Heat‐Induced Dry Tailoring of Porosity in Polymer Scaffolds

The present study evaluates the effect of heat treatment on electrospun poly(lactide‐co‐glycolide) fibrous membranes. Both a temperature (75–150 °C) and a treatment time range (5–40 min) are tested. The effect on the fibrous structure is investigated in terms of morphology, showing that with increasing temperature or longer treatment time the fusion of fibres progresses continuously. Additionally, the tensile properties of the various scaffolds deliver results on the effect of increasing fibre‐to‐fibre linkages. Both modulus and yield increase within the heat treatment procedures. The elevated stiffness of the membranes accompanies a loss in porosity. These findings deliver insights into the tailoring of membranes that might be used in the fabrication of customised scaffolds intended for cell culture in tissue engineering.

     

Porous materials for alkali contaminated environments

This study presents the synthesis of alkali aluminosilicates based on the stoichiometry of KAlSiO₄ by a hydrothermal treatment followed by a sintering step. The aim was to create formed porous samples which could be a potential material in high temperature applications with alkali corrosive conditions. The material composition was adjusted using analysis of variance (ANOVA) to reach resistance to alkali corrosion of the synthesized material. A casting process was established replacing a part of the raw materials by pre-sintered material to produce porous samples. The final samples were characterized with regard to bulk density, refractoriness under load, cold crushing strength and thermal conductivity. The results showed similar properties compared to conventional materials.     

High-Density Real-Time PCR-Based in Vivo Toxicogenomic Screen to Predict Organ-Specific Toxicity

Toxicogenomics, based on the temporal effects of drugs on gene expression, is able to predict toxic effects earlier than traditional technologies by analyzing changes in genomic biomarkers that could precede subsequent protein translation and initiation of histological organ damage. In the present study our objective was to extend in vivo toxicogenomic screening from analyzing one or a few tissues to multiple organs, including heart, kidney, brain, liver and spleen. Nanocapillary quantitative real-time PCR (QRT-PCR) was used in the study, due to its higher throughput, sensitivity and reproducibility, and larger dynamic range compared to DNA microarray technologies. Based on previous data, 56 gene markers were selected coding for proteins with different functions, such as proteins for acute phase response, inflammation, oxidative stress, metabolic processes, heat-shock response, cell cycle/apoptosis regulation and enzymes which are involved in detoxification. Some of the marker genes are specific to certain organs, and some of them are general indicators of toxicity in multiple organs. Utility of the nanocapillary QRT-PCR platform was demonstrated by screening different references, as well as discovery of drug-like compounds for their gene expression profiles in different organs of treated mice in an acute experiment. For each compound, 896 QRT-PCR were done: four organs were used from each of the treated four animals to monitor the relative expression of 56 genes. Based on expression data of the discovery gene set of toxicology biomarkers the cardio- and nephrotoxicity of doxorubicin and sulfasalazin, the hepato- and nephrotoxicity of rotenone, dihydrocoumarin and aniline, and the liver toxicity of 2,4-diaminotoluene could be confirmed. The acute heart and kidney toxicity of the active metabolite SN-38 from its less toxic prodrug, irinotecan could be differentiated, and two novel gene markers for hormone replacement therapy were identified, namely fabp4 and pparg, which were down-regulated by estradiol treatment.     

