Abstract:
PROBLEM TO BE SOLVED: To provide an oral dosage form delayedly releasing active ingredient(s) through floating on gastric juice. SOLUTION: This oral dosage form comprises (a) one or more active ingredient(s), (b) a formulated mixture of polyvinyl acetate and polyvinylpyrrolidone and (c) optionally, another excipient commonly used for producing oral dosage forms.
Abstract:
PROBLEM TO BE SOLVED: To provide an oral administration form exhibiting a delayed active substance release and a high mechanical stability, since the method for adjusting the above releasing profile while maintaining the skeletal and mechanical stability is not publicly known. SOLUTION: This oral administration form exhibiting the delayed active substance release and the high mechanical stability is provided by incorporating a) >=1 active substance, b) a blended mixture consisting of a polyvinyl acetate and polyvinylpyrrolidone, c) a water soluble polymer, or a low molecular weight or high molecular weight lipophilic additive and d) other usually used assistants.
Abstract:
Textile detergent formulation containing a) 0.1 - 10 wt % quaternized glycine nitriles, b) 0.5-40 wt % bleaching agents in the form of peroxo compounds and/or peracids, c) 0.5 - 50 wt % non-ionic and/or anionic tensides and d) 5-85 wt % calcium ion and/or magnesium ion sequestering compounds. The formulation is suitable for household and industrial textile washing, in a dosage of over 2g per litre detergent solution, in particular in a textile: detergent solution bath ratio of 1:10 to 1:2.
Abstract:
The present application describes a process for regenerating a ruthenium catalyst for the hydrogenation of benzene, which comprises flushing the catalyst with inert gas in a regeneration step until the original or part of the original activity is attained.
Abstract:
The invention relates to animal food additives containing a vitamin B6, a method for producing said additives, animal food compounds containing the inventive additive and a method for introducing said additives into the animal food compounds.
Abstract:
The invention relates to a pharmaceutical formulation in the form of agglomerates containing a) 60 - 97 % by weight of sugar or sugar alcohols, b) 1 - 25 % by weight of cross-linked polyvinylpyrrolidone, c) 1 - 15 % by weight of water-insoluble, film-forming polymers, d) 0 - 15 % by weight of water-soluble polymers, and e) 0 - 15 % by weight of other pharmaceutically suitable adjuvants, the sum of components a) to e) adding up to 100 % by weight.
Abstract:
A substantially solid composition, the composition having therein a compound with the structure of Formula (I) wherein A, R1, R2, R3, Y and Z are as defined in the disclosure.
Abstract:
Granules are provided that are useful for oxidizing applications when the granules are dissolved in the presence of an active oxygen source. These granules include a salt having the structure of formula (I), wherein A, R1, R2, R3, Y and Z are as defined in the disclosure. The salt is carried by, coated with, or admixed with a solid particulate such as silica gel, silicic acid, silicate, aluminum oxide, clay, aluminum silicate, or mixtures thereof.
Abstract:
A pharmaceutical formulation in the form of agglomerates comprising a) 60-97% by weight of sugar or sugar alcohols, b) 1-25% by weight of crosslinked polyvinylpyrrolidone, c) 1-15% by weight of water-insoluble, film-forming polymers, d) 0-15% by weight of water-soluble polymers and e) 0-15% by weight of further pharmaceutically customary excipients, the sum of the components a) to e) being 100% by weight.
Abstract:
PCT No. PCT/EP95/04934 Sec. 371 Date Jun. 18, 1997 Sec. 102(e) Date Jun. 18, 1997 PCT Filed Dec. 13, 1995 PCT Pub. No. WO96/20155 PCT Pub. Date Jul. 4, 1996Process for preparing solid, free-flowing water-soluble salts of aryloxy-C1-C4-alkanecarboxylic acids by reacting the aryloxy-C1-C4-alkanecarboxylic acids with a salt-forming base, the salt formation taking place in the melt in the presence or absence of an entraining agent suitable for the azeotropic removal of water or in solution in the presence of an entraining agent suitable for the azeotropic removal of water and, if appropriate, removing the entraining agent from the reaction mixture during the reaction or subsequently and then isolating the solid salts in a customary manner.