Patent Application
20190106725
This invention relates to a biological indicator for monitoring the effectiveness of a sterilization process.
Biological indicators, which typically comprise a carrier and test microorganisms (e.g., bacterial spores) deposited on the carrier, are used to monitor the effectiveness of sterilization processes. The biological indicator is placed in a sterilization chamber and subjected to a sterilization cycle along with the load intended for sterilization (e.g., a medical device). Following the sterilization cycle, the biological indicator is exposed to a growth media and incubated for the purpose of determining if any of the test microorganisms are viable. A successful sterilization cycle is indicated by a complete inactivation (no outgrowth) of the test microorganisms. An unsuccessful sterilization cycle is indicated by an incomplete inactivation (outgrowth detected) of the test microorganisms.
This invention relates to a biological indicator, comprising: a carrier; and a spore deposit on the carrier, wherein from about 70% to about 95% of the area of the spore deposit comprises spores residing in a single spore layer, and the remainder of the area of the spore deposit comprises spores residing in a stacked configuration.
A problem in the art relates to the fact that biological indicators are typically designed to be sterile prior to the end of a sterilization cycle. That is, they are designed in such a manner that for a successful sterilization all of the spores on the biological indicator will be killed prior to the end of the sterilization cycle. In some cases, the biological indicators are designed not to exceed the half cycle (i.e., half way through a typical exposure phase during a sterilization cycle). Many biological indicators become sterile much earlier than at the half cycle due in part to significant spore kill in pre-exposure conditioning phases. For this reason, there are often significant portions of the exposure phase during a sterilization cycle that are not monitored by live spores. This can lead to problems in determining whether a sterilization is successful.
One solution to this problem involves increasing the population bioload of the spores on the carrier. This can be achieved by depositing an inoculum containing a high concentration of the spores on the carrier. This can result in a significant delay until all the spores are killed. A problem with this approach, however, relates to the fact that this often leads to uncontrolled spore stacking. Spore stacking occurs when spores overlie one another such that spores on top protect spores underneath from exposure to a sterilant during a sterilization cycle. Too much spore stacking can lead to false positives where some of the underlying spores survive the full cycle of a sterilization process even though conditions for a successful sterilization are met.
This invention provides a solution to this problem. With this invention it is possible to combine sufficient resistance to extend coverage further into the exposure phase of a sterilization cycle and simultaneously ensure that the spores do not survive the end of a successful sterilization cycle due to excess stacking. This invention involves depositing spores on a carrier in a way in which spore stacking is controlled within predetermined limits to allow the resulting biological indicator to provide coverage throughout a substantial part (e.g., at least about 25%, or at least about 33%, or at least about 50%, or at least about 67%, or at least about 75%, or at least about 90%, or at least about 95%) of the sterilization cycle, but not survive the end of a successful sterilization cycle.
This invention relates to a biological indicator, comprising: a carrier; and a spore deposit on the carrier, wherein from about 70% to about 95%, or from about 80% to about 95%, or from about 90% to about 95%, of the area of the spore deposit comprises spores residing in a single spore layer, and the remainder of the area of the spore deposit comprises spores residing in a stacked configuration. In an embodiment, from about 5% to about 30%, or from about 5% to about 20%, or from about 5 to about 10%, of the area of the spore deposit comprises spores residing in a stacked configuration. The spore deposit may have a total number of spores in the range from about 1×106 to about 1×108 colony forming units (cfu), or from about 1×107 to about 1×108 cfu. The spore deposit may be formed by the deposition of an inoculum (e.g., one or more drops of an inoculum, or from 1 to about 10, or from 2 to about 10, or from 2 to about 8, or from 2 to about 6, or from 2 to about 4, or 2 or 3 drops of an inoculum) on the carrier. The inoculum may comprise water and the spores dispersed in the water. The inoculum may be dried on the carrier to form the spore deposit. In an embodiment, the inoculum deposited on the carrier forms a perimeter upon being deposited on the carrier, and prior to being dried the inoculum is spread to extend the perimeter. The concentration of spores in the inoculum may be in the range from about 1×103 to about 1×106 cfu per microliter, or from about 1×104 to about 1×105 cfu per microliter. The carrier may comprise a hydrophobic substrate. The carrier may comprise metal, glass, ceramics, plastic, or a combination of two or more thereof. The water may comprise tap water, deionized water, distilled water, water purified by osmosis, or a mixture of two or more thereof. The inoculum deposited on the carrier may have a volume in the range from about 10 to about 1000 microliters, or from about 10 to about 500 microliters, or from about 10 to about 50 microliters.
