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DRAFT MALAYSIAN STANDARD 13A007R0 STAGE: PUBLIC COMMENT (40.20) DATE: 01/09/2015 31/10/2015 Test method for Edible-birdnest (EBN) - Determination for nitrite (NO 2 - ) and nitrate (NO 3 - ) contents - Ion Chromatography ICS: 67.050 Descriptors: edible-birdnest, test method, nitrite, nitrate, ion chromatography Copyright 2015 DEPARTMENT OF STANDARDS MALAYSIA

Contents Page Committee representation...ii Foreword...iii 1 Scope...1 2 Normative references.... 1 3 Terms and definitions.... 1 4 Principle... 2 5 Reagents...2 6 Apparatus.... 3 7 Test specimen....3 8 Determination.....4 9 Calculation for nitrite and nitrate amount...5 10 Test report.....5 Annex A The diagram in determination of nitrite content...6 Annex B The diagram in determination of nitrate content...7 STANDARDS MALAYSIA 2015 - All rights reserved i

Committee representation The Industry Standards Committee on Agricultural (ISC A) under whose authority this Malaysian Standard was developed, comprises representatives from the following organisations: Department of Agriculture Malaysia Department of Fisheries Malaysia Department of Standards Malaysia Department of Veterinary Services Farmers Organisation Authority Federal Agricultural Marketing Authority Federation of Livestock Farmers' Associations of Malaysia Forest Research Institute Malaysia Malaysia Fruit Exporters Association Malaysian Agricultural Research and Development Institute Malaysian Association of Standards Users Malaysian Palm Oil Association Malaysian Rubber Board Ministry of Agriculture and Agro-Based Industry Malaysia Ministry of Plantation Industries and Commodities National Seed Association Malaysia SIRIM Berhad (Secretariat) Universiti Putra Malaysia The Working Group on Edible-birdnest (EBN) test method which developed this Malaysian Standard consists of representatives from the following organisations: Department of Chemistry Department of Veterinary Services Department of Veterinary Services (Southern Regional Veterinary Laboratory) Department of Veterinary Services (Eastern Regional Veterinary Laboratory) Ministry of Health Malaysia Permulab Sdn Bhd SIRIM Berhad (Industrial Biotechnology Research Centre) SIRIM Berhad (Secretariat) Sunshine Region Sdn Bhd Universiti Putra Malaysia (Faculty of Veterinary Medicine) ii STANDARDS MALAYSIA 2015 - All rights reserved

Foreword This Malaysian Standard was developed by the Working Group on Edible-birdnest (EBN) test method under the authority of the Industry Standards Committee on Agriculture. Compliance with a Malaysian Standard does not of itself confer immunity from legal obligations. STANDARDS MALAYSIA 2015 - All rights reserved iii

Test method for Edible-birdnest (EBN) - Determination for nitrite (NO 2 ) and nitrate (NO 3 ) contents - Ion Chromatography 1 Scope This Malaysian Standard describes the test method for nitrite ( NO2 ) and nitrate ( NO3 ) in Edible-birdnest (EBN). The test shall be based on the use of ion chromatographic method. 2 Normative references The following normative references are indispensable for the application of this standard. For dated references, only the edition cited applies. For undated references, the latest editions of the normative references (including any amendments) apply. MS 954: Part 14, Methods of test for meat and meat products, Part 14 : Determination of nitrite content MS 954: Part 15, Methods of test for meat and meat products, Part 14 : Determination of nitrate content MS ISO/IEC 17025:2005, General requirements for the competence of testing and calibration laboratories GB 5009.33-2010, Determination of Nitrite and Nitrate in Foods 3 Terms and definitions 3.1 Raw-Clean EBN EBN that has undergone cleaning process may include but not limiting to sorting, drying, soaking, picking of feathers and impurities, moulding, drying, grading and packing. 3.2 Raw-Unclean EBN EBN harvested from caves and ranches which may include but not limiting to sorting, drying, grading, trimming, weighing and packing but, without any cleaning process. There are still visible feathers and impurities. 3.3 Nitrite Nitrite is an anion with the chemical formula NO2. 3.4 Nitrate Nitrate is an anion with the chemical formula NO3. STANDARDS MALAYSIA 2015 - All rights reserved 1

