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The Relationship among Pore-Size Ratings, Bubble Points, and Porosity
Microporous membrane filtration is the technique often applied to the aseptic processing of drug preparations. This is especially appropriate when the ingredients are heat labile. Certain filter performance qualities are of specific interest in such filtrations, namely, the extent of organism removal, the rate of liquid flow, and the total throughput volume. Essentially, it is the numbers and sizes of the pores relative to the number and sizes of suspended particles that determine the filter retention performance, although there are other factors that also affect organism removals (1). The total aggregate space of the pores within the solid filter matrix represents the membrane's porosity. It is constituted of the total number of pores of whatever dimensions. The importance of pore size is obvious. The filter pores are the sites through which the liquid flows. Simultaneously, its suspended particles, such as organisms, are retained at the pores. Ultimately, the throughput is limited by the accumulation of the particles at the pores causing their blockage.
Microporous membranes prepared by the reverse-phase casting process are available from several manufacturers in a series of pore sizes ranging from 0.04 to 8 μm. Curiously, the rating values are not determined by direct pore-size measurements, although several different methods for sizing have been proposed.
Tests such as bubble-point measurements and bacteria challenges are used to assign pore-size ratings. The propriety of translating bubble-point values into pore-size ratings will be discussed later in this article. The assigned numbers are meant to imply particles-size retentions, not dimensional mensurations from which flow properties might also be derived. The bubble points are indicators of the largest size pores present in a membrane; the focus in filtrations being chiefly upon particle retentions.
The significance of pore sizes lies in their implication to particle-size retentions. The quantitative characterization of pore sizes derives from bubble-point measurements coupled with bacterial challenges. These tests are correlative. The former does not compromise subsequent use of the filter. It is a nondestructive test. The latter, although more direct in its diagnosis, is a destructive test in that it contaminates the filter with the test organisms; thus obviating its later application to process filtration.
The organisms used in the microbial challenges differ in accordance with the filter's presumed pore size. The log reduction values necessitated by FDA's definition of a sterilizing filter is the retention of 1 × 107 colony forming units (cfu) per square centimeter of effective filter area (EFA) (2). Such a retention produced against a Brevundimonas diminuta ATCC-19146 confrontation characterizes the 0.2/0.22 μm-rated membranes. Serratia marcescens is the organism commonly used in challenging 0.45 μm-rated membranes. Because Bowman et al. determined that the 0.45 μm-rated membranes retain B. diminuta to approximately the 1 × 105 /cm2 level, that test is sometimes used for testing the 0.45-μm membranes (3). The 0.1 μm-rated pore size is mostly tested against Acholiplasma laidlawii. It is fair to say that the testing of 0.1 μm-rated membranes is not yet fully in place within the industry.
Intermittent bubble-point measurement also is used as a process guide during the membrane-casting operation to ensure that the intended pore-size ratings result. The point being made is that the relevant measurements being performed are of bubble points, not of pore sizes. From these, as will be discussed, pore-size ratings and log reduction values (LRVs) are derived.
The pore-size ratings are the remnants of early efforts at membrane classifications that developments in pharmaceutical filtrations have reduced to rather insignificant utility. Pore-size ratings are administrative devices. They serve only as parts numbers or catalogue listings for filter manufacturers. The selection of filters for sterilizing applications is made primarily on the basis of the LRVs that the various filter types impose upon B. diminuta challenges in accord with FDA's definition of a sterilizing filter (2). The relationship of LRVs to experimentally determined bubble-point values enables use of the latter to identify potential sterilizing membranes subject to verification by microbiological assays performed by the filter manufacturer. The putative pore sizes are affixed accordingly. The membranes that meet FDA's stipulation of retaining the 1 ×107 /cm2 challenge are listed as being rated as 0.2/0.22 μm.
The membrane pores
Microporous membranes can be prepared by various methods. Among these is the track-etch process wherein a polymeric, dielectric film is bombarded with heavy-mass fission fragments, followed by an alkali etch of the radiation-damaged pathway. This process creates pores that are straight through and regularly cylindrical in shape. Their diameters can be accurately measured with scanning electron microscopy. Despite the relative regularity of their pore structures, these membranes do not usually find application in pharmaceutical processing. The membranes used in pharmaceutical processes are almost exclusively prepared by the phase-inversion technique, generally referred to as the "casting method" (4).
