1、July 2014Translation by DIN-Sprachendienst.English price group 12No part of this translation may be reproduced without prior permission ofDIN Deutsches Institut fr Normung e. V., Berlin. Beuth Verlag GmbH, 10772 Berlin, Germany,has the exclusive right of sale for German Standards (DIN-Normen).ICS 85
2、.060!%7=a“2202662www.din.deDDIN EN 16418Paper and board Determination of the cytotoxicity of aqueous extracts usinga metabolically competent hepatoma cell line (HepG2);English version EN 16418:2014,English translation of DIN EN 16418:2014-07Papier und Pappe Bestimmung der Zytotoxizitt von wssrigen E
3、xtrakten unter Verwendung einermetabolisch kompetenten Hepatom-Zelllinie (HepG2);Englische Fassung EN 16418:2014,Englische bersetzung von DIN EN 16418:2014-07Papier et carton Dtermination de leffet cytotoxique dextraits aqueux en utilisant une ligne cellulairedhpatome possdant des enzymes du mtaboli
4、sme (cellules HepG2);Version anglaise EN 16418:2014,Traduction anglaise de DIN EN 16418:2014-07www.beuth.deDocument comprises pagesIn case of doubt, the German-language original shall be considered authoritative.2207.14 2 A comma is used as the decimal marker. National foreword This document (EN 164
5、18:2014) has been prepared by Technical Committee CEN/TC 172 “Pulp, paper and board” (Secretariat: DIN, Germany), Working Group WG 12 “Cytotoxicity” (Secretariat: SFS, Finland). The responsible German body involved in its preparation was the Normenausschuss Papier, Pappe und Faserstoff (Paper, Board
6、 and Pulps Standards Committee), Working Committee NA 074-02-01 AA Chemisch-technische Prfverfahren fr Papier, Pappe, Faserstoff und Chemiezellstoff. The DIN Standard corresponding to the European Standard referred to in Clause 2 of this standard is as follows: EN ISO 3696 DIN ISO 3696 National Anne
7、x NA (informative) Bibliography DIN ISO 3696, Water for analytical laboratory use Specification and test methods DIN EN 16418:2014-07 EUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN 16418 April 2014 ICS 85.060 English Version Paper and board - Determination of the cytotoxicity of aqueous extrac
8、ts using a metabolically competent hepatoma cell line (HepG2) Papier et carton - Dtermination de leffet cytotoxique dextraits aqueux en utilisant une ligne cellulaire dhpatome possdant des enzymes du mtabolisme (cellules HepG2) Papier und Pappe - Bestimmung der Zytotoxizitt von wssrigen Extrakten un
9、ter Verwendung einer metabolisch kompetenten Hepatom-Zelllinie (HepG2) This European Standard was approved by CEN on 8 February 2014. CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national st
10、andard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member. This European Standard exists in three official versions (English, French, German). A version in
11、 any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech R
12、epublic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom. EUROP
13、EAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2014 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 16418:2014 E2 Con
14、tents Page Foreword 3 1 Scope 4 2 Normative references 4 3 Terms and definitions .4 4 Principle 5 5 Reagents .5 6 Cell line .7 6.1 Generating the cell strain 7 6.2 Maintaining the cell strain .7 6.3 Storing the cell strain 8 7 Food simulants used for testing 8 7.1 Reference water (3.1) .8 8 Cleaning
15、 laboratory glassware .8 8.1 Cleaning liquids for laboratory glassware 8 8.2 Cleaning procedure for laboratory glassware 8 9 Equipment 9 9.1 Equipment for the migration test .9 9.2 Cell culture equipment 9 9.3 Equipment used for cytotoxicity testing .9 10 Preparation of specimens 10 10.1 General . 1
16、0 10.2 Paper and board intended for wet contact . 10 11 Cytotoxicity assessment 10 11.1 Principle . 10 11.2 General . 10 11.3 Cell seeding . 11 11.4 Preparation of samples 11 11.5 Cell culture treatment . 11 11.6 Preparation of the chromatography sheet . 12 11.7 Kinetics of uridine incorporation in
17、the cell RNA 12 11.8 Measurements of the RNA synthesis . 12 12 Expression of the results . 13 12.1 Graphic representation of the results 13 12.2 Calculation of percentage RNA synthesis and the validity of the test 14 13 Interpretation of the results . 15 13.1 Results for the reference sample 15 13.2
18、 Results of the positive control sample . 15 13.3 Results for the test sample 15 14 Precision 15 15 Test report . 15 Annex A (informative) 96-well plates configuration 17 Annex B (informative) RNA Synthesis rate inhibition cytotoxicity test work flow 18 Annex C (informative) Validation of the two me
