Breakup dynamics and dripping-to-jetting transition in a Newtonian/shear-thinning multiphase microsystem

The breakup dynamics in non-Newtonian multiphase microsystems is associated with a variety of industrial applications such as food production and biomedical engineering. In this study, we numerically and experimentally characterize the dripping-to-jetting transition under various flow conditions in a Newtonian/shear-thinning multiphase microsystem. Our work can help to predict the formation of undesirable satellite droplets, which is one of the challenges in dispensing non-Newtonian fluids. We also demonstrate the variations in breakup dynamics between shear-thinning and Newtonian fluids under the same flow conditions. For shear-thinning fluids, the droplet size increases when the capillary number is smaller than a critical value, while it decreases when the capillary number is beyond the critical value. The variations highlight the importance of rheological effects in flows with a non-Newtonian fluid. The viscosity of shear-thinning fluids significantly affects the control over the droplet size, therefore necessitating the manipulation of the shear rate through adjusting the flow rate and the dimensions of the nozzle. Consequently, the droplet size can be tuned in a controlled manner. Our findings can guide the design of novel microdevices for generating droplets of shear-thinning fluids with a predetermined droplet size. This enhances the ability to fabricate functional particles using an emulsion-templated approach. Moreover, elastic effects are also investigated experimentally using a model shear-thinning fluid that also exhibits elastic behaviors: droplets are increasingly deformed with increasing elasticity of the continuous phase. The overall understanding in the model multiphase microsystem will facilitate the use of a droplet-based approach for non-Newtonian multiphase applications ranging from energy to biomedical sciences.postprin

Electromagnetic emissions from the IC packaging

The EMC and EMI of the IC packaging are becoming increasingly important to modern electronics. Its EMC, SI, and PI have been broadly attested. But electromagnetic radiations from IC packaging and the corresponding EMI were seldom studied. In this paper, the fundamental principles and properties of the electromagnetic radiations caused by vias and traces in IC packagings are carefully investigated. Various radiation mechanisms are analyzed for different representative scenarios. Numerical simulations are employed to support the analyzing results. © 2012 IEEE.published_or_final_versio

Electromagnetic emissions from the IC packaging

The EMC and EMI of the IC packaging are becoming increasingly important to modern electronics. Its EMC, SI, and PI have been broadly attested. But electromagnetic radiations from IC packaging and the corresponding EMI were seldom studied. In this paper, the fundamental principles and properties of the electromagnetic radiations caused by vias and traces in IC packagings are carefully investigated. Various radiation mechanisms are analyzed for different representative scenarios. Numerical simulations are employed to support the analyzing results. © 2012 IEEE.published_or_final_versio

Adaptação do Questionário de Autonomia nos Adolescentes (QAA) para a língua portuguesa

O presente estudo tem como objectivo principal apresentar a versão portuguesa do Questionário de Autonomia nos Adolescentes, traduzido e adaptado a partir do Adolescent Autonomy Questionnaire (Noom, 1999). De forma a observar as qualidades psicométricas da versão portuguesa procedeu-se à análise da estrutura factorial, análise da fidelidade, análise da sensibilidade e correlações inter- -factores. Os resultados obtidos com uma amostra de 171 adolescentes indicaram, através de análise factorial confirmatória, que o modelo original constituído por três dimensões não se revelou adequado à estrutura correlacional observada. Neste sentido, recorreu-se a uma análise exploratória que reproduziu uma estrutura composta por quatro factores – Auto-determinação; Independência; Autonomia cognitiva e Autonomia emocional. Em termos gerais, observaram-se indícios favoráveis à adequabilidade da presente versão do instrumento para a população adolescente portuguesa em contexto escolar. As diferenças observadas entre os participantes em função da idade (14-16 anos vs. 17-19 anos) são consistentes com os resultados obtidos nos estudos do instrumento original, fornecendo evidências adicionais favoráveis à validade da versão portuguesa.ABSTRACT: The present study aims to adapt and translate the Adolescent Autonomy Questionnaire (Noom, 1999) for the Portuguese context. In order to observe the psychometric qualities of the Portuguese version, the factorial structure, reliability, sensibility and inter-factor correlations were analyzed. Confirmatory factor analysis with a sample of 171 adolescents revealed that the original tridimensional model was not adequate to the observed correlacional structure. Subsequent exploratory factor analysis yielded a structure with four factors – Self-determination, Independence, Cognitive autonomy and Emotional Autonomy. Concerning the psychometric qualities, analysis provided evidences favorable to the suitability of the present version of the questionnaire for the Portuguese adolescent population in educational context. The differences observed between the participants regarding their age (14-16 years vs. 17-19 years) are consistent with the results found in the studies of the original questionnaire, providing additional evidences favorable to the validity of the Portuguese version

