CA2499808A1 - Microdialysis probe with a spiral line - Google Patents
Microdialysis probe with a spiral line Download PDFInfo
- Publication number
- CA2499808A1 CA2499808A1 CA002499808A CA2499808A CA2499808A1 CA 2499808 A1 CA2499808 A1 CA 2499808A1 CA 002499808 A CA002499808 A CA 002499808A CA 2499808 A CA2499808 A CA 2499808A CA 2499808 A1 CA2499808 A1 CA 2499808A1
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- Prior art keywords
- probe
- support body
- membrane
- probe needle
- spiral
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
- A61B5/14525—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using microdialysis
- A61B5/14528—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using microdialysis invasively
Abstract
The invention relates to a microdialysis probe with a probe body, a probe needle for introduction into a tissue, an inlet line and an outlet line for a perfusion solution and a dialysis membrane, comprising at least one hollow channel which forms the outlet for the perfusion solution and which runs at least partly spirally about the probe needle on an external surface of the probe needle. The inlet for the perfusion solution is also preferably embodied with a spiral form about an external surface of the probe needle.
Description
wo 2004/033000 PCT/EP2003/010534 Microdialysis probe with a spiral line The present invention relates to a microdialysis probe, in particular a microdialysis probe for measuring the concentration of a dissolved substance in a tissue.
Microdialysis probes generally comprise a probe body and an injection needle as probe needle for introduction into, for example, a human or animal tissue, the probe needle being completely surrounded by the tissue. The probe needle comprises an inlet line and an outlet line for a perfusion solution. Moreover, in one area of the line for the perfusion solution, a dialysis membrane is arranged which is in contact with the tissue environment. Between the tissue environment and the perfusion solution, the concentration of permeable substances dissolved in the tissue is equalized along the membrane surface.
A conventional microdialysis probe has, for example, a coaxial structure. Two hollow cylinders are arranged one inside the other, the inner hollow cylinder serving as an inlet line for the perfusion solution which, at a transition area in a distal end portion of the probe needle, passes into the area between the inner cylinder and the outer cylinder and is conveyed back within this annular channel. The dialysis membrane can, for example, be arranged in a front area where the perfusion solution turns back or, alternatively, it can form part of the outer hollow cylinder. Microdialysis probes of this type have the disadvantage that the perfusion solution comes into contact with the tissue environment only across a small membrane surface and, at most, across the length of the probe needle, and that a membrane hollow fiber acting as outer cylinder is exposed to the pressure of the tissue, and the outlet line can therefore become blocked. Moreover, in the case of a short probe needle, there is often not enough time left to obtain a complete concentration equalization. By contrast, a long probe needle is unpleasant for the user. With a straight return of the perfusion solution, the flow velocity is too high to permit all of the desired concentration equalization.
Moreover, DE 199 37 099 A1 discloses microdialysis probes in which the inlet line and outlet line for a perfusion solution are arranged next to one another.
For this purpose, two mutually adjacent tubes, for example, are provided which have a flow transfer area for the perfusion solution. It is also possible to arrange, inside a microdialysis membrane in the form of a hollow fiber, a support structure which divides the hollow fiber into different hollow channels, again with the possibility of a flow transfer between the channels being provided. Here too, the inlet line and outlet line have a straight course, with the result that concentration equalization is in some cases not optimal.
The object of the present invention is to make available a microdialysis probe which is comfortable for the user, is easy to produce, has a perfusion solution flow profile optimized for concentration equalization, and has an improved arrangement of the dialysis surface.
The present invention is achieved by the characterizing part of patent claim 1. Advantageous embodiments of the invention are set out in the dependent claims.
Accordingly, in a microdialysis probe with a probe body, and with a probe needle for introduction into a tissue, comprising an inlet line and an outlet line for a perfusion solution, and a dialysis membrane, at least the outlet line of the perfusion solution is formed by a hollow channel which runs at least partly in a spiral formation or helical formation about the probe needle on an outer circumference of said probe needle. The spiral part of the hollow channel preferably extends from a distal end portion of the probe needle, with the needle tip, to the probe body from which the probe needle emerges. The entire hollow channel for the outlet line is preferably provided with a dialysis membrane on its surface facing out from the probe needle. In this way, concentration equalization can take place along the entire length of the spiraling hollow channel. Compared to the prior art with straight lines, the spiral shape of the channel greatly increases the overall length of the outlet line of the perfusion solution, although the length of the needle remains unchanged. In this way, the dwell time of the perfusion solution inside the tissue is considerably lengthened, and its contact surface with the tissue environment is greatly increased.
In a microdialysis probe according to the invention, a hollow channel for the inlet line of the perfusion solution can run inside the probe needle, that is to say right through the spiral hollow channel of the outlet line and as far as the tip of the probe needle.
To form a probe needle of this kind, a cylindrical plastic element with a central bore can be provided, for example, said element having a bore which leads to the outer circumference surface and which opens into the spiral outlet line running around the plastic body.