19、thods (option A and B) . 19 Bibliography . 20 DIN EN 16418:2014-07 (E) EN 16418:20143 Foreword This document (EN 16418:2014) has been prepared by Technical Committee CEN/TC 172 “Pulp, paper and board”, the secretariat of which is held by DIN. This European Standard shall be given the status of a nat
20、ional standard, either by publication of an identical text or by endorsement, at the latest by October 2014 and conflicting national standards shall be withdrawn at the latest by October 2014. Attention is drawn to the possibility that some of the elements of this document may be the subject of pate
21、nt rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Cro
22、atia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and
23、the United Kingdom. DIN EN 16418:2014-07 (E) EN 16418:20144 1 Scope This European Standard specifies a test method for the laboratory assessment of the potential cytotoxic effect of paper and board intended to come into contact with foodstuffs using specifically the HepG2 cell line. Compared to the
24、EN 158451, HepG2 cells are more representative of a human oral exposure to xenobiotics, due to the presence in the cells of phase I, II and III enzymes of the metabolism. 2 Normative references The following documents, in whole or in part, are normatively referenced in this document and are indispen
25、sable for its application. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. EN 645, Paper and board intended to come into contact with foodstuffs - Preparation of a cold water extract EN 64
26、7, Paper and board intended to come into contact with foodstuffs - Preparation of a hot water extract 3 Terms and definitions For the purposes of this document, the following terms and definitions apply. 3.1 reference water tap water which undergoes the following treatment sequence: pre-filtration,
27、reverse osmosis, filtering through activated carbon powder (adsorption) then through cartridges of mixed-bed ion exchange microresins (demineralisation), ultrafiltration (molecular weight cut-off at 10 kDa), and UV photo-oxidation Note 1 to entry: Alternatively, any other purification regime, which
28、produces HPLC-quality water (resistance 18,0 M/cm, total organic carbon 3 ppb, no microorganism) or waters of grade 1 or 2 according to EN ISO 3696, can be used. 3.2 water extract reference water that has been exposed to contact with paper or board Note 1 to entry: See EN 645 or EN 647. 3.3 negative
29、 control water reference water that has been treated according to the same conditions as the water extract but without being in contact to paper or board 3.4 positive control waters 1) fresh 2,5 mg/l solution of potassium dichromate (CAS 7778-50-9) prepared in reference water and sterilized by filtr
30、ation through 0,22 m filter and kept at room temperature in the dark and 2) a stock 2 mg/ml solution of benzo|apyrene (CAS 50-32-8) prepared in dimethylsulfoxide (DMSO) and kept at 4 C in the dark. Dilute this stock solution 1 000 times in reference water before use 3.5 reference sample culture medi
31、um prepared with reference water as specified in 3.1 DIN EN 16418:2014-07 (E) EN 16418:20145 3.6 test sample culture medium prepared with water extract as specified in 3.2 3.7 negative control sample culture medium prepared with negative control water (3.3) alone or with 0,1 % of DMSO (if benzoapyre
32、ne is used as positive control) 3.8 positive control sample culture medium prepared with positive control water as specified in 3.4 3.9 test material a specified quantity of paper or board, that is randomly sampled from a batch 4 Principle The test method specified in this document is intended to ev
33、aluate the cytotoxic effect of water extracts from materials for wet foods intended for human consumption. The test evaluates the impact of the water extract on the rate of RNA (Ribonucleic Acid) synthesis by measuring the incorporation of a radioactive marker (tritiated uridine) in human cells (Hep
34、G2). The food contact paper and board samples to be tested are extracted into the water as described in Clause 10. The extracts then undergo cytotoxicity assessment, and the results obtained are compared to the results of a non-cytotoxic control purified water (for which the rate of RNA synthesis is
35、 considered optimal and arbitrarily set at 100 %). Potassium dichromate and/or benzoapyrene, prepared from stock solutions described in 3.4 and diluted as described in 11.4.4, are used as positive controls. 5 Reagents 5.1 Liquid scintillant, for tritium counts on dry filters 5.2 Culture media The pH
