Previous Pause Next
Home >> Resource Center >>
Patent
Antiviral Vaccines PDF Print E-mail
Friday, 27 March 2009 09:17
Patent # Subject Assignee(s) Inventor(s) Priority application date Publication date
WO 200589792

A new recombinant protein comprising polypeptides bearing epitopes of human papilloma virus (HPV) antigens; useful for treating or preventing HPV infection, or for immunotherapy against the onset of malignant transformation due to HPV infection.

 

BT Pharma (Labège-Innopole, France); INSERM (France); Institut Pasteur (Paris); CNRS (France) la Dant D, le Clerc C, Preville X, Timmerman B 3/18/2004 9/29/2005
WO 200587813

A new composition that comprises contacting an antigen-presenting cell with a chimeric antigen comprising an immune response domain and a target binding domain, which comprises a xenotypic antibody fragment; useful for eliciting a T-cell response against hepatitis B virus and hepatitis C virus infections.

 

ViRexx (Edmonton, Alberta, Canada) George R, Noujaim A, Tyrrell L, Wang D 2/24/2004 9/22/2005
WO 200587799

A new isolated polypeptide that binds specifically to an oligosaccharide; useful in preparing a vaccine for treating or preventing HIV infection.

 

US Dept. of Health & Human Services (Washington, DC, USA) Bewley CA 3/9/2004 9/22/2005
US 20050202045

A method for making a recombinant avian herpesvirus, comprising cotransfecting overlapping subgenomic fragments employing the subgenomic clones and enzymes; useful in producing therapeutic or prophylactic vaccines.

 

Schering-Plough Veterinary Corp. (Kenilworth, NJ, USA) Cochran MD, Cook SM, Wild MA 6/14/2001 9/15/2005
WO 200585445

A novel recombinant varicella herpes-zoster virus comprising a bacterial artificial chromosome vector sequence; useful as a vaccine for treating varicella herpes-zoster virus infection.

 

Osaka University (Osaka, Japan) Gomi Y, Mori Y, Nagaike K, Takahashi M, Yamaishi K 3/5/2004 9/15/2005
EP 1574517

A novel recombinant or synthetic hepatitis C virus E1 envelope protein or its portion comprising one or more disulfide bonds between a specific pair of cysteines; useful as vaccine for hepatitis C virus.

 

Innogenetics (Ghent, Belgium) Bosman A, Depla E, Depraetere S, Verheyden G 3/9/2004 9/14/2005
WO 200581716

A novel nucleic acid encoding chimeric polypeptides such as calreticulin and antigenic peptide from severe acute respiratory syndrome (SARS) coronavirus; useful as a DNA vaccine for SARS coronavirus.

 

Johns Hopkins University (Baltimore, MD, USA) Hung C, Kim TW, Wu T 11/24/2003 9/9/2005
CN 1616654

A method for inactivating and purifying SARS virus; useful for preparing vaccines to combat SARS.

 

Kexing Biological Products (Shenzen, China) Han Z, Zhang J, Zhang Z 11/12/2003 5/18/2005
CN 1616491

A new fusion protein useful as a vaccine for treating and preventing influenza.

 

Qinghua University (Beijing) Chen Y; Liu W 9/29/2004 5/18/2005
CN 1614011

A totally enclosed double-circulating column chromatography process for purifying inactivated virus vaccines.

 

Jiahe Biotechnology (Guangzhou, China) He C; Le W 11/6/2003 5/11/2005
CN 1613503

A technique for preparing a virus vaccine using a bioreactor featuring a disk carrier for increasing the surface area used to grow cells, and a better culture condition created for increasing the culture density.

 

Jiahe Biotechnology (Guangzhou, China) He C, Zhang J 11/6/2003 5/11/2005
IN 200200194 Liposomes containing novel peptide antigens; useful for regulating the immune response and for the development of therapeutic agents for the prevention and treatment of hepatitis B virus–associated diseases. Mogam Biotechnology Research Institute (Yongin, South Korea) Chang JS, Cheong H, Cho SY, Choi MJ, Hwang Y, Kim TY, Lee KU 4/3/2002 3/11/2005
 
Biomedical Devices PDF Print E-mail
Friday, 27 March 2009 09:14
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service (formerly Derwent). The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1725 Duke Street, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) DERWENT (http://www.thomson.com/scientific).

US 20060233850, WO 2006113407

A composition comprising an alginate and a gelatin that is useful as a bioscaffold for the infarct region of a heart or as a coating on a biomedical device (e.g., stent or pacemaker lead).

 

Advanced Cardiovascular System (Santa Clara, CA, USA), Michal ETClaude C, Kwok C, Liao S, Michal ET, Michal G, Qu J4/19/200510/19/2006, 10/26/2006
WO 2006097611, FR 2883299

Use of an organic precursor compound for the formation of a homogeneous organic film on a (semi)conductor electric surface; useful for microelectronic components and biomedical devices.

 

Commissariat Energie Atomique (Paris)Deniau G, Palacin S3/15/20059/21/2006, 9/22/2006
US 20060193894, WO 2006093725

A method for manufacturing biomedical devices (e.g., contact lens, stent, catheters, intraocular lens and implants) involving contacting the surface of the device with humectants and using ultraviolet radiation to produce a stable hydrophilic and antimicrobial coating.

