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The Ohio Journal of - The Ohio Academy of Science

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Vol. 112(1)<br />

1:30 PM<br />

Undergraduate Research Session<br />

Dr. Jeffrey D. Weidenhamer, Presiding<br />

Kettering <strong>Science</strong> Center Lecture Hall Room 112<br />

1:30 Introduction—Dr. Jeffrey D. Weidenhamer—See page 5.<br />

1:40 MENTORING UNDERGRADUATES FOR SUCCESS IN<br />

RESEARCH. S. Tonia Hsieh, sthsieh@temple.edu, Department<br />

<strong>of</strong> Biology, 1900 North 12th St, Temple University,<br />

Philadelphia, PA 19122.<br />

Undergraduate research and inquiry-based learning are<br />

two tools critical for inspiring our future generations<br />

<strong>of</strong> scientists and leaders. While these methods for<br />

engaging students are well-known and <strong>of</strong>ten-practiced at<br />

predominately undergraduate institutions, exploring new<br />

methods for teaching and prioritization <strong>of</strong> undergraduate<br />

research at more research-focused institutions are <strong>of</strong>ten<br />

overlooked. Primary reasons cited for not involving<br />

undergraduates in research include principal investigators<br />

lacking the time to work with undergraduates due to<br />

already over-burdened schedules, the lack <strong>of</strong> preparation<br />

amongst the student body for critical thinking skills<br />

necessary for research, and the (supposed) inability<br />

<strong>of</strong> undergraduates to produce “useful” research. Such<br />

misperceptions are a travesty for scientific progress and<br />

a disservice to an undergraduate population that is filled<br />

with creative, knowledge-hungry students who can play a<br />

critical role driving innovation in even the busiest research<br />

lab. When properly conceived and supported by the right<br />

strategies, undergraduate research can be mentored by a<br />

“time-taxed” assistant pr<strong>of</strong>essor at a research university<br />

and lead to undergraduates presenting talks at national<br />

meetings and co-authoring peer-reviewed publications.<br />

2:30 LEAD AND CADMIUM IN CONSUMER PRODUCTS:<br />

UNDERGRADUATE RESEARCH AT ASHLAND UNIVERSITY<br />

IMPACTING PUBLIC POLICY. Jeffrey D. Weidenhamer,<br />

jweiden@ashland.edu, Department <strong>of</strong> Chemistry, Geology<br />

& Physics, 401 College Ave, Ashland University, Ashland, OH<br />

44805.<br />

Following the death <strong>of</strong> a 4-year-old Minnesota boy after<br />

swallowing a highly leaded bracelet charm, the lead<br />

content <strong>of</strong> children’s jewelry from local dollar stores was<br />

investigated in a course for non-science majors on lead’s<br />

chemistry and toxicity. This blossomed into an ongoing<br />

research effort that has involved science majors in Ashland<br />

University’s analytical chemistry courses and independent<br />

research projects. Jewelry samples and painted toys were<br />

screened for heavy metal content by X-ray fluorescence<br />

(XRF), and lead and cadmium content determined by acid<br />

digestion followed by atomic absorption analysis. Lead and<br />

cadmium bioavailability from jewelry has been determined<br />

using saline extractions to simulate exposure by mouthing<br />

<strong>of</strong> jewelry and dilute HCl extractions to simulate the worstcase<br />

scenario <strong>of</strong> ingestion <strong>of</strong> a jewelry item. Most recently,<br />

cadmium bioavailability was evaluated in 86 components<br />

<strong>of</strong> 57 jewelry items found to contain high levels <strong>of</strong> cadmium<br />

(> 10,000 ppm) by XRF. Saline extraction yielded as much<br />

as 2,200 µg cadmium, and 24-hr dilute HCl extraction<br />

yielded a maximum <strong>of</strong> > 20,000 µg cadmium. <strong>The</strong>se<br />

amounts exceed the maximum amounts recommended by<br />

the United States Consumer Product Safety Commission<br />

(CPSC) by a factor <strong>of</strong> 100, indicating the potential for<br />

dangerous exposures to children who mouth or swallow<br />

this jewelry. <strong>The</strong> undergraduate research projects have<br />

resulted in eight peer-reviewed publications (including<br />

four papers co-authored by six different undergraduates),<br />

and more than a dozen CPSC recalls <strong>of</strong> jewelry and toys<br />

with high lead content as well as the first CPSC recalls <strong>of</strong><br />

consumer products for cadmium contamination.<br />

<strong>The</strong> <strong>Ohio</strong> <strong>Journal</strong> <strong>of</strong> <strong>Science</strong> A-51<br />

