Patent Application
20210393172
The use of a string that is swallowed by a patient has been used for many years to diagnose conditions such as giardia, cancer, pH related conditions such as acid reflux, etc. Typically, such a string comprises a gelatine capsule at one end thereof. The string is typically administered by a clinician or nurse. The problem with this type of string is that the gelatine capsule may stick to the oesophageal lining of the patient which may pose problems for patients, particularly if the patient has oesophageal pathology causing narrowing.
Once the string has been removed from the patient, there is a need for the string to be handled safely, without contamination. This can be difficult, since the string may be relatively long in length.
Eosinophilic esophagitis (EoE) is a disease of the immune system which is known to be increasing in incidence worldwide. The condition causes discomfort when swallowing (dysphagia) and can result in food getting stuck on swallowing (food impaction). The condition is due to the build up of white blood cells (eosinophils) in the oesophagus due to a reaction to foods and/or acid reflux which can inflame or injure oesophageal tissue. Food is a recognised cause for the inflammation, although the mechanism is not clear and available tests such as food allergy testing are often not helpful in deciding which food is the trigger. Typically, the condition has been diagnosed using an endoscope followed by a biopsy. Patient symptoms (e.g. degree and frequency of dysphagia) are not a good indicator of disease activity and the lining of the oesophagus can look normal endoscopically and diagnosis is only made following a biopsy. This poses problems with managing these patients, in particular when monitoring response to treatment. The use of a string with a gelatine capsule at the end to aid swallowing has been problematic with some patients due to oesophageal narrowing and difficulties swallowing the capsule. Eosinophils release various chemicals into the lining of the oesophagus which can adhere to the string. Some, by virtue of their chemical properties, adhere strongly and cannot be removed from the string to enable laboratory analysis. In addition, removing the swallowed string from a patient and placing into a container appropriate for laboratory analysis can pose a risk to the individual (likely to be a doctor or nurse) as it is long and cumbersome and covered with a biological fluid which may lead to a possible infection risk.
Due to some of these markers of eosinophilic inflammation (particularly ECP, eosinophilic cationic protein) being very adherent to the string, in order for these to be measured accurately, the ECP has to be released from the string by chemical processing. This is time consuming and involves manipulation of the string by a laboratory technician.
The present invention seeks to address the above problems.
According to a first aspect, there is provided apparatus comprising a string for insertion into the oesophagus of a patient, the string comprising a proximal end and a distal end, wherein the string forms a structure at the distal end thereof to assist in the insertion of the string into the patient.
Advantageously, the present invention provides apparatus comprising a string that may be easily swallowed by a patient. In addition, the present invention advantageously provides a string collection device that may be used to collect the string once swallowed and to place the string easily into a laboratory container, and apparatus that may be used in a method (e.g. using a centrifuge activated device) for washing (e.g. eluting) components stuck to the string for laboratory analysis. Advantageously, the apparatus of the present invention optimises function during insertion of the string into the oesophagus of a patient, and improves safety and practicality of the nurse or doctor handling the string. Typically, the addition of eluting and neutralising buffer to the string can be time consuming and requires laboratory staff and training. Advantageously, the use of a centrifuge activated device in accordance with the present invention to release the buffer while in the centrifuge eliminates the need for manually performing this step. Advantageously, the use of centrifugation also minimises staff exposure to biological substances such as oesophageal fluid. Preferably, the centrifuge activated device may be provided as one unit. In one embodiment, the centrifuge activated device may be provided as a sealed unit, to ensure that it is kept sterile.
Preferably, the structure provided at the distal end of the string comprises a helical component. In another embodiment, the string may form a compressed pellet of string at the distal end. In another embodiment, the string may be knotted at the distal end. Advantageously, the provision of a string having a structure at the distal end that is formed from the string itself avoids the problems associated with including a non-string component at the distal end (such as gelatine) which may become stuck or cause oesophageal irritation.
Advantageously, the provision of a string having a helical component at the distal end thereof provides a structure that is flexible and soft to assist in swallowing the string. Preferably, the size of the structure at the distal end of the string is optimised such that it is small enough that it does not cause irritation to the oesophagus, whilst still being capable of being swallowed by a patient. Preferably, the string is coiled such that it acts like a spring. Preferably, the size of the structure at the distal end of the string is equivalent to a size 5 capsule (typically 11.1 mm long and 4.9 mm wide) but can be of larger or smaller size if needed.
Preferably, the helical component at the distal end of the string is formed by soaking the distal end of the string in a solution that will confer rigidity on the string once dry, wrapping the distal end of the string around the outer surface of a rod and allowing the string to dry. In one embodiment, the string is wrapped around the outer surface of a metal rod. In one embodiment, the string may be soaked in a solution comprising a sugar. In another embodiment, the string may be soaked in a solution of corn starch, such as 1% corn starch solution. In another embodiment, the string may be steam heated to confer ability to retain a new shape. In one embodiment, the string may be dipped in water (preferably sterile water) and then wound around a metal rod and heated to a temperature of approximately 100° C. for approximately 10 minutes. In one embodiment, the rod may be an aluminium rod. Preferably, once the string has set, the distal end of the string is removed from the outer surface of the rod. Advantageously, the helical component at the distal end of the string provides a structure that is flexible and soft to assist in moving the string down the oesophagus during swallowing and preventing the string from getting stuck in areas of narrowing of the oesophagus if present. Advantageously, the string is of sufficient volume and is flexible enough to assist the patient in swallowing the string. Advantageously, the helical structure at the distal end of the string assists the patient in swallowing the string. Advantageously, when exposed to moisture, for example, in the stomach of a patient, the structure at the distal end of the string unwinds such that the distal end of the string adopts a substantially straight conformation, thus assisting in removal of the string from the patient.
In one embodiment, the structure at the distal end of the string may be coated with a flavouring. In one embodiment, the structure at the distal end of the string may be coated with at least one drop, preferably two to three drops, of flavouring essence, for example, a concentrated flavouring essence. Advantageously, coating the structure at the distal end of the string with a flavouring can encourage swallowing of the string by patients. This is particularly beneficial in children.
Preferably, the string further comprises a structure at the proximal end thereof. Preferably, the structure provided at the proximal end comprises a compressed or knotted portion of the string. Preferably, the structure provided at the proximal end of the string assists in attachment of the string to a cheek of the patient. Advantageously, the provision of a string having a structure at the proximal end thereof assists in attachment of the proximal end of the string to a patient such that the string is not inadvertently detached or swallowed by the patient during insertion of the string, thus improving safety and ease of use.
Preferably, the proximal end of the string is attached to a patient using an attachment means. Preferably, the attachment means comprises tape. Preferably, the tape comprises skin-adhesion grade tape to improve comfort for the patient. Advantageously, the use of tape to secure the string to the patient improves security and reduces the risk of unwanted detachment of the string from the patient. Advantageously, the use of skin-grade adhesion tape prevents or reduces the possibility of the string detaching from the tape, and thus from the patient. Advantageously, the use of skin-grade adhesion tape improves security and comfort for the patient. In one embodiment, the string attachment means may comprise an adhesive removable label to which details regarding the sample type, date sample taken, patient identifiers (such as name, age, date of birth, unique patient identifier such as NHS or hospital number) can be added. Advantageously, this improves sample identification and reduces the risk of sample error (such as sample mix up). In one embodiment, the label may be removed from the string and placed on the tube to which the string will be inserted post-use, prior to sending to the laboratory.
Preferably, the string comprises a medical grade string.
Preferably, the string may be coated with a biological macromolecule. Preferably, the string may be coated with a protein which may act as a marker for a condition. In one embodiment, the string may be coated with a protein such as eosinophilic cationic protein (ECP). In another embodiment, the string may be coated with a dye or other marker. Advantageously, the string acts to capture an element from the oesophagus of a patient that may be useful diagnostically following further analysis.
In another embodiment, the string may be coated with or encompass a pharmaceutical agent for administration to a patient. In this embodiment, the string may assist in the delivery of a drug to a patient. Advantageously, the use of the string to administer a drug assists the patient in swallowing tablets and/or medication and has limited local area of activity (where it lies against the lining of the oesophagus).
Preferably, the string may be used to absorb a component following insertion into the oesophagus of a patient. Preferably, the string is used to absorb and/or capture a component that will be useful diagnostically. Preferably, when the string has been inserted into the oesophagus of a patient, the string absorbs a protein such as eosinophilic cationic protein (ECP). ECP is known to be a marker for the condition eosinophilic esophagitis (EoE), such that the detection of this protein may indicate that the patient is suffering from this condition and the amount of protein detected may indicate how severe the inflammation is, thus providing an indicator of disease activity. Typically, levels of string ECP isolated from the oesophagus of patients with eosinophilic oesophagitis correlates with levels of eosinophils in biopsy specimens from these patients. Typically, a high string ECP level correlates with a high biopsy eosinophil count.
In another embodiment, the string may be used to measure IgG4 levels in a fluid that is absorbed by the string. Advantageously, the presence of IgG4 levels will help to distinguish the condition of reflux oesophagitis from eosinophilic oesophagitis, since IgG4 is only present in the latter condition. Advantageously, the presence of IgG4 antibodies can also be used to test for possible food triggers for eosinophilic oesophagitis (for example, to detect food specific IgG4 antibodies) to help guide a food elimination diet to treat this disease. Advantageously, if a specific IgG4 antibody is detected in relation to a specific food, then eliminating these foods would typically bring the disease into remission.
In one embodiment, the string may be used in a biopsy procedure, for example, to test the presence of one or more cancer cell in a patient. Advantageously, the string may be used to detect the presence of other biological samples in a patient.
