Science communication in bioengineering and biotechnology: Active and collaborative learning project

In a society increasingly dependent on science and technology, the need to equip our students with the most varied digital and communication skills is crucial. Active and collaborative learning among peers is essential for the acquisition of transversal skills. Communication is one of the main tools that the Engineer uses to reach his target audience. Science Communication in Bioengineering and Biotechnology (CCBioTec) is a project on Innovation and Development of Teaching and Learning supported by Center IDEA-UMinho, a structure that emerges to promote and value Innovation and Development of Teaching and Learning at the University of Minho. CCBioTec is transversal to a set of Learning Units (LU) under the responsibility of the Department of Biological Engineering (DEB), including one LU of each year of the Integrated Masters in Biological Engineering and in Biomedical Engineering. The main goals of CCBioTEc are: to foster the awareness of the DEB educational community on the importance of science communication, as well as to develop science communication skills, through the production of short videos (pitches) displaying the explanation, in a simple and dynamic way, of complex concepts of Bioengineering and Biotechnology related with the curricula of each LU. CCBioTec started in the second semester of 2020/21, and it will go on in the 1st semester of 2021/22. The project was designed to be implemented according to the following steps: 1 - Technical and pedagogical training of teachers; 2 - Technical training of students involved in the project - Week CCBioTEC-2021; 3 - Development of materials for Science Communication in Bioengineering and Biotechnology; 4 - CCBioTec-2021 competition. In CCBioTec, teachers presenting himself as a mediator/facilitator of learning, boosting students development of transversal skills, collaborative work, decision making and the expression of ideas, together with the acquisition of knowledge foreseen in the curricular contents of the LU.(undefined)info:eu-repo/semantics/publishedVersio

Ciência na Ponta dos Dedos: Scientific Activities for Children under 10

In the context of the “Projeto” of the 3rd year of “Licenciatura em Biologia Aplicada” it was proposed to develop experimental activities connected with science for 1st to 4th grade students. This initiative was named Ciência na Ponta dos Dedos and was presented in the scope of “Festa da Ciência 2014”, an event of the Escola de Ciências of Universidade do Minho, which happens every year during May (and lasted this year from 12th to 14th of May). The first edition of Ciência na Ponta dos Dedos was offered to 1st grade students (6-7 years old). A mini laboratory where children could see, try and participate in scientific hands-on activities was created for the initiative. The experimental activities were designed and settled in accordance with curricular guidelines, age [1,2,3] and in the scope of the theme “water source of life” through the development of six different activities where the children, organized in groups, had the opportunity to explore aspects connected with the (i) reaction of an acid with sodium bicarbonate in water, (ii) dissolution of different substances in water,(iii) permeability of different soils, (iv) water cycle through the observation of a mini ecosystem, (v) observation on the microscope of the stoma of the plants and (vi) the colouring of carnations by capillarity using several dyes. These activities were carried out in such an environment that kids’ eyes had light up as brightly when doing the science lab activities Children could feel free to express their ideas and participate in the activities to build applicable knowledge in the context of experimental science. This kind of learning comes easier to children if they can touch and make the experiments by themselves, though with a proper supervision, allowing the children to think and to learn that “if I do this, that will happen“, so “in order that to happen, I will have to make this” [2]. In the sequence of these experimental activities, children were asked to fill in an inquiry, previously prepared in order to know their opinion about the activities they performed, including their favourite ones. This survey will also provide some new ideas to improve future similar events.The present communication intends to present the project and its success near the children and their teachers, as well as to highlight the importance of scientific knowledge. Quoting some children: “the activities were very funny and I learned new things”, “I learned why oil does not mix with water” and “I learned that the noses of the plants are in their leaves”. In a developing society it is more and more important that the education system makes science stand out from the early years of school in order to form citizens able to deal efficiently with the challenges and the necessities of the current society [2].info:eu-repo/semantics/publishedVersio

Fluorescence studies on new potential antitumoral 1,3-diarylurea derivatives in the thieno[3,2-b]pyridine series encapsulated in magnetoliposomes

Magnetic nanoparticles of magnetite and of nickel core with silica shell were prepared and either covered with a lipid bilayer or entrapped in liposomes, forming magnetoliposomes. New potential antitumoral 1,3-diarylurea derivatives of thieno[3,2-b]pyridines were then encapsulated in liposomes and magnetoliposomes and their photophysical behavior was investigated.Fundação para a Ciência e a Tecnologia (FCT), FEDER, COMPETE/QREN/EU for financial support to CFUM (PEst-C/FIS/UI0607/2011) and CQ/UM (PEst-C/QUI/UI0686/2011) and to research projects PTDC/QUI/81238/2006 (FCOMP-01-0124-FEDER-007467), PTDC/QUIQUI/111060/2009 (FCOMP-01-0124-FEDER-015603)

