Bernhard Hiebl

Prof. Dr. Bernhard Hiebl

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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 2010 in Expert Review of Medical Devices
Verified
Journal Article
Closed access
ALAndreas Lendlein
Andreas Lendlein
MBMarc Behl
Marc Behl
BHBernhard Hiebl
Bernhard Hiebl
CWChristian Wischke
Christian Wischke
Polymeric materials are clinically required for medical devices, as well as controlled drug delivery systems. Depending on the application, the polymer has to provide suitable functionalities, for example, mechanical functions or the capability to actively move, so that an implant can be inserted in a compact shape through key-hole incisions and unfold to its functional shape in the body. Shape-memory polymers, as described herein regarding their general principle, compositions and architectures, have developed to a technology platform that allows the tailored design of such multifunctionality. In this way, defined movements of implants triggered either directly or indirectly, tailored mechanical properties, capability for sterilization, biodegradability, biocompatibility and controlled drug release can be realized. This comprehensive review of the scientific and patent literature illustrates that this technology enables the development of novel medical devices that will be clinically evaluated in the near future.

1 January 2017 in Experimental Gerontology
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Journal Article
Closed access
BBBabett Bartling
Babett Bartling
SASamiya Al-Robaiy
Samiya Al-Robaiy
HLHolger Lehnich
Holger Lehnich
LBLeonore Binder
Leonore Binder
BHBernhard Hiebl
Bernhard Hiebl
ASAndreas Simm
Andreas Simm

1 January 2011 in Clinical Hemorheology and Microcirculation
Verified
Journal Article
Closed access
PDF file
FJFriedrich Jung
Friedrich Jung
CMC. Mrowietz
C. Mrowietz
BHBernhard Hiebl
Bernhard Hiebl
RFR.P. Franke
R.P. Franke
GPG. Pindur
G. Pindur
RSR. Sternitzky
R. Sternitzky
One thousand two hundred and fifty-six subjects (apparently healthy subjects and patients with cardiovascular diseases) were registered in a prospective study including demographical and clinical data, rheological parameters (hematocrit, plasma viscosity, erythrocyte aggregation, erythrocyte deformability) as well as the erythrocyte velocity in human nailfold capillaries under resting and postischemic conditions. A multivariate regression analysis showed that under resting conditions there was no correlation between rheological parameters and erythrocyte velocity in capillaries. The blood flow regulation seemed to be so effective, that pathological changes of the blood fluidity showed no effect on the velocity of an erythrocyte passing the capillaries. During vessel paralysis in the early phase of the postischemic hyperemia following a stasis of three minutes in the vasculature distal to a pressure cuff at the upper arm a very clear correlation between the plasma viscosity and the maximum postischemic erythrocyte velocity in ipsilateral cutaneous capillaries could be observed (p < 0.0001) while none of the other rheological parameters seemed to play a role. In a subgroup of diabetic patients the erythrocyte aggregation (measured during stasis) also correlated with the erythrocyte velocity (p = 0.0175) besides the plasma viscosity. This shows that a correlation of rheological parameters with the capillary perfusion could only be found during vessel paralysis. In of diabetic patients besides the plasma viscosity also the erythrocyte aggregation correlated with the mean capillary erythrocyte velocity. Theses results are in agreement with the hypothesis from Barras that plasma viscosity determines the perfusion of microvessels. Under certain conditions e.g. diabetic disorder, also the erythrocyte aggregation plays a role.