Cleavable Crosslinkers as Tissue Fixation Reagents for Proteomic Analysis

Formaldehyde fixation is widely used for long‐term maintenance of tissue. However, due to formaldehyde‐induced crosslinks, fixed tissue proteins are difficult to extract, which hampers mass spectrometry (MS) proteomic analyses. Recent years have seen the use of different combinations of high temperature and solubilizing agents (usually derived from antigen retrieval techniques) to unravel formaldehyde‐fixed paraffin‐embedded tissue proteomes. However, to achieve protein extraction yields similar to those of fresh‐frozen tissue, high‐temperature heating is necessary. Such harsh extraction conditions can affect sensitive amino acids and post‐translational modifications, resulting in the loss of important information, while still not resulting in protein yields comparable to those of fresh‐frozen tissue. Herein, the objective is to evaluate cleavable protein crosslinkers as fixatives that allow tissue preservation and efficient protein extraction from fixed tissue for MS proteomics under mild conditions. With this goal in mind, disuccinimidyl tartrate (DST) and dithiobis(succinimidylpropionate) (DSP) are investigated as cleavable fixating reagents. These compounds crosslink proteins by reacting with amino groups, leading to amide bond formation, and can be cleaved with sodium metaperiodate (cis‐diols, DST) or reducing agents (disulfide bonds, DSP), respectively. Results show that cleavable protein crosslinking with DST and DSP allows tissue fixation with morphology preservation comparable to that of formaldehyde. In addition, cleavage of DSP improves protein recovery from fixed tissue by a factor of 18 and increases the number of identified proteins by approximately 20 % under mild extraction conditions compared with those of formaldehyde‐fixed paraffin‐embedded tissue. A major advantage of DSP is the introduction of well‐defined protein modifications that can be taken into account during database searching. In contrast to DSP fixation, DST fixation followed by cleavage with sodium metaperiodate, although effective, results in side reactions that prevent effective protein extraction and interfere with protein identification. Protein crosslinkers that can be cleaved under mild conditions and result in defined modifications, such as DSP, are thus viable alternatives to formaldehyde as tissue fixatives to facilitate protein analysis from paraffin‐embedded, fixed tissue.     

Quasi‐isothermal DSC testing of epoxy adhesives using initial fast heating rates

Three major factors decrease the accuracy of the cure measurement in standard‐isothermal testing using differential scanning calorimetry (DSC). First, cure occurs during the heating step. Second, data are lost during the stabilization period between the dynamic and isothermal step. Third, the baseline selection requires a modification to the protocol. An alternative, which is explored in this study, is the use of fast ramps, which decrease the heating time, but this has been avoided due to overshoot that occurs between the dynamic and isothermal step, which is troublesome for systems with autocatalytic kinetics. By mitigating these factors, a quasi‐isothermal protocol was developed. Therefore, more complete cure kinetics were captured with the implementation of fast DSC to decrease the ramp time and through the optimization of furnace parameters to decrease stabilization time and temperature overshoot. The data suggested this quasi‐isothermal analysis more accurately measured the isothermal curing kinetics of a commercial epoxy adhesive at 110, 115, and 120 °C for fast ramps of 175, 350, and 500 K/min compared to the traditional ramp of 5 K/min. The enthalpy spike at the dynamic to isothermal transition remains an issue; however, an empirical shift can be used to compensate for the enthalpy signal lag. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45425.     

Production of Camphene by Isomerization Reaction on Sulfated ZrO2

Abstract The kinetics of camphene production in liquid phase from α-pinene was experimentally determinedin an isothermal batch reactor.To this end,a sulfated ZrO_2 catalyst was used and the reaction studied in thetemperature range of 370-403K.By analyzing the experimental data,second reaction order for α-pinene wasfound.A kinetic model is presented which includes term for the catalyst load used.The specific rate constant at393K was 2.19×10~(-3)mol.L~(-1),min~(-1),the activation energy being 93kJ.mol~(-1).Both Vaues are within the rangeof literature results.     

Physical and mechanical properties of unsaturated polyester resin matrix from recycled PET (based PG) with corn straw fiber

In this study, composites of unsaturated polyester resin (UPR), synthesized from recycled polyethylene terephthalate (PET), with 10 to 40% in volume of corn straw fiber (CSF), were elaborated and studied the effect of fiber content on their physical and mechanical properties. The content of cellulose (48.97%), hemicellulose (24.06%), and lignin (6.59%) were determined by chemical characterization of CSF. The characteristic bonds of the UPR were identified as a cross-linking network between the styrene monomer (ST) and the unsaturated polyester (UP) through FTIR. Two decomposition stages were observed by TGA–DTG. The results of physical and mechanical properties showed that as the fiber content increased in the UPR, the water absorption increased (0.6% to 2.56%), on the other hand, the density (1218.23 to 1150.28 kg/m³), flexural strength (50.58 to 26.98 MPa), flexural modulus (2.66 to 2.29 GPa), tensile strength (8.62 to 3.65 MPa), tensile modulus (1.18 to 0.43 GPa), and hardness (81.67 to 65.67 Shore D), they decreased. SEM analysis showed some defects in the fiber distribution in the UPR, which affected the mechanical properties of the composites. This research contributes to the development of new material from use of two waste materials for the benefit of the environment.     