Preferably, the string has a length to ensure that, when inserted into a patient, the string is in contact with the entire length of the oesophagus of the patient. Preferably, the string has a length to ensure that the structure at the distal end of the string enters the stomach of the patient. Advantageously, providing a string that has a length such that it is in contact with the entire length of the oesophagus assists in the adequate placing of the string within a patient, thus optimising the procedure.
In some embodiments, segments of the string may be analysed separately following removal of the string from the oesophagus of a patient. In one embodiment, the string may comprise an interval marker. In one embodiment, the interval marker may comprise an ink or dye. In another embodiment, the interval marker may comprise at least one knot provided on the string. Typically, following removal of the string from a patient, the string may be cut at the intervals shown by the interval markers and individual segments may be analysed separately.
Typically, the string may be analysed following insertion into a patient to determine whether the distal end of the string has entered the stomach of the patient. Typically, following removal of the string from a patient, the chemical composition of the distal end of the string may be analysed. In one embodiment, the pH of the distal end of the string may be analysed, for example using a pH indicator dye or paper. Typically, if the distal end of the string has been present in the stomach of the patient, the pH of the distal end of the string will be acidic, due to the acidic nature of the stomach. In another embodiment, following removal of the string from a patient, the distal end of the string may be analysed to test for other stomach markers such as pepsin/pepsinogen or gastrokines.
In one embodiment, the string may be coated with a substance that will provide a stimulus to the oesophageal lining of a patient. In one embodiment, the string may be coated with a substance that will provoke an inflammatory response by the oesophageal lining. Preferably, the substance that provides a stimulus will interact with other biological mediators that are released in response. Typically, the string may be coated with a biological substance, a chemical substance or a food. Typically, the substance may bind to the string and may be measured to determine the effect of the stimulus. In one embodiment, the string may be coated with a cytokine, a weak acid or alkaline substance or a food, such as a whole food or a food component. In one embodiment, the string may be coated with whole milk. In another embodiment, the string may be coated with ovalbumin. In the embodiment wherein the substance providing the stimulus is embedded within the string, the position of the substance on the string may be marked, for example, using a dye or ink or by knotting the string. In this embodiment, string segments on either side of the stimulus can be removed (e.g. cut out) and biological components of inflammation measured. In the embodiment wherein the provoking stimulus is applied to the string, the segment of the string coated with the stimulus may be covered with a protective film to protect the stimulus from being washed away during the swallowing process. Preferably, the protective film comprises a dissolvable substance such as gelatine, wherein the dissolvable substance will dissipate once in place to reveal and/or release the stimulus.
Preferably, following removal of the string from a patient, the string is analysed in a laboratory to check for any biological components that may have bound to the string when it was inserted in the patient.
In one embodiment, the apparatus may comprise a plurality of strings for insertion into the oesophagus of a patient. Preferably, the plurality of strings in combination form a single structure at the distal end thereof. Preferably, the apparatus comprises a plurality of separate strings which combine at the distal end of each string to form a single structure, to assist in insertion of the strings into a patient. Preferably, the structure provided at the distal end of the plurality of strings comprises a helical component. In another embodiment, the structure provided at the distal end of the plurality of strings comprises a compressed pellet. Typically, the swallowing of multiple strings by a patient is difficult. Advantageously, providing a plurality of strings having structure at the distal end thereof assists the patient in swallowing the strings. Preferably, the plurality of strings comprising a structure at the distal end thereof are swallowed by a patient simultaneously. Advantageously, the use of a plurality of strings assists in the detection of more than one component when the strings are subsequently analysed following removal from a patient. Advantageously, the use of a plurality of strings may assist in the detection of one or more chemical, protein or antibody component. This is particularly important since oesophageal diseases can be difficult to detect and may affect different regions of the oesophagus. In the embodiment wherein a single string is inserted into a patient, following removal of the string, the string is typically cut into segments and each segment is analysed in different tests. In this embodiment, it may be possible to miss an area of disease within the oesophagus of a patient, since the oesophageal diseases may be patchy and affect different areas of the oesophagus. Advantageously, the use of multiple strings means that each string contacts substantially the entire lining of the oesophagus and thus, each string may be separately analysed following removal from a patient, thus providing a more accurate result. Typically, the strings are analysed by removing (e.g. cutting) the distal structure from the end of the strings and then analysing each of the strings separately.
In one embodiment, the apparatus of the present invention may be used in human and/or veterinary medicine. Typically, humans and/or animals may chew the string to allow for collection of saliva for analysis using the apparatus of the invention. In another embodiment, the string may be used to collect and test the saliva of humans. Typically, in this embodiment, the saliva of humans may be collected and used to carry out antibody, DNA and/or RNA tests.
According to a second aspect, there is provided a kit for use with the string of the first aspect, the kit further comprising means for removing a sample from the string following insertion into a patient.
Preferably, the kit comprises a string capture rod, string collection apparatus, string extraction apparatus and/or a centrifuge tube.
Preferably, the string capture rod assists in transfer of the string following removal from the oesophagus of a patient to a container, for example, for further laboratory analysis. Advantageously, the use of a string capture rod to transfer the string minimises sample contamination and reduces user risk, i.e. providing for safe handling of the string.
Preferably, the string capture rod comprises a cylindrical element, wherein the string may be wound around the outer surface of the cylindrical element. In one embodiment, the cylindrical element may be telescopic. Advantageously, the use of a telescopic cylindrical element reduces the amount of space taken by the string capture rod, for example, during storage.
Typically, the string capture rod has a length that is between 5 cm and 25 cm, preferably between 10 cm and 20 cm, and most preferably around 16 cm in length.
Preferably, the outer surface of the string capture rod is substantially smooth and comprises a material such as Teflon or polypropylene.
Preferably, at least one end of the cylindrical element is rounded. Preferably, the at least one end of the cylindrical element that is rounded is used to capture the string. Advantageously, the rounded end of the cylindrical element prevents any unwanted tearing of the string during capture by the string capture element. Typically, the distal end of the string is provided with a roughened surface. Advantageously, the roughened surface at the distal end of the string will prevent unwanted release of the string from the capture rod due to the sticky nature of the string when wet.
In one embodiment, the string capture rod may be tapered along the length of the cylinder to assist in removal of the string therefrom.
Preferably, the string capture rod further comprises a guard element. Preferably, the guard element is provided at the end of the string capture rod that is held by a user. Preferably, the guard element comprises a cylindrical portion that is dimensioned such that it fits around the circumference of the cylindrical element. Preferably, the guard element further comprises a circular portion that is substantially perpendicular to the axis of the cylindrical portion of the guard portion and extends therefrom. Typically, the guard element may slide along the longitudinal axis of the cylindrical element of the string capture rod. Typically, the string is wound around the outer surface of the cylindrical element. Preferably, the user then slides the guard element along the longitudinal axis of the cylindrical element to push the string along the cylindrical element and into an appropriate container for transfer to the laboratory. Typically, the guard element may slide along the longitudinal length of the cylindrical element towards the rounded end of the cylindrical element. Advantageously, the guard element provides protection to the string as it prevents the user from coming into contact with the string, thus minimising contamination of the string and protects the user from the patient's oesophageal fluid.
Preferably, the string capture rod comprises a metallic material. In this embodiment, the string capture rod is reusable following sterilisation. In another embodiment, the string capture rod comprises a plastics material. In this embodiment, the string capture rod is disposable. It is preferred that the string capture rod is made from a material that is rigid enough to enable the string to be wound around the rod and smooth enough so as not to hinder the travel of the wound string along the cylinder length of the string capture rod.
In one embodiment, the string collection apparatus may comprise a string removal means. Typically, when the string is wet it adheres to the string capture rod. Advantageously, the string removal element assists in removal of the string from the string capture rod. Preferably, the string removal means may comprise a thimble-like element. Preferably, the string removal element is substantially cylindrical in shape. Preferably, the string removal element comprises a cylindrical wall extending from an upper surface at one end of the cylinder. Preferably, the end of the string removal means opposite to the upper surface is open. In another embodiment, the string removal means may comprise a disk. In one embodiment, the string removal means may comprise a disposable plastics element. Preferably, the string removal means may comprise one or more perforations. Preferably, the upper surface of the string removal means may comprise a hole, wherein the hole is dimensioned such that the string capture rod may pass therethrough. Preferably, the guard element comprises a recess which is shaped such that it may accommodate the string removal means.
Preferably, as the string capture rod passes through the hole in the string removal means, the string is adapted to be removed from the string capture rod. Preferably, the string capture rod is adapted to be inserted through the cylindrical portion of the guard element. Preferably, the string capture rod is adapted to pass through the hole provided in the upper surface of the string removal means. Preferably, the string capture rod is adapted to be withdrawn into the guard element and then to push forwards such that the string removal means is placed into the string holding cup. Preferably, the string removal means is adapted to be held within the string holding cup. Preferably, the string capture rod is removed from the string removal means. Typically, the perforations in the string removal means allow buffer to pass through the string removal means and onto the string.
Preferably, the string collection apparatus comprises a string holding cup. Preferably, the string holding cup holds the string after removal from the oesophagus of a patient. Preferably, the string collection apparatus further comprises a fluid collection tube for holding the string holding cup. Preferably, the string holding cup comprises a cylindrical wall extending from and surrounding a base. Preferably, the base of the string holding cup comprises at least one hole. Preferably, the at least one hole has a diameter which allows the passage of oesophageal secretions through the string holding cup during centrifugation.
Preferably, the at least one hole has a diameter of approximately 0.1 mm. Preferably, the base of the string holding cup has a diameter of approximately 14 mm. Preferably, the end of the string holding cup that is opposite to the base is open. Preferably, the string holding cup is of sufficient diameter to fit the string capture rod. Preferably, the string holding cup is of sufficient diameter to fit the rounded tip of the string capture rod. Preferably, the user may transfer the string from the patient to the string holding cup via the string capture rod.