2:45 UNDERGRADUATE RESEARCH IN POLYMER CHEMISTRY<br />

AT ASHLAND UNIVERSITY: POLYLACTIDE/POLYETHYLENE<br />

GLYCOL STAR BLOCK COPOLYMERS. Perry S. Corbin, pcorbin@<br />

ashland.edu, Ashland University, Department <strong>of</strong> Chemistry/<br />

Geology/Physics, 401 College Ave., Ashland, OH 44805.<br />

<strong>The</strong> synthesis <strong>of</strong> polymers that have varied molecular<br />

architectures and are designed to self-organize into higherorder<br />

structures is critical to the continued development<br />

<strong>of</strong> multifaceted materials. <strong>The</strong> preparation <strong>of</strong> such<br />

polymers has been the goal <strong>of</strong> a long-term undergraduate<br />

research program at Ashland University. Studies have<br />

recently focused on novel four-armed, calixarene- and<br />

resorcinarene-core polylactide (PLA)/polyethylene glycol<br />

(PEG) star block copolymers. <strong>The</strong>se polymers may function<br />

as useful drug-delivery vehicles upon assembling into<br />

aqueous micelles. To synthesize the block copolymers,<br />

PLA star homopolymers were first prepared by tin(II)catalyzed<br />

ring-opening polymerizations <strong>of</strong> L-lactide. To<br />

couple PEG with the PLA chains, the homopolymer end<br />

groups were activated, and, subsequently, reacted with a<br />

nucleophilic, amino-PEG. <strong>The</strong> PLA-PEGs were purified by<br />

dialysis and multiple water washes. <strong>The</strong> disappearance<br />

<strong>of</strong> the signal for the terminal methine hydrogens <strong>of</strong> the<br />

PLA chain ends in nuclear magnetic resonance ( 1 H-NMR)<br />

spectra <strong>of</strong> the activated PLA homopolymers suggested<br />

that the activation proceeded to completion. 1 H-NMR<br />

spectral integrations also allowed the degree <strong>of</strong> PLA-<br />

PEG coupling to be estimated in the second step <strong>of</strong> the<br />

convergent synthesis. Coupling efficiencies were estimated<br />

to be high (>90%). Further fluorescence spectroscopic and<br />

light-scattering studies indicated that aqueous micelles,<br />

indeed, form from the calixarene- and resorcinarenecore<br />

star block copolymers. In addition to the scientific<br />

merit <strong>of</strong> such studies, undergraduates obtain invaluable<br />

research training, develop reasoning skills, and examine<br />

important aspects <strong>of</strong> polymer chemistry—an area that,<br />

in some instances, does not receive its due attention in<br />

undergraduate chemistry curricula.<br />

3:00 FROM PROTEINS TO POLYLACTIDES: APPLICATION<br />

OF MALDI MASS SPECTROMETRY TO UNDERGRADUATE<br />

RESEARCH AT ASHLAND UNIVERSITY. Rebecca W. Corbin,<br />

rcorbin@ashland.edu, Ashland University, Department <strong>of</strong><br />

Chemistry/Geology/Physics, 401 College Avenue, Ashland<br />

OH 44805.<br />

Matrix-assisted laser desorption/ionization (MALDI)<br />

with time-<strong>of</strong>-flight mass spectrometry (TOF MS) is one<br />

<strong>of</strong> the most versatile methods for the characterization<br />

<strong>of</strong> biological as well as synthetic polymer samples.<br />

MALDI-TOF MS serves an important role in a variety <strong>of</strong><br />

interdisciplinary research projects at Ashland University.<br />

Over twelve undergraduates have been involved with<br />

these collaborations. Students learn to prepare samples,<br />

to evaluate matrix-analyte formulations, to optimize<br />

instrumental parameters, and to determine appropriate<br />

data analysis strategies for collaborative projects involving<br />

proteomics as well as polymer synthesis. One proteomics<br />

project involves MALDI-TOF MS analysis <strong>of</strong> recombinant<br />

and purified eye lens crystallins from the zebrafish Danio<br />

rerio. Results indicate the identity <strong>of</strong> specific crystallin<br />

sequences and suggest the presence <strong>of</strong> structurally<br />

modified forms. A second research project is the<br />

identification <strong>of</strong> circadian clock-associated proteins in the<br />

filamentous fungus Aspergillus nidulans. Comparing twodimensional<br />

gel electrophoresis pr<strong>of</strong>iles <strong>of</strong> proteins isolated<br />

at different time points allows the targeting <strong>of</strong> candidates<br />

associated with an internal circadian oscillator. One such<br />

protein, glyceraldehyde-3-phosphate dehydrogenase,<br />

has been identified by tryptic digestion <strong>of</strong> an excised gel<br />

spot followed by MALDI mass fingerprinting. <strong>The</strong> longterm<br />

goal <strong>of</strong> an additional proteomics collaboration is the<br />

identification <strong>of</strong> neuronal interleukin-16 binding partners.<br />

MALDI-TOF MS also proves to be effective for the<br />

characterization <strong>of</strong> synthetic polymers. Specifically, the<br />

acquisition <strong>of</strong> mass spectra from polylactide star polymers<br />

provides information that is complementary to molecular

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