Publications by authors named "J Leban"

The curvature of the lumbar spine plays a critical role in maintaining spinal function, stability, weight distribution, and load transfer. We have developed a mathematical model of the lumbar spine curve by introducing a novel mechanism: minimization of the elastic bending energy of the spine with respect to two biomechanical parameters: dimensionless lumbosacral spinal curvature and dimensionless curvature increment along the spine CI. While most of the biomechanical studies focus on a particular segment of the spine, the distinction of the presented model is that it describes the shape of the thoracolumbar spine by considering it as a whole (non-locally) and thus includes interactions between the different spinal levels in a holistic approach.

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As a part of the biogeochemical cycle, nutrient translocation plays an important role in enhancing the capacity of perennial plants to grow in nutrient-poor soils. Although leaf translocation has been extensively studied, nutrient translocation between wood rings has received considerably less attention, primarily because of methodological constraints. This study aimed to (i) evaluate the effects of different drying techniques on Ca, K, and Mn concentrations, (ii) calibrate a semi-quantitative method for obtaining ring-to-ring nutrient concentrations along wood cores, and (iii) develop a complete calculation chain for nutrient translocation.

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Large-scale syntheses of small molecules and kilo laboratories are crucial steps in drug development, especially in advanced stages. ()-5-((Benzhydrylsulfinyl)methyl)thiazole, ()-CE-123, a potent, selective, and novel atypical DAT inhibitor, has undergone iterative testing as part of the preclinical evaluation step. This required the process transfer, scale-up, and synthesis of a 1 kg preclinical batch.

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Article Synopsis
  • The structural similarities among dopamine, norepinephrine, and serotonin transporters complicate the targeted design of individual transporter inhibitors.
  • Many chemists limit ligand development by reducing chiral centers in compounds, which hinders potential effectiveness.
  • This study highlights the benefits of increasing molecular complexity and using stereoisomers to enhance the selectivity and potency of dopamine transporter inhibitors, while also emphasizing the importance of validating these compounds in vivo.
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The worldwide increase in cognitive decline, both in aging and with psychiatric disorders, warrants a search for pharmacological treatment. Although dopaminergic treatment approaches represent a major step forward, current dopamine transporter (DAT) inhibitors are not sufficiently specific as they also target other transporters and receptors, thus showing unwanted side effects. Herein, we describe an enantiomerically pure, highly specific DAT inhibitor, S-CE-123, synthetized in our laboratory.

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