ES2625351T1 - Método para eliminar bacterias de la sangre utilizando caudal alto - Google Patents
Método para eliminar bacterias de la sangre utilizando caudal alto Download PDFInfo
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- ES2625351T1 ES2625351T1 ES15782250.3T ES15782250T ES2625351T1 ES 2625351 T1 ES2625351 T1 ES 2625351T1 ES 15782250 T ES15782250 T ES 15782250T ES 2625351 T1 ES2625351 T1 ES 2625351T1
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Abstract
Un método ex vivo para eliminar bacterias de una muestra extraída de un sujeto que se sospecha que está infectado con bacterias, comprendiendo el método: poner en contacto una muestra extraída del sujeto con un medio de adsorción para permitir la formación de un complejo adherente, en el que el complejo adherente comprende bacterias y medio de adsorción; y separar la muestra del complejo adherente para producir la muestra con una cantidad reducida de bacterias.
Claims (48)
- 5101520253035404550556065REIVINDICACIONES1. Un metodo ex vivo para eliminar bacterias de una muestra extralda de un sujeto que se sospecha que esta infectado con bacterias, comprendiendo el metodo:poner en contacto una muestra extralda del sujeto con un medio de adsorcion para permitir la formacion de un complejo adherente, en el que el complejo adherente comprende bacterias y medio de adsorcion; y separar la muestra del complejo adherente para producir la muestra con una cantidad reducida de bacterias.
- 2. El metodo de la reivindicacion 1, en el que la muestra se selecciona del grupo que consiste en sangre entera, suero y plasma.
- 3. El metodo de la reivindicacion 2, en el que la muestra es sangre entera.
- 4. El metodo de la reivindicacion 1, en el que el medio de adsorcion es un sustrato solido de area superficial alta que tiene una superficie hidrofila desprovista de adsorbente polisacarldico.
- 5. El metodo de la reivindicacion 4, en el que el sustrato solido comprende una pluralidad de microesferas polimericas rlgidas.
- 6. El metodo de la reivindicacion 5, en el que la microesfera polimerica rlgida es un miembro seleccionado del grupo que consiste en poliuretano, polimetilmetacrilato, polietileno o copollmeros de etileno y otros monomeros, polietilen imina, polipropileno y poliisobutileno.
- 7. El metodo de la reivindicacion 4, en el que el sustrato solido comprende una o una pluralidad de fibras huecas.
- 8. El metodo de la reivindicacion 4, en el que el sustrato solido comprende fibras solidas o hilo tejido fabricado de fibras solidas.
- 9. El metodo de la reivindicacion 4, en el que la superficie hidrofila es una superficie cationica.
- 10. El metodo de la reivindicacion 1, en el que el medio de adsorcion tiene un area superficial alta como resultado de una superficie o topografla rugosa.
- 11. El metodo de la reivindicacion 4, en el que la superficie hidrofila es una superficie con carga neutra.
- 12. El metodo de la reivindicacion 1, en el que las bacterias en la muestra se reducen de aproximadamente aproximadamente 99,9 %.
- 13. El metodo de la reivindicacion 12, en el que las bacterias en la muestra se reducen de aproximadamente aproximadamente 40 %.
- 14. El metodo de la reivindicacion 1, en el que las bacterias son bacterias gram negativas.
- 15. El metodo de la reivindicacion 1, en el que las bacterias son bacterias gram positivas.
- 16. El metodo de la reivindicacion 1, en el que las bacterias se seleccionan del grupo que consiste en Escherichia coli, Klebsiella pneumoniae, Escherichia coli resistente a carbapenemo, Klebsiella pneumoniae resistente a carbapenemo y Klebsiella pneumoniae productora de betalactamasa de espectro ampliado, Enterococcus faecium, Acinetobacter baumannii y Staphylococcus aureus resistente a meticilina (SARM).
- 17. El metodo de la reivindicacion 1, en el que las bacterias se seleccionan del grupo que consiste en Staphylococcus aureus, Staphylococcus aureus resistente a meticilina (SARM) y Escherichia coli.
- 18. El metodo de la reivindicacion 1, en el que la muestra tiene un caudal lineal de aproximadamente 8 cm/min a aproximadamente 1000 cm/min.
- 19. El metodo de la reivindicacion 1, en el que la muestra tiene un caudal volumetrico de aproximadamente 50 ml/min a aproximadamente 5 l/min.
- 20. Un metodo ex vivo para eliminar bacterias de una muestra extralda de un sujeto que se sospecha que esta infectado con bacterias, en el que se sabe que las bacterias tienen una baja afinidad, o ninguna, por sulfato de heparan, comprendiendo el metodo:poner en contacto una muestra extralda del sujeto con un medio de adsorcion para permitir la formacion de un complejo adherente, en el que el medio de adsorcion es un sustrato solido de area superficial alta que tiene al20 % a 20 % a5101520253035404550556065menos un adsorbente polisacarldico en su superficie; yseparar la muestra del complejo adherente para producir la muestra con una cantidad reducida de bacterias.
- 21. El metodo de la reivindicacion 20, en el que la muestra se selecciona del grupo que consiste en sangre entera, suero y plasma.
- 22. El metodo de la reivindicacion 21, en el que la muestra es sangre entera.
- 23. El metodo de la reivindicacion 20, en el que el sustrato solido comprende una pluralidad de microesferas polimericas rlgidas.
- 24. El metodo de la reivindicacion 20, en el que el complejo adherente comprende bacterias y el medio de adsorcion.