Little is known about the numbers, sizes, and shapes of the pores of microporous membrane so prepared. The membrane structure usually is pictured as being analogous to that of a polymeric sponge. A hypothesized oversimplification of the pore passageways is that of irregular and tortuous capillaries that are, therefore, more extended in length than the filter's surface-to-surface thickness. The pores are marked by irregularly restricted diameters that provide the choke-points that interfere with particle passage. However complex, the pores are pictured as being essentially cylindrical and composed of interconnected spaces extending through the depth of the polymer matrix.
The very concept of a definable "pore" is an artificiality when applied to microporous membranes other than the straight-through columnar pores that characterize the track-etched variety. The complex geometry of the sponge-like membrane results in the pores having ratios of cross-sectional areas to perimeters, called the "hydraulic parameters." These vary over the entire thickness of the membrane (5). A membrane's depth can be constructed of several superimposed unit planes that in their aggregate impose their effect on retention and flow rates (6). The "pores" so considered are presumably connected throughout the unit planes to constitute pathways for fluid flows. However, where particle retentions interfere flow redistributions may result through new "pore" alignments. The "pore" concept arises as a hypothetical construct useful in understanding filter performance. Unlike the track-etched pores, they are not integral, structural pathways for fluid flow.
Filtration is not a simple sieving process, except perhaps in the case where the filter is a track-etched membrane with pores passing straight through a much thinner film (~10 μm). As stated however, for the membranes prepared by the casting process (thinness ~150 μm), a fluid on passing through encounters pores of different diameters and surface areas. Particles are separated from the fluid by adsorptive attachments to the pore surfaces as well as by the size exclusion mechanism. Thus, the meaning of the average pore size as reflecting the size of a restrictive diameter within a pore passageway is necessarily an oversimplification. Nevertheless, the events taking place at the pores are depicted as if the pores were continuous and integral paths through the depth of the membrane.
Membrane characteristics are assessed because of their pertinence to aseptic processing. However, the pore-size distribution, despite being an important structural feature that influences both flow and retention, is not among them. It is seldom known or investigated although an ASTM method based on airflow rates enables its assay (9). The reason for not assaying the pore-size distributions of filters is that complete organism removal is dependent upon the largest pores of the pore-size distribution retaining the smallest particle of the particle-size distribution. This is the singular circumstance wherein an absolute filtration can eventuate. Given this felicitous situation, only the size of the largest pore has pertinence. In fact, however, the distributions of neither the pore nor organism sizes are likely to be known by the filtration practitioner. Depending on the relative numbers of pores and particles and their sizes, particles may encounter the larger pores of the distribution to escape removal. These larger pores of a distribution are assayed by bubble-point measurement recorded in pressure units (psi or bar) rather than in dimensional units (μm). The accompanying smaller size pores are ordinarily not quantified or measured because they are not seen to influence retentions.
Methods of pore-size rating
By porosimetry. Numerous methods have been used to assess pore size (10). Early on, mercury porosimetry was the method of choice (11–13). In this procedure, mercury is forced under pressure to penetrate into membrane pores. This process is performed at increasing differential pressures, ΔP. The higher the value of ΔP, the smaller the pores that the fluid metal can intrude. Quantitation of the different pore sizes relates to the volume of mercury that is intruded in filling the pores at each of the progressively increasing differential-pressure stages. Airflow porosimetry studies also have been performed (14, 15).
The porosimetry method is flawed by the assumptions necessary to its application. It is not suited to polymeric materials that are at temperatures above their glass-transition points and whose pores are, therefore, liable to stretching and distortion under the pressures of the intruding fluid. Also, the averaging of volume changes required by the technique may mask the true dimensions of the "pores."
By flow through pores. The engineering principle enabling an orifice's dimensions to be sized using the rates of flow it permits can be applied to determining pore sizes. The rate of flow through a pore at a given differential pressure is essentially inversely proportional to its length and directly so to its width or diameter. Thus, the flow characteristics of single pores are described by the Hagen–Poiseuille Law:
wherein a fluid of viscosity η with an average velocity u of the fluid is related to the tube diameter d and pressure drop, ΔP along a given length z (5).
