Abstract: The object of the present invention is to provide an single-dose package containing an internal adsorbent wherein the internal adsorbent is not trapped in the heat-sealed region thereof. In addition, the object of the present invention is to provide a single-dose package containing internal adsorbent wherein adhesion of the internal adsorbent around the vacuumed open region thereof is slight, whereby the internal adsorbent does not spill out on opening the package. The object of the present invention can be solved by a single-dose package characterized in that the internal adsorbent is tight-packed using a packaging material having a mean specific surface resistivity of from 4.4×109? or more to 1.0×1016? or less at its internal surface, under warming and/or reduced pressure.

Abstract: A dry composition for oral ingestion characterized by comprising as an active ingredient a gas-releasing substance which releases gas by soak with water, and further comprising a gel base in an amount sufficient for gel formation; a gel composition for oral ingestion formed by adding water or a liquid diluent to the dry compound when taking; and a mixed feed obtainable by mixing the gel composition with a feed, are disclosed.

Abstract: 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.

Abstract: The object of the present invention is to provide an single-dose package containing an internal adsorbent wherein the internal adsorbent is not trapped in the heat-sealed region thereof. In addition, the object of the present invention is to provide a single-dose package containing internal adsorbent wherein adhesion of the internal adsorbent around the vacuumed open region thereof is slight, whereby the internal adsorbent does not spill out on opening the package. The object of the present invention can be solved by a single-dose package characterized in that the internal adsorbent is tight-packed using a packaging material having a mean specific surface resistivity of from 4.4×109? or more to 1.0×1016? or less at its internal surface, under warming and/or reduced pressure.

Abstract: A dry composition for oral ingestion characterized by comprising as an active ingredient a gas-releasing substance which releases gas by soak with water, and further comprising a gel base in an amount sufficient for gel formation; a gel composition for oral ingestion formed by adding water or a liquid diluent to the dry compound when taking; and a mixed feed obtainable by mixing the gel composition with a feed, are disclosed.

Abstract: This invention aims to provide a novel taking or having-or-swallowing form for an oral material, such as drugs or foodstuffs. This invention provides an edible film packaging 1 containing an edible film material 10 which has adhesion properties and is softened upon contact with moisture. The edible film packaging 1 is taken or had-or-swallowed while an oral material being encapsulated. Moreover, this invention provides an oral-material taking method, including taking or having-or-swallowing the edible film packaging 1 in which the oral material 2 has been encapsulated as it is without opening or as it is without opening after being immersed in water for a given period of time.

Abstract: A packaging material is formed by a substrate, and an inner sealing layer comprising a polyolefin layer and an aqueous dispersion-type polyester resin layer successively disposed on the substrate. The aqueous dispersion-type amorphous polyester resin layer contains an anionic surfactant or an amphoteric surfactant and is substantially free from an organic solvent having a boiling point of at most 100° C. The thus-formed packaging material is excellent in aroma-retentivity, aroma non-adsorptivity, particulate non-adhesion, low residual solvent and sealability. The packaging material is also free from environmental problem and is therefore suitable as a packaging material for particulate medical supplies and health foodstuff.

Abstract: A housing body (10) for deglutition of a shaped solid (5) for oral ingestion which is stored therein, comprising a generally tubular water-resistant envelope (1); an opening-side end part (A) at one end of the envelope, having an unsealable structure part (2), and capable of forming an opening part (22) by removing the unsealable structure part; a shielding-side end part (B) at the other end of the envelope, having a means for preventing the shaped solid for oral ingestion from release, the means allowing liquid to pass therethrough but not allowing the shaped solid for oral ingestion to pass therethrough; and a storage chamber (6) storing the shaped solid for oral ingestion between the opening-side end part and the shielding-side end part is disclosed.

Abstract: A packaging material is formed by a substrate, and an inner sealing layer comprising a polyolefin layer and an aqueous dispersion-type polyester resin layer successively disposed on the substrate. The aqueous dispersion-type amorphous polyester resin layer contains an anionic surfactant or an amphoteric surfactant and is substantially free from an organic solvent having a boiling point of at most 100° C. The thus-formed packaging material is excellent in aroma-retentivity, aroma non-adsorptivity, particulate non-adhesion, low residual solvent and sealability. The packaging material is also free from environmental problem and is therefore suitable as a packaging material for particulate medical supplies and health foodstuff.

Abstract: The present invention relates to an oral preparation of esculetin with controlled release. The oral preparation of esculetin with controlled release of the present invention comprises a gel-forming polymer base, preferably hydroxypropylmethylcellulose. The preparation may be coated with an enteric polymer base such as hydroxypropylmethylcellulose acetate succinate to thereby enhance solubility in the intestines. When orally administered, the preparation can continuously release esculetin. Thus, the administration frequency and dose can be reduced and a therapeutic effect on arthropathy can be established.

Abstract: Disclosed herein are a divided package of a medicinal adsorbent for internal use, comprising a divided package bag and an adsorbent for internal use which releases air ranging from 1.3 to 10 ml based on one gram of the adsorbent on heating from 10.degree. C. to 30.degree. C. and is packed therein, and having a volume expansion coefficient ranging from 0 to 0.064 ml/.degree.C..multidot.g (adsorbent for internal use) at a temperature of from 10.degree. to 30.degree. C., and a process for producing the same.

Abstract: Disclosed are novel high polymeric substances having saccharide side chains, suitable as a high polymeric material having several functions for medical treatments and a process for preparing thereof.

Abstract: Compounds of 2-substituted-phenyl-5-alkylthiazolidine-4-one having the formula (I) ##STR1## wherein R.sup.1 and R.sup.2 represent respectively a lower alkyl group of 1 to 3 carbon atoms and n denotes an integer of 1 to 3 possess anti-peptic ulcer activity.

Abstract: Compounds of 2-substituted-phenyl-1,3-perhydrothiazine-4-one having the formula (I) ##STR1## wherein R represents a lower alkyl group of 1 to 3 carbon atoms and n denotes an integer of 1 to 3 possess anti-peptic ulcer activity.

Abstract: Disclosed are novel high polymeric substances having saccharide side chains, suitable as a high polymeric material having several functions for medical treatments and a method for producing thereof.