A novel composite of glass fiber paper and reinforcing material that is useful for high speed manufacturing of devices comprising it is disclosed. The composite is formed by pressing into a glass fiber paper, having multimodal (at least bi-modal) composition, a hydrophilic reinforcing material. The composite has anisotropic separation properties that are particularly useful for preparing a fluid fraction from whole blood. The preferred glass fiber paper comprises glass fibers such that there are a plurality of short fibers () having large diameters and long fibers () with smaller diameters. The preferred glass fiber paper also exhibits partial ordering. There are many more of the long fibers () with smaller diameters than of the short fibers () having large diameters. Also disclosed are several blood separator device designs for efficiently separating the fluid fraction of blood from whole blood using the composite.
Method Of Separating A Fluid Fraction From Whole Blood
A novel composite of glass fiber paper and reinforcing material that is useful for high speed manufacturing of devices comprising it is disclosed. The composite is formed by pressing into a glass fiber paper, having multimodal (at least bi-modal) composition, a hydrophilic reinforcing material. The composite has anisotropic separation properties that are particularly useful for preparing a fluid fraction from whole blood. The preferred glass fiber paper comprises glass fibers such that there are a plurality of short fibers () having large diameters and long fibers () with smaller diameters. The preferred glass fiber paper also exhibits partial ordering. There are many more of the long fibers () with smaller diameters than of the short fibers () having large diameters. Also disclosed are several blood separator device designs for efficiently separating the fluid fraction of blood from whole blood using the composite.
Methods And Kits For Detecting Heparin/Platelet Factor 4 Antibodies
David Milunic - Deptford NJ, US Susan Andrelczyk - West Deptford NJ, US
International Classification:
G01N 33/551 G01N 33/553
US Classification:
436524000, 436526000
Abstract:
Methods for determining the presence of heparin/platelet factor 4 antibodies in a sample suspected to contain heparin/platelet factor 4 antibodies are provided, along with apparatus suitable for performing the methods. The method depends upon a color visualization indicating the presence or absence of heparin/platelet factor 4 antibodies in the sample. Preferred methods comprise contacting the sample with particles being complexed to platelet factor 4 (PF4) and which particle-complexed PF4 reacts specifically with heparin/platelet factor 4 antibodies, passing the sample/particle mixture through a filter, and then analyzing the color of the filtrate. The presence of heparin/platelet factor 4 antibodies in the sample is established where the color of the filtrate is substantially different from the color of the receptor-bearing particles.
Rapid Tests For The Detection Of Inhibitors Of Enzymes And Human Exposure To The Same
Yli Remo Vallejo - Newark DE, US David Milunic - Newark DE, US
Assignee:
ANP Technologies Inc. - Newark DE
International Classification:
G01N 21/64
US Classification:
435 20, 4352887
Abstract:
A device and method for the rapid on-site detection of inhibitors of enzymes, such as, acetylcholinesterase is described where the device contains 2 reaction zones containing a reporter enzyme substrate. One reaction zone is for the test sample while the other is for an onboard negative control. Sample and control fluids are preincubated with the enzyme in separate reaction containers, then an aliquot of each reaction mixture is added to designated reaction zones on the test device. A purpose-built reader or an illuminating device, such as, containing an incandescent light source, a diode, a UV light source or any other illumination source that is suitable for the reporter or mere visualization is used to determine the level of reporter.
Apparatus And Method For Conducting An Assay Using Reverse Flow Through A Membrane
The present invention relates to an apparatus and method for conducting an assay using reverse flow through a membrane. More particularly, the present invention is directed to an apparatus and method which allows for the assaying of analytes, such as antigens, in a fluid sample containing such analytes with more accurate and reproducible results.
One-Step Rapid Assay For The Detection Of Inhibitors Of Enzymes
- Newark DE, US David Milunic - Newark DE, US Ray Yin - Newark DE, US Renee Street - Bel Air MD, US De Chen - Newark DE, US
International Classification:
C12Q 1/46
Abstract:
A device and method for the rapid on-site detection of inhibitors of enzymes, such as acetylcholinesterase, is described wherein the device contains all reagents added to a sample pad containing dried releasable enzyme creating a reaction mixture wherein inhibitor deactivates the enzyme, while said reaction mixture travels via a longitudinal membrane to a distal porous pad containing a substrate for the enzyme. The reaction of the enzyme and the substrate results in a product that can generate a measurable signal such as color, fluorescence or luminescence to serve as a reporter. Signal that is generated at this reaction zone is inversely proportional to inhibitor concentration in the test sample. A device containing two such strips, one for a test sample, the other for a negative control fluid as an onboard comparator is described. A purpose-built reader or an illuminating device, such as, containing an incandescent light source, a diode, a UV light source or any other illumination source that is suitable for the reporter or mere visualization is used to determine the level of reporter.
Rapid Tests For The Detection Of Inhibitors Of Enzymes And Human Exposure To The Same
A device and method for the rapid on-site detection of inhibitors of enzymes, such as, acetylcholinesterase is described where the device contains 2 reaction zones containing a reporter enzyme substrate. One reaction zone is for the test sample while the other is for an onboard negative control. Sample and control fluids are preincubated with the enzyme in separate reaction containers, then an aliquot of each reaction mixture is added to designated reaction zones on the test device. A purpose-built reader or an illuminating device, such as, containing an incandescent light source, a diode, a UV light source or any other illumination source that is suitable for the reporter or mere visualization is used to determine the level of reporter.
ANP Technologies, Inc. since Aug 2007
Team Leader, R&D
Akers Biosciences, inc Nov 2002 - Feb 2007
Manager, R&D
Akers Biosciences, Inc Oct 2001 - Nov 2002
Senior Scientist
OraSure Technologies, Inc. Nov 1999 - Oct 2001
Scientist
Diasorin, Inc Jul 1999 - Nov 1999
Scientist
Education:
Cleveland Institute of Technology 2007 - 2011
AASEE, Electronic Engineering
State University of New York at Albany 1980 - 1985
BS, Biology Chemistry
Skills:
Assay Development Protein Purification Validation R&D Chromatography Immunoassays Laboratory Protein Chemistry Quality Assurance Gmp Sds Page Analytical Chemistry Purification In Vitro
David Milunic. My Profile02/21/2007. All Shoutouts. Private Profile. [Restricted to David's friends]. Messaging Off. [Restricted to David's friends] ...