Implantable Organic Electronic Ion Pump Enables ABA Hormone Delivery for Control of Stomata in an Intact Tobacco Plant

Electronic control of biological processes with bioelectronic devices holds promise for sophisticated regulation of physiology, for gaining fundamental understanding of biological systems, providing new therapeutic solutions, and digitally mediating adaptations of organisms to external factors. The organic electronic ion pump (OEIP) provides a unique means for electronically‐controlled, flow‐free delivery of ions, and biomolecules at cellular scale. Here, a miniaturized OEIP device based on glass capillary fibers (c‐OEIP) is implanted in a biological organism. The capillary form factor at the sub‐100 µm scale of the device enables it to be implanted in soft tissue, while its hyperbranched polyelectrolyte channel and addressing protocol allows efficient delivery of a large aromatic molecule. In the first example of an implantable bioelectronic device in plants, the c‐OEIP readily penetrates the leaf of an intact tobacco plant with no significant wound response (evaluated up to 24 h) and effectively delivers the hormone abscisic acid (ABA) into the leaf apoplast. OEIP‐mediated delivery of ABA, the phytohormone that regulates plant's tolerance to stress, induces closure of stomata, the microscopic pores in leaf's epidermis that play a vital role in photosynthesis and transpiration. Efficient and localized ABA delivery reveals previously unreported kinetics of ABA‐induced signal propagation.     

Integration of microfiltration and nanofiltration to promote textile effluent reuse

This study investigates the application of a hybrid microfiltration–nanofiltration (MF–NF) process for textile wastewater reclamation. Indigo blue dye was efficiently retained by an MF membrane, allowing its recovery from the concentrated stream. NF technology was successfully applied to polish textile effluent. The NF membrane was evaluated under different transmembrane pressure (8–15 bars), crossflow velocities (0.21–0.84 cm s^?1), pH (7–11), and feed temperature (20–40 °C). The best NF performance was provided at a pressure of 12 bar and a crossflow rate of 0.63 cm s^?1. The NF performance (in terms of COD, conductivity, colour, and nitrogen removal) was not influenced by pH; however, higher feed pH values resulted in increased membrane fouling. The principal cause of flux decline was due to concentration polarization. Membrane chemical cleaning was sufficient to regain the initial permeability. The NF permeate met the quality requirements for all water demands within the textile industry, while the NF concentrate could be used to wash equipment, print work screens, print paste containers, and floors. The total capital cost (CapEx) of the MF–NF system was estimated at 58,362.50 US dollars and the total operational cost (OpEx) at 0.31 US dollars per cubic metre of effluent.     

Electric current density distribution in planar solid tumor and its surrounding healthy tissue generated by an electrode elliptic array used in electrotherapy

The knowledge of the electric current density distribution generated by an electrode array is very useful in electrotherapy for tumor treatment. We propose an innovative mathematical approach that takes into account planar solid tumor elliptic geometry, electrical differences between it and its surrounding healthy tissue, and positioning of the electrodes with respect to tumor-surrounding healthy tissue interface. We show the distributions of the electric current density in leading order and first correction terms in a heterogeneous planar medium formed by two regions (tumor and its surrounding healthy tissue) in function of these parameters. The results show that when electrodes are completely inserted in tumor and/or its conductivity is higher than that of its surrounding healthy tissue, the electric current density lines concentrate more in tumor and its tumor-surrounding healthy tissue interface. No significant differences are reported between the electric current density distributions in leading-order and first-order correction for each parameter investigated. However, norm of this physical magnitude reveals that these distributions are different when the ratio between radius of the electrodes and radius of the tumor is less than 0.8. We conclude that the analytical modeling presented in this study is of practical interest because it provides a convenient way to visualize the electric current density distributions generated by an electrode elliptic array in order to efficiently destroy the localized planar tumors with the minimum damage to organism, through an increase of the potential applied to the electrodes, the tumor conductivity with respect to its surrounding healthy tissue and insertion of all electrodes into tumor.     