Preferably, the string holding cup fits within a fluid collection tube. Preferably, the fluid collection tube may hold a volume of approximately 15 ml. Preferably, the open end of the string holding cup fits within the fluid collection tube. Preferably, the fluid collection tube is cylindrical and has a base at one end. Preferably, the string holding cup and/or the fluid collection tube comprise a plastics material. Preferably, the string holding cup and/or fluid collection tube may hold a volume of approximately 2 ml.
In one embodiment, the string holding cup may hold a volume of approximately 3 ml. In one embodiment, approximately 300 μl extraction buffer is added to the string holding cup comprising the sample. Typically, a smaller or larger volume of extraction buffer may be added to the string holding cup comprising the sample. Preferably, the string holding cup may be removed from the fluid collection tube to access fluid for laboratory analysis.
Preferably, the string holding cup and the fluid collection tube are placed within a centrifuge tube. Preferably, the centrifuge tube is a 15 ml centrifuge tube. Preferably, the adhesive patient identifier can be removed from the string and placed on the outer surface of the centrifuge tube. Preferably, during centrifugation, the perforations in the string holding cup allow fluid released from the string to be collected at the bottom of the fluid collection tube. Preferably, following centrifugation the string holding cup can be removed from the fluid collection tube and the fluid can be analysed in a laboratory.
Preferably, the inner surface of the fluid collection tube is tapered such that the diameter at a substantially central portion along the longitudinal length of the tube is less than the diameter at the end of the tube. In one embodiment, the inner surface of the fluid collection tube has an indentation at a substantially central portion along the longitudinal length of the tube. In one embodiment, the fluid collection tube has a diameter of approximately 14 mm at the base and a diameter of approximately 19 mm at the opening. Preferably, the fluid collection tube tapers along the length thereof to allow the string holding cup to sit within the fluid collection tube such that it is held in place. Typically, the fluid collection tube may be approximately 40 mm in length. Advantageously, the reduced diameter along the longitudinal length of the inner surface of the fluid collection tube assists in holding the string holding cup in place, allowing the string holding cup to be removed by a user when required, but preventing the string holding cup from slipping further down the length of the fluid collection tube when centrifuged.
Preferably, the string extraction apparatus comprises a cap comprising a retaining ring which is adapted to engage with a container comprising an extraction buffer. Preferably, the string extraction apparatus further comprises a piercing device. Preferably, the string extraction apparatus engages with the string collection apparatus during centrifugation. Preferably, the piercing device sits adjacent to the string holding cup during centrifugation.
Preferably, the piercing device comprises a spike. It is preferred that the piercing device further comprises a disk portion, wherein the spike is positioned at a position substantially at the centre of the disk portion. Preferably, the spike extends from a substantially central portion of the disk portion. Preferably, the disk portion of the piercing device comprises a plastics or metallic material. Preferably, the spike of the piercing device comprises a plastic or metallic material. Preferably, the piercing device comprises at least one hole or perforation. Preferably, the retaining ring sits between the container comprising the extraction buffer and the piercing device and is adapted to prevent contact of the spike of the piercing device with the container comprising the extraction device prior to centrifugation. Preferably, the retaining ring prevents contact of the spike of the piercing device with the container comprising the extraction buffer prior to activation by centrifugation. Advantageously, the retaining ring prevents the container holding the buffer from being punctured prematurely. Preferably, the spike of the piercing device is adapted to puncture the container comprising the extraction buffer during centrifugation. Typically, the g forces of centrifugation push the container comprising the extraction buffer past the retaining ring and onto the piercing device such that the extraction buffer is released. Advantageously, the at least one hole or perforation provided within the piercing device distributes the buffer evenly over the string which is held within the string holding cup.
In one embodiment, the piercing device may comprise an L-shaped piercing device. Preferably, the L-shaped piercing device creates a triangular valve in the cap or stopper of the container comprising the extraction buffer when pierced. Typically, the valve opens under the centrifuge g forces of centrifugation to release the liquid. In one embodiment, the L-shaped piercing device may be provided on a base comprising a plurality of perforations as a support. Typically, the tip of the piercing device may pierce the rubber seal of the container comprising the buffer. Advantageously, a valve is created as the tip pierces the seal of the container which allows the liquid buffer to pass onto the perforated base. Typically, the liquid is then distributed through the perforations and onto the string within the container. Typically, a rubber stopper has self sealing properties such that when the stopper is punctured by a needle, the stopper will seal around the needle which may make it difficult for buffer to be released from the container. Advantageously, the valves created by the unique shape of the piercing device as it cuts through the rubber stopper will address this problem and allows release of buffer from the container.
In another embodiment, the piercing device may comprise a star shaped pyramid piercing device. Advantageously, the use of a piercing device having this shape creates a number of triangular valves in the seal when pierced. The valves open under the centrifuge g forces to release the liquid from the container containing the buffer. The shape of the piercing device may be modified further to contain channels which also aids the flow of buffer along the piercing device and onto the string below. In one embodiment, the piercing device pierces the cap or stopper of the container comprising the extraction buffer and creates four valves. In one embodiment, the cap or stopper comprises a rubber material.
In another embodiment, the kit further comprises a lid which may be placed over and/or may be used to seal the fluid collection tube and/or string holding cup. In one embodiment, the lid may comprise an extraction buffer. In one embodiment, the lid may comprise a release mechanism, wherein when the lid is placed on the fluid collection tube and/or string holding cup, the lid is punctured such that extraction buffer is released into the string holding cup. Typically, when the lid is placed onto the string holding cup and/or fluid collection tube, a puncture device is activated to puncture the lid comprising the extraction buffer. In one embodiment, the puncture device may be provided within the lid. In another embodiment, the puncture device may be provided adjacent to the lid. In one embodiment, the puncture device may comprise a spike. In another embodiment, the extraction buffer may be provided in a container which may be punctured when the lid is placed onto the fluid collection tube and/or string holding cup. In one embodiment, the puncture device may be a piercing device.
In one embodiment, the kit may further comprise a bottle. Typically, the bottle is a buffer holding container or buffer holder. Preferably, the bottle is standardised for use with a centrifuge activated device. Typically, the bottle comprises a buffer. Preferably, the bottle comprises a stopper and/or a cap. It is preferred that the stopper is held in place by the cap. Preferably, the stopper comprises a rubber material. Preferably, the cap is a metallic crimp cap, preferably an aluminium or silver crimp cap. Advantageously, the combination of the stopper and cap provides a liquid tight seal. Preferably, the bottle is used in combination with the string collection apparatus. Preferably, the bottle is dimensioned such that it may be used in combination with the fluid collection tube and/or string holding cup. Preferably, the bottle fits within the lid of the kit. In this embodiment, it is preferred that the piercing device comprises a needle like device. Preferably, the needle like device is sharp to allow the stopper and seal to be punctured. Preferably, the needle like device is hollow to allow the liquid under the g forces of centrifugation to flow through the needle and onto the string that is held within the string holding cup. Preferably, the piercing device comprises an L-shaped piercing device or a star shaped piercing device as described above. Preferably, a disk is provided within the bottle and substantially parallel to the plane of the base of the bottle. Preferably, the disk comprises a plurality of holes, such that as the liquid passes through the needle, the liquid is distributed evenly onto the string.
In one embodiment, the release mechanism comprises a latch member. In this embodiment, the latch holds the buffer in place within the lid when the lid is not attached to the string holding cup and/or fluid collection tube. In this embodiment, the latch member may be released when the cap is placed onto the string holding cup and/or fluid collection tube. Typically, the release of the latch mechanism may result in puncture of the lid and/or container comprising the extraction buffer such that the buffer passes over the string that is held within the string holding cup. In another embodiment, when the lid comprising the extraction buffer is placed onto the fluid collection tube and/or string holding cup, a spike held within or adjacent to the lid and/or fluid collection container punctures the lid and causes release of the extraction buffer. In one embodiment, the spike may be held within the lid and the action of placing the lid onto the fluid collection tube and/or string holding cup causes the spike to puncture the portion of the lid holding the extraction buffer, thus causing release of the extraction buffer.
In one embodiment, the retaining ring and release member may be used together to prevent unwanted puncture of the container comprising the extraction buffer. In one embodiment, the retaining ring comprises a first safety device to prevent unwanted release of the extraction buffer from the container comprising the extraction buffer. In one embodiment, the release member comprises a second safety device to prevent unwanted release of the extraction buffer. Typically, the first safety device may be disarmed during centrifugation when the container comprising the extraction buffer moves past the retaining ring and onto the piercing device such that the extraction buffer is released. Typically, the second safety device may be disarmed by putting the lid onto the fluid collection tube and/or string holding cup, causing the lid to puncture and releasing the extraction buffer held within the lid. In one embodiment, release of the latch member may cause the lid to puncture and cause release of extraction buffer from the lid. In one embodiment, the first and/or second safety device may be disarmed to cause release of the extraction buffer from the container comprising the extraction buffer and/or lid comprising the extraction buffer during centrifugation. Typically, once the extraction buffer has been removed from the lid and/or container comprising the extraction buffer, the extraction buffer passes into the string holding cup where it passes over the string, through the at least one hole provided in the string holding cup and into the fluid collection tube.
In one embodiment, a spring is provided around the piercing unit. Advantageously, the provision of a spring assists in preventing the buffer holder from being pierced prematurely. Typically, the provision of a spring will separate the buffer holder from the piercing unit in transit. Typically, during centrifugation, the spring will be compressed by the buffer holder under g forces which will allow the piercing unit to come into contact with the buffer holder, resulting in the piercing of the buffer holder and subsequent release of buffer.
