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Validation protocol for hold time study of collected water samples
- 1. Validation Protocol for Hold Time Study of Collected Water Samples 1.0 OBJECTIVE Objective of this protocol is to provide documented evidence through the scientific data to establish and verify that on holding water for over a period of 72 hours after collection and subsequent storage does not affect its results for different parameters such as Description, pH, Conductivity, Heavy metals, Nitrates, TOC, Total count and BET. 2.0 SCOPE The scope of this protocol is to evaluate the hold time of water samples upon holding water sample containers for 72 hours while monitoring water quality. 3.0 REFERENCE DOCUMENT Following documents are referred during preparation of the protocol. Water sampling procedure Procedure for analysis of Water 4.0 RESPONSIBILITY 4.1 Quality Control Preparation, review and execution of protocol 4.2 Quality Assurance Review and approval of protocol 5.0 ACCOUNTIBILITY Head of Department 6.0 PROCEDURE 6.1 Pre-Requisite • Pre incubated media/ molten media. • Testing accessories • Water testing reagents • Availability of sterilized glassware. (Where ever applicable) • Availability of pyrogen free glassware. (Where ever applicable) • Testing environment 6.2 Procedure for Hold Time Study 6.2 Procedure for Hold Time Study Test Matrix Raw water Soft water Potabl e water Purifie d water Water for injecti on Pure steam Drinki ng water
- 2. Descri ption Descri ption Descri ption Descrip tion Descrip tion Descrip tion Descri ption pH pH pH pH Conduct ivity pH Hardne ss Hardne ss TDS Conduct ivity Conduct ivity TOC TAMC TAMC TAMC TOC TOC BET TAMC Pathog ens Pathog ens Pathog ens Heavy Metals Heavy Metals TAMC Pathog ens Colifo rms Colifo rms Nitrate Nitrate Colifo rms TAMC TAMC BET Note: Parameter selected in dark shade is considered for hold time study from particular type of water sample. 6.3Test Procedure • Collect samples as per SOP collection of water sample and store the samples up to 3 days at 2-8°C. 6.3.1 Description • Examine the water physically such as Color, Odor. 6.3.2 Heavy Metals • In a glass-evaporating dish evaporate 150 ml of sample to 15 ml on a water bath. Method: Into a small Nessler Cylinder pipette 10.0 ml of lead standard solution (1ppm Pb). Into another Nessler Cylinder pipette 12 ml of test solution as prepared above. To the cylinder containing the standard solution add 2.0 ml of the test solution and mix. To each cylinder add 2 ml of acetate buffer pH 3.5, mix, add 1.2 ml of thioacetamide reagent, allow to stand for 2 minutes and view downwards over a white surface, the color produced with the test solution is not more intense than that produced with the standard solution. 6.3.3 Nitrate • To 5 ml sample in a test tube immersed in ice add 0.4 ml of a 10% w/v solution of Potassium chloride, 0.1 ml of diphenylamine solution and drop wise with shaking 5 ml of sulphuric acid. Transfer the tube to a water bath at 50°C to allow standing for 15 minutes. Any blue color in the solution is not more intense than that in a solution
- 3. prepared at the same time and in the same manner using a mixture of 4.5 ml of nitrate free water and 0.5 ml of nitrate standard solution (2 ppm N03). 6.3.4 Conductivity • Take the 100 ml sample in a suitable container, and stir the test sample by maintaining the temperature 25°C ± 1°C, measure the conductivity with the help of calibrated conductivity meter. 6.3.5 pH • Take 100 ml of sample and add 0.3 ml of saturated KCI solution. Mix the solution well and then measure the pH with the help of Calibrated pH meter. 6.3.6 Total Organic Carbon •Analyze the sample for TOC in a calibrated TOC Analyzer as per the Method for TOC analysis. 6.3.7 Total microbial Count (Pour Plate Method) • Dispense one ml of sample into two petridishes. Approximately add 15-20 ml of R2A / Plate count Agar into each petridishes. Cool the media approximately 45°C (feel on the dorsal side of the hand, it should be bearable). Cover the petridish, mix the sample with the agar by tilting or rotating the dishes and allow the contents to solidify at room temperature. Invert the petridishes and incubate at 30-35°C for 5 days. After incubation, examine the plates for growth, count the number of colonies and express the average for the two plates in terms of the number of colony forming units per ml. 6.3.8 Total microbial Count (Filtration Method) • The procedure gives the use of a single disposable/ autoclaveable filtration funnels and filter holder, using suitable filtration system. •Use sample size as specified in the specification for filtration through the 0.45 m filter. •After completion of filtration of sample, rinse the filter with 100 ml sterile water remove the filter using sterilised forceps and transfer it immediately to the previously prepared petri-dish with appropriate medium (R2A agar/Plate count agar). • Place the membrane carefully so that the air should not be trapped inside the filter, as this will prevent nutrient medium from reaching the entire membrane surface. Replace the lid. Invert the petri dish and incubate at 30-35°C for 5 days. Count the number of colonies on the membrane and express the results as per specification. 6.3.9 Bacterial Endotoxin Test • Refer the SOP for Bacterial Endotoxin Testing.
- 4. • Perform the analysis on 0 hours, 24 hours, 48 hours and 72 hours Related: Sampling, Preservation and Storage Procedure of Water Sample 7.0 ACCEPTANCE CRITERIA Its shall meets the specification of its particular water type. 8.0 CONCLUSION After complete evaluation of the Hold time study for collected water samples a final Hold time study summary report shall be prepared which should essentially contain discussion and conclusion which clearly determine the hold time period for water samples. 9.0 ABBREVIATIONS SOP - Standard operating procedure ° C - Degree Celsius TOC - Total organic carbon Pb - Lead w/v - Weight per volume BET - Bacterial endotoxin test ppm - Parts per million ml - Millilitre TDS - Total dissolved solids %- Percentage TAMC - Total aerobic microbial count N03 - Nitrate KCL- Potassium chloride