Diagnostic protein marker patterns in squamous cervical cancer

Purpose: Cervical cancer is the second most prevalent malignancy of women. Our aim was to identify additional marker protein patterns for objective diagnosis of squamous cervical cancer (SCC). Experimental design: Collected tissue biopsies of SCC, squamous vaginal cancer (SVC), normal cervical and vaginal mucosa were subjected to 2‐DE, SameSpot analysis, MALDI‐TOF‐MS protein identification, and analysis of the expression of selected proteins by immunohistochemistry. Results: In 148 protein spots selected by the difference in expression 99 proteins were identified. A differential protein pattern for SCC was, e.g. over‐expressed (OE) eukaryotic translation initiation factor 3‐2β, neutrophil cytosolic factor 2, annexin A6 (ANXA6), for SVC it was OE cathepsin D, γ‐catenin, RAB2A, for both cancers it was OE apolipoprotein E, tropomyosin 3, HSPA8, and underexpressed cytokeratin 13, osteoglycin. In SCC nuclear expression of neutrophil cytosolic factor 2, PRDX2, HSP27 (nine of ten cases), ANXA6 (nine of ten cases) was observed while tropomyosin 4 was expressed only in two of ten cases. There was 81.1% (43/53) agreement between the expression of protein spots and the immune expression of proteins ( www.proteinatlas.org ). Conclusions and clinical relevance: SCC is characterized by specific tissue marker protein patterns that allow objective detection of the disease. They can become a basis for objective automated cytology‐based screening and improve current diagnostics of SCC.     

Understanding LAG-3 Signaling

Lymphocyte activation gene 3 (LAG-3) is a cell surface inhibitory receptor with multiple biological activities over T cell activation and effector functions. LAG-3 plays a regulatory role in immunity and emerged some time ago as an inhibitory immune checkpoint molecule comparable to PD-1 and CTLA-4 and a potential target for enhancing anti-cancer immune responses. LAG-3 is the third inhibitory receptor to be exploited in human anti-cancer immunotherapies, and it is considered a potential next-generation cancer immunotherapy target in human therapy, right next to PD-1 and CTLA-4. Unlike PD-1 and CTLA-4, the exact mechanisms of action of LAG-3 and its relationship with other immune checkpoint molecules remain poorly understood. This is partly caused by the presence of non-conventional signaling motifs in its intracellular domain that are different from other conventional immunoregulatory signaling motifs but with similar inhibitory activities. Here we summarize the current understanding of LAG-3 signaling and its role in LAG-3 functions, from its mechanisms of action to clinical applications.     

Antibacterial and Anti-biofilm Activity of the Human Breast Milk Glycoprotein Lactoferrin against Group B Streptococcus

Group B Streptococcus (GBS) is an encapsulated Gram-positive human pathogen that causes invasive infections in pregnant hosts and neonates, as well as immunocompromised individuals. Colonization of the human host requires the ability to adhere to mucosal surfaces and circumnavigate the nutritional challenges and antimicrobial defenses associated with the innate immune response. Biofilm formation is a critical process to facilitate GBS survival and establishment of a replicative niche in the vertebrate host. Previous work has shown that the host responds to GBS infection by producing the innate antimicrobial glycoprotein lactoferrin, which has been implicated in repressing bacterial growth and biofilm formation. Additionally, lactoferrin is highly abundant in human breast milk and could serve a protective role against invasive microbial pathogens. This study demonstrates that human breast milk lactoferrin has antimicrobial and anti-biofilm activity against GBS and inhibits its adherence to human gestational membranes. Together, these results indicate that human milk lactoferrin could be used as a prebiotic chemotherapeutic strategy to limit the impact of bacterial adherence and biofilm formation on GBS-associated disease outcomes.     

