This application claims the benefit of pending U.S. Provisional Application No. 61/447,484, filed Feb. 28, 2011; the entirety is hereby expressly incorporated by reference herein.
Dialysis systems for enabling the diffusion of small molecules.
In one embodiment the self-contained dialysis system described includes or utilizes a dialysis device 10, shown in
One embodiment is a dialysis system that contains a generally sealed device configured to receive both a buffer and a dialysis chamber, where positioning the dialysis chamber seals the device. The device is configured to receive a sample to enable dialysis of the sample with respect to the buffer across the membrane. The dialysis device sealingly engages the system such that buffer is generally fluidly isolated from sample in the dialysis device.
One embodiment is a dialysis method, where buffer is placed in a vessel. The dialysis device is accessed including an inner member and an outer member trapping a dialysis membrane therebetween. A sample is placed in the dialysis device. The dialysis device is placed into the vessel as an integral component of the sealing system, thus sealing the vessel.
The outer member 14 can similarly take the form of a generally cylindrical sleeve that is open at its upper and lower ends, and includes a radially outwardly-extending flange 20 at or adjacent to its upper end. The outer member 14 has a lower portion 14a defined by a relative small radius, and an upper portion 14b defined by a radius larger than that of the lower portion 14a. A generally radially extending lip 22 is positioned between the lower 14a and upper 14b portions. As noted above, the illustrated inner 12 and outer 14 members are both generally cylindrical and thus circular in cross section. However, if desired, the inner 12 and outer 14 members can have a variety of other shapes in cross section, so long as the shapes are generally corresponding, such as triangular, square, hexagonal, octagonal, star shaped, irregularly shaped, or other polygons or shapes. The inner 12 and outer 14 members can be made from any of a wide variety of materials that exhibit a low absorbency of proteins and can survive common sterilization procedures, including but not limited to polypropylene.
In the illustrated embodiment the membrane 16 is generally flat and circular, although the membrane 16 can take any of a wide variety of shapes and sizes. The membrane 16 can be made of any of a variety of materials suitable for use in dialysis. In particular, the membrane 16 may be a semi-permeable membrane which allows sufficiently small molecules to pass therethrough, but blocks larger molecules from passing therethrough. In one embodiment, the membrane 16 is made of regenerated cellulose.
In order to assemble the dialysis device 10, the inner member 12, membrane 16 and outer member 14 are arranged in the configuration shown in
In one embodiment, the outer member 14 includes a groove (not shown) on its inner surface positioned immediately above the lip 22. When the inner member 12 is inserted into the outer member 14, the user experiences a slight resistance as the flange 18 approaches the groove until, with sufficient applied force, the flange 18 snaps into place. The groove and snap-fit configuration of the dialysis device 10 is optional and may not necessarily be utilized.
When the dialysis device 10 is properly assembled, as shown in
When the dialysis device 10 is assembled, the inner member 12 protrudes at least slightly axially beyond the bottom of the outer member 14 to ensure that the membrane 16 is exposed to the buffer fluid, as described in greater detail below. In one embodiment, the bottom edge 24 of the inner member 12 is curved, tapered or beveled to minimize tearing or rupturing of the membrane 16 that is stretched thereacross. Further details relating to the dialysis device 10 are disclosed in U.S. Pat. No. 6,039,871, which is expressly incorporated by reference herein in its entirety.
As shown in
The system/tube may include a cap 30, such as a screw cap, which is threadably engageable with the outer surface of the tube 26. In this manner, when the cap 30 is threaded onto the tube 26, the cap 30 seals the tube 26. When the cap 30 is threaded down, the under side of the cap 30 engages the top of the flange 20, thereby forming a sealed engagement therewith, and pressing the flange 20 into sealing engagement upper lip 28 of the tube 26. The engagement of the cap 30 with the flange 20 forms a watertight seal for both the inner cavity 34 of the dialysis device 10 and the inner volume/cavity of the tube 26. The seal allows liquids in both cavities to communicate only through the membrane 16 and prevents accidental leakage, evaporation or contamination of the sample 32 positioned in the dialysis device 10. Thus, in one embodiment the flange 20 is shaped to have generally the same shape as the upper lip 28.
In use, a sample 32 (
In one embodiment the buffer 36 has a volume of between about 15 and about 100 times the volume of the sample 32. This ratio of volumes helps to ensure that sufficient amounts of the small molecules are removed from the sample 32. In one embodiment, after a few hours of dialysis, the sample 32 may show at least a 90% reduction in small molecules. If desired, the dialysis procedure can be enhanced by removing the buffer solution 36 and replacing with a fresh buffer 36. Replacing the buffer 36 in this manner, and allowing sufficient time for dialysis, may, in one embodiment, allow well over 99% of the targeted small molecules to be removed from the sample 32. In one embodiment, the sample 32 has a volume of between about 0.2 and about 1 milliliters, and in one embodiment has a volume of between about 1 and about 4 milliliters. In one embodiment the buffer 36 has a volume of at least about 40 milliliters.
The dialysis system 38 shown in
The dialysis device can also take other forms, e.g., as shown in
Although the invention is shown and described with respect to certain embodiments, it should be clear that modifications and variations will be apparent to those skilled in the art upon reading the specification, and the present invention includes all such modifications and variations.
Number | Date | Country | |
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61447484 | Feb 2011 | US |