The present invention relates to monolithic bodies, uses thereof and processes for the preparation thereof. Certain embodiments of the present invention relate to the use of a monolithic body in the preparation of a radioactive substance, for example a radiopharmaceutical, as part of a microfluidic flow system and a process for the preparation of such a monolithic body.

A first ethylene-based interpolymer comprising, in polymerized form, monomer units derived from ethylene and from a benzocyclobutene (VBCB) structure of Structure 1; wherein n is from 3 to 10; and wherein the ethylene-based polymer comprises, in polymerized form, from 0.02 to 0.70 wt % of the Structure 1, based on the weight of the first ethylene-based interpolymer, as determined by .sup.1H NMR is provided. Further provided is a composition which comprises a second ethylene-based inter-polymer formed by thermally treating a first ethylene-based interpolymer.

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.

The present invention relates to a chromatographic device for isolating and purifying nucleic acids, preferably genomic DNA, by gel filtration chromatography, a method for isolating and purifying nucleic acids, preferably genomic DNA, using this device and a kit comprising this device.

The present invention relates to a chromatographic device for isolating and purifying nucleic acids, preferably genomic DNA, by gel filtration chromatography, a method for isolating and purifying nucleic acids, preferably genomic DNA, using this device and a kit comprising this device.

A sol-gel sorbent or chromatography stationary phase is a particulate metal oxide gel containing polymeric segments uniformly distributed throughout the metal oxide gel. The metal oxide gel is an oxide from silicone or other metal oxide that can have one of the valence bonds attached to an organic group and the remainder occupied by oxygens that can be provided as an oxide or an alkoxide or aryl oxide of the polymeric segments. The particles are used for an SPE sorbent or as a packing for a reversed phase high-performance liquid chromatography (RP-HPLC), a normal phase high-performance liquid chromatography (NP-HPLC) column or a hydrophilic interaction liquid chromatography (HILIC) column.

A sol-gel sorbent or chromatography stationary phase is a particulate metal oxide gel containing polymeric segments uniformly distributed throughout the metal oxide gel. The metal oxide gel is an oxide from silicone or other metal oxide that can have one of the valence bonds attached to an organic group and the remainder occupied by oxygens that can be provided as an oxide or an alkoxide or aryl oxide of the polymeric segments. The particles are used for an SPE sorbent or as a packing for a reversed phase high-performance liquid chromatography (RP-HPLC), a normal phase high-performance liquid chromatography (NP-HPLC) column or a hydrophilic interaction liquid chromatography (HILIC) column.

The present invention relates to a quality control marker and method of using such marker in qualitative and quantitative authentication of Cordyceps sinensis, which is known as a Chinese medicine under the name of Dongchong Xiacao .

A separation medium for removing small molecules from biomacromolecule in aqueous mixtures comprises gel filtration chromatography beads having a nominal protein fractional range of about 1000 Da to about 5000 Da and having an internal adsorbent matrix derived from a hydrophobicized scaffold. The gel filtration chromatography beads remove small molecules that are less than 1500 Da and have log Pow values greater than about −0.5 from biomacromolecules in aqueous mixtures. Devices containing the separation medium are also provided.