 

Johnson & Johnson Vision Care (Jacksonville, FL, USA), Homesley PM, Jen JS, Jones RE, Petisce JHomesley PM, Jen JS, Jones RE, Petisce J2/28/20058/31/2006, 9/8/2006
US 20060172983

New functionalized drugs useful for treating and preventing cancerous disease, reducing pain and inflammation, and in implantable biomedical devices and polymeric compositions, such as bioabsorbable chewing gum.

 

Bezwada Biomedical (Hillsborough, NJ, US)Bezwada RS1/28/20058/3/2006
US 20060145792

A micro-electro-mechanical systems (MEMS) switch for biomedical devices, etc., with a movable conductive plate positioned between upper and lower electrodes, and vertical posts coupled to rings that are integral to the conductive plate.

 

IBM (Armonk, NY, USA)Clevenger L, Dalton T, Hsu LC, Radens C, Wong KH, Yang C1/5/20057/6/2006
US 20060142524, WO 2006071387

A prepolymer used for hydrogel copolymers, with a polymerizable ethylenically unsaturated radical, diradical residue of diisocyanate, diradical residue of polysiloxane diol and diradical residue of diol; useful for increasing oxygen permeability, tensile modulus and water content in biomedical devices, especially ophthalmic devices such as contact lenses, intraocular lenses and ophthalmic implants.

 

Bausch & Lomb (Rochester, NY, USA)Lai Y, Lai YC, Lang W, Quinn ET12/29/20046/29/2006, 7/6/2006
US 20060109045

A voltage-rectifying circuit with a source signal input coupled to an input-judgment circuit and a switching circuit, where the switching circuit has switching units that are transistors; for use in implantable biomedical devices.

 

Neurostream Technologies (Vancouver, BC, Canada)Baru M2/24/20035/25/2006
WO 2006116326, US 20060255293

A method for improving parylene-to-parylene adhesion in, e.g., a biomedical device, comprising providing a device having multiple parylene layers on a substrate in a vacuum chamber, and heating at least two adjacent parylene layers to a temperature that is greater than a deposition temperature at which the parylene layers were formed to enhance adhesion of the parylene layers.

 

California Institute of Technology (Pasadena, CA, USA)Li W, Rodger DC, Tai Y, Tai YC, Tooker A4/21/20054/21/2006, 4/21/2005
US 20060068224, EP 1642653, JP 2006102499

A method for the production of a fluoride-coated biomedical device, comprising exposing a surface of biomedical device to a plasma in presence of solid source of fluorine; useful particularly in implantable orthopedic devices such as knee, hip, shoulder and elbow prostheses.

 

DePuy Products (Warsaw, IN, USA), Grobe G, Heldreth M, Orban J, Paquin D, Spanyer JM, Tarr RRCampbell J, Grobe G, Heldreth M, Orban J, Paquin D, Spanyer J, Spanyer JM, Tarr RR9/30/20043/30/2006, 4/5/2006, 4/20/2006
US 20060054488

A nanotube/polymer composite resistant to ionizing radiation, produced by sonicating single-wall carbon nanotubes, introducing polymethylmethacrylate into the nanotubes to form a polymethylmethacrylate/single-wall nanotube mixture, and sonicating the mixture; used in the manufacture of biomedical devices.

 

Clayton LM, D'Angelo J, Harmon JP, Muisener PAOClayton LM, D'Angelo J, Harmon JP, Muisener PAO11/27/20023/16/2006
JP 2006062208

A fine-structure transfer device with opposing substrate and stamper that are mounted on a temporary mounting surface, so that storage elements move to the same planar position as the substrate mounting surface; used for transferring fine structures (e.g., integrated extra sub micron pattern during fabrication of DNA chips, biodevices, semiconductor multilayer interconnection structures, printed circuit boards (PCB), micro electro mechanical systems, etc.).

 

Hitachi Technology Engineering (Tokyo)Ando T, Kondo Y, Kuwabara K, Miyauchi A, Ogino M, Takahashi K8/27/20043/9/2006
 
Stem Cell Culture PDF Print E-mail
Friday, 27 March 2009 09:11
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

WO 2005063968, EP 1698690, JP 2005516741

A basal medium for producing a culture medium for embryonic stem cell culture, comprising preset amount of components, e.g., l-arginine, l-serine, l-threonine, P-aminobenzoic acid, inositol, nicotinamide, hypoxanthine, calcium pantothenate, linoleic acid, lipoic acid, prolecin dihydrochloride, thymidine, sodium chloride, glucose (anhydrous), sodium pyruvate, sodium selenite and phenol Red.

 

Asashima M, Furue M, GS Platz Co. Ltd. (Tokyo), Okamoto TAsashima M, Furue M, Okamoto T12/26/20037/14/2005, 9/6/2006, 7/19/2007
WO 2007056593, US 20070129353

Nitrogen-containing heterobicyclic compounds useful for the treatment of a cancerous condition, e.g., acute lymphocytic leukemia, cancer of the adrenal cortex, breast cancer, liver cancer, pancreatic cancer and prostate cancer, and a method for eliminating teratoma-forming stem cells prior to transplant into a mammalian subject involving incubating a stem cell culture with the heterobicyclic compound.

 

Institute for Chemical Genomics (Kirkland, WA, USA), Kahn MKahn M11/8/20055/18/2007, 6/7/2007
WO 2007002664, US 20070122392

A cell culture composition comprising a biocompatible matrix comprising cross-linked hyaluronic acid and mammalian embryonic stem cells disposed within the biocompatible matrix, where the composition is free of laminin.

