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Journal of Pharmaceutical Sciences
|
September 1, 1992
Acid-catalyzed hydrolysis of maltosyl-beta-cyclodextrin
F Hirayama, M Yamamoto, K Uekama
Chemical & Pharmaceutical Bulletin
|
January 1, 1975
Inclusion complexes of beta-cyclodextrin with tranquilizing drugs phenothiazines in aqueous solution
M Otagiri, K Uekama, K Ikeda
Chemical & Pharmaceutical Bulletin
|
January 1, 1987
Improvement of chemical instability of carmoful in beta-cyclodextrin solid complex by utilizing some organic acids
M Kikuchi, F Hirayama, K Uekama
Carbohydrate Research
|
December 29, 2000
Crystal structures of heptakis(2,6-di-O-ethyl)cyclomaltoheptaose
K Harata, H Hirayama, K Uekama
Chemical & Pharmaceutical Bulletin
|
January 1, 1975
Inclusion complexes of beta-cyclodextrin with antiinflammatory drugs fenamates in aqueous solution
K Ikeda, K Uekama, M Otagiri
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
May 1, 1979
[Soluble complex formation of 6-ethyl-2,3,6,9-tetrahydro-3-methyl-2,9-dioxothiazolo-[5,4-f]quinoline-8-carboxylic acid (tioxacin) with aliphatic amines (author's transl)]
K Uekama, F Hirayama, N Takasugi
Gan
|
December 1, 1970
Promotion by DNA of the photoinduced radical production from 4-nitroquinoline 1-oxide in aqueous medium at 77 degrees K and its mechanism
T Okano, A Takadate, K Uekama
The Journal of Pharmacy and Pharmacology
|
January 1, 1996
In-vitro evaluation of biphenylyl acetic acid-beta-cyclodextrin conjugates as colon-targeting prodrugs: drug release behaviour in rat biological media
F Hirayama, K Minami, K Uekama
The Journal of Pharmacy and Pharmacology
|
June 1, 1994
In-vivo and in-vitro evaluations of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-beta-cyclodextrin and hydroxypropylcelluloses in dogs
Z Wang, F Hirayama, K Uekama
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
November 1, 1980
[Model analyses of interfacial transfer and absorption behaviors of drugs following dissolution: approach to evaluation procedure of bioavailability (author's transl)]
K Uekama, J Fujisaki, F Hirayama
Page
of 16
Search research articles
Search
Showing results (11-20 of 155) with videos related to
Sort By:
Page
of 16
Journal of Pharmaceutical Sciences
|
September 1, 1992
Acid-catalyzed hydrolysis of maltosyl-beta-cyclodextrin
F Hirayama, M Yamamoto, K Uekama
Chemical & Pharmaceutical Bulletin
|
January 1, 1975
Inclusion complexes of beta-cyclodextrin with tranquilizing drugs phenothiazines in aqueous solution
M Otagiri, K Uekama, K Ikeda
Chemical & Pharmaceutical Bulletin
|
January 1, 1987
Improvement of chemical instability of carmoful in beta-cyclodextrin solid complex by utilizing some organic acids
M Kikuchi, F Hirayama, K Uekama
Carbohydrate Research
|
December 29, 2000
Crystal structures of heptakis(2,6-di-O-ethyl)cyclomaltoheptaose
K Harata, H Hirayama, K Uekama
Chemical & Pharmaceutical Bulletin
|
January 1, 1975
Inclusion complexes of beta-cyclodextrin with antiinflammatory drugs fenamates in aqueous solution
K Ikeda, K Uekama, M Otagiri
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
May 1, 1979
[Soluble complex formation of 6-ethyl-2,3,6,9-tetrahydro-3-methyl-2,9-dioxothiazolo-[5,4-f]quinoline-8-carboxylic acid (tioxacin) with aliphatic amines (author's transl)]
K Uekama, F Hirayama, N Takasugi
Gan
|
December 1, 1970
Promotion by DNA of the photoinduced radical production from 4-nitroquinoline 1-oxide in aqueous medium at 77 degrees K and its mechanism
T Okano, A Takadate, K Uekama
The Journal of Pharmacy and Pharmacology
|
January 1, 1996
In-vitro evaluation of biphenylyl acetic acid-beta-cyclodextrin conjugates as colon-targeting prodrugs: drug release behaviour in rat biological media
F Hirayama, K Minami, K Uekama
The Journal of Pharmacy and Pharmacology
|
June 1, 1994
In-vivo and in-vitro evaluations of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-beta-cyclodextrin and hydroxypropylcelluloses in dogs
Z Wang, F Hirayama, K Uekama
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
November 1, 1980
[Model analyses of interfacial transfer and absorption behaviors of drugs following dissolution: approach to evaluation procedure of bioavailability (author's transl)]
K Uekama, J Fujisaki, F Hirayama
Page
of 16