The present invention provides a multi-stage filter system suitable for the production of drinking water from a wide variety of contaminated water sources. The modular nature of the multi-stage filter system allows for the customization of filter combinations according to the remediation requirements. The multi-stage filter system comprises a coarse filter (S1); an ultrafiltration filter (S2); a graphene-based filter (S3); and a residual nanoparticle filter (S4). The graphene-based filter cartridge comprises few-layer graphene powder; a combination of few-layer graphene powder and pellets comprising a mixture of polyethersulfone, graphene oxide (GO), and dimethylformamide; a composite comprising chitosan, GO, sodium sulfate and ferric chloride; or a combination of few-layer graphene powder, granular activated carbon and a composite comprising chitosan, GO, sodium sulfate and ferric chloride.

A crossflow filtration unit for continuous diafiltration of a feed fluid for obtaining a retentate and a permeate, a corresponding method for diafiltration and the use of the crossflow filtration unit are provided. The crossflow filtration unit includes a diafiltration channel, a flat first filter material, a retentate channel, a flat second filter material, and a permeate collection channel, arranged such that the flat first filter material delimits the diafiltration channel and the retentate channel from one another, and the flat second filter material delimits the retentate channel and the permeate collection channel from one another. The diafiltration channel is fluidly connected to at least one inlet for the diafiltration medium, the retentate channel is fluidly connected to at least one inlet for the feed fluid and to at least one outlet for the retentate. The permeate collection channel is fluidly connected to at least one outlet for the permeate.

This disclosure relates generally to process filtration systems, and more particularly to systems utilizing tangential flow filtration.

The present invention relates to methods for purifying bacterial polysaccharides, in particular for removing impurities from cellular lysates of bacteria producing polysaccharides, comprising: a) acid hydrolysis; b) a first ultrafiltration/diafiltration-(UFDF-1); b) carbon filtration; c) chromatography; and d) a second ultrafiltration/diafiltration-(UFDF-2).

A system for filling multiple sterile containers includes a filter with an inlet port and multiple outlet ports, the outlet ports being pre-attached to sterile containers by respective filling lines of each container. Each container has an interior and each of the respective filling lines are connected to a respective container interior. The respective filling lines are sealed to the outlet ports and the containers such that the container interiors are isolated from an external environment except the inlet port, via the filter, forming a combined interior volume which is sterile. A container that is connectable to an outlet port the system has a bladder, a first tube and a second tube connected to the bladder, and a sterilizing filter. The container, the first tube and the second tube, and the sterilizing filter are sterile before water is flowed through the sterilizing filter into the bladder.

A single-use device for filtration of a large volume of medium including a plurality of single-use filter units, at least some of which, preferably all of which, are connected to each other by rigid pipes. The filter units include at least one prefilter and at least one main filter for virus filtration which is configured as a hollow fiber capsule.

Disclosed are a polysaccharide-peptide composite and a method of preparing the same. The polysaccharide-peptide composite is prepared from a bitter melon peptide (BMP) powder, gardenia fruit oil, a soybean polypeptide powder, an oat dietary fiber powder, a konjac powder, a corn silk, a mulberry leaf extract, a Poria cocos extract, a hawthorn extract, nutritional yeast and a pancreatin. The BMP powder is prepared by temperature-controlled hydrolysis, staged enzymatic hydrolysis and multiple filtrations. The gardenia fruit oil is prepared by staged enzymatic hydrolysis, multi-step centrifugation, filtration and stratification.

A near-zero maintenance integrated purification device for drinking water supply of villages and towns and a method for treating source water using this device are provided to solve the multi-pollution problems caused by microorganisms, turbidity, iron, manganese, taste and odor, and organic matter in the drinking water sources of villages and towns. The device includes a small-spacing folding plate speed sink regulating water tank, a small diameter tube reactor, a granular active carbon (GAC) slow-speed filter tank, a gravity-driven ultrafiltration membrane tank and an ipsilateral U-turn corridor clean water tank. The near-zero maintenance integrated purification device is applicable to different types of water sources (e.g., groundwater, lake water, reservoir water, spring water, snowmelt water, cellar water and rain water, etc.), and could efficiently remove kinds of pollutants, improving the biological and chemical safety of drinking water.

Disclosures herein are directed to first compositions comprising exosomes and extracellular matrix components and their use thereof. Also described are methods and kits wherein these first compositions are packaged and used with second compositions comprising mesenchymal stem cells. The first and second compositions are derived from the same tissue source using tangential flow filtration.

This present disclosure provides a process for concentrating proteins including an ultrafiltering, a diafiltering, and a second ultrafiltering sequence, at elevated temperatures, such as above about 30° C. The disclosure also includes a process of preparing highly concentrated antibody compositions. and highly concentrated antibody products.