36、 of all culture media used shall be 7,4 0,1: pH to be adjusted using a sterile NaOH (or HCl) solution. 5.2.1 Culture media quality and storage All culture media, foetal serum and solutions used for cell culture shall be sterile and of sufficiently high quality to guarantee optimal cell growth (see 1
37、2.2). They shall be stored in compliance with manufacturers instructions, where given. Complete medium with additives and serum should be stored at 4 C for no longer than two weeks. 5.2.2 Medium for routine culture Composition: DIN EN 16418:2014-07 (E) EN 16418:20146 a) minimum Essential Medium Eagl
38、e with Earles salts1), (10x)2)100 ml b) sodium bicarbonate solution1), 7,5 % (m/V) 30 ml c) glutamine solution, 200 mmol/l (or Glutamax I)1), (100x)2)10 ml d) non-essential amino acids solution1), (100x)2)10 ml e) foetal calf serum3)100 ml f) reference water 800 ml 5.2.3 Concentrated culture medium
39、for testing samples A 5,45-fold concentrated culture medium is prepared by successively mixing: a) minimum Essential Medium Eagle with Earls salts1), (10x)2)100 ml b) sodium bicarbonate solution1), 7,5 % (m/V) 30 ml c) glutamine solution, 200 mmol/l (or Glutamax I)1), (100x)2)10 ml d) non-essential
40、amino acids solution1), (100x)2)10 ml e) foetal calf serum3)5 ml The serum concentration of reconstituted treatment medium is reduced to 0,5 % since serum proteins can mask the toxicity of the water extract. 5.3 Solution for rinsing cell lawns Phosphate buffered saline (PBS)1)without Ca2+and Mg2+. 5
41、.4 Cell dissociation reagent 1)Commercially available. Glutamax I is an example of a suitable product available commercially and based on Earles salt with a minimum of the medium necessary. This information is given for the convenience of this European Standard and does not constitute an endorsement
42、 by CEN of this product. 2)10x or 100x imply tenfold or hundredfold concentrated media or solutions. 3)Heat inactivated (56 C for 40 min) before use. Cells are detached using a trypsin/EDTA solution1)(0,25 % m/V trypsin, 1mM N1)EDTA/Na4). 5.5 Trypan blue, at 0,4 % (w/VN2)1)5.6 Dimethyl sulfoxide (DM
43、SO), analytical-grade N1)National footnote: EN 16418 erroneously contains the designation “1mM EDTA/Na4” instead of “1mmol EDTA/Na4”. N2)National footnote: EN 16418 erroneously contains the designation “(w/V)” instead of “m/V)”. DIN EN 16418:2014-07 (E) EN 16418:20147 5.7 Sodium dodecyl sulphate (SD
44、S), for analysis, at 3 % (m/V) 5.8 Trichloroacetic acid (TCA), for analysis 5.9 Ethanol, 95 % to 96 % (v/V) 5.10 5,6-3H uridine Use uridine (35 Ci/mmol to 50 ; 1 mCi/ml or 1,29 TBq/mmol to 1,85, 37MBq/ml): a sterile and non-cytotoxic aqueous solution. On the day of kinetic measurement of uridine inc
45、orporation, the required volume of uridine is taken under sterile conditions and put into a sterile tube to prepare a uridine solution at 10 Ci/ml in culture medium (5.2.3) prepared with reference water (3.1). NOTE The products and materials referred to in the present document are considered non-cyt
46、otoxic if they do not trigger a cytotoxic response, i.e. if the linear regression line generated by measuring the rate of RNA synthesis meets the conditions set out in 13.3. 6 Cell line 6.1 Generating the cell strain The cell line used is HepG2, a human hepatoma cell line. This line shall be generat
47、ed from recognised sources, such as the HB-8065 line of the American Type Culture Collection (ATCC) or European Collection of Cell Cultures (ECACC) No. 85011430. 6.2 Maintaining the cell strain Cells shall be cultured without antibiotics, and checks of absence of mycoplasma shall be run at frequent
48、intervals: a) seed the HepG2 cells in the culture medium (5.2.2) in a flask (9.2.1) and incubate at (37 1) C until a 90 % confluent lawn of growth is formed; b) remove the culture medium, and rinse the cell lawn at least twice with about 10 ml of the rinse medium (5.3); c) cover the cell lawn with 2
49、 ml of the dissociation solution (5.4) and swirl around gently to cover the entire bottom of the flask. Leave on for 1 min and remove excess trypsin/EDTA solution; d) incubate the flask at (37 1) C for 2 min to 5 min. Observe the cells detaching under the inverted microscope periodically tapping on the side of the flask to assist in detachment; e) once the cells are detached, add 10 ml of the culture medium (5.2.2) to stop the reaction. Pipett