 

Massachusetts Institute of Technology (Cambridge, MA, USA), Burdick JA, Gerecht-Nir S, Langer RS, Vunjak-Novakovic GBurdick JA, Gerecht-Nir S, Langer RS, Vunjak-Novakovic G6/22/20051/4/2007, 5/31/2007
US 20070105215

A method for culturing stem cells using ATP-Binding Cassette transporters (ABC transporters) by bringing a stem cell culture into contact with an anti-tumor drug or toxin as a substrate of ABC transporters to allow the substrate to react with the stem cell culture, and reculturing viable cells among the stem cell culture which reacted with the substrate, the viable cells having no substrate introduced in it.

 

Samsung Electronics (Seoul)Kim BC, Lee YS, Song OR11/3/20055/10/2007
US 20070087332

Isolated pulmonary stem cells, which are slowly dividing cells forming individual colonies in vitro, express the marker Oct-4 and undergo terminal differentiation into a mature phenotype; useful for generating new cells to replace diseased and damaged body tissues.

 

Ling T, Yu AL, Yu JCLing T, Yu AL, Yu JC10/17/20054/19/2007
JP 2007089575

A method for producing collagen such as collagen type 14 or collagen type 12, involving introducing a vector containing myodifferentiation inducer factor into a cell; the cell is derived from an animal, preferably mouse mesodermal stem cell culture strain MC3T3-E1, ATDC5 or C3H10T 1/2.

 

Tokyo University of Agriculture and Technology (Tokyo)Arai K9/2/20054/12/2007
WO 2007030469, US 20070077649

A method for culturing a successor cell, e.g., astrocyte, oligodendrocyte or neuron, from a precursor cell, comprising co-culturing a precursor cell with an adult mesenchymal stem cell derived from adipose tissue.

 

Kokai LE, Marra KG, Sammak PJ, University of Pittsburgh (Pittsburgh, PA, USA)Kokai LE, Marra KG, Sammak PJ9/6/20053/15/2007, 4/5/2007
JP 2007037426

A serum-free medium for culturing animal stem cells, obtained by adding an antimicrobial peptide to a basal medium for animal cell culture, which does not contain blood serum; enables excellent and efficient culture and proliferation of animal stem cells equivalent to the medium comprising blood serum, reduces the risk of infection during the culture and obtains cells free from infections such as viral infections and BSE.

 

Futagawa H, To Sell KK (Tokyo)Futagawa H, Kato Y, Nishimura M, Tsuji K8/1/20052/15/2007
WO 2007002210

A composition for culturing a pluripotent mammalian embryonic stem cell, comprising an extracellular matrix and a medium consisting of a basal salt nutrient solution, an activator of insulin-like growth factor family-1 receptor (IGF-1R), serum albumin, an activator of an fibroblast growth factor (FGF) receptor, transferrin, and optionally, a member of the transforming growth factor-beta (TGF-beta) family.

 

Bresagen (Athens, GA, USA), Cythera (San Diego, CA, USA), Robarts Research Institute (London, ON, Canada), University of Georgia Research Foundation (Athens, GA, USA)Baetge EE, Carpenter M, Dalton S, Robins AJ, Schulz TC6/20/20051/4/2007
WO 2006135824

Maintaining pluripotent stem cells, e.g., human embryonic stem cells, involving growing the cells in a basal medium containing substituted 7-amino-1-methyl-3,4-dihydro-1H- pyrimido(4,5-d)pyrimidin-2-one derivative.

 

Scripps Research Institute (La Jolla, CA, USA)Chen S, Ding S, Schultz PG, Yan F6/10/200512/21/2006
 
Antivirals PDF Print E-mail
User Rating :  / 1
Monday, 23 March 2009 09:00
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, VA 22314, USA. Tel: 1 (800) 337–9368 (http://www.thomson.com/scientific).

EP 1674104, WO 2006067606, EP 1827457

The use of new and known uridine derivatives optionally in combination with interferon for preparing a drug having antiviral activity against Flaviviridae and hepatitis C virus.

 

CNRS (Paris), INSERM (Paris)Agrofoglio L, Amblard F, Aucagne V, Durantel D, Escuret V, Joubert N, Trepo C, Zoulim F12/24/20046/28/2006, 6/29/2006, 9/5/2007
JP 2006306836, WO 2007080669

A composition comprising a phenol derivative or its salt as an active ingredient; useful for treating bacterial and viral infections in pharmaceuticals, agrochemicals and as a disinfectant.

 

Micro Biotech (Tokushima, Japan)Higuchi M, Higuchi N, Higuchi T, Koyama H, Shibata H1/11/200511/9/2006, 7/19/2007
US 20070099296

A method of determining whether a test hepatitis C virus (HCV) has an altered susceptibility to a compound, comprising contacting a test host cell with the compound and detecting the activity of the indicator gene.

 

Monogram Biosciences (South San Francisco, CA, USA)Gamarnik A, Parkin NT7/30/19975/3/2007
US 20070087434, JP 2007091671

An antiviral artificial cell comprising an artificial cytoskeleton comprising an electromagnetic wave absorber that generates heat to neutralize a virus when externally irradiated with an electromagnetic wave, an artificial cytomembrane wrapping the artificial cytoskeleton and a nanoparticle having a magnetic spin, rotatably retained on the artificial cytomembrane and having a surface for capturing a virus. Useful as an antiviral drug used in a biofilter for removing virus.

 

Toshiba (Tokyo)Itaya K, Naruse Y9/29/20054/19/2007, 4/12/2007
US 20060142298, WO 2006071564, US 7183284

New aluminium salts of 1,2,3-triazoles useful for treating infection by human immunodeficiency virus.

