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Results 1-10 of 2,103 for Criteria: Office(s):all Language:EN Stemming: true maximize
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TitleCtrPubDate
Int.ClassAppl.NoApplicantInventor
1. WO/2015/099547 FEED COLLECTOR, PARTICULARLY FOR A MULTIPLE SOURCE HEAT PUMPWO02.07.2015
F25B 30/06
PCT/PL2014/000008UNI-HEAT SP. Z.O.O.MATUSIAK, Wiesław
The present invention refers to a feed collector, particularly for a multiple source heat pump. A collector has a water filled body (1) having the form of a reservoir, whose top cap end (24) in the form of a reverse funnel inserted into an ice slurry reservoir (18) located thereover is provided with an ice- breaking pump (25) on the top, said pump having a discharge conduit with an outlet going into an ice slurry reservoir (18), which has a pump (20) for removal of accumulating ice, and in the body (1) of the collector, below the water bath level (27) there is at least one heat exchanger (8), which has the form of a flat chamber filled with a refrigerant medium, enclosed, provided with a pipe and a stub pipe (12J with a cut-off valve (10), said chamber having deformable walls (11), which can deform to at least a small extent when exposed to internal pressure in the chamber of the heat exchanger (8), wherein there is an evaporator (14) in the chamber of the heat exchanger (8), said evaporator favorably having a form of a ribbed coil pipe (2) in Tichelman arrangement, a meander arrangement or a worm arrangement, said coil provided with a radiator (3) fed with compressed gas from the compressor of a heat pump (13).

2. WO/2015/099548 AN ANTIBODY POSSESSING AN AFFINITY FOR EPITHELIAL SECRETORY AND NERVOUS TISSUE, AS WELL AS TUMOUR TISSUE DERIVED FROM THESE TISSUES AS WELL AS THE USE THEREOFWO02.07.2015
C07K 16/12
PCT/PL2014/050080INSTYTUT IMMUNOLOGII I TERAPII DOŚWIADCZALNEJ PANKORZENIOWSKA-KOWAL, Agnieszka
We disclose the use of bacterial antigens and obtained antibodies. The resulting antibodies can be used in the diagnosis of tumors by immunohistochemistry and in the binding of drugs to antibodies for use in cancer therapy.

3. WO/2015/093997 NEW STRAIN OF LACTOBACILLUS DELBRUECKII BACTERIA AND ITS USE FOR THE PRODUCTION OF BEE POLLENWO25.06.2015
C12R 1/225
PCT/PL2014/050061INSTYTUT BIOTECHNOLOGII PRZEMYSŁU ROLNO- SPOŻYWCZEGO IM. PROF.WACŁAWA DĄBROWSKIEGOMISIEWICZ, Anna
The subject of the invention is the Lactobacillus delbrueckii strain of bacteria deposited at the Culture Collection of Industrial Micro-organisms in The Institute of Agricultural and Food Biotechnology in Warsaw under number KKP 1645 p and the use thereof to produce bee pollen.

4. WO/2015/093998 A METHOD FOR DETECTING AN INCREASED RISK OF DEVELOPING SKIN CANCER AND A USE OF A GENOTYPE VARIANT OF THE GRHL3 GENEWO25.06.2015
C12Q 1/68
PCT/PL2014/050078INSTYTUT BIOLOGII DOŚWIADCZALNEJ IM. M. NENCKIEGO POLSKIEJ AKADEMII NAUKKIKULSKA, Agnieszka
The present invention is directed to methods of identifying SNP markers associated with skin cancers, and use of these markers to explain individual susceptibility to skin cancer development. In addition, described SNPs have been identified as potentially crucial for proper GRHL3 protein function.

5. WO/2015/093996 ANTIGEN, INFLUENZA VACCINE, SYSTEM FOR VACCINE MANUFACTURING, METHOD OF ANTIGEN PRODUCTION, AND USE OF ANTIGEN TO PRODUCE AN INFLUENZA VACCINEWO25.06.2015
C07K 14/11
PCT/PL2014/000148INSTYTUT BIOCHEMII I BIOFIZYKI PANKOPERA, Edyta
The subject of the invention is an influenza virus haemagglutinin antigen, an influenza vaccine comprising said antigen, a method of producing said antigen, and use of the antigen as stated above to produce an influenza vaccine. The invention involves a new method of producing said antigen, suitable for use in a vaccine. The outcome as stated in the invention leads to obtaining a highly immunogenic antigen, which does not require contact with the whole virus but just haemagglutinin. The vaccine as described in the invention does not contain the virus or its parts, does not contain cells coming from other organisms or their parts, but only purified haemagglutinin antigen.