At the site of the pore's most restricted diameter its retention and flow properties are defined. Nonetheless, flow rate is influenced by more than the pore's area of constriction. It reflects also the length of the pore. Conceivably, a relatively open pore, less constricted and, therefore, less retentive, may be rendered slower-flowing by its extended length. The area of a filter, however, contains numerous pores. Its rate of flow is defined as its flux. It is the total and simultaneous flow through the many pores of the given filter area that is measured. Flux has the dimensions of volume of flow per unit time, under unit pressure differentials, per unit area of filter. Because several pores are involved, the concept of porosity comes into play.
By porosity one means the percentage of a filter that is its voids or pores; that is, the ratio of space to solid in the membrane matrix. A given porosity can be constituted of a random combination of various numbers of pores, nonuniform in their lengths and diameters and of various shapes. The more numerous the pores, the more likely a higher flux. However, the lengthier the pores, the lower their individual flow rates. Pores of less-restricted diameters would flow faster but would tend to be less retentive. The filter's sieve retention would be decided by the size of its widest restrictive diameters. It is this dimension that will decide the largest particle to escape capture by penetrating the pore.
The possibilities are unlikely of pores of such regularity in size exhibiting identical retention ratings but differing in flow rates. Except for the irregularities introduced by pore-size distributions, organism retention, flux, and porosity should be parallel expressions of the membrane's pore size. This assumes, however, the use of identical polymers, casting solutions, and converting techniques, along with standard systems of measurements. None of these conditions are likely met by competitive filter manufacturers using proprietary practices. Therefore, comparisons, as of flux or of retentions, between filters of various manufacture may not usefully be extended to speculations concerning their structural features or performances.
Ambiguities in pore-size rating
Within any given pore-size designation available in the market, there exists some range to its quantified properties. In its manufacture, a membrane lot may, and indeed will, incur some variation in the in-process bubble-point measurements that are translated into pore size. Each pore-size rating is prepared using a different casting formula. Nonetheless, the preparations do not yield distinct quanta, although the variations within a class are less than those between classes. Each batch or even each filter within a batch of membranes is classified to a single pore-size value, although each of the individual filters comprising the group may have its own bubble point within the range of values that define the given rating.
As Schroeder points out, the pore size–retention correlation is not a step function (26). In its manufacture, a membrane lot will incur some variation. In using nonuniform standards, filter manufacturers might assign their pore-size labels somewhat ambiguously. One fabricator may, on the basis of flux, consider a membrane to be an "open" 0.1 μm. Another filter producer, using a somewhat different rating system might classify it as being a "tight" 0.2 μm. This could give rise to a labeled 0.1 μm, not so handicapped by reduced flows, being compared with a labeled 0.2 μm, not so advantaged by enhanced flows. The more "open" 0.1 μm may not flow faster than an average 0.2 μm but may do so against a "tight" 0.2 μm. Consequently, it becomes an unrewarding exercise to try to compare competitive membranes each rated by their own individual catalogue descriptions as perhaps being of the same pore size, yet exhibiting different flux rates or retentions under test.
Consequences of rating ambiguities
As shown in Table II, Tolliver and Schroeder found that the retention of 0.198 µm latex particles by five commercially available 0.2/0.22 μm-rated membranes differed significantly (21). The particle-retention mechanism was not complicated by adsorptive sequestrations because the solution contained surfactant. Given the size uniformity of latex particles, the variation in retentions based on sieving indicates different reference standards for the like-rated pore sizes. Nonstandard ratings also explain the Lindenblatt et al. (28) report that the flow rates exhibited by four 0.2/0.22 μm-rated membranes, as also of four 0.1 μm-rated filters differed markedly (see Figure 6) (28). Moreover, as indicated in Figure 7, the throughput volumes measured for the nonstandardized similarly rated pores also differed. Comparable data are offered by Jornitz et al. (29).
Pore-size ratings and validation
Until rather recently it was believed that the sterilization of fluids could be achieved by their filtration through a "sterilizing" membrane whose proper and pertinent identity was confirmed by its pore-size rating, which was itself determined by bubble-point measurement. This belief arose from the membrane's successfully withstanding a microbiological challenge of 1 × 107 cfu of B. diminuta per square centimeter of filter surface. On this basis, the membrane, in accord with FDAs definition, was considered a "sterilizing filter."
