Y
Yasuhisa Sakurai
Researcher at University of Tokyo
Publications - 120
Citations - 4548
Yasuhisa Sakurai is an academic researcher from University of Tokyo. The author has contributed to research in topics: Micelle & Copolymer. The author has an hindex of 24, co-authored 120 publications receiving 4449 citations. Previous affiliations of Yasuhisa Sakurai include Kao Corporation & Nikon.
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Journal ArticleDOI
Development of the polymer micelle carrier system for doxorubicin.
T Nakanishi,S. Fukushima,Kazuya Okamoto,Minoru Suzuki,Yasuhiro Matsumura,Masayuki Yokoyama,Teruo Okano,Yasuhisa Sakurai,Kazunori Kataoka +8 more
TL;DR: The result of pre-clinical study of NK911, a polymeric micelle carrier system for doxorubicin (DOX) shows much stronger activity than the free DOX, which can entrap the sufficient amount of DOX in tumor tissue by EPR effect.
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Totally Synthetic Polymer Gels Responding to External Glucose Concentration: Their Preparation and Application to On−Off Regulation of Insulin Release
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Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor
Masayuki Yokoyama,Shigeto Fukushima,Ryuji Uehara,Kazuya Okamoto,Kazunori Kataoka,Yasuhisa Sakurai,Teruo Okano +6 more
TL;DR: It was found that a dimer of adriamycin molecules formed and that this dimer was physically entrapped in the inner core of the micelle as well as intact ADR, indicating that the physicallyEntrapped ADR played a major role in antitumor activity in vivo.
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Enhanced tumor accumulation and prolonged circulation times of micelle-forming poly(ethylene oxide-aspartate) block copolymer-Adriamycin conjugates
TL;DR: Investigation of the biodistribution of poly (ethylene oxide-aspartate) block copolymer-adriamycin conjugates in murine colon adenocarcinoma 26 (C-26) tumor-bearing mice after intravenous injection indicates that ADR associated with the micelleforming PEO-PAsp(ADR) conjugate is more efficaciously delivered to tumor sites than free ADR.
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Thermo-responsive polymer nanoparticles with a core-shell micelle structure as site-specific drug carriers
TL;DR: These micelles have a small diameter with a low critical micelle concentration, providing a carrier that may have long blood circulation times and a low RES uptake and are valuable for site-specific delivery of drugs using changes in temperature as a trigger.