Marc Pignitter

Prof. Dr. Marc Pignitter

Physiological Chemistry, Faculty of Chemistry, University of Vienna
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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26 March 2013 in Journal of Agricultural and Food Chemistry
Verified
Journal Article
Closed access
MEMiriam M. Ehrnhöfer-Ressler
Miriam M. Ehrnhöfer-Ressler
KFKristina Fricke
Kristina Fricke
Marc PignitterMarc Pignitter
Marc Pignitter
JWJoel M. Walker
Joel M. Walker
JWJessica Walker
Jessica Walker
VSVeronika Somoza
Veronika Somoza

1 June 2019 in LWT
Verified
Journal Article
Closed access
SGSilke Grosshagauer
Silke Grosshagauer
RSRaphael Steinschaden
Raphael Steinschaden
Marc PignitterMarc Pignitter
Marc Pignitter

26 June 2023 in Food Hydrocolloids
Verified
Journal Article
Closed access
CWChao Wu
Chao Wu
ZLZhe Liu
Zhe Liu
LZLanyi Zhi
Lanyi Zhi
BJBo Jiao
Bo Jiao
HHHui Hu
Hui Hu
Aimin ShiAimin Shi
Aimin Shi

26 March 2021 in Communications Earth & Environment
Verified
Journal Article
Open access
PDF file
GSGabriel Sigmund
Gabriel Sigmund
CSCristina Santín
Cristina Santín
Marc PignitterMarc Pignitter
Marc Pignitter
NTNathalie Tepe
Nathalie Tepe
SDStefan Doerr
Stefan Doerr
Thilo HofmannThilo Hofmann
Thilo Hofmann
Globally landscape fires produce about 256 Tg of pyrogenic carbon or charcoal each year. The role of charcoal as a source of environmentally persistent free radicals, which are precursors of potentially harmful reactive oxygen species, is poorly constrained. Here, we analyse 60 charcoal samples collected from 10 wildfires, that include crown as well as surface fires in forest, shrubland and grassland spanning different boreal, temperate, subtropical and tropical climate. Using electron spin resonance spectroscopy, we measure high concentrations of environmentally persistent free radicals in charcoal samples, much higher than those found in soils. Concentrations increased with degree of carbonization and woody fuels favoured higher concentrations. Moreover, environmentally persistent free radicals remained stable for an unexpectedly long time of at least 5 years. We suggest that wildfire charcoal is an important global source of environmentally persistent free radicals, and therefore potentially of harmful reactive oxygen species.

26 August 2022 in Nanomaterials
Verified
Journal Article
Open access
PDF file
CWChao Wu
Chao Wu
ZLZhe Liu
Zhe Liu
LZLanyi Zhi
Lanyi Zhi
BJBo Jiao
Bo Jiao
YTYanjie Tian
Yanjie Tian
Aimin ShiAimin Shi
Aimin Shi
High internal phase Pickering emulsion (HIPPE) is a type of emulsion stabilized by solid particles irreversibly adsorbed on an interfacial film, and the volume fraction of the dispersed phase (Φ) is larger than the maximum packing volume fraction (Φmax). Proteins, polysaccharides, and their composite particles can be used as good particle stabilizers. The contact angle can most intuitively demonstrate the hydrophilicity and hydrophobicity of the particles and also determines the type of emulsions (O/W or W/O type). Particles’ three-phase contact angles can be adjusted to about 90° by compounding or modification, which is more conducive to emulsion stability. As a shear thinning pseudoplastic fluid, HIPPE can be extruded smoothly through 3D printer nozzles, and its high storage modulus can support the structure of printed products. There is huge potential for future applications in 3D printing of food. This work reviewed the biomacromolecules that can be used to stabilize food-grade HIPPE, the stabilization mechanism of the emulsions, and the research progress of food 3D printing to provide a reference for the development of advanced food products based on HIPPE.

13 November 2013 in Food & Function
Verified
Journal Article
Closed access
PDF file
JWJessica Walker
Jessica Walker
KSKatharina Schueller
Katharina Schueller
LSLisa-Marie Schaefer
Lisa-Marie Schaefer
Marc PignitterMarc Pignitter
Marc Pignitter
LELaura Esefelder
Laura Esefelder
VSVeronika Somoza
Veronika Somoza
Resveratrol has been shown to exploit various biological activities, including an anti-inflammatory activity. However, resveratrol is metabolized by phase II enzymes post-absorption to predominantly form glucuronides and sulfates. To investigate the anti-inflammatory effects of resveratrol and its dominating sulfated and glucuronated metabolites formed in vivo, U-937 macrophages were chosen as an immune-competent model system, known to release cytokines upon lipopolysaccharide stimulation. U-937 cells were stimulated with lipopolysaccharides from Escherichia coli (E. coli-LPS) to evoke an inflammatory reaction, and pre- or co-incubated with 1 or 10 μM of resveratrol (RES), resveratrol-3-sulfate (R3S), resveratrol-disulfates (RDS), resveratrol-3-glucuronide or resveratrol-4′-glucuronide. Time dependent gene expression of IL-6, IL-1α/β and IL-1R by qPCR was studied at 1 h, 3 h, 6 h, 9 h, and 24 h of incubation, and the release of IL-6 and TNF-α, after 6 h was analysed by means of non-magnetic or magnetic bead analysis. As a result, 10 μM resveratrol completely inhibited the E. coli-LPS-induced release of IL-6, while resveratrol-3-sulfate and resveratrol-disulfates decreased it by respective 84.2 ± 29.4% and 52.3 ± 39.5%. Whereas TNF-α release was reduced by 48.1 ± 15.4%, 33.0 ± 10.0% and 46.7 ± 8.7% by RES, R3S and RDS, respectively. These results show that not only resveratrol but also resveratrol-3-sulfate and resveratrol-disulfates exhibit an anti-inflammatory potential by counteracting an inflammatory challenge in U-937 macrophages at plasma representative concentrations.