Abstract: The disclosure relates to a dosage forms and combinations of dosage forms useful for effective oral administration of drugs which are otherwise unsuitable for oral administration, owing to acid- and/or protease-mediated degradation. The dosage forms include a self-microemulsifying drug delivery system (SMEDDS) with which the drug is combined and an antacid. When co-administered to a mammal, the dosage form(s) can prevent drug degradation by the strong acid and digestive enzymes normally present in the gastric environment, and can improve water-soluble drug absorption in gastrointestinal (GI) tract. The dosage forms can be used to effectively administer insulin by an oral route, for example, such as in the form of a powder that can be stored for long periods and reconstituted with water or another fluid shortly before administration.

Abstract: The present invention is directed to flumioxazin suspension concentrates containing a polyoxyethylene polyarylphenol phosphate or phosphate ester acid salts thereof. The present invention is further directed to a method of controlling weeds by applying compositions of the present invention.

Abstract: The present invention is directed to an aqueous herbicidal composition containing one or more low water solubility herbicides, hydroxyethyl cellulose, and an inorganic compound selected from the group consisting of silicon dioxide, aluminum oxide, magnesium aluminum silicate, attapulgite and mixtures thereof. The present invention is further directed to a method of controlling weeds by applying compositions of the present invention.

Abstract: A hydrogel condom containing an antioxidant can provide increased sexual pleasure, thus improving usage and resulting in prevention of disease and prevention of unwanted pregnancies.

Abstract: An all 25(b) botanical food grade, all purpose cleaner, anti-microbial and disinfectant includes a microemulsion that contains effective amounts of the ingredients of thyme oil, wintergreen oil, a surfactant, citric acid, and isopropanol. The ingredients combined with water to produce a clear microemulsion for application as a cleaner/disinfectant as well as treating growing and harvested crops, animals and pets for pesticide purposes and as a dust suppressant and to disrupt bioaerosols in the air and/or remove them from the air. Areas of treatment can include hospitals, homes, construction sites, open areas outside, laboratories, and the like.

Abstract: A trichome and pistil maturing bud finisher plant treatment formula to which plants, pollinators, and humans respond favorably but which deters insects and contagions. The formulas include a series of edible spices claimed in specific ratios. The spices comprise food grade products manufactured for human consumption and specifically comprise Garlic, Ginger, Cinnamon, Turmeric, Clove, Black Pepper, Powdered Ancho Chili, Coriander, Cayenne, Cumin, Fenugreek, Nutmeg, and Oregano. In the bud finisher formula, these spices are mixed with potassium bicarbonate in a first container in relative quantities. Meanwhile, the bud finisher formula requires mixing sesame oil with apple cider vinegar, also in a particular ratio. The bud finisher formula matures pistils and trichomes. An alternative bud shield formula excludes the potassium bicarbonate and apple cider vinegar to also mature trichomes but matures pistils at a slower rate. After dilution the plant treatment formula is applied to all surfaces of the plant.

Abstract: A valve structuring designed for use in all water installations, water inlets for houses, kitchen installations and embedded shower filters as a stop valve, in the areas to perform on-off control, in faucets with the purpose of providing water savings and to use in domestic and industrial type kitchen faucets as a stop valve. The valve is designed for use as an on-off valve in air installations that operate with air.

Abstract: The present Invention relates to pharmaceutical compositions of (3S,11aR)—N-[(2,4-difluorophenyhmethyl]-2,3,5,7,11,11a-hexahydro-6-hydroxy-3-methyl-5,7-dioxo-oxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamide, useful in the treatment or prevention of Human Immunodeficiency Virus (HIV) infections.

Abstract: Disclosed is a method of enhancing bud break in plants, comprising administering a combination of an amine polymer delivery agent and a sulfur containing compound to said plants. Disclosed also is a formulation comprising an amine polymer delivery agent and a sulfur containing compound. In addition, the use of such a formulation for enhancing bud break in plants is also disclosed.

Abstract: A hand held spray device is disclosed. The spray device includes a body with a reservoir, an actuator with an actuator exit orifice, a valve in fluid communication with the actuator exit orifice and the reservoir and a propellant and antiperspirant composition stored in the reservoir. The propellant has a concentration from about 30% to about 70% by weight of the total fill of materials stored within the reservoir and a boiling point at 1 atmosphere from about ?10° C. to about 10° C. The antiperspirant composition includes a liquid carrier and an antiperspirant active.