Contrary to common belief, B. diminuta was not selected to be the model organism because it was thought to be the smallest microbe—smaller organisms were known for decades (30). Rather, it was chosen as likely to be the smallest organism that might commonly be encountered in nonsterile pharmaceutical preparations. Therefore, its filtrative removal was considered as indicating with a high probability that the membrane used was a sterilizing filter. Using this type filter, identified by its bubble point, was assumed, with this caveat, to ensure a sterile effluent.
Over time, it became evident that positive conclusions based on pore-size ratings were subject to modification by the physicochemical specificity of the organism-suspending fluid, by the individuality of the organism type in its size-changing response to the fluid, in the possible change in pore size induced by the fluid, and by the adsorptive qualities of the filter resulting from its particular polymeric composition. All of these factors are influenced by the filtration conditions in their numerous varieties, but especially by the transmembrane pressure.
A filter may not sterilize the same preparation under different filtration conditions, especially under dissimilar differential pressures (31). A given membrane may or may not retain a particular organism type suspended in a different drug vehicle (3, 31). The organism type need not remain constant in size but may alter in response to its suspending fluid (32–34). The effect of the vehicle upon the polymeric membrane may cause a change in its pore sizes (24). What had once seemed simple is now recognized as being quite complex. Pore-size ratings alone are not sufficient to ensure the validation of a sterilizing filtration.
Given the above, it is surprising that The European Medicines Agency (EMEA) has stipulated certain requirements for a bioburden confronting the sterilizing filter. Its 1996 Notes for Guidance states, "In most situations NFT 10 cfu/100 mL will be acceptable depending on the volume to be filtered in relation to the diameter of the filter. If this requirement is not met, it is necessary to use a prefiltration through a bacteria-retaining filter to obtain a sufficiently low bioburden" (35). In recommending the use of a bioburden-reducing filter when the level of 10 cfu/100 mL is exceeded, the EMEA guideline states, "The type of bacteria-retentive filter and its pore size should also be described in the application. Pore sizes of 0.22 μm are acceptable without further justification" (emphasis added). It would seem that validation by pore size is still acceptable to the EMEA.
Conclusions cannot be made regarding the sterile filtration of microorganisms unless methods of quantifying them by culturing and counting are available. Organisms such as the L-forms, nanobacteria, and "viable but nonculturable" entities may not be amenable to such analyses. Concerns about their presence may be justified but without the means to cultivate and count them, it is impossible to attest to their complete absence. It follows that a sterilizing filter can be judged only by its performance in the removal of identifiable and culturable organisms known to be present in the drug preparation (36).
Bubble points and "the largest pores"
An alternative approach focuses on measuring the set of "largest pores" of a filter. These are the least resistant to fluid flow. They, if any, would be the most likely to permit organism passage. The measurement is of the pores' constricted diameters rather than of their lengths. It is at these choke points that the size of a particle just large enough to be retained is defined. The pore diameter varies along the length of the pore passageway and differs among the various pores of the filter; hence, pore-size distributions characterize the microporous membranes.
It is the size of the smallest diameter of such a largest pore that is measured by the bubble-point test. As more accurately stated by the Aerospace Recommended Practice, "No bubble point test measures actual pore size but only allows correlation of the measured capillary pressure with some dimensional characteristics of the pore structures" (37). Although not an absolute measure of specific pore sizes, the pressure levels designating bubble points bear the pore sizes a strong relationship on the basis of the capillary rise experience and provide an indication of their magnitude (38).
The other means of measuring filter integrity are the equal of the bubble point for that purpose. They all are accepted as being of equal reliability when properly performed. The forward flow method—often if somewhat erroneously, identified as a single-point diffusive airflow procedure—is an example. The "diffused air" that is measured, however, is the product of Fick's Law of Diffusion that reflects porosity, the total volume of all the pores regardless of their sizes, and not the diameters of its largest pores:
in which N is the permeation rate, D is the diffusivity of gas in the liquid, H is the solubility coefficient of gas in the liquid, L is the membrane thickness, (P 1–P2) is the differential pressure, and p is the total porosity.
By contrast, the air quantified in the bubble point reflects, albeit inexactly, that which passes only through the set of largest pores in accord with the capillary rise equation. It is the implications to pore size and, therefore, to particle retentions that suit the use of the bubble-point test for this purpose.
