Surgery – Diagnostic testing – Measuring or detecting nonradioactive constituent of body...
Reexamination Certificate
2001-07-20
2003-07-08
Jacyna, J. Casimer (Department: 3751)
Surgery
Diagnostic testing
Measuring or detecting nonradioactive constituent of body...
C600S352000, C600S365000, C600S366000, C604S019000
Reexamination Certificate
active
06591126
ABSTRACT:
BACKGROUND AND SUMMARY OF THE INVENTION
The invention concerns a microdialysis system comprising a microdialysis probe that can be inserted in organic tissue and has a dialysis membrane to separate a probe channel filled with perfusion fluid from the tissue, a sensor cell for the preferably electrochemical detection of components and especially glucose in the perfusion fluid that is conveyed from the microdialysis probe and a transport device to convey the perfusion fluid through the probe channel of the microdialysis probe to the sensor cell.
In a measuring system of this type known from WO 97/42868, the transport device has a dialysate pump downstream of the microdialysis probe embedded in the body tissue which sucks perfusion fluid from a reservoir through the probe and passes it on to the extracorporeal sensor cell while dialysate is formed. In this suction transport the operating pressure of the pump is adjusted according to the desired delivery rate to overcome the obstacles to flow in the suction branch. The small bore flow cross-sections thus result in a significant negative pressure difference (underpressure) of the perfusion fluid in the probe channel relative to the interstitial fluid. Consequently tissue fluid is practically sucked by ultrafiltration through the dialysis membrane into the probe. It has even been observed in in vitro experiments that the entire solution at the outlet of the probe is derived from ultrafiltration. Although in suction operation the actual flow rate of the dialysate solution leaving the microdialysis probe corresponds to the set value, the origin of the liquid (ultrafiltrate from body tissue or perfusate) is uncertain. Another disadvantage is that the function of the dialysis membrane can be impaired by a negative pressure gradient. In particular this can lead to a reduction of the active exchange surface by accumulation of macromolecules on the tissue side or by constructional factors and thus the amount of dialysate obtained is also reduced.
Conversely when the perfusion fluid is pressure fed by a perfusate pump in the delivery branch of the microdialysis probe, the problem arises that perfusion fluid, and hence essentially water, is discharged through the dialysis membrane into the tissue as a result of the required overpressure. This is disadvantageous since the tissue fluid around the probe is diluted, the tissue glucose has to diffuse into the probe channel against a counterflow of water molecules and the flow rate of perfusion fluid at the outlet cannot be determined due to the loss of liquid. A further disadvantage is that when the pump fails there is a risk that reagent solution added to the outlet branch can eventually pass into the body tissue via the microdialysis probe.
Based on this, the object of the invention is to eliminate the said disadvantages and to improve a microdialysis system of the type described above in such a manner that the dialysis function is reliable and defined.
A combination of features as stated in claim 1 is proposed as a solution to this object. Advantageous embodiments and further developments of the invention result from the dependent claims.
The essence of the invention is to utilize a combined push-pull transport of perfusion fluid to optimize the diffusion processes across the dialysis membrane. Accordingly the invention proposes that the transport device has a pressure pump unit which is connected on the pressure side with the inlet of the probe channel and a suction pump unit connected on the suction side with the outlet of the probe channel which operates simultaneously with the pressure pump unit. This allows a desired pressure level to be set in the region of the microdialysis membrane between the positive output pressure of the pressure pump unit and the negative input pressure of the suction pump unit. In this connection it is advantageous that the pressure pump unit is exclusively connected on the pressure side with the inlet and the suction pump unit is exclusively connected on the suction side with the outlet of the probe channel. This can be achieved by the pressure pump unit and the suction pump unit each being connected to the probe channel of the microdialysis probe by a non-branching duct which is preferably a flexible hose. This ensures defined flow conditions and guarantees that the mass flow through any flow cross-sections in the respective duct is of equal magnitude in the same time interval.
In a preferred embodiment the delivery rates of the pressure and suction pump unit are matched and are preferably essentially equal in order to reduce the effective pressure difference between the perfusion and tissue fluid across the dialysis membrane. This achieves an equilibrium at a low pressure level between the perfusion fluid and the tissue fluid across the dialysis membrane such that no ultrafiltration occurs and the origin of the solution which leaves the probe channel as well as its delivery rate and flow rate are known and defined. This also ensures that glucose passes through the dialysis membrane solely as a result of diffusion. At the same time this prevents the membrane from being sucked onto the probe lumen and thus maintains the effective membrane surface.
As a result of the push-pull operation it is possible to operate the dialysis process at low perfusion rates. The delivery rate of the pressure and suction pump unit is preferably less than 1 &mgr;l, preferably less than 0.1 &mgr;l per minute.
For long-term operation it is preferable that the suction side of the pressure pump unit is connected to a reservoir of perfusion fluid whereas the pressure side of the suction pump unit is connected to a flow chamber of the sensor cell which preferably terminates in a collecting vessel. The sensor cell or the sensor unit has an electrode arrangement operating electrochemically which allows a measuring signal to be detected in the flow chamber that correlates with the glucose content of the dialysate in a known manner. Basically it is also possible that the suction pump unit is downstream of the sensor cell so that the flow chamber is integrated in the suction path.
In order to chemically process the dialysate a reagent pump unit can be provided which is used to meter a reagent solution, in particular an enzyme solution, into the perfusion fluid upstream of the sensor cell. A further improvement, also with regard to reducing the risk of contamination, is achieved by connecting the pressure side of the reagent pump unit and of the suction pump unit preferably via a Y connector to a connecting duct leading to the sensor cell.
A technically advantageous embodiment of the system envisages that the pressure pump unit, the suction pump unit and optionally the reagent pump unit each consist of a flexible pump tube of a multichannel peristaltic pump that are actuated by a common rotating piston.
The microdialysis probe preferably comprises a double-lumen catheter which has a micropore dialysis membrane preferably made of hollow fibres in the area of its distal end, the outside of which is embedded in the tissue and the inside of which is filled with perfusion fluid.
REFERENCES:
patent: 5237993 (1993-08-01), Skrabal
patent: 5640954 (1997-06-01), Pfeiffer et al.
patent: 6190316 (2001-02-01), Hirabayashi et al.
patent: 44 26 694 (1996-02-01), None
patent: 0 367 752 (1990-05-01), None
patent: 0 940 151 (1999-08-01), None
patent: WO 97/42868 (1996-05-01), None
Hoerauf Christian
Roeper Josef
Schoemaker Michael
Jacyna J. Casimer
Knauer Richard T.
Roche Diagnostics Corporation
Woodburn Jill L.
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