Trypsin immobilization on discs of polyvinyl alcohol glutaraldehyde/polyaniline composite

Discs of polyvinyl alcohol cross-linked with glutaraldehyde (PVAG) were synthesized and covered with polyaniline activated with glutaraldehyde (PANIG). Trypsin was covalently immobilized on this composite yielding a preparation containing 21.1 units per disc. The FT-IR spectra of the discs showed bands of PVA (3300 cm^?1, 2930 cm^?1 and 1440 cm^?1) and PANI (1594 cm^?1 and 1100 cm^?1). The best immobilization conditions were: trypsin concentration at 0.2 mg mL^?1, pH 7.6 and 60 min of incubation, similar to polyaniline–trypsin systems reported in the literature. The PVAG–PANIG–trypsin derivative showed an optimal pH and an optimal temperature of 7.0 and 35 °C, respectively. Hydrolysis of casein showed variations in the size of the products, revealing differences between the immobilized enzyme and the mechanism catalyzed by the native enzyme.     

Optimisation of osmotic dehydration process of guavas by response surface methodology and desirability function

Response surface methodology was used to assess the effects of osmotic solution concentration (40–60°Brix), process temperature (20–40 °C) and vacuum pulse application time (0–20 min) at 100 mbar on water loss (WL), weight reduction (WR), solid gain (SG), water activity (a_w), colour parameters and mechanical properties of guava slices. Optimal process conditions were determined through the desirability function approach and quality characteristics of osmotically dehydrated guavas were analysed. Only models obtained for WL, WR and a_w were suitable to describe the experimental data. The desirability function showed that optimal conditions for osmotic dehydration of guavas were: osmotic solution concentration at 60°Brix, process temperature at 32 °C and 20 min of vacuum pulse application. Under optimal conditions, colour and mechanical properties of treated guavas were similar to fresh fruit, presenting WL of 29.01 g/100 g, WR of 25.91 g/100 g, SG of 3.10 g/100 g and a_w of 0.979.     

Mass transfer kinetics and regressional‐desirability optimisation during osmotic dehydration of pumpkin,kiwi and pear

Mass transfer kinetics and optimisation of osmotic dehydration (OD) of fruits and vegetables with diverse structures were studied. Different concentrations of sucrose (20–60 °Brix) and process times (0–24 h) were used. Magee’s model was appropriate for predicting water loss (WL), while Azuara’s model fitted well solids gain (SG) data and represented more accurately the evolution of the complete process close to equilibrium. Polynomial equations for each kinetic variable [WL, SG and weight reduction (WR) – for pumpkin, kiwi and pear] using multiple linear regression were fitted for a selected range of experimental data (30–240 min, 20–60 °Brix). A complete solution algorithm for desirability function was coded in Matlab^® 7.2 (Mathworks, Natick, MA, USA) with the aim to optimise osmotic dehydration process in terms of WL, SG and WR; optimal conditions were found for each fruit. Besides, an optimal common zone was identified for OD corresponding to process time from 114 to 240 min and sucrose concentration from 54 to 60 °Brix.     

Polydiacetylene as a Biosensor: Fundamentals and Applications in the Food Industry

Biosensors offer the potential for real-time pathogen detection. Polydiacetylene (PDA) is an ideal choice for use as a sensor due to its unique optical properties. PDA molecules can form thin films or vesicles that change color from deep blue to red in response to different stimuli, like temperature, pH, and the presence of biological molecules. PDA films and vesicles have been proven to be promising devices for the detection of bacteria and bacterial toxins. Langmuir troughs (for films) and microcalorimetry (for vesicles) are among the many techniques used to characterize PDA films and vesicles. In order to enable more applications of PDA films, it is imperative to elucidate and gain a deeper understanding of the molecular interactions associated with their color change. In addition, it is necessary to transfer the PDA film onto a solid support like plastic in order to incorporate PDA biosensors into an intelligent packaging system. Through the use of such a system, consumers can monitor food quality, thereby preventing foodborne outbreaks. In this review, we discuss the formation of PDA films and vesicles, their characteristics, and their potential applications as biosensors. The possibility to incorporate PDA biosensors into an intelligent packaging system to be used in the food industry is also explored.