摘要:
PROBLEM TO BE SOLVED: To provide a solid stick topical composition containing a corticosteroid.SOLUTION: There is provided a solid stick topical composition comprising a corticosteroid formulation. The solid stick including an outer protective covering also includes: at least one wax present in an amount sufficient such that the stick is solid at 25°C; propyleneglycol in an amount of 5 to 20 wt.%; and an emulsifier present in an amount of 0.2 to 2.0 wt.% based on the total weight of the composition to emulsify the propyleneglycol and petrolatum. The solid stick is contained in a protective covering so that during application it does not come into contact with the hand holding the stick.
摘要:
PROBLEM TO BE SOLVED: To improve the centering of a core of a compression coating tablet.SOLUTION: A pin punch assembly is positioned so as to contact with a top portion of bottom fill powder 19 in a metal mold 17. A roll 13 applies pressure on a protrusion 11 on a pin with a non-punching end of the pin 3 as a fixed position. The pressure compresses a spring 9 so as to project out the pin from a housing, by moving the pin to the housing 1. When the pin moves, an impression or a cup is punched and put in a bottom fill. The size of the impression directly depends on the size of the pin. The depth of the impression directly depends on the height of the protrusion positioned at the top portion of the pin. Next, the pin goes out from the roll, and returns to an original position by action of the spring and a key 5 intercepting the pin at this position.
摘要:
PROBLEM TO BE SOLVED: To provide a method and a composition for treating insomnia.SOLUTION: A dosage form includes a drug substance useful in the treatment of insomnia. The dosage form is adapted to release the drug substance after a lag time during which substantially no drug substance is released, and the lag time is about at least one hour after administration of the dosage form.
摘要:
PROBLEM TO BE SOLVED: To improve the moisture resistance of dry powder formulations for inhalation and to improve the storage stability of the formulations.SOLUTION: For improving the moisture resistance of dry powder formulations for inhalation and improving the storage stability of the formulations, the formulations contain a phamaceutically not effective carrier of not-inhalable particle size and a finely divided phamaceutically effective substance of inhalable particle size. For the improvement, magnesium stearate is used in the formulations. One of the features of the inventive dry powder is that a high fine particle dosage or fine particle fraction can be maintained under relatively extreme temperature and humidity conditions.
摘要:
Irritation upon injection of a formulation containing propofol is reduced or substantially eliminated by administering a stable, sterile, and antimicrobial aqueous dispersion comprising a water-insoluble microdroplet matrix of mean diameter from about 50 nm to about 1000 nm consisting essentially of about 1% to about 15% of propofol, up to about 7% of a propofol-soluble diluent, and about 0.8% to about 4% of a surface stabilizing amphiphilic agent. The aqueous phase includes a pharmaceutically acceptable water-soluble polyhydroxy tonicity modifier. The propofol-containing dispersion is devoid of additional bactericidal or bacteriostatic preservative agents.
摘要:
PROBLEM TO BE SOLVED: To provide a drug dispensing container, giving a dose to a patient only when the dispensing container is placed in a correct positional direction. SOLUTION: This drug dispensing container includes: a housing for storing a drug; a cap connected to the housing; and a gravity actuated lock device for locking the cap, wherein when the container is held in a first directional position, the container is in the non-locked state, and when the container is tilted or rotated, the container is locked by the gravity. A lock device includes: a first lock element connected to a cap, and moved according to the cap in the housing; and a second lock element moved on the contour part formed on the inner surface of the housing by the action of gravity to engage with the first lock element in response to tilting or rotary movement of the container dislocated from the first directional position. The second lock element is formed of material freely moved on receiving the action of gravity even in the presence of electrostatic field. COPYRIGHT: (C)2007,JPO&INPIT
摘要:
PROBLEM TO BE SOLVED: To provide: a controlled-release formulation that releases an active agent with an ascending release rate in response to the change in pH when it reaches gastrointestinal tract after its administration to a patient; a method of producing the same; and a method of using the same.SOLUTION: Solid controlled-release multilayer formulations for oral dosage contains: a core layer comprising one or more active agents and one or more enteric materials; and two or more barrier layers comprising one or more swellable, erodible, or gellable polymers, wherein the one of the barrier layers is provided on the upper side of the core layer and the other(s) thereof are/is provided on the lower side of the core layer.