In a preferred embodiment of the invention, alongside the spiral hollow channel for the outlet line, another spiral hollow channel is provided for the inlet line of the perfusion solution. The two hollow channels for the inlet line and the outlet line run into one another in a reverse turn area at the distal end portion of the probe needle. In this case, a dialysis membrane is preferably provided both on the surface of the spiral inlet line facing out from the probe needle and also that of the spiral outlet line. In principle, it is a possible to provide the dialysis membrane only in some areas of the probe needle. However, it is advantageous for the dialysis membrane to be arranged along the entire length of the hollow channels.
The dialysis membrane can, for example, be a hollow fiber which at the same time forms the hollow channel for the outlet line, and possibly also the inlet line.
The use of a membrane hollow fiber has the advantage that, inside the tissue, no transitions between the material of the membrane and the material of the needle are required. Both the inlet line and the outlet line are preferably formed by a single membrane hollow fiber which makes a reverse turn in a distal end portion of the probe tip.
To form the probe needle, an elongate support body or a frame can be used on which the membrane fiber is arranged in the manner according to the invention. The inlet line in the form of the hollow fiber can be routed through the middle area of the support body or frame and can emerge from the support body only at the distal end portion of the support body and run back in a spiral formation around the support body to the probe housing. It is preferable, however, for the inlet line also to run in a spiral formation around the outside of the probe needle or support body to the distal end portion of the needle. At the end portion, the hollow fiber membrane reverses and runs in a spiral formation, in the spaces between the inlet channel, back to the probe housing and thus forms the outlet line of the perfusion liquid. For this purpose, the probe needle is preferably formed by a cylindrical support body which, on its outer circumference surface, has at least one recess which is open to the outside in the form of a depression and which runs in a spiral formation around at least part of the support body, but preferably along the entire length of said support body. In the case of a support body designed like this, a membrane hollow a fiber can be embedded in the depression. For this purpose, the depressions are preferably as deep as the external diameter of the membrane hollow fiber. In this way, the membrane hollow fiber is flush with the surface of the support body and is not exposed to a pressure exerted by the tissue. It is also possible, however, for the depressions to be made less deep so that part of the membrane hollow fiber protrudes above the circumference surface of the support body, as a result of which the dialysis surface can be increased in size.
It is also possible for a dialysis membrane in the form of a hollow fiber to be tucked over a cylindrical support body with a spiral recess for the inlet and outlet line, this dialysis membrane having an internal diameter approximately the same as the external diameter of the support body. At least those areas of the support body having the recess should be covered by the hollow fiber membrane. The hollow fiber membrane can, for example, be secured on the circumference surfaces of the support body which lie between the depressions. For this purpose, it is possible to use an adhesive agent or glue for example. The space between the tucked-over hollow fiber and the recess then forms the hollow channel at least for the inlet line of the perfusion solution, but preferably also for the outlet line of the perfusion solution. If the membrane hollow fiber is closed off in an area of the tip, that is to say if it forms a kind of membrane sock, then, in this embodiment too, there are no transitions at all between the material of the membrane and the material of the probe needle inside the tissue.
In a further embodiment of a microdialysis probe according to the present invention having a cylindrical support body with a spiral recess or depressions, a dialysis membrane in the form of a membrane layer or a membrane sheet is wound about the outer circumference 6 a of the support body. The abutting edges of the membrane layer are sealed tight, and the membrane layer is secured in the areas between the recess on the circumference surface of the support body. In this way, the hollow channels for the outlet line and inlet line of the perfusion solution are again obtained between the membrane layer and the recess. In the last two embodiments described, the dialysis surface corresponds to the width of one recess times the length of the spiral depression. The perfusion solution can make contact with the tissue environment along the entire length of the probe needle inside the tissue.
When applying the dialysis membrane, it must be generally noted that it swells in a moist environment and its surface thus increases in size. This must be taken into account particularly if the membrane is secured across relatively large surface areas or if its diameter has to be adapted to the diameter of the support body.
In one embodiment in which both the inlet line and also the outlet line run in a spiral formation about the probe needle, these form a kind of double helix. The pitch of the spiral has to be adapted to a desired flow velocity or to a desired dwell time of the perfusion solution in the tissue. A support body which forms the probe needle can, for example, be made of various plastics such as liquid-crystalline polymers, polybutylene terephthalate (PBT), or also of PE or PET.
Such materials can be worked by inj ection molding, for example. During the actual production of a cylindrical blank for the support body, depressions for the inlet and outlet lines can be formed in said blank, or they can be provided in said blank at a later stage by means of finishing work such as milling, cutting or etching.
The area forming the distal end portion of such a cylindrical support body or frame is generally cut obliquely in order to form a tip for introduction into _ 7 _ a tissue. The distal end portion of the support body is preferably beveled in such a way that the user experiences minimal pain and the tissue environment is minimally changed, such as is described, for example, in the patent application entitled "Injection needle tip" filed by the Applicant of the present application and bearing the same application date.
