40results about How to "Improves friability" patented technology

Methods of administering and pharmaceutical compositions of a biphenyl sulfonamide compound which is a dual angiotensin and endothelin receptor antagonist are disclosed for treating diseases.

A process for preparing a pharmaceutical dosage form or core wherein an absorption/compression agent is introduced into the formulation extra-granularly, and a pharmaceutical tablet prepared by said process.

A cellulose powder which has an average degree of polymerization of 150 to 450, an average particle diameter of 30 to 250 μm, an apparent specific volume exceeding 7 cm³/g, and a retention of polyethylene glycol having a molecular weight of 400 to 190% or higher.

The object of the present invention is to provide an adsorbent for oral administration, which can: obviate sandy texture of granules-formed adsorbent for oral administration, reduce the volume administered compared to encapsulated adsorbent for oral administration, and be easy to take.

The object of the present invention is solved by a tablet-formed pharmaceutical composition consisting of 65% or more by weight of particulate substance as an active ingredient and one or more additives, characterized in that:

• (a) the particulate substance does not exhibit water solubility and swelling property in water, has a distortion rate of 2% or less when subjected to a pressure of 2 MPa, and has a fracture strength of 5 MPa or more,
• (b) the tablet-formed pharmaceutical composition comprises one or more particle-formulating additives wherein the amount of the particle-formulating additives is 1% or more by weight in total with respect to the weight of the tablet-formed pharmaceutical composition,

and a thin layer of the particle-formulating additive can be formed when 0.5 mL of solution or dispersion liquid of the particle-formulating additive of 1% by weight is dropped on a plane surface of fluorine resin and heat-dried.

The invention discloses a plant colonic-coated hollow capsule, which is prepared by treating 80-95 percent of zein powder and 5-20 percent of a plasticizer serving as raw materials in a more than or equal to 80 percent ethanol solution or a more than or equal to 70 percent acetone solution with a known process and equipment. The quality of the capsule is accordant with the specifications in the colonic-coated hollow capsule standard of the Chinese Pharmacopoeia of the version 2010, the capsule is not disintegrated in an enteric process, is disintegrated on a colonic part within one hour, and has three years of shelf life.

The invention relates to a toughening forming auxiliary of a hard capsule taking starch as a matrix for food, healthcare products, medicines and the like, and a starch hard capsule for the food, healthcare products, medicines and the like, prepared from the toughening forming auxiliary of a hard capsule taking starch as a matrix in combination with a starch matrix. The toughening forming auxiliary for preparing a hard capsule taking starch as a matrix consists of 5-50wt% of carrageenan and 50-95wt% of ghatti gum. According to the toughening forming auxiliary provided by the invention, the toughening forming auxiliary is added into the starch matrix, so that the glue-dip forming is assisted by the gelation effect of the carrageenan, and a final capsule shell is toughened by the net structure generated in gelation and a natural polysaccharide carbohydrate chain structure in the ghatti gum; meanwhile, the disintegration of the hard capsule can be effectively promoted by the good solubility and emulsifiability of the ghatti gum, thus the prepared starch hard capsule has excellent flexibility and can be quickly disintegrated.

Tablets are prepared with friability reducing agents to yield tablets that are more resistant to breakage or crumbling, but with satisfactory hardness. The friability reducing agents include low molecular weight polyethylene glycol as well as similar agents exhibiting at least three percent (3%) hydroxide moieties and a water solubility of at least eighty percent (80%) (w/w %) in room temperature water. The tablets may comprise an active agent and excipient of almost any type, and about 0.1-about 0.5% by weight friability reducing agent. They exhibit a hardness of at least eighty percent (80%) of the same tablet prepared without the friability reducing agent.

The invention provides a method for preparing voglibose particles. The particles are prepared through a one-step prilling process,the friability is low,and the roundness is good. Voglibose can be dissolved out fast,the content uniformity is good,and the voglibose particles are suitable for being further prepared into capsules,tables (including dispersible tablets and orally disintegrating tablets)and granules. According to the preparation idea,the voglibose is added into a polar solvent containing a water-soluble adhesive,and the mixture is sprayed into a one-step pelletizer containing a diluent and a disintegrating agent in a top spraying prilling mode. The preparation method is easy to operate,the labor intensity is reduced,and the preparation method is suitable for large-scale production.

It is intended to provide tablets which have a favorable texture in taking and excellent compressing characteristics, friability and mechanical strength. Tablets which are produced by blending a powdery or granular mixture comprising (1) an effective amount of a pharmacologically active substance and (2) 50% by weight or more of a water-soluble filler based on the powdery or granular mixture with (3) a compressing characteristic improving agent containing moisture at least in an amount corresponding to the equilibrated moisture content at 25° C. under a humidity of 12% and having an average particle size of 100 μm or less, at a ratio of from 1 to 50% by weight based on the above mixture, and then compressing the resultant mixture.