In another embodiment, a clip may be provided around the piercing unit. Advantageously, the provision of a clip assists in preventing the buffer holder from being pierced prematurely. Typically, the provision of a clip will separate the buffer holder from the piercing unit in transit. Typically, during centrifugation, the clip will move into the buffer holder under g forces which will allow the piercing unit to come into contact with the buffer holder, resulting in the piercing of the buffer holder and subsequent release of buffer. Typically, the clip comprises a plastics material. In one embodiment, the clip may be spring loaded.
In some embodiments, a component within the oesophageal fluid may stick to the string and may require removal from the string using an extraction and/or release buffer. In one embodiment, the extraction or release buffer can be added to the string prior to centrifugation. In another embodiment, the extraction or release buffer can be added to the string during centrifugation, i.e. during a centrifuge activated mechanism, wherein the extraction buffer is released onto the string by g forces acting on the tube during centrifugation. In one embodiment, the extraction or release buffer may require neutralisation which can be achieved by providing a neutralisation buffer within the fluid collection tube. Preferably, centrifugation is used to obtain an oesophageal sample for laboratory analysis. In one embodiment, the pH of the sample may be measured following centrifugation. Preferably, ECP that is collected by the oesophageal string test adheres to the string and centrifugation alone is typically not sufficient to remove it from the string. Typically, the addition of a low pH buffer to the string allows release of the ECP.
In one embodiment, the kit may comprise a string holder. Preferably, the string holder comprises a disc region comprising a front conical projection onto which the string is wound and a rear cylinder where the remaining string is wrapped. Typically, the disc region comprises a flexible material. Advantageously, the string holder may be used to preserve the shape and integrity of the coil provided at the proximal end of the string. Typically, the string is coiled around the string holder and then placed in a sealed package until ready for use. Advantageously, the provision of a sealed package allows the string to be kept sterile. Typically, once removed from the packaging the string may be unwound from the rear cylinder and the distal end of the string is fixed to the check of a patient as described above. Preferably, the string which is wound around the front conical projection remains in place until the patient is ready to swallow the string. Typically, at this point, gentle squeezing of the outer edge of the string holder compresses the conical holder, thus reducing the diameter of the holder and allowing the string to be removed therefrom. Typically, the string holder comprises a plurality of segments, assisting in the compression of the string holder to facilitate removal of the string therefrom. Typically, the released coil of string can then be placed in the mouth of the patient and swallowed. Typically, following use, the string holder may be discarded. Typically, the string holder comprises a plastics material. Typically, the plastics material is smooth, stiff and flexible. In one embodiment, the string holder may be packed in packaging that also includes a centrifuge activated device. In one embodiment, the string holder and/or centrifuge activated device may be packaged in a packaging that also includes a set of instructions for how to use the string holder and/or centrifuge activated device.
In one embodiment, the string holder may also comprise a string capture rod. Advantageously, combining the string transport device and string collection device allow for the provision of a dual purpose unit. In this embodiment, the string can be captured and then stored using one unit. This embodiment can be used to store and transport the string but can also be used to collect the string once used and dispense into the tube with the centrifuge activated device.
In another embodiment, a DNA and/or RNA stabilising buffer may be used to reduce and/or prevent degradation of the sample prior to analysis. In one embodiment, the DNA and/or RNA stabilising buffer may comprise a TE buffer comprising 10 mM Tris (pH 8.0) with HCl and 1 mM EDTA. Advantageously, the addition of DNA and/or RNA stabilising agents to a sample may prevent contaminants in the saliva of a patient from breaking down nucleotides. In addition, the use of DNA and/or RNA stabilising agents in a buffer can help to stabilise a sample until it can be processed.
In a further embodiment, protein stabilising agents may be added to the buffer, such as protease inhibitors and/or metal chelators. Advantageously, the use of a protein stabilising agent may prevent degradation prior to analysis, and/or may assist in stabilising a sample where specific protein analysis may be needed.
In another embodiment, enzymes may be added to a buffer to remove free DNA and/or RNA that may act as a contaminant.
Typically, ECP that is collected by the oesophageal string test adheres to the string and centrifugation alone is not sufficient to remove it from the string. Typically, the addition of a low pH buffer to the string allows the release of ECP.
Preferably, the use of a DNA and/or RNA stabilising buffer and/or protein stabilising agent may assist in stabilising the sample prior to testing in a laboratory.
Advantageously, the use of a DNA and/or RNA stabilising buffer and/or protein stabilising agent may assist in stabilising a saliva sample prior to testing in a laboratory, thus improving the performance of the test.
Typically, the string may be analysed following insertion into a patient to determine whether the distal end of the string has entered the stomach of the patient. Typically, following removal of the string from a patient, the chemical composition of the distal end of the string is analysed. In one embodiment, the pH of the distal end of the string may be analysed, for example using a pH indicator dye or paper. Typically, if the distal end of the string has been present in the stomach of the patient, the pH of the distal end of the string will be acidic, due to the acidic nature of the stomach. In another embodiment, following removal of the string from a patient, the distal end of the string may be analysed to test for other stomach markers such as pepsin or gastrokines. It is preferred that the pH indicator and/or stomach markers are provided with the kit of the invention.
Advantageously, the kit of the present invention assists in obtaining a sample from a swallowed string and/or packaging the string for laboratory analysis.
Preferably, the kit comprises a centrifuge activated device (which may also be known as a CAD). Preferably, the centrifuge activated device comprises a buffer holder, a piercing device and a mechanism to prevent the buffer holder from being pierced prior to centrifugation. In one embodiment, the buffer holder may be a bottle. Preferably, the centrifuge activated device may be used in a method (e.g. using a centrifuge activated device) for washing (e.g. eluting) components stuck to the string for laboratory analysis. Advantageously, the apparatus of the present invention optimises function during insertion of the string into the oesophagus of a patient, and improves safety and practicality of the nurse or doctor handling the string. Typically, the addition of eluting and neutralising buffer to the string can be time consuming and requires laboratory staff and training. Advantageously, the use of a centrifuge activated device in accordance with the present invention to release the buffer while in the centrifuge eliminates the need for manually performing this step. Advantageously, the use of centrifugation also minimises staff exposure to biological substances such as oesophageal fluid.
Preferably, the mechanism to prevent the buffer holder from being pierced prior to centrifugation comprises a spring or retaining clip.
Preferably, the centrifuge activated device may be provided as one unit. In one embodiment, the centrifuge activated device may be provided as a sealed unit, to ensure that it is kept sterile.
Preferably, the centrifuge activated device is activated by centrifugation where the g forces cause piercing of the buffer holder and releasing the buffer.
According to a third aspect, there is provided a method of providing a structure at the distal end of the string of the apparatus of the first aspect of the invention, comprising the step of modifying the string to form a structure at the distal end of the string. Preferably, the string is modified to form a helical structure at the distal end. Preferably, the method comprises the steps of coating the distal end of the string in a solution which will confer rigidity to the string when dry, wrapping the distal end of the string around a rod to form a helical structure and allowing the string to dry. In one embodiment, the string may be soaked in a solution comprising a sugar. In another embodiment, the string may be soaked in a solution of corn starch, for example, 1% corn starch solution. Preferably, the string is steam heated to confer the ability to retain a new shape to the distal end of the string. In one embodiment, the string may be dipped in water (preferably sterile water), wound around the outer surface of a metal rod and heated to a temperature of approximately 100° C. for approximately 10 minutes. Preferably, once the string has set, the distal end of the string is removed from the outer surface of the rod. Advantageously, the helical component at the distal end of the string provides a structure that is flexible and soft to assist in insertion into the oesophagus of a patient, yet rigid to assist in the patient swallowing the string. Preferably, the size of the structure at the distal end of the string is optimised such that it is small enough that it does not cause irritation to the oesophagus, whilst still being capable of being swallowed by a patient. Preferably, size of the structure at the distal end of the string is equivalent to a size 5 capsule, for example, having a length of approximately 11.1 mm and a width of approximately 4.9 mm. In other embodiments, a smaller or larger size of structure at the distal end of the string can be used if needed.
According to a fourth aspect, there is provided a method of determining the presence of a substance within the oesophageal lining a patient using the apparatus of the first aspect, the method comprising the steps of providing a structure at the distal end of the string to assist the patient in swallowing the string, removing the string from the oesophagus of the patient and testing the string to check for the presence of the substance. In one embodiment, the method comprises the step of applying a marker such as a protein or dye to the string prior to insertion into the patient. Preferably, the string may be coated with a biological macromolecule. Preferably, the string may be coated with a protein which may act as a marker for a condition. In one embodiment, the string may be coated with the protein eosinophilic cationic protein (ECP). In another embodiment, the string may be coated with a dye or other marker. In one embodiment, the marker may be applied to the string during centrifugation.
Preferably, method comprises the step of absorbing a component from the oesophageal lining following insertion into the oesophagus of a patient. Preferably, when the string has been inserted into the oesophagus of a patient, the string absorbs a protein such as eosinophilic cationic protein (ECP). ECP is known to be a marker for the condition eosinophilic esophagitis (EoE), such that the detection of this protein may indicate that the patient is suffering from this condition. Typically, ECP can be released from the string using a low pH buffer. Typically, the ECP can be released from the string using a buffer comprising approximately 0.1 Molar glycine at approximately pH 2.8. Typically, this buffer can then be neutralised using an approximately 1 Molar Tris buffer at around pH 14. Typically, approximately 300 μl buffer, preferably comprising glycine, is used to elute the ECP protein into approximately 80 μl Tris buffer.