Thermal Assisted Oxygen Annealing for High Efficiency Planar CH3NH3PbI3 Perovskite Solar Cells

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Creation of Laryngeal Grafts from Primary Human Cells and Decellularized Laryngeal Scaffolds

Current reconstruction methods of the laryngotracheal segment fail to replace the complex functions of the human larynx. Bioengineering approaches to reconstruction have been limited by the complex tissue compartmentation of the larynx. We attempted to overcome this limitation by bio-engineering laryngeal grafts from decellularized canine laryngeal scaffolds recellularized with human primary cells under one uniform culture medium condition. First, we generated laryngeal scaffolds with preserved glycosaminoglycan content and biomechanical properties by detergent perfusion-decellularization over nine days. We proofed biocompatibility by absence of a CD3 lymphocyte response to subcutaneously implanted scaffolds in immune-competent rats. We then developed a uniform culture medium that strengthened the endothelial barrier over 5 days after an initial growth phase. Simultaneously, this culture medium supported airway epithelial cell and skeletal myoblast growth while maintaining their full differentiation and maturation potential. We then applied the uniform culture medium composition to whole laryngeal scaffolds seeded with endothelial cells from both carotid arteries and external jugular veins and generated re-endothelialized arterial and venous vascular beds. Under the same culture medium condition, we bio-engineered epithelial monolayers onto laryngeal mucosa and repopulated intrinsic laryngeal muscle. We were then able to demonstrate early muscle formation in heterotopic transplantations in immuno-deficient mice. The model supported the formation of three humanized laryngeal tissue compartments under one uniform culture condition, possibly a key factor in developing, complex, multicellular, ready-to-transplant tissue grafts

ITPKC Single Nucleotide Polymorphism Associated with the Kawasaki Disease in a Taiwanese Population

Kawasaki disease (KD) is characterized by systemic vasculitis with unknown etiology. Previous studies from Japan indicated that a gene polymorphism of ITPKC (rs28493229) is responsible for susceptibility to KD. We collected DNA samples from 1,531 Taiwanese subjects (341 KD patients and 1,190 controls) for genotyping ITPKC. In this study, no significant association was noted for the ITPKC polymorphism (rs28493229) between the controls and KD patients, although the CC genotype was overrepresented. We further combined our data with previously published case/control KD studies in the Taiwanese population and performed a meta-analysis. A significant association between rs28493229 and KD was found (Odds Ratio:1.36, 95% Confidence Interval 1.12–1.66). Importantly, a significant association was obtained between rs28493229 and KD patients with aneurysm formation (P = 0.001, under the recessive model). Taken together, our results indicated that C-allele of ITPKC SNP rs28493229 is associated with the susceptibility and aneurysm formation in KD patients in a Taiwanese population

Optically trapped bacteria pairs reveal discrete motile response to control aggregation upon cell–cell approach

