Patent Application
20220347671
The present techniques generally relate to apparatus for a device for performing liquid dilutions in a systematic manner.
Serial dilutions are typically required in biological and chemical processes. A dilution involves taking a known volume (e.g. 1 ml) of a stock solution and adding it to a known volume of a diluent (e.g. 9 ml, to produce a ten-fold dilution). The diluent may be any suitable liquid, such as distilled water or a buffer. The process can be repeated for successive dilutions (serial dilutions) by using a diluted solution from one dilution as the stock for the next dilution. At each stage, 1 ml of the previous dilution may be added to 9 ml of diluent, such that each stage results in a further ten-fold change (reduction) in concentration. This process can be laborious if a large change in concentration is required for subsequent processing/use.
Typically, samples which need to be kept under aseptic or sterile conditions need to be diluted in a laboratory setting. This requires access to aseptic/sterile conditions, the knowledge and skills to perform the dilutions, a sterile diluent, and laboratory equipment to facilitate the process.
Background information can be found in the following patent literature: WO2018/186823 which discloses a biological fluid dilution device having a moveable piston tube with a metering groove that can measure a precise volume of biological fluid; CN106053162 which discloses a solution preparing and measuring device having a liquid distribution barrel for preparing liquid and a liquid collection tube to measure the liquid; and US2019/025163 which discloses a specimen processing device that includes one or more vessels that are each coupled to a metering reservoir by a plurality of syphons configured to deliver a metered and equivalent volume of liquid to each vessel. However, these documents disclose devices that are complex from a mechanical point of view (e.g. have complex components to facilitate the flow of liquid), and complex from a manufacturing point of view (which increases the cost of the device and makes it less desirable). In many biology and chemistry laboratories, cheap, single-use devices and components are desirable, as these reduce the need to carefully clean, decontaminate and sterilise the devices and components for re-use. In contrast, these documents disclose devices that are complex and so are likely to be expensive and not suitable for single-use, and may not be easily used outside a laboratory setting (e.g. in the field/during field work).
The present applicant has identified the need for a device that enables easier dilutions without requiring a laboratory setting.
According to the present techniques, there is provided a hand-held liquid handling device for diluting a liquid sample, comprising: at least two chambers connected together and arranged to contain liquid; and at least one liquid transfer mechanism arranged to transfer a controlled volume of liquid from one chamber to an adjacent chamber. In some cases, a liquid transfer mechanism may be provided in a housing between adjacent chambers. In other cases, a liquid transfer mechanism may be provided in a housing of each chamber.
Preferred features are set out in the appended dependent claims.
Implementations of the present techniques will now be described, by way of example only, with reference to the accompanying drawings, in which:
Broadly speaking, embodiments of the present techniques provide a liquid handling device that enables a user to more easily and efficiently perform sample dilutions, without requiring the user to perform any calculations or be in a controlled environment (e.g. a laboratory or sterile/aseptic environment). Advantageously, this may enable a user to perform sample dilutions and subsequent sample processing outside of a laboratory, such as during field work, or in environments, regions or countries where access to sterile/aseptic environments may be difficult or non-existent. The device may be used to dilute any liquid sample, such as biological samples, chemical samples, or environmental samples (e.g. liquid samples taken from a river or lake, or soil samples that are mixed with liquid). Advantageously, the liquid handling device is mechanically-operated by a user, such that the device may be used even when no power source is available. Furthermore, the liquid handling device is a hand-held device, which means the device is compact and easy to transport and use for field work.
In the example shown in
Thus, the at least two chambers 104 of the device may comprise: a first chamber for holding a stock solution; and a second chamber for holding a diluent; wherein the liquid transfer mechanism is provided between the first chamber and the second chamber, and arranged to transfer a controlled volume of stock solution from the first chamber into the second chamber. Alternatively, the at least two chambers 104 of the device may comprise: a first chamber for holding a first diluent; and a second chamber for holding a second diluent. The first and second diluents may be the same or different.
