Is mercury in fluorescent lamps the only risk to human health? A study of environmental mobility of toxic metals and human health risk assessment.

Although fluorescent lamps (FL) are extensively used worldwide, recycling rates in some countries are still low. If disposed of inappropriately and broken, FL can cause soil contamination. Hg toxicity in FL is extensively discussed in the literature; however, few studies address the other toxic metals present in the phosphorous powder of FL (PPFL). This paper presents a characterization of the environmental mobility with sequential extraction scheme (SES) of Cd, Cu, Hg, Mn, Ni, Pb, and Zn in PPFL, and modeling the potential risks to human health, in case of direct disposal in soils. An after thermal treatment waste was used for safety reasons. The SES method included five fractions, and the quantification was performed by flame atomic absorption spectrometry (FAAS). Human health risk assessment (HHRA) was conducted using RISC4® software. The PPFL showed the following mobility sequence: Cu (85%) > Ni (81%) > Hg (80%) > Zn (77%) > Cd (75%) > Mn (6%) > Pb (2%), which suggests that Cu, Ni, Zn, and Cd, besides Hg, could be of environmental concern in terms of availability. HHRA showed the potential hazard of Cd, for both children and adults, in the hypothetical scenario of vegetable ingestion, considering vegetables grown in soils contaminated with FL waste. The thermal treatment does not completely remove Hg from the matrix, and the residual Hg still poses a risk to children. These results show that Hg and Cd can be hazardous to humans and reinforce the importance of the correct disposal and treatment of PPFL.

Electronic pillbox-enabled self-administered therapy versus standard directly observed therapy for tuberculosis medication adherence and treatment outcomes in Ethiopia (SELFTB): protocol for a multicenter randomized controlled trial.

BACKGROUND: To address the multifaceted challenges associated with tuberculosis (TB) in-person directly observed therapy (DOT), the World Health Organization recently recommended that countries maximize the use of digital adherence technologies. Sub-Saharan Africa needs to investigate the effectiveness of such technologies in local contexts and proactively contribute to global decisions around patient-centered TB care. This study aims to evaluate the effectiveness of pillbox-enabled self-administered therapy (SAT) compared to standard DOT on adherence to TB medication and treatment outcomes in Ethiopia. It also aims to assess the usability, acceptability, and cost-effectiveness of the intervention from the patient and provider perspectives. METHODS: This is a multicenter, randomized, controlled, open-label, superiority, effectiveness-implementation hybrid, mixed-methods, two-arm trial. The study is designed to enroll 144 outpatients with new or previously treated, bacteriologically confirmed, drug-sensitive pulmonary TB who are eligible to start the standard 6-month first-line anti-TB regimen. Participants in the intervention arm (n = 72) will receive 15 days of HRZE-isoniazid, rifampicin, pyrazinamide, and ethambutol-fixed-dose combination therapy in the evriMED500 medication event reminder monitor device for self-administration. When returned, providers will count any remaining tablets in the device, download the pill-taking data, and refill based on preset criteria. Participants can consult the provider in cases of illness or adverse events outside of scheduled visits. Providers will handle participants in the control arm (n = 72) according to the standard in-person DOT. Both arms will be followed up throughout the 2-month intensive phase. The primary outcomes will be medication adherence and sputum conversion. Adherence to medication will be calculated as the proportion of patients who missed doses in the intervention (pill count) versus DOT (direct observation) arms, confirmed further by IsoScreen urine isoniazid test and a self-report of adherence on eight-item Morisky Medication Adherence Scale. Sputum conversion is defined as the proportion of patients with smear conversion following the intensive phase in intervention versus DOT arms, confirmed further by pre-post intensive phase BACTEC MGIT TB liquid culture. Pre-post treatment MGIT drug susceptibility testing will determine whether resistance to anti-TB drugs could have impacted culture conversion. Secondary outcomes will include other clinical outcomes (treatment not completed, death, or loss to follow-up), cost-effectiveness-individual and societal costs with quality-adjusted life years-and acceptability and usability of the intervention by patients and providers. DISCUSSION: This study will be the first in Ethiopia, and of the first three in sub-Saharan Africa, to determine whether electronic pillbox-enabled SAT improves adherence to TB medication and treatment outcomes, all without affecting the inherent dignity and economic wellbeing of patients with TB. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04216420. Registered on 2 January 2020.

A Digital Controlled Pulse Generator for a Possible Tumor Therapy Combining Irreversible Electroporation With Nanosecond Pulse Stimulation.

