Neus Fabregat-Cabello

ORCID: 0000-0002-5898-8176
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About
Contact & Profiles
Research Areas
  • Vitamin D Research Studies
  • Hormonal and reproductive studies
  • Pharmacological Effects and Assays
  • Effects and risks of endocrine disrupting chemicals
  • Pesticide Residue Analysis and Safety
  • Analytical Chemistry and Chromatography
  • Pharmaceutical and Antibiotic Environmental Impacts
  • Metabolomics and Mass Spectrometry Studies
  • Analytical chemistry methods development
  • Vitamin C and Antioxidants Research
  • Mass Spectrometry Techniques and Applications
  • Mercury impact and mitigation studies
  • Diabetes Treatment and Management
  • Pharmacological Effects and Toxicity Studies
  • Chromium effects and bioremediation
  • Antibiotics Pharmacokinetics and Efficacy
  • Analytical Methods in Pharmaceuticals
  • Adrenal Hormones and Disorders
  • Blood Pressure and Hypertension Studies
  • Mycotoxins in Agriculture and Food
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Estrogen and related hormone effects
  • Antibiotic Use and Resistance
  • Eating Disorders and Behaviors
  • Biotin and Related Studies

University of Liège
2016-2022

Centre Hospitalier Universitaire de Liège
2020

Instituto de Investigación Sanitaria La Fe
2019

Institute of Pesticides and Environmental Protection
2016

Universitat Jaume I
2013-2016

Universidad de Oviedo
2012

This study deals with one of the major concerns in mycotoxin determinations: matrix effect related to LC-MS/ MS systems electrospray ionization sources. To this end, a first approach, has been evaluated two ways: monitoring signal compound (added mobile phase) during entire chromatographic run, and by classical post-extraction addition. The was focused on nine selected mycotoxins: aflatoxin B 1 , fumonisins 2 3 ochratoxin A, deoxynivalenol, T-2 HT-2 toxins zearalenone various sample extracts...

10.3920/wmj2014.1872 article EN World Mycotoxin Journal 2015-09-30

We present here a new environmental measurement method for the rapid extraction and accurate quantification of Cr(VI) in solid samples. The quantitative is achieved 10 minutes by means focused microwave assisted using 50 mmol/L Ethylendiamintetraacetic acid (EDTA) at pH as extractant. In addition, it enables separation Cr species anion exchange chromatography mobile phase which 1:10 dilution extracting solution. Thus, neutralization or acidification steps are prone to cause interconversion...

10.1021/es3022864 article EN Environmental Science & Technology 2012-10-23

A stable isotope dilution liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed for the determination of 24,25-dihydroxyvitamin D<sub>3</sub> (24,25(OH)<sub>2</sub>D<sub>3</sub>) and 25-hydroxyvitamin D<sub>3</sub>/D<sub>2</sub> (25(OH)D<sub>3</sub>/D<sub>2</sub>) in human aqueous humor samples.

10.1039/c9ay01896d article EN Analytical Methods 2019-01-01
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