In one embodiment, segments of the string may be analysed separately following removal of the string from the oesophagus of a patient. In one embodiment, the method may comprise the step of providing an interval marker on the string. In one embodiment, the interval marker may comprise an ink or dye. In another embodiment, the interval marker may comprise at least one physical marker such as a knot provided on the string. Typically, following removal of the string from a patient, the string may be cut at the intervals shown by the interval markers and individual segments may be analysed separately. Typically, the segments may be measured to analyse variance in pH and/or differences in chemical and/or biological marker levels along the length of the string.
In one embodiment, the method comprises the step of coating the string with a substance that will provide a stimulus to the oesophageal lining of the patient. In one embodiment, the string may be coated with a substance that will provoke an inflammatory response by the oesophageal lining of the patient. Preferably, the substance that provides a stimulus will interact with other biological mediators that are released in response. Typically, the method comprises the step of coating the string with a biological substance, a chemical substance or a food. In one embodiment, the method comprises the step of coating the string with a cytokine, a weak acid or alkaline substance or a food, such as a whole food or a food component. In one embodiment, the method comprises the step of coating the string with whole milk. In another embodiment, the method comprises the step of coating the string with ovalbumin. In one embodiment, the method comprises the step of marking the string using a dye or providing a knot within the string to act as a marker. In this embodiment, string segments on either side of the stimulus can be removed (e.g. cut out) and biological components of inflammation measured. In the embodiment wherein the provoking stimulus is applied to the string, the method comprises the step of coating the section of the string provided with the stimulus with a protective film to protect the stimulus from being washed away during the swallowing process. Preferably, the protective film comprises a dissolvable substance such as gelatine, wherein the dissolvable substance will dissipate once in place to reveal the stimulus.
Preferably, the method comprises the step of analysing the string following removal from the oesophagus of the patient to check for any biological components that may have bound to the string when it was inserted in the patient.
Typically, the method comprises the step of using a string capture rod to transfer the string following removal from a patient to a string collection apparatus. Advantageously, the use of a string transfer rod to transfer the string minimises sample contamination and reduces user risk. Preferably, the string is wound around the outer surface of the cylindrical element of the string capture rod. Preferably, the user then slides the guard element of the string capture rod along the longitudinal axis of the string capture rod such that the string is pushed along the cylindrical element and into an appropriate container, e.g. for transfer to the laboratory.
Preferably, the string is transferred from the string capture rod to a string collection apparatus comprising a string holding cup. Preferably, the string holding cup holds the string after removal from the oesophagus of a patient. Preferably, the user transfers the string from the patient to the string holding cup via the string capture rod.
Preferably, the method further comprises the step of providing a string removal means, such as a thimble like element, to assist in removal of the string from the string capture element. Preferably, as the string capture rod passes through the hole in the string removal means, the string is removed from the surface of the string capture rod. Preferably, the string capture rod is inserted through the cylindrical portion of the guard element. Preferably, the string capture rod is passed through the hole provided in the upper surface of the string removal means. Preferably, the string removal means is housed within the recess of the guard element. Preferably, the string capture rod is withdrawn into the guard element and then pushed forwards such that the string removal means is placed into the string holding cup. Preferably, the string removal means is held within the string holding cup and the string capture rod is removed from the string removal means. Typically, the perforations in the string removal means allow buffer to pass through the perforations in the string removal means and onto the string.
In one embodiment, the method comprises the use of a string holder comprising a disc region comprising a front conical projection onto which the string is wound and a rear cylinder where the remaining string is wrapped. Typically, the disc region comprises a flexible material. Advantageously, the string holder may be used to preserve the shape and integrity of the coil provided at the proximal end of the string. Typically, the string is coiled around the string holder and then placed in a sealed package until ready for use. Advantageously, the provision of a sealed package allows the string to be kept sterile. Typically, once removed from the packaging the string is unwound from the rear cylinder and the distal end of the string is fixed to the check of a patient as described above. Preferably, the string which is wound around the front conical projection remains in place until the patient is ready to swallow the string. Typically, at this point, gentle squeezing of the outer edge of the string holder compresses the conical holder, thus reducing the diameter of the holder and allowing the string to be removed therefrom. Typically, the released coil of string can then be placed in the mouth of the patient and swallowed. Typically, following use, the string holder may be discarded. Typically, the string holder comprises a plastics material. Typically, the plastics material is smooth, stiff and flexible. In one embodiment, a robot may be used to wrap the string around the string holder and seal the string holder in a package.
In one embodiment, the string holder may also comprise a string capture rod. Advantageously, combining the string transport device and string collection device allow for the provision of a dual purpose unit. In this embodiment, the string can be captured and then stored using one unit. This embodiment can be used to store and transport the string but can also be used to collect the string once used and dispense into the tube with the centrifuge activated device.
Preferably, the method further comprises the step of providing a fluid collection tube which is dimensioned to hold the string holding cup.
Preferably, the method further comprises the step of providing a string extraction apparatus to assist in extracting the marker from the string. Preferably, the method comprises the step of providing a cap comprising a retaining ring, wherein the retaining ring engages with a container comprising an extraction buffer. Preferably, the string extraction apparatus engages with the string collection apparatus during centrifugation. Preferably, prior to centrifugation, the string is placed within the string holding cup of the string collection apparatus and the string collection apparatus and string extraction apparatus are placed within a centrifuge tube.
Preferably, the spike of the piercing device punctures the container comprising the extraction buffer during centrifugation. Typically, the extraction buffer is then transferred into the string holding cup, washes over the string and passes through the at least one hole provided within the base of the string holding cup. Typically, as the extraction buffer washes over the string it causes a component such as a protein that has bound to the string to be removed. Preferably, the component passes into the fluid collection tube where it can then be taken for further tests in the laboratory.
In one embodiment, the lid may comprise an extraction buffer. In this embodiment, when the lid is placed over the string holding cup and/or fluid collection tube, a release mechanism provided within or adjacent to the lid causes the lid to be punctured, thus removing the extraction buffer from the lid such that it passes over the string within the string holding cup and into the fluid collection tube.
In one embodiment, the lid may comprise a bottle, wherein the bottle may be standardised for use in a centrifuge. Preferably, the bottle may be used in combination with a string holding cup. Preferably, the bottle comprises an extraction buffer. Preferably, the bottle further comprises a stopper and seal. Preferably, the stopper is pierced with a piercing device to release buffer from the buffer and into the string holding cup, wherein the string is held within the string holding cup.
Preferably, the string holding cup and the fluid collection tube are placed within a centrifuge tube. Preferably, the centrifuge tube is a 15 ml centrifuge tube. Preferably, the adhesive patient identifier can be removed from the proximal end of the string and placed on the outer surface of the centrifuge tube. Preferably, during centrifugation, the perforations in the string collection cup allow fluid released from the string to be collected at the bottom of the fluid collection tube. Preferably, following centrifugation the string collection cup can be removed from the fluid collection tube and the fluid can be analysed in a laboratory.
According to a fifth aspect, there is provided a method of administering a drug to a patient using apparatus comprising a string in accordance with the first aspect. Preferably, the method comprises the step of applying a pharmaceutical substance to the distal end of the string which has been adapted to assist the patient in swallowing the string. In another embodiment, the method comprises the step of placing a pharmaceutical substance within the interior of the portion at the distal end of the string which has been adapted to assist the patient in swallowing the string. Advantageously, the method of administering a drug to a patient helps the patient in swallowing tablets and/or medication.
According to a sixth aspect, there is provided a method of removing a substance from apparatus comprising a string according to the first aspect of the invention using the process of centrifugation. Advantageously, the use of a centrifuge activated device aims to improve the consistency of removal of substances that are adhered to the string and to save laboratory staff time, minimise exposure to biological substances and simplify the process. Typically, the addition of eluting and neutralising buffer to the string can be time consuming and requires laboratory staff and training. Advantageously, the use of a centrifuge activated device to release the buffer while in the centrifuge eliminates the need for manually performing this step. Advantageously, the use of centrifugation also minimises staff exposure to biological substances such as oesophageal fluid.
Preferably, the method comprises the step of placing a string after removal from the oesophagus of a patient into a string collection apparatus according to the second aspect of the invention, placing the string collection apparatus and a string extraction apparatus according to the second aspect of the invention into a centrifuge tube and using the process of centrifugation to release extraction (i.e. elution) buffer onto the string. Preferably, during centrifugation, the piercing structure of the piercing device pierces the container comprising the extraction buffer such that the extraction buffer washes over the string and causes elution of a substance that is bound to the string. In one embodiment, a neutralisation buffer may be provided within the fluid collection tube to neutralise the extraction buffer. Preferably, following elution, the substance that was bound to the string is collected for testing in a laboratory.
Preferably, the act of centrifugation forces the spike to puncture the container comprising the extraction buffer and to release the extraction buffer onto the string.
Preferably, the forces applied to the system during centrifugation force the container holding the extraction buffer past the retaining ring onto the spike of the piercing device. Typically, the buffer is released and passes through at least one hole provided within the piercing device and onto the string that is held within the string holding container.
In one embodiment, the lid of the string holding cup comprises an extraction buffer release mechanism. In this embodiment, when the lid is positioned over the string holding cup and/or fluid collection tube, a release mechanism provided within or adjacent to the lid causes the lid to be punctured, thus removing the extraction buffer from the lid such that it passes over the string and into the fluid collection tube.
In one embodiment, the release mechanism and retaining ring or spring may provide first and second safety devices to prevent unwanted release of the extraction buffer. Typically, the lid is placed onto the fluid collection tube and/or string holding cup to activate the release mechanism such that the lid is punctured and extraction buffer is released. Typically, during centrifugation, the g forces of centrifugation force the buffer holding container past the retaining ring and onto the spike provided on the piercing device. Typically, the extraction buffer is released and passes through perforations of the piercing device and onto the string that is held within the string holding cup. Typically, the retaining ring and/or spring may be used to prevent piercing of the buffer holder or bottle during storage and/or transit.
