IP Library Granted Patent US 8,187,250
Granted Patent B2
US 8,187,250 · App. 11/700,690 · Granted May 29, 2012

Peritoneal dialysis methods and apparatus

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,187,250
App. No.
11/700,690
Granted
May 29, 2012
Kind
B2
Abstract

A peritoneal-based (“bloodless”) artificial kidney processes peritoneal fluid without need for additional fluids (“waterless”). Fluid is separated into a protein-rich stream and a protein-free stream. The protein-rich stream is regenerated using a sorbent assembly, and its protein composition can be modified by removal of selected protein(s) (“dialysate-pheresis”). It is then reconstituted with additives and returned into the peritoneal cavity, thereby reducing protein-loss and providing oncotic-pressure for ultrafiltration. The protein-free stream is used to produce free water, and an alkaline or acid fluid for optimization of the composition of the regenerated stream. The unused protein-free stream can be used to “reverse flush” the separator to maintain its patency and the excess discarded for fluid-balance regulation. Compared to prior art, immobilization of urease allows more protein rich fluid to be regenerated and re-circulated into the peritoneal cavity for toxin removal and allows practicable development of portable and wearable artificial kidneys.

Claims (23)

1. A method of processing a substantially blood-free fluid derived from a peritoneal cavity of a person, comprising:

separating the substantially blood-free fluid into a relatively protein-rich fluid and a relatively protein-free fluid such that a stream of the relatively protein-rich fluid averages at least 15% (by vol) of a stream of the substantially blood-free fluid over at least some period of time;

processing the relatively protein-rich fluid with a sorbent having an at least substantially immobilized urease to produce a purified regenerated fluid, wherein the urease is immobilized with greater than Van der Waals forces;

depositing at least some of the purified regenerated fluid back into the peritoneal cavity; and

wherein at least 80% of the substantially blood-free fluid is re-circulated into the peritoneal cavity as the purified regenerated fluid over a period of 8 hours.

2. The method of claim 1 , wherein the step of depositing occurs concurrently with the step of separating.

3. The method of claim 1 , wherein the step of depositing occurs intermittently with the step of separating.

4. The method of claim 1 , further comprising using a filter to filter out the relatively protein-free fluid from the relatively protein-rich fluid.

5. The method of claim 1 , further comprising controlling at least two of: (a) a cation in the purified fluid; (b) an anion in the purified fluid; (c) a gas; and (d) a glucose level in the purified fluid.

6. The method of claim 1 , further comprising re-circulating to the person at least 80% of the substantially blood-free fluid as the purified fluid over a period of 4 hours.

7. The method of claim 1 , further comprising re-circulating at least 90% of the substantially blood-free fluid as the purified fluid over a period of 8 hours.

8. The method of claim 1 , further comprising re-circulating the substantially blood-free fluid as the purified fluid at a rate sufficient to provide at least 20 liters of purified fluid over a 10 hour period.

9. The method of claim 1 , further comprising re-circulating the substantially blood-free fluid as the purified fluid at a rate sufficient to provide at least 48 liters of purified fluid over a 24 hour period.

10. The method of claim 1 , wherein the step of processing occurs at least 40 hours during a period of seven consecutive days.

11. The method of claim 1 , wherein the step of processing occurs at least 126 hours during a period of seven consecutive days.

12. The method of claim 1 , further comprising embodying the steps of separating and processing in a device, and the person wearing the device.

13. The method of claim 1 , further comprising processing at least a portion of the relatively protein-free fluid through at least one of a reverse osmosis unit and an ion-exchanger, and then adding a resulting product into a stream containing the relatively protein-rich fluid.

14. A method of processing a substantially blood-free fluid derived from a peritoneal cavity of a person, comprising:

separating the substantially blood-free fluid into a relatively protein-rich fluid and a relatively protein-free fluid such that a stream of the relatively protein-rich fluid averages at least 15% (by vol) of a stream of the substantially blood-free fluid over at least some period of time;

processing the relatively protein-rich fluid with a sorbent having an at least substantially immobilized urease to produce a purified regenerated fluid, wherein the urease is immobilized with greater than Van der Waals forces;

depositing at least some of the purified regenerated fluid back into the peritoneal cavity;

wherein at least 90% of the substantially blood-free fluid is re-circulated into the peritoneal cavity as the purified regenerated fluid over a period of 8 hours; and

further comprising a step of processing at least a portion of the relatively protein-free fluid through at least one of a reverse osmosis unit and an ion-exchanger, and then adding a resulting product into a stream containing the relatively protein-rich fluid.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2009
From: ROBERTS, MARTIN; LEE, DAVID B.N.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA; THE US GOVERNMENT REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS
Reel/Frame 022496/0481 →
Continuity (3)
Provisional Application 60763254 · Jan 30, 2006
Provisional Application 60763337 · Jan 30, 2006
Related Publication 20070179431A1 · Aug 2, 2007