A method and apparatus involving the configuration of an open capillary channel for size-based separation of analytes is described. The open capillary channel contains numerous turns of defined angles separated by intervening linear or curvilinear segments of capillary tubing. The configuration of the channel allows analyte differentiation based on diffusion coefficients and thus separates analytes by size.

A method and apparatus involving the configuration of an open capillary channel for size-based separation of analytes is described. The open capillary channel contains numerous turns of defined angles separated by intervening linear or curvilinear segments of capillary tubing. The configuration of the channel allows analyte differentiation based on diffusion coefficients and thus separates analytes by size.

The present invention relates to compounds and their uses, in particular, compounds in the form of prodrugs that promote transport of a pharmaceutical agent to the lymphatic system and subsequently enhance release of the parent drug.

A method for deconvoluting the molecular weight characteristics of the copolymer or rubber in an impact copolymer (ICP) comprising at least one copolymer or rubber and at least one homopolymer such as polypropylene, as well as a method of determining the comonomer characteristics of the rubber in an ICP, the methods comprising in part eluting a solubilized ICP through a gel permeation chromatographic (GPC) column to form an eluate comprising the rubber and/or polypropylene, measuring the Infrared (IR) absorption of at least the primary monomer-derived unit stretch frequency and the comonomer-derived unit in elution volume slices to determine the amount of comonomer, measuring the concentration of ICP using any detector, and determining the mass concentration, comonomer composition, and the total comonomer content of the ICP through the appropriate mathematical transformations.

Herein disclosed is an economical standalone system that replaces conventional monomer purification methods needed to perform chemical reactions that require reactants with a high degree of purity. Chemical reactions, such as anionic polymerization, can produce highly monodisperse homopolymers and block copolymers, however to do so they require very high purity reactants along with a moisture and oxygen free atmosphere. The system and method uses traditional column purification methods, but incorporates them into an economical, standalone, compact, and hazard free system. This method is different in view of safety, cost of cleaning procedure, time commitment, space availability, design and operational ease; helping researchers save time by cutting down the operating commitment by 90% and most importantly making it safer.

Herein disclosed is an economical standalone system that replaces conventional monomer purification methods needed to perform chemical reactions that require reactants with a high degree of purity. Chemical reactions, such as anionic polymerization, can produce highly monodisperse homopolymers and block copolymers, however to do so they require very high purity reactants along with a moisture and oxygen free atmosphere. The system and method uses traditional column purification methods, but incorporates them into an economical, standalone, compact, and hazard free system. This method is different in view of safety, cost of cleaning procedure, time commitment, space availability, design and operational ease; helping researchers save time by cutting down the operating commitment by 90% and most importantly making it safer.

Apatite pretreatment methods are provided. The method is applied to the apatite solid surface prior to first chromatographic use. In one embodiment, the method may be achieved by contacting an apatite solid surface with a phosphate buffered solution at a pH of at least about 6.5 and contacting the apatite solid surface with a solution having a hydroxide.

Methods for purifying biological macromolecules are provided. Aspects of the subject methods include contacting the biological macromolecule with an exemplary hydroxamate affinity tag to produce a tagged moiety followed by purification of the tagged moiety by immobilized metal affinity chromatography (IMAC). Also provided are kits comprising an exemplary subject hydroxamate affinity tag, an IMAC resin and a metal ion configured for loading onto the resin, wherein the metal ion is capable of binding to a compound containing the hydroxamate affinity tag.

Methods for purifying biological macromolecules are provided. Aspects of the subject methods include contacting the biological macromolecule with an exemplary hydroxamate affinity tag to produce a tagged moiety followed by purification of the tagged moiety by immobilized metal affinity chromatography (IMAC). Also provided are kits comprising an exemplary subject hydroxamate affinity tag, an IMAC resin and a metal ion configured for loading onto the resin, wherein the metal ion is capable of binding to a compound containing the hydroxamate affinity tag.

A process for removing iodine using gold particles includes contacting a solution including iodine, with gold particles. The iodine is adsorbed onto the gold particles and then removed. A device for removing iodine using gold particles includes gold particles in a stationary phase and is configured to contact a solution including iodine, with gold particles, to thus adsorb the iodine onto the gold particles and remove the iodine.