Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Masato Terakawa"'
Autor:
Masataka Katashima, Fumiaki Koizumi, Manabu Murakami, Hiromitsu Kageyama, Akihiro Ohnishi, Masato Terakawa
Publikováno v:
Clinical Pharmacology & Therapeutics. 66:501-508
Purpose We compared the pharmacokinetics of the inhaled novel neutrophil elastase inhibitor FK706 between healthy nonsmokers and smokers. Methods Six healthy nonsmokers and six smokers inhaled 50 to 400 mg FK706 in two different doses. Series of plas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cf9846a211adfca975a3f232df4730
https://doi.org/10.1016/s0009-9236(99)70013-5
https://doi.org/10.1016/s0009-9236(99)70013-5
Autor:
Atsunori Kaibara, Masato Terakawa, Kiyoshi Yamaoka, Kenji Tabata, Takehisa Hata, Shingo Suzuki
Publikováno v:
Drug Metabolism and Pharmacokinetics. 14:286-293
A computer program, MOMENT (EXCEL), for moment analysis was developed on Microsoft Excel®. MOMENT (EXCEL) written in Visual Basic for Applications® can handle time course not only of blood concentration but also of urinaly or bilialy excretion acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fa4363c560b8d7d0b6411b6de10e093
https://doi.org/10.2133/dmpk.14.286
https://doi.org/10.2133/dmpk.14.286
Autor:
Toshifumi Shiraga, Shin-ichi Ninomiya, Kouji Takeshita, Yoshio Esumi, Yoshinori Teramura, Akio Kawamura, Akira Kagayama, Masato Terakawa
Publikováno v:
Drug Metabolism and Pharmacokinetics. 14:385-391
The penetration and absorption of tacrolimus (FK506) in the skin of rat after a single topical application of 14C-labeled FK506 (14C-FK506) ointment under occlusive dressing was studied by semimicroautoradiography of the skin and by counting radioact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5601fa7d5cf3d88a1e8d582f9697403
https://doi.org/10.2133/dmpk.14.385
https://doi.org/10.2133/dmpk.14.385
Publikováno v:
Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics. 25:603-613
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14043c1d43906c0fce5658fa4ac0ea26
https://doi.org/10.3999/jscpt.25.603
https://doi.org/10.3999/jscpt.25.603
Autor:
Koji Ishibashi, Toshiaki Amamoto, Akinori Urae, Hiromitsu Kageyama, Nami Iyota, Masato Terakawa, Shin Irie
Publikováno v:
Drug Metabolism and Pharmacokinetics. 9:793-798
The effect of food intake on the bioavailability of vamicamide, a new anticholinergic drug, was studied in six healthy male volunteers. Each subject, in a two-way crossover manner, was given a single 18-mg oral dose of vamicamide after overnight fast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c348294095523c665c056398d6353a9
https://doi.org/10.2133/dmpk.9.793
https://doi.org/10.2133/dmpk.9.793
Autor:
Nami Iyota, Masato Terakawa
Publikováno v:
Drug Metabolism and Pharmacokinetics. 9:799-808
The pharmacokinetic data of vamicamide, a new anticholinergic drug, collected from healthy male subjects were analysed to estimate population pharmacokinetic parameters. A total of 48 subjects participated in three single-dose studies and three multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da4f44bef509f664aceac79cb4be1013
https://doi.org/10.2133/dmpk.9.799
https://doi.org/10.2133/dmpk.9.799
Autor:
Masato Terakawa, Mitsuyoshi Nalcashima, Akira Sugiyama, Mitsutaka Kanamaru, Toshihiko Uematsu, S. Nagashima, Atsuhiro Mizuno
Publikováno v:
The Journal of Clinical Pharmacology. 33:1122-1131
The pharmacokinetics, and aldose reductase (AR) inhibitory and uricosuric activities of FK366 were studied in healthy volunteers given a single oral dose of 150, 300, or 600 mg after fasting, 600 mg after a meal, or 300 mg twice a day for 8 days afte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d775b364d5ddec5fc63f2a66a19c0141
https://doi.org/10.1002/j.1552-4604.1993.tb01950.x
https://doi.org/10.1002/j.1552-4604.1993.tb01950.x
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:515-520
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfac604a81a8e8f1cee15354f1d963fa
https://doi.org/10.2133/dmpk.8.515
https://doi.org/10.2133/dmpk.8.515
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:1047-1056
The pharmacokinetics of quinotolast sodium, a new anti-allergic drug, were studied in six elderly and six young healthy male volunteers after single oral dosing with 5mg of the drug. The mean maximum plasma concentration of unchanged drug increased s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb4f7c151a68847c5cc4b7eb157d50aa
https://doi.org/10.2133/dmpk.8.1047
https://doi.org/10.2133/dmpk.8.1047
Autor:
Koji Ishibashi, Masataka Katashima, Hisayuki Sekino, Masato Terakawa, Seiichi Fujiwara, Noboru Nakamichi
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:1029-1040
Quinotolast sodium, a new anti-allergic drug, was studied in six healthy male volunteers to evaluate its pharmacokinetics in steady-state conditions after oral dosing. The subjects were given a single dose of 5mg, and after a two-day washout period,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8268b30716f6fcfd17e4a16932de4db
https://doi.org/10.2133/dmpk.8.1029
https://doi.org/10.2133/dmpk.8.1029