6. WO/2015/093993 TRANSMISSION GEAR ENGAGEMENT SYSTEMWO25.06.2015
F16D 63/00
PCT/PL2013/000166PRZEMYSŁOWY INSTYTUT AUTOMATYKI I POMIARÓW PIAPZBOIŃSKI, Mariusz
The invention relates to a gear engagement system in a transmission, especially a planetary gear, that allows for applying the solution in various fields of technology, in particular in robotics or remotely controlled models. The transmission gear engagement system has a toothed wheel (1) with internal and/or external teeth in the housing (2), with claws (3) notched on the front surface as well as a coaxial ring (5) opposite to the toothed wheel (1) with claws (4) matched to the claws (3) of the toothed wheel (1). The ring (5) is connected on both sides with two symmetrical cams (6) by means of the connector (9), and the cams (6) are connected with the driving claw (7). The ring (5), together with toothed wheel (1), is located inside the housing (2); however, the cams (6), driving claw(7), springs (11) and actuator (8) are located outside the housing (2), where the connector (9) and the spring mount elements (10) pass through the housing (2) wall. The driving claw (7) is connected with the actuator (8), and at the same time, at least three spring (10) spring mount elements (11) are located radially on the ring (5), where the other ends of the springs (11) are fixed to the housing (2).

7. WO/2015/093995 A METHOD OF MANUFACTURING A MULTILAYER POLYMER PROTECTIVE COATING FOR IMPLANT MATERIALS WITH A CONTROLLED DRUG RELEASE FUNCTIONWO25.06.2015
A61L 27/34
PCT/PL2014/000145UNIWERSYTET JAGIELLOŃSKIBRZYCHCZY-WŁOCH Monika
The method of forming a multilayer protective coating for implant materials with a controlled drug release function, wherein a 6 to 20 μηι-thick: parylene layer is applied onto the surface of an implant by chemical vapour deposition, and then treated with oxygen plasma at 0.2 to 1 mbar pressure for 15 to 60 minutes, using a plasma generator of 10 to 60 W power, and then the treated parylene layer is coated with the mixture of lactide and glycolide solutions in the molar ratio of lactide to glycolide of 1 : 1 to 100: 1 together with the drug substance in the amount of 5% to 10% w/w of the polymer material and a polymerisation initiator, and then the polymerisation is performed and the obtained layer is dried.

8. WO/2015/093994 THE METHOD FOR MANUFACTURING OF VARDENAFIL AND ITS SALTSWO25.06.2015
C07D 487/04
PCT/PL2014/000135Zakłady Farmaceutyczne POLPHARMA S.A.SZRAMKA, Roman
The method of synthesizing vardenafil base, in anhydrous conditions, by chlorosulfonation of 2- (2-etoxy-phenyl)-5-methyl-7-propyl-iH-imidazo[5,l-fJ[l,2,4]triazin-4-one in a mixture of thionyl chloride and sulfurochloridic acid followed by amidation of the product, 4-etoxy-3-(5- methyl-4-oxo-7-propyl-3,4-dihydroimidazo[5,l-f][l,2,4]triazin-2-yl)benzene-sulfonic acid chloride with N-ethylpiperazine, in an aprotic solvent, in the presence of an inorganic base and the method of conversion the product, vardenafil base, to yield vardenafil monohydrochloride trihydrate having a melting point of 234 °C by contacting with water of the anhydrous modification V of vardenafil monohydrochloride in an organic solvent. The subject of the invention is also the anhydrous modification V of vardenafil monohydrochloride and its use in the preparation of vardenafil monohydrochloride trihydrate having a melting point of 234 °C.

