Abstract:
An electromagnetic immune tissue invasive system includes a primary device housing (1100 of Figure 30). The primary device housing having a control circuit therein (1110 of Figure 30). A shielding (1160 of Figure 30) is formed around the primary device housing (1100 of Figure 30) to shield the primary device housing and any circuits therein from electromagnetic interference. A lead system (1150 of Figure 30) transmits and receives signals between the primary device housing (1100 of Figure 30). The lead system (1150 of Figure 30) is either a fiber optic system or an electrically shielded electrical lead system.
Abstract:
An apparatus for regulating the concentration of insulin within the blood of a living organism, wherein said apparatus is comprised of an in vitro cell culture for producing insulin, an in vitro cell culture for producing glucagon, an in vitro cell culture for producing somatostatin, means for measuring the concentration of glucose within the blood of such living organism, means for measuring the concentration of insulin within the blood of such living organism, means for delivering a specified amount of insulin to the blood of such living organism, means for delivering a specified amount of glucagon to the blood of such living organism, means for delivering a specified amount of somatostain to the blood of such living organism, and means for reducing the amount of insulin within such blood of such living organism.
Abstract:
An electronic database for identification of enzyme substrate and enzyme inhibitor structures that are structurally similar to a submitted chemical structure is provided. The enzyme substrate and enzyme inhibitor structures can be linked by numerous parameters, such as by Enzyme Classification Number. The database can be used to identify potential therapeutics for newly discovered enzymes or enzymes families.
Abstract:
The invention relates to compositions and co-crystals each comprising VX-950 and a co-crystal former selected from the group consisting of 4-hydroxybenzoic acid, 4-amino salicylic acid, phenylalanine, threonline, tartaric acid, adipic acid, succinic acetate, proline, methyl 4-hydroxybenzoate, anthranilic acid, and d-Biotin. Also within the scope of this invention are methods of making and using the same.
Abstract:
A process for the in vivo treatment of the bodily fluid of a biological organism is presented, wherein the organism is implanted with a capture device containing a target specific binding agent. The bodily fluid of the donor is brought into contact with the binding agent and the desired cellular components are allowed to bind with the binding agent.
Abstract:
An electromagnetic immune tissue invasive system includes a primary device housing (1100 of Figure 30). The primary device housing having a control circuit therein (1110 of Figure 30). A shielding (1160 of Figure 30) is formed around the primary device housing (1100 of Figure 30) to shield the primary device housing and any circuits therein from electromagnetic interference. A lead system (1150 of Figure 30) transmits and receives signals between the primary device housing (1100 of Figure 30). The lead system (1150 of Figure 30) is either a fiber optic system or an electrically shielded electrical lead system.
Abstract:
A temperature gradient calorimeter and method of calculating heats of reactions is disclosed. The calorimeter has a two dimensional array of reaction chambers located in a thermally conductive substrate. A first heat transfer medium is in thermal contact with the thermal conductive substrate and is located at one region of the array of reaction chambers. A second heat transfer medium is in thermal contact with the thermal conductive substrate and is located on the opposite side of the array from the first heat transfer medium. The first and second heat transfer mediums are at two different temperatures. That temperature difference produces a temperature gradient across the array of reaction chambers. The fluorescence intensities are measured for reactant samples located in the array of reaction chambers. By inserting the fluorescence intensity data into thermodynamic equations expressing the degree of advancement and the heat of reaction, the heat of reaction for the reaction process of the sample can be determined.
Abstract:
The present disclosure relates to co-crystals comprising N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide (Compound 1) and a co-former and methods for their preparation. The present disclosure further relates to pharmaceutical compositions comprising the co-crystal forms, as well as methods of treatment therewith and kits.
Abstract:
The invention relates to compositions and co-crystals each comprising VX-950 and a co-crystal former selected from the group consisting of 4-hydroxybenzoic acid, 4-amino salicylic acid, phenylalanine, threonline, tartaric acid, adipic acid, succinic acetate, proline, methyl 4-hydroxybenzoate, anthranilic acid, and d-Biotin. Also within the scope of this invention are methods of making and using the same.
Abstract:
The present invention relates to solid state forms of N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide (Compound 1), pharmaceutical compositions thereof and methods therewith.