分子修飾の代謝に関する研究
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- Improving the pharmacokinetic and pharmacodynamic properties of drug chemical conversion to a chimera drug
- M. Otagiri, T. Imai, A. Fukuhara
- J. Control. Release, 62, 223-229 (1999)
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- Characterization of urinary metabolites of a new benzofuroquinoline derivative, 3,9-bis(N,N-dimethyl carbamoyloxy)-5H-benzofuro[3,2-c]-quinoline-6-one (KCA-098), in dogs.
- T.Yamada, A. Yamamoto, M. Fujioka, M. Miyagi, N. Saito, T. Imai, M.Otagiri
- Pharmazie, 54 (9), 672-677 (1999)
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- In vitro identification of the human cytochrome P-450 enzymes involved in the N-demethylation of azelastine
- T. Imai, M. Taketani, T.Suzu, K. Kusube, M. Otagiri
- Drug Metab. Dispos., 27(8) 942-946 (1999).
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- Characterization of Esterase Involved in the Stereoselective Hydrolysis of Ester-Type Prodrugs of Propranolol in Rat Liver and Plasma.
- Y. Yoshigae, T. Imai, M. Taketani and M. Otagiri
- Chirality, 11 (1) 10-13 (1999).
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- Species Differences in Stereoselective Hydrolase Activity in Intestinal Mucosa.
- Y. Yoshigae, T. Imai, A. Horita, H. Matsukane, M. Otagiri
- Pharm. Res., 15(4) 626-631 (1998)
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- Species Differences in the Disposition of Propranolol Prodrugs Derived from Hydrolase Activity in Intestinal Mucosa.
- Y. Yoshigae, T Imai, T. Aso and M. Otagiri
- Life Sciences, 62(14) 1231-1241 (1998)
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- Stereospecific Activity and Nature of Metabolizing Esterases for Propranolol Prodrug in Hairless Mouse Skin, Liver and Plasma.
- S. Ahmed, T. Imai, Y. Yoshigae and M. Otagiri
- Life Sciences, 61(19), 1879-1887 (1997).
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- Stereoselectivity in Cutaneous Hydrolysis and Transdermal Transport of Propranolol Prodrug.
- S. Ahmed, T. Imai, M. Otagiri
- Enantiomer, 2(3-4) 181-191 (1997).
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- Species Differences for Stereoselective Hydrolysis of Propranolol Prodrugs in Plasma and Liver.
- Y. Yoshigae, T. Imai, A. Horita and M. Otagiri
- Chirality, 9(7), 661-666 (1997).
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- Alteration of Pharmacokinetics and Nephrotoxicity of Cisplatin by Alginates
- T. Imai, K. Fujii, S. Shiraishi, M. Otagiri
- J. Pharm. Sci., 86(2) 244-247 (1997).
Caco2膜透過性に関する研究
- Simultaneous Use of Sodium Deoxycholate and Dipotassium Glysyrrhizinate Enhances the Cellular Transport of Poorly Absorbed Compounds across Caco-2 Cell Monolayers.
- M. Sakai, T. Imai, H. Ohtake, H. Azuma and M. Otagiri
- J. Pharm. Pharmacol., 51(1) 27-33 (1999).
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- In Vitro and In Vivo Evaluation of the Enhancing Activity of Glycyrrhizin on the Intestinal Absorption of Drugs
- T. Imai, M. Sakai, H. Ohtake, H. Azuma and M. Otagiri
- Pharm. Res., 16(1) 80-86 (1999).
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- Cytotoxicity of Absorption Enhancers in Caco-2 Cell Monolayers.
- M. Sakai, Teruko Imai, H. Ohtake and M. Otagiri
- J .Pharm. Pharmacol., 50 (10) 1101-1108 (1998) .
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- Effects of Absorption Enhaners on Cytoskeletal Actin Filaments in Caco-2 Cell Monolayers.
- M.Sakai, T. Imai, H.Ohtake, H.Azuma and M. Otagiri
- Life. Sci., 63(1) 45-54 (1998).
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- Effects of Absorption Enhancers on the Transport of Model Compounds in Caco-2 Cell Monolayers: Assessment by Confocal Laser Scanning Microscopy.
- M. Sakai, T. Imai, H. Ohtake, H. Azuma and M. Otagiri
- J. Pharm. Sci., 86(7) 779-785 (1997).
製剤設計に関する研究
- Comparison of the pharmaceutical properties of sustained-release gel beads prepared by alginate having different molecular size with commercial sustained-release tablet.
- T. Imai, C. Kawasaki, T. Nishiyama, M. Otagiri
- Pharmazie, 55, 218-222 (2000).
- A strategy for the immediate-release of indomethacin from a sustained-release preparation using a chitosan hydrolysate.
- T. Imai, S. Shiraishi, M. Otagiri
- S.T.P. Pharm. Sci., 10(1) 57-62 (2000).
- Effect of grinding with hydroxypropyl cellulose on the dissolution and particle size of a poorly water-soluble drug.
- T. Yamada, N. Saito, T. Imai, M. Otagiri
- Chem. Pharm. Bull., 47(9), 1311-1313 (1999).
- Casein Hydrolysate as a Rapid and/or Enteric Dissolving Additive for Oral Drugs.
- T. Imai, T. Nishiyama, M. Shameem and M. Otagiri
- Pharm. Develop. Tech., 3(2) 225-232 (1998).
- Mutual Effect of Egg Albumin and Fatty Acids on Bioavailability of dl-?-Tocopherol.
- T. Imai, K. Nohdomi, M. Shameem, H. Matsumoto, T. Satoh and M. Otagiri
- Int. J. Pharm., 155(1) 45-52 (1997).