The irreversible electroporation with microsecond electric pulses is a new ablation technique adopted in the tumor therapy worldwide. On the other hand, the nsPEF (nanosecond pulsed electric field) has been proved to provide a means to induce immunogenic cell death and elicits antitumor immunity, which is under intensive in-vitro and in-vivo studies and in clinical trials. Normally, one needs two different types of electric pulse generators for producing the pulses in the ranges of nanosecond and microsecond, respectively. In order to realize these two types of tumor treatments in complementary and optimize electrical pulse parameters, we have developed a compact high-voltage pulse generator with a wide pulse width tuning range, based on a capacitor discharging configuration digitally controlled by a silicon carbide MOSFET switching array through a pair of optic-coupler drivers. The developed digital pulse generator is capable of adjusting: pulse width over 100-100 µs, voltage over 0-2 kV and repetition rate up to 1.2 kHz. The pulse generator is designed in simulation, implemented and verified in experiments. The pulse generator is shown to deliver a complementary treatment on Murine melanoma B16 cell lines, i.e., triggering the cell early apoptosis under the 300 ns pulse stimulation while a complete killing under the 100 ns pulses. The pulse generator is further demonstrated to induce antitumor immunity in a preliminary in vivo study on the mice model.

E-noise: An increasingly relevant health risk.

This article briefly reviews and discusses the current status of major non-communicable diseases (mNCDs), definition of e-noise, its possible link as a risk factor for cardiovascular diseases and other mNCDs, and proposes possible mechanisms and hypotheses on that link, and how to control e-noise in the future. E-noise is defined as signal from electronic products and instruments that emit radiation and electromagnetic fields. It includes not only the acoustic but also non-acoustic noise. Just like road traffic and aircraft noises, e-noise may not only lead to hearing loss and health problems such as fatigue, stress, irritability, headache, and insomnia, but may also endanger cardiovascular health and result in hypertension, ischemic heart disease (myocardial infarction), arrhythmia (atrial fibrillation) and stroke; brain and metabolic problems such as obesity and diabetes; mental and cognitive impairment; as well as changing of humans' long-evolved cortisol and circadian rhythms after long-term exposure. Even short-term exposure to excessive e-noise may lead to heightened stress responses and low quality of life. In conclusion, e-noise is a potential danger in our world, and further studies are needed of its effects on mechanisms of aging, disease, and human health.

Characterization of Levels of Extremely Low Frequency Magnetic Fields Emitted From Portable Hand-Held Fans.

This study aims to assess the levels of extremely low frequency magnetic fields (ELF-MF) emitted from portable hand-held fans (HHFs) and their principal frequency and to identify factors influencing these levels. We collected a total of eleven models of HHF and monitored the ELF-MF as a function of fan speed and distance from the fan. EMDEX II was used to monitor the ELF-MF. An SMP2 EMF-meter equipped with a P400 field probe was used to determine the levels of ELF-MF and the frequency spectrum. Ten of the fans, excluding only one bladeless-fan model, emitted a high level of ELF-MF near the source of the HHF direct-current motor. The maximum measured level of ELF-MF ranged from 14.07 to 218.7 µT. All measurements of the ELF-MF taken within 10 cm from the HHFs showed values higher than 1.0 µT. ELF-MF levels were found to decrease markedly with distance, regardless of the HHF product. The level of ELF-MF rose noticeably with increased fan speed. The speed of and distance from the HHF significantly influenced the level of ELF-MF. All principal frequencies ranged from 1 to 300 Hz, which falls in the typical range of ELF. Bioelectromagnetics. 2019;40:569-577. © 2019 Bioelectromagnetics Society.

Technical Note: Characterization of the new microSilicon diode detector.

PURPOSE: Dosimetric properties of the new microSilicon diode detector (60023) have been studied with focus on application in small-field dosimetry. The influences of the dimensions of the sensitive volume and the density of the epoxy layer surrounding the silicon chip of microSilicon have been quantified and compared to its predecessor (Diode E 60017) and the microDiamond (60019, all PTW-Freiburg, Germany). METHODS: Dose linearity has been studied in the range from 0.01 to 8.55 Gy and dose-per-pulse dependence from 0.13 to 0.86 mGy/pulse. The effective point of measurement (EPOM) was determined by comparing measured percentage depth dose curves with a reference curve (Roos chamber). Output ratios were measured for nominal field sizes from 0.5 × 0.5  cm2 to 4 × 4 cm2 . The corresponding small-field output correction factors, k, were derived with a plastic scintillation detector as reference. The lateral dose-response function, K(x), was determined using a slit beam geometry. RESULTS: MicroSilicon shows linear dose response (R2  = 1.000) in both low and high dose range up to 8.55 Gy with deviations of only up to 1% within the dose-per-pulse values investigated. The EPOM was found to lie (0.7 ± 0.2) mm below the front detector's surface. The derived k for microSilicon (0.960 at seff  = 0.55 cm) is similar to that of microDiamond (0.956), while Diode E requires larger corrections (0.929). This improved behavior of microSilicon in small-fields is reflected in the slightly wider K(x) compared to Diode E. Furthermore, the amplitude of the negative values in K(x) at the borders of the sensitive volume has been reduced. CONCLUSIONS: Compared to its predecessor, microSilicon shows improved dosimetric behavior with higher sensitivity and smaller dose-per-pulse dependence. Profile measurements demonstrated that microSilicon causes less perturbation in off-axis measurements. It is especially suitable for the applications in small-field output factors and profile measurements.

