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Kazunori Iwanaga

Division of Pharmaceutics

Osaka University of Pharmaceutical Sciences

Osaka 569-1094

Japan

[email]@gly.oups.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Division of Pharmaceutics, Osaka University of Pharmaceutical Sciences, Osaka 569-1094, Japan. 2003 - 2012

References

  1. Effects of furanocoumarins in Kampo extract-based medicines on rat intestinal absorption of CYP3A and P-glycoprotein substrate drugs in vivo. Iwanaga, K., Arimune, K., Miyazaki, M., Shibano, M., Taniguchi, M., Baba, K., Kakemi, M. Arch. Pharm. Res. (2012) [Pubmed]
  2. Application of organogels as oral controlled release formulations of hydrophilic drugs. Iwanaga, K., Kawai, M., Miyazaki, M., Kakemi, M. Int. J. Pharm (2012) [Pubmed]
  3. Characterization of organogel as a novel oral controlled release formulation for lipophilic compounds. Iwanaga, K., Sumizawa, T., Miyazaki, M., Kakemi, M. Int. J. Pharm (2010) [Pubmed]
  4. Furanocoumarin derivatives in Kampo extract medicines inhibit cytochrome P450 3A4 and P-glycoprotein. Iwanaga, K., Hayashi, M., Hamahata, Y., Miyazaki, M., Shibano, M., Taniguchi, M., Baba, K., Kakemi, M. Drug Metab. Dispos. (2010) [Pubmed]
  5. Disposition of lipid-based formulation in the intestinal tract affects the absorption of poorly water-soluble drugs. Iwanaga, K., Kushibiki, T., Miyazaki, M., Kakemi, M. Biol. Pharm. Bull. (2006) [Pubmed]
  6. Usefulness of microspheres composed of gelatin with various cross-linking density. Iwanaga, K., Yabuta, T., Kakemi, M., Morimoto, K., Tabata, Y., Ikada, Y. J. Microencapsul (2003) [Pubmed]
 
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