57 research outputs found
Neighborhood fast food restaurants and fast food consumption: A national study
<p>Abstract</p> <p>Background</p> <p>Recent studies suggest that neighborhood fast food restaurant availability is related to greater obesity, yet few studies have investigated whether neighborhood fast food restaurant availability promotes fast food consumption. Our aim was to estimate the effect of neighborhood fast food availability on frequency of fast food consumption in a national sample of young adults, a population at high risk for obesity.</p> <p>Methods</p> <p>We used national data from U.S. young adults enrolled in wave III (2001-02; ages 18-28) of the National Longitudinal Study of Adolescent Health (n = 13,150). Urbanicity-stratified multivariate negative binomial regression models were used to examine cross-sectional associations between neighborhood fast food availability and individual-level self-reported fast food consumption frequency, controlling for individual and neighborhood characteristics.</p> <p>Results</p> <p>In adjusted analysis, fast food availability was not associated with weekly frequency of fast food consumption in non-urban or low- or high-density urban areas.</p> <p>Conclusions</p> <p>Policies aiming to reduce neighborhood availability as a means to reduce fast food consumption among young adults may be unsuccessful. Consideration of fast food outlets near school or workplace locations, factors specific to more or less urban settings, and the role of individual lifestyle attitudes and preferences are needed in future research.</p
Volume 01
Introduction from Dean Dr. Charles Ross
Three Decades of Digging: Undergraduate Archeology at Longwood by Jessica Fields and Stephanie Neeley
Interactions of Allelopathy and Heat Stress in Plants by Derek W. Hambright and Mary E. Lehman
Inertial Electrostatic Confinement D-D Fusion Device: Construction and Simulation by Andrew R. Grzankowski
Shackled Nim by Zachary Johnson
Development of GC-MS and Chemometric Methods for the Analysis of Accelerants in Arson Cases by Boone M. Prentice
A Comparison of Image Analysis Methods in cDNA Microarrays by Ashley M. Swandby
Perceived Sexual Activity of Short and Long-Term Relationships by Victoria Morgan and Katie Williamson
Elderly Male Communication by Kristine G. Bender
Three Poems: âAdam and Eve and an Orange Treeâ, âThe Name of Everything Before Dyingâ, and âThe âPoet Voiceââ by Katelyn N. Romaine
There\u27s Nothing Like Dancing, After All : Marriage and Gender in the Dance Scenes of Jane Austen\u27s Novels by D. Nicole Swann
Two Poems: âAge Nine with Motherâ and âThe Apple That Crawls Away From the Treeâ by Jessica Fox
Untitled by Mike McAteer
Room 9 by Alex Grabiec
Two Photographs: âGracieâ and âEmilyâ by Laura Nodtvedt
Bowling Lanes Night by Nick Costa
Two Paintings: âCan and Kettleâ and âScarecrowâ by Rachel Wolfe
Exploring Henrik Ibsen\u27s âPerr Gyntâ by Zack Dalton
Creative Writing Scholarship at Longwood University
Music Scholarship at Longwood â Senior Recital Arianne K. Burrus
Longwood University Theater â Peer Gyn
Mass spectrometry instrumentation and ion/ion reaction method development for the fundamental analysis of gas phase biomolecules
Mass spectrometry (MS) and tandem mass spectrometry (MSn) approaches play vital roles in the molecular analysis of many different types of analytes (e.g., proteins, peptides, etc.). The typical molecular mass spectrometry experiment involves making/sampling ions, probing ions, and transmitting/measuring ions. While the work described herein covers a broad range of technical mass spectrometry instrumentation and experimentation topics on each of these three main segments, the fundamental study of physical and chemical ionic behaviors is a common theme throughout. A technique which has been previously developed to manipulate droplets generated via electrospray ionization (ESI) during the ionization process (viz. the making/sampling phase) was quantified using a mathematical model. This technique involves the controlled introduction of volatile acidic and basic reagents into the interface region of the mass spectrometer where electrospray droplets are undergoing desolvation on the sub-millisecond time scale. Quantitative pH results from this model show good correlation with experimental results. Several projects were also completed involving ion transmission phases. One such projected was the construction and implementation of a miniature ion funnel interface, based off of the design reported by Julian et al. This interface is designed to increase the transmission efficiency (~100x) of ions generated via atmospheric ionization techniques into the high vacuum region of the mass spectrometer. Once the ions are inside the mass spectrometer, it was discovered that introducing a monopolar DC field during a number steps in a typical 3-D ion trap MS experiments