 

Bristol-Myers Squibb (Princeton, NJ, USA), Kadow JF, Regueiro-Ren AKadow JF, Regueiro-Ren A12/29/20046/29/2006, 7/6/2006, 2/27/2007
JP 2006335756

A medical treatment method, or antiviral drug or riboflavin (vitamin B2) drug for viral infection, preferably AIDS caused by HIV, having an envelope, involving using diethyl ether or a substance such as pancreas lipase, bile acid, chitosan, acetone, ethanol, newlase etc., where the concentration of the substance is not altered.

 

Uchiyama MUchiyama M6/6/200512/14/2006
WO 2006091798

A method for lowering viral load of a virus, where the virus causes a chronic viral infection and is resistant to an antiviral drug, comprising administering to a host a medicament comprising the antiviral drug, where the antiviral drug is capable of selecting for a predetermined antiviral drug-resistant mutation in a viral protein, thus creating an antiviral drug-resistant virus; and a synthetic peptide of 9–15 amino acids, comprising the antiviral drug resistant mutation in the viral protein, where the peptide induces an antiviral cytotoxic T lymphocyte response.

 

US Department of Health and Human Services (Washington, DC, USA)Berzofsky JA, Broder S, Catanzaro A, Okazaki T, Snyder JT, Yarchoan R2/22/20058/31/2006
WO 2006084275, US 20060177483

A method for making a system for delivering drugs (e.g., antibiotic, anti-inflammatory, antihistamine, antiviral agent, cancer drug or anesthetic) involving forming a recognitive polymer hydrogel into contact lenses.

 

Auburn University (Auburn, AL, USA), Byrne ME, Venkatesh S, Ewing WR, Huang Y, Mikkilineni A, Sitkoff DF, Sun C, Yu GByrne ME, Venkatesh S, Ewing WR, Huang Y, Mikkilineni A, Sitkoff DF, Sun C, Yu G2/4/20058/10/2006
WO 2006077427

A combination useful for treating infections caused by a glycosylated envelope protein bearing virus, comprising a viral entry inhibitor and an adjunctive agent selected from glycosylation modulator, alkovir and glycovir (e.g., glucovir).

 

MNL Pharma (Ceredigion, UK)Carroll MW, Nash RJ, Slingsby JH1/21/20057/27/2006
WO 2006065125

A method for determining whether a compound (e.g., an antiviral drug) can be transported through active transport by breast cancer resistance protein (BCRP) into the milk or colostrum of a lactating mammal, by determining whether the compound is a BCRP substrate.

 

Het Nederlands Kanter Instituut (Amsterdam)Jonker JW, Schinkel AH, van Herwaarden AE12/16/20046/22/2006
 
Antibodies PDF Print E-mail
Monday, 23 March 2009 08:59
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

WO 2007081680

Diagnosing whether a subject has, or is at risk for developing, pancreatic cancer or pancreatic acinar cell carcinoma, involving measuring the level of the microRNA (miRNA) gene in a test sample.

 

Ohio State University Research Foundation (Columbus, OH, USA)Calin GA, Croce CM1/5/20067/19/2007, 12/27/2007
WO 2007124072, US 20070281314

A method of isolating an miRNA sample from skin comprising applying an adhesive tape to a target area of the skin in a manner to isolate an epidermal sample, where the epidermal sample contains miRNA, where the tape comprises a rubber adhesive, and where the tape is pliable, thus isolating an epidermal sample adhering to the adhesive tape.

 

Dermtech International (San Diego, CA, USA)Benson NR4/20/200611/1/2007, 12/6/2007
WO 2007021896, US 20070123482, US 20070213292

A method of reducing the amount of an miRNA in a cell in a subject for treating, e.g., hemolytic anemia, arthrogryposis complex congenita, pituitary ectopia, rhabdomyolysis or hyperkalemia by administering an antagomir to the subject, where the oligonucleotide agent is substantially single-stranded.

 

Rockefeller University (New York), Alnylam (Cambridge, MA, USA), Manoharan M, Rajeev KG, Stoffel MManoharan M, Rajeev KG, Stoffel M8/10/20052/22/2007, 5/31/2007, 9/13/2007
WO 2007095614

A new array of oligonucleotide probes comprising probes that selectively bind a mature mRNA and a platform on which the probes are immobilized; useful for identifying miRNAs in a sample.

 

University of Louisville Research Foundation (Louisville, KY, USA)Wang E2/15/20068/23/2007
JP 2007179274

An miRNA search method involving determining the base sequence data of a stem loop structure extracted from nucleic-acid-base sequence data, which becomes the base-sequence candidate of an miRNA.

 

Fujitsu (Tokyo), Toyobo (Osaka, Japan), Toyobo Gene Analysis (Tsuruga, Japan)Arakawa T, Kawasaki H, Mizuno T, Taira K12/27/20057/12/2007
WO 2007073737

A method of detecting the tissue origin of cancer comprising contacting a sample derived from a sample containing tumor cells with detection probe, which is a member from a collection of detection probes, the collection of detection probes being capable of specifically identifying target RNA sequences in all miRNAs of the mammal.

 

Exiqon (Vedbaek, Denmark)Echwald SM, Glue C, Jacobsen N, Litman T, Moller S12/29/20057/5/2007
WO 2007064301

A nanoparticle useful for detecting an analyte molecule, e.g., miRNA, comprising a transition metal oxide and a capping agent having a ligand group and a functional group.

