Devices, systems, and methods herein relate to performing dialysis to manage a chronic condition such as end-stage renal disease. These systems and methods may allow a patient to orally ingest a potable dialysate and excrete the dialysate via the urinary tract. In some variations, a method may include delivering a dialysate via the esophagus of a patient and draining the dialysate into a bladder of the patient. Delivering the dialysate may further comprise delivering the dialysate through the nasopharynx or oropharynx. Delivering the dialysate through the oropharynx may comprise the patient drinking the dialysate.

Provided herein are membrane separation systems and methods suitable for use in separating carbonylation catalyst from a beta-lactone product stream. Such membrane separation systems utilize a cross flow separation technique and employ a sweep stream.

Disclosed are apparatus and methods for blood and other biological fluid purification using a membrane with cell containing vascular channel systems and filtration channel systems. Also disclosed are methods of making the apparatus as well as methods of making membranes.

Disclosed are apparatus and methods for blood and other biological fluid purification using a membrane with cell containing vascular channel systems and filtration channel systems. Also disclosed are methods of making the apparatus as well as methods of making membranes.

Provided herein are membrane separation systems and methods suitable for use in separating carbonylation catalyst from a beta-lactone product stream. Such membrane separation systems utilize a cross flow separation technique and employ a sweep stream.

A hollow fiber module includes hollow fiber cartridges. A port receives a second solution to be treated in a shell side volume and another port for discharging the treated second solution. A first end cap has an inlet for a first solution and a distributer for distributing the first solution to a first end of the hollow fiber cartridges. A second end cap has a collector for collecting the treated first solution from the second end of the hollow fiber cartridges and an outlet for the treated first solution. A first connector has an inlet for the second solution and a distributer for distributing the second solution to a port of the hollow fiber cartridges. A second connector has a collector for collecting the treated second solution from the other port of the hollow fiber cartridges and an outlet for the treated second solution.

A hollow fiber module includes hollow fiber cartridges. A port receives a second solution to be treated in a shell side volume and another port for discharging the treated second solution. A first end cap has an inlet for a first solution and a distributer for distributing the first solution to a first end of the hollow fiber cartridges. A second end cap has a collector for collecting the treated first solution from the second end of the hollow fiber cartridges and an outlet for the treated first solution. A first connector has an inlet for the second solution and a distributer for distributing the second solution to a port of the hollow fiber cartridges. A second connector has a collector for collecting the treated second solution from the other port of the hollow fiber cartridges and an outlet for the treated second solution.

The present disclosure relates to diffusion and/or filtration devices comprising hollow fiber membranes, e.g., ultrafilters for water purification, plasma filters, or capillary dialyzers for blood purification; housings and end caps for the devices; and methods for the production of the devices.

The present invention provides a method for producing lipid particles that have a desired particle diameter, the method comprising: (A) a step for preparing, in a first mixing region, a primary dilution by mixing a first solution containing a lipid and an alcohol with a second solution containing water; (B) a step for feeding the primary dilution from the first mixing region to a second mixing region through a liquid feed pipe within a prescribed time; and (C) a step for preparing a secondary dilution by mixing the primary dilution with a third solution containing water in the second mixing region, wherein the steps (A)-(C) are continuously carried out, and the particle diameter of the lipid particles is controlled by adjusting at least one condition selected from the group consisting of the concentration of the alcohol and the concentration of the lipid in the primary dilution, the prescribed time, and the temperature during mixing.

The present invention provides a method for producing lipid particles that have a desired particle diameter, the method comprising: (A) a step for preparing, in a first mixing region, a primary dilution by mixing a first solution containing a lipid and an alcohol with a second solution containing water; (B) a step for feeding the primary dilution from the first mixing region to a second mixing region through a liquid feed pipe within a prescribed time; and (C) a step for preparing a secondary dilution by mixing the primary dilution with a third solution containing water in the second mixing region, wherein the steps (A)-(C) are continuously carried out, and the particle diameter of the lipid particles is controlled by adjusting at least one condition selected from the group consisting of the concentration of the alcohol and the concentration of the lipid in the primary dilution, the prescribed time, and the temperature during mixing.