Abstract: A method is provided for mineralizing a dental surface or subsurface including contacting the dental surface with a protein disrupting agent and stabilized amorphous calcium phosphate (ACP) or amorphous calcium fluoride phosphate (ACFP).
Abstract: The present disclosure provides an electrode and an feedthrough for an implantable medical device. In one embodiment, the implantable electrode and the implantable feedthrough both comprise electrically insulating diamond material and electrically conductive diamond material that form an interface. Further, the present disclosure provides method for fabricating the implantable electrode and the feedthrough.
Type:
Application
Filed:
December 3, 2013
Publication date:
April 3, 2014
Applicants:
National ICT Australia Limited, The University of Melbourne
Inventors:
Hamish Meffin, Kate Fox, David Garrett, Kumaravelu Ganesan, Steven Prawer, Samantha Lichter, Igor Aharonovich
Abstract: The present invention relates to a phosphopeptide-stabilized amorphous calcium phosphate and/or amorphous calcium fluoride phosphate complex, wherein the complex is formed at a pH of below 7.0. Methods of making such complexes are also provided. The complexes are useful in dental applications, in particular in dental remineralisation.
Abstract: A method is provided for mineralizing a dental surface or subsurface including contacting the dental surface with a protein disrupting agent and stabilized amorphous calcium phosphate (ACP) or amorphous calcium fluoride phosphate (ACFP).
Abstract: The present invention provides a phosphopeptide or phosphoprotein (PP) stabilised amorphous calcium phosphate or amorphous calcium fluoride phosphate complex having a calcium ion greater than about 30 moles of calcium per mole of PP.
Abstract: A continuous process for the functionalization of fullerenes is disclosed. The process offers numerous advantages in comparison to traditional batch processes. The functionalized fullerenes may find use in the fabrication of hetero-junction devices.
Type:
Application
Filed:
December 21, 2011
Publication date:
February 13, 2014
Applicant:
The University of Melbourne
Inventors:
David Jones, Wing Ho Wallace Wong, Andrew Holmes, Helga Seyler
Abstract: The invention relates to methods of medically treating mammals with Eustachian tube dysfunctions, such as Ménière's disease, vertigo, Otitis Media (including Otitis Media with Effusion (OME), Acute Otitis Media (AOM) and Aerotitis Media (AM)) as well as other disorders which are characterized by ET dysfunction.
Abstract: The present invention relates to isolated Porphyromonas gingivalis polypeptides and nucleotides. The polypeptides include an amino acid sequence selected from the group consisting of: SEQ. ID. NO. 110; SEQ. ID. NO. 111; SEQ. ID. NO. 112; SEQ. ID. NO. 113; SEQ ID NO: 120; SEQ. ID. NO. 123; SEQ. ID. NO. 124; SEQ. ID. NO. 125; SEQ. ID. NO. 130; SEQ. ID. NO. 131; SEQ. ID. NO. 132; SEQ. ID. NO. 133; SEQ. ID. NO. 135; SEQ. ID. NO. 136; SEQ. ID. NO. 137; SEQ. ID. NO. 138; SEQ. ID. NO. 143; SEQ. ID. NO. 144; SEQ. ID. NO. 145; SEQ. ID. NO. 146; SEQ. ID. NO. 147; SEQ. ID. NO. 148; and amino acid sequences at least 95% identical thereto.
Type:
Grant
Filed:
February 21, 2012
Date of Patent:
February 4, 2014
Assignees:
CSL Limited, The University of Melbourne
Inventors:
Bruce C. Ross, Ian G. Barr, Michelle A. Patterson, Catherine T. Agius, Linda J. Rothel, Mai B. Margetts, Dianna M. Hocking, Elizabeth A. Webb
Abstract: A rapid and sensitive analyte detection assay is based on whispering gallery modes of fluorescently labelled microspheroidal particles. Ligands for the analyte, such as nucleic acids, are anchored to the particles. The fluorescent labels may comprise fluorophores or quantum dots. In the latter case, the particles may comprise melamine formaldehyde. The assay may be used to detect analytes in aqueous samples.
Type:
Grant
Filed:
November 20, 2009
Date of Patent:
December 31, 2013
Assignees:
Genera Biosystems Limited, The University of Melbourne
Inventors:
Karl Frederick Poetter, Edin Nuhiji, Paul Mulvaney
Abstract: The present invention relates to a phosphopeptide-stabilized amorphous calcium phosphate and/or amorphous calcium fluoride phosphate complex, wherein the complex is formed at a pH of below 7.0. Methods of making such complexes are also provided. The complexes are useful in dental applications, in particular in dental remineralization.
Abstract: The present invention provides a phosphopeptide or phosphoprotein (PP) stabilized amorphous calcium phosphate or amorphous calcium fluoride phosphate complex having a calcium ion greater than about 30 moles of calcium per mole of PP.
