Development of PHBV electrospun fibers containing a borate bioactive glass doped with Co, Cu, and Zn for wound dressings.

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) nanofibers embedded with borate glasses of 45B5 composition doped with Co2+, Cu2+, and Zn2 +(46.1 B2O326.9-X CaO24.4 Na2O2.6 P2O5, X CoO/CuO/ZnO mol % (X = 0-5)) were produced by electrospinning for wound healing applications. Prior to their addition, the glasses exhibited two broad halos typical of a vitreous borate network, which were mainly composed of ring-type metaborate structural units. The particle distribution in the PHBV nanofibers embedded with 45B5 borate bioactive glasses is present in isolated and agglomerated states, being partially coated by a polymeric layer-except for the cobalt-doped glass, which resulted in a successful encapsulation with 100% embedding efficiency. The incorporation of the glasses reduced the PHBV crystallinity degree and its decomposition temperature, as well as its mechanical properties, including Young's modulus, tensile strength, and elongation at break. The neat PHBV fibers and those containing the cobalt-doped glasses demonstrated great cytocompatibility with human keratinocytes (HaCat), as suggested by the high cell viability after 7 days of exposure. Further studies are needed to fully understand the wound healing potential of these fibers, but our results significantly contribute to the area.

Structural and thermoluminescence properties of lithium borate glass matrices under UV and beta radiation.

In the present work, glass samples in the (100 - x)B2O3-xLi2O binary system, with x varying from 30 to 50 mol%, were prepared using the conventional melting and moulding method, with the main objective of evaluating the thermoluminescence response when exposing these materials to ultraviolet (UV) radiation. Complementary analysis based on density, optical absorption on the UV-visible region (UV-vis absorbance), Fourier transform infrared spectroscopy on the medium region, X-ray diffraction, and differential thermal analysis measurements were performed. Thermoluminescence measurements of vitreous samples showed glow curves with at least one peak with a maximum temperature of ~170°C after exposure to UV radiation in the temperature range 50-250°C. Samples were also exposed to beta radiation in the temperature range 25-275°C, also showing single peaks with a maximum temperature of ~150°C.

Synthesis, characterization and thermoluminescence properties of MgB4O7 phosphor co-doped with Tm and Dy.

The luminescent and dosimetric properties of the MgB4O7 phosphor co-doped with Tm and Dy ions (MgB4O7:Tm,Dy) obtained by the solution combustion technique were investigated. With the prepared material, sintered dosimeters in pellet form were made. The MgB4O7 dosimeters doped with Tm and Dy with 0.25 and 0.10 mol% respectively and sintered at 1223 K for 3 h showed a sensitivity almost 11 times greater than the sensitivity of the TLD-100 commercial dosimeter. The TL response as a function of the gamma dose showed linearity up to 50 Gy followed by a supralinearity region and, above 500 Gy, the saturation region of the electron traps is reached. The fading of the main TL peak was negligible in the first five days after irradiation reaching 13% after 60 days and the lower detection limit was 43 µGy. The kinetic parameters were determined using the deconvolution method revealing general and second order kinetics. The morphology, crystallography and photoluminescence of the prepared phosphor samples are also reported.

A store-operated Ca2+-entry in Trypanosoma equiperdum: Physiological evidences of its presence.

The Trypanosomatidae family encompasses many unicellular organisms responsible of several tropical diseases that affect humans and animals. Livestock tripanosomosis caused by Trypanosoma brucei brucei (T. brucei), Trypanosoma equiperdum (T. equiperdum) and Trypanosoma evansi (T. evansi), have a significant socio-economic impact and limit animal protein productivity throughout the intertropical zones of the world. Similarly, to all organisms, the maintenance of Ca2+ homeostasis is vital for these parasites, and the mechanism involved in the intracellular Ca2+ regulation have been widely described. However, the evidences related to the mechanisms responsible for the Ca2+ entry are scarce. Even more, to date the presence of a store-operated Ca2+ channel (SOC) has not been reported. Despite the apparent absence of Orai and STIM-like proteins in these parasites, in the present work we demonstrate the presence of a store-operated Ca2+-entry (SOCE) in T. equiperdum, using physiological techniques. This Ca2+-entry is induced by thapsigargin (TG) and 2,5-di-t-butyl-1,4-benzohydroquinone (BHQ), and inhibited by 2-aminoethoxydiphenyl borate (2APB). Additionally, the use of bioinformatics techniques allowed us to identify putative transient receptor potential (TRP) channels, present in members of the Trypanozoon family, which would be possible candidates responsible for the SOCE described in the present work in T. equiperdum.

