Abstract This study aimed to estimate the allelopathic intensity of four Asteraceae invasive plant species (IPS), including Conyza canadensis (L.) Cronq., Erigeron annuus (L.) Pers., Bidens pilosa (L.), and Aster subulatus Michx., by testing the effect of leaf extracts on the seed germination and seedling growth (SGe and SGr) of lettuce (Lactuca sativa L.) in combination with two particle sizes of silver nanoparticles. These four IPS decreased the germination of lettuce seeds but increased the growth of lettuce seedlings. The allelopathic intensity of the four IPS decreased in the following order: B. pilosa > C. canadensis > E. annuus > A. subulatus. Silver nanoparticles decreased the SGe and SGr of lettuce. The 20 nm silver nanoparticles affected the competition intensity for water and the absorption of inorganic salts by lettuce more intensively than the 80 nm nanoparticles. Silver nanoparticles intensify the allelopathic intensity of the four invasive plant species on the SGe and SGr of lettuce. The allelopathic intensity of B. pilosa was higher than that of the other three IPS when they were polluted with silver nanoparticles. Thus, silver nanoparticles could facilitate the invasion process of the four IPS, particularly B. pilosa, via an increase in the intensity of allelopathy.

Poly(3-hydroxybutyrate) (PHB) has been proposed to be a potential candidate to be used as biomaterial. However, its poor processability, high brittleness and rigidity have limited its applicability. Transesterification reactions with poly(ε-caprolactone) (PCL), one of the most promising biomedical materials, emerge as an attractive alternative to improve its mechanical properties. In this work, poly(3-hydroxybutyrate-b-ε-caprolactone) (PHB-b-PCL) was prepared straightforwardly by transesterification of the parent homopolymers by reactive extrusion in the presence of stannous octanoate. After purification by solvent fractionation, PHB-b-PCL was characterized by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy of carbon (13C NMR) and hydrogen (1H NMR) and, subsequently, submitted to electrospinning. The results indicate that PHB was modified, showing lower crystallinity as compared to the original homopolymers. The electrospun mats are tough and flexible and analysis by scanning electron microscopy indicates the formation of uniformly smooth morphology with average fiber diameter of 900-1200 nm and voids in the range between a few microns up to a few tens of microns, suitable for cell diffusion in biomedical applications.

ABSTRACT Objective This study aimed to present the impact of age and gender on thyroid hormone levels in a large Chinese population with sufficient iodine intake. Subjects and methods A total of 83643 individuals were included and were stratified by age and gender. The median, 2.5th and 97.5th of thyrotropin (TSH), free triiodothyronine (FT3), free thyroxine (FT4) and FT3/FT4 ratio were calculated for both genders for every decade from 18 to over 80 years. TSH, FT3, FT4, FT3/FT4 distribution in each age group was evaluated for females and males using smoothing splines in the generalized additive models (GAM). TSH concentrations were compared in the different age groups in gender. Results In the over 80s age group, the TSH level (median: 2.57 mIU/L, 2.5th-97.5th: 0.86-7.56 mIU/L) was significantly higher than other age groups, irrespective to gender (P<0.001). Females had a higher TSH value than males in all age groups (P<0.001). Results of the smoothing curves showed that TSH increased with age, FT3 concentration was higher in males than in females and the tendency of the FT3/FT4 ratio was basically similar to that of FT3. TSH concentration in the 50s age group (median 2.48 mIU/L for females versus 2.00 mIU/L for males) was significantly higher than that in the 30s age group (median 2.18 mIU/L for females versus median 1.85 mIU/L for males). Conclusions In accord with increasing TSH values during aging, females and older adults have lower FT3 values and lower FT3/FT4 ratios, while the FT4 values remain stable.