 

Agency for Science, Technology and Research (Singapore)Gao Z11/30/20055/7/2007
JP 2007075095

A microarray for miRNA detection comprising a capture probe of endogenic low–molecular weight RNA. The microarray enables comprehensive and efficient analysis and detection of miRNA and can correctly track time-dependent expression change of miRNA by conducting a relative miRNA expression analysis.

 

Mitsubishi Rayon Co. (Tokyo), Kokuritsu Seishin Shinkei Center (Tokyo)Fukushima T, Hojo H4/11/20053/29/2007
US 20070066521

A method of inhibiting the effects of miRNA and/or small interfering RNAs (siRNAs) on gene expression that comprises providing to a system a protein which comprises a sequence of 140 amino acids (SEQ ID NO: 1; A-AC4) or 100 amino acids (SEQ ID NO: 2; S-AC4).

 

Fauquet CMFauquet CM4/13/20053/22/2007
US 20070059739, WO 2007032817

A method of purifying mature miRNAs comprises lysing the sample, degrading the additional nucleic acids and liberating the mature miRNAs.

 

Applera (Foster City, CA, USA)Lao KQ9/12/20053/15/2007, 3/22/2007
US 20070054287

Diagnosing a biological condition, e.g., cancer, comprising amplifying a target miRNA from a test sample to provide a derived miRNA quantity, where the target miRNA is from a tissue of interest, comparing the derived miRNA quantity to an expectation miRNA quantity from a background tissue, and diagnosing the biological condition.

 

Applera (Foster City, CA, USA)Bloch W5/31/20053/8/2007
 
microRNAs PDF Print E-mail
Monday, 23 March 2009 08:58
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

WO 2007081680

Diagnosing whether a subject has, or is at risk for developing, pancreatic cancer or pancreatic acinar cell carcinoma, involving measuring the level of the microRNA (miRNA) gene in a test sample.

 

Ohio State University Research Foundation (Columbus, OH, USA)Calin GA, Croce CM1/5/20067/19/2007, 12/27/2007
WO 2007124072, US 20070281314

A method of isolating an miRNA sample from skin comprising applying an adhesive tape to a target area of the skin in a manner to isolate an epidermal sample, where the epidermal sample contains miRNA, where the tape comprises a rubber adhesive, and where the tape is pliable, thus isolating an epidermal sample adhering to the adhesive tape.

 

Dermtech International (San Diego, CA, USA)Benson NR4/20/200611/1/2007, 12/6/2007
WO 2007021896, US 20070123482, US 20070213292

A method of reducing the amount of an miRNA in a cell in a subject for treating, e.g., hemolytic anemia, arthrogryposis complex congenita, pituitary ectopia, rhabdomyolysis or hyperkalemia by administering an antagomir to the subject, where the oligonucleotide agent is substantially single-stranded.

 

Rockefeller University (New York), Alnylam (Cambridge, MA, USA), Manoharan M, Rajeev KG, Stoffel MManoharan M, Rajeev KG, Stoffel M8/10/20052/22/2007, 5/31/2007, 9/13/2007
WO 2007095614

A new array of oligonucleotide probes comprising probes that selectively bind a mature mRNA and a platform on which the probes are immobilized; useful for identifying miRNAs in a sample.

 

University of Louisville Research Foundation (Louisville, KY, USA)Wang E2/15/20068/23/2007
JP 2007179274

An miRNA search method involving determining the base sequence data of a stem loop structure extracted from nucleic-acid-base sequence data, which becomes the base-sequence candidate of an miRNA.

 

Fujitsu (Tokyo), Toyobo (Osaka, Japan), Toyobo Gene Analysis (Tsuruga, Japan)Arakawa T, Kawasaki H, Mizuno T, Taira K12/27/20057/12/2007
WO 2007073737

A method of detecting the tissue origin of cancer comprising contacting a sample derived from a sample containing tumor cells with detection probe, which is a member from a collection of detection probes, the collection of detection probes being capable of specifically identifying target RNA sequences in all miRNAs of the mammal.

 

Exiqon (Vedbaek, Denmark)Echwald SM, Glue C, Jacobsen N, Litman T, Moller S12/29/20057/5/2007
WO 2007064301

A nanoparticle useful for detecting an analyte molecule, e.g., miRNA, comprising a transition metal oxide and a capping agent having a ligand group and a functional group.

 

Agency for Science, Technology and Research (Singapore)Gao Z11/30/20055/7/2007
JP 2007075095

A microarray for miRNA detection comprising a capture probe of endogenic low–molecular weight RNA. The microarray enables comprehensive and efficient analysis and detection of miRNA and can correctly track time-dependent expression change of miRNA by conducting a relative miRNA expression analysis.

 

Mitsubishi Rayon Co. (Tokyo), Kokuritsu Seishin Shinkei Center (Tokyo)Fukushima T, Hojo H4/11/20053/29/2007
US 20070066521

A method of inhibiting the effects of miRNA and/or small interfering RNAs (siRNAs) on gene expression that comprises providing to a system a protein which comprises a sequence of 140 amino acids (SEQ ID NO: 1; A-AC4) or 100 amino acids (SEQ ID NO: 2; S-AC4).

 

Fauquet CMFauquet CM4/13/20053/22/2007
US 20070059739, WO 2007032817

A method of purifying mature miRNAs comprises lysing the sample, degrading the additional nucleic acids and liberating the mature miRNAs.

