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In recent years, Glove Integrity Testing has been profoundly discussed and numerous articles have been written on this topic. However, many doubts still remain within the industry due to the lack of norms and clear guidance available. In 2008 Annex 1 to EU Guidelines to Good Manufacturing Practice reiterated the importance of having glove integrity testing:
“25. Monitoring should be carried out routinely and should include frequent leak testing of the isolator and glove/sleeve system.”
Over the course of the past few years different industry specific associations have conducted statistical studies about the frequency in which this type of testing is performed in the pharma industry and the results indicated that the test is executed normally prior to each batch of a production run.
However as far as performance requirements the question is still open: which hole diameter should I be able to detect?
The theoretical answer would probably be 1μm (bacteria spores diameter), but the practical answer is much larger due to technological limitations at this time.
The methodologies of testing available today are many, but few of them may be automated and many times they are not suitable for the routine.
Moreover today it is difficult to find equipment to test the integrity of gloves that comes with performance qualification (PQ) and this is mainly due to the lack of test repeatability. Although there are many different methods available in the industry, the method used by the greatest portion of the users to test the integrity of the gloves is the Positive Pressure Decay method which follows the international standard ISO 14644-7 Annex E.5.
The ISO 14644 Part 7 doesn’t detail specific methodologies for the Positive Pressure Decay. In terms of acceptance criteria many different interpretations can be reached. The box below shows what the ISO norm states about the test procedure and the results.
Many questions can arise from such a simple test procedure and such a wide interpretation of the results. What is the performance of this method? Which hole diameters will I be able to detect?
The first step is to create a mathematical model which can describe an inflated glove with an orifice, as this will provide you with a formula relating to the hole diameter for the expected pressure drop. Unfortunately the calculation is very complex due to different elastic properties of the glove material (different elastomers, thickness, and sizes) so different strategies need to be followed.
The glove materials available in the industry vary (Hypalon, Butadyl, Neoprene, EPDM). In particular, Hypalon is a mixture of polymers such as plastic and rubber, with a very different reaction to stress and elasticity. These gloves, very common in aseptic applications, result in more of a challenge to integrity testing than other types of materials. Thickness and size, together with the flange mounting, greatly contribute to the determination of a customized testing procedure for each kind of glove material. Therefore an experimental approach needs to be strictly followed.
For the positive pressure decay method, performance tests may be carried out in different ways, such as calibrated hole on the flange, needle inserted through the glove or pinholes on the glove (1) . Based on our experience, the calibrated hole method is the most appropriate and precise method of the three listed above, so this configuration, together with the Automatic Glove Tester (2), was used for this study. After testing gloves of different sizes and materials currently available in the market, we were able to collect a significant amount of data to support the methodology described below that is based on the comparison between these two systems:
The expected behavior of the two systems should be like the one shown in the graph below.
To achieve a Qualified Performance the following activities have to be performed:
Characterization of the Closed System: Study the pressure decay curve at several inflatable pressures (< 1000 Pa) (3) and collect a statistica set of data from these tests.
Characterization of the Open System: Study the pressure decay curve at several inflatable pressures (< 1000 Pa) for the hole whose performance we are trying to prove and collect a statistical set of data from these tests (4).
From the two sets of curves the following test parameters are then defined:
The objective is to locate the value of these paremeters so that they will correspond to a significant difference between the Pressure Drop of the Open System (ΔPos) and the Pressure Drop of the Closed System (ΔPcs), i.e. ΔPcs – ΔPos . The statistical deviation of the collected data needs to be as small as possible and the accuracy of the pressure transmitters must be considered in order to reach an effective and valuable acceptance criteria. Basically what we look for is a large difference between the slopes of the two curves based on the collected data of the two systems during testing: a smaller difference between the two curves may result in a longer overall test procedure time until a significant difference is observed.
As such, the equipment and the test can be easily validated while the specific glove and fixing mechanism (flange and counterflange, o-ring, etc.) is characterized in terms of “normal leakage” (Closed System curve). Before running the test, it is important that the integrity of the machine running the test is also verified and assured.
With the method described above a variety of hole diameters can be detected developing the correct test parameters.However the detection limits are primarily influenced by the precision of the adopted transmitters, statistics involved and time constraints.
Using this method with a calibrated hole of 100 μm a high level of reproducibility and a very, very low frequency of false positives has been observed. This means that an automatic glove tester machine may be easily validated. Lower detection limits may be achieved by the use of smaller calibrated hole sizes, but this practice will impact the reproducibility and the probability of false positives.
Data collected and PQ protocols in this study are available upon request.