BS EN 13623:2020
$167.15
Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of bactericidal activity against Legionella of chemical disinfectants for aqueous systems. Test method and requirements (phase 2, step 1)
Published By | Publication Date | Number of Pages |
BSI | 2020 | 42 |
This document specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant products intended to be used for treatment in aqueous systems against Legionella pneumophila that form a homogeneous, physically stable preparation when diluted with buffered ferrous hard water or hard water. Whenever Legionella pneumophila poses a risk to human health, this method is suitable for water used in cooling towers and water for general purposes, like spas, pools, showers and other uses. The method is not suitable for electro-chemical disinfection.
The document applies to products used as a single application shock treatment in order to kill Legionella pneumophila. It is not suitable for the evaluation of those products that are dosed continuously into water systems to control the growth of Legionella pneumophila.
The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used.
This method corresponds to a phase 2 step 1 test.
This method does not take into account the fact that Legionella pneumophila is often found in cells of amoebae and/or biofilms and that thereby a product’s activity against the bacteria may be reduced.
EN 14885 specifies in detail the relationship of the various tests to one another and to “use recommendation”.
PDF Catalog
PDF Pages | PDF Title |
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2 | undefined |
7 | 1 Scope 2 Normative references 3 Terms and definitions |
8 | 4 Requirements 5 Test methods 5.1 Principle |
9 | 5.2 Materials and reagents 5.2.1 Test organism 5.2.2 Culture media and reagents 5.2.2.1 General 5.2.2.2 Water |
10 | 5.2.2.3 Buffered Charcoal Yeast Extract (BCYE) Agar |
11 | 5.2.2.4 BCYE Broth 5.2.2.5 Neutralizer 5.2.2.6 Rinsing liquid (for membrane filtration) 5.2.2.7 Hard water for general purposes (HWGP) |
12 | 5.2.2.8 Interfering substance (yeast extract) 5.2.2.9 Page’s Saline 5.2.2.10 Buffered ferrous hard water for treatment of cooling water (BFHW) |
13 | 5.3 Apparatus and glassware 5.3.1 General 5.3.2 Usual microbiological laboratory equipment) |
14 | 5.4 Preparation of test organism suspensions and test solutions 5.4.1 Test organism suspension (test suspension N and validation suspension NV) 5.4.1.1 General 5.4.1.2 Preservation and stock cultures of test organism |
15 | 5.4.1.3 Working cultures of test organism 5.4.1.4 Test suspensions (N) 5.4.1.5 Validation suspension (NV, NVB) 5.4.1.6 Incubation and counting of the test and validation suspensions |
16 | 5.4.2 Product test solution 5.5 Procedure for assessing the bactericidal activity of the product 5.5.1 General 5.5.1.1 Experimental conditions (obligatory and additional) |
17 | 5.5.1.2 Choice of test method 5.5.1.3 General instructions for validation and control procedures 5.5.1.4 Equilibration of temperature 5.5.1.5 Precautions for manipulation of test organisms |
18 | 5.5.2 Dilution-neutralization method) 5.5.2.1 General 5.5.2.2 Test Na – determination of bactericidal concentrations 5.5.2.3 Experimental conditions control A – validation of the selected experimental conditions and/or verification of the absence of any lethal effect in the test conditions |
19 | 5.5.2.4 Neutralizer control B – verification of the absence of toxicity of the neutralizer 5.5.2.5 Method validation C – dilution-neutralization validation 5.5.2.6 Incubation and counting of the test mixture and the control and validation mixtures |
20 | 5.5.3 Membrane filtration method) 5.5.3.1 General 5.5.3.2 Test Na– determination of the bactericidal concentrations 5.5.3.3 Experimental conditions control A – validation of the selected experimental conditions and/or verification of the absence of any lethal effect in the test conditions |
21 | 5.5.3.4 Filtration control B – validation of the filtration procedure 5.5.3.5 Method validation C – validation of the membrane filtration method or counting of the bacteria on the membranes which have previously been in contact with the mixture of product and interfering substance 5.5.3.6 Incubation and counting of test mixture and the control and the validation mixtures 5.6 Experimental data and calculations 5.6.1 Explanation of terms and abbreviations 5.6.1.1 Overview of the different suspensions and test mixtures |
22 | 5.6.1.2 VC-values 5.6.2 Calculation 5.6.2.1 General |
23 | 5.6.2.2 Determination of VC-values |
24 | 5.6.2.3 Calculation of N and N0 5.6.2.4 Calculation of Na |
26 | 5.6.2.5 Calculation of NV and NV0 5.6.2.6 Calculation of A, B and C |
27 | 5.7 Verification of methodology 5.7.1 General 5.7.2 Control of weighted mean counts 5.7.3 Basic limits 5.8 Expression of results and precision 5.8.1 Reduction |
28 | 5.8.2 Control of active and non-active product test solution (5.4.2) 5.8.3 Bactericidal concentration 5.8.4 Precision, repetition 5.9 Interpretation of results – conclusion 5.9.1 General 5.9.2 Bactericidal activity for general purposes 5.9.3 Bactericidal activity for specific purposes 5.10 Test report |
30 | Annex A (informative)Referenced strains in national collections |
31 | Annex B (informative)Determination of the bactericidal activity against Legionella pneumophila |
34 | Annex C (informative)Neutralizer |
36 | Annex D (informative)Graphical representation of test procedures D.1 Dilution-neutralization method |
38 | D.2 Membrane filtration method |