Abstract: A formulation or preparation for treating and preventing arterial and venous thrombi is provided. This preparation includes a non-metal containing photodynamic dye and a fat soluble vitamin. A method of administration for treatment and prophylaxis of arterial and venous thrombi is also provided. This method includes steps of: combining a non-metal containing photodynamic dye and a fat soluble vitamin; combining the non-metal containing photodynamic dye and fat soluble vitamin with a sodium solution; and administering the combination of non-metal containing photodynamic dye, fat soluble vitamin, and sodium solution as an intravenous drip.
Abstract: A carrier for cell culture comprising a water-containing polymer gel containing chitosan, wherein the water-containing polymer gel is coated with collagen and/or alginic acid, and a carrier for cell culture, which comprises a gel layer containing chitosan and an inorganic layer adjacently provided to the gel layer.
Abstract: The present invention relates to the use of staphylokinase for the preparation of a pharmaceutical composition for treating arterial thrombosis, such as e.g. myocardial infarction. It is demonstrated that staphylokinase can be particularly useful as a thrombolytic agent for the lysis of platelet-rich clots. Furthermore it is demonstrated that staphylokinase, unlike streptokinase, does not induce antibody induction upon repeated administration.
Type:
Grant
Filed:
July 14, 1993
Date of Patent:
August 9, 1994
Assignees:
Leuven Research & Development vcw, Desire J. Collen
Inventors:
Desire J. Collen, Jean-Marie Stassen, Henri R. Lijnen
Abstract: Heparins, heparin fractions or fragments, optionally salified with pharmaceutically acceptable cations, having molecular weight ranging from 1.000 to 30.000 D, characterized by an EDTA content lower than 0.1%, by the absence, in the .sup.1 H--NMR spectra, of the signals due to EDTA between 2.50 and 4.00 p.p.m. and substantially free from bleeding effect and optionally free from signals, in the .sup.13 C--NMR spectrum, from 80 to 86 ppm.
Type:
Grant
Filed:
September 24, 1990
Date of Patent:
May 5, 1992
Assignee:
Sanofi S.A.
Inventors:
Benito Casu, Annamaria Naggi, Pasqua Oreste, Giangiacomo Torri, Giorgio Zoppetti, Giancarlo Sportoletti, Francesco De Santis
Abstract: The present invention provides a low molecular weight anti-viral factors isolated from the serum of a hyperimmune regressor line chicken and methods of purifying same. The factors are useful in the treatment and prevention of certain disease states.
Type:
Grant
Filed:
June 20, 1989
Date of Patent:
October 15, 1991
Inventors:
Craig E. Whitfill, Nicholas R. Gyles, John A. Thoma
Abstract: A topical composition comprising LYCD together with known topically active useful medicinal agents such as anti-wrinkling, antibiotic, anticancer, antifungal, antiinflammatory such as anti-acne, antiviral, wound healing, and hair-growing agents. The LYCD works together with the other active agents to achieve a synergistic result more effective than can be obtained from the topical agents individually, and more effective than could be predicted from the mere addition of the known efficacies of the individual ingredients.
Abstract: A process for the preparation of a factor VIII:C-deficient plasma is made available, in which a starting plasma is consecutively treated with antibodies against von Willebrand factor and antibodies against factor VIII:Ag. The deficient plasma prepared in this way contains less than 0.5% residual activity of factor VIII:C.
Type:
Grant
Filed:
March 4, 1988
Date of Patent:
June 4, 1991
Assignee:
Behringwerke Akitengesellschaft
Inventors:
Udo Becker, Norbert Heimburger, Konrad Braun
Abstract: There is disclosed a composition and process for disinfecting or essentially sterilizing blood fractions and components of blood. The composition is formed by adding a chlorine dioxide liberating compound with a weak organic acid and a heat activated saccharide.
Abstract: A composition for the treatment of the skin comprises a fraction of a mechanically obtained lysate of yeast cultures of the species Saccharomyces cerevisiae. The translation system contained in the compositions of the invention are obtained by lysing cultures of Saccharomyces cerevisiae. The application of such composition, in any suitable form, such as a cream, ointment, gel or the like, to skin promotes protein biosynthesis by the skin cells so that the metabolism of the extracellular matrix of the skin is restored to the physiologically correct balance and the skin is revitalized.
Type:
Grant
Filed:
August 23, 1988
Date of Patent:
May 28, 1991
Assignee:
HEYL Chemisch-parmazeutische Fabrik GmbH & Co KG
Inventors:
Thomas Bunte, Wolfgang Parr, Eduard Heyl
Abstract: The present invention relates to pharmaceutical compositions for cerebral and neuronal diseases containing physiologically active substances extracted from infected tissues. The physiologically active substances of the present invention have NGF-like nerve growth stimulating effect. Therefore, the substances of the invention are useful as drugs for various cerebral and neuronal diseases such as dementia, post-herpetic neuralgia, brain edema and spino-cerebellar degeneration.