Synthesis of novel 1-Aryl-3-[2-,3- Or 4-(Thieno[3,2-b]Pyridin-7-Ylthio)Phenyl]Ureas and evaluation as VEGFR2 Tyrosine kinase inhibitors

Vascular endothelial growth factor receptor 2 (VEGFR2) tyrosine kinase is involved in cancer and in angiogenesis. Herein, we report the synthesis of novel1-aryl-3-[2-, 3- or 4-{thieno[3,2-b ]pyridin-7-ylthio) phenyl]ureas as VEGFR2 inhibitors by promoting the regioselective attack of the thiol group of the 4-aminothiophenol in the chlorine nucleophilic displacement on 7-chlorothieno[3,2-b]pyridine 1, obtaining the aminated compounds Za- c. These were reacted with arylisocyanates to give the corresponding 1,3-diarylureas 3a-c, 4a-c and Sa-c (see scheme).Foundation for the Science and Technology (FCT–Portugal) for financial support through the NMR Portuguese network (Bruker 400 Avance III-Univ Minho). FCT and FEDER (European Fund for Regional Development)-COMPETE/QREN/EU for financial support through the research unities PEst-C/QUI/UI686/2011 and PEst-OE/AGR/UI0690/2011, the research project PTDC/QUI- QUI/111060/2009 and the post-Doctoral grant attributed to R.C.C. (SFRH/BPD/68344/2010

Key initiatives to successfully manage collaborative university-industry R&D: IC-HMI case study

This paper describes the results of a qualitative study to identify the key management initiatives in a successful university-industry (UI) collaborative funded program between the University of Minho (UMinho) and Bosch Car Multimedia Portugal (Bosch), named IC-HMI. The IC-HMI program embraced an overall investment of 54.7 M€ and involved around 500 people throughout the Program's duration (2015-2018). While the literature provides some advice on managing programs and projects, the specific context of UI R&D collaboration is being scarcely reported, demanding a strong research effort to produce effective guidelines. The IC-HMI is considered a successful program for several reasons, as evidenced by the decision of UMinho and Bosch partners to develop a subsequent R&D collaborative program from 2018 to 2021, doubling its investment. The success attained with the IC-HMI program could be somehow explained by key management initiatives adopted, such as the: creation of Program and Project Management Office, definition and communication of a Governance Model, creation of Project Charters, promotion of Alignment Stakeholders Workshops, Project Progress Meetings and creation of Project Transition Plans, among other key initiatives reported in this paper.This research is sponsored by the Fundação para a Ciência e a Tecnologia FCT (SFRH/BPD/111033/2015), and by the Portugal Incentive System for R&D. Project in co-promotion nº 039479/2018 (FoF 2018-2021)

Repurposing of statins for Buruli Ulcer treatment: antimicrobial activity against Mycobacterium ulcerans

Mycobacterium ulcerans causes Buruli Ulcer, a neglected infectious skin disease that typically progresses from an early non-ulcerative lesion to an ulcer with undermined edges. If not promptly treated, these lesions can lead to severe disfigurement and disability. The standard antibiotic regimen for Buruli Ulcer treatment has been oral rifampicin combined with intramuscular streptomycin administered daily for 8 weeks. However, there has been a recent shift toward replacing streptomycin with oral clarithromycin. Despite the advantages of this antibiotic regimen, it is limited by low compliance, associated side effects, and refractory efficacy for severe ulcerative lesions. Therefore, new drug candidates with a safer pharmacological spectrum and easier mode of administration are needed. Statins are lipid-lowering drugs broadly used for dyslipidemia treatment but have also been reported to have several pleiotropic effects, including antimicrobial activity against fungi, parasites, and bacteria. In the present study, we tested the susceptibility of M. ulcerans to several statins, namely atorvastatin, simvastatin, lovastatin and fluvastatin. Using broth microdilution assays and cultures of M. ulcerans-infected macrophages, we found that atorvastatin, simvastatin and fluvastatin had antimicrobial activity against M. ulcerans. Furthermore, when using the in vitro checkerboard assay, the combinatory additive effect of atorvastatin and fluvastatin with the standard antibiotics used for Buruli Ulcer treatment highlighted the potential of statins as adjuvant drugs. In conclusion, statins hold promise as potential treatment options for Buruli Ulcer. Further studies are necessary to validate their effectiveness and understand the mechanism of action of statins against M. ulcerans