In an embodiment, the biological indicator may be positioned in a first compartment of an indicator device, the first compartment being adapted to permit the spores to be brought into contact with a sterilant during a sterilization process. The indicator device may further comprise a second compartment containing a growth media, the second compartment being adapted to maintain the growth media separate from the spores during the sterilization process, and the second compartment being adapted to permit the growth media to contact the spores after the sterilization process is completed. The indicator device may be referred to as a self-contained biological indicator. The indicator device may be positioned in a test pack.
The spores may comprise bacterial spores. The spores may comprise spores of the Bacillus or Clostridia genera. The spores may comprise spores of Geobacillus stearothermophilus, Bacillus atrophaeus, Bacillus sphaericus, Bacillus anthracis, Bacillus pumilus, Bacillus coagulans, Clostridium sporogenes, Clostridium difficile, Clostridium botulinum, Bacillus subtilis globigii, Bacillus cereus, Bacillus circulans, or a mixture of two or more thereof. In an embodiment, the spores may comprise Geobacillus stearothermophilus spores.
This invention relates to a sterilization process, comprising: exposing an article to be sterilized and the above-indicated biological indicator to a sterilant. The sterilant may comprise vaporous hydrogen peroxide, ethylene oxide, steam, peracetic acid, oxone, or a combination of two or more thereof.
This invention relates to a process for determining the effectiveness of a sterilization process, comprising: exposing an article to be sterilized and the above-indicated biological indicator to a sterilant; and incubating the biological indicator in the presence of a growth media to determine whether the sterilization process is effective.
This invention relates to a process for making a biological indicator, comprising: (A) forming an inoculum comprising water and spores, the concentration of the spores in the inoculum being in the range from about 1×103 to about 1×106 colony forming units per microliter; (B) depositing the inoculum on a carrier, the volume of the inoculum being deposited on the carrier being in the range from about 10 to about 1000 microliters; and (C) drying the inoculum to form a spore deposit on the carrier, wherein from about 70% to about 95%, or from about 80% to about 95%, or from about 90% to about 95%, of the area of the spore deposit comprises spores residing in a single spore layer, with the remainder of the spore deposit comprising spores residing in a stacked configuration.
All ranges and ratio limits disclosed in the specification and claims may be combined in any manner. It is to be understood that unless specifically stated otherwise, references to “a,” “an,” and/or “the” may include one or more than one, and that reference to an item in the singular may also include the item in the plural.
The phrase “and/or” should be understood to mean “either or both” of the elements so conjoined, i.e., elements that are conjunctively present in some cases and disjunctively present in other cases. Other elements may optionally be present other than the elements specifically identified by the “and/or” clause, whether related or unrelated to those elements specifically identified unless clearly indicated to the contrary. Thus, as a non-limiting example, a reference to “A and/or B,” when used in conjunction with open-ended language such as “comprising” can refer, in one embodiment, to A without B (optionally including elements other than B); in another embodiment, to B without A (optionally including elements other than A); in yet another embodiment, to both A and B (optionally including other elements); etc.
