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Featured researches published by Masao Ueno.


Journal of Pharmacy and Pharmacology | 1990

Rapidly Absorbed Solid Oral Formulations of Ibuprofen Using Water-soluble Gelatin

Teruko Imai; Susumu Kimura; Takeo Iijima; Tetsu Miyoshi; Masao Ueno; Masaki Otagiri

Abstract— Rapidly absorbed oral dosage forms of ibuprofen using water‐soluble gelatin (hydrolysate of common gelatin: mean mol. wt: 6000) have been studied and compared with tablets prepared with common gelatin (mean mol. wt: 100 000) and commercial tablets. Spray‐dried and speed‐kneaded powders, two types of granules and tablets were prepared with water‐soluble gelatin. The in‐vitro dissolution rates of water‐soluble gelatin preparations were significantly faster than those of commercial tablets, whereas the tablets prepared using common gelatin had slower dissolution rates than commercial tablets. Water‐soluble gelatin enhanced the dissolution rate of ibuprofen by improving the wettability of the drug particle surface by water, without any interaction in solution and the solid state. The absorption behaviour of various preparations was evaluated in four beagle dogs. The peak concentration time (tmax) of the water‐soluble gelatin preparations was significantly shorter than that of tablets prepared with common gelatin and commercial tablets. The maximum concentration (cmax) and the area under the serum concentration‐time curve (AUC0–10 h) were similar in all cases. The serum concentration profiles of water‐soluble gelatin solid preparations were almost the same as those of the solutions. On the other hand, the profiles of the common gelatin tablets were similar to those of the commercial tablets. The mean absorption time (MAT) from water‐soluble gelatin preparations was about 0.7 h, while the MAT from commercial tablets and common gelatin tablets was about 1.2 h. The differences in the MAT of water‐soluble gelatin preparations and commercial tablets or common gelatin tablets were the same as the differences in mean dissolution time (MDT) in gastrointestinal fluid. The MDTs of the water‐soluble gelatin preparations were from 1 to 5 min, so both disintegration and dissolution steps were rapid. The water‐soluble gelatin preparations were stable at 40°C and 70% RH for at least 30 days. The results suggest that the water‐soluble gelatin is a useful additive to solid ibuprofen formulations as it may initiate a more rapid and uniform dissolution and absorption of the drug.


Chemical & Pharmaceutical Bulletin | 1994

Applicaiotn of the Solid Dispersion Method to the Controlled Release of Medicine. VI. Release Mechanism of a Slightly Water Soluble Medicine and Interaction between Flurbiprofen and Hydroxypropyl Cellulose in Solid Dispersion

Hiroshi Yuasa; Tetsuya Ozeki; Hiroyuki Takahashi; Yoshio Kanaya; Masao Ueno


Archive | 1988

Pharmaceutical preparations containing non-steroidal anti-inflammatory agents

Takeo Iijima; Masaki Otagiri; Masao Ueno; Tetsu Miyoshi


Chemical & Pharmaceutical Bulletin | 1989

Enhancement of the dissolution rates of poorly water-soluble drugs by water-soluble gelatin

Teruko Imai; Tetsuyuki Nishiyama; Masao Ueno; Masaki Otagiri


Chemical & Pharmaceutical Bulletin | 1993

Application of the Solid Dispersion Method to the Controlled Release of Medicine. III. Control of the Release Rate of Slightly Water Soluble Medicine from Solid Dispersion Granules

Hiroshi Yuasa; Hiroyuki Takahashi; Tetsuya Ozeki; Yoshio Kanaya; Masao Ueno


Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan | 1989

Dissolution and absorption behavior of meclizine dihydrochloride from soft gelatin capsules

Susumu Kimura; Teruko Imai; Yorishige Imamura; Masao Ueno; Takeo Iijima; Masaki Otagiri


Journal of pharmacobio-dynamics | 1989

Enhanced Dissolution of Poorly Water-Soluble Drugs by Water-Soluble Gelatin

Teruko Imai; Susumu Kimura; Tetsuyuki Nishiyama; Masaki Otagiri; Tetsu Miyoshi; Masao Ueno


Archive | 1988

Nichtsteroide Antientzündungswirkstoffe enthaltende pharmazeutische Zubereitungen.

Takeo Iijima; Masaki Otagiri; Masao Ueno; Tetsu Miyoshi


Archive | 1988

Nichtsteroide antientzuendungswirkstoffe enthaltende pharmazeutische zubereitungen.

Takeo Iijima; Masaki Otagiri; Masao Ueno; Tetsu Miyoshi


Archive | 1988

Nichtsteroide antientzuendungswirkstoffe enthaltende pharmazeutische zubereitungen. Nonsteroidal antientzuendungswirkstoffe containing pharmaceutical preparations.

Takeo Iijima; Masaki Otagiri; Masao Ueno; Tetsu Miyoshi

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Yoshio Kanaya

Taisho Pharmaceutical Co.

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