A powerful on line ABTS+-CE-DAD method to screen and quantify major antioxidants for quality control of Shuxuening Injection.

A novel method of on-line 2,2'-Azinobis-(3-ethylbenzthiazoline-6-sulphonate)-Capillary Electrophoresis-Diode Array Detector (on-line ABTS+-CE-DAD) was developed to screen the major antioxidants from complex herbal medicines. ABTS+, one of well-known oxygen free radicals was firstly integrated into the capillary. For simultaneously detecting and separating ABTS+ and chemical components of herb medicines, some conditions were optimized. The on-line ABTS+-CE-DAD method has successfully been used to screen the main antioxidants from Shuxuening injection (SI), an herbal medicines injection. Under the optimum conditions, nine ingredients of SI including clitorin, rutin, isoquercitrin, Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside, kaempferol-3-O-rutinoside, kaempferol-7-O-ß-D-glucopyranoside, apigenin-7-O-Glucoside, quercetin-3-O-[2-O-(6-O-p-hydroxyl-E-coumaroyl)-D-glucosyl]-(1-2)-L-rhamnoside, 3-O-{2-O-[6-O-(p-hydroxyl-E-coumaroyl)-glucosyl]}-(1-2) rhamnosyl kaempfero were separated and identified as the major antioxidants. There is a linear relationship between the total amount of major antioxidants and total antioxidative activity of SI with a linear correlation coefficient of 0.9456. All the Relative standard deviations of recovery, precision and stability were below 7.5%. Based on these results, these nine ingredients could be selected as combinatorial markers to evaluate quality control of SI. It was concluded that on-line ABTS+-CE-DAD method was a simple, reliable and powerful tool to screen and quantify active ingredients for evaluating quality of herbal medicines.

A collapsed-cone based transit EPID dosimetry method.

PURPOSE: To develop a transit-dose portal dosimetry method based on a commercial collapsed-cone algorithm. METHODS: A Varian Clinac21EX (Varian Medical Systems, USA), equipped with an amorphous-silicon EPID aS1000, was used. Dose calculations were performed with the collapsed-cone algorithm of Pinnacle3 v8.0 m (Philips Medical Systems, USA). A model for the energy of 6 MV was made in Pinnacle3 and afterwards validated for clinical use. A virtual phantom with different densities was contoured and superimposed on the patient images, simulating the presence of the EPID during the treatment. Corrections for photon spectral variations were introduced using Matlab (Mathworks, USA). Transit dosimetry was verified with an anthropomorphic phantom, on which different treatment fields were simulated in locations of skull, thorax and pelvis. In addition, a prostate treatment with IMRT was administered thereon. Dose distributions were compared with gamma index. RESULTS: The dose differences at the central point did not exceed 2%, except for the 20 x 20 cm2 field size centered in the skull. The model presented in this work, assumes that the dimensions of the solid water phantom, are infinite, except for the thickness. The mean values for the gamma index pass rates were 85.62% for (3%, 3 mm), 91.73% (4%, 3 mm) and 95.68% (5%, 3 mm). CONCLUSIONS: The value of 95% for γ (5%, 3 mm) can be established as the value below which the origin of the discrepancies should be investigated. It should be considered that the proposed method is complementary and not a substitute for pre-treatment dosimetry.

Micro-coil-induced Inhomogeneous Electric Field Produces sound-driven-like Neural Responses in Microcircuits of the Mouse Auditory Cortex In Vivo.