The word “or” should be understood to have the same meaning as “and/or” as defined above. For example, when separating items in a list, “or” or “and/or” shall be interpreted as being inclusive, i.e., the inclusion of at least one, but also including more than one, of a number or list of elements, and, optionally, additional unlisted items. Only terms clearly indicated to the contrary, such as “only one of” or “exactly one of,” may refer to the inclusion of exactly one element of a number or list of elements. In general, the term “or” as used herein shall only be interpreted as indicating exclusive alternatives (i.e. “one or the other but not both”) when preceded by terms of exclusivity, such as “either,” “one of,” “only one of,” or “exactly one of.”
The phrase “at least one,” in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements. This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase “at least one” refers, whether related or unrelated to those elements specifically identified. Thus, as a non-limiting example, “at least one of A and B” (or, equivalently, “at least one of A or B,” or, equivalently “at least one of A and/or B”) can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.
The transitional words or phrases, such as “comprising,” “including,” “carrying,” “having,” “containing,” “involving,” “holding,” and the like, are to be understood to be open-ended, i.e., to mean including but not limited to.
The term “bacteria” refers to a domain of prokaryotic microorganisms. The bacteria may be unicellular microorganisms. The cells may be described as prokaryotic because they lack a nucleus. The bacteria cells may have one of four major shapes: bacillus (rod shaped), coccus (spherical shape), spirilla (spiral shape), or vibrio (curved shape). The bacteria may have a peptidoglycan wall. The bacteria may divide by bacteria fission. The bacteria may possess flagella for motility. The bacteria may be classified as either Gram-positive or Gram-negative when using Gram staining. The bacteria may be divided based on their response to gaseous oxygen into the following groups: aerobic (living in the presence of oxygen), anaerobic (living without oxygen), and facultative anaerobic (can live in both environments). The bacteria may be classified as heterotrophs or autotrophs. Autotrophs make their own food by using the energy of sunlight or chemical reactions, in which case they are called chemoautotrophs. Heterotrophs obtain their energy by consuming other organisms. The bacteria that use decaying life forms as a source of energy may be called saprophytes.
The term “spore” refers to a unit of asexual reproduction that may be adapted for dispersal and survival for extended periods of time under unfavorable conditions. Spores are highly resistant, dormant cell types. Endospores (or simply spores) form within the vegetative mother cell in response to adverse changes in the environment, most commonly nutrient depletion. The mother cell undergoes an asymmetrical cell division, where it replicates its genetic material, which is then surrounded by multiple concentric and spore specific layers. The mother cell then disintegrates, releasing the mature dormant spore which requires neither nutrients, water nor air for survival and is protected against a variety of trauma, including extremes of temperature, radiation, and chemical assault.
The term “bacterial spore” refers to a spore produced by bacteria.
The term “biological indicator” refers to an article that can be used to determine the efficacy of a sterilization process. The biological indicator may comprise spores deposited on a carrier. The spores may be referred to as test microorganisms.
The term “carrier” refers to a support onto which spores may be deposited to form a biological indicator.
The term “spore stacking” refers to a spore deposit wherein spores are stacked on top of one another. The spores on top tend to shield spores underneath from exposure to a sterilant during a sterilization process. Spore stacking can be detected using light microscopy and electron microscopy.
The term “single spore layer” refers to a layer of spores wherein no spore stacking occurs. A spore deposit with a single spore layer has a thickness of one spore. A single spore layer may be referred to as a monodispersed spore layer. With this invention spore deposits are used wherein from 70% to about 95%, or from about 80% to about 95%, or from about 90% to about 95% of the area of the spore deposit may comprise spores that reside in a single spore layer, with the remainder of the spore deposit comprising spores residing in a stacked configuration. From about 5% to about 30%, or from about 5% to about 20%, or from about 5% to about 10% of the area of the spore deposit may comprise spores residing in a stacked configuration.