ABSTRACT Objective: To analyze the compositions of upper urinary tract stones and investigate their distributions in different gender and age groups. Materials and Methods: Patients diagnosed with upper urinary tract stone disease between December 2014 and March 2018 were retrospectively reviewed. Patient's age, gender, BMI, comorbidities, stone event characteristics, and compositions were collected, and proportions of stone components in different gender and age groups were analyzed. Results: A total of 1532 stone analyses were performed (992 from males and 540 from females). The mean age was younger in males (p <0.001). Males included more cases with larger BMI, hyperuricemia, and obesity, while females had more urinary tract infections. Multiple components were present in 61.8% of stones. Calcium oxalate (CaOx) (67.0%) was the most common component, followed by uric acid (UA) (11.8%), infection stone (11.4%), calcium phosphate (CaP) (8.0%), cystine (1.1%), brushite (0.4%), and 2, 8-dihydroxyadenine (0.2%). Men contributed with more CaOx stones than women at age 30-49 years (all p <0.01) and more UA stones at 30-59 years (all p <0.05). Women contributed with more infection stones than men in age groups 30-49 and 60-69 years (all p <0.05), and more CaP stones at 30-49 years. The prevalence peak was 50-59 years in men and 60-69 years in women. Both genders had the lowest prevalence in adolescence. Prevalence of UA stones increased while that of infection stones decreased with aging in both genders. Conclusions: Age and sex had a strong association with distribution of stone compositions in this Chinese cohort.

BACKGROUND: Rural settings where molecular tuberculosis diagnostics are not currently available need easy-to-use tests that do not require additional processing or equipment. While acid-fast bacilli (AFB) smear is the most common and often only tuberculosis diagnosis test performed in rural settings, it is labour intensive, has less-than-ideal sensitivity, and cannot assess tuberculosis drug susceptibility patterns. OBJECTIVE: The objective of this study was to determine the feasibility of a multidrug-resistant (MDR) or extensively drug-resistant (XDR)-tuberculosis coloured agar-based culture test (tuberculosis CX-test), which can detect Mycobacterium tuberculosis growth and evaluate for drug susceptibility to isoniazid, rifampicin and a fluoroquinolone (i.e. ciprofloxacin) in approximately 14 days. METHOD: In this study, 101 participants were enrolled who presented to a rural health clinic in central Malawi. They were suspected of having active pulmonary tuberculosis. Participants provided demographic and clinical data and submitted sputum samples for tuberculosis testing using the AFB smear and tuberculosis CX-test. RESULTS: The results showed a high level of concordance between the AFB smear (12 positive) and tuberculosis CX-test (13 positive); only one sample presented discordant results, with the molecular GeneXpert MTB/RIF® test confirming the tuberculosis CX-test results. The average time to a positive tuberculosis CX-test was 10 days. Of the positive samples, the tuberculosis CX-test detected no cases of drug resistance, which was later confirmed by the GeneXpert MTB/RIF®. CONCLUSION: These findings demonstrate that the tuberculosis CX-test could be a reliable low-cost diagnostic method for active pulmonary tuberculosis in high tuberculosis burden rural areas.

Abstract Block copolymers and blends comprised by liquid crystalline oligoester and polystyrene were prepared and their thermal stability were characterized by thermogravimetric analysis (TGA). The samples have shown three main decomposition temperatures due to (1) lost of flexible chain and decomposition of mesogenic segment, (2) decomposition of polystyrene and (3) final decomposition of oligoester rigid segment. Both copolymers and polymer blends presented lower thermal stability compared to polystyrene and oligoester. The residual mass after heating at 600 °C in copolymers and polymer blends were lower than those found in the oligoesters. A degradative process of aromatic segments of oligoester induced by decomposition of polystyrene is suggested.

Abstract Polymeric membranes were developed using a SPEEK (sulfonated poly(ether ether ketone)) polymer matrix, containing titanium oxide (TiO2) (incorporated by sol-gel method). SPEEK with different sulfonation degrees (SD): 63% and 50% were used. The influence of sulfonation degree on membrane properties was investigated. The thermal analysis (TGA and DTGA) and X-ray diffraction (XRD) were carried out to characterize the membranes and electrochemical impedance spectroscopy (EIS) was carried out to evaluate the proton conductivity of the membranes. The proton conductivities in water were of 3.25 to 37.08 mS.cm-1. Experimental data of impedance spectroscopy were analyzed with equivalent circuits using the Zview software, and the results showed that, the best fitted was at 80 °C.

