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New inhibitors of the PPAR beta/delta receptor

Novel substances are selective ligands which selectively inhibit PPAR receptors of the beta/delta subtype (PPAR: peroxisome proliferator-activated receptor) are offered for product develop-ment. The three well-known PPAR subtypes alpha, beta/delta and gamma regulate upon activation by ligands the activity of their respective target genes.

Production of photocatalytically active titanium dioxide surfaces with anatase content for e.g. biocompatible implants

Implantation technology allows the production of photocatalytically effective TiO2 in titanium or titanium alloy surfaces.

New bifunctional Prodrugs with cleavable linker for targeted tumor therapy (ADC)

Scientists at the University of Göttingen in Germany developed new and highly potent drugs with cleavable chemical linkers to develop tumor specific antibodies for selective tumor therapy (ADC). The soluble prodrugs are activated into highly cytotoxic drugs only in targeted tumor cells.

Quantum Simulation 2.0: Atoms Chat Long Distance

Simulations are a popular tool to study physical processes that cannot be investigated experimentally in detail. For example, scientists are challenged to…

PET-tracer-based visualization of the intensity and localization of peripheral longlasting pain

Pain is probably the most common symptom and sensation of a disease, and a big individual and socioeconomic challenge. Diagnostic tools are limited and do not result in clear mechanism-based insight into the etiology of the individual pain. PET-tracers are widely used as diagnostic and therapeutic tools in several types of cancer, besides other applications of visualization in various medical indications. However, there are so far only few reports, which utilize PET-tracer and PET-scan for the detection of pain (see references). The inventors have provided proof that an established PET-tracer for use in cancer can be also utilized for the detection of pain as a second medical application. They found this tracer to be enriched at the peripheral site of pain (see figure). The amount of tracer-enrichment strongly correlated with the measured change in pain sensitivity. On behalf of the University of Cologne and of the Witten/Herdecke University, PROvendis offers access to rights for commercial use as well as the opportunity for further co-development and evaluation.

Genetic coding of electron spin resonance markers

Electron spin resonance (ESR) spectroscopy provides data about the structure and dynamics of large molecules and permits the examination of biologically-relevant systems, which play a role in the regulation of the expression of illness-related genes. However, magnetic markings must be affixed to strategically-selected points of protein structures, because most biological structures do not contain unpaired electrons.
At the University of Konstanz, a molecular structure and the corresponding process were developed, with which the incorporation of ESR markers into peptide structures are largely independent of existing amino acid residues. The incorporation of the markers can be done specifically in any protein structure. The peptide structure experiences no essential changes, which makes an examination using ESR spectroscopy possible in intracellular and in vivo fashion.

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