The invention provides lipoic acid tablets with few types and small dose of accessories and a preparation method thereof. The preparation method comprises the steps of weighing filler and an adhesive, and preparing accessory tablets by a conventional tabletting process; putting the prepared accessory tablets into an efficient coating pan; weighing lipoic acid and sieving; spraying the sieved lipoic acid powder to coat the accessory tablets layer by layer by a spray gun by taking a sodium carboxymethylcellulose solution as a spray; drying and airing in a thermostatic chamber to obtain the lipoic acid tablets. The content of main drug is high, and the compliance is improved; by adopting few types and small dose of accessories, the adverse effect of the accessories is reduced, and the cost of raw materials is also reduced; the temperature of the operation process is strictly controlled, and the sticking phenomenon generated in lipoic acid tabletting is avoided by pressing the accessory tablets not containing lipoic acid; by adopting the spraying-coating process, color spots are avoided; moreover, the content uniformity, friability, chroma uniformity and stability of the lipoic acid tablets are all remarkably improved.

The invention relates to a method for preparing hippophae rhamnoides seed micro powder capsules. The method for preparing the hippophae rhamnoides seed micro powder capsules comprises the following steps of: performing vacuum drying on hippophae rhamnoides seeds; adding konjac glucomannan-acrylic graft copolymer (KAC) which serves as an anticaking agent into the hippophae rhamnoides seeds; performing low-temperature superfine pulverization on the mixture; and encapsulating the mixture, and performing irradiation sterilization at the temperature of 600 DEG C. The method has the advantages of making full use of the hippophae rhamnoides seeds, generating no by-products, keeping the primitivity of the hippophae rhamnoides seeds, avoiding destruction to heat-sensitive and unstable active ingredients, reserving the effective active ingredients and the original various nutritional ingredients in the hippophae rhamnoides seeds to the utmost extent, and being favorable for absorption. An adopted anti-caking agent can solve the problems that the superfine powder is aggregated easily and is difficult to disperse due to superfine particle sizes, and if the added content of the anti-caking agent is less, the anti-caking performance is higher so that the purity of the capsule hippophae rhamnoides seed powder reaches over 99.6 percent. Besides, the method for preparing the hippophae rhamnoides seed micro powder capsules is simple, has less equipment investments, a low production cost and no three wastes outputs, is suitable for application in hippophae rhamnoides producing areas with underdeveloped economy, and is environment-friendly industrialized technology.

The invention discloses a hydroxypropyl methyl cellulose plant empty capsule which is prepared through the following method: dissolving hydroxypropyl methyl cellulose in a mixed solvent of an organic solvent and water, preparing a hydroxypropyl methyl cellulose solution with the mass percentage of 10 to 33 percent, and making capsules by using the hydroxypropyl methyl cellulose solution, wherein the organic solvent is ethyl alcohol and/or acetone. The hydroxypropyl methyl cellulose plant empty capsule has the advantages that the capsule is disintegrated fast, is not brittle and has extremely low weight loss on drying; furthermore, according to the preparation method of the capsule, no heating is needed, so that energy consumption is reduced; no gelatinizer is added, so that influence on disintegration due to the gelatinizer is avoided; the capsule is cured and molded only through volatilization of the organic solvent, so that the hydroxypropyl methyl cellulose plant empty capsule is suitable for filling of certain medicines having special requirements.

The invention belongs to the technical field of pharmaceutical preparations and particularly relates to chitosan tablets and a preparation method thereof. The chitosan tablets comprise tablet cores and coating layers, wherein the tablet cores comprise components in parts by weight as follows: 70-76 parts of chitosan, 3-6 parts of crospovidone, 7-12 parts of calcium hydrogen phosphate, 8-12 parts of microcrystalline cellulose, 1-3 parts of aerosil and 4-6 parts of sodium carboxymethyl cellulose; the coating layers are prepared from raw materials in parts by weight as follows: 4-6 parts of zein, 7-9 parts of hydroxypropyl methoxyl cellulose, 3-5 parts of polyethylene glycol and 80-84 parts of ethyl alcohol with the volume fraction of 30%-40%. The chitosan tablets have bright and clean appearance and are stable in physical and chemical properties and long in shelf life, and the disintegration time, hardness, friability and the like agree with related regulations of the Chinese pharmacopoeia.

The present invention relates to acerola cherry tabletted candies and a preparation method thereof. The candies consist of cherry powder, an excipient, a sweetening agent, an adhesive and a lubricant; the acerola cherry tabletted candies specifically comprise 25-33.35% of acerola cherry powder, 28.6-29.3% of sorbitol, 15-25% of microcrystalline cellulose, 1-8% of D-mannitol, 0.1-1% of stevioside, 10.65-20% of blueberry powder, 0.01-0.05% of sucralose and 0.3-1% of magnesium stearate. The tabletted candies are obtained by adopting the technologies of sieving, weighing, premixing, total mixing and direct pressing. The acerola cherry tabletted candies are simple in preparation process, stable in hardness, friability and taste, have blueberry flavor, are moderate in sourness and sweetness and convenient to eat, and have the beneficial effects of enhancing immunity, improving skin state, whitening, regulating intestinal flora and the like.