In another embodiment, the extraction buffer may be held within a container comprising a valve that is normally in the closed position. In this embodiment, the force applied to the system during centrifugation causes the valve to open, thus releasing the extraction buffer from the container and onto the string.
In another embodiment, the piercing device sits within the container holding the extraction buffer and is activated by the g forces that are applied to the system during centrifugation.
According to a seventh aspect, there is provided a string holder for use with the string of the first aspect and/or the kit of the second aspect. Preferably, the string holder comprises a disc region comprising a front conical projection onto which the string is wound and a rear cylinder where the remaining string is wrapped. Typically, the disc region comprises a flexible material. Advantageously, the string holder may be used to preserve the shape and integrity of the coil provided at the proximal end of the string. Typically, the string is coiled around the string holder and then placed in a sealed package until ready for use. Advantageously, the provision of a sealed package allows the string to be kept sterile. Typically, once removed from the packaging the string is unwound from the rear cylinder and the distal end of the string is fixed to the check of a patient as described above. Preferably, the string which is wound around the front conical projection remains in place until the patient is ready to swallow the string. Typically, at this point, gentle squeezing of the outer edge of the string holder compresses the conical holder, thus reducing the diameter of the holder and allowing the string to be removed therefrom. Typically, the string holder comprises a plurality of segments, assisting in the compression of the string holder to facilitate removal of the string therefrom. Typically, the released coil of string can then be placed in the mouth of the patient and swallowed. Typically, following use, the string holder may be discarded. Typically, the string holder comprises a plastics material. Typically, the plastics material is smooth, stiff and flexible.
In one embodiment, the string holder may also comprise a string capture rod. Advantageously, combining the string transport device and string collection device allow for the provision of a dual purpose unit. In this embodiment, the string can be captured and then stored using one unit. This embodiment can be used to store and transport the string but can also be used to collect the string once used and dispense into the tube with the centrifuge activated device.
According to an eight aspect, there is provided a centrifuge activated device (CAD). Preferably, the centrifuge activated device comprises a buffer holder, a piercing device and a mechanism to prevent the buffer holder from being pierced prior to centrifugation. In one embodiment, the buffer holder is a bottle. Preferably, the centrifuge activated device may be used in a method (e.g. using a centrifuge activated device) for washing (e.g. eluting) components stuck to the string for laboratory analysis. Advantageously, the apparatus of the present invention optimises function during insertion of the string into the oesophagus of a patient, and improves safety and practicality of the nurse or doctor handling the string. Typically, the addition of eluting and neutralising buffer to the string can be time consuming and requires laboratory staff and training. Advantageously, the use of a centrifuge activated device in accordance with the present invention to release the buffer while in the centrifuge eliminates the need for manually performing this step. Advantageously, the use of centrifugation also minimises staff exposure to biological substances such as oesophageal fluid.
Preferably, the mechanism to prevent the buffer holder from being pierced prior to centrifugation comprises a spring or retaining clip.
Preferably, the centrifuge activated device may be provided as one unit. In one embodiment, the centrifuge activated device may be provided as a sealed unit, to ensure that it is kept sterile.
Preferably, the centrifuge activated device is activated by centrifugation where the g forces cause piercing of the buffer holder and releasing the buffer.
The invention will now be further described by way of illustrative example, wherein:
With reference to
In the embodiment shown in
The proximal end is the end of the string that is nearest the user rather than the patient.
The helical component 8 at the distal end of the string is formed by soaking the distal end of the string in a solution that will confer rigidity on the string once dry, wrapping the distal end of the string around a rod and allowing the string to dry. The string may be soaked in a solution of corn starch, for example, 1% corn starch solution. Alternatively, the string may be dipped in sterile water, wound around the outer surface of a metal rod, and then heated to a temperature of approximately 100° C. for approximately 10 minutes. Advantageously, the helical component at the distal end of the string provides a structure that is flexible and soft to assist in insertion into the oesophagus of a patient, yet rigid to assist in the patient swallowing the string.
The string further comprises a structure at the proximal end 4 thereof, wherein the structure provided at the proximal end comprises a compressed or knotted portion of the string. The structure provided at the proximal end 4 of the string assists in attachment of the string to a cheek of the patient. Advantageously, the provision of a string having a structure at the proximal end thereof assists in attachment of the proximal end of the string to a patient such that the string is not inadvertently detached or swallowed by the patient during insertion of the string, thus improving safety and ease of use.
The proximal end of the string is attached to a patient using an attachment means in the form of a skin-adhesion grade tape to improve comfort for the patient. Advantageously, the use of tape to secure the string to the patient improves security and reduces the risk of unwanted detachment of the string from the patient. The string attachment means may comprise an adhesive removable label to which details regarding the sample type, date sample taken, patient identifiers (such as name, age, date of birth, unique patient identifier such as NHS or hospital number) can be added. Advantageously, this improves sample identification and reduces the risk if sample error (such as sample mix up). The label may be removed from the string and placed on the tube to which to string will be inserted post-use, prior to sending to the laboratory.
The string 2 that is used in
The string may be coated with a biological macromolecule, such as a protein which may act as a marker for a condition. In another embodiment, the string may be coated with a dye or other marker. In another embodiment, the string may be coated with or encompass a pharmaceutical agent for administration to a patient.
The structure at the distal end of the string may be coated with a flavouring. In one embodiment, the structure at the distal end of the string may be coated with at least one drop, preferably two to three drops, of flavouring essence. Advantageously, coating the structure at the distal end of the string with a flavouring can encourage swallowing of the string by patients. This is particularly beneficial in children.
In one embodiment, the string is used to absorb a biological component following insertion into the oesophagus of a patient. Preferably, when the string has been inserted into the oesophagus of a patient, the string absorbs a protein such as eosinophilic cationic protein (ECP). ECP is known to be a marker for the condition eosinophilic esophagitis (EoE), such that the detection of this protein may indicate that the patient is suffering from this condition.
The string may be used to measure IgG4 levels in the fluid that is absorbed by the string. Advantageously, the presence of IgG4 levels will help to distinguish reflux oesophagitis from eosinophilic oesophagistis, since IgG4 is only present in the latter. Advantageously, the presence of IgG4 antibodies can also be used to test for possible food triggers for eosinophilic oesophagitis (for example, food specific IgG4 antibodies) to help guide a food elimination diet to treat this disease. Advantageously, if a specific IgG4 antibody is detected in relation to a specific food, then eliminating these foods would bring the disease into remission.
The string has a length to ensure that, when inserted into a patient, the string is in contact with the entire length of the oesophagus of the patient. Preferably, the string has a length to ensure that the structure at the distal end of the string enters the stomach of the patient. Advantageously, providing a string that has a length such that it is in contact with the entire length of the oesophagus assists in the adequate placing of the string within a patient.
In some embodiments, segments of the string may be analysed separately following removal of the string from the oesophagus of a patient. In one embodiment, the string may comprise an interval marker which may comprise an ink or dye. In another embodiment, the interval marker may comprise at least one knot provided on the string. In this embodiment, following removal of the string from a patient, the string may be cut at the intervals shown by the interval markers and individual segments may be analysed separately.
The string may be analysed following insertion into a patient to determine whether the distal end of the string has entered the stomach of the patient. Typically, following removal of the string from a patient, the chemical composition of the distal end of the string is analysed. In one embodiment, the pH of the distal end of the string may be analysed, for example using a pH indicator dye or paper. Typically, if the distal end of the string has been present in the stomach of the patient, the pH of the distal end of the string will be acidic, due to the acidic nature of the stomach. In another embodiment, following removal of the string from a patient, the distal end of the string may be analysed to test for other stomach markers such as pepsin or gastrokines.
In one embodiment, the string may be coated with a substance that will provide a stimulus to oesophageal lining of the patient, for example, wherein the substance will provoke an inflammatory response by the oesophageal lining. The substance that provides a stimulus will typically interact with other biological mediators that are released in response. In one embodiment, the string may be coated with a cytokine, a weak acid or alkaline substance or a food, such as a whole food or a food component. In one embodiment, the string may be coated with whole milk. In another embodiment, the string may be coated with ovalbumin. In the embodiment wherein the substance providing the stimulus is embedded within the string, the position of the substance on the string will be marked, for example, using a dye or ink or by knotting the string. In this embodiment, string segments on either side of the stimulus can be removed (e.g. cut out) and biological components of inflammation measured using the kit as shown in
As shown in
The apparatus of the present invention may be used in human and/or veterinary medicine. Typically, humans and/or animals may chew a string to collect saliva for analysis using the apparatus of the invention. In another embodiment, the string may be used to collect and test the saliva of humans. Typically, in this embodiment, the saliva of humans may be collected and used to carry out antibody, DNA and/or RNA tests.
Following removal of the string from a patient, the string is analysed in a laboratory to check for any biological components that may have bound to the string when it was inserted in the patient.
Levels of string ECP isolated from the oesophagus of patients with eosinophilic oesophagitis correlates with levels of eosinophils in biopsy specimens from these patients. A high string ECP correlates with a high biopsy eosinophil count. The results of this study is shown in the Graph of
ECP collected by the oesophageal string test adheres to the string and centrifugation alone is not sufficient to remove it from the string. The addition of a low pH buffer to the string allows release of the ECP as shown in the graph of
With reference to
The kit comprises a string capture rod 12, string collection apparatus 14, string extraction apparatus 16 and/or a centrifuge tube.
As shown in
The string capture rod 12 comprises a cylindrical element 18, wherein the string may be wound around the outer surface of the cylindrical element. The cylindrical element may be telescopic. Advantageously, the use of a telescopic cylindrical element 18 reduces the amount of space taken by the string capture rod, for example, during storage.
