Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tadanori Yano"'
Autor:
Haruo Oyashiki, Tadanori Yano
Publikováno v:
JOURNAL OF THE BREWING SOCIETY OF JAPAN. 90:416-423
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::785b319115931123935c52d6f4834633
https://doi.org/10.6013/jbrewsocjapan1988.90.416
https://doi.org/10.6013/jbrewsocjapan1988.90.416
Autor:
Masataka Ichikawa, Tadanori Yano, Mikiro Nakashima, Shigeru Goto, Shuji Satoh, Kenji Matsuyama
Publikováno v:
Biological and Pharmaceutical Bulletin. 17:1395-1398
The suitability of sampling via microdialysis for a lipophilic drug, valproate (VPA), was evaluated by the elimination rate constant of VPA solution in an in vitro experimental first-order elimination system. The elimination rate constant of VPA in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54ff24ca9378eaa8da231026ce82a1a4
https://doi.org/10.1248/bpb.17.1395
https://doi.org/10.1248/bpb.17.1395
Publikováno v:
European Journal of Pharmaceutical Sciences. 1:117-123
An inclusion complex of prostaglandin E 1 (PGE 1 ) with β-cyclodextrin (β-Cyd) or O-carboxymethyl-O-ethyl-β-cyclodextrin (CME-β-CyD) was made as topical preparations in a fatty alcohol/propylene glycol ointment base. When the PGE 1 preparations w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c0b9d3906c71ecd3419f0b6094668ac
https://doi.org/10.1016/0928-0987(93)90001-q
https://doi.org/10.1016/0928-0987(93)90001-q
Autor:
Kenji Matsuyama, Yukiko Nakaboh, Shuji Satoh, Masataka Ichikawa, Mikiro Nakashima, Tadanori Yano
Publikováno v:
Pharmaceutical Research. 11:684-686
Microdialysis was applied to determine the in vivo transdermal absorption of methotrexate (MTX) in rats with or without a new penetration enhancer, l-[2-(decylthio)ethyl]azacyclopentan-2-one (HPE-101). A solution composed of 2.5 mM MTX and 3% (w/v) H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::600de326f16375525463533138f9a26d
https://doi.org/10.1023/a:1018972112077
https://doi.org/10.1023/a:1018972112077
Publikováno v:
The Journal of pharmacy and pharmacology. 45(9)
The penetration enhancer, 1-[2-(decylthio)ethyl]azacyclopentan-2-one (HPE-101), significantly enhanced the excretion of topically applied [14C]indomethacin when dissolved in dipropylene glycol, triethylene glycol, diethylene glycol, 1,3-butylene glyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54fdb3e8f31264099db397e7e4e6cc59
https://pubmed.ncbi.nlm.nih.gov/7903363
https://pubmed.ncbi.nlm.nih.gov/7903363
Publikováno v:
The Journal of pharmacy and pharmacology. 44(2)
The optimal prescription of transdermal preparations of prostaglandin E1 (PGE1) for treatment of peripheral vascular diseases has been investigated. The chemical stability of PGE1 in fatty alcohol/propylene glycol (FAPG) ointment was markedly improve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67e10f7e6dad69b4d2865ce49401e4ae
https://pubmed.ncbi.nlm.nih.gov/1352811
https://pubmed.ncbi.nlm.nih.gov/1352811
Publikováno v:
Journal of pharmacobio-dynamics. 14(12)
Plasters containing methyl salicylate with and without l-menthol and dl-camphor were prepared and topically applied on hairless mouse skin to investigate the effects of l-menthol and dl-camphor on the skin penetration and hydrolysis of methyl salicyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05d7ec1d69d0f6fc1a691aad089153b6
https://pubmed.ncbi.nlm.nih.gov/1812275
https://pubmed.ncbi.nlm.nih.gov/1812275
Autor:
Ryuhei Kodama, Toshikazu Sonoda, Tadanori Yano, Kazuhide Furukawa, Hidetoshi Amano, Kanji Noda, Hiroyuki Ide
Publikováno v:
Xenobiotica. 5:601-609
1. The maximum concentration of radioactivity in blood occurred 2-4 h after oral administration of [14C]H-88 in mouse, rabbit and man. With rat, a maximum concentration was obtained 24 h after administration of the drug at a dose level of 60 mg/kg, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::748c662ca24544aec7ecb4a4f02cd2ba
https://doi.org/10.3109/00498257509056130
https://doi.org/10.3109/00498257509056130
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 6(6)
1. The main route of elimination of d-limonene administered orally was via the urine in animals and man, 75-95% of the administered radioactivity being excreted in the urine during 2-3 days. Faecal excretion accounted for less than 10% of the dose in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdbc52f89a669f24de3d50fd2646183c
https://pubmed.ncbi.nlm.nih.gov/969565
https://pubmed.ncbi.nlm.nih.gov/969565
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 5(1)
1. Following oral administration of [14C] H-88 to rat, mouse, quinea-pig and hamster, 40-65% and 5-15% of radioactivity was excreted in urine and faeces respectively during 3 or 4 days. In rabbit, monkey and man, more than 80% of radioactivity was ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7d94996d5ed201b8e19a7d9e781a770
https://pubmed.ncbi.nlm.nih.gov/1080313
https://pubmed.ncbi.nlm.nih.gov/1080313