The term “area of the spore deposit” refers to the area of a spore deposit that is measured after an inoculum containing the spores is deposited on the carrier and dried. Drying refers to sufficient drying to allow the spore deposit to be used as a biological indicator in a sterilization process. The spore deposit can be formed using an ink jet printer to deposit the inoculum on the carrier. The area of the spore deposit that is in the form of a single spore layer can be determined during production on an ink jet printer by monitoring the deposition using a fiduciary camera and knowing the concentration of the inoculum dispensed by the printer (in the nano to picoliter range), or by use of a light microscope to get overall view of the deposit, or by an electron microscope which allows resolution of individual spores.
The term “inoculated carrier” refers to a carrier onto which an inoculum containing spores has been deposited.
The term “inoculum” refers to a composition containing water and spores dispersed in the water. The inoculum can be used to inoculate a carrier. The inoculum can be used to form a biological indicator by depositing the inoculum on a carrier, and then drying the inoculum leaving a spore deposit on the carrier.
The carrier may comprise a hydrophobic substrate. The term “hydrophobic substrate” refers to a substrate that repels a drop of water such that the drop of water beads up when deposited on the substrate. In an embodiment, a drop of water deposited on the hydrophobic substrate will bead up with a contact angle greater than 90°. The contact angle may be measured using a contact angle goniometer.
The spores used with the inventive biological indicator may be used as test microorganisms during a sterilization process. Test microorganisms are typically selected from those microorganisms that are more resistant to the sterilization process being evaluated than the organisms to be killed by the sterilization process. Spores, especially bacterial spores, which are difficult to kill, are often used as test microorganisms for sterilization processes. The killing of the test microorganisms during a sterilization process is indicative of a successful sterilization process.
The term “killing” spores refers to rendering spores incapable of reproduction, metabolism and/or growth. The term “dead” spores refers to spores which have been rendered incapable of reproduction, metabolism and/or growth.
The term “live” spores refers to spores that are capable of reproduction, metabolism and/or growth.
The term “log reduction” is a mathematical term to show the number of spores used as test microorganisms that are killed by contacting the spores with a sterilant during a sterilization process. A “4 log reduction” means that the number of live spores at the end of the sterilization process is reduced by 10,000-fold. A “5 log reduction” means that the number of live spores is reduced by 100,000-fold. A “6 log reduction” means that the number of live spores is reduced by 1,000,000-fold. Thus, for example, if a carrier has 1,000,000 live spores on it, a 6-log reduction would reduce the number of live spores to 1.
The term “sterilization” is used to refer to a process wherein there is a total absence of living test microorganisms on the biological indicator remaining after the sterilization process has been completed. However, processes that are less rigorous than sterilization processes including, for example, disinfection, sanitization, decontamination, cleaning processes, and the like, may be of value and are taken into account with this invention. Unless otherwise indicated, the term “sterilization” is used herein to refer to sterilization processes as well as less rigorous processes such as disinfection, sanitation, decontamination, cleaning, and the like.
The term “sterilant” refers to any medium that can be used to sterilize a substrate (e.g., a medical device, the interior of a room, etc.). The sterilant may comprise a liquid or a gas. The sterilant may comprise vaporous hydrogen peroxide, steam, ethylene oxide, peracetic acid, ozone, or a combination of two or more thereof.
The sterilization process provided for herein may employ any of the above-indicated sterilants. The sterilization process may be conducted for an effective period of time to achieve at least a 4 log reduction, or at least a 5 log reduction, or at least a 6 log reduction in the number of spores used as test microorganisms which are capable of reproduction, metabolism and/or growth. When at least a 6 log reduction is achieved, the process may be referred to as a sterilization process. When a 4 log reduction or a 5 log reduction is achieved, the process may be considered to be less rigorous than a sterilization process, but nevertheless useful for various disinfection, sanitization, decontamination and/or cleaning applications.
The inoculum may comprise water and the spores. The water may comprise tap water, deionized water, distilled water, water purified by osmosis, or a mixture of two or more thereof.