The string capture rod 12 has a length of approximately 16 cm.
The outer surface of the string capture rod 12 is substantially smooth and comprises a material such as Teflon or polypropylene.
At least one end of the cylindrical element is rounded, wherein the at least one end of the cylindrical element that is rounded is used to capture the string. Advantageously, the smooth rounded end of the cylindrical element prevents any unwanted tearing of the string during capture by the string capture element. Typically, the string is very sticky with respect to the string capture rod when the string is wet. Providing the string with a roughened distal end has the effect that the string will stick avidly to the string capture rod. Providing the string capture rod with a smooth distal end will assist in removal of the string from the string capture rod.
The string capture rod 12 further comprises a guard element 20 that is provided at the end 22 of the string capture rod that is held by a user. The guard element comprises a cylindrical portion 24 that is dimensioned such that it fits around the circumference of the cylindrical element. The guard element further comprises a circular portion 26 that is substantially perpendicular to the axis of the cylindrical portion 24 of the guard element 20 and extends therefrom. The guard element may slide along the longitudinal axis of the cylindrical element of the string capture rod. The string is wound around the cylindrical element and the user then slides the guard element along the longitudinal axis of the cylindrical element to push the string along the cylindrical element and into an appropriate container for transfer to the laboratory. Advantageously, the guard element provides protection to the string as it prevents the user from coming into contact with the string, thus minimising contamination of the string and protecting the user from the patient's oesophageal fluid.
In one embodiment, the string capture rod 12 comprises a metallic material. In this embodiment, the string capture rod 12 is reusable following sterilisation. In another embodiment, the string capture rod 12 comprises a plastics material. In this embodiment, the string capture rod is disposable. It is preferred that the string capture rod 12 is made from a material that is rigid enough to enable the string to be wound around the rod and smooth enough so as not to hinder the travel of the wound string along the cylinder length.
With reference to
Advantageously, the string holder 150 allows the string to be packaged and protects the string and particularly the coiled part of the string from damage prior to use.
With reference to
With reference to
With reference to
The string holding cup 28 fits within a fluid collection tube 30, wherein the open end of the string holding cup fits within the fluid collection tube 82. The fluid collection tube is cylindrical and has a base at one end. Typically, the string holding cup and/or the fluid collection tube comprise a plastics material. In the embodiment shown in
The string holding cup 28 and the fluid collection tube 30 are placed within a centrifuge tube. Typically, the centrifuge tube is a 15 ml centrifuge tube. The adhesive patient identifier can be removed from the proximal end of the string and placed on the outer surface of the centrifuge tube. During centrifugation, the perforations in the string collection cup allow fluid released from the string to be collected at the bottom of the fluid collection tube. Following centrifugation the string holding cup can be removed from the fluid collection tube and the fluid can be analysed in a laboratory.
The fluid collection tube 30 comprising perforations can also be seen in
The inner surface 34 of the fluid collection tube 30 is tapered such that the diameter at a substantially central portion along the longitudinal length of the tube is less than the diameter at the end of the tube. Advantageously, the reduced diameter along the longitudinal length of the inner surface of the fluid collection tube assists in holding the string holding cup in place, allowing the string holding cup to be removed by a user when required, but preventing the string holding cup from slipping further down the length of the fluid collection tube when centrifuged.
With reference to
The piercing device 42 comprises a spike 44. In the embodiment shown in
With reference to
A similar embodiment is shown in
In the embodiment shown in
In the embodiment shown in
In the embodiment shown in
In another embodiment, the kit comprises a lid which may be used to seal the fluid collection tube 30 and/or string holding cup 28. In one embodiment, the lid may comprise an extraction buffer. In one embodiment, the lid may comprise a release mechanism, wherein when the lid is placed on the fluid collection tube 30 and/or string holding cup 28, the extraction buffer is released into the string holding cup 28. In one embodiment, the release mechanism comprises a latch member. In this embodiment, the latch member may be released when the cap is placed on the string holding cup and/or fluid collection tube. Typically, the release of the latch mechanism may result in puncture of the lid comprising the extraction buffer such that the buffer passes over the string that is held within the string holding cup. In another embodiment, when the lid comprising the extraction buffer is placed onto the fluid collection tube and/or string holding cup, a spike held within or adjacent to the lid and/or fluid collection container punctures the lid and causes release of the extraction buffer. In one embodiment, the spike may be held within the lid and the action of placing the lid onto the fluid collection tube and/or string holding cup causes the spike to puncture the portion of the lid holding the extraction buffer, thus causing release of the extraction buffer.
In one embodiment, the retaining ring 38 and release member may be used together to prevent unwanted puncture of the container comprising the extraction buffer. In one embodiment, the retaining ring 38 comprises a first safety device to prevent unwanted release of the extraction buffer from the container comprising the extraction buffer. In one embodiment, the release member comprises a second safety device to prevent unwanted release of the extraction buffer. In this embodiment, the second safety device is disarmed by putting the lid onto the fluid collection tube 30 and/or string holding cup 28. In one embodiment, the first and/or second safety device may be disarmed to cause release of the extraction buffer from the container comprising the extraction buffer and/or lid comprising the extraction buffer, for example, during centrifugation.
With reference to
There is also provided a method of providing a structure at the distal end of the string 2 of the apparatus of
There is also provided a method of determining the presence of a substance within a patient using the apparatus of
The method may comprise the step of absorbing a component following insertion into the oesophagus of a patient. In one embodiment, when the string has been inserted into the oesophagus of a patient, the string absorbs a protein such as eosinophilic cationic protein (ECP). ECP is known to be a marker for the condition eosinophilic esophagitis (EoE), such that the detection of this protein may indicate that the patient is suffering from this condition and falling ECP levels indicate response to treatment.
Segments of the string may be analysed separately following removal of the string from the oesophagus of a patient. In one embodiment, the method may comprise the step of providing an interval marker on the string. In one embodiment, the interval marker may comprise an ink or dye. In another embodiment, the interval marker may comprise at least one knot provided on the string. Typically, following removal of the string from a patient, the string may be cut at the intervals shown by the interval markers and individual segments may be analysed separately.
In one embodiment, the method comprises the step of coating the string with a substance that will provide a stimulus to the oesophageal lining of the patient. In one embodiment, the string may be coated with a substance that will provoke an inflammatory response by the oesophageal lining of the patient. Typically, the substance that provides a stimulus will interact with other biological mediators that are released in response. Typically, the method comprises the step of coating the string with a biological substance, a chemical substance or a food. In one embodiment, the method comprises the step of coating the string with a cytokine, a weak acid or alkaline substance or a food, such as a whole food or a food component. In one embodiment, the method comprises the step of coating the string with whole milk. In another embodiment, the method comprises the step of coating the string with ovalbumin. In one embodiment, the method comprises the step of marking the string using a dye or providing a knot within the string to act as a marker. In this embodiment, string segments on either side of the stimulus can be removed (e.g. cut out) and biological components of inflammation measured as indicated above (see Adaption 3). In the embodiment wherein the provoking stimulus is applied to the string, the method comprises the step of coating the section of the string provided with the stimulus with a protective film to protect the stimulus from being washed away during the swallowing process. In this embodiment, the protective film comprises a dissolvable substance such as gelatine, wherein the dissolvable substance will dissipate once in place to reveal the stimulus.
The method further comprises the step of analysing the string following removal from the oesophagus of the patient to check for any biological components that may have bound to the string when it was inserted in the patient.
The method comprises the step of using a string capture rod 12 to transfer the string following removal from a patient to a string collection apparatus. Advantageously, the use of a string transfer rod to transfer the string minimises sample contamination and reduces user risk. The string is wound around the outer surface of the cylindrical element 18 of the string capture rod. The user then slides the guard element 20 of the string capture rod along the longitudinal axis of the string capture rod such that the string is pushed along the cylindrical element and into an appropriate container for transfer to the laboratory.
The string 2 is transferred from the string capture rod 12 to a string collection apparatus 14 comprising a string holding cup 28. The string holding cup 28 holds the string 2 after removal from the oesophagus of a patient. The user transfers the string from the patient to the string holding cup 28 via the string capture rod 12.
The method further comprises the step of providing a fluid collection tube 30 which is dimensioned to hold the string holding cup 28.
The method further comprises the step of providing a string extraction apparatus 16 to assist in extracting the biological marker from the string. The method comprises the step of providing a cap 36 comprising a retaining ring 38, wherein the retaining ring 38 engages with a container 40 comprising an extraction buffer. The string extraction apparatus 16 engages with the string collection apparatus 14 during centrifugation. Prior to centrifugation, the string 2 is placed within the string holding cup 28 of the string collection apparatus 14 and the string collection apparatus 14 and string extraction apparatus 16 are placed within a centrifuge tube.
During centrifugation, the spike 44 of the piercing device 42 punctures the container 40 comprising the extraction buffer. The extraction buffer is then transferred into the string holding cup 28, washes over the string 2 and passes through the at least one hole 27 provided within the base of the string holding cup 28. Typically, as the extraction buffer washes over the string it causes a biological component such as a protein that has bound to the string to be removed. The biological component passes into the fluid collection tube where it can then be taken for further tests in the laboratory.
The string holding cup 28 and the fluid collection tube 30 are placed within a centrifuge tube. In one embodiment, the centrifuge tube is a 15 ml centrifuge tube. The adhesive patient identifier can be removed from the string and placed on the outer surface of the centrifuge tube. During centrifugation, the perforations 27 in the string holding cup allow fluid released from the string to be collected at the bottom of the fluid collection tube 30. Following centrifugation the string holding cup 28 can be removed from the fluid collection tube 30 and the fluid can be analysed in a laboratory.
