PREPARATION CONTAINING ACTIVE SUBSTANCE

    公开(公告)号:JPH06172160A

    公开(公告)日:1994-06-21

    申请号:JP19824593

    申请日:1993-08-10

    Applicant: BASF AG

    Abstract: PURPOSE: To provide a solid granular active substance-contg. preparation. CONSTITUTION: This solid granular active substance-contg. preparation is obtd. by tightly mixing the active substance with a water-soluble melt consisting of a) 10 to 90 wt.% water-soluble polymer A having a viscosity Va of 1,000 to 120,000 cPs, b) 10 to 90 wt.% water-soluble polymer B having a viscosity Vb of 1 to 500 cPs (where the viscosities Va and Vb are those of 2 wt.% aq. solns. at 20 deg.C and are measured by a capillartity method stipulated in ASTM D2363-72) as a carrier material and processing and molding the melt to particles.

    PREPARATION OF SLOW RELEASE SOLID PHARMACEUTICALS

    公开(公告)号:JPH0656651A

    公开(公告)日:1994-03-01

    申请号:JP15209393

    申请日:1993-06-23

    Applicant: BASF AG

    Abstract: PURPOSE: To obtain a drug excellent in storage stability and persisting property by applying a regenerated and aqueous dispersion liquid of a specified binder on the core containing the effective substance. CONSTITUTION: An aqueous dispersion liquid of a binder is obtd. by emulsion polymn. with a pharmaceutically allowed material such as methylmethacrylate. The obtd. dispersion liquid, a water-soluble and pharmaceutically allowed spray assistant having >=60 deg.C glass transition temp. such as methylcellulose by 5 to 50 wt.% of the binder, and a pharmaceutically allowed adhesion preventive such as talc by 0 to 50 wt.% are spray-dried together and then again prepared as a regenerated and aqueous dispersion liquid. The obtd. liquid is applied on the core containing the effective substance to obtain the drug of the purpose.

    PHARMACEUTICAL PREPARATION IN SOLID RETARDING FORM

    公开(公告)号:JPH05194197A

    公开(公告)日:1993-08-03

    申请号:JP31006092

    申请日:1992-11-19

    Applicant: BASF AG

    Abstract: PURPOSE: To prepare a sustained release formulation of a solid pharmaceutical preparation by an extruding and continuous forming method for allowing the treatment to successively progress with a high throughput when the material loss is slight. CONSTITUTION: A sustained release formulation is prepared by melt-extruding a mixture of an active ingredient of a pharmaceutical preparation with a polymer melt comprising (a) a water-insoluble poly(meth)acrylate, (b) a water-soluble hydroxyalkyl cellulose having 2-3 carbon atoms in the hydroxyalkyl group or hydroxyalkylmethyl cellulose, or a N-vinylpyrrolidone polymer having vinyl acetate, or a mixture of preceding two, (c) one or more conventional pharmaceutical auxiliaries, and successively forming the molten mixture.

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