The probe needle of the microdialysis probe can be designed itself to pierce the skin. However, it is also possible to use an insertion aid for the probe needle.
This is especially advantageous when wide areas of the membrane are arranged unprotected on the surface of the support body.
According to the invention, it is in principle also possible to provide several spiraling inlet lines and/or outlet lines alongside one another on the outer circumference of the probe needle.
With a microdialysis probe having the design according to the invention, the path along which the perfusion solution is in contact with the tissue environment is lengthened, without thereby having to make the probe needle longer. Conversely, it is possible to produce the same length of line, but on a shorter probe needle.
This makes a microdialysis probe more comfortable for the user. Since, compared to an outlet line taking up the entire diameter of the probe needle, the lines according to the invention have a relatively small diameter, the ratio of surface to volume is improved, with the result that more perfusion liquid can come into contact with an outside surface of the dialysis membrane and, consequently, with the tissue environment.
The invention is explained in more detail on the basis of illustrative embodiments, which are to be understood as non-limiting, and with reference to the drawing, in g _ which:
Figure 1 shows a perspective view of a first embodiment of a probe needle according to the invention with a spiral inlet and outlet line, and Figure 2 shows a perspective view of a second embodiment of the present invention, with a spiral outlet line and a rectilinear inlet line.
In Figure 1, a cylindrical support body (1) or frame is shown which forms a probe needle for a microdialysis probe. In a starting area of the support body inserted into a probe body, a recess or depression (3) begins which initially runs in the longitudinal direction of the support body (1), on the outer surface thereof. In a middle area (4) of the support body, the depression (3) merges into a spiral course. The spiral course extends to just before a distal end portion (2) of the support body (1) and forms, to that point, the depression for an inlet line of a perfusion solution.
Before the distal end portion (2), the depression (3) makes a reverse turn (5) and extends from there in a spiral formation between the first spiral course for the inlet line and back to the starting area of the support body (1), thereby forming the depression for the outlet line of the perfusion liquid. In this way, two interlaced spiral courses are obtained, that is to say a kind of double helix.
A membrane hollow fiber, for example, can then be introduced into the course of the recess or depression (3), said membrane hollow fiber following the course of the depression, that is to say from a starting area of the support body (1) along the depression (3) through the area (4) and via the deflection (5) to the distal end portion (2) of the support body (1) and then back through the spiral area (4) to the starting area of the support body (1). It is also possible, as has been described above, for a membrane hollow fiber with an internal diameter corresponding approximately to the external diameter of the support body (1) to be tucked over the support body (1) and secured in the intermediate spaces of the surface between the depressions (3), in which case the inlet and outlet lines are formed by the depression closed off by the membrane. Finally, it is likewise possible, as has been described above, for a membrane layer or a membrane sheet to be wound around the support body (1) and connected at a seam. The support body (1) with the dialysis membrane applied to it then forms the totality of the probe needle and is inserted into a probe body from which the perfusion solution is conveyed into/withdrawn from the inlet/outlet line.
Figure 2 shows a further embodiment of a microdialysis probe according to the invention with a cylindrical support body (1) which likewise has a spiral recess or depression (3) on its outer surface. This depression is provided for the outlet line of the perfusion solution.
As the inlet line of the perfusion solution, a rectilinear hollow channel (6) is provided in a middle area of the support body (1) along the longitudinal axis of the support body, which hollow channel (6) runs from a starting area of the support body (1) to just before the distal end portion (2) of the support body.
Just before the end portion (2), the hollow channel (6) is deflected in the direction of the outer circumference surface of the support body (1) so that it emerges from the outer circumference surface and forms the reverse turn (5). The outlet opening of the rectilinear hollow channel opens out into the spiral depression (3). In this way, a continuous hollow channel can, on the one hand, form the inlet line running from a starting area of the support body to its distal end portion (2) and, on the other hand, can form the outer spiraling outlet line back to the starting area of the support body (1).
In the illustrative embodiment shown in Figure 2, a membrane hollow fiber (7) closed at the tip (1) and in the form of a membrane sock is arranged over the support body (1). The membrane hollow fiber has an internal diameter slightly greater than the external diameter of the support body (1). The membrane hollow fiber (7) is secured in the intermediate areas (8) between the spiral course of the depression on the support body (1), as a result of which a hollow channel for the outlet line of the perfusion solution is formed between the membrane hollow fiber and the support body.
In the example shown, the support body (1) is completely enclosed by the dialysis membrane. When such a probe needle is inserted, there are no transition points between the material of the membrane and the material of the support body within the tissue.
The probe needle made up of support body (1) and membrane hollow fiber (7) is attached to a probe body (9) from which the inlet line is supplied with perfusion solution and into which the perfusion solution is returned via the outlet line after the concentration equalization.