9. WO/2015/088365 MICROSTRUCTURED MULTICORE OPTICAL FIBRE (MMOF), A DEVICE AND THE FABRICATION METHOD OF A DEVICE FOR INDEPENDENT ADDRESSING OF THE CORES OF MICROSTRUCTURED MULTICORE OPTICAL FIBREWO18.06.2015
PCT/PL2014/050077INPHOTECH SP. O. O.NASIŁOWSKI, Tomasz
Microstructured multicore optical fibre with a microstructure area, in which, at least two basic cells are embedded, where each of them contains a core, preferably made of glass, specifically including doped silica glass or polymer, together with the surrounding it longitudinal areas with lower refraction index vs. that of the cladding, which areas may adopt the shape of holes, filled with gas, in particular with the air or a fluid or a polymer or spaces of another glass with doping allowing to reduce refractive index(further referred to as holes), embedded in a matrix of glass, in particular of silica glass or polymer. The refraction index of the holes is decreased vs. that of the matrix of glass, in particular of silica glass or polymer. The basic cell is characterised by the diameter of D2 core, the diameter of D3 core and the distance between adjacent holes, corresponding to lattice constant Λ. The centres of the holes are localised on the vertices and the middle points of the sides of the hexagon, the centre of which is designated by the core; the length of side c of the hexagon, created by the centres of holes, is equal to the preferably doubled lattice constant Λ. The juxtaposed, at least, two basic cells are surrounded by the cladding, preferably made of glass, in particular of silica glass or polymer. Device for addressing cores of the multicore optical fibre, characteristic in that it contains single-core, single-mode optical fibres, with parallel layout in the capillary, (further referred to as single-mode optical fibres), in the number, corresponding to the number of the cores of the multicore optical fibre, while the capillary with single-mode optical fibres is connected with the multicore optical fibre, e.g., the microstructured optical fibre, according to this invention, while the cross-sections of the optical fibres in the capillary and the cross- section of the multicore optical fibre are parallel in their configuration. The fabrication method of the device for addressing cores consists in: 1. an analysis of the structure of multicore optical fibre and determination of the number of cores of the multicore optical fibre, the diameter of cores and the distances among them, 2. measurement of the diameters of the cores and of the claddings of single-mode optical fibres, with which the multicore optical fibre is connected, and the scale of tapering of the single-mode optical fibres is deteremined, 3. removal of the cladding of single-mode optical fibres and cleaning their surface, 4. etching, preferably with hydrofluoric acid, the exposed and cleaned fragments of the single-mode optical fibres, so that after their possible tapering and mutual reassembly, the alignment of the cores of the multicore optical fibre was possible with the cores of the single-mode optical fibre, 5. tapering of single-mode optical fibres, according to the calculated scale of tapering, allowing to achieve the diameters of their cores equal to the dimensions of the diameters of the cores of the multicore optical fibre (provided its preferable), 6. preparation of a capillary by its tapering to the size, allowing for insertion of single- mode optical fibres and glass rods, so that the inserted element shad no freedom of movement or that their movement was limited, 7. laying of single-mode optical fibres and glass rods in the capillary, 8. tapering and clamping of the laid and spliced structure in the capillary by its heating and tensing, while, if it is necessary, the multicore optical fibre is also tapered, 9. cleaving the capillary with the laid and spliced structure under right angle to the axis of the longitudinal capillary, preferably with a cleaver for optical fibres with various outer diameters and internal structures, with a possibility of controlled stretching of the fibre, preferably the capillary surface is polished, together with structure, laid in the capillary, 10. cleaving the multicore optical fibre and preferably polishing its surface, 11. orientation of the capillary vs. the multicore optical fibre, together with the structure, laid and welded in its inside, 12. connection of the multicore optical fibre with the capillary and the structure in its inside by means of any disclosed technology, preferably by splicing.

10. WO/2015/088364 METHOD OF GENERATING GRAPHICAL ACCESS PASSWORDSWO18.06.2015
G06F 21/36
PCT/PL2013/000162NORD-SYSTEMS Sp.z o.o.BRANDT, Łukasz
Method of generating graphical access passwords for computer, network and physical systems of, access control based on process of selecting fields from two-dimensional array or moving fields containing particular base symbol associated with zero or more optional parameters like color to two- dimensional array, processing of that value and generating of new processed value. New value is generated in automatic manner. Base symbols, fields composing two-dimensional array and other parameters are combined in order to create alphabet containing symbols that are used to represent passwords. Subsequently sequence of n-bits long values is generated under restriction that n is integer number sufficient to unequivocal representation of all alphabet symbols. These values are assigned to alphabet symbol with the use of pseudo-random mask of alphabet size. By means of two- dimensional user interface password is created in the scope of alphabet. Chosen password opens access to protected resources.


Results 1-10 of 2,103 for Criteria: Office(s):all Language:EN Stemming: true
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