The new 2020 draft of EU GMP Annex 1, which regulates the manufacture, control and release of sterile pharmaceutical products in the EU, gives greater weight to quality risk management (QRM) than its current version. Hence there is a need to know more about the manufacturing processes used and the microbial contamination risks of the manufactured product. This study investigates the feasibility of modifying the most frequently used active air sampling method in two different ways to enhance the knowledge about these risks: increasing the volume of sampled air and sampling onto the same plate at regular intervals.
An environmental monitoring plan must include the determination of sampling locations, monitoring frequencies, and monitoring methods. Incubation conditions should be based on a documented risk assessment and knowledge of the process and operations to be performed in the area. The specific limits or frequencies specified in the draft should be considered as the minimum requirement. They are based on historical experience of issues that have previously been identified and have impacted the safety of patients.
The well-known environmental monitoring methods based on volumetric air samplers, settle plates, contact plates, and swabs are recommended to be applied frequently. In general, there is no need to change the well-established procedures, which have been proven to be efficient. In order to achieve continuous viable air monitoring, it is recommended to use settle plates in combination with active air samplers.
Newly included rapid or automated methods can fulfill the requirement to perform continuous airborne viable monitoring, but the 2020 EU GMP Annex 1 draft states the limits in colony forming units (CFUs). Where different or new technologies generate results in units other than CFUs, the manufacturer should scientifically justify the limits set in another unit and, where possible, correlate them with colony counts.
However, it is mandatory to validate and demonstrate the equivalence or superiority of these methods over the established methodology. The metrics used to measure biocontamination may yield units related to the technology used that are not readily comparable to the results of the cultural method, which reports in CFU. Establishing and understanding how to translate the results might take time.
For this reason, it is worthwhile to look at alternatives to such real-time methods. One method, sequential sampling, is based on air samplers in combination with culture media, like the conventional method is, but covers a longer period of the manufacturing process. The MAS-100 NT® air sampler offers the build-in option to perform sequential sampling, meaning a determined air sample volume of up to 2000 liters is taken in up to 50 intervals over the course of up to 24 hours, during which the same settle plate is used every time. Not needing to change the plate for a new one avoids secondary contamination caused by the act of replacing the plate and thus the risk of false-positive results.
• To determine if dehydration of the culture medium impacts the accuracy of results when larger volumes of up to 4000 liters of ambient air are sampled (Part 1).
• To compare the effectiveness of conventional and sequential (interval) sampling by counting the CFUs after the incubation period (Part 2).
Active air sampling was performed in a non-controlled environment with intense human activity to detect a broad range of airborne microorganisms and, furthermore, to achieve higher microbial counts than in a controlled environment.
Newly calibrated MAS-100 NT® microbial air samplers (cat. no. 1091910001) were used in combination with TSA with LTHThio sedi.-ICR settle plates (cat. no 1467860120; same batch for all trials) for all sampling.
Drying of settle plates' agar media was performed by a MAS-100 NT® air sampler in advance of sampling to simulate the influence that the sampling of a larger air volume has on the water loss of these media. This was done under a laminar flow hood to avoid contamination and thus enable only the colony counts of the air drawn during the ensuing sampling step. Half of the plates were incubated immediately after the initial drying step to serve as negative controls to establish the cleanness of the air in the laminar flow hood. All air sampling was performed in a non-controlled area and started with a 1-minute delay to avoid contamination caused by the presence of the lab technician.
Relative humidity and temperature were recorded with a calibrated instrument during sampling to evaluate the effects of these factors on water loss.
The colonies of microorganisms on the agar media were counted after 1 or 3 days of incubation and expressed as colony forming units (CFUs).
The aim of this part of the study was to measure drying of the agar media as a function of the sampled air volume.1
Four MAS-100 NT® microbial air samplers were used at sampling locations positioned about three meters apart. The reference and test plates alternated, and the order was changed after every run. This ensured that every air sampler with every type of plate would sample air at every one of the locations, and in turn.
The test procedure is shown in Figure 1. The first step was to dry plates, with half the number of these to be used as negative controls and the other half as test plates. The second step was to perform side-by-side tests with pre-dried test plates and reference plates without prior drying. The reference plates (fresh plates, not pre-dried) served to determine if water loss of the pre-dried plates had led to lower recovery rates.
The water loss of each plate was determined by weighing before and after the initial drying step, as well as at the end of the subsequent sampling procedure. For initial drying, two different air sample volumes of 2000 or 3000 liters were applied per plate. As the air sampling volume for the test added 1000 liters per plate, the total air volume per test plate was 3000 or 4000 liters (Table 2). For each selected sample volume 10 runs were performed in parallel in a side-by-side test.
After sampling, the plates were incubated at 30 to 35 °C for 1 to 3 days, after which the colonies on the settle plates were counted and the values corrected according to Feller statistics.
Figure 1.(Test procedure for Part 1: For each sampling volume 20 plates were pre-dried (e.g. for the total air volume of 3000 liters, 20 plates were pre-dried with 2000 liters)
In conventional air sampling a specific air volume is sampled at a certain time onto a different agar plate for each measurement. In sequential air sampling, on the other hand, several samples are taken at regular intervals over the course of a certain period (e.g. a whole day) using the same plate1. According to the following sentence the interval was apparently 30 minutes (the total measurement period was 2 hours).
