Looking for assistance to interpret ATP swab results
Hi
We are doing ATP checking in the morning plus conventional micro swabbing after the ATP before production proceed: (M-F monitoring because we wash our equipment everyday)
LIMITS:
ATP 0-100 Passed
ATP 101-150 re-clean machine and pass
ATP 151 above re-clean machine and re-test ATP
TPC <100 pass
Can you help me explain the data below.
AREA ATP, RLU TPC, cfu/cm2 Coliform, cfu/cm2
1 250 <10 <10
2 9 TNTC TNTC
3 20 TNTC TNTC
*** TPC, Coliform of final product produced are all within specifications
Thanks.
Hi,
You can never correlate the data between ATP vs cfu/plate count, full stop.
Both are different method altogether.
Rgds
Hi Fuse,
IMO you need more data. Difficult to give an opinion based on 1 datum /area.
Do you clean, check ATP, sanitize, check micro. or ??
Were all the cleaned surfaces visually satisfactory ?
Are areas 1,2,3 likely to be similarly "contaminated" ?
ATP and micro.data are 2 ways of evaluating the "cleanliness" of a surface.
As noted in previous post microbiological testing may or may not correlate with ATP readings, since the two techniques measure different parameters. Microbiological methods detect residual micro-organisms (usually bacteria), which should decrease as a result of cleaning/sanitization (C/S). The magnitude of any decrease will depend on the method, materials and chemicals used. ATP bioluminescence is a measure of cleanliness that detects organic soiling (OS) (microbial and non-microbial ATP). (The non-microbial contribution to total ATP is frequently much greater than microbial.)
Despite the above comments, there are some published correlations also.
Verification cleaning efficiency, ATP vs micro..pdf 465.97KB 233 downloads
Ideally one would obviously like to achieve satisfactory results for both.
If all the data is representative of the routine C/S procedure and quantitatively reliable, suggests that -
Area 1 is OS unsatisfactory but micro.satisfactory (with respect to TPC/coliform)
Areas 2,3 are OS satisfactory but micro. unsatisfactory (with respect to TPC/coliform) (how much unsatisfactory depends on the quant. meaning of TNTC)
(I daresay you knew that already).
i suggest you should establish a baseline for both test procedures/sampling points/routine cleaning-sanitizing process. I think this is recommended by ATP unit suppliers.
Hi Fuse,
IMO you need more data. Difficult to give an opinion based on 1 datum /area. ----
In a week time, data will show up/down trend on tpc results
Do you clean, check ATP, sanitize, check micro. or ??
Prior to production we will sanitize the machine and will do atp check and conventional swabbing
after production finish our cleaning procedure is as follow:
--rinse of the seasoning from the machine using hot water
--use an alkaline chlorinated detergent for foaming and leave it for approx 10 mins
-- rinsing the machine using normal water and afterwards put sanitizer
Were all the cleaned surfaces visually satisfactory ? yes
Are areas 1,2,3 likely to be similarly "contaminated" ? NO
ATP and micro.data are 2 ways of evaluating the "cleanliness" of a surface.
As noted in previous post microbiological testing may or may not correlate with ATP readings, since the two techniques measure different parameters. Microbiological methods detect residual micro-organisms (usually bacteria), which should decrease as a result of cleaning/sanitization (C/S). The magnitude of any decrease will depend on the method, materials and chemicals used. ATP bioluminescence is a measure of cleanliness that detects organic soiling (OS) (microbial and non-microbial ATP). (The non-microbial contribution to total ATP is frequently much greater than microbial.)
Despite the above comments, there are some published correlations also.
Verification cleaning efficiency, ATP vs micro..pdf
Ideally one would obviously like to achieve satisfactory results for both.
If all the data is representative of the routine C/S procedure and quantitatively reliable, suggests that -
Area 1 is OS unsatisfactory but micro.satisfactory (with respect to TPC/coliform)
Areas 2,3 are OS satisfactory but micro. unsatisfactory (with respect to TPC/coliform) (how much unsatisfactory depends on the quant. meaning of TNTC)
(I daresay you knew that already).
i suggest you should establish a baseline for both test procedures/sampling points/routine cleaning-sanitizing process. I think this is recommended by ATP unit suppliers.
Need to read more about this matter. thanks for the info.
As a practical matter, I've found that many data points are needed for ATP analysis as the test is not as precise as we would like it to be. Use the same machine, same program, same sites over time to get data you can analyze.
Hi Fuse,
Thks for comments.
Here are some procedures /link for (1) setting baselines, (2) a (random) couple of Correlation studies (3) an investigation of some possible variables which somewhat supports RMAV's post.
(1)
bas1 - hygiena atp thresholds.pdf 330.85KB 102 downloads
bas2 - neogen faq.pdf 383.85KB 72 downloads
bas3 - Scigiene ATP Monitoring.pdf 1.61MB 68 downloads
http://www.testkitcentral.com/faq.html
(2)
Correlation example ATP-micro.2014.pdf 314.48KB 77 downloads
Correlation example2 ATP-micro.2014.pdf 699.1KB 64 downloads
(3)
Cleanliness Evaluation,2002, ATP compared to Micro.data.pdf 407.32KB 101 downloads
Does anyone have updated info on this?