3.5 Ion chromatography A process that allows the separation of ions and polar molecules based on their affinity to the ion exchanger. 3.6 Eluent Mobile phase used to extract solute or ion bound to a matrix as shown in the figure below: Mobile phase 3.7 Reagents A reagent is a substance or compound that is added to a system in order to bring about a chemical reaction, or added to see if a reaction occurs. 3.8 Ultra-pure water (UPW) Water, where, organic and inorganic compounds, dissolved and particulate matter, volatile and non-volatile, reactive and inert, hydrophilic and hydrophobic, and dissolved gases have been removed. Its conductivity of 18.2 MΩ.cm is maintained. 4 Principle An EBN aqueous extract is subjected to ion exchange chromatography. The ion exchange column is eluated using potassium hydroxide. The eluate is measured using conductivity detector and quantified. 5 Reagents Use only reagents of recognised analytical grade, unless otherwise stated. 5.1 Ultra-pure water (UPW) 5.2 Eluent generator for Potassium hydroxide (KOH). 5.3 Nitrite ion (NO2 - ) stock solution (1000 mg/l, aqueous solution). 5.4 Nitrate ion (NO3 - ) stock solution (1000 mg/l, aqueous solution). 2 STANDARDS MALAYSIA 2015 - All rights reserved

5.5 Mixed Standard Solution, Nitrite and Nitrate. 5.5.1 Pipette 10 ml of nitrite ion (NO2 - ) stock solution and 10 ml nitrate ion (NO3 - ) stock solution into 100 ml volumetric flask, adjust to the mark with water. 5.5.2 Mix well 1 ml of this mixed solution contains 100 µg of nitrite ion and 100 µg of nitrate ion. 5.6 Working Mixed Standard Solution Prepare a working mixed standard solution between 0.1 mg/l to 10 mg/l. 6 Apparatus 6.1 Ion Chromatography System Dionex inclusive of a conductivity detector, suppressor or equivalent (refer to manufacturer procedure). 6.1.1 Automated Sampler. 6.1.2 Anion exchange column (Analytical Column: AS19 or equivalent (4 x 250mm, 5 µm particle diameter) 6.1.3 Guard Column: AG 19 or equivalent (4 x 50 mm, 5 µm particle diameter) - a column used before the separator column to protect it from contaminants, such as particulate matter or irreversibly attained materials. 6.1.4 Software (Chromeleon or equivalent) for data analysis 6.2 Dry mixer 6.3 Analytical balance: readability 0.1 mg and 1 mg. 6.4 Centrifuge: 10000 rpm with 5 ml or 10 ml centrifuge tubes. 6.5 Membrane filter: 0.45 µm 6.6 Syringe: 1 ml and 5 ml 6.7 Polypropylene plastic ware Should be soaked in distilled water and dried. 7 Test specimen Preparation of EBN sample 7.1. Pre-treatment The EBN samples shall be a representative from a single batch. The samples must be treated as received. There are 2 techniques of sample preparation available as below: 7.1.1 Sample preparation technique 1 STANDARDS MALAYSIA 2015 - All rights reserved 3

7.1.1.1 Weigh 0.25 to 2.5 g into centrifuge tube and add 10 ml to 100 ml UPW. 7.1.1.2 Vortex the sample solution vigorously to ensure complete mixing of the samples. 7.1.1.3 Heat the sample solution at 70 C to 90 C in a waterbath shaker for 15 minutes. 7.1.1.4 Centrifuge the solution from 5 000 rpm to 10 000 rpm for 10 minutes at room temperature. 7.1.1.5 Filter the supernatant with membrane filter (0.45 micron). 7.1.1.6 The sample ready for analysis (minimum 5 ml per injection). 7.1.1.7 The sample should be analysed within a day. 8 Determination 8.1 Chromatographic conditions for reference 8.1.1 Chromatographic column High capacity anionic exchange column compatible to gradient elution capable of separating anions (NO3 -, NO2 - ). 8.1.2 Elution solution 8.1.2.1 KOH *solution with its concentration of 6 mmol/l-70mmol/l, elution gradient is 6 mmol/i for 30 minutes, 70 mmol/1 for 5 minutes and 6 mmol/1 for 5 minutes. Flow rate is 1.0 ml/min. Note: *the solution depends on the column capacity and type. 8.1.2.2 Sample volume: 20 µl to 25 µl (enabled to be modified according to the content of ion to be measured). 8.1.3 Determine and calibrate a standard curve 8.1.3.1 Inject 20 µl to 25 µl of the prepared working standard solution. 8.1.3.2 Inject 20 µl to 25 µl of blank sample (ultrapure water). 8.1.3.3 Plot and verify the linearity of the standard curve (R 2 =0.99 to 1.0). NOTE: Calibration of the equipment based on MS ISO/IEC 17025:2005 8.2 Quality control procedure 8.2.1. Prepare blank sample or known samples in triplicate. 8.2.2 Prepare spike sample by adding known concentration of standard in triplicate. 4 STANDARDS MALAYSIA 2015 - All rights reserved