Abstract Low cost UV-Ozone reactor using a high pressure mercury vapor lamp of 80 watts without outer bulb showed good results for treatment of ITO films used as anode electrode in the assembly of P-OLED (polymer-organic light emitting diode) devices. This study revealed 20 minutes as effective treatment time and it was verified also that the effect of UV-Ozone treatment loses its efficiency as the elapsed time increases. It was analyzed with measurements of contact angle using a droplet of PEDOT:PSS polymer. P-OLEDs devices were mounted with architecture: ITO/PEDOT:PSS/PVK/Alq3/Al. The PVK polymer was diluted in organic solvent of 1,2,4-trichlorobenzene with concentrations of: 5, 10, 20 and 30 mg/mL. Results revealed better performance of P-OLED devices for concentration of 5 mg/mL resulting in lower threshold voltage, elevation of electrical current and similar diode curve.

Um novo material contendo grupos fluoreno e quinolina foi obtido por síntese direta através da reação de Suzuki e mostrou-se ser facilmente solúvel em solventes orgânicos comuns. A estrutura química da macromolécula foi confirmada através da caracterização por medidas de ressonância magnética nuclear de 1H (1H NMR), infravermelho com transformada de Fourier (FTIR), calorimetria diferencial de varredura (DSC), análise termogravimétrica (TGA) e cromatografia de permeação em gel (GPC). Em solução, o material apresentou duas absorções máximas em 314 e 245 nm, juntamente com um alto rendimento quântico de fluorescência (82%) e uma emissão máxima em 419 nm. O band gap do material foi estimado em cerca de 2,60 eV por voltametria cíclica, entretanto o band gap óptico para o filme fino determinado por espectroscopia UV-Vis apresentou valor maior, 3,10 eV. A divergência foi atribuída a interações de transferência de carga, devido à presença de grupos doador e aceptor no copolímero.

A new oligomer having fluorenylene and quinolinylene groups was straightforwardly synthesized by Suzuki reaction and proven to be readily soluble in common organic solvents. The chemical structure of the copolymer was confirmed and characterized by 1H nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and gel permeation chromatography (GPC) measurements. In solution, the oligomer presented two absorption maxima at 314 and 245 nm, along with a high fluorescence quantum yield (82%), characterized by an emission maximum at 419 nm. The band gap of the material was estimated to be around 2.60 eV by cyclic voltammetry, however the optical band gap for the thin film observed by UV-Vis spectroscopy was 3.10 eV. The divergence was attributed to charge transfer interactions due to the presence of donor and acceptor units in the copolymer.

The formation of the crystalline phase of polypropylene in the presence of four different types of CaCO3 was studied. All composites were prepared by melt mixing and extrusion and the concentration of CaCO3 was maintained at 5 wt %. Furthermore, in another series of composites, 5 wt % of polypropylene-graft-maleic anhydride (PP-g-MA) was added for comparison. The tensile strength, flexural modulus and impact resistance of the composites were determined. The composites were also analyzed by DSC (differential scanning calorimetry) and WAXD (wide angle x-ray diffractometry) in order to understand and quantify the beta crystalline phase. The results indicated that the composite having the smallest CaCO3 size and PP-g-MA presented the best combined mechanical properties, therefore, the highest impact resistance, flexural modulus and tensile strength were observed, which were attributed to the proportionally higher concentration of beta crystalline phase.