There is also provided a method of administering a drug to a patient using apparatus comprising a string as shown in
There is also provided a method of removing a substance from apparatus comprising a string 2 as shown in
The method comprises the step of placing a string after removal from the oesophagus of a patient into a string collection apparatus as shown in
The act of centrifugation forces the spike 44 to puncture the container 40 comprising the extraction buffer and to release the extraction buffer onto the string.
The forces applied to the system during centrifugation force the container 40 holding the extraction buffer past the retaining ring 38 onto the spike 44 of the piercing device 42. The extraction buffer is released and passes through the at least one hole 48 provided within the piercing device 42 and onto the string 2 that is held within the string holding container 28.
In another embodiment, the extraction buffer may be held within a container comprising a valve that is normally in the closed position. In this embodiment, the force applied to the system during centrifugation causes the valve to open, thus releasing the elution buffer from the container and onto the string.
In another embodiment, the piercing sits within the container holding the extraction buffer and is activated by the g forces that are applied to the system during centrifugation.
In use, the distal end of a string 2 is adapted by soaking the string in a solution comprising, for example, 1% corn starch. The distal end 6 of the string is wound around the outer surface of a metal rod and allowed to dry. Once the string has dried, a protein such as eosinophilic cationic protein (ECP) is applied to the distal end of the string. The string is inserted into the oesophagus of a patient. Advantageously, the provision of the structure provided at the distal end of the string assists in the patient swallowing the string.
The proximal end 4 of the string comprises a structure such as a knotted portion of the string to facilitate attachment of the string to the cheek of a patient. The string may be attached to the patient using medical grade tape. A patient identifier may be added to the proximal end of the string.
The string 2 is then removed from the oesophagus of the patient and transferred to a fluid collection apparatus 14 using a string capture rod 12. The string is wound around the outer surface of the cylindrical element 18 of the string capture rod 12 and the user slides a guard element 20 along the longitudinal length of the cylindrical element 18 to push the string into a string holding cup 28. The string holding cup is held within a fluid collection tube 30.
The string extraction apparatus 16 is placed adjacent to the string collection apparatus 14 and both the string extraction apparatus and the string collection apparatus are placed into a centrifugation tube. The cap of the string extraction apparatus 16 comprises a retaining ring 28 which is adjacent to a container 40 comprising an extraction buffer. A piercing device 42 is positioned adjacent the container comprising the extraction buffer. Prior to centrifugation, the piercing device does not engage the container comprising the extraction buffer. During centrifugations, the forces applied to the system cause the piercing device to puncture the container comprising the extraction buffer. The extraction buffer passes into the string holding cup 28 and washes over the string and through the holes 27 provided in the string holding cup 28. The fluid then passes into the fluid collection tube for further analysis in a laboratory. A neutralisation buffer may be provided within the fluid collection tube to neutralise the extraction buffer, if required.
A DNA and/or RNA stabilising buffer may be used to reduce and/or prevent degradation of the sample prior to analysis. In one embodiment, the DNA and/or RNA stabilising buffer may comprise a TE buffer comprising 10 mM Tris (pH 8.0) with HCl and 1 mM EDTA. Advantageously, the addition of DNA and/or RNA stabilising agents to a sample may prevent contaminants in the saliva of a patient from breaking down nucleotides. In addition, the use of DNA and/or RNA stabilising agents in a buffer can help to stabilise a sample until it can be processed.
In a further embodiment, protein stabilising agents may be added to the buffer, such as protease inhibitors and/or metal chelators. Advantageously, the use of a protein stabilising agent may prevent degradation prior to analysis, and/or may assist in stabilising a sample where specific protein analysis may be needed.
In another embodiment, enzymes may be added to a buffer to remove free DNA and/or RNA that may act as a contaminant.
Preferably, the use of a DNA and/or RNA stabilising buffer and/or protein stabilising agent may assist in stabilising the sample prior to testing in a laboratory.
Advantageously, the use of a DNA and/or RNA stabilising buffer and/or protein stabilising agent may assist in stabilising a saliva sample prior to testing in a laboratory, thus improving the performance of the test.
Typically, the string may be analysed following insertion into a patient to determine whether the distal end of the string has entered the stomach of the patient. Typically, following removal of the string from a patient, the chemical composition of the distal end of the string is analysed. In one embodiment, the pH of the distal end of the string may be analysed, for example using a pH indicator dye or paper. Typically, if the distal end of the string has been present in the stomach of the patient, the pH of the distal end of the string will be acidic, due to the acidic nature of the stomach. In another embodiment, following removal of the string from a patient, the distal end of the string may be analysed to test for other stomach markers such as pepsin or gastrokines. It is preferred that the pH indicator and/or stomach markers are provided with the kit of the invention.
Preferably, a string capture rod may be used to transfer the string following removal from a patient to a string collection apparatus. Advantageously, the use of a string transfer rod to transfer the string minimises sample contamination and reduces user risk. Preferably, the string is wound around the outer surface of the cylindrical element of the string capture rod. Preferably, the user then slides the guard element of the string capture rod along the longitudinal axis of the string capture rod such that the string is pushed along the cylindrical element and into an appropriate container, e.g. for transfer to the laboratory.
Preferably, the string is transferred from the string capture rod to a string collection apparatus comprising a string holding cup. Preferably, the string holding cup holds the string after removal from the oesophagus of a patient. Preferably, the user transfers the string from the patient to the string holding cup via the string capture rod.
A string removal means, such as a thimble like element, may be used to assist in removal of the string from the string capture element. Preferably, as the string capture rod passes through the hole in the string removal means, the string is removed from the surface of the string capture rod. Preferably, the string capture rod is inserted through the cylindrical portion of the guard element. Preferably, the string capture rod is passed through the hole provided in the upper surface of the string removal means. Preferably, the string removal means is housed within the recess of the guard element. Preferably, the string capture rod is withdrawn into the guard element and then pushed forwards such that the string removal means is placed into the string holding cup. Preferably, the string removal means is held within the string holding cup and the string capture rod is removed from the string removal means. Typically, the perforations in the string removal means allow buffer to pass through the perforations in the string removal means and onto the string.
A string holder may be used comprising a disc region comprising a front conical projection onto which the string is wound and a rear cylinder where the remaining string is wrapped. Typically, the disc region comprises a flexible material. Advantageously, the string holder may be used to preserve the shape and integrity of the coil provided at the proximal end of the string. Typically, the string is coiled around the string holder and then placed in a sealed package until ready for use. Advantageously, the provision of a sealed package allows the string to be kept sterile. Typically, once removed from the packaging the string is unwound from the rear cylinder and the distal end of the string is fixed to the check of a patient as described above. Preferably, the string which is wound around the front conical projection remains in place until the patient is ready to swallow the string. Typically, at this point, gentle squeezing of the outer edge of the string holder compresses the conical holder, thus reducing the diameter of the holder and allowing the string to be removed therefrom. Typically, the released coil of string can then be placed in the mouth of the patient and swallowed. Typically, following use, the string holder may be discarded. Typically, the string holder comprises a plastics material. Typically, the plastics material is smooth, stiff and flexible. In one embodiment, a robot may be used to wrap the string around the string holder and seal the string holder in a package.
In one embodiment, the string holder may also comprise a string capture rod. Advantageously, combining the string transport device and string collection device allow for the provision of a dual purpose unit. In this embodiment, the string can be captured and then stored using one unit. This embodiment can be used to store and transport the string but can also be used to collect the string once used and dispense into the tube with the centrifuge activated device.
A fluid collection tube may then be used which is dimensioned to hold the string holding cup.
Preferably, a string extraction apparatus may be used to assist in extracting the marker from the string. Preferably, the cap may comprise a retaining ring, wherein the retaining ring engages with a container comprising an extraction buffer. Preferably, the string extraction apparatus engages with the string collection apparatus during centrifugation. Preferably, prior to centrifugation, the string is placed within the string holding cup of the string collection apparatus and the string collection apparatus and string extraction apparatus are placed within a centrifuge tube.
Preferably, the spike of the piercing device punctures the container comprising the extraction buffer during centrifugation. Typically, the extraction buffer is then transferred into the string holding cup, washes over the string and passes through the at least one hole provided within the base of the string holding cup. Typically, as the extraction buffer washes over the string it causes a component such as a protein that has bound to the string to be removed. Preferably, the component passes into the fluid collection tube where it can then be taken for further tests in the laboratory.
In one embodiment, the lid may comprise an extraction buffer. In this embodiment, when the lid is placed over the string holding cup and/or fluid collection tube, a release mechanism provided within or adjacent to the lid causes the lid to be punctured, thus removing the extraction buffer from the lid such that it passes over the string within the string holding cup and into the fluid collection tube.
In one embodiment, the lid may comprise a bottle, wherein the bottle may be standardised for use in a centrifuge. Preferably, the bottle may be used in combination with a string holding cup. Preferably, the bottle comprises an extraction buffer. Preferably, the bottle further comprises a stopper and seal. Preferably, the stopper is pierced with a piercing device to release buffer from the buffer and into the string holding cup, wherein the string is held within the string holding cup.
Preferably, the string holding cup and the fluid collection tube are placed within a centrifuge tube. Preferably, the centrifuge tube is a 15 ml centrifuge tube. Preferably, the adhesive patient identifier can be removed from the proximal end of the string and placed on the outer surface of the centrifuge tube. Preferably, during centrifugation, the perforations in the string collection cup allow fluid released from the string to be collected at the bottom of the fluid collection tube. Preferably, following centrifugation the string collection cup can be removed from the fluid collection tube and the fluid can be analysed in a laboratory.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1818843.3 | Nov 2018 | GB | national |
| 1903657.3 | Mar 2019 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2019/053272 | 11/19/2019 | WO | 00 |