The device 100 may be provided as a pre-formed device, such that the at least two chambers 104 are already connected together. In this case, the at least two chambers may be fixedly connected together, and a user may not be able to separate individual chambers 104 from the device without damaging the device 100. For example, the at least two chambers may be connected together by any or more of: heat sealing, an adhesive, and a UV-cured adhesive. It will be understood that this is a non-exhaustive list of example mechanisms for fixedly connecting together the chambers.
Alternatively, the device 100 may be provided as a kit comprising two or more chambers and one or more liquid transfer mechanisms, which a user may be able to assemble as they require. In this case, each chamber 104 may comprise at least one fastening mechanism for releasable connection of the chamber to at least one other chamber. The fastening mechanism may be or comprise a screw thread or clipping mechanism. This may enable a user to connect together as many chambers as they require, according to the number of serial dilutions they need to perform.
The device 100 may comprise at least one sample aperture 103 for adding liquid to the device or removing liquid from the device. The device 100 may comprise a single sample aperture 103 on the chamber corresponding to the final dilution in the series (which in the example of
To prevent contamination or liquid leakage, and ensure aseptic technique and the sterility of the samples within the chambers is maintained, the or each sample aperture 103 may comprise a seal (not shown) for covering the sample aperture. The seal may be a removable seal, such as a removable film. The seal may be resealable to allow repeated access to the sample aperture 103. The seal may be a pierceable seal. The sampling aperture 103 may be sealed using a film such as any one of the following: Polyvinyl chloride film, polyethylene wrap, cellophane, tape, acetate, or a thermoplastic flexible plastic film. Alternatively, the sampling aperture 103 may be sealed with a push-fit seal such as a bung, plug, stopper or cork, any of which may be formed from a suitable material such as hardened rubber, silicone, polypropylene or natural cork. It will be understood that these are non-limiting and non-exhaustive examples of seals for the sampling aperture 103. The seal may be broken by the end-user to allow a sample to be removed. When the seal is broken, the end-user should use aseptic technique or conduct the experiment in a biological safety cabinet if sterility is still required.
Each chamber 104 of the at least two chambers may comprise at least one mating surface 208 which contacts a mating surface of an adjacent chamber. For example, mating surface 208 of chamber 104a contacts the mating surface of chamber 104b when the two chambers are connected together. The mating surface 108 of each chamber 104 may comprise a channel 206, and when two chambers are connected together the channel 206 of each mating surface forms a housing for the liquid transfer mechanism 106 that is located between adjacent chambers 104. The liquid transfer mechanism 106 may be insertable into the housing formed between adjacent chambers. Thus, in some cases, the or each liquid transfer mechanism 106 may be provided in the device 100 after the chambers 104 have been connected together.
The mating surface 208 of each chamber 104 comprises an aperture (not visible in
The or each liquid transfer mechanism 106 of the device 100 may comprise: a rotatable container 202 provided between the at least two chambers 104; and a handle 210 extending outside of the device for rotating the rotatable container 202. The rotatable container 202 is provided within the housing formed between two chambers 104 when the mating surfaces of the two chambers come into contact. The rotatable container 202 is depicted as being substantially cylindrical, but it will be understood that the container 202 may have any suitable shape or form. The or each rotatable container comprises an aperture 204.