In principle, it is also possible to choose, for the probe tip, a support body which has no depressions for forming the lines or for receiving a membrane hollow fiber. A hollow fiber membrane can be wound in a spiral formation around a smooth cylindrical support body of this kind and can be secured at certain intervals to the support body by means of an adhesive agent. When a probe needle of this kind is located in the tissue, the pressure of the perfusion solution within the lines must be great enough to withstand the external pressure exerted by the tissue and thus ensure that the line is not closed.
To configure a dialysis membrane in the spiral fashion described here, it is possible, for example, to employ a method as described in the patent application entitled "Microdialysis probe and method for the production thereof" which is from the same Applicant as the present invention and bears the same application date. In said method, the dialysis membrane first lies on a shaping means and is brought into a predetermined shape by bending or forming of the shaping means. An adhesive agent or a connecting means such as adhesive cement or glue is then applied at least partially to a bending point of the dialysis membrane, so that the membrane is maintained in the predetermined shape.
After the adhesive agent has been applied, the shaping means is removed from the dialysis membrane. The shaping means can be a filament which is pulled through the hollow fiber membrane. The shape is defined by the spiral course of the microdialysis membrane according to the invention.
The invention has been described by way of illustration on the basis of different embodiments; the embodiments shown are not intended to limit the scope of the invention, and modifications and refinements are to be considered as belonging to the invention.
List of reference numbers (1) support body (2) distal end portion (3) depression (4) spiral area (5) reverse turn (6) rectilinear hollow channel (7) membrane hollow fiber (8) intermediate area (9) probe body
Microdialysis probes generally comprise a probe body and an injection needle as probe needle for introduction into, for example, a human or animal tissue, the probe needle being completely surrounded by the tissue. The probe needle comprises an inlet line and an outlet line for a perfusion solution. Moreover, in one area of the line for the perfusion solution, a dialysis membrane is arranged which is in contact with the tissue environment. Between the tissue environment and the perfusion solution, the concentration of permeable substances dissolved in the tissue is equalized along the membrane surface.
A conventional microdialysis probe has, for example, a coaxial structure. Two hollow cylinders are arranged one inside the other, the inner hollow cylinder serving as an inlet line for the perfusion solution which, at a transition area in a distal end portion of the probe needle, passes into the area between the inner cylinder and the outer cylinder and is conveyed back within this annular channel. The dialysis membrane can, for example, be arranged in a front area where the perfusion solution turns back or, alternatively, it can form part of the outer hollow cylinder. Microdialysis probes of this type have the disadvantage that the perfusion solution comes into contact with the tissue environment only across a small membrane surface and, at most, across the length of the probe needle, and that a membrane hollow fiber acting as outer cylinder is exposed to the pressure of the tissue, and the outlet line can therefore become blocked. Moreover, in the case of a short probe needle, there is often not enough time left to obtain a complete concentration equalization. By contrast, a long probe needle is unpleasant for the user. With a straight return of the perfusion solution, the flow velocity is too high to permit all of the desired concentration equalization.
Moreover, DE 199 37 099 A1 discloses microdialysis probes in which the inlet line and outlet line for a perfusion solution are arranged next to one another.
For this purpose, two mutually adjacent tubes, for example, are provided which have a flow transfer area for the perfusion solution. It is also possible to arrange, inside a microdialysis membrane in the form of a hollow fiber, a support structure which divides the hollow fiber into different hollow channels, again with the possibility of a flow transfer between the channels being provided. Here too, the inlet line and outlet line have a straight course, with the result that concentration equalization is in some cases not optimal.
The object of the present invention is to make available a microdialysis probe which is comfortable for the user, is easy to produce, has a perfusion solution flow profile optimized for concentration equalization, and has an improved arrangement of the dialysis surface.
The present invention is achieved by the characterizing part of patent claim 1. Advantageous embodiments of the invention are set out in the dependent claims.
Accordingly, in a microdialysis probe with a probe body, and with a probe needle for introduction into a tissue, comprising an inlet line and an outlet line for a perfusion solution, and a dialysis membrane, at least the outlet line of the perfusion solution is formed by a hollow channel which runs at least partly in a spiral formation or helical formation about the probe needle on an outer circumference of said probe needle. The spiral part of the hollow channel preferably extends from a distal end portion of the probe needle, with the needle tip, to the probe body from which the probe needle emerges. The entire hollow channel for the outlet line is preferably provided with a dialysis membrane on its surface facing out from the probe needle. In this way, concentration equalization can take place along the entire length of the spiraling hollow channel. Compared to the prior art with straight lines, the spiral shape of the channel greatly increases the overall length of the outlet line of the perfusion solution, although the length of the needle remains unchanged. In this way, the dwell time of the perfusion solution inside the tissue is considerably lengthened, and its contact surface with the tissue environment is greatly increased.
In a microdialysis probe according to the invention, a hollow channel for the inlet line of the perfusion solution can run inside the probe needle, that is to say right through the spiral hollow channel of the outlet line and as far as the tip of the probe needle.
