ISO 18184 test method

Determination of Antiviral Activity of Textile Products

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Quick understanding of the test

ISO 18184 test method - This International Standard (ISO 18184: 2019) specifies testing method for the determination of the antiviral activity of the textile products against viruses.

ISO 18184 test method evaluates the antiviral activity of textile products, ensuring their effectiveness in reducing virus viability on porous surfaces.
Applicable for a wide range of textiles, including woven, non-woven, and knitted fabrics, activewear, socks, healthcare products, and more.

Mandatory test strains

  • Samples are challenged with the test virus.
  • After incubation, samples are neutralized with a suitable neutralizing solution.
  •  Virus recovered in the neutralizing solution is then serially diluted, and the infectious titre of the recovered virus is determined using plaque assays or TCID50 assays.

Benefits

Turnaround Time

  • Standard turnaround: 4 weeks.
  • Fast Track program: 2โ€“3 weeks (based on the virus strain).

Results

The antiviral efficacy of the textile is determined by measuring the log reduction in the infectious virus titre.

Passing criteria

As per ISO 18184, Log reduction value between 2 and 3 indicates good antiviral performance, while a log reduction value of 3 or higher signifies excellent antiviral performance.

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Abstract

In the last two decades, there were multiple viruses breakouts (SARS-CoV-1, MERS, SARS-CoV-2) causing large-scale damage to human lives. During this time, the general awareness of products protecting against such breakout increased multi-fold, and because of this, many antiviral products were launched in the marketplace. The antiviral products for textiles were also launched and with that, there was a need for a unified test method to evaluate the antiviral efficacy of different products on textile products. ISO 18184 was first introduced in 2014 and later revised in 2019, is a test method to evaluate the antiviral activity of textile products.

Products that can be tested with ISO 18184

ISO 18184 can be used to evaluate the antiviral activity of different textile products, such as 

  • woven, non-woven & knitted fabrics, 
  • yarns,
  • activewear,
  • socks
  • daily wear,
  • health care products such as scrubs, masks, & surgical clothes,
  • and other home textiles.

ISO 18184 is used for textile products that are hydrophilic in nature. For hydrophobic textiles, ISO 21702 shall be used to evaluate antiviral activity.

ISO 18184 is also a commonly used method for evaluating the efficacy of antiviral face masks.

Know here โ€“ Face Mask Antiviral Testing standards: ISO 18184 vs. JIS L 1922

Sample Preparation

Control Sample โ€“ 9 sterilized control (untreated) specimens with a mass of 0.4g ยฑ 0.05g are required for ISO 18184 testing.

  • 3 control specimens are used to determine the infectious titre of the virus immediately after inoculation.
  • 3 control specimens are used to determine the infectious titre of the remaining virus after inoculation for a โ€œcontact timeโ€ (Standard โ€œcontact timeโ€ is 2 hours, but can go up to 24 hours).
  • 3 control specimens are used for cytotoxicity analysis.

Test samples โ€“ 6 sterilized test (treated) samples with a mass of 0.4g ยฑ 0.05g are required for ISO 18184 testing. 

  •  3 treated specimens to determine the infectious titre of the remaining virus after inoculation is in contact with the treated specimen, same as the control specimen.
  • 3 treated specimens are used for cytotoxicity analysis.

We test using following organisms: SARS CoV-2, Beta Coronavirus (OC-43) (ATCC VR-1558), Human Coronavirus (229E) (ATCC VR-740), Influenza A (H1N1) (ATCC VR-1469), Influenza A (H3N2) (ATCC VR-1679), Adenovirus, Norovirus, Poliovirus, Vaccinia virus, Feline Calicivirus

ISO 18184 Test Procedure

  • Control and treated samples are placed in separate sterile plates.
  • The 200 uL of the virus is inoculated on both the control and the treated samples.
  • Immediately after the inoculation of the virus, 20 ml of SCDLP ( used as a neutralizing solution) is added to 3 control samples.
  • After a specific contact period, 20 ml of  SCDLP broth is added to 3 treated and 3 untreated samples to recover the remaining virus. 
  • The wash-out solution is serially diluted up to 10 dilutions, and the infectious titre of the recovered virus is determined either by Plaque assay or by TCID50 assay. Other assays can also be used based on the virus strain.

Antiviral Activity and Performance Standard

The antiviral activity is determined by the following equation.

Mv = Log10 (Va) โ€“ Log10 (Vc)

Where,

Mv is the antiviral activity value

Log10 (Va) is the logarithm average of 3 infectivity titre value immediately after inoculation of the control specimen

Log10 (Vc) is the logarithm average of 3 infectivity titre value after specific contact time with the test specimen.

As per the ISO 18184, If the log value is between 2 and 3, the antiviral performance of the textile product is considered good. If the log value is greater than or equal to 3, then the antiviral performance of textile product is considered excellent.

Antiviral activity value (Mv)

Efficacy Rating

2 โ‰ค Mv < 3

Good Effect Level

Mv โ‰ฅ 3

Excellent Effect Level

Table 1: Antiviral performance standard

The ISO 18184 is a very robust test method. If followed properly, the results are accurate and repeatable in both inter-laboratory testing and intra-laboratory testing. In the ISO 18184 test protocol, the steps are given for Influenza A (H3N2 and H1N1), and Feline calicivirus, but the protocol can be used for other viruses also after appropriate validations.

At Microbe Investigations Switzerland, we evaluate the efficacy of a wide range of antimicrobial textile materials such as woven, non-woven & knitted fabrics and textile clothes used in health care settings.

We measure the antiviral activity on textile materials using standard methods like JIS L 1922 and ISO 18184, while ISO 20743, JIS L 1902, and AATCC 147 are standard protocols used for assessing the antibacterial activity of textile materials.

We also offer a comprehensive array of testing services to determine the antimicrobial efficacy of plastics, coatings, and surface disinfectants.

To request a quote or for more information on ISO 18184 testing, get a free consultation from our experts.

Frequently Asked Questions

DR. Martinoz Scholtz

MIS Labs
1. What is the ISO 18184 test?

The ISO 18184 is an antiviral textile test that measures virucidal antimicrobial activity on textiles and other porous materials. Test standard is designed to test the ability of textiles and other similar materials to kill virus. Standard virus exposure times range from 2 hours to less than 24 hours.

2. What are the Products that can be tested with ISO 18184 test?

The ISO 18184 can be used to evaluate the antiviral activity of different textile products such as yarn, woven, non-woven, knitted, etc. used in different areas such as healthcare products (scrubs, masks), active-wear, socks, home textiles, daily wear, etc. 

3. What is the Turnaround Time for ISO 18184 test?

The turnaround time for ISO 18184 test is 4 weeks. We also offer โ€œFast Trackโ€ program, where the turnaround time is 2-3 weeks depending on the virus strain.

4. On how many (viruses) can your ISO 18184 testing lab perform tests on?

At Microbe Investigations Switzerland, we understand the need for accuracy and speed. We test for the ISO 18184 using the following viruses: SARS CoV-2 (Omicron, Delta, Wuhan variant), Betacoronavirus 1 (OC43) (ATCC VR-1558), Human coronavirus 229E (ATCC VR-740), Influenza A (H1N1) (ATCC VR-1469), Influenza A (H3N2) (ATCC VR-1679), Human Poliovirus type 1 (LSc-2ab), Human Adenovirus type 5 (ATCC VR-5), and Murine Norovirus (S99).

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