could result in significant enhancements in instrument performance (e.g., ion accumulation efficiency, ion/ion reaction control, mass analysis). The final phase of a mass spectrometry experiment involves measuring and detecting the ions. A novel method for performing mass analysis in a 3-D ion trap was developed and characterized which involves scanning the quadrupolar DC potential applied to the ion trap while holding the RF potential. This `downscan\u27 can offer some advantages over the traditional RF scan for ions of high m/z values, including a larger scanable mass range as well as the opportunity for improved resolution at high mass. Perhaps more chemically interesting is the work herein devoted to the development and characterization of several different methods to structurally interrogate ions (viz. the probing phase). The design and development of two ion activation approaches using a 3-D ion trap mass spectrometer, dipolar direct current collision induced dissociation (DDC CID) and photodissociation (PD), have been other major areas of research. Interesting characteristics of DDC CID, relative to the conventional single-frequency resonance excitation approach commonly employed, are its non-resonant or broad-band nature and the fact that ions of all m/z values are activated simultaneously. Key to the information derived from activation techniques such as the one mentioned above and from reactions performed inside the mass spectrometer is the ion type. Our research group is actively pursuing targeted chemical derivatization techniques that can be performed via ion/ion reactions ( viz. reactions involving a cation and anion) in the gas-phase as part of MSn workflows for biopolymer characterization. Here, this targeted gas-phase chemistry is extended to analytes containing carboxylic acid groups and carboxylate groups using carbodiimide and fixed charge ammonium reagents, respectively. In the spirit of exploring a wider range of chemistries, studies have been conducted involving non-covalently-bound cluster ions as reagent ion types. Relatively stable non-covalent cluster-type ion complexes have been used as multi-functional reagents in ion/ion reactions. This type of methodology allows for multiple covalent modifications to be achieved in a single ion/ion encounter and at the `cost\u27 of only a single analyte charge. These experiments spurred further investigation into the surprisingly gas phase reactive behavior of arginine residues cationized with sodium towards sulfo-NHS ester reagents. Additionally, another area of research aims to implement a means to cool a 3-D ion trap so as to extend the lifetimes of solvated ions, which are typically short lived under ambient MS conditions. This instrumentation opens up numerous avenues for both fundamental and applicative studies of a wide variety of different chemical reactions, allowing the study of solution-phase-limited reactions using the inherent benefits of mass spectrometric analysis. This instrumentation design currently involves the use of copper blocks connected to the end-cap electrodes that are be cooled via their attachment to a custom built, in-vacuum liquid nitrogen dewar
Ion/Ion Reactions with âOniumâ Reagents: An Approach for the Gas-phase Transfer of Organic Cations to Multiply-Charged Anions
xvii,; 246 hlm,; 21 c
Electrospray Droplet Exposure to Gaseous Acids for the Manipulation of Protein Charge State Distributions
Identification of Phosphatidylcholine Isomers in Imaging Mass Spectrometry Using Gas-Phase Charge Inversion Ion/Ion Reactions
Photoactive Chromium(III)-Cyclam Complexes with Axially Bound \u3cem\u3egeminal\u3c/em\u3e-Diethynylethenes
Standard Reticle Slide To Objectively Evaluate Spatial Resolution and Instrument Performance in Imaging Mass Spectrometry
Spatial
resolution is a key parameter in imaging mass spectrometry
(IMS). Aside from being a primary determinant in overall image quality,
spatial resolution has important consequences on the acquisition time
of the IMS experiment and the resulting file size. Hardware and software
modifications during instrumentation development can dramatically
affect the spatial resolution achievable using a given imaging mass
spectrometer. As such, an accurate and objective method to determine
the working spatial resolution is needed to guide instrument development
and ensure quality IMS results. We have used lithographic and self-assembly
techniques to fabricate a pattern of crystal violet as a standard
reticle slide for assessing spatial resolution in matrix-assisted
laser desorption/ionization (MALDI) IMS experiments. The reticle is
used to evaluate spatial resolution under user-defined instrumental
conditions. Edgespread analysis measures the beam diameter for a Gaussian
profile and line scans measure an âeffectiveâ spatial
resolution that is a convolution of beam optics and sampling frequency.