To form a probe needle of this kind, a cylindrical plastic element with a central bore can be provided, for example, said element having a bore which leads to the outer circumference surface and which opens into the spiral outlet line running around the plastic body.
In a preferred embodiment of the invention, alongside the spiral hollow channel for the outlet line, another spiral hollow channel is provided for the inlet line of the perfusion solution. The two hollow channels for the inlet line and the outlet line run into one another in a reverse turn area at the distal end portion of the probe needle. In this case, a dialysis membrane is preferably provided both on the surface of the spiral inlet line facing out from the probe needle and also that of the spiral outlet line. In principle, it is a possible to provide the dialysis membrane only in some areas of the probe needle. However, it is advantageous for the dialysis membrane to be arranged along the entire length of the hollow channels.
The dialysis membrane can, for example, be a hollow fiber which at the same time forms the hollow channel for the outlet line, and possibly also the inlet line.
The use of a membrane hollow fiber has the advantage that, inside the tissue, no transitions between the material of the membrane and the material of the needle are required. Both the inlet line and the outlet line are preferably formed by a single membrane hollow fiber which makes a reverse turn in a distal end portion of the probe tip.
To form the probe needle, an elongate support body or a frame can be used on which the membrane fiber is arranged in the manner according to the invention. The inlet line in the form of the hollow fiber can be routed through the middle area of the support body or frame and can emerge from the support body only at the distal end portion of the support body and run back in a spiral formation around the support body to the probe housing. It is preferable, however, for the inlet line also to run in a spiral formation around the outside of the probe needle or support body to the distal end portion of the needle. At the end portion, the hollow fiber membrane reverses and runs in a spiral formation, in the spaces between the inlet channel, back to the probe housing and thus forms the outlet line of the perfusion liquid. For this purpose, the probe needle is preferably formed by a cylindrical support body which, on its outer circumference surface, has at least one recess which is open to the outside in the form of a depression and which runs in a spiral formation around at least part of the support body, but preferably along the entire length of said support body. In the case of a support body designed like this, a membrane hollow a fiber can be embedded in the depression. For this purpose, the depressions are preferably as deep as the external diameter of the membrane hollow fiber. In this way, the membrane hollow fiber is flush with the surface of the support body and is not exposed to a pressure exerted by the tissue. It is also possible, however, for the depressions to be made less deep so that part of the membrane hollow fiber protrudes above the circumference surface of the support body, as a result of which the dialysis surface can be increased in size.
It is also possible for a dialysis membrane in the form of a hollow fiber to be tucked over a cylindrical support body with a spiral recess for the inlet and outlet line, this dialysis membrane having an internal diameter approximately the same as the external diameter of the support body. At least those areas of the support body having the recess should be covered by the hollow fiber membrane. The hollow fiber membrane can, for example, be secured on the circumference surfaces of the support body which lie between the depressions. For this purpose, it is possible to use an adhesive agent or glue for example. The space between the tucked-over hollow fiber and the recess then forms the hollow channel at least for the inlet line of the perfusion solution, but preferably also for the outlet line of the perfusion solution. If the membrane hollow fiber is closed off in an area of the tip, that is to say if it forms a kind of membrane sock, then, in this embodiment too, there are no transitions at all between the material of the membrane and the material of the probe needle inside the tissue.
In a further embodiment of a microdialysis probe according to the present invention having a cylindrical support body with a spiral recess or depressions, a dialysis membrane in the form of a membrane layer or a membrane sheet is wound about the outer circumference 6 a of the support body. The abutting edges of the membrane layer are sealed tight, and the membrane layer is secured in the areas between the recess on the circumference surface of the support body. In this way, the hollow channels for the outlet line and inlet line of the perfusion solution are again obtained between the membrane layer and the recess. In the last two embodiments described, the dialysis surface corresponds to the width of one recess times the length of the spiral depression. The perfusion solution can make contact with the tissue environment along the entire length of the probe needle inside the tissue.
When applying the dialysis membrane, it must be generally noted that it swells in a moist environment and its surface thus increases in size. This must be taken into account particularly if the membrane is secured across relatively large surface areas or if its diameter has to be adapted to the diameter of the support body.
In one embodiment in which both the inlet line and also the outlet line run in a spiral formation about the probe needle, these form a kind of double helix. The pitch of the spiral has to be adapted to a desired flow velocity or to a desired dwell time of the perfusion solution in the tissue. A support body which forms the probe needle can, for example, be made of various plastics such as liquid-crystalline polymers, polybutylene terephthalate (PBT), or also of PE or PET.
Such materials can be worked by inj ection molding, for example. During the actual production of a cylindrical blank for the support body, depressions for the inlet and outlet lines can be formed in said blank, or they can be provided in said blank at a later stage by means of finishing work such as milling, cutting or etching.
