Anders E. Daugaard

Dr. Anders E. Daugaard

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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4 January 2019 in Environmental Science & Technology
Verified
Journal Article
Closed access
Nanna B. HartmannNanna B. Hartmann
Nanna B. Hartmann
THThorsten Hüffer
Thorsten Hüffer
RTRichard C. Thompson
Richard C. Thompson
MHMartin Hassellöv
Martin Hassellöv
AVAnja Verschoor
Anja Verschoor
MWMartin Wagner
Martin Wagner

15 January 2016 in Macromolecular Rapid Communications
Verified
Journal Article
Closed access
PDF file
FMFrederikke B. Madsen
Frederikke B. Madsen
ADAnders E. Daugaard
Anders E. Daugaard
SHSøren Hvilsted
Søren Hvilsted
ASAnne Skov
Anne Skov


1 June 2018 in International Journal of Nanomedicine
Verified
Journal Article
Open access
PSPriyanka Singh
Priyanka Singh
SPSantosh Pandit
Santosh Pandit
JGJørgen Garnæs
Jørgen Garnæs
STSanja Tunjic
Sanja Tunjic
VMVenkata Mokkapati
Venkata Mokkapati
Ivan MijakovicIvan Mijakovic
Ivan Mijakovic
Cannabis sativa (hemp) is a source of various biologically active compounds, for instance, cannabinoids, terpenes and phenolic compounds, which exhibit antibacterial, antifungal, anti-inflammatory and anticancer properties. With the purpose of expanding the auxiliary application of C. sativa in the field of bio-nanotechnology, we explored the plant for green and efficient synthesis of gold nanoparticles (AuNPs) and silver nanoparticles (AgNPs). The nanoparticles were synthesized by utilizing an aqueous extract of C. sativa stem separated into two different fractions (cortex and core [xylem part]) without any additional reducing, stabilizing and capping agents. In the synthesis of AuNPs using the cortex enriched in bast fibers, fiber-AuNPs (F-AuNPs) were achieved. When using the core part of the stem, which is enriched with phenolic compounds such as alkaloids and cannabinoids, core-AuNPs (C-AuNPs) and core-AgNPs (C-AgNPs) were formed. Synthesized nanoparticles were character-ized by UV–visible analysis, transmission electron microscopy, atomic force microscopy, dynamic light scattering, Fourier transform infrared, and matrix-assisted laser desorption/ionization time-of-flight. In addition, the stable nature of nanoparticles has been shown by thermogravimetric analysis and inductively coupled plasma mass spectrometry (ICP-MS). Finally, the AgNPs were explored for the inhibition of Pseudomonas aeruginosa and Escherichia coli biofilms. The synthesized nanoparticles were crystalline with an average diameter between 12 and 18 nm for F-AuNPs and C-AuNPs and in the range of 20–40 nm for C-AgNPs. ICP-MS analysis revealed concentrations of synthesized nanoparticles as 0.7, 4.5 and 3.6 mg/mL for F-AuNPs, C-AuNPs and C-AgNPs, respectively. Fourier transform infrared spectroscopy revealed the presence of flavonoids, cannabinoids, terpenes and phenols on the nanoparticle surface, which could be responsible for reducing the salts to nanoparticles and further stabilizing them. In addition, the stable nature of synthesized nanoparticles has been shown by thermogravimetric analysis and ICP-MS. Finally, the AgNPs were explored for the inhibition of P. aeruginosa and E. coli biofilms. The nanoparticles exhibited minimum inhibitory concentration values of 6.25 and 5 µg/mL and minimum bactericidal concentration values of 12.5 and 25 µg/mL against P. aeruginosa and E. coli, respectively.

12 November 2018 in Artificial Cells, Nanomedicine, and Biotechnology
Verified
Journal Article
Closed access
Priyanka SinghPriyanka Singh
Priyanka Singh
SPSantosh Pandit
Santosh Pandit
MBMariam Beshay
Mariam Beshay
VMV.R.S.S. Mokkapati
V.R.S.S. Mokkapati
JGJørgen Garnaes
Jørgen Garnaes
Ivan MijakovicIvan Mijakovic
Ivan Mijakovic
Bacterial biofilm represents a major problem in medicine. They colonize and damage medical devices and implants and, in many cases, foster development of multidrug-resistant microorganisms. Biofilm development starts by bacterial attachment to the surface and the production of extracellular polymeric substances (EPS). The EPS forms a structural scaffold for dividing bacterial cells. The EPS layers also play a protective role, preventing the access of antibiotics to biofilm-associated microorganisms. The aim of this work was to investigate the production nanoparticles that could be used to inhibit biofilm formation. The applied production procedure from rhizome extracts of Rhodiola rosea is simple and environmentally friendly, as it requires no additional reducing, stabilizing and capping agents. The produced nanoparticles were stable and crystalline in nature with an average diameter of 13–17 nm for gold nanoparticles (AuNPs) and 15–30 nm for silver nanoparticles (AgNPs). Inductively coupled plasma mass spectrometry analysis revealed the concentration of synthesized nanoparticles as 3.3 and 5.3 mg/ml for AuNPs and AgNPs, respectively. Fourier-transform infrared spectroscopy detected the presence of flavonoids, terpenes and phenols on the nanoparticle surface, which could be responsible for reducing the Au and Ag salts to nanoparticles and further stabilizing them. Furthermore, we explored the AgNPs for inhibition of Pseudomonas aeruginosa and Escherichia coli biofilms. AgNPs exhibited minimum inhibitory concentrations of 50 and 100 µg/ml, against P. aeruginosa and E. coli, respectively. The respective minimum bactericidal concentrations were 100 and 200 µg/ml. These results suggest that using the rhizome extracts of the medicinal plant R. rosea represents a viable route for green production of nanoparticles with anti-biofilm effects. A schematic representation of the green synthesis, characterization and biofilm inhibition application of nanoparticles produced by extracts of R. rosea.

11 May 2016 in Polymer International
Verified
Journal Article
Closed access
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Jon TrifolJon Trifol
Jon Trifol
DPDavid Plackett
David Plackett
CSCecile Sillard
Cecile Sillard
PSPeter Szabo
Peter Szabo
JBJulien Bras
Julien Bras
ADAnders E. Daugaard
Anders E. Daugaard