8.3 Preparation of test sample 8.3.1 Inject 20 µl to 25 µl of blank sample (ultrapure water). 8.3.2 Inject 20 µl to 25 µl of test sample. 9 Calculation for nitrite and nitrate amount The amount of nitrite (NO2 - ) and nitrate (NO3 - ) in samples are calculated using the formula below: where A c co V F A = ( c co ) x V x F x 1 000 w x 1 000 the amount of nitrite or nitrate in the sample, mg/kg; the amount of nitrite or nitrate in the samples obtain from the curve calibrated, mg/l; the amount of nitrite or nitrate in blank solution, mg/l; the volume of sample solution, ml; dilution factor of sample solution; w weight of sample, g. NOTE. The amount of nitrite (NO 2 - ) in the sample, expressed as sodium nitrite is calculated as a multiply with 1.5 The amount of nitrate (NO3 - ) in the sample, expressed as sodium nitrate is calculated as A multiply with 1.37. 10 Test report 10.1 Report the test result to the nearest milligram per kilogram. 10.2 The test report shall also contain the following information: 10.2.1 reference to this national standard; 10.2.2 all details required for the complete identification of the sample; 10.2.3 any departure from the specified procedure or any circumstances which affected the results STANDARDS MALAYSIA 2015 - All rights reserved 5

Annex A (informative) The diagram in determination of nitrite content Spin the sample then filter, pipette, and take 15ml (V 1 ) Add water, and reagents then, incubate, etc Pipette, 40ml (V 3 ) the solution then filtrate Add reagents for color formation Soak sample in water 200 ml (V 0 ) Bird nest (M= 5g) A Mark 500 ml (V 2 ) B 0 Mark 50ml C Mark Abs 538nm D 6 STANDARDS MALAYSIA 2015 - All rights reserved

Annex B (informative) The diagram in determination of nitrate content Reduction and determination of nitrate 20ml (V 2 ) Buffer Eluent V 1 B 1 Mark 500 500 ml ml (V o ) Bird nest 30 ml F Reduction column 80-90ml Eluent 100ml (V 3 ) G 40ml (V 4 ) Mark Reagents added for color formation 50ml H Abs 538nm I STANDARDS MALAYSIA 2015 - All rights reserved 7

Acknowledgements Members of the Working Group on Edible-birdnest (EBN) test method Dr Fadzilah A ini Abdul Kadir (Chairman) Ms Irma Munirah (Secretary) Hajah Azizon bt Abdullah Ms Faridah @Faridzah Ismail/Dr Ketty Goh Siew Lin Department of Veterinary Services SIRIM Berhad Department of Veterinary Services (Eastern Regional Veterinary Laboratory) Department of Veterinary Services (Southern Regional Veterinary Laboratory) Ms Lim Hooi Sung/Ms Nurul Izzah Abd Rahman Ms Hazly Mohamed/Ms Sathya Darshini Raja Ram Ms Thavamanithevi Subramaniam Prof Dr Saleha Abdul Aziz Mr Kho Dak Yung/Mr Mr Low Siang Tim Department of Chemistry Ministry of Health Malaysia (Food Safety and Quality Division) SIRIM Berhad (Industrial Biotechnology Research Centre) Universiti Putra Malaysia (Faculty of Veterinary Medicine) Permulab Sdn Bhd Sunshine Region Sdn Bhd STANDARDS MALAYSIA 2015 - All rights reserved