 

Applera (Foster City, CA, USA)Lao KQ9/12/20053/15/2007, 3/22/2007
US 20070054287

Diagnosing a biological condition, e.g., cancer, comprising amplifying a target miRNA from a test sample to provide a derived miRNA quantity, where the target miRNA is from a tissue of interest, comparing the derived miRNA quantity to an expectation miRNA quantity from a background tissue, and diagnosing the biological condition.

 

Applera (Foster City, CA, USA)Bloch W5/31/20053/8/2007
 
Drug Discovery Automation PDF Print E-mail
Monday, 23 March 2009 08:57
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

JP 2008020275

An automatic solid phase extractor consisting of a vibration excitation device that provides vibration to a container filled with liquid, such as a pharmaceutical liquid; for use during drug discovery screening.

 

Hitachi Koki (Tokyo)Toi H7/12/20061/31/2008
WO 2007148130

A de novo iterative synthesis method for drug discovery that selects a compound having the desired pharmacophoric fit with a seed structure and synthesizing, assaying and comparing the compound to the structure to determine whether the compound has synthetically desirable properties.

 

Cresset Biomolecular Discovery (Letchworth, UK), Cresset Therapeutics (Philadelphia, PA, USA)Mackay M, Vinter J, Warrington B6/19/200612/27/2007
EP 1859866, US 20070274871

A well plate of non-unitary construction with side walls containing surface energy that provides a specific contact angle for aqueous solution contained in the well in an ambient environment to suppress meniscus formation; for growing cells and handling liquid samples in fields such as gene sequencing, combinatorial chemistry, drug discovery and proteomics, in automated and integrated systems.

 

Genetix (New Milton, UK)Jiang Y5/23/200611/28/2007, 11/29/2007
US 7292263

A robotic charge coupled device microscope for crystal recognition with a lighting system comprising a cluster of high brightness white LEDs; useful in structural, rational drug discovery, etc.

 

University of California (Oakland, CA, USA)Segelke BW, Toppani D3/16/200511/6/2007
JP 2007161453

An automatic storage apparatus for use in a drug discovery research environment, with a hand plate that moves in contact with the surrounding walls of the storage rack to obtain positional information of the storage rack in all directions.

 

Tsubakimoto Chain Co. (Osaka, Japan)Oshimo J, Shibata N12/15/20056/28/2007
WO 2006036737, US 20060094059, EP 1797427

A high-throughput, completely automated method of identifying a new therapeutic use for a test entity, e.g., a drug or drug candidate, involving testing the activity of the test entity against a protein complex in a cell and using the results obtained to identify new activity of the test entity; useful for large-scale drug discovery.

 

Odyssey Thera (San Ramon, CA, USA)MacDonald ML, Michnick SW, Owens S, Westwick JK, Yu H9/22/20044/6/2006, 5/4/2006, 6/20/2007
JP 2007046956

A dispensing apparatus comprising a chip remover arranged at the back of the dispensing mechanism to remove the used chip from the dispensing head and a chip holder to hold the unused chip; useful for drug discovery.

 

Juki Corp. (Tokyo)Okubo K8/8/20052/22/2007
WO 2006133555, US 20060292549

A system for testing the psychotropic activity of a compound comprising a silicon die having a surface for the growth of a neuronal network; useful for the automated screening of a compound in the field of drug discovery and neuroscience.

 

Neurosilicon (Calgary, Canada)Colicos MA6/15/200512/21/2006, 12/28/2006
EP 1653235

A method of controlling the usage of reservoirs in a liquid handling area of an automated liquid handling system, involving determining and removing the content of a reservoir where the reagent is not expected to be used within a predetermined time interval; useful in drug discovery and development.

 

Automation Partnership Cambridge (Royston, UK)Grant PS, Oakeshott RBS10/27/20045/3/2006
JP 2005348615

A sample thawing apparatus that uses a sequence of several acicular nozzles to eject warm water to thaw a sample sealed in a container, such as deep-well plates or microtubes; for use in drug discovery research.

 

Tsubakimoto Chain Co. (Osaka, Japan)Oshimo J, Shibata N, Komada M6/8/200412/22/2005
 
Drug Screening PDF Print E-mail
Monday, 23 March 2009 08:56
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

US 20080054913, WO 2008030503

A candidate drug screening method for iontophoretic delivery, involving applying alternating current to a bulk solution, and ranking the drug candidate based on the measured impedance response of the bulk solutionincluding the drug candidate.

 

Transcu Ltd. (Singapore)Smith GA9/5/20063/6/2008, 3/13/2008
US 7338775

Determining activity of an ATPase or kinase that catalyzes a biochemical reaction producing adenosine diphosphate (ADP); useful in drug screening.

 

Myriad Genetics (Salt Lake City, UT, USA)Hunsaker T, Ostanin K2/9/20053/4/2008
WO 2008024473

Mapping genomic interactions for use in diagnostics, drug screening or research studies by contacting a genomic interaction library with unique primers and amplifying the second genomic library with a single pair of PCR primers.

 

University of Massachusetts Medical School (Shrewsbury, MA, USA)Dekker J, Dostie J8/24/20062/28/2008
JP 2008022743

A spheroid useful in drug screening, toxicity evaluation of therapeutic agents and generating pathological condition model animals. The spheroid is anchored to the solid phase and contains an exogenous cell coagulant.