Metabolic activity of hydro-carbon-oxo-borate on a multispecies subgingival periodontal biofilm: a short communication.

OBJECTIVE: This study evaluated the metabolic activity of hydro-carbon-oxo-borate complex (HCOBc) on a multispecies subgingival biofilm as well as its effects on cytotoxicity. MATERIALS AND METHODS: The subgingival biofilm with 32 species related to periodontitis was formed in the Calgary Biofilm Device (CBD) for 7 days. Two different therapeutic schemes were adopted: (1) treatment with HCOBc, 0.12% chlorhexidine (CHX), and negative control group (without treatment) from day 3 until day 6, two times a day for 1 min each time, totaling 8 treatments and (2) a 24-h treatment on a biofilm grown for 6 days. After 7 days of formation, biofilm metabolic activity was determined by colorimetry assay, and bacterial counts and proportions of complexes were determined by DNA-DNA hybridization. Both substances' cytotoxicity was evaluated by cell viability (XTT assay) and clonogenic survival assay on ovary epithelial CHO-K1 cells and an osteoblast precursor from calvaria MC3T3-E1 cells. RESULTS: The first treatment scheme resulted in a significant reduction in biofilm's metabolic activity by means of 77% by HCOBc and CHX treatments versus negative control. The total count of 11 and 25 species were decreased by treatment with hydro-carbon-oxo-borate complex and CHX, respectively, compared with the group without treatment (p < 0.05), highlighting a reduction in the levels of Porphyromonas gingivalis, Tannerella forsythia, Prevotella intermedia, and Fusobacterium periodontium. CHX significantly reduced the count of 10 microorganisms compared to the group treated with HCOBc (p < 0.05). HCOBc and CHX significantly decreased the pathogenic red-complex proportion compared with control-treated biofilm, and HCOBc had even a more significant effect on the red complex than CHX had (p ≤ 0.05). For the second treatment scheme, HCOBc complex and CHX significantly decreased 61 and 72% of control biofilms' metabolic activity and the counts of 27 and 26 species, respectively. HCOBc complex did not significantly affect the proportions of formed biofilms, while CHX significantly reduced red, orange, and yellow complexes. Both substances exhibited similar cytotoxicity results. CONCLUSIONS: This short communication suggested that the HCOBc complex reduced a smaller number of bacterial species when compared to chlorhexidine during subgingival biofilm formation, but it was better than chlorhexidine in reducing red-complex bacterial proportions. Although HCOBc reduced the mature 6-day-old subgingival multispecies biofilms, it did not modify bacterial complexes' ratios as chlorhexidine did on the biofilms mentioned above. Future in vivo studies are needed to validate these results. CLINICAL RELEVANCE: HCOBc complex could be used to reduce red-complex periodontal bacterial proportions.

Silver Nanoparticles Enhance Thermoluminescence and Photoluminescence Response in Li2B4O7 Glass Doped with Dy3+ and Yb3.