The area forming the distal end portion of such a cylindrical support body or frame is generally cut obliquely in order to form a tip for introduction into _ 7 _ a tissue. The distal end portion of the support body is preferably beveled in such a way that the user experiences minimal pain and the tissue environment is minimally changed, such as is described, for example, in the patent application entitled "Injection needle tip" filed by the Applicant of the present application and bearing the same application date.
The probe needle of the microdialysis probe can be designed itself to pierce the skin. However, it is also possible to use an insertion aid for the probe needle.
This is especially advantageous when wide areas of the membrane are arranged unprotected on the surface of the support body.
According to the invention, it is in principle also possible to provide several spiraling inlet lines and/or outlet lines alongside one another on the outer circumference of the probe needle.
With a microdialysis probe having the design according to the invention, the path along which the perfusion solution is in contact with the tissue environment is lengthened, without thereby having to make the probe needle longer. Conversely, it is possible to produce the same length of line, but on a shorter probe needle.
This makes a microdialysis probe more comfortable for the user. Since, compared to an outlet line taking up the entire diameter of the probe needle, the lines according to the invention have a relatively small diameter, the ratio of surface to volume is improved, with the result that more perfusion liquid can come into contact with an outside surface of the dialysis membrane and, consequently, with the tissue environment.
The invention is explained in more detail on the basis of illustrative embodiments, which are to be understood as non-limiting, and with reference to the drawing, in g _ which:
Figure 1 shows a perspective view of a first embodiment of a probe needle according to the invention with a spiral inlet and outlet line, and Figure 2 shows a perspective view of a second embodiment of the present invention, with a spiral outlet line and a rectilinear inlet line.
In Figure 1, a cylindrical support body (1) or frame is shown which forms a probe needle for a microdialysis probe. In a starting area of the support body inserted into a probe body, a recess or depression (3) begins which initially runs in the longitudinal direction of the support body (1), on the outer surface thereof. In a middle area (4) of the support body, the depression (3) merges into a spiral course. The spiral course extends to just before a distal end portion (2) of the support body (1) and forms, to that point, the depression for an inlet line of a perfusion solution.
Before the distal end portion (2), the depression (3) makes a reverse turn (5) and extends from there in a spiral formation between the first spiral course for the inlet line and back to the starting area of the support body (1), thereby forming the depression for the outlet line of the perfusion liquid. In this way, two interlaced spiral courses are obtained, that is to say a kind of double helix.
A membrane hollow fiber, for example, can then be introduced into the course of the recess or depression (3), said membrane hollow fiber following the course of the depression, that is to say from a starting area of the support body (1) along the depression (3) through the area (4) and via the deflection (5) to the distal end portion (2) of the support body (1) and then back through the spiral area (4) to the starting area of the support body (1). It is also possible, as has been described above, for a membrane hollow fiber with an internal diameter corresponding approximately to the external diameter of the support body (1) to be tucked over the support body (1) and secured in the intermediate spaces of the surface between the depressions (3), in which case the inlet and outlet lines are formed by the depression closed off by the membrane. Finally, it is likewise possible, as has been described above, for a membrane layer or a membrane sheet to be wound around the support body (1) and connected at a seam. The support body (1) with the dialysis membrane applied to it then forms the totality of the probe needle and is inserted into a probe body from which the perfusion solution is conveyed into/withdrawn from the inlet/outlet line.
Figure 2 shows a further embodiment of a microdialysis probe according to the invention with a cylindrical support body (1) which likewise has a spiral recess or depression (3) on its outer surface. This depression is provided for the outlet line of the perfusion solution.
As the inlet line of the perfusion solution, a rectilinear hollow channel (6) is provided in a middle area of the support body (1) along the longitudinal axis of the support body, which hollow channel (6) runs from a starting area of the support body (1) to just before the distal end portion (2) of the support body.
Just before the end portion (2), the hollow channel (6) is deflected in the direction of the outer circumference surface of the support body (1) so that it emerges from the outer circumference surface and forms the reverse turn (5). The outlet opening of the rectilinear hollow channel opens out into the spiral depression (3). In this way, a continuous hollow channel can, on the one hand, form the inlet line running from a starting area of the support body to its distal end portion (2) and, on the other hand, can form the outer spiraling outlet line back to the starting area of the support body (1).
In the illustrative embodiment shown in Figure 2, a membrane hollow fiber (7) closed at the tip (1) and in the form of a membrane sock is arranged over the support body (1). The membrane hollow fiber has an internal diameter slightly greater than the external diameter of the support body (1). The membrane hollow fiber (7) is secured in the intermediate areas (8) between the spiral course of the depression on the support body (1), as a result of which a hollow channel for the outlet line of the perfusion solution is formed between the membrane hollow fiber and the support body.
In the example shown, the support body (1) is completely enclosed by the dialysis membrane. When such a probe needle is inserted, there are no transition points between the material of the membrane and the material of the support body within the tissue.
The probe needle made up of support body (1) and membrane hollow fiber (7) is attached to a probe body (9) from which the inlet line is supplied with perfusion solution and into which the perfusion solution is returned via the outlet line after the concentration equalization.
