectiveness. Finally, there is a need to develop improved standard test methods that more closely reflect clinical use conditions and provide success criteria linked to clinical outcomes.
The authors thank Dr. John Mitchell for his critical review of this manuscript.
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