The bubble-point equation, based on the capillary rise equation, involves a reciprocal relationship between its value and the size of the "largest pore" diameter. It is the pore diameter that is being sought.
in which P is the bubble-point pressure, d is the pore diameter, λ is the surface tension, and θ is the wetting angle.
As the applied differential pressure rises, the water layers in the largest pores thin. Successively the next smaller pores are likewise affected and so forth. Eventually the water is expelled from them. The affected pores progressively increase in number from a very few. In the process the air that underwent diffusion becomes added to by the bulk airflow occurring through the vacated pores that also increase progressively in amount. The collected air is then, strictly speaking, not composed completely of diffused air. To this extent, the term "diffusive airflow" is a misnomer (39).
The capillary rise situation
Bubble-point measurements are based on the capillary rise phenomenon. When glass capillaries are dipped into water the liquid rises within them. The rise is motivated by hydrogen bonding of water molecules to the capillary's hydrophilic silicate walls. Given capillaries of different radii, the water rises highest in the narrowest capillaries because the ratio of wall area to liquid volume is greatest and the attractive force of the hydrogen bond more directly affects a larger proportion of the water molecules. In the capillaries with wider lumens there is, in effect, a free-standing column of water not in direct contact with the glass walls. Fewer of the water molecules directly experience the intermolecular forces attracting them to the silicate moieties. As a result, the liquid rises to a lesser extent in the wider capillaries and can be expelled by lesser air pressures. The water within the capillaries of the widest diameters is expelled first.
In performing the bubble-point measurement, a water-filled membrane is suitably positioned and retained in a holder so that a progressively increasing air pressure can be directed against its upstream face. It is assumed that membrane pores act like simple, round capillaries in their imbibition of water and in their being emptied under a differential pressure. The water filling the pores prevents frank air passage until the applied air pressure becomes large enough to expel the blocking water from the widest pores. The passage of air then escaping through the vacated passageways is evidenced by the appearance of bubbles in a downstream pool; hence the term "bubble point."
The vacating of the liquid by an imposed air pressure represents a work function, namely, a forced separation, (removal) of the wetting liquid from the polymer surface (40). The bubble-point pressures reflect the various strengths of the bonding interactions between different polymers wet by different liquids. The air pressure needed to separate the water molecules from the pore walls, as occurs upon emptying the pores, quantifies the work function involved. A given polymer type with different liquids, or a given liquid paired with various polymeric type membranes, results in bonds of different strengths and is different as well for each pore size.
Thus, different bubble points (delta pressures) quantify the force expelling the wetting liquid from the pores. Pore-size ratings, were they but assessable, could be applied to all filter types. The rating of whatever pore size, were it to represent the dimensions of a passageway, would not change with the filter type. As stated, however, the bubble-point value, presumably for the same size pore, is different for each polymer–liquid couple—whether for each polymeric membrane with different liquids or for a given liquid with different type filters. Rating filters by bubble-point values peculiar to each solid–liquid couple of each membrane type and to each pore size would be too cumbersome to be practical.
In practice the membrane is measured by bubble point, which is then rather arbitrarily translated into a pore size rating. The translation rests on a conjunction of two items: FDA defined a sterilizing filter as being one that withstands the challenge of 1 × 107 cfu of B. diminuta per square centimeter of EFA. In addition, several experimenters found that an inverse straight-line relationship existed between the log reduction values and the bubble-point levels for the various polymeric-type membrane filters. The higher the bubble point, the smaller the restricted pore diameter and the greater the LRV value (see Figure 8) (41). One could, therefore, read from a graph the bubble-point value of a given filter–liquid couple that would correspond to the LRV of a "sterilizing" membrane.
Integrity test values used in membrane making
In casting the polymer solution in the form of a wet-film preparatory to its conversion to a finished, dry microporous membrane, the manufacturer seeks to predict by periodic testing in the wet casting-state the properties that will eventuate in the dried, finished product. Essentially, what is sought in the wet stage is the foretelling of the proper integrity test value of the finished dry filter. The considerable complexities of the solvent evaporation, washing, and drying stages of the fabrication process are involved in negotiating the change from casting solution to dry membrane. The translation of the characteristics of the wet cast film into those of the dry membrane requires a considerable experience in producing membranes.