Lithium borate glass matrices doped with Dy3+ and Yb3+, containing silver nanoparticles in different concentrations are synthesized and characterized in this work. The Scanning Transmission Electron Microscopy confirms formation of silver nanoparticles in the samples. Absorption spectra of the samples show the presence of a broadband spectrum associated due to the surface plasmon effect of the silver nanoparticles. A strong surface plasmon band bellow 400 nm appears after the annealing process, due to the formation of silver nanoparticles with radius of 5-15 nm. The transition peaks of Dy3+ are also observed at 386, 446, 798, 917, 1088, 1265 and 1669 nm. Additionally, a large peak at 976 nm belonging to the absorption band corresponding to the Yb3+ is observed. Emission spectra under 406 nm pumping show two prominent bands at 506 and 590 nm belonging to the Dy3+ transitions 4F9/2 → 6H15/2 and 4F9/2 → 6H13/2, respectively. The fluorescence in the 480 nm and 525 nm spectral ranges enhanced with the silver nanoparticles contained in the samples. Is the first time, the luminescence studies of the lithium borate matrix doped with Dy3+ and Yb3+ containing silver nanoparticles is done. The basic parameters defining the lasing-amplifying potential of the glass matrices as a function of silver nanoparticles concentration are calculated. The Thermoluminescence response to UV irradiation also exhibits significant enhancement with the increment of silver nanoparticles in the samples.

Evaluation of optimal storage time of tuberculous lesions stored in sodium borate / Avaliação do tempo de armazenamento do borato de sódio na conservação de lesões tuberculosas

Preservation of specimens during transportation between abattoirs and diagnostic laboratories defines a critical stage in the definitive diagnosis of bovine tuberculosis by the isolation of Mycobacterium bovis. A 2-step study was designed to verify the maximum time that tissue samples can be stored in saturated sodium borate solution (SSB) with the highest detection of M. bovis isolates. Ninety hamsters were inoculated intraperitoneally with a suspension of M. bovis strain AN5 and were humanely euthanized after 40 days. Their spleens were collected and stored in SSB during four distinct periods (30, 60, 90 and 120 days) with incubation at two temperatures (27C and 37C). The control group was cultured on the day of euthanasia. Sixty-nine suspected tuberculous lesions samples were collected in the abattoir and were stored in SSB for three periods (30, 60 and 90 days) at 27C in the laboratory. The bovine control group was cultured on the day of entry in the laboratory. Both experiments were analyzed separately based on the growth proportion of isolates and the number of colonies. SSB was able to maintain the viability of most M. bovis at high temperatures for up to 30 days. A progressive decline was observed with other storage periods at 27C, and no growth was obtained after 60-day storage at 37C. Despite the loss in viability of M. bovis, SSB is the most favorable choice to preserve specimens during transportation across a large country with high variation in environmental temperature. The sensitivity of M. bovis detection by bacteriological examination is inversely proportional to storage time. Therefore, the storage of tuberculous lesion specimens in SSB is recommended to not exceed 30 days at 27°C before cultivation.(AU)

A conservação de espécimes durante o transporte entre abatedouros e laboratórios de diagnóstico define uma etapa crítica no diagnóstico definitivo da tuberculose bovina pelo isolamento de Mycobacterium bovis. Um estudo de duas fases foi delineado para verificar o tempo máximo de armazenamento que amostras teciduais podem ser mantidas em solução saturada de borato de sódio (SSB) com a mais alta detecção de isolados de M. bovis. Noventa hamsters foram inoculados com suspensão de M. bovis cepa AN5 por via intraperitoneal e, após 40 dias, submetidos à eutanásia humanitária. Os baços foram coletados, armazenados em SSB por quatro períodos distintos (30, 60, 90 e 120 dias) e incubados a duas temperaturas (27 e 37C). O grupo controle foi cultivado no mesmo dia da eutanásia. Sessenta e nove amostras de lesões suspeitas de tuberculose foram coletadas em abatedouro e armazenadas em SSB por três períodos (30, 60 e 90 dias) a 27C no laboratório. O grupo controle bovino foi cultivado no dia da entrada no laboratório. Ambos os experimentos foram analisados separadamente baseados na proporção de crescimento de isolados e no número de colônias. A SSB foi capaz de manter a maioria de M. bovis viáveis em altas temperaturas por até 30 dias. Houve um declínio progressivo nos outros períodos de armazenamento a 27C, e não houve crescimento a partir de 60 dias a 37C. Apesar da perda de viabilidade de M. bovis, a SSB é a escolha mais favorável para preservar as amostras durante o transporte em um grande país com alta variação de temperatura ambiente. A sensibilidade de detecção de M. bovis por exames bacteriológicos é inversamente proporcional ao tempo de armazenamento. Portanto, é recomendado que o armazenamento de amostras de lesões tuberculosas em SSB não exceda 30 dias a 27°C antes do cultivo.(AU)