This work studies the influence of the film deposition process on light emission performance and on threshold voltage of OLEDs, with architecture glass/ITO/PEDOT:PSS/PVK/Alq3/Al. The commercial PVK was dissolved in different solvents such as: chloroform, tetrahydrofuran, 1,2,4-trichlorobenzene and trimethylpentane. OLEDs were characterized by current-voltage and revealed a significant influence of the solvents, although all devices emitted green electroluminescence. A difference in threshold voltage up to 10 V was observed among OLEDs prepared from different solvents. The 1,2,4-trichlorobenzene showed best performance, presenting lowest treshold voltage (≈ 6 V), followed by tetrahydrofuran (≈ 8 V), trimethylpentane (≈ 14 V) and chloroform (≈ 16 V).

Neste trabalho, foram sintetizados copolímeros à base de estireno (STY), divinilbenzeno (DVB) e metacrilato de metila (MMA) com propriedades magnéticas pela técnica de polimerização em suspensão. Os copolímeros foram caracterizados quanto a sua morfologia, ao teor de ferro incorporado, a densidade aparente, a distribuição de tamanho de partículas e as suas propriedades magnéticas. Foi avaliado o efeito da concentração de MMA sobre as características das partículas poliméricas obtidas. Copolímeros que não utilizaram MMA foram, em geral, os que apresentaram maior incorporação de ferro e melhor controle morfológico. Quando a temperatura foi alterada de 80 ºC para 70 ºC e a velocidade de agitação de 480 rpm para 360 rpm, houve aumento no teor de ferro incorporado nas partículas poliméricas.

In this work, copolymers based on styrene (STY), divinylbenzene (DVB) and methyl methacrylate (MMA) with magnetic properties were synthesized using the suspension polymerization technique. The copolymers were characterized according to morphology, iron content incorporated, bulk density, particle size distribution and magnetic properties. The effect of MMA content on the characteristics of polymeric particles was investigated. Generally, copolymers without MMA presented the biggest iron content incorporated and the best morphologic control. When the temperature was decreased from 80 ºC to 70 ºC and the stirring speed was reduced from 480 rpm to 360 rpm the iron content in the polymeric particles increased.

Magnetic composites have a wide range of potential technological applications; however the evaluation of this material for extraction of phenolic compounds has not been sufficiently studied. Due to its high toxicity and solubility the removal of phenolic compounds from the aquatic environments has critical importance. In this work polymeric composites were prepared by anchoring Ni and Co particles on sulfonatedpoly(styrene-co-divinylbenzene) PS-DVB. The PS-DVB beads were synthesized by suspension polymerization and reacted with acetyl sulfate, aiming to obtain sulfonated copolymers. All materials were capable of removing phenol from aqueous solutions. The phenol adsorption kinetics was influenced by the polymer porosity and swelling capacity in water. The composite derivative of the more porous copolymer impregnated with nickel (C1SNi) was the most efficient in phenol removal, with the sorption equilibrium being established more rapidly than for the other composites. The pseudo second-order model was more adequate to describe the phenol adsorption process for the composite C1SNi. The Langmuir model describes successfully the phenol removal by this composite.

This paper describes the preparation of magnetic copolymer obtained from suspension polymerization of styrene (Sty) and divinylbenzene (DVB) in the presence of iron particles treated and not treated with oleic acid. The magnetic copolymers were characterized according to their morphology, particle size distribution and magnetic properties. The results show that incorporation of iron particles significantly changed the particles’ morphology. All samples presented higher saturation magnetization than the values reported in the literature and the particle size distribution was more monodisperse when the polymerization was conducted with 5%wt of benzoyl peroxide (BPO).

Commercial copolymers based on styrene and divinylbenzene containing sulfonic acid groups were used as support for the incorporation of silver nanoparticles. These nanoparticles were obtained in situ by the reduction of Ag+ by using hydroxylamine in the presence of a protective agent. These materials were characterized with determination of the silver content and their morphological characteristics. The antibacterial activity of the final products against Escherichia coli was evaluated and the results show that the synthesized copolymers had antibacterial effect varying from 54 to 100%. The most efficient composite was made with small, well distributed particles.