The wet testing involved is usually proprietary. Presumably, the test values of any of the integrity tests, including the forward flow, based on diffusive airflows, may be serving this purpose. Experimentally determined bubble points are the guiding measuring units known to the authors to be used. Although the membrane is classified in terms of pore-size ratings, the category is determined on the basis of bubble-point values. The higher the bubble-point value, the smaller the pore-size rating and the more likely the retention of smaller organisms. The grouping by bubble point inexorably gives rise to a spectrum of values for each pore-size rating.
Care is taken that membranes intended for sterilization filtrations are not of too low a bubble-point value; this would signify a too open pore arrangement susceptible to organism passage. On the other hand, tighter filters are seen as a guarantee against violating the threshold value that was experimentally established as being capable of removing 1 × 107 cfu of B. diminuta per square centimeter of EFA. In fact, in a responsible address to dependable quality membrane, manufacturers add a (nonstandard) safety margin to the threshold value of the product that is released to the market.
Bubble point, organism retention
The bubble point had been shown by several experimenters to correlate directly with the log reduction values (LRV) characteristic of a given filter type confronted by a particular type organism (25, 41–43) (see Figure 9). B. diminuta ATCC 19146 was the organism whose different degrees of retention, expressed as LRVs, was shown to correspond to specific bubble-point pressure levels. Establishing the capability of a filter to sustain a challenge level of 1 × 107 cfu of B. diminuta per cm2 of efa, expressed as its bubble point, defines its qualification as a "sterilizing filter." This performance accords with FDA's definition of a sterilizing filter (2). The following equation describes the relationship of the bubble point to the pore's diameter, the dimension most influential on its retention properties:
in which θ represents the angle of wetting, λ is the liquid's surface tension, D signifies the pore diameter, and P is the bubble-point pressure in psi.
The equation is correct in indicating the reciprocal relationship of the bubble-point pressure with the restrictive pore width. The critical sensitivity of the wetting action, however, disallows calculating the dimensional size of the pore by way of the equation. Obtaining retentions of 1 × 107 /cm2 requires more than a particular pore-size rating. It is dependent also on the suspending fluid's compatibility with both organisms and filter in terms of size alterations of the microbes and pores; on the filtration conditions, especially the differential pressure, temperature and viscosity; and on the numbers, shapes, and size distributions of both the pores and the organisms.
The correlation of a bubble-point pressure level with an (LRV) organism retention of 1 × 107 cfu/cm2 EFA was established for the B. diminuta organism cultivated in a prescribed manner (31). This relationship need not necessarily be the same for B. diminuta cultivated to a different size or for other organisms having a different size or size distribution. The more recent recognition that certain organisms, B. diminuta not included, may diminish in size after exposure for a period of time to given drug preparations renders uncertain that a filter found "sterilizing" in one application will necessarily be sterilizing in another (23). No pore-size rating in itself can ensure a sterile effluent. Ralstonia pickettii and Berkholderia cepacia in particular have been studied for their size decrease after undergoing exposure to certain drug preparations.
The point being made is that the filter manufacturer's bubble point was established within a protocol of specified operational steps. Deviations from these may impugn conclusions not so specifically arrived at. The testing is usually outsourced to testing services, intending bias-free results. Correlating the bubble-point values of the various pore-sized filters with the LRVs required for the various filter types using organisms of interest is not a standard protocol. In any case, meeting the manufacturer's bubble point does not exempt the filtration process from the requirement of being validated.
To repeat, the pore-size rating is not assigned on the basis of an actual pore size measurement but according to bubble-point values that have been found to be characteristic of membranes suitable for sterilizing applications. That this identification is warranted is confirmed by a follow-up microbiological assay demonstrating that the membrane does indeed withstand the classic 1 × 107 cfu/cm2 B. diminuta confrontation.
An appropriate bacterial challenge is performed to determine the membrane's suitability for the "sterilizing" grade identification before bestowing the 0.2/0.22-μm pore-size rating. The testing is used by each of the individual filter manufacturers using a program based on an American Society for Testing and Materials procedure (27). However, there is not an industry-wide standard for the specifics of the organism challenge test. For example, the organism content of the bacterial test suspension is calculated to furnish the target 1 × 107 cfu challenge per square centimeter of filter surface, but the total organism load is dispensed in from 2 to 20 L of (usually) saline lactose broth. Interestingly, there is reason to believe that the concentration of the organism suspension may influence the sterility of the effluent (1, 44, 45).
