6 research outputs found

    Improving MRI-based Knee Disorder Diagnosis with Pyramidal Feature Details

    Get PDF
    This paper presents MRPyrNet, a new convolutional neural network (CNN) architecture that improves the capabilities of CNN-based pipelines for knee injury detection via magnetic resonance imaging (MRI). Existing works showed that anomalies are localized in small-sized knee regions that appear in particular areas of MRI scans. Based on such facts, MRPyrNet exploits a Feature Pyramid Network to enhance small appearing features and Pyramidal Detail Pooling to capture such relevant information in a robust way. Experimental results on two publicly available datasets demonstrate that MRPyrNet improves the ACL tear and meniscal tear diagnosis capabilities of two state-of-the-art methodologies. Code is available at https://git.io/JtMPH

    Proceedings of the Scientific-Practical Conference "Research and Development - 2016"

    Get PDF
    talent management; sensor arrays; automatic speech recognition; dry separation technology; oil production; oil waste; laser technolog

    Proceedings of the Scientific-Practical Conference "Research and Development - 2016"

    Get PDF
    talent management; sensor arrays; automatic speech recognition; dry separation technology; oil production; oil waste; laser technolog

    [<sup>18</sup>F]fluorination of biorelevant arylboronic acid pinacol ester scaffolds synthesized by convergence techniques

    Get PDF
    Aim: The development of small molecules through convergent multicomponent reactions (MCR) has been boosted during the last decade due to the ability to synthesize, virtually without any side-products, numerous small drug-like molecules with several degrees of structural diversity.(1) The association of positron emission tomography (PET) labeling techniques in line with the “one-pot” development of biologically active compounds has the potential to become relevant not only for the evaluation and characterization of those MCR products through molecular imaging, but also to increase the library of radiotracers available. Therefore, since the [18F]fluorination of arylboronic acid pinacol ester derivatives tolerates electron-poor and electro-rich arenes and various functional groups,(2) the main goal of this research work was to achieve the 18F-radiolabeling of several different molecules synthesized through MCR. Materials and Methods: [18F]Fluorination of boronic acid pinacol esters was first extensively optimized using a benzaldehyde derivative in relation to the ideal amount of Cu(II) catalyst and precursor to be used, as well as the reaction solvent. Radiochemical conversion (RCC) yields were assessed by TLC-SG. The optimized radiolabeling conditions were subsequently applied to several structurally different MCR scaffolds comprising biologically relevant pharmacophores (e.g. β-lactam, morpholine, tetrazole, oxazole) that were synthesized to specifically contain a boronic acid pinacol ester group. Results: Radiolabeling with fluorine-18 was achieved with volumes (800 μl) and activities (≤ 2 GBq) compatible with most radiochemistry techniques and modules. In summary, an increase in the quantities of precursor or Cu(II) catalyst lead to higher conversion yields. An optimal amount of precursor (0.06 mmol) and Cu(OTf)2(py)4 (0.04 mmol) was defined for further reactions, with DMA being a preferential solvent over DMF. RCC yields from 15% to 76%, depending on the scaffold, were reproducibly achieved. Interestingly, it was noticed that the structure of the scaffolds, beyond the arylboronic acid, exerts some influence in the final RCC, with electron-withdrawing groups in the para position apparently enhancing the radiolabeling yield. Conclusion: The developed method with high RCC and reproducibility has the potential to be applied in line with MCR and also has a possibility to be incorporated in a later stage of this convergent “one-pot” synthesis strategy. Further studies are currently ongoing to apply this radiolabeling concept to fluorine-containing approved drugs whose boronic acid pinacol ester precursors can be synthesized through MCR (e.g. atorvastatin)
    corecore