The spores may comprise bacterial spores. The spores may comprise spores of the Bacillus or Clostridia genera. The spores may comprise spores of Geobacillus stearothermophilus, Bacillus atrophaeus, Bacillus sphaericus, Bacillus anthracis, Bacillus pumilus, Bacillus coagulans, Clostridium sporogenes, Clostridium difficile, Clostridium botulinum, Bacillus subtilis globigii, Bacillus cereus, Bacillus circulans, or a mixture of two or more thereof. The spores may comprise spores of Geobacillus stearothermophilus. The concentration of spores in the inoculum may range from about 1×103 to about 1×106 colony-forming units (cfu) per microliter (μl), or from about 1×104 to about 1×105 cfu/μl.
The carrier may comprise a hydrophobic substrate. The carrier may comprise a non-porous material. The carrier may comprise a solid material. The carrier may comprise any material that does not dissolve or deteriorate during the sterilization or incubation processes. The carrier may comprise any material that does not combust with a high concentration of an oxidizing sterilant. The carrier may comprise metal, glass, ceramics, plastic, or a combination of two or more thereof. The metal may comprise aluminum or steel. The plastic may comprise a polyolefin, polystyrene, polycarbonate, polymethacrylate, polyacrylamide, polyimide, polyester, and the like. The carrier may comprise a film. The carrier may comprise a surface within a biological indicator, for example, a self-contained biological indicator (SCBI).
The spore deposit may have a central region and a peripheral region. See, for example,
By increasing the volume of the inoculum, while holding the total number of spores deposited the same, it is possible to disproportionately increase the area of the central region with little or no stacking relative to the peripheral region with stacking.
The carrier may be positioned in an indicator device, for example, a self-contained biological indicator (SCBI). The carrier may comprise a surface in a compartment of an indicator device. The carrier may be inoculated with the inoculum. The biological indicator may comprise a SCBI with two separate compartments. One of the compartments may contain the inoculated carrier or an inoculated interior surface. The other compartment may contain a growth media. The growth media may be in a frangible glass vial that can be broken just prior to incubation. In use, the biological indicator and the article to be sterilized are exposed to a sterilant during a sterilization process. Then following sterilization, the biological indicator is activated to allow for the test microorganisms to come into contact with the growth media. The biological indicator may then be incubated to determine whether the sterilization process is effective.
The indicator device may comprise a SCBI, which may be in the form illustrated in
When used in a sterilization process, the cap 110 is held in an open position as illustrated in
After the sterilization process is complete, the SCBI 100 is activated by screwing the cap 110 downward into a closed position as shown in
While in container 120, the spores and the growth media may be incubated for a sufficient period of time to determine the viability of the spores. At the end of the incubation period, the SCBI may be evaluated to determine whether any spores survive the sterilization process. If the spores survive the sterilization process, the sterilization process is not considered to have been successful. On the other hand, if the spores are killed, then the sterilization process is considered to be successful.
The SCBI 100 may be used with a test pack as depicted in
Another modification of the above forms of the biological indicator may be a rapid read or fast acting biological indicator. In this form the biological indicator may be mated to a dedicated instrument (reader) that detects early signals of spore viability.
The biological indicator may be used to release loads or validate sterilization chamber functionality in healthcare settings. The biological indicator may also be used to determine if biological indicator waste has been properly decontaminated. In the scientific setting, the biological indicator may be used to validate the functionality of sterilization chambers, release loads of goods, or validate that a process meets required functionality. A valid biological indicator for a given process requires a specific resistance and therefore biological indicator manufacturers may strive to manufacture the biological indicator with targeted resistance characteristics.