 

Scivax KK (Sakado, Japan)Gocho T, Ozawa F, Shimada J, Tanaka S7/19/20062/7/2008
US 20080027651

A potential efficacy-determining method for treating neural disorders, for example, schizophrenia, involving determining the outcome-representing efficacy of a test composition for treating a disorder; the method allows rapid screening of chemical compositions for various psychiatric and neurological disorders, even when no suitable animal models exist, so that the accuracy of screening of the drug compositions is improved.

 

Matthysse S, Siekmeier PMatthysse S, Siekmeier P11/14/20051/31/2008
WO 2007132526

A shuttle-type conveyor for use in the drug screening field; has a controller that controls the shuttle transfer portion to remove and convey microplates to a delivery stand by raising or lowering the base.

 

Is Technology (Tokodai, Japan), Rorze Corp. (Hiroshima, Japan)Munakata T, Yamasaki Y, Yamashita S5/16/200611/22/2007
US 20070269834

A screening method for a drug candidate agent or composition of more than one drug candidate agent of possible clinical value in the treatment of a neurological disease, comprising using an indicator system for explicitly measuring stress protein expression or other protein modifications indicative of oxidative stress in the cultured fibroblast cells to identify as a drug candidate.

 

Shapiro HKShapiro HK8/25/200311/22/2007
JP 2007304783

A design-of-experiment method for drug screening, involving allocating a predicted value to experiment candidate data for generating new training data and repeating this process until storing a preset number of experiment candidate data.

 

NEC (Tokyo)Osoda T5/10/200611/22/2007
JP 2007278960

A cell electrophysiology sensor with an opening of a through-hole provided in the wall surface that is opened towards the through-hole of the holding plate; for drug screening in pharmacology.

 

Matsushita Denki Sangyo (Osaka, Japan)Hiraoka S, Nakatani M, Ushio K4/11/200610/25/2007
US 20070218475

A method of identifying an agent that binds to a protein identifying chemical ligands for cellular proteins by contacting a cell containing a pharmacologically relevant protein with labeled agents, and detecting binding of agents to the cell.

 

Beachy PA, Chen JK, Taipale AJNBeachy PA, Chen JK, Taipale AJN11/22/20059/20/2007
WO 2007090649

A bioelectronic device comprising a cell and an extracellular planar potential-sensitive electrode; useful as a sensor or in a drug screening procedure.

 

The Max Planck Society for the Advancement of Science (Munich)Fromherz P, Peitz I2/10/20068/16/2007
 
Biological Imaging PDF Print E-mail
Monday, 23 March 2009 08:56
Patent #SubjectAssignee(s)Inventor(s)Priority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

WO 2006123148, EP 1886107

An electromagnetic radiation pulse (e.g., ultraviolet pulse)-measuring apparatus having a beam-splitter that splits the pulse into two sub-pulses, where spectrally-sheared up-converted replicas of the pulse are produced; useful for telecommunication, material processing and biological imaging.

 

Isis Innovation (Oxford, UK)Gorya S, Radunsky AS, Walmsley IA5/20/200511/23/2006, 2/3/2008
US 20080009558, WO 2008008559

A method of preparing polymer nanoparticles for biological imaging, involving producing a mixture of acrylate, polymerization initiator that is activated by microwave irradiation, cross-linker that creates intra-particle cross-links during polymerization and water based solvent.

 

Regents of the University of California (Oakland, CA, USA)An Z, Hawker C, Stucky G7/10/20061/10/2008, 1/17/2008
US 20070159694

An optical beam with an inhomogeneous polarization state in which polarization rotates in a continuous and counterclockwise manner while traversing a circular path around a beam axis in a clockwise direction; used for optical inspection, lithography and biological imaging, such as confocal microscopy for dark-field confocal inspection of biological samples and spectroscopic imaging.

 

University of Rochester (Rochester, NY, USA)Biss DP, Brown TG1/12/20047/12/2007
US 7232913

A novel chromophore used as a photo polymerization initiator for a composition used for biological imaging.

 

Bazan GC, Benmansour H, Gorohmaru H, Hong W, Koehler B, Kojima T, Maeda S, Mikhailovsky A, Shigeiwa M, Woo HY, Regents of the University of California (Oakland, CA, USA)

 

Bazan GC, Benmansour H, Gorohmaru H, Hong JW, Koehler B, Kojima T, Maeda S, Mikhailovsky A, Shigeiwa M, Woo HY9/28/20046/19/2007
US 20070122440

A method of producing nanoparticles as micro-reactor vessels by combining two reactant mixtures and flash precipitating under conditions to react the polymeric reactants and form precipitated nanoparticles comprising a block and/or graft copolymer.

 

Anacker J, Hoye TR, Macosko CW, Prud HRKAnacker J, Hoye TR, Macosko CW, Prud HRK7/20/20055/31/2007
CN 1967248

A biologically functional fluorescent magnetic nanometer particle and its preparation method and application. The particle has core-shell structure, including fluorescent material and magnetic material of the kernel layer; the shell layer formed by fluorescent transparent material; and the modified layer above the shell layer surface with an organic functional group.

 

Shanghai Normal University (Shanghai)Chen W, Shen H, Zhou L, Zhu L11/15/20055/23/2007
WO 2007054552, FR 2893131

A nanoparticles quantifying and/or detecting method for in vitro diagnosis, etc., involving illuminating through an upper or lower surface of a flat solid support, made of glass, using a white light source or polychromatic light to illuminate the nanoparticles present on the upper surface.

