Patents by Inventor Takashi Imagawa

Takashi Imagawa 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).

  • Publication number: 20210124791
    Abstract: To construct an information system or an information network focusing on a physical medium and provide a predetermined information composed of a series of information or the like that has a relation in terms of a time and/or a place and/or a context. The information providing system includes an ID storage medium that is attached to a specific physical medium to store a unique ID identifying a specific tangible object, an information recording means of making a computer realize a function of recording an ID of one tangible object in a storage means when a user reads out the ID storage medium at a specific location, where the ID storage medium is physically present, by a terminal device having an ability to read the ID of the ID storage medium, and an information retrieving means of providing the user with a function of retrieving information about the tangible object uniquely corresponding to the ID recorded in the storage means.
    Type: Application
    Filed: August 13, 2020
    Publication date: April 29, 2021
    Inventor: Takashi Imagawa
  • Patent number: 9056128
    Abstract: There is provided an adjuvant capable of enlarging an ablation area and reducing ablation unevenness in a dielectric heating-assisted cancer treatment such as radiofrequency ablation used for treatment of hepatic cancer. The adjuvant includes a conductive substance such as a metal element (e.g., iron) and a pharmaceutically acceptable carrier of lipid dispersion, polymer solution or polymer dispersion.
    Type: Grant
    Filed: January 30, 2004
    Date of Patent: June 16, 2015
    Assignee: OTSUKA PHARMACEUTICAL FACTORY, INC.
    Inventors: Hirokazu Uyama, Takamichi Murakami, Takashi Imagawa
  • Publication number: 20100099639
    Abstract: The present invention provides a W/O/W multiple emulsion composition composed of an internal aqueous phase, an oil phase, and an external aqueous phase, the internal aqueous phase containing an ionic physiologically active substance and a physiologically acceptable compound having a molecular weight of 1,000 or less and generating a polyvalent counterion with two or more valencies for the ionic physiologically active substance. The W/O/W emulsion composition of the present invention not only can stably encapsulate a useful substance in its internal aqueous phase at a high encapsulation ratio, but also has high safety.
    Type: Application
    Filed: October 26, 2007
    Publication date: April 22, 2010
    Applicant: CONTROLLED LIPO TECHS, INC.
    Inventors: Toshimitsu Terao, Takashi Imagawa, Hironobu Yanagie, Masazumi Eriguchi
  • Publication number: 20090192230
    Abstract: The present invention provides a propofol-containing fat emulsion that can be administered with reduced vascular pain without incorporating a local anesthetic such as lidocaine; and a process for producing the same. The fat emulsion comprises 0.1 to 5 w/v % of propofol, 2 to 20 w/v % of an oily component, 0.4 to 10 w/v % of an emulsifier and 0.02 to 0.3 w/v % of at least one compound selected from the group consisting of cyclodextrins, cyclodextrin derivatives and pharmacologically acceptable salts thereof, and is in the form of a fat emulsion.
    Type: Application
    Filed: January 6, 2005
    Publication date: July 30, 2009
    Inventors: Koichi Takeda, Kenji Matsuda, Toshimitsu Terao, Tadaaki Inoue, Takashi Imagawa, Shigeru Masumi
  • Publication number: 20090069445
    Abstract: This invention provides a propofol-containing fat emulsion preparation including: 0.1 to 2 w/v % of propofol, 10 to 20 w/v % of an oily component, and 2 to 5 w/v % of an emulsifier, the weight of the oily component being in the range of about 5 to about 200 times the weight of propofol, the weight of the emulsifier being in the range of about 0.9 to about 50 times that of propofol, and the average size of emulsion particles being 180 nm or less, and a method for preparing the same. Propofol-containing fat emulsion preparation of this invention alleviates the vascular pain that occurs during the administration thereof without incorporating a local anesthetic, such as lidocaine or the like, therein.
    Type: Application
    Filed: April 7, 2006
    Publication date: March 12, 2009
    Applicant: Otsuka Pharmaceutical Factory, Inc
    Inventors: Koichi Takeda, Kenji Matsuda, Toshimitsu Terao, Tadaaki Inoue, Takashi Imagawa, Shigeru Masumi
  • Publication number: 20080128314
    Abstract: The present invention provides a pharmaceutical composition which can permit a sparingly water-soluble drug substance to be solubilized or dispersed in a pharmaceutically allowable liquid medium (e.g., fat emulsion, etc.), characterized in that said pharmaceutical composition contains (a) a base (e.g., polyethylene glycol, etc.), (b) a sparingly water-soluble drug substance and (c) a fatty acid or its pharmaceutically allowable salt. The pharmaceutical composition can be mixed with a pharmaceutically allowable liquid medium to produce a pharmaceutical preparation for administration, such as an injectable solution, etc., wherein mixing can be performed for a shortened period of time and the sparingly water-soluble drug substance can be uniformly solubilized or dispersed in a liquid medium.