In principle, it is also possible to choose, for the probe tip, a support body which has no depressions for forming the lines or for receiving a membrane hollow fiber. A hollow fiber membrane can be wound in a spiral formation around a smooth cylindrical support body of this kind and can be secured at certain intervals to the support body by means of an adhesive agent. When a probe needle of this kind is located in the tissue, the pressure of the perfusion solution within the lines must be great enough to withstand the external pressure exerted by the tissue and thus ensure that the line is not closed.
To configure a dialysis membrane in the spiral fashion described here, it is possible, for example, to employ a method as described in the patent application entitled "Microdialysis probe and method for the production thereof" which is from the same Applicant as the present invention and bears the same application date. In said method, the dialysis membrane first lies on a shaping means and is brought into a predetermined shape by bending or forming of the shaping means. An adhesive agent or a connecting means such as adhesive cement or glue is then applied at least partially to a bending point of the dialysis membrane, so that the membrane is maintained in the predetermined shape.
After the adhesive agent has been applied, the shaping means is removed from the dialysis membrane. The shaping means can be a filament which is pulled through the hollow fiber membrane. The shape is defined by the spiral course of the microdialysis membrane according to the invention.
The invention has been described by way of illustration on the basis of different embodiments; the embodiments shown are not intended to limit the scope of the invention, and modifications and refinements are to be considered as belonging to the invention.
List of reference numbers (1) support body (2) distal end portion (3) depression (4) spiral area (5) reverse turn (6) rectilinear hollow channel (7) membrane hollow fiber (8) intermediate area (9) probe body
Claims (9)
1. A microdialysis probe with a probe body, and with a probe needle for introduction into a tissue, comprising an inlet line and an outlet line for a perfusion solution, and a dialysis membrane, at least the outlet line of the perfusion solution being formed by a hollow channel (4) which runs at least partly in a spiral formation about the probe needle (1) on an outer circumference of said probe needle (1).
2. The microdialysis probe as claimed in claim 1, characterized in that a hollow channel for the inlet line of the perfusion solution runs inside the probe needle (1) through the spiral hollow channel (4) of the outlet line.
3. The microdialysis probe as claimed in claim 1, characterized in that a hollow channel for the inlet line of the perfusion solution runs in a spiral formation on the outer circumference of the probe needle (1) alongside the hollow channel (4) for the outlet line.
4. The microdialysis probe as claimed in one of the preceding claims, characterized in that the dialysis membrane (7) is provided at least partly on a surface of the partly spiral hollow channel (4) facing out from the probe needle (1) for the inlet line and/or outlet line.
5. The microdialysis probe as claimed in one of the preceding claims, characterized in that the dialysis membrane (7) is a hollow fiber which forms at least the hollow channel (4) for the outlet line.
6. The microdialysis probe as claimed in one of the preceding claims, characterized in that the hollow channel (4) for the inlet line and the outlet line is formed by a single dialysis membrane (7) in the form of a hollow fiber which makes a reverse turn (5) in a distal end portion (2) of the probe tip.
7. The microdialysis probe as claimed in one of the preceding claims, characterized in that the probe needle (1) is formed by a cylindrical support body which, on its outer circumference surface, has at least one recess (3) which is open to the outside and which runs in a spiral formation around at least part of the support body.
8. The microdialysis probe as claimed in claim 6, characterized in that a dialysis membrane (7) in the form of a hollow fiber is tucked over the support body (1), at least in the area with the recess (3).
9. The microdialysis probe as claimed in claim 6, characterized in that a dialysis membrane in the form of a membrane layer is wound about the outer circumference of the support body (1), at least in the area with the recess (3).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10246207.0 | 2002-10-04 | ||
| DE10246207A DE10246207B4 (en) | 2002-10-04 | 2002-10-04 | Microdialysis probe with spiral line |
| PCT/EP2003/010534 WO2004033000A1 (en) | 2002-10-04 | 2003-09-22 | Microdialysis probe with a spiral line |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2499808A1 true CA2499808A1 (en) | 2004-04-22 |