- 25. El metodo de la reivindicacion 23, en el que la microesfera polimerica rlgida es un miembro seleccionado del grupo que consiste en poliuretano, polimetilmetacrilato, polietileno o copollmeros de etileno y otros monomeros, polietilen imina, polipropileno y poliisobutileno.
- 26. El metodo de la reivindicacion 20, en el que el sustrato solido comprende una o una pluralidad de fibras huecas.
- 27. El metodo de la reivindicacion 20, en el que el al menos un absorbente polisacarldico es un miembro seleccionado del grupo que consiste en heparina, heparan sulfato, acido hialuronico, acido sialico, hidratos de carbono con secuencias de manosa y quitosano.
- 28. El metodo de la reivindicacion 27, en el que el al menos un absorbente polisacarldico es heparina o heparan sulfato.
- 29. El metodo de la reivindicacion 28, en el que el al menos un absorbente polisacarldico es heparina.
- 30. El metodo de la reivindicacion 29, en el que las microesferas se recubren con aproximadamente de 0,27 mg a aproximadamente 10 mg de heparina por gramo de microesfera.
- 31. El metodo de la reivindicacion 30, en el que la microesfera se recubre con 2+0,5 mg de heparina por gramo de microesfera.
- 32. El metodo de la reivindicacion 20, en el que las bacterias en la muestra se reducen de aproximadamente 20 % a aproximadamente 99,9 %.
- 33. El metodo de la reivindicacion 20, en el que las bacterias en la muestra se reducen de aproximadamente 20 % a aproximadamente 40 %.
- 34. El metodo de la reivindicacion 20, en el que las bacterias en la muestra fracasan en un ensayo de union a heparina in vitro.
- 35. El metodo de la reivindicacion 16, en el que las bacterias son bacterias gram negativas.
- 36. El metodo de la reivindicacion 16, en el que las bacterias son bacterias gram positivas.
- 37. El metodo de la reivindicacion 20, en el que las bacterias se seleccionan del grupo que consiste en Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, Enterococcus faecium, Escherichia coli resistente a carbapenemo, Klebsiella pneumoniae resistente a carbapenemo y Klebsiella pneumoniae productora de betalactamasa de espectro ampliado.
- 38. El metodo de la reivindicacion 20, en el que la muestra tiene un caudal lineal de aproximadamente 8 cm/min a aproximadamente 1000 cm/min.
- 39. El metodo de la reivindicacion 20, en el que la muestra tiene un caudal volumetrico de aproximadamente 50 ml/min a aproximadamente 5 l/min.
- 40. Un metodo ex vivo para eliminar bacterias de una muestra extralda de un sujeto que se somete a dialisis, comprendiendo el metodo:poner en contacto una muestra extralda del sujeto con un cartucho de adsorcion que comprende medios de adsorcion, en el que el cartucho de adsorcion esta en serie con un cartucho de dialisis para permitir la formacion de un complejo adherente; yseparar la muestra del complejo adherente para producir la muestra con una cantidad reducida de bacterias.51015202530
- 41. El metodo de la reivindicacion 40, en el que la muestra tiene un volumen de sangre total menor de 200 ml.
- 42. El metodo de la reivindicacion 40, en el que el cartucho de adsorcion tiene una altura de columna entre 1 cm-50 cm.
- 43. El metodo de la reivindicacion 40, en el que el cartucho de adsorcion tiene un diametro de columna entre 1 cm- 50 cm.
- 44. El metodo de la reivindicacion 40, en el que el cartucho de adsorcion es proximal al sujeto en comparacion con el cartucho de dialisis.
- 45. El metodo de la reivindicacion 40, en el que el cartucho de adsorcion es distal al sujeto en comparacion con el cartucho de dialisis.
- 46. El metodo de la reivindicacion 40, en el que el complejo adherente comprende bacterias y medios de adsorcion.
- 47. El metodo de la reivindicacion 40, en el que la muestra tiene un caudal lineal de aproximadamente 8 cm/min a aproximadamente 1000 cm/min.
- 48. El metodo de la reivindicacion 40, en el que la muestra tiene un caudal volumetrico de aproximadamente 50 ml/min a aproximadamente 5 l/min.
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- 2015-04-17 WO PCT/US2015/026340 patent/WO2015164198A1/en not_active Ceased
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| Publication number | Publication date |
|---|---|
| WO2015164198A1 (en) | 2015-10-29 |
| JP2022125040A (ja) | 2022-08-26 |
| JP2021045573A (ja) | 2021-03-25 |
| CA2946294C (en) | 2023-03-21 |
| AU2015250107A1 (en) | 2016-11-17 |
| CN106255520B (zh) | 2022-08-12 |
| US20170035956A1 (en) | 2017-02-09 |
| BR112016024569A8 (pt) | 2021-06-01 |
| US11844895B2 (en) | 2023-12-19 |
| MX2016013873A (es) | 2017-03-09 |
| EP3134146A1 (en) | 2017-03-01 |
| US20200171233A1 (en) | 2020-06-04 |
| CA2946294A1 (en) | 2015-10-29 |
| EP3134146B1 (en) | 2024-12-25 |
| BR112016024569A2 (pt) | 2017-08-15 |
| EP3134146A4 (en) | 2018-01-10 |
| JP2017513636A (ja) | 2017-06-01 |
| BR112016024569B1 (pt) | 2023-01-03 |
| JP7184864B2 (ja) | 2022-12-06 |
| CN106255520A (zh) | 2016-12-21 |
| DE15782250T1 (de) | 2017-08-10 |
| AU2020200029B2 (en) | 2022-07-28 |
| KR20170020749A (ko) | 2017-02-24 |
| ES2625351T3 (en) | 2025-04-07 |
| AU2020200029A1 (en) | 2020-01-30 |
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