Magnetic stimulation is widely used in neuroscience research and clinical treatment. Despite recent progress in understanding the neural modulation mechanism of conventional magnetic stimulation methods, the physiological mechanism at the cortical microcircuit level is not well understood due to the poor stimulation focality and large electric artifact in the recording. To overcome these issues, we used a sub-millimeter-sized coil (micro-coil) to stimulate the mouse auditory cortex in vivo. To determine the mechanism, we conducted the first direct electrophysiological recording of micro-coil-driven neural responses at multiple sites on the horizontal surface and laminar areas of the auditory cortex. The laminar responses of local field potentials (LFPs) to the magnetic stimulation reached layer 6, and the spatiotemporal profiles were very similar to those of the acoustic stimulation, suggesting the activation of the same cortical microcircuit. The horizontal LFP responses to the magnetic stimulation were evoked within a millimeter-wide area around the stimulation coil. The activated cortical area was dependent on the coil orientation, providing useful information on the effective position of the coil relative to the brain surface for modulating cortical circuitry activity. In addition, numerical calculation of the induced electric field in the brain revealed that the inhomogeneity of the horizontal electric field to the surface is critical for micro-coil-induced cortical activation. The results suggest that our micro-coil technique has the potential to be used as a chronic, less-invasive and highly focal neuro-stimulator, and is useful for investigating microcircuit responses to magnetic stimulation for clinical treatment.

Portal MV imaging with thin-film high-energy current X-ray detectors: A Monte Carlo study.

PURPOSE: We investigate the potential of the recently introduced high-energy current (HEC) thin-film detector as an alternative design to existing electronic portal imaging devices (EPID). The HEC radiation detectors employ multiple nano-/micrometer layers made of disparate atomic number (Z) conductors separated by solid or gaseous (e.g., air) dielectrics. The HEC detector may be designed as an external structure or an auxiliary device integrated into the existing EPID. METHOD: Using Geant4 Monte Carlo simulations, we compare the image contrast of a HEC detector to that of a commercial EPID device (AS500) for a 2.5 MV X-ray beam. The detector response was modeled using a series of monoenergetic incident photons with detector signal scored as the energy deposition in the air gaps (HEC) and in the phosphor layer (EPID). Las Vegas (LV) phantom was employed to test the spatial resolution and contrast of the single- and multielement HEC detector. The HEC detector pixel size was the same as for AS500 (0.78 mm × 0.78 mm). In addition, image contrast of a water/bone phantom using both the multielement HEC and EPID detectors was simulated and compared. RESULTS: The HEC detector has higher relative response to low-energy photons compared to EPID. The multielement HEC has 32.3 times greater response at 100 keV than at 500 keV, while the EPID without copper plate shows a factor of 6.8 between the same energies. LV phantom images indicate that the image contrast is approximately the same for single- and multielement HEC detectors, but the latter has lower noise. Both single- and multielement HEC could resolve a 2 mm diameter hole with an image magnification factor of 1.2. In the present design, the HEC detector has much less material (9.66 mg/cm2 gold) compared to EPID (133 mg/cm2 Gd2 O2 S) to interact with incident photons. For imaging bony structures, the HEC detector needs about nine times greater photon flux as the EPID to acquire data at same uncertainty level. Despite this, the HEC sensor requires less than 1 cGy dose to obtain images with statistical uncertainty better than 2.5%. In the case when the field diameter is 10 cm, the multielement HEC image contrast is 14.3% higher than that of EPID with copper removed. When the field diameter is decreased to 5 cm, HEC contrast is 27.1% better than the EPID contrast. CONCLUSION: It is demonstrated that the image contrast of HEC detectors are comparable and in some cases better than that of the standard EPID design. This opens a potential for complementary HEC and EPID designs that may better utilize the kV portion of the spectrum.

New experimental model for single liver lobe hyperthermia in small animals using non-directional microwaves.

PURPOSE: Our aim was to develop a new experimental model for in vivo hyperthermia using non-directional microwaves, applicable to small experimental animals. We present an affordable approach for targeted microwave heat delivery to an isolated liver lobe in rat, which allows rapid, precise and stable tissue temperature control. MATERIALS AND METHODS: A new experimental model is proposed. We used a commercial available magnetron generating 2450 MHz, with 4.4V and 14A in the filament and 4500V anodic voltage. Modifications were required in order to adjust tissue heating such as to prevent overheating and to allow for fine adjustments according to real-time target temperature. The heating is controlled using a virtual instrument application implemented in LabView® and responds to 0.1° C variations in the target. Ten healthy adult male Wistar rats, weighing 250-270 g were used in this study. The middle liver lobe was the target for controlled heating, while the rest of the living animal was protected. RESULTS: In vivo microwave delivery using our experimental setting is safe for the animals. Target tissue temperature rises from 30°C to 40°C with 3.375°C / second (R2 = 0.9551), while the increment is lower it the next two intervals (40-42°C and 42-44°C) with 0.291°C/ s (R2 = 0.9337) and 0.136°C/ s (R2 = 0.7894) respectively, when testing in sequences. After reaching the desired temperature, controlled microwave delivery insures a very stable temperature during the experiments. CONCLUSIONS: We have developed an inexpensive and easy to manufacture system for targeted hyperthermia using non-directional microwave radiation. This system allows for fine and stable temperature adjustments within the target tissue and is ideal for experimental models testing below or above threshold hyperthermia.