The rotatable mechanism 202 may be rotatable by a user of device 100 by operating the handle 210. The handle 210 may take any suitable form. rotatable mechanism 202 may be rotated between at least: a first position in which the aperture 204 of the rotatable container 202 aligns with the aperture in the channel 206 of a first chamber 104a (or 104b) of the two chambers; and a second position in which the aperture 204 of the rotatable container 202 aligns with the aperture in the channel 206 of a second chamber 104b (or 104c) of the two chambers. In the first position, liquid from the first chamber 104a (or 104b) fills the rotatable container 202, and in the second position, liquid from the rotatable container 202 is transferred to the second chamber 104b (or 104c). The rotatable mechanism 202 may also be rotated to a third position in which the aperture 204 of the rotatable container 202 is closed, i.e. is not aligned with any apertures whereby liquid flow is prevented. Preferably, the rotatable container is only able to rotate in one direction or by a predefined amount, so that liquid may only be transferred in one direction to perform the dilution. (In other words, it may not be possible for liquid to be transferred from chamber 104c to chamber 104b, or from chamber 104b to chamber 104a, as this would interfere with the dilution process). This controlled amount rotation may be achieved by the locking mechanism as described in more detail in relation to
It will be appreciated that the rotatable liquid transfer mechanism 106 is just one suitable form to ensure the correct transfer of liquid from one chamber to another chamber. The skilled person would understand that the liquid transfer mechanism 106 may take any suitable form, for example, a sliding mechanism or a button operated mechanism.
In embodiments where the first chamber 104a in the dilution device 100 to which the original stock sample/solution is added comprises a lid 102, then the chamber 104a may comprise a screw thread 200 to allow mating with complimentary threads in the lid 102. As explained above, the lid 102, if present, may take any form and this is merely one example.
The rotatable container 202 is hollow. The rotatable container 202 may be designed to have a specific volume so that a required, controlled volume of liquid is transferred from one chamber to the adjacent chamber in the device 100. For example, the rotatable container 202 may be able to hold exactly 1 ml of liquid. The skilled person would understand that the predetermined volume of liquid, and the volume of diluent in each chamber 104, depends on the required dilution factor.
The sealing unit 208 and the tap 106 may be formed from a suitable polymer, for example polycarbonate. The skilled person would understand that other polymers would be suitable, for example, polypropylene, polyethene, polybutylene terephthalate, polyester, polycarbonate or polysulfone.
When carrying out a serial dilution, it is important that the user is aware of exactly how much liquid is being transferred each time a dilution is carried out. Thus, if any sample was to leak out of the rotatable container 202 during rotation, the serial dilutions would not be accurate and may lead to experimental failures. To prevent leaking, an O-ring or similar seal may be provided around apertures 302, 204. The mating surfaces 208 and the liquid transfer mechanism 106 may be shaped such that the liquid transfer mechanism 106 sits tightly in the housing formed between the mating surfaces 208 which may reduce the likelihood of leaking and which may produce a leak-proof push-fit seal when appropriate materials are used. Alternatively, another suitable push-fit seal may be used.
In
In contrast to the example of
The at least one liquid transfer mechanism 106 of the device may comprise a first liquid transfer mechanism 106a and a second liquid transfer mechanism 106b. The at least two chambers 104 of the device may comprise: a first chamber 104a for holding a stock solution and a housing 107 for the first liquid transfer mechanism 106a; and a second chamber 104b for holding a diluent and a housing 107 for the second liquid transfer mechanism 106b; and wherein the first liquid transfer mechanism 106a is arranged to transfer a controlled volume of stock solution from the first chamber 104a into the second chamber 104b. Alternatively, the at least two chambers 104 of the device may comprise: a first chamber 104a for holding a first diluent; and a second chamber 104b for holding a second diluent. The first and second diluents may be the same or different.
The device 100′ may be provided as a pre-formed device, such that the at least two chambers 104 are already connected together. In this case, the at least two chambers may be fixedly connected together, and a user may not be able to separate individual chambers 104 from the device without damaging the device 100′. For example, the at least two chambers may be connected together by any or more of: heat sealing, an adhesive, and a UV-cured adhesive. It will be understood that this is a non-exhaustive list of example mechanisms for fixedly connecting together the chambers.
Alternatively, the device 100′ may be provided as a kit comprising two or more chambers and one or more liquid transfer mechanisms, which a user may be able to assemble as they require. In this case, each chamber 104 may comprise at least one fastening mechanism for releasable connection of the chamber to at least one other chamber. The fastening mechanism may be or comprise a screw thread (see e.g.
