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59 results about "Uremic toxins" patented technology

Uremic toxins. a name given to the many products of metabolism that accumulate in the body with renal failure, and in association with uremia, because of impaired renal degradation and/or excretory capacity.

Systems and methods related to degradation of uremic toxins

The present invention generally relates to the treatment of uremic toxins in vivo using uremic toxin-treating enzymes, and/or cells capable of producing uremic toxin-treating enzymes or otherwise reacting with uremic toxins. Non-limiting examples of cases where the treatment of uremic toxins is desired include renal disease or dysfunction, gout, subjects receiving chemotherapy, or the like. In one aspect, the treatment includes an oral delivery composition able to reduce the blood concentration of one or more non-protein nitrogen compounds in vivo. The composition, in some cases, may comprise one, two, or more uremic toxin-treating enzymes, such as urease, uricase or creatininase. The oral delivery composition may be able to deliver the uremic toxin-treating enzymes, substantially undigested, to the intestines, where the enzymes can interact with uremic toxins transported to the intestines from the bloodstream. In another aspect, the treatment includes an oral delivery composition comprising a cell able to reduce the concentration of one or more uremic toxins in vivo. In some cases, the cell may be designed to overexpress one, two, or more uremic toxin-treating enzymes, such as urease, uricase or creatininase, for example, by transfecting the cell with a corresponding gene. In some embodiments, a species able to react with or otherwise sequester by-products of the uremic toxin-treating enzyme reactions may be included with the oral delivery composition. For example, if the by-product is ammonium, the species may be a sorbent able to adsorb ammonium, an enzyme able to react with the ammonium, or the like.
Owner:BROWN UNIVERSITY

Nano molybdenum sulfide and application thereof as efficient adsorbent for uremic toxin

The invention relates to nano molybdenum sulfide and application of the nano molybdenum sulfide as an efficient adsorbent for uremia toxin. The technical problems that in the prior art, an adsorption material in a dialysate purification device capable of wearing an artificial kidney is difficult to store, the adsorption efficiency is low, and the biocompatibility is poor are solved. The nano molybdenum sulfide has a two-dimensional ultrathin nanosheet structure, a large number of defects exist on a basal plane due to the interlayer spacing, and the molybdenum disulfide with wide interlayer spacing and rich lattice defects can be used as an efficient adsorbent for uremia toxins. The invention reports that molybdenum disulfide with wide interlayer spacing and rich lattice defects is used for adsorbing uremia toxins urea, creatinine and uric acid for the first time. Compared with commercial MoS2, activated carbon, narrow-interlayer-spacing MoS2 with lattice defects and narrow-interlayer-spacing MoS2 without lattice defects, the dialysate purification material with high adsorbability, high selectivity and high stability is obtained by analyzing and researching the adsorption performance of the material under different conditions (adsorbent dosage, adsorption time, temperature and the like).
Owner:CENT SOUTH UNIV

Oscillator for clinical laboratory

The invention discloses an oscillator for a clinical laboratory. The oscillator structurally comprises a test tube shaft sleeve ring, a square frame groove, a ball rubber concave cap push seat, an integrated circuit seat, an indication lampshade, a contact switch seat and a rotating speed adjusting knob; according to the invention, the test tube shaft sleeve ring is matched with the ball rubber concave cap push seat; the urine test tube is locked by the test tube shaft sleeve ring to perform rotary oscillation; a spherical swing pipe inclined strut shaking effect is formed at the bottom of thesettled uranidin and urotoxin through the concave arc thick ring frame and the semispherical groove seat, it is guaranteed that the whole ball cap push rod frame and the balance weight paddle frame push lining form a segmented pressure effect; settled urotoxin floccules can be matched with centrifugal oscillation in the fluid to diffuse sufficient toxin data saturation, so the accurate value of the amount of data harmful to inspection is increased, the oblique alignment frame of the test tube twisting and shaking rubber-coated tray in the later period can conveniently adapt to the inertia rotation effect, the protection of the test tube wall toughness rated value is improved, the effect of lifting settled flocculated thick fluid during data inspection is guaranteed, and full oscillation inspection is achieved.
Owner:重庆市第四人民医院

Systems and methods related to degradation of uremic toxins

The present invention generally relates to the treatment of uremic toxins in vivo using uremic toxin-treating enzymes, and / or cells capable of producing uremic toxin-treating enzymes or otherwise reacting with uremic toxins. Non-limiting examples of cases where the treatment of uremic toxins is desired include renal disease or dysfunction, gout, subjects receiving chemotherapy, or the like. In one aspect, the treatment includes an oral delivery composition able to reduce the blood concentration of one or more non-protein nitrogen compounds in vivo. The composition, in some cases, may comprise one, two, or more uremic toxin-treating enzymes, such as urease, uricase or creatininase. The oral delivery composition may be able to deliver the uremic toxin-treating enzymes, substantially undigested, to the intestines, where the enzymes can interact with uremic toxins transported to the intestines from the bloodstream. In another aspect, the treatment includes an oral delivery composition comprising a cell able to reduce the concentration of one or more uremic toxins in vivo. In some cases, the cell may be designed to overexpress one, two, or more uremic toxin-treating enzymes, such as urease, uricase or creatininase, for example, by transfecting the cell with a corresponding gene. In some embodiments, a species able to react with or otherwise sequester by-products of the uremic toxin-treating enzyme reactions may be included with the oral delivery composition. For example, if the by-product is ammonium, the species may be a sorbent able to adsorb ammonium, an enzyme able to react with the ammonium, or the like.
Owner:BROWN UNIVERSITY
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