 

Centre National Recherche Scientifique (Paris)Fort E, Le Moal ER, Leveque-Fort SP, Ricolleau C11/9/20055/18/2007, 5/11/2007
US 20070034011

A dynamic focusing apparatus that has an annular transducer, transmitter and receiver. The annular transducer includes different frequency responses at different surface positions and adjusts frequency characteristics of a transmit waveform or receive filter; used for ultrasonic imaging, for example, in biological or medical imaging and non-destructive testing.

 

Li PLi P7/25/20052/15/2007
CN 1885347

A method for using dynamic digit model to detect CT angiography reconstruction algorithm performance.

 

Shanghai Jiao Tong University (Shanghai)Liu Z, Zhao J, Zhuang T7/6/200612/27/2006
US 20060118696

A near-field imaging apparatus useful in a system for collecting image data of macromolecules, comprises a near-field microscope and a precision optical probe coupled to the microscope for noninvasively imaging inside a cell without destruction.

 

O'Connell D, O'Connell-Rodwell C, Nanopoint (Honolulu, HI, USA)O'Connell D, O'Connell-Rodwell C11/8/20016/8/2006
 
Mass Spectrometry PDF Print E-mail
Monday, 23 March 2009 08:54
Patent numberDescriptionAssigneeInventorPriority application datePublication date

Source: Thomson Scientific Search Service. The status of each application is slightly different from country to country. For further details, contact Thomson Scientific, 1800 Diagonal Road, Suite 250, Alexandria, Virginia 22314, USA. Tel: 1 (800) 337-9368 (http://www.thomson.com/scientific).

WO 2008051093

A method for improving the signal intensity of precursor ionsconstrained in a carrier gas in a selected ion flow mass spectrometry (SIFT-MS) instrument, involving applying electrical potential to aflow tube to lower the diffusive loss of ions within the tube.

 

Syft Techologies (Christchurch, NZ)Peck GC, Wilson PF10/19/20065/2/2008
US 20080102536

A manufacturing method for an analytical sample by secondary ion mass spectrometry, involving separating a thin film and thin-film stack body from the substrate.

 

Semiconductor Energy Laboratory Co. (Atsugi-shi, Japan)Toriumi S10/31/20065/1/2008
JP 2008102020

A mass spectrometry sample stand for analyzing micro samples, comprising a crystalline substance with reverse perovskite structure provided between a base material and an analysis target object. Since the reverse perovskite structure has electrical conductivity as the metal is located in the surroundings, the thermal conductivity is also good and the analysis target object can be ionized efficiently. Hence high spatial resolution can be obtained, even if high energy is applied and temperature rises.

 

Toppan Printing Co. (Tokyo)Furuta K10/19/20065/1/2008
JP 2008096353

A mass spectrometer for analyzing a protein sample that selectsthe ionic species that are dissociated out of ions generated by the ionization of sample using valence of the ion, determined from mass spectrum data without interference peak.

 

Hitachi Technologies (Tokyo)Kurosawa T, Morishima D, Nishida T, Takeda A10/13/20064/24/2008
JP 2008095504

An inductively-coupled-plasma-source-mass-spectrometry apparatus that supplies additional gas to the intermediate position of alow-vacuum side stage and reduces partial pressure of hydrogengas in the high-vacuum chamber. The rapid increase of partialpressure of hydrogen gas can be prevented and durability of theturbo molecular pump can be increased, allowing the analysisprocess to be performed continuously and stably.

 

Agilent Technologies (Santa Clara, CA, USA)Kitamoto A10/5/20064/24/2008
US 20080087817

A mass spectrometry system for analyzing metal species within a cell or tissue, with an integrated ionization source with an electrospray ionization source that generates a potential difference across a capillary tube and mass spectrometer interface.

 

Li G, Lopez-Avila VLi G, Lopez-Avila V10/13/20064/17/2008
US 20080087809

A tandem mass spectrometer with an electrode system positioned between mass analyzers to selectively deflect ions from an ion path for detection.

 

Crawford RK, Fischer SM, Russ CWCrawford RK, Fischer SM, Russ CW10/13/20064/17/2008
US 20080083873

An electrospray ionization system for liquid chromatography mass spectroscopy with a valve coupled to the inlet of a specific nozzle for selectively nebulizing one of a secondary and calibration liquid. Less expensive and allows for easier optimization of the secondary sprayer, and provides an effective way of introducing a secondary stream of liquid droplets into primary stream of electrosprayed droplets toreference correct time-of-flight mass spectra.

 

Giardina MGiardina M10/9/20064/10/2008
WO 2008035124

A silica particle useful as matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF-MS) matrix materialfor the adsorption of polar organic compounds (e.g., dioxins, furans, steroids or sterols) and for partial desorption of adsorbed compounds.

 

Analytical Nano Technologies (Sedgefield, UK)Rowell F, Sundar L9/22/20063/27/2008
WO 2007145361

A method of detecting lipid-antigen of microorganisms for diagnosing diseases associated with Mycoplasma infections (e.g., asthma),involving analyzing the sample by mass spectrometry and detectingthe spectrum peak specific to lipid antigen.

 

M Bio Technology (Tokyo)Matsuda K, Shingu Y6/14/200612/21/2007
WO 2007106816

A new substrate compound for mass spectrometric analysis of enzymes (e.g., alpha-galactosidase A); eliminates the need of detergents, user-unfriendly solvents (e.g., chloroform), and liquid-liquid and solid phase extraction steps. The process is also less time consuming than prior art processes.

 

PerkinElmer (Boston)Cerda B3/13/20069/20/2007
 
<< Start < Prev 1 2 Next > End >>

Page 1 of 2