Eek
Arne Eek, Trosa SE
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20090200335 | Spray Device, Method for Spraying a Certain Quantity of Fluid and a Process for Manufacturing the Device - A device and a method for spraying a certain quantity of fluid. The device includes a casing with a cavity for accommodating a liquid reservoir and a pump which delivers a specific quantity fluid upon activation. The device further includes a nozzle through which the flow of fluid passes in the form of spray droplets together with an activating device which acts upon the base of the reservoir due to the application of opposing forces to the casing, basically at right angles to the pumping movement of the device. | 08-13-2009 |
Arne Eek, Sodertalje SE
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20090170854 | New Use - The present invention relates to a new use of certain pharmaceutically active compounds in the treatment and/or prevention of medicament induced gastric ulcer. More particularly the invention is directed to the use of said compounds, and pharmaceutically acceptable salts thereof, for the treatment and/or prevention of NSAID (non-steroidal antiinflammatory drugs) induced gastric ulcer as well as a pharmaceutical composition in the unit dosage form for the prevention of NSAID induced gastric ulcer in a mammal comprising an NSAID together with a 6-carboxamido-imidazo[1,2-a]pyridine compounds. Other pharmaceutically active compounds used in the present invention comprises COX-2 inhibitors, NO-NSAIDs and bisphosphonates. | 07-02-2009 |
Bjorn C.j. Eek, Long Beach, CA US
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20110003770 | METHOD AND PHARMACEUTICAL TO TREAT SPINAL DISCS - Methods for reducing chronic pain caused by a disrupted spinal disc are described. In one method, a physiologically acceptable amount of an injectable is injected into the disc. The injectable is obtained from a stock solution comprising chondroitin sulphate, glucosamine HCl, aqueous solution of dextrose; sodium carboxymethylcellulose, and a buffer substance in quantity to bring the pH of the stock solution to a value above about 6.0. Water is also added to dilute the stock solution. The stock solution may further comprise an anesthetic such as bupivicaine. | 01-06-2011 |
20110312913 | METHOD AND PHARMACEUTICAL TO TREAT SPINAL DISCS - Methods for reducing chronic pain caused by a disrupted spinal disc are described. In one method, a solution is injected into the disc. The solution includes chondroitin sulphate, glucosamine HCl, and dextrose. The solution may optionally include dimethyl sulfoxide and/or an anesthetic such as bupivicaine. | 12-22-2011 |
20120295867 | METHOD AND PHARMACEUTICAL TO TREAT SPINAL DISCS - Methods for reducing chronic pain caused by a disrupted spinal disc are described. In one method, a solution is injected into the disc. The solution includes chondroitin sulphate, glucosamine HCl, and dextrose. The solution may optionally include dimethyl sulfoxide and/or an anesthetic such as bupivicaine. | 11-22-2012 |
20140066389 | METHOD AND PHARMACEUTICAL TO TREAT SPINAL DISCS - Methods for reducing chronic pain caused by a disrupted spinal disc are described. In one method, a solution is injected into the disc. The solution includes chondroitin sulphate, ghicosamine HCl, and dextrose. The solution may optionally include dimethyl sulfoxide and/or an anesthetic such as bupivicaine. | 03-06-2014 |
Jan Eek, Aa Delft NL
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20150014206 | STACKABLE CRATES AND METHOD FOR THE TRANSPORTATION OF LIVING PLANT MATERIAL EMPLOYING THE SAME - Stackable crates ( | 01-15-2015 |
Konrad Eek, Norman, OK US
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20100139047 | Ergonomic Tool Handle Accessory - A handle accessory provides an attachment portion that attaches to a rod handle of a tool such as a mop or broom, and a grasping portion that projects out into space from the attachment portion. In a preferred embodiment, the grasping portion consists of two lengths of material that project from the attachment portion and meet to form an acute interior angle. That is, the attachment portion and the grasping portion form a triangle. | 06-10-2010 |
Margus Eek, Harjumaa EE
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20090187041 | ESTERS OF (2-HYDROXY-3-OXO-CYCLOPENT-1-ENYL) ACETIC ACID AND THEIR USE FOR PREPARING (-)-R-HOMOCITRIC ACID GAMMA-LACTONE, (+)-S-HOMOCITRIC ACID GAMMA-LACTONE AND THE CORRESPONDING (-)-R-HOMOCITRIC ACID AND (+)-S-HOMOCITRIC ACID SALTS - Archiral (2-hydroxy-3-oxo-cyclopent-1-enyl) acetic acid) alkyl, alkylphenyl and phenyl esters, and a simple and efficient method for the synthesis of both enantiomers of homocitric acid gamma-lactone and the corresponding salts from these esters are described. The method is based on asymmetric oxidation of esters, and the steps of basic and acidic hydrolysis and final acidic lactonization of the homocitric acid into homocitric acid gamma-lactone. The homocitric acid salts are obtained after basic treatment of homocitric acid gamma-lactone. The esters, conditions and reagents used in chemical conversion and separating products are important constituents affording efficient and simple method for production of homocitric acid gamma-lactone and homocitric acid salts. | 07-23-2009 |
Margus Eek, Tallinn EE
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20130317109 | PROCESS FOR THE PREPARATION OF LACOSAMIDE - There is provided a process for the preparation of Lacosamide (which is a useful medicament) of formula I, which comprises an enantioselective enzymatic acylation. | 11-28-2013 |
20140187789 | NEW PROCESSES FOR PREPARING 4-SUBSTITUTED IMIDAZOLES - There is provided a novel process for the preparation of a compound of formula (I), (Formula (I)). There is also provided novel processes to intermediates of the compound of formula (I), as well as novel intermediates themselves. | 07-03-2014 |
Margus Eek, Viimsi Vald EE
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20150299105 | NEW PROCESS - There is provided a process for the preparation of Lacosamide in a particular polymorphic form, which process involves the isolation of a salt of formula I: according to the methods defined in the application. | 10-22-2015 |
Rob Eek, Lantau Island HK
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20080200734 | CRYSTALLIZATION PROCESSES FOR PRODUCING BISPHENOLS - Processes for producing bisphenols (e.g., bisphenol A (BPA)) having a purity greater than 99.7% are described, such processes including reacting a phenol and acetone in the presence of an acidic catalyst to form a product mixture comprising a bisphenol; removing at least a portion of the bisphenol from the product mixture in the form of a bisphenol/phenol adduct by crystallization, filtration and washing to provide bisphenol/phenol adduct crystals; and removing at least a portion of the phenol from the bisphenol/phenol adduct crystals to provide the bisphenol having a purity of more than 99.7%; wherein the crystallization comprises continuous suspension crystallization and is carried out in at least three crystallization devices arranged such that the product mixture is first cooled in a first stage of the crystallization to a temperature of 50 to 70° C. in a first crystallization device and a second crystallization device connected in parallel, and subsequently cooled in a second stage of the crystallization to a temperature of 40 to 50° C. in a third crystallization device connected downstream in series to the first and second crystallization devices, and wherein a total dwell time of the product mixture in the crystallization is more than 4 hours. | 08-21-2008 |