Production of Green Star/Linear PLA Blends by Extrusion and Injection Molding: Tailoring Rheological and Mechanical Performances of Conventional PLA

In this work, bio-based products composed of blends of a star-shaped poly(d ,l -lactide) (star-PDLLA) and a conventional linear poly(l -lactide) (linear-PLLA) are produced by typical large-scale manufacturing techniques for thermoplastic blends. In the first case, the two polymers are blended through melt extrusion, producing pellets that are subsequently compression-molded into the final bio-based polymer films. Alternatively, the star/linear poly(lactide) (PLA) materials are developed by direct blending through injection molding, a process that generally applies after a preblending extrusion step to ensure proper mixing. Thermomechanical degradation induced by the different processes is evaluated, and the performances of the final star/linear PLA products are thoroughly compared. The effect of the short-branched, amorphous, star polymeric component on thermal, mechanical, and rheological properties of the conventional PLLA is comprehensively investigated, revealing that the star-PDLLA incorporation promotes the formation of a more flexible and tougher material with reduced capability of crystallization. Most importantly, star-PDLLA decreases the melt viscosity of the final material, while increasing the shear-thinning behavior, hence facilitating melt flow during manufacturing. Such properties lead to enhanced material ductility and processability, with respect to typically brittle and viscous conventional PLLA-based materials. Moreover, the tuning of final material performances can be achieved by simply varying the star-PDLLA content.     

Chemorheological time‐temperature‐transformation‐viscosity diagram: Foamed EPDM rubber compound

Thermal analysis, rheometry, and kinetic modeling are used to generate a comprehensive processability diagram for thermosetting and elastomeric resins. A chemorheological “time‐temperature‐transformation‐viscosity” diagram is proposed to fully characterize curing reactions toward process' on‐line control, optimization, and material design. Differential scanning calorimetry and thermogravimetric techniques are used to measure total reaction heat, degree of vulcanization, and cure kinetics. The viscosity, as a function of temperature and cure degree, is obtained from parallel plate rheometry. The auto‐catalytic Kamal–Sourour model, including a diffusion‐control mechanism, is used to model cure kinetics, while the Castro–Macosko model serves to model the rheological behavior. Non‐linear least‐squares regression and numerical integration are used to find models' parameters and to construct the chemorheological diagram. The usefulness of the proposed methodology is illustrated in the context of an industrial‐like Ethylene Propylene Diene Termononer rubber compound that includes a chemical blowing agent. Even though the rubber formulation contains crosslinking agents, primary and secondary accelerators, promoters, activators, and processing aids, the chemorheological diagram is obtained consistently, validating the proposed methodology to any thermosetting or elastomeric resin. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43966.     

Identification of a novel protein synthesis inhibitor active against gram-positive bacteria

In an effort to identify novel antibacterial chemotypes, we performed a whole‐cell screen for inhibitors of Staphylococcus aureus growth and pursued those compounds with previously uncharacterized antibacterial activity. This process resulted in the identification of a benzothiazolium salt, ABTZ‐1, that displayed potent antibacterial activity against Gram‐positive pathogens. Several clinically desirable qualities were demonstrated for ABTZ‐1 including potent activity against multidrug‐resistant clinical isolates of methicillin‐resistant S. aureus (MRSA) and vancomycin‐resistant enterococci (VRE), retention of this activity in human serum, and low hemolytic activity. The antibacterial activity of ABTZ‐1 was attributed to its inhibition of bacterial translation, as this compound prevented the incorporation of [³⁵S]methionine into S. aureus proteins, and ABTZ‐1‐resistant strains were cross‐resistant to known inhibitors of bacterial translation. ABTZ‐1 represents a promising new class of antibacterial agents.