    Type: Application
    Filed: March 10, 2006
    Publication date: June 5, 2008
    Inventors: Koichi Takeda, Kenji Matsuda, Toshimitsu Terao, Tadaaki Inoue, Takashi Imagawa
  • Publication number: 20060147551
    Abstract: There is provided an adjuvant capable of enlarging an ablation area and reducing ablation unevenness in a dielectric heating-assisted cancer treatment such as radiofrequency ablation used for treatment of hepatic cancer. The adjuvant includes a conductive substance such as a metal element (e.g., iron) and a pharmaceutically acceptable carrier of lipid dispersion, polymer solution or polymer dispersion.
    Type: Application
    Filed: January 30, 2004
    Publication date: July 6, 2006
    Inventors: Hirokazu Uyama, Takamichi Murakami, Takashi Imagawa
  • Patent number: 6177059
    Abstract: A complex comprising a lipid and a conjugate of GPIb and lipid having a functional group, and use thereof. The GPIb-lipid complex of the present invention is extremely useful as a platelet substitute, a pharmaceutical agent for the prophylaxis and treatment of angiopathy, vascular damages and thrombosis, a diagnostic for vWF deficiency and the like, a biological or medical reagent, a reagent for screening platelet aggregation suppressant or antithrombosis, and the like. The GPIb-lipid complex of the present invention is also useful as a diagnostic for finding the location of vascular lesion or thrombus formation, or a therapeutic agent therefor, since it accumulates at vascular lesions.
    Type: Grant
    Filed: December 3, 1998
    Date of Patent: January 23, 2001
    Assignee: Yoshitomi Pharmaceutical Industries, Ltd.
    Inventors: Hiroshi Matsuda, Kaeko Kamide, Yasuo Amatsuji, Takashi Imagawa, Yasuo Ikeda, Mitsuru Murata
  • Patent number: 5575986
    Abstract: A compound of the following formula ##STR1## wherein m is an integer of 1 to 3, R.sub.1 and R.sub.2 are the same or different and each is hydrogen atom or lower alkyl, and R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are the same or different and each is hydroxy or a group of the formula ##STR2## (wherein n is 0 or 1, X is --NH-- or --O--, Y is alkylene, A is hydrogen atom, lower alkyl, lower alkoxy, halogen atom or trifluoromethyl, and B is alkyl or alkenyl), with the proviso that two or three of R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are hydroxyl groups and that when two of them are hydroxyl groups, the cases where R.sub.3 and R.sub.5 are hydroxy, and R.sub.4 and R.sub.6 are hydroxy are excluded; a complex compound comprising said compound and a metallic atom; and a diagnostic agent containing said complex compound. The above compound is useful as a chelating agent and the complex compound comprising said compound and a metallic atom exhibits superior characteristics as a contrast medium for image diagnosis.
    Type: Grant
    Filed: April 19, 1995
    Date of Patent: November 19, 1996
    Assignee: The Green Cross Corporation
    Inventors: Fumio Mori, Tadashi Okano, Kazuki Murakami, Masakazu Shintome, Hiromichi Mukai, Ikuko Miyagi, Takashi Imagawa, Sang-Won Kim, Taro Marukawa, Takahiro Kozuka
  • Patent number: 5455412
    Abstract: A scanner is so arranged that a quantity of light reaching a CCD sensor can be kept constant with a change in reading position. In case a light source and a reading optical unit are driven independent of each other, variations in feed amount inevitably occur. To deal with it, a test chart of a specified length is first read to measure moving amounts of the light source and the reading optical unit. Then, the reading optical unit is moved by a predetermined amount. The light source is moved as effecting a correction based on the moving amounts initially measured. Then, a one-line reading process is carried out to scan an image on a document.
