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Dive into the research topics where Tatsunobu Yoshioka is active.

Publication


Featured researches published by Tatsunobu Yoshioka.


European Journal of Pharmaceutics and Biopharmaceutics | 2016

Oral tacrolimus oil formulations for enhanced lymphatic delivery and efficient inhibition of T-cell's interleukin-2 production.

Takayuki Yoshida; Kiyo Nakanishi; Tatsunobu Yoshioka; Yuuki Tsutsui; Atsushi Maeda; Hiromu Kondo; Kazuhiro Sako

Oral oil formulations have been reported to deliver drugs into the lymph. Lymphatic delivery of immunomodulatory drugs can more efficiently expose the drugs to T-cells in lymph, consequently induce higher efficacy and lower side effects. In this study, effects of tacrolimus oral oil formulations on drug blood exposure, and on inhibition of T-cells interleukin-2 (IL-2) production were investigated in rats. Oil formulations (sunflower oil, cacao butter, medium chain triglyceride, and palm oil) dissolving tacrolimus showed lower drug blood concentration than a solid dispersion formulation (SDF). The sunflower oil, and cacao butter formulations suppressed drug blood exposure to 50% of the SDF, and inhibited T-cells IL-2 production similar to the SDF. In vitro digestion tests indicated that slower digestion of the oils might reduce amount and rate of tacrolimus blood absorption. The cacao butter formulations showed 3.0 times more rapid tacrolimus absorption to lymphatic fluid than the SDF. Ratio of the rate constants of absorption into lymph to that into blood was higher in oil formulations (15 times in cacao butter, 15 times sunflower oil, and 3.5 times palm oil) than in the SDF. These results indicated that the oral oil formulations might be suitable for reduced tacrolimus blood concentration for low systemic side effects, and keep high lymph concentration for high efficacy in organ transplantation patients.


Archive | 2000

Stable pharmaceutical composition for oral use

Kazuhiro Sako; Toyohiro Sawada; Keiichi Yoshihara; Tatsunobu Yoshioka; Shunsuke Watanabe


Archive | 2001

Timed-release compression-coated solid composition for oral administration

Toyohiro Sawada; Kazuhiro Sako; Tatsunobu Yoshioka; Shunsuke Watanabe


Archive | 2001

Drug delivery system for averting pharmacokinetic drug interaction and method thereof

Toyohiro Sawada; Kazuhiro Sako; Tatsunobu Yoshioka; Shunsuke Watanable


Journal of Controlled Release | 2007

Enhanced pharmacological activity of recombinant human interleukin-11 (rhIL11) by chemical modification with polyethylene glycol

Akira Takagi; Noboru Yamashita; Tatsunobu Yoshioka; Yuuki Takaishi; Kyoko Sano; Hideto Yamaguchi; Atsushi Maeda; Katsumi Saito; Yoshinobu Takakura; Mitsuru Hashida


Archive | 2001

Time-release coated solid compositions for oral administration

Toyohiro Sawada; Kazuhiro Sako; Tatsunobu Yoshioka; Shunsuke Watanabe


Journal of Controlled Release | 2006

Incorporation into a biodegradable hyaluronic acid matrix enhances in vivo efficacy of recombinant human interleukin 11 (rhIL11).

Akira Takagi; Noboru Yamashita; Tatsunobu Yoshioka; Yuuki Takaishi; Kiyo Nakanishi; Shigeo Takemura; Atsushi Maeda; Katsumi Saito; Yoshinobu Takakura; Mitsuru Hashida


Archive | 2001

Drug delivery system for avoiding pharmacokinetic interaction between drugs and method thereof

Toyohiro Sawada; Kazuhiro Sako; Tatsunobu Yoshioka; Shunsuke Watanabe


Archive | 2007

Cefdinir-containing pharmaceutical composition

Tatsunobu Yoshioka; Yoshiyuki Murakami; Noboru Yamashita; Shigemitsu Tomei; Katsumi Saito; Akira Takagi


Archive | 2000

Stable medicinal compositions for oral use

Kazuhiro Sako; Toyohiro Sawada; Keiichi Yoshihara; Tatsunobu Yoshioka; Shunsuke Watanabe

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Atsushi Maeda

Tokyo University of Agriculture and Technology

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