摘要:
Disclosed is an electronic device capable of controlling a power supply interrupt according to the state of water leakage. A portable telephone (1) is equipped with a water leakage detection unit (60) that detects a physical quantity which changes according to the state of water leakage and a CPU (49) that interrupts a power supply in response to the detection result from the water leakage detection unit (60). When the electrostatic capacity detected by the water leakage detection unit (60) is greater than or equal to a threshold value A and less than a threshold value B, the CPU (49) continues to interrupt the power supply until a time T1 elapses, and when the electrostatic capacity detected by the water leakage detection unit (60) is equal to or greater than the threshold value B, said CPU continues to interrupt the power supply until a time T2 which is longer than the time T1 elapses.
摘要:
A therapeutic method for treating a skin wound involving administering to a patient in need thereof a composition containing pharmaceutically effective amounts of the following components: (1) a peptide consisting of the amino acid sequence represented by Ser-Ser-Ser-Arg (SEQ ID NO: 1) or pharmaceutically acceptable salts thereof and (2) a peptide consisting of the amino acid sequence represented by Phe-Gly-Leu-Met-NH2 (SEQ ID NO: 2) or substance P or pharmaceutically acceptable salts thereof, together with a pharmaceutically acceptable additive.
摘要翻译:一种治疗皮肤伤口的治疗方法,包括向有需要的患者施用含有药学有效量的以下成分的组合物:(1)由Ser-Ser-Ser-Arg(SEQ ID NO: (2)由Phe-Gly-Leu-Met-NH 2(SEQ ID NO:2)或物质P表示的氨基酸序列或其药学上可接受的盐,以及 药学上可接受的添加剂。
摘要:
A method for treating a corneal disorder or for promoting skin wound healing comprising administering to a patient in need thereof a composition containing pharmaceutically effective amounts of (i) a first peptide comprising an amino acid sequence containing the following consecutive amino acids: Ser-Ser-Ser-Arg (SEQ ID NO: 1), or an analog thereof or a pharmaceutically acceptable salt thereof and (ii) a second peptide comprising an amino acid sequence containing the following consecutive amino acids with a terminal —NH2 group: Phe-Gly-Leu-Met-NH2 (SEQ ID NO: 2), or an analog thereof or a pharmaceutically acceptable salt thereof, together with a pharmaceutically acceptable carrier.
摘要翻译:一种治疗角膜病症或促进皮肤伤口愈合的方法,包括向有需要的患者施用含有药学有效量的组合物(i)包含含有以下连续氨基酸的氨基酸序列的第一肽:Ser-Ser- Ser-Arg(SEQ ID NO:1)或其类似物或其药学上可接受的盐,和(ii)包含具有末端-NH 2基团的下列连续氨基酸的氨基酸序列的第二肽:Phe-Gly- Leu-Met-NH 2(SEQ ID NO:2)或其类似物或其药学上可接受的盐以及药学上可接受的载体。
摘要:
An object of the present invention is to research a therapeutic agent for a keratoconjunctival disorder. A compound represented by the following general formula (1) or a salt thereof exhibits an excellent improving effect on corneal disorder models, and therefore is useful as a therapeutic agent for a keratoconjunctival disorder such as dry eyes, corneal ulcer, keratitis or conjunctivitis. In the formula, the ring Y represents a substituted or unsubstituted nitrogen-containing heterocyclic ring; R1 represents a carboxy group or a substituted or unsubstituted nitrogen-containing 5-membered heterocyclic ring; and R2 and R3 may be the same or different and represent a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or unsubstituted alkylcarbonyl group. In the formula, X represents
摘要翻译:本发明的目的是研究一种治疗角化结膜疾病的药物。 由以下通式(1)表示的化合物或其盐对角膜障碍模型显示出优异的改善效果,因此可用作干眼症,角膜溃疡,角膜炎或结膜炎等角膜结膜疾病的治疗剂。 式中,Y表示取代或未取代的含氮杂环; R 1表示羧基或取代或未取代的含氮5元杂环; 并且R 2和R 3可以相同或不同,表示氢原子,取代或未取代的烷基或取代或未取代的烷基羰基。 在该式中,X表示
摘要:
An object of the present invention is to research a new medicinal use of E-4-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy) benzyloxyimino]-4-phenylbutyric acid, Z-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy) benzyloxyimino]-2-(4-phenoxyphenyl)acetic acid, 2-[2-propyl-3-[3-[2-ethyl-4-(4-fluorophenyl)-5-hydroxyphenoxy]propoxy]phenoxy] benzoic acid, 2(S)-methoxy-3-[4-[3-(4-phenoxyphenoxy)propoxy]phenyl] propionic acid, or a salt thereof. Any of the above-mentioned carboxylic acid compounds and a salt thereof exhibit an excellent improving effect on corneal disorder models and are useful as a therapeutic agent for a keratoconjunctival disorder such as dry eyes, corneal ulcer, keratitis, conjunctivitis, superficial punctate keratopathy, corneal epithelial defects, conjunctival epithelial defects, keratoconjunctivitis sicca, superior limbic keratoconjunctivitis or filamentary keratitis.
摘要:
An object of the present invention is to provide an eyedrop which has a relatively low viscosity before instillation but is thickened on the eyeball surface at instillation. The eyedrop containing a viscous agent for ophthalmic use, which comprises a combination of hydroxyethylcellulose and dextran, exhibits a specific and synergistic thickening effect in the coexistence of mucin. Therefore, the eyedrop of the present invention is thickened on the eyeball surface upon contact with mucin in the precorneal tear film at instillation, whereby a desired pharmacological efficacy or refreshing feel can be sustained.
摘要:
Object of the present invention is to search a novel pharmaceutical use of 5-[4-(6-methoxy-1-methyl-1H-benzimidazol-2-ylmethoxy) benzyl] thiazolidine-2, 4-dione being a condensed heterocyclic compound, or a salt thereof. 5-[4-(6-methoxy-1-methyl-1H-benzimidazol-2-ylmethoxy) benzyl] thiazolidine-2, 4-dione or a salt thereof can exert an excellent effect to promote healing in a dry eye model, and is useful as a therapeutic agent for keratoconjunctival disorders such as dry eyes, corneal ulcer, keratitis, conjunctivitis, superficial punctate keratopathy, corneal epithelial defects, conjunctival epithelial defects, keratoconjunctivitis sicca, superior limbic keratoconjunctivitis and filamentary keratitis.
摘要:
Based on research for compounds that can display a corneal epithelial migration promoting effect in ophthalmology, the present invention provides P2Y receptor agonist corneal epithelial migration promoters, such as phosphoric acid compounds having an adenosyl group, uridyl group, xanthosyl group, guanosyl group, or thymidyl group, or their salts, with excellent corneal epithelial migration promoting effects.
摘要:
The object of the present invention is to find new effects of natriuretic peptides in an ophthalmological field. The present invention provides eyedrops for promoting lacrimal secretion or for treating keratoconjunctival disorders containing the natriuretic peptide as active ingredient. The natriuretic peptides are atrial natriuretic peptides (ANP), brain natriuretic peptides (BNP) and C-type natriuretic peptides (CNP). Typical examples of the keratoconjunctival disorder are dry eye, corneal erosion and corneal ulcer.
摘要:
The image forming device according to the present invention performs resolution conversion processing or scaling processing of a binary image and outputs a processed image. The present image forming device is provided with an edge detecting section, which, during resolution conversion or scaling of the binary image, detects edges of the image and detects lengths and shapes of the edges, and with an interpolated/skipped line producing section, which performs resolution conversion processing or scaling processing based on the lengths and shapes of edges detected by the edge detecting section.