In an example, the kit provided to end users may comprise a plurality of chambers 104 and liquid transfer mechanisms 106. The liquid transfer mechanisms 106 may be provided as already assembled into the chambers 104, or may be provided separately for insertion by the end user—the former may be required if some or all of the chambers 104 in the kit are pre-filled with a diluent (such chambers may be referred to as a “regular” chamber). The kit may also comprise one or more lids 102. The kit may comprise a plurality of chambers 104 which are already coupled to a liquid transfer mechanism 106 and to a lid 102. If end users wish to add their own diluent to a chamber 104, some or all of the chambers 104 in the kit may not be pre-filled (such chambers may be referred to as a “starter” chamber). The lid 102 may be removed by the end user to enable them to add diluent to the chamber 104. A seal may be provided at one or both ends of the chamber 104, such that a seal covers one or both mating portions of the chamber 104 (i.e. the end that is mated to a lid or the end to be mated to another chamber 104). If some or all of the chambers 102 are pre-filled with diluent, the seal on the end of the chamber 104 that is mated to a lid 10 helps to keep the diluent liquid within the chamber 104 sterile even when the lid is removed.
For example, if an end user wishes to perform three serial dilutions, they would take one “starter” chamber and two “regular” chambers from the kit. They would remove the lids from the “regular” chambers and join the two regular chambers together by, for example, screwing/threading them together in such a way that the chambers are joined together, but the seals between the chambers have not yet been broken (which, as explained herein, may be achieved by further twisting/turning one chamber relative to another). The “starter” chamber is coupled to the first “regular” chamber, and again the seal between the “starter” chamber and the first “regular” chamber may not be broken at this stage. The lid of the “starter” chamber may not be removed until liquid is to be added to the “starter” chamber. This is because a seal may not be provided on the “starter” chamber below the lid, and therefore the lid needs to be retained on the chamber until the sample is added to prevent contamination.
Alternatively, all chambers—“starter” and “regular” chambers—may comprise a seal on both ends of the chamber regardless of whether they are pre-filled with liquid. This ensures that even if the lid is removed from a chamber, the contents of the chamber remain sterile and unexposed to the external environment due to the presence of the seal. In this case, a seal of the chamber may be broken either by mating the chamber to another chamber (as described herein), or by a scoring or cutting mechanism provided within each lid. The scoring or cutting mechanism within each lid may operate in the same way as the cutting mechanism of each chamber, i.e. screwing on a lid to a chamber secures the lid to the chamber, but turning the lid further to tighten the lid engages the cutting mechanism of the lid with the seal on the chamber.
Each chamber 104 of device 100′ may comprise at least one sample aperture 103 for adding liquid to the device or removing liquid from the device, as described above with respect to
Each chamber 104 may be couplable to a lid 102 and to another chamber 104. For example, the chamber in which the original stock solution is provided may comprise a lid 102 to enable the stock solution to be added to the device 100′. The lid 102 may be any one of: a screw cap, a flip-cap or a plug, a foil layer, aluminium foil, Polyvinyl chloride film, polyethylene wrap or a thermoplastic flexible plastic film.
To prevent contamination or liquid leakage, and ensure aseptic technique and the sterility of the samples within the chambers is maintained, the or each sample aperture 103 may comprise a seal (not shown) for covering the sample aperture. The seal may be a removable seal, such as a removable film. The seal may be resealable to allow repeated access to the sample aperture 103. The seal may be a pierceable seal. The sampling aperture 103 may be sealed using a film such as any one of the following: Polyvinyl chloride film, polyethylene wrap, cellophane, tape, acetate, or a thermoplastic flexible plastic film. Alternatively, the sampling aperture 103 may be sealed with a push-fit seal such as a bung, plug, stopper or cork, any of which may be formed from a suitable material such as hardened rubber, silicone, polypropylene or natural cork. It will be understood that these are non-limiting and non-exhaustive examples of seals for the sampling aperture 103. The seal may be broken by the end-user to allow a sample to be removed. When the seal is broken, the end-user should use aseptic technique or conduct the experiment in a biological safety cabinet if sterility is still required.
