Patents by Inventor Kazunari Akiyoshi

Kazunari Akiyoshi has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 8759322
    Abstract: The present invention provides a hydrophobic group-introduced hyaluronic acid derivative comprising at least one repeating unit represented by the formula (I): wherein R1, R2, R3, R4, Z, n, Ra, Y, and X1 are as defined in the specification.
    Type: Grant
    Filed: November 5, 2009
    Date of Patent: June 24, 2014
    Assignees: National University Corporation Tokyo Medical and Dental University, Chugau Seiyaku Kabushiki Kaisha
    Inventors: Kazunari Akiyoshi, Takashi Nakai, Tai Hirakura, Tsuyoshi Shimoboji
  • Publication number: 20110212901
    Abstract: The present invention provides a hydrophobic group-introduced hyaluronic acid derivative comprising at least one repeating unit represented by the formula (I): wherein R1, R2, R3, R4, Z, n, Ra, Y, and X1 are as defined in the specification.
    Type: Application
    Filed: November 5, 2009
    Publication date: September 1, 2011
    Applicants: NATIONAL UNIVERSITY CORPORATION TOKYO MEDICAL AND DENTAL UNVERSITY, CHUGAI SEIYAKU KABUSHIKI KAISHA
    Inventors: Kazunari Akiyoshi, Takashi Nakai, Tai Hirakura, Tsuyoshi Shimoboji
  • Publication number: 20110206729
    Abstract: A mucosal vaccine for the prevention or treatment of microbial infections is described that is capable of inducing vaccine antigen-specific immune responses in an organism without the addition of a mucosal adjuvant. The mucosal vaccine comprises a composite of a nanogel comprising a hydrophilic polysaccharide having a cationic functional group and a hydrophobic cholesterol added thereto as a side chain and a vaccine antigen. The vaccine is administered via a mucosal route.
    Type: Application
    Filed: October 30, 2009
    Publication date: August 25, 2011
    Inventors: Kazunari Akiyoshi, Hiroshi Kiyono, Yoshikazu Yuki, Tomonori Nochi
  • Publication number: 20100221345
    Abstract: An object of the present invention is to provide an osteogenic biomaterial which achieves long-term sustained release and localized functional expression of a substance which promotes the formation of bone tissue. The present inventors have found out that a nanogel efficiently encloses an osteogenesis promoting substance to suppress the substance from diffusion into blood, and that the nanogel functions as a carrier for local administration of the osteogenesis promoting substance. Furthermore, they have found out that the osteogenesis promoting substance-containing nanogel can be cross-linked with a water-soluble polymer to allow sustained release of the osteogenesis promoting substance at a local area over a long period of time. Based on these findings, the present invention was completed.
    Type: Application
    Filed: January 17, 2007
    Publication date: September 2, 2010
    Applicant: NATIONAL UNIVERSITY CORPORATION TOKYO MEDICAL AND
    Inventors: Kazunari Akiyoshi, Masaki Noda
  • Publication number: 20100204102
    Abstract: The present invention provides a composition comprising a hyaluronic acid derivative having a crosslinking group(s) and a hydrophilic polysaccharide derivative having a hydrophobic group(s), wherein the hyaluronic acid derivative having a crosslinking group(s) is prepared by crosslinkage formation reaction in hyaluronic acid or a derivative thereof having a crosslinkable group(s) in the presence of the hydrophilic polysaccharide derivative wherein the hydrophilic polysaccharide derivative may have a crosslinkable group(s).
    Type: Application
    Filed: April 30, 2008
    Publication date: August 12, 2010
    Inventors: Kazunari Akiyoshi, Nobuyuki Morimoto, Tai Hirakura, Tsuyoshi Shimoboji
  • Publication number: 20080279918
    Abstract: It is intended to efficiently inject into a target cell, a substance charged within a liposome. The present inventors have found that connexin synthesized within a liposome is introduced as connexon having a gap junction function into the liposome membrane. Specifically, the liposome according to the present invention is a liposome in which connexon composed of connexin synthesized by an in-vitro protein synthesis system is incorporated in a state of having a gap junction function.
    Type: Application
    Filed: November 2, 2005
    Publication date: November 13, 2008
    Applicants: National University Corporation Tokyo Medical and Dental University, Dai Nippon Printing Co., Ltd.
    Inventors: Ikuo Morita, Kazunari Akiyoshi, Shinichiro Nomura
  • Publication number: 20070253940
    Abstract: The present invention provides a platelet-rich plasma with high activities in an easy and economical manner. The platelet-rich plasma is obtained by aggregating and precipitating erythrocytes from collected whole blood selectively and facilitatively without employing centrifugation. For example, the plasma is obtained by the addition of a polymer having a residue of an organic phosphate compound. Specifically, the polymer having a residue of an organic phosphate compound can be added to whole blood and allowed to stand for a specific time, thereby to selectively and facilitatively aggregate and precipitate erythrocytes to give a supernatant. The supernatant contains much platelets which exist in their extremely intact state similar as in a living body and simultaneously provides a platelet-rich plasma with high activity comprising much plasma proteins such as fibrinogen and leukocytes.
    Type: Application
    Filed: January 28, 2005
    Publication date: November 1, 2007
    Applicant: TORAY INDUSTRIES, INC.
    Inventors: Emi Sumida, Shohei Kasugai, Kazunari Akiyoshi, Yasuhiko Iwasaki
  • Publication number: 20050170327
    Abstract: An object of this invention is to provide platelet-rich plasma having high activity easily and at low cost. The object is achieved by a method for preparing platelet-rich plasma comprising a step of adding a water-soluble polymer compound to whole blood obtained by blood collection. For example, by adding poly-L-glutamic acid to whole blood and allowing the mixture to stand still for a definite period, it is possible to obtain platelet-rich plasma having high activity that contains blood plasma components containing much fibrinogen in addition to platelets in the supernatant and blood cell components including white blood cells. This invention also includes the platelet-rich plasma and the use thereof as well as a kit for preparing platelet-rich plasma.
    Type: Application
    Filed: August 1, 2003
    Publication date: August 4, 2005
    Inventors: Emi Sumida, Shohei Kasugai, Kazunari Akiyoshi, Yasuhiko Iwasaki
  • Patent number: 6566516
    Abstract: A high purity polysaccharide containing hydrophobic group is produced by a process involving a first process step of producing an isocyanate group-containing hydrophobic compound, wherein one mole of a hydroxyl group-containing hydrocarbon having 12-50 carbon atoms or of a sterol is reacted with a diisocyanate represented by OCN—R1—NCO in which R1 is a hydrocarbyl of 1-50 carbon atoms, a second process step of producing the polysaccharide containing hydrophobic group composed of the hydrocarbon group of 12-50 carbon atoms or of the steryl group, wherein the isocyanate group-containing hydrophobic compound obtained in the first process step is reacted with one or more polysaccharides, and a purification step in which the reaction product in the second process step is purified using a solvent based on a ketone.
    Type: Grant
    Filed: April 25, 2000
    Date of Patent: May 20, 2003
    Assignees: NOF Corporation
    Inventors: Junzo Sunamoto, Kazunari Akiyoshi, Ryuzo Hosotani, Akio Hayashi, Hiroki Fukui
  • Publication number: 20020143160
    Abstract: 1.
    Type: Application
    Filed: March 6, 2002
    Publication date: October 3, 2002
    Applicant: NOF CORPORATION
    Inventors: Junzo Sunamoto, Kazunari Akiyoshi, Ryuzo Hosotani, Akio Hayashi, Hiroki Fukui