Masashi Nakakura
Kyowa Hakko Kirin Co., Ltd.
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Publication
Featured researches published by Masashi Nakakura.
International Journal of Pharmaceutics | 2010
Atsushi Ishihara; Masahiro Yamauchi; Hiroko Kusano; Yukiteru Mimura; Masashi Nakakura; Masaaki Kamiya; Ayato Katagiri; Masaki Kawano; Hisao Nemoto; Toshiyuki Suzawa; Motoo Yamasaki
We examined the effect on drug delivery of liposomes with surfaces that were modified with branched oligoglycerols (BGLs) and explored possible formulation advantages to increase drug exposure. BGL012 is a branched oligoglycerol derivative with a cascade-like structure of 12 glycerol units, characterized as a widely spread structure in aqueous solution. We prepared BGL-phospholipid derivatives (BGL-PEs), including BGL012, by coupling 1,2-distearoylphosphatidylethanolamine to BGLs. BGL012-PE modification of the liposomes (BGL012L) achieved a long circulation time after intravenous injection in rats. The circulation lifetime of BGL012L was almost the same as that of polyethylene glycol (PEG)-modified liposomes. The surface of BGL012L induced the formation of a fixed aqueous layer and reduced protein adsorption on the liposome surface, without strong interference with the binding reaction on the liposome. Thus, the newly synthesized branched oligoglycerol derivatives are considered to have useful hydrophilic and physical properties for modifying the liposome surface to increase drug exposure.
Journal of Drug Targeting | 1995
Masashi Nakakura; Mitsuru Terajima; Yasuki Kato; Eiji Hayakawa; Kunio Ito; Tokuyuki Kuroda
The effects of concentration, amperage and duration on the antidiuretic response induced by iontophoretic delivery of desmopressin acetate (DDAVP) were examined using a diabetes insipidus model in rats. A higher current density brought about a larger and longer antidiuretic response. Prolonged iontophoretic duration caused an overdose. Repeated short iontophoretic treatments with lower current density maintained a constant response with a short lag time and a rapid disappearance of pharmacological response immediately after cessation of the final treatment. This type of iontophoresis substantially reduced the inter-subject variability of response as compared to the response using an intranasal route of administration.
Archive | 1995
Masashi Nakakura; Yuji Ueno; Eiji Hayakawa; Tokuyuki Kuroda
Biological & Pharmaceutical Bulletin | 2007
Masahiro Yamauchi; Kyoko Tsutsumi; Masayuki Abe; Yoichi Uosaki; Masashi Nakakura; Noboru Aoki
Archive | 2004
Yuji Ueno; Takashi Kayashita; Atsushi Ishihara; Masashi Nakakura; Kyoko Yamauchi
Chemical & Pharmaceutical Bulletin | 1993
Yasuki Kato; Watanabe K; Masashi Nakakura; Toshihito Hosokawa; Eiji Hayakawa; Kunio Ito
Biochimica et Biophysica Acta | 2006
Masahiro Yamauchi; Hiroko Kusano; Etsuko Saito; Takeshi Iwata; Masashi Nakakura; Yasuki Kato; Noboru Aoki
Journal of Controlled Release | 2006
Masahiro Yamauchi; Hiroko Kusano; Etsuko Saito; Takeshi Iwata; Masashi Nakakura; Yasuki Kato; Takaaki Uochi; Shiro Akinaga; Noboru Aoki
Biological & Pharmaceutical Bulletin | 1996
Masashi Nakakura; Yasuki Kato; Eiji Hayakawa; Kunio Ito; Tokuyuki Kuroda
Archive | 1995
Masashi Nakakura; Eiji Hayakawa; Tokuyuki Kuroda