Bi-structured matrix for solid reactants purification and handling and methods for obtaining said matrix

Patent metadata

Field	Value
Publication number	US-2018147556-A1
Application number	US-201515534872-A
Country	US
Kind code	A1
Filing date	Dec 11, 2015
Priority date	Dec 11, 2014
Publication date	May 31, 2018
Grant date	—

Abstract

Bi-structured matrix for purification and handling of solid reagents, which comprises at least a polymer solid carrier coated with at least one hydrosoluble polymer, and manufacturing processes. The solid carrier may be, among others, cross-linked polyurethane foam or a micropipette tip. The hydrosoluble polymer may be, among others, polyvinylalcohol, agarose, hydroxyethylcellulose or combinations thereof. The matrix may further comprise a polymer produced from monomers of glycidyl metacrylate (GMA), dimethyl acrylamide (DMAAm), 2-hydroxyethyl metacrylate, metacrylic acid, or combinations thereof.

First claim

1 - 46 . (canceled)

47 . A bi-structured matrix for solid reactants purification and handling comprising at least a polymeric solid carrier coated with at least one hydrosoluble polymer.

48 . The matrix according to claim 47 , wherein the solid carrier is selected from the group comprising cross-linked polyurethane foam and micropipette tips.

49 . The matrix according to claim 47 , wherein the hydrosoluble polymer is selected from the group comprising polyvinyl alcohol, agarose, hydroxyethylcellulose, and combinations thereof.

50 . The matrix according to claim 47 , further comprising a monomer selected from the group consisting of glycidyl metacrylate monomers (GMA), dimethyl acrylamide (DMAAm), 2-hydroxyethyl metacrylate, metacrylic acid, and combinations thereof.

51 . The matrix according to claim 50 , wherein the monomer is glycidyl metacrylate (GMA).

52 . The matrix according to claim 51 , further comprising functional groups selected from the group consisting of sulfonic, iminodiacetic acid (IDA) y ethylenediamine (EDA).

53 . The matrix according to claim 47 , comprising a cross-linked polyurethane foam solid carrier, coated with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, hydroxyethylcellulose, and glycidyl metacrylate (GMA) monomers bound to said hydrosoluble polymer.

54 . The matrix according to claim 47 , comprising a cross-linked polyurethane foam solid carrier coated with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, hydroxyethylcellulose, glycidyl metacrylate (GMA) monomers bound to the hydrosoluble polymer and sulfonic groups bound to the glycidyl metacrylate (GMA) monomers.

55 . The matrix according to claim 47 , comprising a cross-linked polyurethane foam solid carrier coated with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, hydroxyethylcellulose, glycidyl metacrylate (GMA) monomers bound to the hydrosoluble polymer and iminodiacetic acid (IDA) bound to the glycidyl metacrylate (GMA) monomers.

56 . The matrix according to claim 47 , comprising a pipette tip as a solid carrier internally coated with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose and hydroxyethylcellulose.

57 . The matrix according to claim 47 , comprising a pipette tip as a solid carrier internally coated with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, hydroxyethylcellulose, and silica particles.

58 . The matrix according to claim 57 , wherein the silica particles have a diameter of between 0.015 and 40 microns.

59 . A process for manufacturing a matrix according to claim 47 , comprising the following steps:
a) contacting a polymer solid carrier with at least one hydrosoluble polymer until obtaining a polymer solid carrier coated with a hydrosoluble polymer; b) drying the solid carrier coated with the hydrosoluble polymer and immersing it in an irradiation solution; and c) irradiating with a source of 60-Cobalt and drying the bi-structured matrix obtained.

60 . The process according to claim 59 , comprising after step a) a step wherein the solid carrier coated with the hydrosoluble polymer is immersed in a clotting agent selected from the group consisting of 2-propanol, ethanol, 1-propanol, and dioxane.

61 . The process according to claim 59 , wherein the solid carrier is selected from the group comprising cross-linked polyurethane foam and micropipette tips.