All the 0.2/0.22-μm rated membranes of commerce do meet FDA's definition of "sterilizing" membrane, but all do not retain B. diminuta organisms to the same extent. The relative influences of such parameters as bacterial density, volume of test solution, test duration, applied pressure differential, and so forth, have largely not been investigated. Therefore, the distinctions found among different membranes are of an unknown significance. They may reflect the variations in the nonstandard testing.
Consequently, the filters qualified by their fabricators as being suitable for sterilizing trials are labeled and purveyed either as 0.2 or 0.22-μm rated, depending upon their manufacturer. This "pore size" label is affixed to the membranes that exhibit the bubble point, identifying it as a "sterilizing filter." The label signifies that the membrane type did meet FDA's definition of sterilizing filter in the B. diminuta microbial challenge test performed by the filter manufacturer and that it, therefore, has the potential to perform similarly in other filtrations. Whether it would in fact do so would require validation of the filtration process wherein it was used.
The pore sites of a filter are where the liquid flow manifests itself, where the particle removals take place, and consequently where the throughput volume is defined by the filter blockage. Important though they be, pore sizes are not appraised by direct measurements. They are determined by way of experimentally performed bubble points whose values are transmuted into pore-size ratings. Each filter manufacturer confers its own pore-size designations to its filters. There is no industry standard. In the process, the pore-size ratings, which in any case are not numerical description of the pores' dimensions, are reduced in their significance to parts number in the fabricator's catalogue.
The bubble-point values identify the pores with the largest diameters, those through which suspended particles are most likely to escape capture. In conjunction with information on organism sizes, a coupling of correct pore sizes can be used to attain complete organism removals. It has been established that a correlation exists between bubble-point values and the log-reduction values for the various membrane types. This enables the identification of the filters that can accomplish the removal of 1 × 107 cfu of B. diminuta per square centimeter of EFA, as confirmed by microbiological assays. Such filters are "sterilizing filters" as defined by FDA. This designation qualifies the filter for sterilizing applications. Its actual performance as a sterilizing filter requires validation.
The logic of the above is weakened by the absence of industry standards. The direct assessments of pore sizes are difficult. The converting of bubble-point measurements into pore sizes is encumbered by the complexity of bubble-point values being so highly peculiar to the pairing of the membrane (polymer) type with its particular wetting liquid and for being different again for each pore-size rating of the solid–liquid couple.
It would seem that membrane users would be faced with considerable problems in their choosing the filters best suited for given applications. On the basis of experience, however, the filter user finds that assigned pore-size numbers do offer a level of practical guidance, for example, to particle retentions. Albeit indirectly, bubble points can be interpreted as bearing a relationship to particle sizes. Moreover, although the guidance of formal standards is largely absent, the foci both of filter manufacturers and users are strongly directed to the needs of a federally regulated industry. In this manner, even proprietary actions undergo a peer review. In addition, the development of tools and techniques necessary to pharmaceutical manufacture are shared through numerous technical communications: papers, books, lectures, courses, congresses, and so forth. The need of the industry to meet the requirements set by the regulating agencies promotes shared experiences and cooperative approaches to industry-wide problems. These technical contacts do compensate to an extent for the lack of formal standards. Coupled to a user's experience, the assigned pore-size numbers can offer a level of practical guidance. Nevertheless, it is the bubble points that can be and are measured experimentally. However complicated their values, they can be quantified. It is upon these measurements that, on the basis of experience, the practical applications of filters should be ventured.
Maik W. Jornitz is the group vice-president of global product management, bioprocess of Sartorius North America and is a director of the
PDA, Russel E.
Madsen, Jr., is the president of The Williamsburg Group, LLC, and Theodore H. Meltzer* is a consultant for Capitola Consulting Company, firstname.lastname@example.org
*To whom all correspondence should be addressed.
Submitted: Aug. 11, 2006. Accepted: Oct. 12, 2006.
Keywords: filtration, integrity tests, pore-size ratings
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