H. Nakagami

发表

Solid Dispersions of Indomethacin and Griseofulvin in Non-porous Fumed Silicon Dioxide, Prepared by Melting

H. Nakagami, 1991 .

Evaluation of solid dispersions on a molecular level by the Raman mapping technique.

Susumu Hasegawa, Etsuo Yonemochi, Hiroaki Nakagami, 2008, International journal of pharmaceutics.

Effect of crystallinity of microcrystalline cellulose on the compactability and dissolution of tablets.

T. Suzuki, H. Nakagami, 1999, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

The relationship between the drug concentration profiles in plasma and the drug doses in the colon.

S. Tajiri, Shuichi Yada, H. Nakagami, 2010, Chemical & pharmaceutical bulletin.

Development of a method for the determination of caffeine anhydrate in various designed intact tablets [correction of tables] by near-infrared spectroscopy: a comparison between reflectance and transmittance technique.

E. Yonemochi, K. Terada, Tatsuya Suzuki, 2008, Journal of pharmaceutical and biomedical analysis.

Evaluation of rapidly disintegrating tablets manufactured by phase transition of sugar alcohols.

S. Ando, Y. Kuno, H. Nakagami, 2005, Journal of controlled release : official journal of the Controlled Release Society.

Improvement of low bioavailability of a novel factor Xa inhibitor through formulation of cationic additives in its oral dosage form.

M. Akashi, S. Yamashita, S. Sakuma, 2011, International journal of pharmaceutics.

Prediction of recrystallization behavior of troglitazone/polyvinylpyrrolidone solid dispersion by solid-state NMR.

Tomoyuki Watanabe, K. Higashi, K. Moribe, 2010, International journal of pharmaceutics.

Effect of the type of lubricant on the characteristics of orally disintegrating tablets manufactured using the phase transition of sugar alcohol.

E. Yonemochi, K. Terada, Y. Kuno, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Phase Separation of an IgG1 Antibody Solution under a Low Ionic Strength Condition

Kiichi Fukui, Susumu Uchiyama, Masanori Noda, 2010, Pharmaceutical Research.

Development of a method for nondestructive NIR transmittance spectroscopic analysis of acetaminophen and caffeine anhydrate in intact bilayer tablets.

Hiroshi Teramoto, Etsuo Yonemochi, Hiroaki Nakagami, 2010, Journal of pharmaceutical and biomedical analysis.

Evaluation of infrared-reflection absorption spectroscopy measurement and locally weighted partial least-squares for rapid analysis of residual drug substances in cleaning processes.

Manabu Kano, Shinji Hasebe, Hiroshi Nakagawa, 2012, Analytical chemistry.

Development of controlled release matrix pellets by annealing with micronized water-insoluble or enteric polymers.

H. Nakagami, M. Kojima, 2002, Journal of controlled release : official journal of the Controlled Release Society.

Chemical mapping of hydration and dehydration process of theophylline in tablets using terahertz pulsed imaging.

K. Terada, Tatsuya Suzuki, N. Wakiyama, 2012, Chemical & pharmaceutical bulletin.

Dosage form design and in vitro/in vivo evaluation of cevimeline extended-release tablet formulations.

S. Tajiri, H. Nakagami, T. Kanamaru, 2010, International journal of pharmaceutics.

Development of an abdominal magnetic resonance (MR) contrast agent formulation with Oral Magnetic Particles (OMP, Ferristene).

C. Chen, H. Nakagami, T. Konno, 1998, Pharmaceutica acta Helvetiae.

Colonoscopic method for estimating the colonic absorption of extended-release dosage forms in dogs.

S. Tajiri, Shuichi Yada, H. Nakagami, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Quantification of pharmaceutical polymorphs and prediction of dissolution rate using theophylline tablet by terahertz spectroscopy.

K. Terada, Tatsuya Suzuki, Jin Hisazumi, 2011, Chemical & pharmaceutical bulletin.

Quantitative estimation of intra-subject variability in bioequivalence studies of generic solid oral dosage forms by multiple regression analysis

Shigenori Wada, Seiya Kagatani, Hiroaki Nakagami, 2021 .

Impact of gastrointestinal residence time of extended-release (ER) tablets on in vivo evaluation of ER tablets

S. Tajiri, H. Nakagami, T. Kanamaru, 2010 .

Investigation of water mobility and diffusivity in hydrating micronized low-substituted hydroxypropyl cellulose, hydroxypropylmethyl cellulose, and hydroxypropyl cellulose matrix tablets by magnetic resonance imaging (MRI).

H. Nakagami, M. Kojima, 2002, Chemical & pharmaceutical bulletin.

Effect of Crystallinity of Microcrystalline Cellulose on Granulation in High-shear Mixer

Tatsuya Suzuki, H. Nakagami, Kazuichi Watanabe, 1994 .

Colonoscopic method for estimating the colonic absorption of extended-release dosage forms in dogs.

S. Tajiri, Shuichi Yada, H. Nakagami, 2010, European journal of pharmaceutics and biopharmaceutics.

Effect of preparation method on properties of orally disintegrating tablets made by phase transition.

S. Ando, Y. Kuno, H. Nakagami, 2008, International journal of pharmaceutics.

Film Formation with Coating Systems of Aqueous Suspensions and Latex Dispersions of Ethylcellulose

H. Nakagami, Taketoshi Keshikawa, 1994 .

Bioequivalence Study of Ezetimibe Tablets After a Single Oral Dose of 10 mg in Healthy Japanese Subjects Under Fasting Conditions

S. Kagatani, H. Nakagami, Shigenori Wada, 2023, Clinical pharmacology in drug development.

Evaluation of solid dispersions on a molecular level by the Raman mapping technique.

E. Yonemochi, K. Terada, S. Hasegawa, 2008, International journal of pharmaceutics.

Computer optimization for the formulation of controlled-release theophylline tablet made of micronized low-substituted hydroxypropylcellulose and methylcellulose

Kozo Takayama, Tsuneji Nagai, Hiroaki Nakagami, 1994 .