Development and application of LED arrays for use in phototherapy research.

Lasers/LEDs demonstrate therapeutic effects for a range of biomedical applications. However, a consensus on effective light irradiation parameters and efficient and reliable measurement techniques remain limited. The objective here is to develop, characterise and demonstrate the application of LED arrays in order to progress and improve the effectiveness and accuracy of in vitro photobiomodulation studies. 96-well plate format LED arrays (400-850 nm) were developed and characterised to accurately assess irradiance delivery to cell cultures. Human dental pulp cells (DPCs) were irradiated (3.5-142 mW/cm2 : 15-120 s) and the biological responses were assessed using MTT assays. Array calibration was confirmed using a range of optical and analytical techniques. Multivariate analysis of variance revealed biological responses were dependent on wavelength, exposure time and the post-exposure assay time (P < 0.05). Increased MTT asbsorbance was measured 24 h post-irradiation for 30 s exposures of 3.5 mW/cm2 at 470, 527, 631, 655, 680, 777, 798 and 826 nm with distinct peaks at 631 nm and 798 nm (P < 0.05). Similar wavelengths were also effective at higher irradiances (48-142 mW/cm2 ). LED arrays and high throughput assays provide a robust and reliable platform to rapidly identify irradiation parameters which is both time- and cost-effective. These arrrays are applicable in photobiomodulation, photodynamic therapy and other photobiomedical research.

Evaluación de tecnología sanitaria: eficacia y seguridad del uso del dispositivo estimulador del nervio vago / Evaluation of health technology: efficacy and safety of the use of the vagus nerve stimulator device

INTRODUCCIÓN: Antecedentes: El presente informe está referido a la evaluación de la eficacia y seguridad del dispositivo médico Estimulador del Nervio Vago (ENV) en pacientes con el diagnóstico de Epilepsia Resistente a Fármacos, solicitado por el Hospital Edgardo Rebagliati Martins. Aspectos Generales: La Epilepsia, es un transtorno neurológico de tendencia crónica que afecta a adultos y niños; en el mundo, unos 50 millones de personas padecen de epilepsia y es la causa de defunción más común de caso neurológico a nival mundial. La Epilepsia se caracteriza por convulsiones recurrentes, que pueden ser episodios de movimientos involuntários que afectan una parte del cuerpo (convulciones parciales) o a todo el cuerpo (convulciones generalizadas) que puede acompañarse de pérdida de conciencia y de control de los esfínteres. Tecnología Sanitaria de Interés: El dispositivo Estimulador del Nervio Vago es similar a un marcapaso, el cual se conecta mediante una vía al nervio que cruza por el lado izquierdo dek cuello. Este dispositivo es colocado por debajo de la clavícula, este aparato es programado para generar estímulos eléctros repetidos, a intensidades seleccionadas y regulares, que, al estimular el nervio vago, tiene como objetivo el reducir la frencuencia de crisis epilépticas. METODOLOGÍA: Estrategia de Búsqueda: Se realizó una búsqueda sistemática de la evidencia científica con respecto a la seguridad y eficacia del dispositivo denominado Estimulador del Nervio Vago (ENV) usado en pacientes con epilepsia fármaco resistente que no son tributarios de tratamiento quirúrgico por lesión cerebral focal. Se realizó una búsqueda en las bases de datos: Pubmed, Tripdatabase, Science Direct, Embase, EBSCO; además, de la información proporcionada por grupos internacionales o agencias internacionales de que realizan revisiones sistemáticas, evaluación de tecnologías sanitarias y guías de práctica clínica, tales como The Cochrane Library, el Instituto Nacional de Salud y Excelencia en Cuidado (NICE), The National Guideline Clearinhouse (NGC), The Canadian Agency for Drugs and Technologies in Health (CADTH). Finalmente, se hizouna búsqueda en www.clinicaltrials.gov, para poder identificar ensayos aún en elaboración o que no hayan sido publicados. RESULTADOS: Lugeo de la búsqueda realizada se encontró evidencia científica que evaluaron la eficacia y seguridad del dispositivo ENV para pacientes con epilepsia fármaco resistente que no son tributarios de tratamiento quirúrgico por lesión cerebral focal. Sinopsis de la Evidenvia: Se encontró evidencia acerca de la eficacia del dispositivo Estimulador del Nervio Vago (ENV) usado en pacientes con epilepsia fármaco resistente que no son tributarios de tratamiento quirúrgico por lesión cerebral focal: -Guías de Práctica Clínica (GPC): 02 Guías de Práctica Clínica; -Revisiones Sistemáticas (RS) y Metanálisis (ME): 02 selecionadas; -Evaluaciones de Tecnología Sanitaria (ETS) y Económicas: 02 ETS; -Estudios Experimentales: Incluidos en los estudios de revisiones sistemáticas y metanálisis; -Estudios Observacionales: ninguno seleccionado; -Ensayos clínicos en proceso: ninguno. Conclusiones: Esta evaluación de tecnología santiaria llevada a cabo por el Instituto de Evaluación de Tecnologías en Salud e Investigación (IETSI) ha determinado que el uso del dispositivo Estimulador del nervio vago como tratamiento adyuvante para la Epilepsia Refractaria es eficaz para la reducción de las crisis epilépticas, ya que su efecto alcanzaría en la reducción de las crisis epilépticas, ya que su efecto alcanzaría en la reducción de hasta un 50% de las crisis epilépticas en el 50% de los pacientes tratados con el dispositivo. El dispositivo estimulador del nervio vago se muestra seguro en los pacientes con epilpsia refractaria, ya que los eventos adversos reportados no han impedido su uso en los pacientes con epilepsia refractaria. Se ha determinado que el uso del Dispositivo estimulador del nervio vago no disminuye la cantidad de medicamentos antiepilépticos en los pacientes con epilepsia refractaria. El dispositvo ENV debe utilizarse como terapia adyuante para la reducción de las crisis epilépticas. Hace falta mayores estudios que evidencien el efecto del dispositivo Estimulador del Nervio Vago en la calidad de vida de los pacientes o en la disminución de sus controles médicos o el número de hospitalizaciones. A pesar de que los resultados mostrados en la evidencia científica revisada no son alentadores, los médicos especialistas neurólogos y nerucirujanos, expresaron que el dispositivo estimulador del nervio vago representa la última alternativa que tienen este tipo de pacientes como tratamiento paliativo para disminuir la frecuencia de convulciones hasta en un 50% en un grupo de entre 30% a 50% de ellos, loo que podría traducirse en una mejora al menos modesta de su calidad de vida. El Instituto de Evaluación de Tecnologías en Salud e Investigación aprueba el uso del dispositivo estimulador del nervio vago para pacientes con epilepsia refractaria. La aprobación del uso de este dispositivo tiene una vigencia de 02 años a partir d ela fecha de publicación.