62 . The process according to claim 59 , wherein the hydrosoluble polymer is selected from the group comprising polyvinyl alcohol, agarose, hydroxyethylcellulose, and combinations thereof.

63 . A process for manufacturing the matrix according to claim 53 , comprising the following steps:
a) contacting a cross-linked polyurethane foam solid carrier with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, and hydroxyethylcellulose until obtaining a polymer solid carrier coated with a hydrosoluble polymer; b) immersing the solid carrier coated with the hydrosoluble polymer obtained in the previous step, in a clotting agent selected from the group consisting of 2-propanol, ethanol, 1-propanol, and dioxane; c) drying the solid carrier coated with the hydrosoluble polymer of the previous step and immersing in an irradiation solution comprising glycidyl metacrylate (GMA) monomers; and d) irradiating with a source of 60-Cobalt and drying the bi-structured matrix obtained.

64 . The process according to claim 63 , wherein the irradiation solution comprises ethanol/water.

65 . The process according to claim 63 , wherein the irradiation solution comprises an amount of between 2% and 6% of the glycidyl metacrylate (GMA) monomer.

66 . A process for manufacturing the matrix according to claim 54 , comprising the following steps:
a) contacting a cross-linked polyurethane foam solid carrier with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, and hydroxyethylcellulose until obtaining a polymer solid carrier coated with a hydrosoluble polymer; b) immersing the solid carrier coated with the hydrosoluble polymer obtained in the previous step, in a clotting agent selected from the group consisting of 2-propanol, ethanol, 1-propanol, and dioxane; c) drying the solid carrier coated with the hydrosoluble polymer of the previous step and immersing it in an irradiation solution comprising glycidyl metacrylate (GMA) monomers; d) irradiating with a source of 60-Cobalt and drying the bi-structured matrix obtained; and e) incubating the matrix obtained in the previous step with an aqueous solution comprising sodium sulfite and isopropanol, and drying.

67 . The process according to claim 66 , wherein the irradiation solution comprises ethanol/water.

68 . The process according to claim 66 , wherein the irradiation solution comprises an amount of between 2% and 6% of the glycidyl metacrylate (GMA) monomer.

69 . A process for manufacturing the matrix according to claim 55 , comprising the following steps:
a) contacting a cross-linked polyurethane foam solid carrier with a hydrosoluble polymer selected from the group consisting of polyvinyl alcohol, agarose, and hydroxyethylcellulose until obtaining a polymer solid carrier coated with a hydrosoluble polymer; b) immersing the solid carrier coated with the hydrosoluble polymer obtained in the previous step, in a clotting agent selected from the group consisting of 2-propanol, ethanol, 1-propanol, and dioxane; c) drying the solid carrier coated with the hydrosoluble polymer of the previous step and immersing it in an irradiation solution comprising glycidyl metacrylate (GMA) monomers; d) irradiating with a source of 60-Cobalt and drying the bi-structured matrix obtained; e) incubating the matrix obtained in the previous step with a solution comprising iminodiacetic acid (IDA) and dimethyl sulfoxide (DMSO); and f) incubating next in the presence of and acid and drying.

70 . The process according to claim 69 , wherein the irradiation solution comprises ethanol/water.

71 . The process according to claim 69 , wherein the irradiation solution comprises an amount of between 2% and 6% of the glycidyl metacrylate (GMA) monomer.

72 . A process for manufacturing the matrix according to claim 5

Assignees

• Consejo Nacional De Investigaciones Cientificas Y Tecn Conicet
• Univ Nacional De Quilmes
• Inis Biotech Llc

Inventors

• Sanchez Mirna
• Grasselli Mariano
• Martinez Leandro J

Classifications

• B01J20/3291

  Characterised by the shape of the carrier, the coating or the obtained coated product · CPC title

• B01L2200/16

  Reagents, handling or storing thereof · CPC title

• B01L2200/12

  Specific details about manufacturing devices · CPC title

• B01J20/261

  obtained by reactions only involving carbon to carbon unsaturated bonds (macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds per se C08F) · CPC title

• C07K1/16

  by chromatography · CPC title