New 1,3-diarylureas linked by C-C Suzuki coupling to the methyl 3-aminothieno[3,2-b]pyridine-2-carboxylate moiety: synthesis and fluorescence studies in solution and in lipid membranes

New six fluorescent 1,3-diarylureas linked by C-C Suzuki coupling to the 6-position of the methyl 3-aminothieno[3,2-b]pyridine-2-carboxylate moiety were prepared by reaction of the amino groups on the ortho or meta positions relative to the C-C bond of the Suzuki coupling products, with different para-substituted arylisocyanates (H, OMe, CN), in high to excellent yields. The fluorescence properties of the 1,3-diarylureas in solution and in lipid membranes of egg-yolk phosphatidylcholine (Egg-PC), dipalmitoyl phosphatidylcholine (DPPC), dipalmitoyl phosphatidylglycerol (DPPG) or dioctadecyldimethylammonium bromide (DODAB), with or without cholesterol (Ch), were studied. The six 1,3-diarylureas have reasonable fluorescence quantum yields in several solvents (between 0.02 and 0.69) and present a moderately solvent sensitive emission, but are not fluorescent in alcohols and water. The compounds bearing the arylurea moiety in the meta position relative to the C-C bond, especially with the OMe and CN substituents, present the better solvatochromic properties. Incorporation of the six compounds in lipid membranes indicates that all the compounds are deeply located in the hydrophobic region of the lipid bilayers, feeling the transition between the rigid gel phase and fluid phases.To the Foundation for the Science and Technology (FCT, Portugal) for inancial support to the NMR portuguese network (PTNMR, Bruker Avance III 400-Univ. Minho). To the FCT and FEDER (European Fund for Regional Development)-COMPETE-QREN-EU for financial support to the Research Centres, CQ/UM [PEst-C/QUI/UI0686/2011 (FCOMP-01-0124-FEDER-022716)] and CFUM [PEst-C/FIS/UI0607/2011 (F-COMP-01-0124-FEDER-022711)], and to the research projects PTDC/QUI/81238/2006 (FCOMP-01-0124-FEDER-007467) (photophysical studies) and PTDC/QUI-QUI/111060/2009 (F-COMP-01-0124-FEDER-015603) (organic synthesis)

Synthesis, antiangiogenesis evaluation and molecular docking studies of 1-Aryl-3-[(thieno[3,2-b]pyridin-7-ylthio)phenyl]ureas: Discovery of a new substitution pattern for type II VEGFR-2 Tyr kinase inhibitors

The synthesis and biological evaluation of novel 1-aryl-3-[2-, 3- or 4-(thieno[3,2-b]pyridin-7-ylthio)phenyl]ureas 3, 4 and 5 as VEGFR-2 tyrosine kinase inhibitors, are reported. The 1-aryl-3-[3-(thieno[3,2-b]pyridin-7-ylthio)phenyl]ureas 4a-4h, with the arylurea in the meta position to the thioether, showed the lowest IC50 values in enzymatic assays (10-206 nM), the most potent compounds 4d-4h (IC50 10-28 nM) bearing hydrophobic groups (Me, F, CF3 and Cl) in the terminal phenyl ring. A convincing rationalization was achieved for the highest potent compounds 4 as type II VEGFR-2 inhibitors, based on the simultaneous presence of: (1) the thioether linker and (2) the arylurea moiety in the meta position. For compounds 4, significant inhibition of Human Umbilical Vein Endothelial Cells (HUVECs) proliferation (BrdU assay), migration (wound-healing assay) and tube formation were observed at low concentrations. These compounds have also shown to increase apoptosis using the TUNEL assay. Immunostaining for total and phosphorylated (active) VEGFR-2 was performed by Western blotting. The phosphorylation of the receptor was significantly inhibited at 1.0 and 2.5 microM for the most promising compounds. Altogether, these findings point to an antiangiogenic effect in HUVECs.To the Foundation for Science and Technology (FCT–Portugal) for financial support through the NMR Portuguese network (Bruker 400 Avance III-Univ Minho). FCT and FEDER (European Fund for Regional Development)-COMPETE/QREN/EU for financial support through the research unities PEst-C/QUI/UI686/2013-2014, PEst-OE/SAU/UI0038/2013 and 2014 and PEst OE/AGR/UI0690/2013 and 2014, the research project PTDC/QUI-QUI/111060/2009, the PhD grant attributed to V.M. (SFRH/BD/77373/2011) and the post-Doctoral grant attributed to R.C.C. (SFRH/BPD/68344/2010), also financed by the POPH and FSE