A method of separating a mixture of fluids may comprise contacting an absorbent material with a mixture of fluids comprising a first fluid and a second fluid having different polarities, wherein the absorbent material selectively absorbs the first fluid to provide a permeate comprising the first fluid and a retentate comprising the second fluid. The absorbent material comprises a zwitterionic polymer, the zwitterionic polymer being a polymerization product of reactants comprising a zwitterionic monomer and a (meth)acrylate crosslinker. The zwitterionic monomer is selected from the group consisting of: a zwitterionic monomer of Formula I, R—(CH.sub.2).sub.m—NR′.sub.2.sup.+—(CH.sub.2).sub.n-A.sup.−, wherein R is selected from a carboxyamide, a (meth)acrylate, and an alkyl; m is an integer of from 0 to 5; each R′ is independently selected from hydrogen and an alkyl; n is an integer of from 1 to 5; and A.sup.− is SO.sub.3.sup.− or CO.sub.2.sup.−; a zwitterionic monomer of Formula II, R—(CH.sub.2).sub.m-A.sup.−-(CH.sub.2).sub.n—NR′.sub.3.sup.+, wherein R is an (meth)acrylate; m is an integer of from 1 to 5; A is PO.sub.4.sup.−; n is an integer of from 1 to 5; and each R′ is independently selected from hydrogen and an alkyl; carboxybetaine diacrylamide; (3-methacryloylamino-propyl)-(2-carboxy-ethyl)-dimethylammonium; 3-[Dimethyl-(2-hydroxyethyl)ammonio]-1-propanesulfonate; 1-methylpyridinium 3-sulfonate; and combinations thereof.

An object of the present invention is to provide an ion-exchange membrane for simply and inexpensively separating and purifying exosomes present in a biological sample such as serum. The invention relates to a cellulose-based ion-exchange membrane containing a cellulose-based polymer having at least one hydroxyl group or acetyl group at the 2-, 3-, or 6-position being replaced with a positively charged compound. The invention also relates to a method for purifying exosomes, including subjecting a sample containing exosomes to membrane permeation by using the cellulose-based ion-exchange membrane to allow for adsorption of the exosomes, bringing the membrane into contact with a washing liquid to remove impurities, and bringing the membrane into contact with an eluent to allow for desorption of the exosomes.

An object of the present invention is to provide a chemical liquid purification method by which a chemical liquid capable of inhibiting the occurrence of short in a semiconductor substrate manufactured by a photolithography process is obtained. Another object of the present invention is to provide a chemical liquid manufacturing method and a chemical liquid. The chemical liquid purification method of the present invention includes a purification step of filtering a liquid to be purified by using a filter, in which a filter satisfying a condition 1 or a condition 2 in the following test is used as the filter. Test: 1,500 ml of a test liquid formed of the organic solvent is brought into contact with the filter for 24 hours under a condition of 23° C., and a content of particles containing at least one kind of metal selected from the group consisting of Fe, Al, Cr, Ni, and Ti in the test liquid after the contact satisfies a predetermined condition.

The present invention relates to a separation of viruses of an essentially spherical shape from viruses with a rod-like shape that are comprised in a sample, wherein the sample comprising the viruses is subjected to filtration.

The present invention relates to a separation of viruses of an essentially spherical shape from viruses with a rod-like shape that are comprised in a sample, wherein the sample comprising the viruses is subjected to filtration.

Viral filters include a filter member featuring a first surface and a second surface and having a thickness extending between the first and second surfaces in a first direction, and a plurality of channels formed in the filter member, each of the channels having a channel axis, where during use, a solution carrying a viral load flows in a direction parallel to the first surface, and at least a portion of the viral load enters the membrane through the first surface and propagates in the first direction, and where for at least 50% of the channels in the filter member, the channel axis is oriented at an angle of between 5 degrees and 85 degrees relative to the first direction.

A gas separation membrane has a gas separation layer containing a crosslinked cellulose resin. The crosslinked cellulose resin has a particular linking structure in a crosslinked structure. The gas separation layer contains an organic solvent in a particular amount.

This invention describes a method and a device for efficient isolation of extracellular vesicles from animal and human biological fluids, as well as from culture fluid using equipment of standard diagnostic laboratories, that is, without the use of ultracentrifugation. These method and device can be applied for the diagnosis of various human diseases, as well as for therapeutic purposes, if the purified vesicles are used as an agent for drug delivery to the cells of the body. The device for the purification of extracellular vesicles contains at least two membrane filters: the first filter containing a membrane with pore sizes in the range from 400 to 600 nm, connected to the second filter containing a membrane with pores in the range from 95 to 200 nm. At the same time, the membranes of these filters are made of materials that practically do not bind biological polymers.

Copper based nanoparticle composite compositions, methods, and systems for purification and sterilization of contaminated water are provided.

A filtration membrane comprising cellulose fibres, the membrane having a pore size distribution such that the modal pore diameter is between 10 nm and 25 nm and/or wherein less than 5% of the pore volume comprises pores of greater than 40 nm and having a total porosity greater than 30%.