Each chamber 104 may comprise at least one mating portion 500. The mating portion 500 may be mated with/connected to a lid 102 or to the mating portion 500 of another chamber 104. The mating portion 500 may comprise a fastening mechanism for releasable connection to at least one other chamber (or to a lid). The at least one fastening mechanism of one chamber may be one of a thread or a groove, and is connectable to the other of a thread or a groove of another chamber. The fastening mechanism may comprise a screw mechanism to connect together two chambers (or a chamber to a lid), as visible in
The at least one mating portion 500 of each chamber 104 may comprise at least one seal (not shown) to keep the chamber 104 sterile/aseptic before use, and which must be removed in order for liquid to be transferred from one chamber to another. The seal may also prevent liquid in one chamber from flowing or moving into an adjacent chamber until the liquid transfer mechanism is activated/used. The seal may therefore comprise or be made of a non-permeable membrane layer. Each mating portion 500 of each chamber 104 may comprise a seal. Alternatively, each chamber 104 may comprise an open end and a sealed end. The open end of a chamber 104 may mate with the sealed end of another chamber 104. The sealed end/seal may be formed of a film layer which may be, for example, a layer of aluminium foil, Polyvinyl chloride film, polyethylene wrap or a thermoplastic flexible plastic film.
The mating portion 500 of each chamber 104 may comprise a cutting mechanism 502 for breaking the seal of an adjacent chamber when two chambers are connected together. That is, in order for a controlled volume of liquid from one chamber 104 to be transferred into an adjacent chamber 104, at least one seal may need to be broken. Breaking the seal may include semi-scoring or otherwise partially cutting through each seal so that liquid transfer between the chambers may occur but so that the seal is not detached entirely from its respective chamber. In this way, the seal remains at least partially attached to the chamber and is not free or loose therein. The cutting mechanism may comprise any one or more of: a sharp edge, a sharp tooth, multiple sharp teeth, a serrated edge, a piercing element, a piercing and cutting element, a slicing element, and a scoring element. The cutting mechanism may be part of the fastening mechanism.
The cutting mechanism may be activated by rotating one chamber relative to an adjacent chamber. For example, if two chambers 104 are connected by screwing the chambers together, twisting/turning one chamber relative to the other by some amount may screw the two chambers together, and twisting/turning one chamber by a further amount may activate the cutting mechanism. For example, twisting one chamber by a quarter or a half rotation may connect the two chambers together, and twisting one chamber by a further quarter or half rotation may cause the cutting mechanism of one or both chambers to engage with the seal therebetween. In this way, once two chambers are connected together, liquid can be moved from one chamber (via activation of the liquid transfer mechanism 106) into another without exposing the liquid to external contaminants.
Each liquid transfer mechanism 106 of the device 100′ may comprise a rotatable container 202 in the housing of a chamber 104, and a handle 210, coupled to one end of the rotatable container 202, which extends outside of the device for rotating the rotatable container 202. The rotatable container 202 is depicted as being substantially cylindrical, but it will be understood that the container 202 may have any suitable shape or form. The or each rotatable container comprises an aperture 204 (see
The rotatable container 202 may be rotatable by a user of device 100′ by operating the handle 210. The handle 210 may take any suitable form. The rotatable container may be rotated between at least: a first position in which the aperture 204 of the rotatable container 202 aligns with a first aperture 301a in a first chamber 104a of the two chambers; and a second position in which the aperture 204 of the rotatable container 202 aligns with a second aperture 301b in the first chamber 104a of the two chambers; wherein in the first position, liquid from the first chamber 104a fills the rotatable container 202, and in the second position, liquid from the rotatable container 202 is transferred to the second chamber 104b. Each chamber 104 of device 100′ may be considered to have a liquid containing portion 504 and a mating portion 500. The first aperture 301a of the chamber 104 may be within the liquid containing portion 504, and the second aperture 301b of the chamber 104 may be within one of the mating portions 500. The liquid transfer mechanism 106 may be provided in a housing 107 located between the liquid containing portion 504 and a mating portion 500 of each chamber 104. Thus, the rotatable container 202 transfers liquid from the liquid containing portion 504 to a mating portion 500. The mating portion 500 is connected to a liquid containing portion 504 of another chamber, and thus, liquid is transferred to this adjacent chamber.