12 April 2019 in PLOS ONE
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Journal Article
Open access
PDF file
SMSinja Mertens
Sinja Mertens
MVMiriam Vogt
Miriam Vogt
PGPeter Gass
Peter Gass
RPRupert Palme
Rupert Palme
BHBernhard Hiebl
Bernhard Hiebl
SCSabine Chourbaji
Sabine Chourbaji
Mice are social animals hence group-housing of mice is preferred over individual housing. However, aggression in group-housed male mice under laboratory housing conditions is a well-known problem leading to serious health issues, including injury or death. Therefore, group-housed mice are frequently separated for welfare reasons. In this study, we investigated the effect of 3 different handling methods (tail, forceps, tube) in 2 different housing conditions (single vs. group) on the variance of aggression-associated parameters in male C57BL/6NCrl mice over 8 weeks. Blood glucose concentration, body weight, body temperature, plus number and severity of bite wounds and barbering intensity in group-housed mice were recorded. An assessment of nest complexity was also performed weekly. Feces were collected in week 3 and 7 for analysis of corticosterone metabolites. We also monitored the level of aggression by recording the behavior of group-housed animals after weekly cage cleaning. An open field test followed by a social novel object test, a light/dark box test, a hotplate and a resident-intruder test were performed at the end of the 8-week handling period. Post-mortem, we assessed organ weights. We found that forceps-handled mice, independent of the housing condition, had significantly higher levels of stress-induced-hyperthermia and enhanced aggression after cage cleaning, and they performed worse in the nest complexity test. In addition, handling male mice by the tail seems to be most effective to reduce aggressiveness after transferring animals into new cages, thereby representing an appropriate refinement.

24 August 2010 in Journal of Materials Chemistry
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Journal Article
Closed access
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NSNico Scharnagl
Nico Scharnagl
SLSeahyoung Lee
Seahyoung Lee
BHBernhard Hiebl
Bernhard Hiebl
ASAdam Sisson
Adam Sisson
ALAndreas Lendlein
Andreas Lendlein
The next generation of biomaterials for regenerative therapies requires the development of substances, which are able to influence and activate specific phenotype characteristics of cells and tissues. Research towards this aim has resulted in an increasing number of reports about material induced cellular functions and cell-cell interactions. In this context, polymeric materials, which are not intended to degrade can provide helpful in-vitro tools to gain more detailed knowledge about the cell-substrate crosstalk and the resulting cell specific effects. This review aims to consolidate current strategies to induce specific effects on adhesive cells which are related to defined characteristics of two-dimensional systems starting with the molecular dimension, following up with the nanostructure and ending with the surface microstructure. This includes approaches to induce direct or indirect biological responses towards cells by systematic changes in material properties such as hydrophilicity or elasticity. These properties are explained as a function of chemical composition such as the type and ratio of copolymers used for linear polymers, or the geometric arrangement of branching points for network polymer architectures. Surface topographical features are identified to strongly influence cell-substrate interactions and techniques are described to control the surface patterning of polymeric materials on the nano- or microscale. Finally we offer a strategy on how to develop complex and multifunctional materials, which might fulfill the requirements of cell and tissue adapted biomaterials for regenerative therapies.

3 January 2011 in The International Journal of Artificial Organs
Verified
Journal Article
Closed access
SPSusanna Piluso
Susanna Piluso
BHBernhard Hiebl
Bernhard Hiebl
SGStanislav N. Gorb
Stanislav N. Gorb
AKAlexander Kovalev
Alexander Kovalev
ALAndreas Lendlein
Andreas Lendlein
ANAxel T. Neffe
Axel T. Neffe
Biopolymers of the extracellular matrix are attractive starting materials for providing degradable and biocompatible biomaterials. In this study, hyaluronic acid-based hydrogels with tunable mechanical properties were prepared by the use of copper- catalyzed azide-alkyne cycloaddition (known as “click chemistry”). Alkyne-functionalized hyaluronic acid was crosslinked with linkers having two terminal azide functionalities, varying crosslinker density as well as the lengths and rigidity of the linker molecules. By variation of the crosslinker density and crosslinker type, hydrogels with elastic moduli in the range of 0.5–4 kPa were prepared. The washed materials contained a maximum of 6.8 mg copper per kg dry weight and the eluate of the gel crosslinked with diazidostilbene did not show toxic effects on L929 cells. The hyaluronic acid-based hydrogels have potential as biomaterials for cell culture or soft tissue regeneration applications.