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116results about How to "Reduce cell death" patented technology

Buffer solution for electroporation and a method comprising the use of the same

The invention relates to a buffer solution for suspending animal or human cells and for dissolving biologically active molecules in order to introduce said biologically active molecules into the cells using an electric current and to a method for introducing biologically active molecules into animal or human cells using an electric current and a buffer solution. The inventive buffer solution has a buffering capacity of at least 20 mmol*I−1*pH−1 and an ionic strength of at least 200 mmol*I−1 during a change to the pH value from pH 7 to pH 8 and at a temperature of 25° C. The use of a buffer solution of this type in the corresponding method allows biologically active molecules to be introduced into animal and human cells with a high degree of transfection efficiency and at the same time a low cell mortality. Different cell types, in particular dormant and actively dividing cells of low activity, can be successfully transfected in said buffer solution.
Owner:LONZA COLOGNE

Cell culture treatment apparatus and cell culture treatment method

The present invention provides a cell culture treatment device for culturing, treating and collecting cells, which includes a flow path, a cell-retaining section, a solution inlet, a solution outlet, a cell collection port and a lid. The present invention also provides an device for easily, efficiently separating and collecting the cells thereby in a short period of time, and provides a method therefor.
Owner:CANON KK

Methods and compositions of monoclonal antibodies specific for beta-amyloid proteins

This invention provides methods and compositions for the detection, diagnosis and treatment of amyloid-associated diseases, in particular, diseases comprising deposition of amyloid assemblies, fibrils, filaments, tangles, or plaques. A preferred composition comprises monoclonal antibodies that specifically bind amyloid proteins, peptides or fragments and change the conformation.
Owner:DIAGENICS INT CORP

Method, Device and System for Targetted Cell Lysis

ActiveUS20130261683A1High permittivityIrreversible electroporationElectrotherapySurgical instrument detailsElectric fieldBiology
A method, device and system employs particles, such as nanoparticles, and an electric or electro-magnetic field, to cause cell death in target cells by non-thermal means. The method of causing targeted cell death comprises the steps of: introducing a particle to the interior of a target cell and exposing the target cell to a transient electromagnetic field for a sufficient time interval in order to cause cell death. The invention overcomes problems associated with similar methods as a result of the fact that a smaller electric field is applied because the particle enhances the effect of the electric field in its immediate vicinity, so reducing the field strength needed to achieve cell lysis and thereby reducing the risk of damage to healthy cells that may be in its vicinity. Apparatus for performing the method; as well as techniques of delivering particles and for producing particles are also described.
Owner:BIOVICES IPR HLDG AS +1

Cell transplantation

The present invention provides polymers for use in preventing damage to the membranes of cells in fat grafts. Mixing of a triblock copolymer such as poloxymer P188 with adipocytes or adipose tissue to be transplanted into a subject is thought to stabilize the membranes of the cells leading to more successful fat transplantation in soft tissue reconstruction or augmentation. Such methods may also be used in the transplantation of adult stem cells or other cells derived from fat tissue. Other agents such as lipoic acid may also be added to the polymer / cell compositions for cell transplantation.
Owner:THE GENERAL HOSPITAL CORP

Antagonists of a non-selective cation channel in neural cells

InactiveUS20100092469A1Reduce mortalityReduces stroke sizeBiocideNervous disorderDiseaseNervous system
The present invention is directed to a combination of therapeutic compounds and treatment methods and kits using the combination. In particular, one of the combination affects the NCca-ATP channel of neural tissue, including neurons, glia and blood vessels within the nervous system. Exemplary SUR1 and / or TRPM4 antagonists that inhibit the NCca-ATP channel may be employed in the combination. The combination therapy also employs one or more of a non-selective cation channel blocker and / or an antagonist of VEFG, NOS, MMP, or thrombin. Exemplary indications for the combination therapy includes the prevention, diminution, and / or treatment of injured or diseased neural tissue, including astrocytes, neurons and capillary endothelial cells, that is due to ischemia, tissue trauma, brain swelling and increased tissue pressure, or other forms of brain or spinal cord disease or injury, for example. In other embodiments, there are methods and compositions directed to antagonists of TRPM4, including at least for therapeutic treatment of traumatic brain injury, cerebral ischemia, central nervous system (CNS) damage, peripheral nervous system (PNS) damage, cerebral hypoxia, or edema, for example.
Owner:THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPT OF VETERANS AFFAIRS

