B01F23/66

Method for producing test pieces of water-insoluble material for MALDI mass spectrometry and method for quantitative analysis of water-insoluble material using MALDI mass spectrometry

The present invention relates to a method for producing test pieces in which the thickness of the samples of homogeneous water-insoluble material is uniform, and to a method for quantitative analysis of water-insoluble material by analyzing such test pieces using MALDI mass spectrometry. Specifically, the test pieces can be produced by: adding a volatile solvent to a mixture of water-insoluble material and matrix; placing, in a pellet cup made of water-soluble material, and pressing, with even pressure, the sample obtained by mixing the mixture of water-insoluble material and matrix until the solvent has evaporated; and melting the pellet cup with water.

Device for mixing powders by cryogenic fluid

A device for mixing powders by cryogenic fluid, characterised in that it comprises at least: a chamber for mixing powders, comprising a cryogenic fluid; a chamber for supplying powders in order to allow the powders to be introduced into the mixing chamber; means for agitation in the mixing chamber so as to allow the mixing of the powders placed in suspension in the cryogenic fluid.

Method for Producing Test Pieces of Water-Insoluble Material for Maldi Mass Spectrometry and Method for Quantitative Analysis of Water-Insoluble Material Using Maldi Mass Spectrometry

The present invention relates to a method for producing test pieces in which the thickness of the samples of homogeneous water-insoluble material is uniform, and to a method for quantitative analysis of water-insoluble material by analyzing such test pieces using MALDI mass spectrometry. Specifically, the test pieces can be produced by: adding a volatile solvent to a mixture of water-insoluble material and matrix; placing, in a pellet cup made of water-soluble material, and pressing, with even pressure, the sample obtained by mixing the mixture of water-insoluble material and matrix until the solvent has evaporated; and melting the pellet cup with water.

Device for mixing powders by cryogenic fluid and generating vibrations

A device for mixing powders by a cryogenic fluid, characterised in that it comprises: a chamber for mixing the powders, comprising a cryogenic fluid, provided with means for forming a fluidised powder bed; a chamber for supplying powders in order to allow the powders to be introduced into the mixing chamber; a chamber for supplying cryogenic fluid in order to allow the cryogenic fluid to be introduced into the mixing chamber; a system for generating vibrations in the fluidised powder bed; and a system for controlling the system for generating vibrations.

DEVICE FOR MIXING POWDERS BY CRYOGENIC FLUID
20180318778 · 2018-11-08 ·

A device for mixing powders by cryogenic fluid, characterised in that it comprises at least: a chamber for mixing powders, comprising a cryogenic fluid; a chamber for supplying powders in order to allow the powders to be introduced into the mixing chamber; means for agitation in the mixing chamber so as to allow the mixing of the powders placed in suspension in the cryogenic fluid.

DEVICE FOR MIXING POWDERS BY CRYOGENIC FLUID AND GENERATING VIBRATIONS
20180318779 · 2018-11-08 ·

A device for mixing powders by a cryogenic fluid, characterised in that it comprises: a chamber for mixing the powders, comprising a cryogenic fluid, provided with means for forming a fluidised powder bed; a chamber for supplying powders in order to allow the powders to be introduced into the mixing chamber; a chamber for supplying cryogenic fluid in order to allow the cryogenic fluid to be introduced into the mixing chamber; a system for generating vibrations in the fluidised powder bed; and a system for controlling the system for generating vibrations.

Solid dispersions of insoluble drug and preparation method thereof

The present invention relates to a solid dispersion characterized in that it comprises carbamic acid 3-(4-benzyloxy-phenyl)-isoxazol-5-ylmethyl ester as an active ingredient and a water-soluble polymer having a glass transition temperature lower than the melting point of the active ingredient as a carrier, and it is prepared via melt extrusion. The solid dispersion of the present invention remarkably increases the solubility and dissolution rate of the active ingredient which is an insoluble drug to efficiently improve the bioavailability when it is orally administered.

SOLID DISPERSIONS OF INSOLUBLE DRUG AND PREPARATION METHOD THEREOF

The present invention relates to a solid dispersion characterized in that it comprises carbamic acid 3-(4-benzyloxy-phenyl)-isoxazol-5-ylmethyl ester as an active ingredient and a water-soluble polymer having a glass transition temperature lower than the melting point of the active ingredient as a carrier, and it is prepared via melt extrusion. The solid dispersion of the present invention remarkably increases the solubility and dissolution rate of the active ingredient which is an insoluble drug to efficiently improve the bioavailability when it is orally administered.

Solid dispersions of insoluble drug and preparation method thereof

The present invention relates to a solid dispersion characterized in that it comprises carbamic acid 3-(4-benzyloxy-phenyl)-isoxazol-5-ylmethyl ester as an active ingredient and a water-soluble polymer having a glass transition temperature lower than the melting point of the active ingredient as a carrier, and it is prepared via melt extrusion. The solid dispersion of the present invention remarkably increases the solubility and dissolution rate of the active ingredient which is an insoluble drug to efficiently improve the bioavailability when it is orally administered.

Antiperspirant compositions and methods for making same

A consumer product comprising packaging including a product chamber and an outer jacket at least partially surrounding the product chamber; and an antiperspirant composition disposed within the product chamber, wherein the composition exhibits an average standard deviation of less than or equal to about 5 of penetration peak force measurements taken in accordance with a penetration test method as defined herein.