Evaluation of optimal storage time of tuberculous lesions stored in sodium borate / Avaliação do tempo de armazenamento do borato de sódio na conservação de lesões tuberculosas

Preservation of specimens during transportation between abattoirs and diagnostic laboratories defines a critical stage in the definitive diagnosis of bovine tuberculosis by the isolation of Mycobacterium bovis. A 2-step study was designed to verify the maximum time that tissue samples can be stored in saturated sodium borate solution (SSB) with the highest detection of M. bovis isolates. Ninety hamsters were inoculated intraperitoneally with a suspension of M. bovis strain AN5 and were humanely euthanized after 40 days. Their spleens were collected and stored in SSB during four distinct periods (30, 60, 90 and 120 days) with incubation at two temperatures (27C and 37C). The control group was cultured on the day of euthanasia. Sixty-nine suspected tuberculous lesions samples were collected in the abattoir and were stored in SSB for three periods (30, 60 and 90 days) at 27C in the laboratory. The bovine control group was cultured on the day of entry in the laboratory. Both experiments were analyzed separately based on the growth proportion of isolates and the number of colonies. SSB was able to maintain the viability of most M. bovis at high temperatures for up to 30 days. A progressive decline was observed with other storage periods at 27C, and no growth was obtained after 60-day storage at 37C. Despite the loss in viability of M. bovis, SSB is the most favorable choice to preserve specimens during transportation across a large country with high variation in environmental temperature. The sensitivity of M. bovis detection by bacteriological examination is inversely proportional to storage time. Therefore, the storage of tuberculous lesion specimens in SSB is recommended to not exceed 30 days at 27°C before cultivation.

A conservação de espécimes durante o transporte entre abatedouros e laboratórios de diagnóstico define uma etapa crítica no diagnóstico definitivo da tuberculose bovina pelo isolamento de Mycobacterium bovis. Um estudo de duas fases foi delineado para verificar o tempo máximo de armazenamento que amostras teciduais podem ser mantidas em solução saturada de borato de sódio (SSB) com a mais alta detecção de isolados de M. bovis. Noventa hamsters foram inoculados com suspensão de M. bovis cepa AN5 por via intraperitoneal e, após 40 dias, submetidos à eutanásia humanitária. Os baços foram coletados, armazenados em SSB por quatro períodos distintos (30, 60, 90 e 120 dias) e incubados a duas temperaturas (27 e 37C). O grupo controle foi cultivado no mesmo dia da eutanásia. Sessenta e nove amostras de lesões suspeitas de tuberculose foram coletadas em abatedouro e armazenadas em SSB por três períodos (30, 60 e 90 dias) a 27C no laboratório. O grupo controle bovino foi cultivado no dia da entrada no laboratório. Ambos os experimentos foram analisados separadamente baseados na proporção de crescimento de isolados e no número de colônias. A SSB foi capaz de manter a maioria de M. bovis viáveis em altas temperaturas por até 30 dias. Houve um declínio progressivo nos outros períodos de armazenamento a 27C, e não houve crescimento a partir de 60 dias a 37C. Apesar da perda de viabilidade de M. bovis, a SSB é a escolha mais favorável para preservar as amostras durante o transporte em um grande país com alta variação de temperatura ambiente. A sensibilidade de detecção de M. bovis por exames bacteriológicos é inversamente proporcional ao tempo de armazenamento. Portanto, é recomendado que o armazenamento de amostras de lesões tuberculosas em SSB não exceda 30 dias a 27°C antes do cultivo.

