Method for diagnosing dry eyes
    51.
    发明授权
    Method for diagnosing dry eyes 失效
    干眼症诊断方法

    公开(公告)号:US5884630A

    公开(公告)日:1999-03-23

    申请号:US773520

    申请日:1996-12-23

    申请人: Hiroshi Fujishima

    发明人: Hiroshi Fujishima

    IPC分类号: A61B3/10 A61B5/11 A61B19/00

    摘要: Dry eyes are more objectively and exactly diagnosed on the basis a rate of decrease in corneal surface temperature due to the heat vaporization in tear evaporation as determined by measuring corneal surface temperatures in time course from one blinking to next blinking of eyes of patients by an infrared radiation thermometry.

    摘要翻译: 根据通过测量角膜表面温度在时间过程中通过红外线测量患者眼睛的眨眼到下一次眼睛的角度来确定由于泪液蒸发中的热蒸发而导致的角膜表面温度降低的速率,干眼睛被更客观地和准确地诊断 放射测温。

    Parenchymal hepatocyte growth factors
    52.
    发明授权
    Parenchymal hepatocyte growth factors 失效
    实质肝细胞生长因子

    公开(公告)号:US5807711A

    公开(公告)日:1998-09-15

    申请号:US525505

    申请日:1995-09-22

    CPC分类号: C07K14/4753

    摘要: A novel parenchymal hepatocyte growth factor originating in a human or animal liver, having an estimated molecular weight according to nonreductive SDS-PAGE of about 63,000 to about 69,000, an estimated molecular weight according to reductive SDS-PAGE of about 32,000 to about 36,000 and an estimated molecular weight according to gel filtration of about 60 to about 70 Kd; and having an activity of effecting the growth of parenchymal hepatocyte has been obtained from the hemihepatectomized tissue. Furthermore, a gene coding for the above substance has been obtained from the mRNA of the above tissue and it has thus become possible to mass-produce the above substance.

    摘要翻译: PCT No.PCT / JP94 / 00455 Sec。 371日期1995年9月22日 102(e)1995年9月22日PCT 1994年3月22日PCT公布。 公开号WO94 / 21678 日期1994年9月29日一种来源于人或动物肝脏的新型实质肝细胞生长因子,根据非还原性SDS-PAGE估计的分子量为约63,000至约69,000,根据还原性SDS-PAGE估计的分子量为约32,000 约36,000,并且根据凝胶过滤估计的约60至约70Kd的分子量; 并且具有影响实质肝细胞生长的活性已从半肝切除组织获得。 此外,从上述组织的mRNA获得编码上述物质的基因,因此可以大量生产上述物质。

    Prostaglandin derivatives
    53.
    发明授权
    Prostaglandin derivatives 失效
    前列腺素衍生物

    公开(公告)号:US5545666A

    公开(公告)日:1996-08-13

    申请号:US290745

    申请日:1995-04-19

    CPC分类号: C07C405/0016

    摘要: A prostaglandin derivative represented by formula ##STR1## wherein R.sup.1 represents a hydrogen atom or a C.sub.1 -C.sub.6 alkyl group, and R.sup.2 represents a cyclohexyl group or a cyclopentylmethyl group. This compound has physiological activities such as platelet aggregation-inhibiting action, renal blood vessel and coronary blood vessel-dilating actions and the like, and is useful for treatment of renal failure and diseases of circulatory organs.

    摘要翻译: PCT No.PCT / JP93 / 01493 Sec。 371日期1995年04月19日 102(e)1995年4月19日PCT PCT 1993年10月18日PCT公布。 公开号WO94 / 08959 日本1994年4月28日由式表示的前列腺素衍生物,其中R1表示氢原子或C1-C6烷基,R2表示环己基或环戊基甲基。 该化合物具有血小板聚集抑制作用,肾血管和冠状血管扩张作用等的生理活性,可用于治疗肾衰竭和循环器官疾病。

    Method of producing fine coated pharmaceutical preparation
    54.
    发明授权
    Method of producing fine coated pharmaceutical preparation 失效
    生产精细涂层药物制剂的方法

    公开(公告)号:US5017383A

    公开(公告)日:1991-05-21

    申请号:US395594

    申请日:1989-08-18

    IPC分类号: A61K9/50

    CPC分类号: A61K9/5089

    摘要: A method of producing a fine coated pharmaceutical preparation, which includes cooling fine liquid droplets composed of a liquid medium, a drug dissolved or suspended in the liquid medium, and as required, a binder to a temperature of not higher than the freezing point of the liquid medium to form frozen particles of the drug and as required the binder, adjusting the particle sizes of the fine frozen particles, mixing the fine frozen particles with a fine powder of a coating material having a particle diameter smaller than the particles at a temperature higher than the freezing point of the liquid medium to cause the fine powder of the coating material to adhere to the surfaces of the particles, and then removing the liquid medium from the resulting coated particles.

    Peptide serine protease inhibitor
    55.
    发明授权
    Peptide serine protease inhibitor 失效
    肽丝氨酸蛋白酶抑制剂

    公开(公告)号:US4963654A

    公开(公告)日:1990-10-16

    申请号:US309161

    申请日:1989-02-13

    申请人: Nobuhiko Katunuma

    发明人: Nobuhiko Katunuma

    IPC分类号: C07K14/81

    CPC分类号: C07K14/811

    摘要: A peptide having an amino acid sequence of the following formula ##STR1## is provided as an inhibitor of trypsin and trypsin-like serine proteases.

    摘要翻译: 具有下式Ile-Ala-Ala-Cys-Asn-Leu-Pro-Ile-Val-Gln-Gly-Pro-Cys-Arg-Ala-Phe-Ala-Glu-Leu-Leu的氨基酸序列的肽 -Ala-Phe-Asp-Ala-Ala-Gln-Gly-Lys-Cys-Ile-Gln-Phe-Ile-Tyr-Gly-Gly-Cys-Lys-Gly-Asn-Asn-Asn-Lys-Phe-Tyr -Ser-Glu-Pro-Lys-Cys-Lys-Trp-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Gly-Tyr作为胰蛋白酶和胰蛋白酶样丝氨酸蛋白酶的抑制剂。

    Orally administrable pharmaceutical preparation of improved flavoring
characteristics
    59.
    发明授权
    Orally administrable pharmaceutical preparation of improved flavoring characteristics 失效
    口服给药的药物制剂具有改善的调味特性

    公开(公告)号:US4892740A

    公开(公告)日:1990-01-09

    申请号:US147860

    申请日:1988-01-25

    摘要: An orally administrable pharmaceutical preparation of improved flavoring characteristics composed of a core material containing a drug and a coated layer applied to its surface, said coated layer being composed of a particulate polymeric substance having an average particle diameter of not more than 60 microns and being soluble in gastric juice; and a process for producing said orally administrable pharmaceutical preparation, which comprises causing minute liquid droplets of a volatile liquid containing a drug and optionally a gastric juice-soluble polymeric substance to fall onto a powder bed composed of a gastric juice-soluble particulate polymeric substance having an average particle diameter of not more than 60 microns to coat the surface of the liquid droplets with the gastric juice-soluble particulate polymeric substance, and drying the coated particles.