The rotatable container 202 may also be rotated to a third position in which the aperture 204 of the rotatable container 202 is closed, i.e. is not aligned with any apertures whereby liquid flow is prevented. Preferably, the rotatable container is only able to rotate in one direction or by a predefined amount, so that liquid may only be transferred in one direction to perform the dilution. (In other words, it may not be possible for liquid to be transferred from chamber 104b to chamber 104a, as this would interfere with the dilution process). This controlled amount rotation may be achieved by the locking mechanism as shown in
The rotatable container 202 is hollow. The rotatable container 202 may be designed to have a specific volume so that a required, controlled volume of liquid is transferred from one chamber to the adjacent chamber in the device 100′. For example, the rotatable container 202 may be able to hold exactly 1 ml of liquid. The skilled person would understand that the predetermined volume of liquid, and the volume of diluent in each chamber 104, depends on the required dilution factor.
The locking mechanism may prevent movement of the liquid transfer mechanism 106 after the controlled volume of liquid has been transferred from one chamber to the adjacent chamber. The locking mechanism may comprise: an endstop 404 on the housing 107 of the chamber 104; and a protrusion 402 on the liquid transfer mechanism 106, wherein interaction of the protrusion 402 with the endstop 404 prevents movement of the liquid transfer mechanism 106 after the liquid transfer has occurred. This may prevent the rotatable container 202 from rotating further and, for example, transferring more liquid and impacting the dilution process. The skilled person would understand that any suitable locking mechanism may be used to prevent the liquid transfer mechanism 106 from moving once the liquid transfer has taken place. For example, the locking mechanism may comprise an overhang or arm that may engage with the protrusion 402 to prevent clockwise or anti-clockwise rotation.
As noted above, the liquid transfer mechanism 106 may comprise a handle 210 coupled to one end of the rotatable container 202. The liquid transfer mechanism 106 may further comprise a plurality of resiliently deformable fingers 207 disposed around another end (i.e. the opposite end to where the handle 210 is provided) of the rotatable container, wherein the fingers 207 hold the rotatable container 202 within the housing 107. The fingers 207 may be pushed towards each other when the liquid transfer mechanism 106 is inserted into housing 107, and the fingers 207 may expand or revert to their original expanded/open state once in the housing 107, thereby exerting a force on the housing 107 that retains the liquid transfer mechanism 106 in place. Other mechanisms may be provided in addition or alternatively to retain the liquid transfer mechanism 106 within the housing 107 of chamber 104. For example, each finger 207 may have a groove that engages with a lip or protrusion on an inner surface of housing 107, such that the engagement locks the liquid transfer mechanism 106 in place.
As mentioned above, the lid 102 of the device 100, 100′ may comprise a cutting mechanism (not shown) for breaking the seal of the chamber to which the lid 102 is attached. Breaking the seal may be required if liquid is to be added to a chamber (e.g. to add a stock solution to the first chamber in the series). Breaking the seal may include semi-scoring or otherwise partially cutting through the seal. The cutting mechanism of the lid 102 may comprise any one or more of: a sharp edge, a sharp tooth, multiple sharp teeth, a serrated edge, a piercing element, a piercing and cutting element, a slicing element, and a scoring element. The cutting mechanism may be part of the fastening mechanism of the lid.