Determinación de la dureza total en agua con EDTA empleando una solución amortiguadora inodora de borato / Total hardness water determination by EDTA using a olorless buffer borate

La determinación de Dureza Total con EDTA en agua usando una solución amortiguadora de amonio pH 10 tiene la desventaja de generar vapores de gas amoníaco que suelen ser molestos o ser potencialmente dañinos para el sistema respiratorio del operario. El objetivo de este estudio fue utilizar una solución amortiguadora inodora de borato pH 10 en sustitución de una solución amortiguadora de amonio a pH 10 para la determinación de la dureza total en agua por la metodología de la norma COVENIN 2408-86 y determinar si existía diferencia estadísticamente significativa entre ambos procedimientos. Se determinó la Dureza Total usando la solución amortiguadora inodora de borato en 13 muestras de agua con diferentes grados de dureza (suave, dura y muy dura); los resultados obtenidos se compararon con los valores del procedimiento de referencia. La solución amortiguadora permitió una visualización rápida y definida del punto final durante la ejecución de la determinación volumétrica, los resultados mostraron que no existe diferencia estadísticamente significativa (p≤0,05) en los valores de dureza al emplear ambas soluciones amortiguadoras. Se concluyó que el empleo de la solución amortiguadora inodora de borato para la cuantificación de dureza total en agua es una alternativa a la solución amortiguadora de amonio.

Total Hardness determination EDTA in water using ammonium buffer solution pH 10 has the disadvantage of generating ammonia gas vapors are usually upset or be potentially harmful to the respiratory system operator. The aim of this study was to use a buffer solution pH 10 borate odorless replacing ammonium buffer solution at pH 10 for the determination of total water hardness in the methodology of COVENIN 2408-86 standard and determine whether there was difference statistically significant between the two procedures. Total Hardness was determined using borate buffer odorless in 13 water samples with different degrees of hardness (soft, hard and very hard); the results obtained were compared with the reference method values. The buffer allowed rapid and sharp display of the end point during the execution of the volumetric determination, the results showed that there was no statistically significant difference (p≤ 0,05) in hardness values by using two buffers. It was concluded that the use of borate buffer odorless for quantification of total hardness water is an alternative to the ammonium buffer.

Chronic administration of methylmalonate on young rats alters neuroinflammatory markers and spatial memory.

The methylmalonic acidemia is an inborn error of metabolism (IEM) characterized by methylmalonic acid (MMA) accumulation in body fluids and tissues, causing neurological dysfunction, mitochondrial failure and oxidative stress. Although neurological evidence demonstrate that infection and/or inflammation mediators facilitate metabolic crises in patients, the involvement of neuroinflammatory processes in the neuropathology of this organic acidemia is not yet established. In this experimental study, we used newborn Wistar rats to induce a model of chronic acidemia via subcutaneous injections of methylmalonate (MMA, from 5th to 28th day of life, twice a day, ranged from 0.72 to 1.67 µmol/g as a function of animal age). In the following days (29th-31st) animal behavior was assessed in the object exploration test and elevated plus maze. It was performed differential cell and the number of neutrophils counting and interleukin-1 beta (IL-1ß) and tumor necrosis factor-alpha (TNF-α) levels in the blood, as well as levels of IL-1ß, TNF-α, inducible nitric oxide synthase (iNOS) and 3-nitrotyrosine (3-NT) in the cerebral cortex were measured. Behavioral tests showed that animals injected chronically with MMA have a reduction in the recognition index (R.I.) when the objects were arranged in a new configuration space, but do not exhibit anxiety-like behaviors. The blood of MMA-treated animals showed a decrease in the number of polymorphonuclear and neutrophils, and an increase in mononuclear and other cell types, as well as an increase of IL-1ß and TNF-α levels. Concomitantly, MMA increased levels of IL-1ß, TNF-α, and expression of iNOS and 3-NT in the cerebral cortex of rats. The overall results indicate that chronic administration of MMA increased pro-inflammatory markers in the cerebral cortex, reduced immune system defenses in blood, and coincide with the behavioral changes found in young rats. This leads to speculate that, through mechanisms not yet elucidated, the neuroinflammatory processes during critical periods of development may contribute to the progression of cognitive impairment in patients with methylmalonic acidemia.