    Type: Grant
    Filed: April 26, 1994
    Date of Patent: October 3, 1995
    Assignee: Sharp Kabushiki Kaisha
    Inventors: Takashi Imagawa, Fumikazu Nagano
  • Patent number: 5453264
    Abstract: A compound of the following formula ##STR1## wherein m is an integer of 1 to 3, R.sub.1 and R.sub.2 are the same or different and each is hydrogen atom or lower alkyl, and R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are the same or different and each is hydroxy or a ##STR2## (wherein n is 0 or 1, X is --NH-- or --O--, Y is alkylene, A is hydrogen atom, lower alkyl, lower alkoxy, halogen atom or trifluoromethyl, and B is alkyl or alkenyl), with the proviso that two or three of R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are hydroxyl groups and that when two of them are hydroxyl groups, the cases where R.sub.3 and R.sub.5 are hydroxy, and R.sub.4 and R.sub.6 are hydroxy are excluded; a complex compound comprising said compound and a metallic atom; and a diagnostic agent containing said complex compound. The above compound is useful as a chelating agent and the complex compound comprising said compound and a metallic atom exhibits superior characteristics as a contrast medium for image diagnosis.
    Type: Grant
    Filed: March 3, 1994
    Date of Patent: September 26, 1995
    Assignee: The Green Cross Corporation
    Inventors: Fumio Mori, Tadashi Okano, Kazuki Murakami, Masakazu Shintome, Hiromichi Mukai, Ikuko Miyagi, Takashi Imagawa, Sang-Won Kim, Taro Marukawa, Takahiro Kozuka
  • Patent number: 5275956
    Abstract: The concentration of an organic chlorine compound contained in a gaseous medium is measured in situ by feeding the gaseous medium to a reaction zone and oxidizing the chlorine compound to produce a reactive gas capable of reacting with a chemiluminescent compound to cause chemiluminescence. The reactive gas is contacted with the chemiluminescent compound contained in a cell to cause chemiluminescence whose intensity is proportional to the amount of the reactive gas produced by the oxidation of the organic compound. The concentration of an organic chlorine compound contained in an aqueous medium may also be measured by the similar method after separating the organic chlorine compound as vapors from the aqueous medium. A device suitable for the above measurement is also disclosed.
    Type: Grant
    Filed: November 18, 1992
    Date of Patent: January 4, 1994
    Assignee: Director-General of Agency of Industrial Science and Technology
    Inventors: Kenji Bansho, Hiroaki Tao, Akira Miyazaki, Takashi Imagawa
  • Patent number: 4771296
    Abstract: A transfer ribbon feed arrangement for use in a transfer type recording apparatus which transfers onto a recording sheet by sequentially feeding the transfer ribbon includes a feed roller disposed on the feed side of the transfer ribbon for feeding the transfer ribbon from the feed roller, a take-up roller for winding up the transfer ribbon around it and a tension unit disposed on the feed side of the transfer ribbon for applying a constant load on the transfer ribbon to keep it under a constant tension.
    Type: Grant
    Filed: October 17, 1986
    Date of Patent: September 13, 1988
    Assignee: Sharp Kabushiki Kaisha
    Inventors: Mitsuhiro Shimada, Yuichiro Mori, Fumio Shiozaki, Susumu Nonaka, Takashi Imagawa
  • Patent number: 4751519
    Abstract: According to the recording apparatus of the present invention, recording papers are wound by the winding member while the end portions of the recording papers are tightly held. The recording papers can therefore be correctly reciprocated. Furthermore, before recording is effected by the recording head, the recording papers are one wound back by the winding member to an initial position, thereby removing strains or deflections of the recording papers. Also, in the case of a color printer of thermal transcription, images in each of the four colors can be accurately overlapped without disagreement.
    Type: Grant
    Filed: September 22, 1986
    Date of Patent: June 14, 1988
    Assignee: Sharp Kabushiki Kaisha
    Inventors: Mitsuhiro Shimada, Yuichiro Mori, Takashi Imagawa, Fumio Shiozaki, Susumu Nonaka
  • Patent number: 4684633
    Abstract: A prostaglandin emulsion composition comprising a prostaglandin emulsified with a phosphatidylethanolamine-free phospholipid, the composition being suitable for intravenous administration.
    Type: Grant
    Filed: January 14, 1985
    Date of Patent: August 4, 1987
    Assignee: The Green Cross Corporation
    Inventors: Takashi Imagawa, Kazumasa Yokoyama, Yutaka Mizushima
  • Patent number: 4265888
    Abstract: Acetylsalicylates with basic amino acids such as DL-lysine is stabilized in the form of solid preparation by admixing anhydrous calcium chloride therewith. The preparation containing calcium chloride is prevented from hydrolysis and can be stored for a long period of time even at a relatively high room temperature. The preparation is further prevented from discarolation when glycine is added thereto.
    Type: Grant
    Filed: January 8, 1980
    Date of Patent: May 5, 1981
    Assignee: The Green Cross Corporation
    Inventors: Yoshio Kagitani, Takashi Imagawa, Hirohisa Inahara, Ryozo Watanabe