Abstract: Procedures are disclosed for eliminating immune competent cells from a population of human epidermal cells. The cells free of immune competent cells are used for growing tissue sheets suitable for transplantation to recipients unrelated to the donor.
Abstract: The present invention relates to physiologically active substances extracted from infected tissues inoculated with a poxvirus. The substances of the present invention have excellent actions to improve blood flow and recover functions of diseased tissues, thus are useful as drugs for various diseases caused by blood flow disorders.
Abstract: A preparation for activating hemocytes of bivalves for pearl production containing a mitogen as an effective component, and a method for producing pearl through nucleus insertion operation of a bivalve for pearl production which comprises treating a section of the mantle part of a donor to be inserted with a mitogen.By the treatment with the present preparation, hemocytes of the wound site due to the nucleus insertion operation are activated, tissue growth of the section of the mantle part of the donor is accelerated and a good pearl sac is formed around the nucleus. As a result, the number ejected nuclei is decreased and the pearl quality and production amount are enhanced.These effects are further enhanced by using a mitogen treated with an aluminum adjuvant or the like.
Type:
Grant
Filed:
August 2, 1988
Date of Patent:
September 4, 1990
Assignee:
Juridical Foundation The Chemo-Sero-Therapeutic Research Institute
Abstract: A process and nourishing agent for treating and nourishing the scalp and hair to promote conditions for the natural growth of hair on a human head for the reversal of male pattern baldness in individual cases. The process includes the steps of cleansing the scalp and hair, opening the pores and follicles in the scalp and softening and removing clogging deposits from the pores and hair follicles, and then applying to the scalp a nourishing agent comprising a mixture of chalaza extracted from chicken eggs, unflavored powdered gelatin, and aqueous saline solution. In the preferred form of the invention, the pores of the scalp and hair follicles are opened and sanitized by repeated applications of a benzoic acid mixture and heat, and the clogging deposits and foreign matter are softened and separated by the application of a carbamide peroxide solution and heat.
Abstract: The invention relates to a process for the fermentation of carbohydrates by bacteria of the genus Xanthomonas for the production of a polysaccharide of the xanthane type, in which the source of nitrogen consists of a gelatin with a molecular weight of less than 5000.Application: preparation of xanthane.
Abstract: The body composition of poultry is improved by a hormonal strategy that involves either:(1). increasing plasma levels of thyroid hormone by about 2- to 3-fold during the finishing phase (e.g., for chickens, 3 to 6 or 7 weeks-of-age) by providing feed containing 0.1 to 1 ppm of metabolically-active thyroid hormone of the formula: ##STR1## wherein R1 is the residue of a carboxylic acid such as an alpha-amino acid or an aliphatic carboxylic acid, e.g. L-alanine, D-alanine, acetic acid, or propionic acidR3 is iodine (I)R5 is iodine (I) or hydrogen (H)R3' is iodine (I) or the residue of an aliphatic carboxylic acid such as butyric acid, or propionic acidR5' is iodine (I) or hydrogen (H)R4' is hydroxy (OH)(2). increasing plasma levels of metabolically-active thyroid hormone by 2- to 3-fold and increasing plasma levels of growth hormone or glucagon by 2- to 10-fold for 15 to 30% of each day with any suitable method during the finishing phase of poultry growth.
Abstract: A lipid powder having a cross-linked coating thereon comprises a core lipid powder and a water-soluble coating agent coating the core lipid powder. The water-soluble coating agent contains cross-linked protein. A process for preparing lipid powders each having a cross-linked coating thereon comprises the steps of emulsifying lipid and a water-soluble coating agent containing protein to obtain an emulsion, adding a cross-linking agent for the protein the the emulsion to thereby cross-link the protein, atomizing and drying the emulsion containing the cross-linked protein to terminate the cross-linking reaction and to obtain lipid powders each coated with the water-soluble coating agent, and cooling the coated lipid powders.
Abstract: A human placenta-derived antiocoagulating substance is prepared by homogenizing a human plancenta, subjecting the resulting homogenate to centrifugal separation, extracting the thus-obtained sediment with a chelating agent, and then separating and purifying the extract. The substance has a molecular weight of 73,000.+-.2,000 as measured in reduced and non-reduced states by SDS-polyacrylamide gel electrophoresis. Its isoelectric point ranges from 6.2 to 6.6 as measured by isoelectric column electrophoresis using an ampholyte. It is inactivated by a heat treatment at 50.degree. C. for 30 minutes, is stable in a pH range of 5.5-8.5 (37.degree. C.) and is also stable in plasma at 37.degree. C. for 15 minutes. It can prolong the recalcification time, prothrombin time and activated partial thromboplastic time.