The patterned crystal violet reticle was also used to diagnose issues
with IMS instrumentation such as intermittent losses of pixel data
Enhanced Ion Transmission Efficiency up to <i>m</i>/<i>z</i> 24âŻ000 for MALDI Protein Imaging Mass Spectrometry
The
molecular identification of species of interest is an important
part of an imaging mass spectrometry (IMS) experiment. The high resolution
accurate mass capabilities of Fourier transform ion cyclotron resonance
mass spectrometry (FT-ICR MS) have recently been shown to facilitate
the identification of proteins in matrix-assisted laser desorption/ionization
(MALDI) IMS. However, these experiments are typically limited to proteins
giving rise to ions of relatively low <i>m</i>/<i>z</i> due to difficulties transmitting and measuring large molecular weight
ions of low charge states. Herein we have modified the source gas
manifold of a commercial MALDI FT-ICR MS to regulate the gas flow
and pressure to maximize the transmission of large <i>m</i>/<i>z</i> protein ions through the ion funnel region of
the instrument. By minimizing the contribution of off-axis gas disruption
to ion focusing and maximizing the effective potential wall confining
the ions through pressure optimization, the signal-to-noise ratios
(S/N) of most protein species were improved by roughly 1 order of
magnitude compared to normal source conditions. These modifications
enabled the detection of protein standards up to <i>m</i>/<i>z</i> 24âŻ000 and the detection of proteins from
tissue up to <i>m</i>/<i>z</i> 22âŻ000 with
good S/N, roughly doubling the mass range for which high quality protein
ion images from rat brain and kidney tissue could be produced. Due
to the long time-domain transients (>4 s) required to isotopically
resolve high <i>m</i>/<i>z</i> proteins, we have
used these data as part of an FT-ICR IMS-microscopy data-driven image
fusion workflow to produce estimated protein images with both high
mass and high spatial resolutions
Multiple Time-of-Flight/Time-of-Flight Events in a Single Laser Shot for Improved Matrix-Assisted Laser Desorption/Ionization Tandem Mass Spectrometry Quantification
Quantitative matrix-assisted
laser desorption/ionization time-of-flight
(MALDI TOF) approaches have historically suffered from poor accuracy
and precision mainly due to the nonuniform distribution of matrix
and analyte across the target surface, matrix interferences, and ionization
suppression. Tandem mass spectrometry (MS/MS) can be used to ensure
chemical specificity as well as improve signal-to-noise ratios by
eliminating interferences from chemical noise, alleviating some concerns
about dynamic range. However, conventional MALDI TOF/TOF modalities
typically only scan for a single MS/MS event per laser shot, and multiplex
assays require sequential analyses. We describe here new methodology
that allows for multiple TOF/TOF fragmentation events to be performed
in a single laser shot. This technology allows the reference of analyte
intensity to that of the internal standard in each laser shot, even
when the analyte and internal standard are quite disparate in <i>m</i>/<i>z</i>, thereby improving quantification while
maintaining chemical specificity and duty cycle. In the quantitative
analysis of the drug enalapril in pooled human plasma with ramipril
as an internal standard, a greater than 4-fold improvement in relative
standard deviation (<10%) was observed as well as improved coefficients
of determination (<i>R</i><sup>2</sup>) and accuracy (>85%
quality controls). Using this approach we have also performed simultaneous
quantitative analysis of three drugs (promethazine, enalapril, and
verapamil) using deuterated analogues of these drugs as internal standards
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