Abstract: The present invention relates to an oral composition and an immunogenic composition for the suppression of the pathogenic effects of the intra-oral bacterium Porphyromonas gingivalis associated with periodontal disease.
Type:
Application
Filed:
March 28, 2013
Publication date:
November 21, 2013
Applicant:
The University of Melbourne
Inventors:
Eric Charles Reynolds, Neil Martin O'BRIEN-SIMPSON, Nada SLAKESKI
Abstract: The present invention relates generally to a method for the treatment and prophylaxis of pain. In accordance with the present invention, it is proposed that antagonists of GM-CSF are effective in the treatment of pain. Antagonists of GM-CSF include, but are not limited to, antibodies which are specific for GM-CSF or the GM-CSF receptor. The present invention further provides transgenic animals, such as a GM-CSF knock-out mouse, useful for testing antagonists in certain disease models.
Abstract: The present invention relates to non-steroidal compounds useful in the treatment of inflammatory conditions and pharmaceutical compositions comprising them.
Type:
Grant
Filed:
April 14, 2008
Date of Patent:
September 17, 2013
Assignee:
The University of Melbourne
Inventors:
Alastair Stewart, Martin Banwell, Brenda Leung, Anu Augustine, Jacki Kitching, Thomasz Bilski
Abstract: This invention relates to a method for treating or preventing a disease by raising an innate immune response in a subject, the method comprising administering to the subject an effective amount of a composition comprising a TLR2 moiety in solution, wherein the TLR2 moiety comprises a TLR2 agonist and wherein the disease is not treated or prevented by a humoral or cellular immune response directed against the TLR2 moiety.
Type:
Application
Filed:
September 22, 2011
Publication date:
September 5, 2013
Applicant:
THE UNIVERSITY OF MELBOURNE
Inventors:
David Charles Jackson, Amabel Tan, Weiguang Zeng
Abstract: The present invention relates to a Mycoplasma hyopneumoniae vaccine strain comprising a mutation in at least one of the genes listed or as deposited with the National Measurements Institute (Australia) under accession number NM04/41259, which strain is temperature sensitive and attenuated, a vaccine comprising such strains and methods and uses thereof.
Type:
Grant
Filed:
May 19, 2010
Date of Patent:
September 3, 2013
Assignees:
Bioproperties Pty Ltd., The University of Melbourne
Inventors:
Rima Youil, Youssef Abs El-Osta, Glenn Browning, Phillip Markham
Abstract: The present invention provides a process for the preparation of a multilayer film, in particular, a cross-linked multilayer macromolecular film.
Type:
Grant
Filed:
March 10, 2011
Date of Patent:
July 30, 2013
Assignee:
The University of Melbourne
Inventors:
Francesco Caruso, Greg Guanghua Qiao, Anton Richard Blencowe, Tor Kit Goh, Luke Andrew Connal, Georgina Kate Such
Abstract: The present invention relates to a synthetic immunogen represented by the general formula 1, useful for generating long lasting protective immunity against various intracellular pathogens which are the causative agents of tuberculosis, leishmaniasis, AIDS, trypanosomiasis, malaria and also allergy, cancer and a process for the preparation thereof. The developed immunogen is able to circumvent HLA restriction in humans and livestock. The invention further relates to a vaccine comprising the said immunogen for generating enduring protective immunity against various diseases. The said vaccine is targeted against intracellular pathogens, more particularly the pathogen M. tuberculosis in this case. In the present invention, promiscuous peptides of M. tuberculosis are conjugated to TLR ligands especially; Pam2Cys to target them mainly to dendritic cells and therefore elicit long-lasting protective immunity.
Type:
Application
Filed:
September 14, 2011
Publication date:
July 18, 2013
Applicants:
UNIVERSITY OF MELBOURNE, COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH
Inventors:
Javed Naim Agrewala, Uthaman Gowthaman, David Jackson, Weiguang Zeng
Abstract: The present invention relates generally to a method for the treatment and prophylaxis of pain. In accordance with the present invention, it is proposed that antagonists of GM-CSF are effective in the treatment of pain. Antagonists of GM-CSF include, but are not limited to, antibodies which are specific for GM-CSF or the GM-CSF receptor. The present invention further provides transgenic animals, such as a GM-CSF knock-out mouse, useful for testing antagonists in certain disease models.
Abstract: The present invention relates to an oral composition and an immunogenic composition for the suppression of the pathogenic effects of the intra-oral bacterium Porphyromonas gingivalis associated with periodontal disease.
Type:
Grant
Filed:
June 9, 2010
Date of Patent:
April 30, 2013
Assignee:
The University of Melbourne
Inventors:
Eric C. Reynolds, Neil Martin O'Brien-Simpson, Nada Slakeski