Sandra Huber

Dr. Sandra Huber

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2011 in Environment International
Verified
Journal Article
Closed access
LHLine S. Haug
Line S. Haug
SHSandra Huber
Sandra Huber
GBGeorg Becher
Georg Becher
CTCathrine Thomsen
Cathrine Thomsen

21 May 2007 in Journal of Environmental Monitoring
Verified
Journal Article
Closed access
PDF file
JBJonathan L. Barber
Jonathan L. Barber
UBUrs Berger
Urs Berger
CCChakra Chaemfa
Chakra Chaemfa
SHSandra Huber
Sandra Huber
AJAnnika Jahnke
Annika Jahnke
KJKevin C. Jones
Kevin C. Jones
Air samples were collected from 4 field sites in Europe: 2 sites from the UK, Hazelrigg (semi-rural) and Manchester (urban); 1 site from Ireland: Mace Head (rural); and 1 site from Norway: Kjeller (rural). Additionally, air samples were taken from indoor locations in Tromsø, Norway. Air samples were collected using high-volume air samplers employing sampling modules containing glass-fibre filters (GFFs, particle phase), and glass columns with a polyurethane foam (PUF)–XAD-2–PUF sandwich (gaseous phase). Typical outdoor air volumes required for the determination of per- and polyfluorinated alkyl substances (PFAS) ranged from 500–1800 m3. GFFs and PUF–XAD columns were analysed separately to obtain information on phase partitioning. All air samples were analysed for volatile, neutral PFAS, with selected GFF samples halved for analysis of both neutral and airborne particle-bound ionic PFAS. Volatile PFAS were extracted from air samples by cold-column immersion with ethyl acetate, and were analysed by gas chromatography–mass spectrometry in the positive chemical ionisation mode (GC–PCI–MS). Ionic PFAS were extracted from GFFs by sonication in methanol, and were analysed by liquid chromatography–time-of-flight–mass spectrometry (LC–TOF–MS) using electrospray ionisation in the negative ion mode (ESI−). Perfluorooctanoate (PFOA) was often the predominant analyte found in the particulate phase at concentrations ranging from 1–818 pg m−3, and 8:2 fluorotelomer alcohol (FTOH) and 6:2 FTOH were the prevailing analytes found in the gas phase, at 5–243 pg m−3 and 5–189 pg m−3, respectively. These three PFAS were ubiquitous in air samples. Many other PFAS, both neutral and ionic, were also present, and levels of individual analytes were in the 1–125 pg m−3 range. Levels of some PFAS exceeded those of traditional persistent organic pollutants (POPs). In this study, the presence of 12:2 FTOH and fluorotelomer olefins (FTolefins), and ionic PFAS other than perfluorooctane sulfonate (PFOS) and PFOA, are reported in air samples for the first time. Concentrations of neutral PFAS were several orders of magnitude higher in indoor air than outdoor air, making homes a likely important diffuse source of PFAS to the atmosphere. Our repeated findings of non-volatile ionic PFAS in air samples raises the possibility that they might directly undergo significant atmospheric transport on particles away from source regions, and more atmospheric measurements of ionic PFAS are strongly recommended.

13 April 2010 in Environmental Science & Technology
Verified
Journal Article
Closed access
SHStuart Harrad
Stuart Harrad
CWCynthia A. de Wit
Cynthia A. de Wit
MAMohamed Abou-Elwafa Abdallah
Mohamed Abou-Elwafa Abdallah
CBCaroline Bergh
Caroline Bergh
JBJustina A. Björklund
Justina A. Björklund
TWThomas Webster
Thomas Webster

1 April 2021 in Environmental Research
Verified
Journal Article
Open access
MAMaria Averina
Maria Averina
JBJan Brox
Jan Brox
SHSandra Huber
Sandra Huber
AFAnne-Sofie Furberg
Anne-Sofie Furberg
Prevalence of obesity, hypertension and dyslipidemia has been increasing in children and adolescents worldwide. Exposure to environmental pollutants may contribute to this development. Our aim was to study associations between perfluoroalkyl substances (PFAS) and dyslipidemia, hypertension and obesity in a population-based sample of adolescents. Serum PFAS concentrations were measured in 940 adolescents, mean age 16.4 (SD 1.3) years, from the cross-sectional Fit Futures study by the UHPLC-MS/MS method. The following endpoints were used: hypertension (systolic blood pressure over 130 mmHg and/or diastolic blood pressure over 80 mmHg); obesity (body mass index over 2 z-score, WHO charts for adolescents); dyslipidemia (total cholesterol ≥ 5.17 mmol/L, and/or LDL-cholesterol ≥ 3.36 mmol/l, and/or apolipoprotein B ≥ 1.10 g/L). Perfluorooctane sulfonate (PFOS), perfluorononanoate (PFNA), perfluorodecanoate (PFDA) and perfluoroundecanoate (PFUnDA) serum concentrations were positively associated with apolipoprotein B, total- and LDL cholesterol. The highest vs. lowest quartiles of total PFAS (∑PFAS), PFNA and PFDA concentrations were positively associated with the risk of dyslipidemia: OR 2.24 (95% CI 1.10-4.54), OR 2.30 (95% CI 1.16-4.57) and 2.36 (95% CI 1.08-5.16), respectively. The highest vs. lowest quartiles of ∑PFAS, perfluorohexane sulfonate (PFHxS), PFOS, perfluorooctanoate (PFOA) concentrations were positively associated with the risk of hypertension: OR 1.91 (95% CI 1.12-3.26), OR 2.06 (95% CI 1.16-3.65), 1.86 (95% CI 1.08-3.19) and 2.08 (95% CI 1.17-3.69) respectively. PFHxS and perfluoroheptane sulfonate (PFHpS) concentrations were positively associated with obesity. This cross-sectional study showed a possible link between several PFAS and dyslipidemia, hypertension and obesity in Norwegian adolescents.

18 March 2011 in Environmental Science & Technology
Verified
Journal Article
Closed access
LHLine S. Haug
Line S. Haug
SHSandra Huber
Sandra Huber
MSMartin Schlabach
Martin Schlabach
GBGeorg Becher
Georg Becher
CTCathrine Thomsen
Cathrine Thomsen

1 October 2012 in Chemosphere
Verified
Journal Article
Closed access
MMMorten K. Moe
Morten K. Moe
SHSandra Huber
Sandra Huber
JSJohan Svenson
Johan Svenson
AHAn Hagenaars
An Hagenaars
MPMartial Pabon
Martial Pabon
DHDorte Herzke
Dorte Herzke