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Dive into the research topics where Scott M. Norton is active.

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Featured researches published by Scott M. Norton.


Journal of Electroanalytical Chemistry | 2002

Electrochemical synthesis and optical readout of striped metal rods with submicron features

Brian D. Reiss; R. Griffith Freeman; Ian D. Walton; Scott M. Norton; Patrick C. Smith; Walter G. Stonas; Christine D. Keating; Michael J. Natan

Abstract Fluorescent molecules are widely used as identification tags in both analytical and bioanalytical chemistry. This manuscript describes an electrochemical approach to the manufacture of submicron metal barcodes for application as identification tags. These Nanobarcodes™ identification tags (NBCs), are prepared via the sequential electrodeposition of various metals within an alumina template. The striped particles grow as replicas of the pores of the membrane, and can be released from the membrane through chemical treatment. The striping pattern of NBCs can be read out via optical microscopy, and allows for the synthesis of large numbers of distinguishable tags. Herein, we address the synthesis of these NBCs and the use of software that can be used to identify specific NBCs in optical microscope images containing several distinct species of NBCs.


Nanobiotechnology | 2005

Encoded metal nanoparticle-based molecular beacons for multiplexed detection of DNA

Michael Y. Sha; Mark Yamanaka; Ian D. Walton; Scott M. Norton; Rebecca L. Stoermer; Christine D. Keating; Michael J. Natan; Sharron G. Penn

In this paper we describe a molecular beacon format assay in which encoded nanowire particles are used to achieve multiplexing. We demonstrate this principle with the detection of five viral pathogens; Hepatitis A virus, Hepatitis C virus, West Nile Virus, Human Immune Deficiency virus and Severe Acute Respiratory Syndrome virus. Oligonucleotides are designed complementary to a target sequence of interest containing a 3′ universal fluorescence dye. A 5′ thiol causes the oligonucleotides to self-assemble onto the metal nanowire. The single-stranded oligonucleotide contains a self-complementary hairpin stem sequence of 10 bases that forces the 3′ fluorophore to come into contact with the metallic nanowire surface, thereby quenching the fluorescence. Upon addition of target DNA, there is hybridization with the complementary oligonucleotides. The resulting DNA hybrid is rigid, unfolds the hairpin structure, and causes the fluorophore to be moved away from the surface such that it is no longer quenched. By using differently encoded nanowires, each conjugated with a different oligonucleotide sequence, multiplexed DNA assays are possible using a single fluorophore, from a multiplexed RT-PCR reaction.


Methods of Molecular Biology | 2005

Use of Nanobarcodes® Particles in Bioassays

R. Griffith Freeman; Paul A. Raju; Scott M. Norton; Ian D. Walton; Patrick C. Smith; Lin He; Michael J. Natan; Michael Y. Sha; Sharron G. Penn

We have developed striped metal nanoparticles, Nanobarcodes particles, which can act as encoded substrates in multiplexed assays. These particles are metallic, encodeable, machine-readable, durable, submicron-sized tags. The power of this technology is that the particles are intrinsically encoded by virtue of the difference in reflectivity of adjacent metal stripes. This chapter describes protocols for the attachment of biological molecules, and the subsequent use of the Nanobarcodes particles in bioassays.


Advances in nucleic acid and protein analyses, manipulation, and sequencing. Conference | 2000

Microvolume Laser Scanning cytometry platform for biological marker discovery

Ian D. Walton; Louis J. Dietz; Gary Frenzel; Jerry Chen; Jim Winkler; Scott M. Norton; Aaron B. Kantor

Modern chemical synthesis and screening technologies have the ability to create large numbers of lead components but still do not answer questions of efficacy, dosing, toxicity and optimal patient population. SurroMed was founded to develop discovery technologies for new biological markers that will answer these questions. Biological markers will be derived from the results of many different assays; cell surface, serum factors and others, many performed using whole blood and other fluids and tissues. We report on the design of a Microvolume Laser Scanning Cytometer (MLSC) and disposable capillary arrays to be used in biological marker discovery. The MLSC machines are used primarily for cell surface assays, though they are suitable for other fluorescence assays as well. Each capillary requires a very small sample volume per assay, less than twenty micro- liters, and so allows hundreds of assays to be performed on a single ten milliliter blood draw. The new MLSC is capable of optimally detecting four fluorescence colors at different scan rates. HeNe excitation and red emission permits the use of whole blood, so that no lysing or cell separation is required. The MLSC instrument and disposable capillary arrays are in routine use for biological marker discovery at SurroMed.


BiOS 2000 The International Symposium on Biomedical Optics | 2000

Cell enumeration and characterization in microvolume laser scanning cytometry: a multicolor image-processing package

Scott M. Norton; Jim Winkler; Louis J. Dietz

MLSC is an alternative to flow cytometry that has many advantages in clinical environments such as minimal sample preparation, low sample volume, and direct measurement of absolute cell counts. However, MLSC requires an added image- processing step to produce the industry-standard FCS output format. The image processing program needs to handle multiple binary images, representing different detection channels; it needs to determine the background fluorescence level in each channel; the overall noise in each channel such that it can enumerate cell from noise; it needs to ignore extraneous signal such as bubbles, dust particles and other artifacts; and it needs to characterize each recognized cell to report parameters such as weighted flux, size, ellipticity, and ratios and correlations between the signal in other channels at the same location. We have developed an image processing solution, SurroImage that meets the above criteria and performs well in a clinical research setting.


electronic imaging | 2004

Nanobarcodes particles as covert security tags for documents and product security

Sharron G. Penn; Scott M. Norton; Ian D. Walton; Richard Griffith Freeman; Glenn Davis

At Nanoplex Technologies, Inc. we have developed Nanobarcodes particles, which are encodeable, machine-readable, durable, sub-micron sized taggants which have application for document and product security. We will present results on the use of Nanobarcodes particles in a number of authentication and anti-counterfeiting applications. We also focus on the software component in recognition of particles imaged against varied backgrounds.


Analytical Chemistry | 2003

Quantification of proteins and metabolites by mass spectrometry without isotopic labeling or spiked standards

Weixun Wang; Haihong Zhou; Hua Lin; Sushmita Roy; Thomas A. Shaler; Lander R. Hill; Scott M. Norton; Praveen Kumar; Markus Anderle; Christopher H. Becker


Archive | 1999

Optical architectures for microvolume laser-scanning cytometers

Louis J. Dietz; Ian D. Walton; Scott M. Norton


Analytical Chemistry | 2002

Particles for multiplexed analysis in solution: detection and identification of striped metallic particles using optical microscopy.

Ian D. Walton; Scott M. Norton; Arjuna Balasingham; Lin He; Dominador F. Oviso; Dimpy Gupta; Paul A. Raju; and Michael J. Natan; R. Griffith Freeman


Archive | 2002

Mass spectrometric quantification of chemical mixture components

Christopher H. Becker; Curtis A. Hastings; Scott M. Norton; Sushmita Roy; Weixun Wang; Haihong Zhou; Thomas Andrew Shaler; Praveen Kumar; Markus Anderle; Hua Lin

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Ian D. Walton

Pennsylvania State University

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Rebecca L. Stoermer

Pennsylvania State University

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Christine D. Keating

Pennsylvania State University

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R. Griffith Freeman

Pennsylvania State University

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Lin He

North Carolina State University

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