Bojan Sarkanj

Prof. Bojan Sarkanj

Department of Food Technology, University North, Koprivnica, Croatia
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

View All Publications
1 August 2018 in Analytica Chimica Acta
Verified
Journal Article
Open access
BSBojan Sarkanj
Bojan Sarkanj
CEChibundu N. Ezekiel
Chibundu N. Ezekiel
Paul C. TurnerPaul C. Turner
Paul C. Turner
Wilfred A. AbiaWilfred A. Abia
Wilfred A. Abia
MRMichael Rychlik
Michael Rychlik
BWBenedikt Warth
Benedikt Warth
There is a critical need to better understand the patterns, levels and combinatory effects of exposures we are facing through our diet and environment. Mycotoxin mixtures are of particular concern due to chronic low dose exposures caused by naturally contaminated food. To facilitate new insights into their role in chronic disease, mycotoxins and their metabolites are quantified in bio-fluids as biomarkers of exposure. Here, we describe a highly sensitive urinary assay based on ultra-high performance liquid chromatography - tandem mass spectrometer (UHPLC-MS/MS) and 13C-labelled or deuterated internal standards covering the most relevant regulated and emerging mycotoxins. Utilizing enzymatic pre-treatment, solid phase extraction and UHPLC separation, the sensitivity of the method was significantly higher (10-160x lower LODs) than in a previously described method used for comparison purpose, and stable isotopes provided compensation for challenging matrix effects. This method was in-house validated and applied to re-assess mycotoxin exposure in urine samples obtained from Nigerian children, adolescent and adults, naturally exposed through their regular diet. Owing to the methods high sensitivity, biomarkers were detected in all samples. The mycoestrogen zearalenone was the most frequently detected contaminant (82%) but also ochratoxin A (76%), aflatoxin M1 (73%) and fumonisin B1 (71%) were quantified in a large share of urines. Overall, 57% of 120 urines were contaminated with both, aflatoxin M1 and fumonisin B1, and other co-exposures were frequent. These results clearly demonstrate the advanced performance of the method to assess lowest background exposures (pg mL-1 range) using a single, highly robust assay that will allow for the systematic investigation of low dose effects on human health.

1 August 2013 in Food Chemistry
Verified
Journal Article
Closed access
BSBojan Sarkanj
Bojan Sarkanj
MMMaja Molnar
Maja Molnar
MČMilan Čačić
Milan Čačić
LGLars Gille
Lars Gille

1 November 2018 in Food and Chemical Toxicology
Verified
Journal Article
Open access
OOOluwaseun T. Ojuri
Oluwaseun T. Ojuri
CEChibundu N. Ezekiel
Chibundu N. Ezekiel
MSMichael Sulyok
Michael Sulyok
Obinna EzeokoliObinna Ezeokoli
Obinna Ezeokoli
OOOluwawapelumi A. Oyedele
Oluwawapelumi A. Oyedele
RKRudolf Krska
Rudolf Krska
This study assessed, for the first time, the mycotoxicological risks from consumption of complementary foods by infants and young children in Nigeria. Molds belonging to Aspergillus aculeatinus, A. flavus, A. luchuensis, A. tubingensis, A. welwitschiae and Geotrichum candidum were recovered from the complementary foods. Twenty-eight major mycotoxins and derivatives, and another 109 microbial metabolites including chloramphenicol (a bacterial metabolite), were quantified in 137 food samples by LC-MS/MS. Aflatoxins and fumonisins co-contaminated 42% of the cereal- and nut-based food samples, at mean concentrations exceeding the EU limits of 0.1 and 200 μg/kg set for processed baby foods by 300 and six times, respectively. Milk contained mainly beauvericin, chloramphenicol and zearalenone. The trichothecenes, T-2 and HT-2 toxins, were quantified only in infant formula and at levels three times above the EU indicative level of 15 μg/kg for baby food. Chronic exposure estimate to carcinogenic aflatoxin was high causing low margin of exposure (MOE). Exposures to other mycotoxins either exceeded the established reference values by several fold or revealed low MOEs, pointing to important health risks in this highly vulnerable population. The observed mycotoxin mixtures may further increase risks of adverse health outcomes of exposure; this warrants urgent advocacy and regulatory interventions.

1 December 2013 in Food and Chemical Toxicology
Verified
Journal Article
Closed access
BSBojan Sarkanj
Bojan Sarkanj
BWBenedikt Warth
Benedikt Warth
SUSilvio Uhlig
Silvio Uhlig
WAWilfred A. Abia
Wilfred A. Abia
MSMichael Sulyok
Michael Sulyok
IBInes Banjari
Ines Banjari

1 April 2019 in Food Control
Verified
Journal Article
Open access
OOOluwaseun T. Ojuri
Oluwaseun T. Ojuri
CEChibundu N. Ezekiel
Chibundu N. Ezekiel
MEMari K. Eskola
Mari K. Eskola
BSBojan Sarkanj
Bojan Sarkanj
ABAkinola D. Babalola
Akinola D. Babalola
RKRudolf Krska
Rudolf Krska

10 December 2014 in Analytical and Bioanalytical Chemistry
Verified
Journal Article
Open access
PDF file
BWBenedikt Warth
Benedikt Warth
PFPhilipp Fruhmann
Philipp Fruhmann
GWGerlinde Wiesenberger
Gerlinde Wiesenberger
BKBernhard Kluger
Bernhard Kluger
BSBojan Sarkanj
Bojan Sarkanj
RSRainer Schuhmacher
Rainer Schuhmacher

Abstract

We report the identification of deoxynivalenol-3-sulfate and deoxynivalenol-15-sulfate as two novel metabolites of the trichothecene mycotoxin deoxynivalenol in wheat. Wheat ears which were either artificially infected with Fusarium graminearum or directly treated with the major Fusarium toxin deoxynivalenol (DON) were sampled 96 h after treatment. Reference standards, which have been chemically synthesized and confirmed by NMR, were used to establish a liquid chromatography-electrospray ionization (LC-ESI)-MS/MS-based “dilute and shoot” method for the detection, unambiguous identification, and quantification of both sulfate conjugates in wheat extracts. Using this approach, detection limits of 0.003 mg/kg for deoxynivalenol-3-sulfate and 0.002 mg/kg for deoxynivalenol-15-sulfate were achieved. Matrix-matched calibration was used for the quantification of DON-sulfates in the investigated samples. In DON-treated samples, DON-3-sulfate was detected in the range of 0.29–1.4 mg/kg fresh weight while DON-15-sulfate concentrations were significantly lower (range 0.015–0.061 mg/kg fresh weight). In Fusarium-infected wheat samples, DON-3-sulfate was the only detected sulfate conjugate (range 0.022–0.059 mg/kg fresh weight). These results clearly demonstrate the potential of wheat to form sulfate conjugates of DON. In order to test whether sulfation is a detoxification reaction in planta, we determined the ability of the sulfated DON derivatives to inhibit in vitro protein synthesis of wheat ribosomes. The results demonstrate that both DON-sulfates can be regarded as detoxification products. DON-15-sulfate was about 44× less inhibitory than the native toxin, and no toxicity was observed for DON-3-sulfate in the tested range.

ᅟ