The biological indicator may be used by subjecting it to the same sterilization medium and treatment as the articles for which sterile conditions may be sought. Sterilant (e.g., vaporous hydrogen peroxide, ethylene oxide, steam, peracetic acid, ozone, etc.) may pass into the area where the biological indicator is located thereby exposing the biological indicator to the same sterilization process as the articles being sterilized. Following sterilization, growth media may be brought into contact with the biological indicator. The growth media may be in the form of a liquid. The growth media may comprise a buffered aqueous solution. Any procedure whereby the biological indicator is brought into contact with the growth media under conditions which allow for growth of live test microorganisms (i.e., spores), if any exists, may be used. The growth media may be present in the sterilization chamber in powder or tablet form and, after sterilization, sterile water may be added such that the biological indicator comes into contact with the aqueous incubation medium.
The growth media may comprise one or more nutrient sources. The nutrient source may be used to provide energy for the growth of any of the test organisms that may survive the sterilization process. Examples of the nutrient sources may include pancreatic digest of casein, enzymatic digest of soybean meal, sucrose, dextrose, yeast extract, L-cystine, and mixtures of two or more thereof.
A microbial growth indicator, which changes color or native state, in the presence of viable test organisms may be used with the growth media. The growth indicator may be dispersed or solubilized in the growth media and impart an initial color to the growth media. The growth indicator may also impart a color change in the growth media upon test organism growth. Growth indicators which may be employed include pH-sensitive dye indicators (such as bromothymol blue, bromocresol purple, phenol red, etc. or combinations thereof), oxidation-reduction dye indicators (such as methylene blue, etc.). The use of these microbial growth indicators may result in a change in color in response to a phenomenon of microorganism growth, such as changes in pH, oxidation-reduction potentials, enzymatic activity, as well as other indications of growth.
The growth media may further comprise one or more pH buffers, one or more neutralizers, one or more agents for maintaining osmotic equilibrium, or a mixture of two or more thereof.
The pH buffers may include K2HPO4, KH2PO4, (NH4)2HPO4, 2,2-Bis(hydroxylmethyl)-2,2′,2″-nitrilothiethanol (Bis Tris), 1, 3-Bis[tris(hydroxymethyl)methylamino] propane (Bis-Tris Propane), 4-(2-Hydroxyethyl)piperazine-ethanesulfonic acid (HEPES), 2-Amino-2-(hydroxymethyl)-1,3-propanediol (Trizma, Tris base), N-[Tris(hydroxymethyl)methyl]glycine (Tricine), Diglycine (Gly-Gly), N,N-Bis(2-hydroxyethyl)glycine (Bicine), N-(2-Acetamido)iminodiacetic acid (ADA), N-(2-Acetamido)-2-aminoethanesulfonic acid (aces), 1,4-Piperazinediethanesulfonic acid (PIPES), Beta-Hydroxy-4-morpholinepropanesulfonic acid (MOPSO), N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 3-(N-Morpholino)propanesulfonic acid (MOPS), 2-[(2-Hydroxy-1,1-bis(hydroxylmethyl)ethyl)amino]ethanesulfonic acid (TES), 3-(N,N-Bis[2-hydroxyethyl]amino)-2-hydroxypropanesulfonic acid (DIPSO), 4-(N-Morpholino)butanesulfonic acid (MOBS), 2-Hydroxy-3-[tris(hydroxymethyl)methylamino]-1-propanesulfonic acid (TAPSO), 4-(2-Hydroxyethyl)piperazine-1-(2-hydroxypropanesulfonic acid hydrate (HEPPSO), Piperazine-1,4-bis(2-hydroxypropanesulfonic acid) dihydrate (POPSO), 4-(2-Hydroxyethyl)-1-piperazine propanesulfonic acid (EPPS), N-(2-Hydroxyethyl)piperazine-N′-(4-butanesulfonic acid) (HEPBS), [(2-Hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]-1-propanesulfonic acid (TAPS), 2-Amino-2-methyl-1,3-propanediol (AMPD), N-tris(Hydroxymethyl)methyl-4-aminobutanesulfonic acid (TABS), N-(1,1-Dimethyl-2-hydroxyethyl)-3-amino-2-hydroxypropanesulfonic acid (AMPSO), 2-(Cyclohexylamino)ethanesulfonic acid (CHES), 3-(Cyclohexylamino)-2-hydroxyl-1-propanesulfonic acid (CAPSO), 2-Amino-2-methyl-1-propanol (AMP), 3-(Cyclohexylamino)-1-propanesulfonic acid (CAPS), 4-(Cyclohexylamino)-1-butanesulfonic acid (CABS), 2-(N-Morpholino)ethanesulfonic acid hydrate (MES), N-(2-Acetamido)-2-aminoethanesulfonic acid (ACES), and mixtures of two or more thereof.