Simultaneous Determinations of Eleven Bioactive Components in Suanzaoren Decoction Granules by High-Performance Liquid Chromatography and Its Application to the Quality Control in Productive Processes.

A simple and reliable method using high-performance liquid chromatography coupled with a photodiode array detector (HPLC-PDA) was firstly established for the determinations of eleven bioactive compounds (neomangiferin, mangiferin, spinosin, liquiritin apioside, liquiritin, fumalic acid, 6'''-feruloylspinosin, senkyunolide I, isoliquiritin, glycyrrhizic acid and senkyunolide A) in Suanzaoren decoction (SZRD) extract and its granules. The chromatographic analysis was performed on a C18 column at 30°C. Excellent linear behaviors over the investigated concentration ranges were observed with the values of R(2) being higher than 0.9990 for all analytes. The developed method showed good precision and accuracy with overall intra- and inter-day variations of less than 2.0%, and overall recoveries in the range of 97.2 - 102.1%. The validated method was successfully applied to the determination of eleven components in SZRD samples from different production batches, including SZRD extract, lab-made SZRD granules and clinical medicine. This accurate and reliable HPLC-PDA method will be helpful for improving the quality evaluation of SZRD granules and its quality control in productive processes.

Evaluación del ambiente electromagnético en salas de rehabilitación / Evaluation of the electromagnetic environment in rehabilitation wards

Se realizó un estudio del ambiente electromagnético en 2 departamentos de electroterapia del municipio Palma Soriano de Santiago de Cuba, a fin de obtener el patrón de distribución para diferentes modos de operatividad y explotación del equipamiento médico-terapéutico. Para la caracterización electromagnética de los ambientes evaluados se elaboró un protocolo de medición a partir del análisis de normas internacionales y se empleó un medidor isotrópico que mostró los resultados a través de mapas de contorno. El equipo electromédico Magnetomed, modelo 7200 fue el que más aportó, aunque el valor máximo de la inducción magnética obtenido (19,7 µT) estuvo por debajo del límite de exposición establecido y por encima del límite de exposición sugerido por el Grupo de Trabajo Bioiniciativa. Se recomienda limitar la permanencia de personas en sus proximidades mientras está en funcionamiento.