The cutting mechanism may be activated by rotating the lid relative to the chamber. For example, if a lid 102 is attached to a chamber 104 by screwing the lid onto the chamber, twisting/turning the lid relative to the chamber by some amount may screw the two together, and twisting/turning the lid by a further amount may activate the cutting mechanism. For example, twisting the lid by a quarter or a half rotation may connect the lid to the chamber, and twisting the lid by a further quarter or half rotation may cause the cutting mechanism of the lid to engage with the seal of the chamber.
The at least two chambers 104 of the devices 100 and 100′ may be pre-filled with a diluent. The diluent may be a sterile diluent. The diluent may be, for example, sterile distilled water, or a Tris-HCl, sodium acetate, peptone buffer/phosphate buffer. The sterile diluent may be a liquid growth media, for example, a lysogeny broth (LB), Dulbecco's Modified Eagle Medium, minimal essential media, Dey-Engley Neutralizing Broth, or a phage buffer.
The device 100, 100′ may be arranged to perform one or more dilutions according to a predetermined dilution factor, such as, for example, 10−1, 10−2, 10−3, 10−4, 10−4, 10−5, 10−6, 10−7, 10−8, 10−9, 5−1, 2−1, and 3−1. The predetermined volume of (sterile) diluent required for the dilution may be, for example, 1 ml, 5 ml, 10 ml, 15 ml, 20 ml, 25 ml, 30 ml, 40 ml, 50 ml, 100 ml.
The device 100, 100′ may be able to dilute any type of liquid sample, such as, for example a biological sample, a chemical sample, and an environmental sample. Serial dilutions are often required in biology to accurately create highly diluted solutions as well as solutions for experiments. They may also be used to reduce the concentration of organisms or cells contained within a sample. In such cases, aseptic technique is required to prevent contamination of a sample. The liquid handling device 100, 100′ may be used for the serial dilution of an input sample, under aseptic conditions.
The liquid handling device 100, 100′ may be used for diluting biological samples, such as bacteria or mammalian cell cultures, where aseptic technique is crucial to experimental success. Therefore, the components of the liquid handling device 100, 100′ may be formed from a non-reactive material. The device 100, 100′ may be formed from a polymer or plastic. For example, the device 100, 100′ may be formed of polypropylene, which has resistance to temperatures up to 135° C. and may be auto-claved, meaning the inner cavity of the liquid handling device 100, 100′ should remain sterile. The components of the liquid handling device 100, 100′ may be formed from any one of: polypropylene, polyethene, polybutylene terephthalate, polyester, polycarbonate and polysulfone.
The device 100, 100′ may be a single-use device. Alternatively, it may be possible to sterilise the device 100, 100′ for reuse.
Each component of the liquid handling device 100, 100′ may be manufactured via injection moulding.
As previously described, serial dilutions are important in microbiology and cell culturing. They may be required to reduce the concentration of organisms or cells contained within a sample. In this situation it may be important to reduce the chance of contaminating the cultured sample when transferring an aliquot to the liquid handling device 100, 100′. Thus, the end-user may use the liquid handling device 100, 100′ as a receptacle for culturing a sample. Alternatively, the chamber in which the original stock solution is added (e.g. chamber 104a in
The predetermined volume of sterile diluent may be added during manufacture of the liquid handling device 100, 100′.
The predetermined volume of sterile diluent may be added following assembly of the liquid handling device 100, 100′, via the sampling port 103. The sampling port 103 may then be sealed and the liquid handling device 100, 100′ may be sterilised before being shipped to an end-user. The skilled person would understand that any suitable method for sterilisation could be used, for example, electron beam or gamma irradiation, steam autoclaving at a suitable temperature or Ethylene Oxide gas.
Those skilled in the art will appreciate that while the foregoing has described what is considered to be the best mode and where appropriate other modes of performing present techniques, the present techniques should not be limited to the specific configurations and methods disclosed in this description of the preferred embodiment. Those skilled in the art will recognise that present techniques have a broad range of applications, and that the embodiments may take a wide range of modifications without departing from any inventive concept as defined in the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1907538.1 | May 2019 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2020/065080 | 5/29/2020 | WO |