Therapeutic agents targeting the NCCa-ATP channel and methods of use thereof

ActiveUS20060100183A1Reduces and decrease and inhibits activationInhibition is effectiveBiocideNervous disorderMedicineNeuron
The present invention is directed to therapeutic compositions targeting the NCCa-ATP channel of an astrocyte, neuron or capillary endothelial cell and methods of using same. More specifically, antagonists of the NCCa-ATP channel are contemplated. The compositions are used to prevent cell death and to treat secondary damage associated with spinal cord injury.
Owner:U S GOVERNMENT REPRESENTED BY THE DEPT OF VETERANS AFFAIRS

CELL CULTURE HYDROGEL WITH pH INDICATOR

The invention provides devices, compositions and methods for maintaining conditions in a cell culture and for measurement of conditions in the cell culture. In particular, the invention provides hydrogel materials, apparatus and methods for several non-invasive techniques of maintaining glucose and pH levels in cell cultures at near-optimal levels and the non-invasive measurement of pH levels in cell cultures.
Owner:UNIVERSITY OF MASSACHUSETTS LOWELL

Pyruvate dehydrogenase kinases as therapeutic targets for cancer and ischemic diseases

InactiveUS20090209618A1Treating and preventing neoplasiaReduced activityCompound screeningBiocideMedicinePyruvate dehydrogenase activity
The invention provides therapeutic and prophylactic compounds and methods for altering the activity of pyruvate dehydrogenase kinase (e.g. PDK1, PDK2, PDK3, PDK4). Such therapies are useful for the treatment of neoplasia. The invention further provides therapeutic and prophylactic compounds and methods of altering pyruvate dehydrogenase activity to treat or prevent cell death related to ischemia.
Owner:THE JOHN HOPKINS UNIV SCHOOL OF MEDICINE

Dimeric Smac Mimetics

The invention provides small molecule mimics of the Smac peptide that are dimers or dimer-like compounds having two binding domains connected by a linker These compounds are useful to promote apoptosis. The invention includes pharmaceutical compositions comprising such compounds and methods to use them to treat conditions including cancer and autoimmune disorders.
Owner:JOYANT PHARMA INC

Use of AAV replication machinery for improved protein production

The present invention provides a method for enhanced production of a gene product of interest in a cell, using the AAV replication machinery. The present invention further relates to a cell for use in the method of the invention and a non-human transgenic animal or a transgenic plant comprising a cell of the invention.
Owner:UNIQURE IP BV

Use of AAV replication machinery for improved protein production

ActiveUS20110119777A1Increase copy numberIncrease viable life-spanAnimal cellsBryophytesGMO PlantsGenetically modified animal
The present invention provides a method for enhanced production of a gene product of interest in a cell, using the AAV replication machinery. The present invention further relates to a cell for use in the method of the invention and a non-human transgenic animal or a transgenic plant comprising a cell of the invention.
Owner:UNIQURE IP BV

Small molecule inhibitors of necrosis

The invention features methods for decreasing necrosis. The invention also features methods for treating a subject with a condition in which necrosis occurs. The invention further features chemical compounds used to decrease necrosis.
Owner:PRESIDENT & FELLOWS OF HARVARD COLLEGE

Prepn process of acidophilic lactobacillus milk tablet

The preparation process of acidophilic lactobacillus milk tablet adopts inducing mutation breeding method to breed high temperature mutant acidophilic lactobacillus strain, i. e., acidophilic lactobacillus LA201 strain. Meanwhile, matter capable of lowering the death rate of acidophilic lactobacillus is extracted from the Chinese herbal medicine extract liquid and microbe culture liquid. The breeding of high temperature acidophilic lactobacillus strain and the protecting agent make it possible to produce acidophilic lactobacillus milk tablet in available milk powder producing high temperature spray drying apparatus and conventional tabletting.
Owner:SHAANXI UNIV OF SCI & TECH

Use of Bone-Marrow Derived Stem Cells to Treat Ischemia

InactiveUS20090155220A1Restore peripheral circulationRescue lossBiocideMammal material medical ingredientsLimb ischemiaMedicine
Disclosed are cellular compositions and methods for preventing, treating or reducing the severity of tissue ischemia, particularly limb ischemia in a mammal. One inventive method includes administering a therapeutically effective amount of a cellular composition comprising a novel isolated multi-potent human bone marrow-derived stem cell (BMSC) having undetectable or negligible levels of markers of other known stem cells isolated from bone marrow. These cells can be expanded in vitro and formulated into cellular compositions and grafts capable of differentiating into components of functional new blood vessels when directly administered into ischemic limb tissue.
Owner:STEWARD RES & SPECIALTY PROJECTS
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