Aggregation of bacteria plays a key role in the formation of many biofilms. The critical first step is cell–cell approach, and yet the ability of bacteria to control the likelihood of aggregation during this primary phase is unknown. Here, we use optical tweezers to measure the force between isolated Bacillus subtilis cells during approach. As we move the bacteria towards each other, cell motility (bacterial swimming) initiates the generation of repulsive forces at bacterial separations of ~3 μm. Moreover, the motile response displays spatial sensitivity with greater cell–cell repulsion evident as inter-bacterial distances decrease. To examine the environmental influence on the inter-bacterial forces, we perform the experiment with bacteria suspended in Tryptic Soy Broth, NaCl solution and deionised water. Our experiments demonstrate that repulsive forces are strongest in systems that inhibit biofilm formation (Tryptic Soy Broth), while attractive forces are weak and rare, even in systems where biofilms develop (NaCl solution). These results reveal that bacteria are able to control the likelihood of aggregation during the approach phase through a discretely modulated motile response. Clearly, the force-generating motility we observe during approach promotes biofilm prevention, rather than biofilm formation

Emergent heterogeneous microenvironments in biofilms: substratum surface heterogeneity and bacterial adhesion force-sensing

Phenotypically-heterogeneous micro-environments emerge as biofilms mature across different environments. Phenotypic-heterogeneity in biofilm sub-populations not obeying quorum sensing-dictated, collective group-behavior, may be considered as a strategy allowing non-conformists to survive hostile conditions. Heterogeneous phenotype development has been amply studied with respect to gene expression and genotypic changes, but 'biofilm genes' responsible for pre-programmed development of heterogeneous micro-environments in biofilms have never been discovered. Moreover, the question of what triggers the development of phenotypically-heterogeneous micro-environments has never been addressed. The definition of biofilms as 'surface-adhering and surface-adapted' microbial communities contains the word 'surface' twice. This leads us to hypothesize that phenotypically-heterogeneous micro-environments in biofilms develop as an adaptive response of initial colonizers to their adhering state, governed by the forces through which they adhere to a substratum surface. No surface is entirely homogeneous, while adhering bacteria can substantially contribute to stochastically occurring surface heterogeneity. Accordingly, bacterial adhesion forces sensed by initial colonizers differ across a substratum surface, leading to differential mechanical deformation of the cell wall and membrane, where many environmental sensors are located. Bacteria directly adhering to heterogeneous substratum domains therewith formulate their own local responses to their adhering state and command non-conformist behavior, leading to phenotypically-heterogeneous micro-environments in biofilms

An integrated model system to gain mechanistic insights into biofilm-associated antimicrobial resistance in Pseudomonas aeruginosa MPAO1

open access articlePseudomonas aeruginosa MPAO1 is the parental strain of the widely utilized transposon mutant collection for this important clinical pathogen. Here, we validate a model system to identify genes involved in biofilm growth and biofilm-associated antibiotic resistance. Our model employs a genomics-driven workflow to assemble the complete MPAO1 genome, identify unique and conserved genes by comparative genomics with the PAO1 reference strain and genes missed within existing assemblies by proteogenomics. Among over 200 unique MPAO1 genes, we identified six general essential genes that were overlooked when mapping public Tn-seq data sets against PAO1, including an antitoxin. Genomic data were integrated with phenotypic data from an experimental workflow using a user-friendly, soft lithography-based microfluidic flow chamber for biofilm growth and a screen with the Tn-mutant library in microtiter plates. The screen identified hitherto unknown genes involved in biofilm growth and antibiotic resistance. Experiments conducted with the flow chamber across three laboratories delivered reproducible data on P. aeruginosa biofilms and validated the function of both known genes and genes identified in the Tn-mutant screens. Differential protein abundance data from planktonic cells versus biofilm confirmed the upregulation of candidates known to affect biofilm formation, of structural and secreted proteins of type VI secretion systems, and provided proteogenomic evidence for some missed MPAO1 genes. This integrated, broadly applicable model promises to improve the mechanistic understanding of biofilm formation, antimicrobial tolerance, and resistance evolution in biofilms