CHEMICAL ANALYSIS FACILITY CORE Accurate and sensitive qualitative and quantitative determination of toxicants forms a core element of CEED?s mission. The Chemical Analysis Facility Core (CAF) maintains state-of-the-art measurement capabilities to identify and quantify levels of chemicals in the total environment; characterizing potential internal dose (from environmental matrices), metabolites and biologically effective doses in target tissues. The goal of this Facility Core is to provide Center investigators assistance in experimental design, sample preparation, assay development, training, and access to technologies. These analysis tools are necessary for accurate assessment of chemical exposures for targeted metabolite analyses (biological response indicators) that can be linked to mechanisms of pathogenesis. Analysis of toxicants and their metabolites in a variety of biological and environmental matrices (e.g., blood, urine, sputum, cellular extracts, water, soil, dust) is performed within the CAF using mass spectrometrically-based techniques. The CAF also generates detailed mechanistic and metabolomic information on toxicants and chemo preventive or therapeutic agents and supports rapid response initiatives and new sensor development. The CAF uses inductively- coupled plasma mass spectrometry (ICPMS) for the bulk of its elemental analysis, gas chromatography/mass spectrometry (GC/MS) for semi-volatile and volatile molecular analytes, and high/ultra-performance liquid chromatography/mass spectrometry (HPLC/MS) for nonvolatile and polar chemical analysis. Through University funding (see Facilities and Resources section) the CAF continues to expand its capacities in metabolomics for discovery of biomarkers that bridge exposure to resultant biological responses and, ultimately, disease pathogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES005022-33
Application #
9927645
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
33
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Rbhs-School of Public Health
Department
Type
DUNS #
078795880
City
Piscataway
State
NJ
Country
United States
Zip Code
08854
Lee, Heedoo; Zhang, Duo; Laskin, Debra L et al. (2018) Functional Evidence of Pulmonary Extracellular Vesicles in Infectious and Noninfectious Lung Inflammation. J Immunol 201:1500-1509
Del Giudice, Marco; Barrett, Emily S; Belsky, Jay et al. (2018) Individual differences in developmental plasticity: A role for early androgens? Psychoneuroendocrinology 90:165-173
Barrett, E S; Hoeger, K M; Sathyanarayana, S et al. (2018) Anogenital distance in newborn daughters of women with polycystic ovary syndrome indicates fetal testosterone exposure. J Dev Orig Health Dis 9:307-314
George, Blessy; Joy, Melanie S; Aleksunes, Lauren M (2018) Urinary protein biomarkers of kidney injury in patients receiving cisplatin chemotherapy. Exp Biol Med (Maywood) 243:272-282
Vail, Gwyndolin; Roepke, Troy A (2018) Membrane-initiated estrogen signaling via Gq-coupled GPCR in the central nervous system. Steroids :
Tiethof, Angela K; Richardson, Jason R; Hart, Ronald P (2018) Knockdown of Butyrylcholinesterase but Not Inhibition by Chlorpyrifos Alters Early Differentiation Mechanisms in Human Neural Stem Cells. Toxics 6:
Liu, Anna B; Tao, Siyao; Lee, Mao-Jung et al. (2018) Effects of gut microbiota and time of treatment on tissue levels of green tea polyphenols in mice. Biofactors :
Rockafellow-Baldoni, Megan; Spayd, Steven E; Hong, Jun-Yan et al. (2018) Arsenic Exposure and Cancer Risk Reduction with Local Ordinance Requiring Whole-House Dual-Tank Water Treatment Systems. Hum Ecol Risk Assess 24:1256-1267
Jabbar, Shaima; Reuhl, Kenneth; Sarkar, Dipak K (2018) Prenatal alcohol exposure increases the susceptibility to develop aggressive prolactinomas in the pituitary gland. Sci Rep 8:7720
Radbel, Jared; Le-Hoang, Oanh; Vayas, Kinal N et al. (2018) Effect of World Trade Center Dust Exposure and Chronic Intermittent Hypoxia on Macrophage Matrix Metalloproteinase-12 Expression in Mice. Ann Am Thorac Soc 15:S125-S126

Showing the most recent 10 out of 819 publications