The neutralizers may include but are not limited to sodium thioglycollate, sodium thiosulfate, catalase, sodium bisulfate, sodium bisulfite lecithin, polysorbate 20, polysorbate 80, calcium bicarbonate, and mixtures of two or more thereof.
The agents for maintaining osmotic equilibrium may include sodium salt, potassium salts, magnesium salts, manganese salts, calcium salts, metallic salts, sodium chloride, potassium chloride, magnesium sulfate, iron chloride, and mixtures of two or more thereof.
The growth media may comprise an aqueous composition comprising: water; from about 0.01 to about 100 grams per liter (gift or from about 0.1 to about 50 g/l, of one or more nutrient sources; from about 1.0×10-5 to about 10 g/l, or from about 1.0×10-4 to about 1.0 g/l of one or more microbial growth indicators; up to about 5000 g/l, or from about 0.001 to about 5000 g/l, or from about 0.1 to about 1000 g/l, of one or more pH buffers; up to about 100 g/l, or from about 0.01 to about 100 g/l, or from about 0.1 to about 50 g/l, of one or more neutralizers; up to about 50 g/l, or from about 0.1 to about 50 g/l, or from about 0.1 to about 25 g/l, of one or more agents for maintaining osmotic equilibrium.
Spores of Geobacillus stearothermophilus are suspended in water to form an inoculum. The concentration of spores in the inoculum is either (A) 1×105 cfu per microliter or (B) 0.5×105 cfu per microliter. A 20 microliter drop of (A) and a 40 microliter drop of (B) are deposited on a glass slide. The same number of spores (2×106) are deposited with each of (A) and (B). The surface area at the base of the deposited drop increases from 0.141 cm2 for drop (A) to 0.224 cm2 for drop (B), i.e., an increase of 59%. This is shown in Table 1. The circumference of the deposited drops increases from 1.333 cm for drop (A) to 1.679 cm for drop (B), an increase of 26%. This is shown in Table 2. The ratio of circumference to surface area decreases from 9.454 for drop (A) to 7.496 for drop (B), a decrease of 21%. This is shown in Table 3.
These results indicate that by increasing the volume of the inocula from 20 to 40 microliters, the area of the deposit with the monodispersed spores (i.e., spores residing in a single spore layer) increases more than the non-monodispersed peripheral region or circumference where stacking occurs.
The drops (A) and (B) from Example 1 are dried to form spore deposits. The spore deposits are shown in
The spores from Example 1 are suspended in water to form an inoculum. The concentration of spores in the inoculum is 1×105 cfu per microliter. A 20 microliter drop (A) and two 10 microliter drops (C) are deposited on a glass plate. The 20 microliter drop (A) corresponds to drop (A) in Example 1. One of the spore deposits from drop (C) is shown in
By distributing the same inocula across two separate deposits, the resulting combined circumference exceeds the combined increase in the area achieved. This means that it is possible to control the ratio of circumference to surface area to make adjustments in the proportions of spores that are monodisperse (i.e., single spore layer) versus stacked. This can be used to modify the required exposure times for the inventive biological indicator to achieve different partial and all kill times.
While the invention has been explained in relation to various embodiments, it is to be understood that various modifications thereof will become apparent to those skilled in the art upon reading the specification. Therefore, it is to be understood that the invention disclosed herein includes any such modifications that may fall within the scope of the appended claims.
