ВОИС - Поиск по национальным патентным фондам и фондам PCT

1.WO/2002/089216METHOD FOR INCREASING THE OUTPUT POWER OF PHOTOVOLTAIC CELLS

WO - 07.11.2002

Класс МПК F24S 23/30 № заявки PCT/DZ2001/000004 Заявитель HIHI, Bachir Изобретатель HIHI, Bachir

The invention concerns a method for increasing the output power of any photovoltaic cell using a linear concentration by means of a mutliprism and for using a special transparent film which can absorb up to 93 % of ultraviolet rays so that the temperature at the surface of the photovoltaic cells is acceptable.

2.WO/2001/085134PHARMACEUTICAL SOLID COMPOSITIONS AND PROCESS FOR THE PRODUCTION OF MOUTH DISSOLVING TABLETS

WO - 15.11.2001

Класс МПК A61K 9/00 № заявки PCT/IN2000/000055 Заявитель EMCURE PHARMACEUTICALS LTD Изобретатель MEHTA, Satish

Solid pharmaceutical compositions containing various ingredients for the production of Mouth dissolving Tablets (MDT) are described. Also described herewith the process using the said compositions which when processed as per the process described herein produce tablets containing active pharmaceutical ingredients preferably the Non Steroid Analgesics. The compositions are prepared by spraying the granulating solution on the dry-mix consisting of polyalcohol and the active ingredient in fluidized bed dryer containing such spraying facility. The tablets prepared using the compositions described using the process show remarkable fast disintegration in the mouth cavity without any action like chewing, even in absence of any carrier like water or hot/cold drinks. The tablets being rapid disintegrating can be easily administered to the aged, children and non-cooperating patients.

3.WO/1998/046580DEACYLATION PROCESS AND PRODUCT

WO - 22.10.1998

Класс МПК C07K 9/00 № заявки PCT/US1998/007359 Заявитель ELI LILLY AND COMPANY Изобретатель BRIGGS, Barbara, Shreve

The present invention is directed to deacyl teicoplanin, and to a process for preparing deacyl teicoplanin by reacting teicoplanin with ECB deacylase. Deacyl teicoplanin can be alkylated to produce compounds useful for their antibacterial activity.

4.WO/1998/056406STABLE INSULIN FORMULATIONS

WO - 17.12.1998

Класс МПК A61K 38/28 № заявки PCT/US1998/012218 Заявитель ELI LILLY AND COMPANY Изобретатель DEFELIPPIS, Michael, Rosario

The present invention provides a monomeric insulin analog formulation stabilized against aggregation in which the buffering agent is either TRIS or arginine. The stable formulations of the present invention are useful for treating diabetes, and are particularly advantageous in treatment regimes requiring lengthy chemical and physical stability, such as, in continuous infusion systems.

5.WO/2000/031285GENE DELIVERY VECTORS PROVIDED WITH A TISSUE TROPISM FOR SMOOTH MUSCLE CELLS, AND/OR ENDOTHELIAL CELLS

WO - 02.06.2000

Класс МПК A61K 38/00 № заявки PCT/NL1999/000717 Заявитель INTROGENE B.V. Изобретатель HAVENGA, Menzo, Jans, Emco

The invention provides a nucleic acid delivery vehicle with or having been provided with at least a tissue tropism for smooth muscle cells and/or endothelial cells. In one aspect said nucleic acid delivery vehicle is a virus capsid or a functional part, derivative and/or analogue thereof. Preferably said virus capsid is an adnovirus capsid. Preferably said adenovirus is a subgroup B adenovirus, preferably adenovirus 16. Preferably said tissue tropism is provided by at least a tissue tropism determining part of an adenovirus fiber protein or a functional derivative and/or analogue thereof. The invention further presents methods for the treatment of diseases, preferably cardiovascular diseases.

6.WO/2003/048186SURFACE SIMULATION SYNTHETIC PEPTIDES USEFUL IN THE TREATMENT OF HYPER-VARIABLE VIRAL PATHOGENS

WO - 12.06.2003

Класс МПК C07K 14/16 № заявки PCT/US2002/037664 Заявитель CREVECOEUR, Harry Изобретатель CREVECOEUR, Harry

Synthetic peptides and methods for configuring the amino acid sequences thereof are disclosed which are especially useful in the preparation of vaccines intended for the prophylaxis and treatment of viral pathogens exhibiting high mutation rates such as HIV-1. The high mutation rates of such viral pathogens result in extreme variance in the linear sequence of viral protein residues, such as the variable linear sequences of gp 120 of HIV-1. To be effective and provide broad-spectrum and/or cross-clad coverage against hypervariable viruses such as HIV-1, vaccines must target common denominators of all infective strains of such a virus. These functional common denominators lie in the 3-dimensional configuration of proteins essential for host cell binding and infectivity. The disclosed peptides and methods for configuring same are derived from the 3 dimensional relationships of conserved residues of viral proteins defining conformational epitopes necessary and required for viral pathogenicity.

7.WO/1998/031686SUBSTITUTED 4-(6-FLUORO-(1H)-INDOL-3-YL)-1,2,3,6-TETRAHYDROPYRIDINE FOR THE TREATMENT OF CNS-DISORDERS

WO - 23.07.1998

Класс МПК C07D 513/06 № заявки PCT/GB1998/000113 Заявитель ELI LILLY AND COMPANY LIMITED Изобретатель FAIRHURST, John

A pharmaceutical compound of formula (I), in which R¹ is hydrogen, C_1-4 alkyl, C_1-4 alkoxy or halo, and R² is hydrogen, C_1-4 alkyl or C_1-4 alkoxy; or a salt thereof. The compounds of the invention and their pharmaceutically acceptable salts are indicated for use in the treatment of disorders of the central nervous system.

8.WO/1998/035819METHOD TO REPAIR POLYETHYLENE CONTAINMENT SUMPS

WO - 20.08.1998

Класс МПК B29C 73/02 № заявки PCT/US1998/002852 Заявитель AMOCO CORPORATION Изобретатель LYZINSKI, David

A method of repairing polyethylene fuel containment sumps used in underground storage systems in gasoline and diesel service stations without 'welding' the polyethylene, using suitable surface preparation, priming of the affected area, and sealing with a two part rubber compound.

9.WO/1998/052589ALKYLATED HEXAPEPTIDES

WO - 26.11.1998

Класс МПК A61K 38/00 № заявки PCT/US1998/008986 Заявитель ELI LILLY AND COMPANY Изобретатель THOMPSON, Richard, Craig

The present invention is directed to N¹-alkylated derivatives of desleucyl A82846B. These derivatives are useful as antibacterials and also as starting materials from which further antibacterial compounds are prepared.

10.WO/1998/046221METHOD FOR TREATING FUNGAL INFECTIONS

WO - 22.10.1998

Класс МПК A61K 31/395 № заявки PCT/US1998/007269 Заявитель ELI LILLY AND COMPANY Изобретатель SHIH, Chuan

The present invention provides a method for controlling fungal growth, mycotic infections, yeast infections and parasitic infections using a therapeutically effective amount of a compound selected from Compounds (I-V). Further provided is a method for providing mdr inhibition using a therapeutically effective amount of a compound of formula (IA). Also provided is an antifungal composition comprising at least five percent (5%) by weight of a compound selected from Compounds (I-V).

1 / 438 815

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