Figure 2.(Photo of the three air sampling locations for Part 2. The distance between the sampling locations was approx. three meters)
Inactivity and active air sampling alternated for sequential sampling. Over 2 hours, 1000 liters of air were sampled, 200 liters at the start and subsequently 200 liters every 30 minutes. Conventional sampling was performed at the same intervals, but the plates were exchanged for new ones every time, and the sampling volume was 1000 liters each (Table 1).
All agar plates were pre-dried under the laminar flow hood with an air volume of 1000 liters. Therefore, at the end of the experiment, the total sampling volume was 2000 liters for each plate. The relative humidity was 44% on the day of the experiment. The CFUs were counted after a 3-day incubation at 32.5 °C.
None of the negative control plates showed growth after incubation, suggesting that no contamination occurred during the initial drying step in the laminar flow hood.
The test trials were performed in four different series to determine the influence of water loss on the recovery rates of the ICR plates at different temperature and relative humidity values.
The water loss per agar plate is shown in Figure 3.
According to the product specifications each settle plate is filled with 30 mL of agar medium, which weighs about 30 grams. A weight loss of, for example, 6 grams was considered to be a 20 percent weight loss, and thus a 20 percent loss of water. Weighing of the plates was performed with the Petri dish lid in place.
As expected, the plates at the higher humidity of 52 to 54% during drying and sampling (series 3 and 4) lost less weight and thus less water than those at the lower humidity of 37 to 38% (series 1 and 2), see Figure 3. At both humidity values, the water loss was almost linearly proportional to the total air volume drawn, with the rate of water loss slowing only very slightly as the air volumes increased.
Figure 3.Average water loss of the settle plates' agar media in grams at different total air volumes for series 1/2 (left) and 3/4 (right)
The CFU counts of the reference plates and the pre-dried plates of the same series were very similar (Figure 4). This indicates that colony formation was not impaired by the water loss. Had water loss impaired colony formation, the fresh reference plates would have yielded significantly higher counts than the corresponding pre-dried plates.
Figure 4.CFUs per fresh reference plate and 2000 or 3000 liter pre-dried plate for series 1/2 (left) and 3/4 (right) after a one-day incubation at 32.5 °C.
The different absolute levels of total CFUs between series 1/2 and series 3/4 are due to differences in the number of microbes in the air on the days the sampling took place. This is evidenced by the similar count levels of the corresponding reference plates.
Figure 5 illustrates the number of colonies counted on the pre-dried plates as a percentage of those on the reference plates, as well as the amount of water lost after initial drying and after air sampling following that drying step, calculated via the weight lost after drying/sampling. It shows that the numbers of recovered colonies on the pre-dried plates did not differ significantly from those of the reference plates without pre-drying, despite a significant loss of water having occurred (e.g. 2000 L series 1: 98% recovery rate and 25% total water loss; 2000 L series 3: 93% recovery rate and 20% total water loss).
In five of the ten plates of series 2 (3000 liters pre-drying volume plus 1000 liters air sampling at 37 to 38% relative humidity) the agar had shrunk after a two-day incubation at 32.5 °C (Figure 6). After only 24 hours of incubation at 32.5 °C, no agar shrinkage had been visible, and neither was agar shrinkage observed even after two days where the relative humidity had been a higher 52 to 54% (series 4, Figure 3). This underlines the relevance of the environmental conditions (temperature and relative humidity) during sampling (see series 4).
Figure 6.Settle plate with shrinkage at the edges of the agar
Sequential and conventional sampling were compared with regards to the suitability of these methods to recover colonies on settle plates, each after a 1000-liter initial drying step in a laminar flow hood and a subsequent 1000-liter sampling step in the non-controlled environment. The average numbers of colonies recovered per cubic meter of sampled air are shown in a boy-blot illustration (Figure 7). This indicates that sequential and conventional sampling yield similar colony counts.
All plates were weighed before and after the pre-drying step, and again after the side-by-side test procedure. The water loss during pre-drying and sampling had amounted to between 4.74 and 5.39 grams per plate, which is equivalent to 15.8% and 17.9% of the agar media's weight.
Figure 7.CFUs per m3 of sampled air for conventional and sequential air sampling (SQS) at the 3 collection points (see figure 2 and table 2 for the test set-up). The SQS value is the average count of the two SQS locations.
By adding a long prior drying step before sampling the usual air volume of 1000 liters, it has been possible to simulate the influence that the sampling of up to 4000 liters has on the water loss of TSA settle media plates used in combination with the MAS-100 NT® microbial air sampler, as well as the effects this has on microbiological detection. The test results reveal an almost linear water loss over sampling time (and thus also over air volume). However, in the air volume range tested, the significant water loss caused by evaporation was shown not to impair the ICR settle plates' suitability for microbiological detection. Hence it is possible to sample up to 4000 liters without impacting the quality of results, allowing longer and/or more comprehensive active air sampling in manufacturing facilities. The simultaneously processed undried reference plates suggested that the determined higher or lower absolute colony counts were due to different contamination levels on the days of the experiment.
The object of the second set of experiments was to determine whether sequential air sampling would lead to different colony counts than conventional sampling. In sequential air sampling, the air sampler is programmed to sample air on a single agar plate at certain intervals over a pre-defined period of time. This period can, for example, cover a whole working process during which, unlike for conventional air sampling, it would not be necessary to replace the agar plate several times, which would avoid the risk of contamination on the plate (and thus false-positive results) caused by the manual act of plate replacement by a QC attendant. The comparison revealed that the result quality of sequential air sampling is comparable to that of the conventional sampling method, suggesting that this alternative method may be preferable for manufacturing activities over a longer period of time during the course of a day.
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