Abstract:
Exemplary embodiments are generally directed to beverage chillers for chilling a hot beverage so that the hot beverage can be served as a chilled beverage in real time on demand fashion. The beverage chillers include a beverage collection section, a heat exchanger section, and a dispensing section fluidically connected relative to each other. The beverage collection section receives a beverage in a hot state. The heat exchanger section chills the beverage from the hot state to a predetermined chilled temperature. The dispensing section dispenses the beverage at or near the predetermined chilled temperature. Exemplary embodiments are also directed to methods and systems for chilling a hot beverage in real time on demand fashion.
Abstract:
Disclosed are compositions for inhibiting transmission of a sexually transmitted infection that contain one or more polyanionic microbicides, such as carrageenans, including lambda carrageenan, as well as water-soluble metal salts and specified antiretro viral agents comprising NNRTIs and NRTIs. Also disclosed are methods for making and using the compositions.
Abstract:
The present invention relates antidotes to anticoagulants targeting factor Xa. The antidotes are factor Xa protein derivatives that bind to the factor Xa inhibitors thereby substantially neutralizing them but do not assemble into the prothrombinase complex. The derivatives describe herein lack or have reduced intrinsic coagulant activity. Disclosed herein are methods of stopping or preventing bleeding in a patient that is currently undergoing anticoagulant therapy with a factor Xa inhibitor.
Abstract:
The present invention provides methods and compositions useful in the treatment or prevention of cardiovascular disorders in individuals for whom therapy with a COX-1 enzyme inhibitor is not feasible due to sensitivity, intolerance, or resistance to the inhibitor. Additionally, the invention provides methods of treating cardiovascular disorders in an individual who is receiving a therapeutically effective dose of a TP modulator and is instructed or advised to avoid and/or not to take aspirin or another COX-1 inhibitor.
Abstract:
An instrument for capturing an image of thrombus formation, blood coagulation, recruitment of circulating inflammatory or tumour cells in a blood sample. The instrument comprises a member defining a channel therethrough, a fluid handling assembly that permits the blood sample to move through the channel at a flow rate, and an imaging assembly including a microscopy device. The imaging assembly is disposed relative to the channel so as to capture light rays defining the image of thrombus formation in the channel.
Abstract:
The present invention concerns naphthalene and quinoline derivatives of formula (I), processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals. R, R 1 , R 2 , R 3 , R 4 , X and W are defined as in claim I.
Abstract translation:本发明涉及式(I)的萘和喹啉衍生物,其制备方法,含有它们的药物组合物及其作为药物的用途。 R 1,R 1,R 2,R 3,R 4,X和W如权利要求1中所定义, 一世。
Abstract:
Wet barrel fire hydrants (10) which feature additional structure for reducing the potential that those with ill intent can foul municipal water supplies by- introducing toxins or other materials into fire hydrants. Various embodiments include valves which close off portions of the hydrant or water conduit otherwise available for receipt of toxic or other materials when the fire hydrant nozzle cap is unscrewed and open and/or a pump is connected to the nozzle (14). Such valves preferably open automatically when water is flowing from the water supply through the nozzle (14), but close off portions of the barrel when the nozzle (14) is open and water is not flowing through the nozzle (14).
Abstract:
A compound of formula (I) or a pharmaceutically acceptable salt, solvate or N-oxide thereof: wherein A represents a pyrrole, pyrazole, imidazole or triazole ring; B represents a benzene, pyridine or pyrimidine ring; M represents the residue of an azetidine, pyrrolidine or piperidine ring; E represents a covalent bond or an optionally substituted straight or branched alkylene chain containing from 1 to 4 carbon atoms; Z represents hydrogen, -CORa, -C0 2 R b , -CONK c R d , -CONR c OR b , -COCO 2 R b , - COCONR c R d , -COCH2NR c R d , -COCH2NR c CONK c R d , COCH2NR c CO 2 R b , -NR c COR a , - NR c CO2R b , -NR c CONR c R d , -S0 2 R e , -SO 2 NR c R d or -SO2NR c C0 2 R b ; or Z represents an optionally substituted phenyl, heteroaryl or C 3-7 heterocycloalkyl group; R 1 and R 2 independently represent hydrogen, halogen, cyano, nitro, C 1-6 alkyl, trifluoromethyl, hydroxy, C 1-6 alkoxy, difluoromethoxy, trifluoromethoxy, C 1-6 alkylsulphonyl, amino, C 1-6 alkylamino, di(C 1-6 )alkylamino, aminocarbonyl or C 2-6 alkoxycarbonyl; R 3 represents hydrogen, C 1-6 alkyl, -CH2CONR c R d or -SO 2 R e ; R 4 represents hydrogen, C 1-6 alkoxy, oxo, -CO2R b or -CONK c R d . The compounds of the present invention are potent inhibitors of JNK.
Abstract:
The present invention provides novel compositions and methods for inhibiting restenosis, thrombosis, and/or inflammation in a patient undergoing a vascular intervention. More particularly, the present invention provides intravascular devices coated with one or more spleen tyrosine kinase (Syk) inhibitors. Methods for inhibiting restenosis, thrombosis, and/or inflammation in a patient by treatment with such intravascular devices are also provided. In addition, the present invention provides methods for treating sickle cell disease using Syk inhibitors.
Abstract:
Disclosed are compositions for inhibiting transmission of a sexually transmitted infection that contains one or more carrageenans, including lambda carrageenan. Also disclosed are methods for making and using the compositions.