A study of the electromagnetic environment was carried out in 2 electrotherapy departments of Palma Soriano in Santiago de Cuba, in order to obtain the distribution pattern for different operability ways and exploitation of the medical-therapeutic equipment. For the electromagnetic characterization of the evaluated environments a measurement protocol was elaborated starting from the analysis of international standards and an isotropic measure was used that showed the results through contour maps. The electro-medical device Magnetomed, model 7200 was the one that contributed the most, although the maximum value of the obtained magnetic induction (19.7 µT) was below the established exhibition limit and above the exhibition limit suggested by the Bioiniciativa Work Group. It is recommended to limit the permanency of people around, while it is in operation.

Wood-Derived Materials for Green Electronics, Biological Devices, and Energy Applications.

With the arising of global climate change and resource shortage, in recent years, increased attention has been paid to environmentally friendly materials. Trees are sustainable and renewable materials, which give us shelter and oxygen and remove carbon dioxide from the atmosphere. Trees are a primary resource that human society depends upon every day, for example, homes, heating, furniture, and aircraft. Wood from trees gives us paper, cardboard, and medical supplies, thus impacting our homes, school, work, and play. All of the above-mentioned applications have been well developed over the past thousands of years. However, trees and wood have much more to offer us as advanced materials, impacting emerging high-tech fields, such as bioengineering, flexible electronics, and clean energy. Wood naturally has a hierarchical structure, composed of well-oriented microfibers and tracheids for water, ion, and oxygen transportation during metabolism. At higher magnification, the walls of fiber cells have an interesting morphology-a distinctly mesoporous structure. Moreover, the walls of fiber cells are composed of thousands of fibers (or macrofibrils) oriented in a similar angle. Nanofibrils and nanocrystals can be further liberated from macrofibrils by mechanical, chemical, and enzymatic methods. The obtained nanocellulose has unique optical, mechanical, and barrier properties and is an excellent candidate for chemical modification and reconfiguration. Wood is naturally a composite material, comprised of cellulose, hemicellulose, and lignin. Wood is sustainable, earth abundant, strong, biodegradable, biocompatible, and chemically accessible for modification; more importantly, multiscale natural fibers from wood have unique optical properties applicable to different kinds of optoelectronics and photonic devices. Today, the materials derived from wood are ready to be explored for applications in new technology areas, such as electronics, biomedical devices, and energy. The goal of this study is to review the fundamental structures and chemistries of wood and wood-derived materials, which are essential for a wide range of existing and new enabling technologies. The scope of the review covers multiscale materials and assemblies of cellulose, hemicellulose, and lignin as well as other biomaterials derived from wood, in regard to their major emerging applications. Structure-properties-application relationships will be investigated in detail. Understanding the fundamental properties of these structures is crucial for designing and manufacturing products for emerging applications. Today, a more holistic understanding of the interplay between the structure, chemistry, and performance of wood and wood-derived materials is advancing historical applications of these materials. This new level of understanding also enables a myriad of new and exciting applications, which motivate this review. There are excellent reviews already on the classical topic of woody materials, and some recent reviews also cover new understanding of these materials as well as potential applications. This review will focus on the uniqueness of woody materials for three critical applications: green electronics, biological devices, and energy storage and bioenergy.

Light-emitting diodes at 940nm attenuate colitis-induced inflammatory process in mice.

Inflammatory bowel disease (IBD) presents intense inflammatory infiltrate, crypt abscesses, ulceration and even loss of function. Despite the clinical relevance of IBD, its current therapy remains poorly effective. Infrared wavelength phototherapy shows therapeutic potential on inflammation. Our goal was to evaluate whether light-emitting diodes (LED) at 940nm are capable of mitigating the colitis-induced inflammatory process in mice. Forty male Swiss mice were assigned into five groups: control; control treated with LED therapy; colitis without treatment; colitis treated with LED therapy; colitis treated with Prednisolone. Experimental colitis was induced by acetic acid 7.5% (pH2.5) rectal administration. LED therapy was performed with light characterized by wavelength of 940nm, 45nm bandwidth, intensity of 4.05J/cm(2), total power of 270mW and total dose of 64.8J for 4min in a single application. Colitis-induced intestinal transit delay was inhibited by LED therapy. Colitis caused an increase of colon dimensions (length, diameter, total area) and colon weight (edema), which were inhibited by LED therapy. LED therapy also decreased colitis-induced tissue gross lesion, myeloperoxidase activity, microscopic tissue damage score and the presence of inflammatory infiltrate in all intestinal layers. Furthermore, LED therapy inhibited colitis-induced IL-1ß, TNF-α, and IL-6 production. We conclude LED therapy at 940nm inhibited experimental colitis-induced colon inflammation in mice, therefore, rendering it a promising therapeutic approach that deserves further investigation.