Abstract: The patent discloses self-emulsifying formulations of bisphosphonates or bisphosphonic acids in the prevention and treatment of conditions involving calcium or phosphate metabolism. The dosage forms are either capsules, or tablets, or other controlled release drug delivery systems, or devices that contain self-emulsifying formulation of such bisphosphonates or bisphosphonic acids.

Abstract: A herbicidal composition comprises an aqueous solution of a plurality of salts of glyphosate wherein said glyphosate is in anionic form accompanied by low molecular weight non-amphiphilic cations, wherein a major amount but less than 100% of the low molecular weight non-amphiphilic cations are potassium cations, and wherein the composition has a measured pH of at least about 4.8.

Abstract: Provided is a compound of formula (I) or an N-oxide thereof, wherein Het1 represents Het1-1, Het1-2, Het1-3, Het1-4 or Het1-5, and the remaining variable groups are as defined in the specification. The compound of formula (I) or N-oxide compound thereof has an excellent control effect against arthropod pests.

Abstract: A compound represented by formula (I) or an N-oxide compound thereof is provided with excellent control efficacies against harmful arthropods, wherein A1 represents a nitrogen atom or a CR4; R4 represents a hydrogen atom, a OR27, a NR27R28, a cyano group, a nitro group, or a halogen atom; hereinafter referred to as “Het”, represents Het-1, Het-2, Het-3, or Het-4: wherein #1 represents the binding position of Het and T, and #2 represents the binding position of Het and T represents T-1, T-2, T-3, T-4, T-5, T-6, or T-7: R1 represents a C1-C10 chain hydrocarbon group having one or more halogen atoms or the like; and R2 represents a C1-C6 alkyl group optionally having one or more halogen atoms or the like.

Abstract: Pharmaceutical composition of memantine for administering orally which comprises a premixture comprising: i) between 74 and 85% w/w total of the premixture of a granulate of pellets comprising memantine between 10 and 15% w/w total of the premixture; coated by first coating of polyvinylpyrrolidone and a second coating comprising between 80 and 95% w/w total of the coating of cationic copolymer of dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate and between 5 and 20% w/w total of the coating of magnesium stearate; ii) between 4 and 7% w/w total of the premixture of sucralose; iii) between 11 and 19% w/w total of the premixture of essences. All the components have a particle size smaller than 710 microns. The composition can be a suspension, a powder for preparing a suspension or an oral disintegrating tablet. It can also be used to be administered through a nasogastric tube.

Abstract: A hand held spray device is disclosed. The spray device has a body with a reservoir to house a total fill of material, an actuator having an actuator exit orifice, a valve in fluid communication with the actuator exit orifice and the reservoir, and a propellant and antiperspirant composition stored in the reservoir. The propellant has a concentration from 30% to 70% by weight of the total fill of materials stored within the reservoir. The antiperspirant composition includes a non-volatile silicone fluid having a concentration from about 30% to about 70% by weight of the antiperspirant composition, an antiperspirant active, an organoclay material and at least one liquid activation enhancer, and optionally a liquid fragrance material.

Abstract: The present invention relates to compounds of Formula (I): wherein R1 is as defined herein, or an acceptable salt, solvate, prodrug or hydrate thereof. The compounds of Formula I are inhibitors of metalloenzymes, such as lanosterol demethylase (CYP51).

Abstract: The present invention relates to formulations and methods of arthropod control employing formulations comprising certain essential oils formulated as soaps using a saponified or partially saponified formulation comprising a mixture of fatty acids, geraniol, and peppermint oil.

Abstract: The present invention relates to methods for increasing absorption of compounds of interest by nematode worms through the design of carrier systems containing said compound of interest and expressing chemoattractive tags at their surface.

Abstract: Stents and methods for producing stents are provided. The stent includes a polymeric substrate comprised of 10-50% (w/w) of alginate and 45-85% (w/w) of gelatine and further includes a polymeric biodegradable resin for coating said polymeric substrate. The stent can also include a contrast agent. The stent can further include a crosslinking agent. The method for producing the stent includes dissolving the alginate and gelatine in water and stirring to obtain a polymeric substrate. The method also includes adding a crosslinking agent to the substrate, injecting the substrate into a mold to obtain the stent, placing the stent in a first alcohol solution, and placing the stent in a crosslinking agent solution. The method further includes placing the stent in a second alcohol solution, and a series of interchanging drying and immersing steps.