Family
ID=32086842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002499808A Abandoned CA2499808A1 (en) | 2002-10-04 | 2003-09-22 | Microdialysis probe with a spiral line |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US20050277820A1 (en) |
| EP (1) | EP1545651A1 (en) |
| JP (1) | JP2006501909A (en) |
| AU (1) | AU2003280339A1 (en) |
| CA (1) | CA2499808A1 (en) |
| DE (1) | DE10246207B4 (en) |
| WO (1) | WO2004033000A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10246207B4 (en) * | 2002-10-04 | 2008-04-03 | Disetronic Licensing Ag | Microdialysis probe with spiral line |
| DE10247023B4 (en) | 2002-10-09 | 2006-07-20 | Disetronic Licensing Ag | Microdialysis probe and method for its production |
| JP4658656B2 (en) * | 2005-03-25 | 2011-03-23 | 雅之 北野 | Inspection probe and inspection method |
| GB2442209B (en) | 2006-09-28 | 2012-01-18 | Probe Scient Ltd | Molecular exchange device |
| GB2457469B (en) * | 2008-02-13 | 2012-11-07 | Probe Scient Ltd | Molecular exchange device |
| GB2457468B (en) | 2008-02-13 | 2012-11-21 | Probe Scient Ltd | molecular exchange device |
| US10251993B2 (en) | 2016-02-26 | 2019-04-09 | Feng Chen | Hemodialysis device |
| EA202191966A1 (en) * | 2019-03-05 | 2021-12-08 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | PENTACYCLIC HETEROCYCLIC COMPOUND |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4016863A (en) * | 1975-08-27 | 1977-04-12 | Brantigan John W | Tissue tonometer device for use in measuring gas in body tissue |
| DE2734248A1 (en) * | 1977-07-29 | 1979-02-08 | Fresenius Chem Pharm Ind | PORTABLE ARTIFICIAL KIDNEY |
| DE2734247C2 (en) * | 1977-07-29 | 1984-07-19 | Fresenius AG, 6380 Bad Homburg | Device for continuous chemical analysis in the living body |
| DE2737922A1 (en) * | 1977-08-23 | 1979-03-08 | Fresenius Chem Pharm Ind | ARTIFICIAL ENDOCRINE DRUESE |
| US4516580A (en) * | 1981-12-28 | 1985-05-14 | Polanyi Michael L | Continuous blood gas monitoring |
| SE434214B (en) * | 1982-12-01 | 1984-07-16 | Carl Urban Ungerstedt | DIALYSIS PROBLEM, INTENDED FOR INFORMATION IN BIOLOGICAL Tissues |
| US4726381A (en) * | 1986-06-04 | 1988-02-23 | Solutech, Inc. | Dialysis system and method |
| US4774955A (en) * | 1986-06-04 | 1988-10-04 | Solutech, Inc. | Programmable dialyzer system analyzer and method of use |
| US4763658A (en) * | 1986-06-04 | 1988-08-16 | Solutech, Inc. | Dialysis system 2nd method |
| US4765339A (en) * | 1986-06-04 | 1988-08-23 | Solutech, Inc. | Closed loop dialysis system |
| US4901727A (en) * | 1988-05-05 | 1990-02-20 | The Boc Group, Inc. | Micro-probe for gas sampling |
| GB9320850D0 (en) * | 1993-10-09 | 1993-12-01 | Terwee Thomas H M | Monitoring the concentration of a substance or a group of substances in a body fluid of a human or an animal |
| DE19714572C1 (en) * | 1997-04-09 | 1998-06-25 | Haindl Hans | Catheter for measuring chemical parameters in biological tissue |
| US6272370B1 (en) * | 1998-08-07 | 2001-08-07 | The Regents Of University Of Minnesota | MR-visible medical device for neurological interventions using nonlinear magnetic stereotaxis and a method imaging |
| US6561996B1 (en) * | 1998-05-19 | 2003-05-13 | Transvivo, Inc. | Apparatus and method for in vivo hemodialysis |
| DE19937099C2 (en) | 1999-08-06 | 2001-07-12 | Disetronic Licensing Ag | Microdialysis probe |
| DE10246207B4 (en) * | 2002-10-04 | 2008-04-03 | Disetronic Licensing Ag | Microdialysis probe with spiral line |
| US20050137471A1 (en) * | 2003-12-18 | 2005-06-23 | Hans-Peter Haar | Continuous glucose monitoring device |
-
2002
- 2002-10-04 DE DE10246207A patent/DE10246207B4/en not_active Expired - Lifetime
-
2003
- 2003-09-22 CA CA002499808A patent/CA2499808A1/en not_active Abandoned
- 2003-09-22 EP EP03770947A patent/EP1545651A1/en not_active Withdrawn
- 2003-09-22 AU AU2003280339A patent/AU2003280339A1/en not_active Abandoned
- 2003-09-22 WO PCT/EP2003/010534 patent/WO2004033000A1/en not_active Application Discontinuation
- 2003-09-22 JP JP2004542365A patent/JP2006501909A/en active Pending
-
2005
- 2005-04-01 US US11/096,708 patent/US20050277820A1/en not_active Abandoned
-
2007
- 2007-11-15 US US11/940,636 patent/US7828763B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP1545651A1 (en) | 2005-06-29 |
| US20080228131A1 (en) | 2008-09-18 |
| US20050277820A1 (en) | 2005-12-15 |
| AU2003280339A1 (en) | 2004-05-04 |
| DE10246207B4 (en) | 2008-04-03 |
| WO2004033000A1 (en) | 2004-04-22 |
| JP2006501909A (en) | 2006-01-19 |
| US7828763B2 (en) | 2010-11-09 |
| DE10246207A1 (en) | 2004-05-06 |
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Legal Events
| Date | Code | Title | Description |
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| FZDE | Discontinued |