S. Yokohama

发表

Influence of water soluble fillers in hydroxypropylmethylcellulose matrices on in vitro and in vivo drug release.

H. Nakashima, T. Sonobe, K. Sako, 2002, Journal of controlled release : official journal of the Controlled Release Society.

Timed-release formulation to avoid drug-drug interaction between diltiazem and midazolam.

K. Sako, M. Hayashi, T. Sawada, 2003, Journal of pharmaceutical sciences.

Effect of food on gastrointestinal transit of liquids in cynomolgus monkeys

J. Watanabe, H. Kondo, S. Yokohama, 2003, Biopharmaceutics & drug disposition.

Release of recombinant human bone morphogenetic protein 2 from a newly developed carrier.

T. Uchida, T. Sonobe, K. Nozaki, 2003, International journal of pharmaceutics.

Potential Use of Cyclodextrins to Enhance the Solubility of YM466 in Aqueous Solution

Katsutoshi Nakamura, Keiichi Tokihiro, Yukihisa Motomura, 2003, Drug development and industrial pharmacy.

Characteristics of the gastric pH profiles of unfed and fed cynomolgus monkeys as pharmaceutical product development subjects

T. Shinoda, H. Nakashima, H. Kondo, 2003, Biopharmaceutics & drug disposition.

Intestinal absorption mechanisms of γ-butyrolactone-γ-carbonyl-L-histidyl-L-prolinamide citrate (DN-1417) and thyrotropin-releasing hormone (TRH)

T. Shimamoto, S. Yokohama, T. Yoshioka, 1985 .

Absorption of gamma-butyrolactone-gamma-carbonyl-L-histidyl-L-prolinamide citrate (DN-1417), an analog of thyrotropin-releasing hormone, in rats and dogs.

S. Yokohama, T. Yoshioka, N. Kitamori, 1984, Journal of pharmacobio-dynamics.

Intestinal absorption mechanisms of thyrotropin-releasing hormone.

S. Yokohama, K. Yamashita, T. Yoshioka, 1984, Journal of pharmacobio-dynamics.

A new recombinant human bone morphogenetic protein-2 carrier for bone regeneration.

T. Uchida, M. Murai, T. Sonobe, 2001, International journal of pharmaceutics.

The improved dissolution and prevention of ampoule breakage attained by the introduction of pretreatment into the production process of the lyophilized formulation of recombinant human Interleukin-11 (rhIL-11).

S. Yokota, S. Yokohama, A. Okada, 2004, International journal of pharmaceutics.

Gastrointestinal transit of liquids in unfed cynomolgus monkeys

J. Watanabe, Yutaka Takahashi, H. Kondo, 2003, Biopharmaceutics & drug disposition.

Effect of Colonic Lactulose Availability on the Timing of Drug Release Onset in Vivo from a Unique Colon-Specific Drug Delivery System (CODES™)

Jinhe Li, Shigeharu Yokohama, Jinhe Li, 2003, Pharmaceutical Research.

A new index, the core erosion ratio, of compression-coated timed-release tablets predicts the bioavailability of acetaminophen.

M. Fukui, K. Sako, M. Hayashi, 2003, International journal of pharmaceutics.

Absorption of thyrotropin-releasing hormone after oral administration of TRH tartrate monohydrate in the rat, dog and human.

H. Toguchi, S. Yokohama, K. Yamashita, 1984, Journal of pharmacobio-dynamics.

Radioimmunoassay of thyrotropin-releasing hormone (TRH) in rat, dog, and human blood.

H. Toguchi, S. Yokohama, K. Yamashita, 1983, Journal of pharmacobio-dynamics.

A new stressed test to predict the foreign matter formation of minodronic acid in solution.

T. Sonobe, T. Sawada, S. Yokohama, 2003, International journal of pharmaceutics.

Failure of stability prediction for minodronic acid injectable by accelerated stability testing.

T. Sonobe, S. Yokohama, Katsutoshi Nakamura, 2002, International journal of pharmaceutics.

Stabilization of minodronic acid in aqueous solution for parenteral formulation.

K. Saito, T. Sonobe, S. Yokohama, 2001, International journal of pharmaceutics.

Characteristics of intestinal absorption of adinazolam and in vivo evaluation of oral sustained release tablets of adinazolam in beagle dogs

S. Yokohama, K. Tahara, T. Nishihata, 1993 .

Blood level and brain distribution of thyrotropin-releasing hormone (TRH) determined by radioimmunoassay after intravenous administration in rats.

Y. Nagai, S. Yokohama, Y. Hirooka, 1980, Journal of pharmacobio-dynamics.

Common solubilizers to estimate the Caco-2 transport of poorly water-soluble drugs.

Yutaka Takahashi, H. Kondo, S. Yokohama, 2002, International journal of pharmaceutics.