Method for testing validity period of wet wipe product
A determination method and technology of validity period, applied in the field of the validity period of wet wipes products, can solve the problems of insufficient validity period arguments, insufficient basis, non-compliance, etc., and achieve the effect of shortening the test period and ensuring the accuracy
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0044] Embodiment 1 prepares test solution
[0045] Sterilize the front end of the scissors in an infrared heating sterilizer for injection needles for at least 5 seconds, then cool for at least 5 seconds, cut open the sample packaging bag, cut 20g of sample from the upper part of the sample into a 180ml jar containing solution D, and mark it briefly The digital batch number, sampling date. Place the jar on a shaker and oscillate at a speed of 190-220 rpm for at least 10 minutes to obtain a test solution with a mass-volume ratio of 1:10.
Embodiment 2
[0046] The mensuration of embodiment 2 total amount of aerobic bacteria and mold yeast
[0047] Install the membrane filter on the device, take out 10ml of 1:10 test solution, after filtering, take 100ml of solution D to rinse, after filtering, sterilize the tip of the tweezers in an infrared heating sterilizer for injection needles for at least 5 seconds, take out After cooling for at least 5 seconds, stick the primary membrane on the pre-marked TSAWLP plate with tweezers, and place the TSAWLP plate in a 30-35°C incubator for 3-5 days. Stick another membrane on the pre-labeled SDAWLP plate, and place the SDAWLP plate in a 20-25°C incubator for 5-7 days.
[0048] The preparation method of the solution D is as follows: dissolve 1g of peptone in 1000ml of purified water, then add 1ml of Tween-80, after the dissolution is complete, adjust the pH to 7.1±0.2, and sterilize at 121°C for 20 minutes, namely have to.
[0049] The detection results are as described in Table 1, wherein...
Embodiment 3
[0055] The detection of embodiment 3 Staphylococcus aureus
[0056] Take 10ml of 1:10 test solution and filter it, rinse and filter with 100ml solution D, put the filter membrane into 100ml soybean-casein digest broth (TSB), and incubate at 30-35℃ for 18-24 hours At 20 o'clock, the initial enrichment solution A was obtained. Use an inoculation loop to pick a ring from the initial enrichment solution A and spread it evenly on Mannitol Sodium Chloride Agar (MSA), and incubate it upside down at 30-35°C for 18-72 hours; if there are yellow colonies on the MSA plate or the periphery is yellow If there is no growth of white colonies that match the above-mentioned morphological characteristics or suspected growth on the plate, or there are consistent or suspected growth of colonies but The result of Gram staining was negative, and it was judged that Staphylococcus aureus was not detected in the test product. The test results are shown in Table 2.
[0057] Table 2 Detection of Stap...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