Exploring bitterness of traditional Chinese medicine samples by potentiometric electronic tongue and by capillary electrophoresis and liquid chromatography coupled to UV detection.

Instrumental bitterness assessment of traditional Chinese herbal medicine (TCM) preparations was addressed in this study. Three different approaches were evaluated, high-performance liquid chromatography coupled to UV detector (HPLC), capillary electrophoresis coupled to UV detector (CE) and a potentiometric multisensor system - electronic tongue (ET). Most studies involving HPLC and CE separations use these as selective instruments for quantification of individual substances. However we employed these techniques to provide chromatographic or electrophoretic sample profiles. These profiles are somewhat analogous to the profiles produced by the ET. Profiles from all instruments were then related to professional sensory panel evaluations using projections on latent structures (PLS) regression. It was found that all three methods allow for bitterness assessment in TCM samples in terms of human sensory panel with root mean squared errors of prediction ca. 0.9 within bitterness scale from 0 (no bitterness) to 6 (maximal bitterness).

A piecewise-focused high DQE detector for MV imaging.

PURPOSE: Electronic portal imagers (EPIDs) with high detective quantum efficiencies (DQEs) are sought to facilitate the use of the megavoltage (MV) radiotherapy treatment beam for image guidance. Potential advantages include high quality (treatment) beam's eye view imaging, and improved cone-beam computed tomography (CBCT) generating images with more accurate electron density maps with immunity to metal artifacts. One approach to increasing detector sensitivity is to couple a thick pixelated scintillator array to an active matrix flat panel imager (AMFPI) incorporating amorphous silicon thin film electronics. Cadmium tungstate (CWO) has many desirable scintillation properties including good light output, a high index of refraction, high optical transparency, and reasonable cost. However, due to the 0 1 0 cleave plane inherent in its crystalline structure, the difficulty of cutting and polishing CWO has, in part, limited its study relative to other scintillators such as cesium iodide and bismuth germanate (BGO). The goal of this work was to build and test a focused large-area pixelated "strip" CWO detector. METHODS: A 361 × 52 mm scintillator assembly that contained a total of 28 072 pixels was constructed. The assembly comprised seven subarrays, each 15 mm thick. Six of the subarrays were fabricated from CWO with a pixel pitch of 0.784 mm, while one array was constructed from BGO for comparison. Focusing was achieved by coupling the arrays to the Varian AS1000 AMFPI through a piecewise linear arc-shaped fiber optic plate. Simulation and experimental studies of modulation transfer function (MTF) and DQE were undertaken using a 6 MV beam, and comparisons were made between the performance of the pixelated strip assembly and the most common EPID configuration comprising a 1 mm-thick copper build-up plate attached to a 133 mg/cm(2) gadolinium oxysulfide scintillator screen (Cu-GOS). Projection radiographs and CBCT images of phantoms were acquired. The work also introduces the use of a lightweight edge phantom to generate MTF measurements at MV energies and shows its functional equivalence to the more cumbersome slit-based method. RESULTS: Measured and simulated DQE(0)'s of the pixelated CWO detector were 22% and 26%, respectively. The average measured and simulated ratios of CWO DQE(f) to Cu-GOS DQE(f) across the frequency range of 0.0-0.62 mm(-1) were 23 and 29, respectively. 2D and 3D imaging studies confirmed the large dose efficiency improvement and that focus was maintained across the field of view. In the CWO CBCT images, the measured spatial resolution was 7 lp/cm. The contrast-to-noise ratio was dramatically improved reflecting a 22 × sensitivity increase relative to Cu-GOS. The CWO scintillator material showed significantly higher stability and light yield than the BGO material. CONCLUSIONS: An efficient piecewise-focused pixelated strip scintillator for MV imaging is described that offers more than a 20-fold dose efficiency improvement over Cu-GOS.

Multi-frequency bioimpedance in equine muscle assessment.

Multi-frequency BIA (mfBIA) equipment has been shown to be a non-invasive and reliable method to assess a muscle as a whole or at fibre level. In the equine world this may be the future method of assessment of training condition or of muscle injury. The aim of this study was to test if mfBIA reliably can be used to assess the condition of a horse's muscles in connection with health assessment, injury and both training and re-training. mfBIA measurements was carried out on 10 'hobby' horses and 5 selected cases with known anamnesis. Impedance, resistance, reactance, phase angle, centre frequency, membrane capacitance and both extracellular and intracellular resistance were measured. Platinum electrodes in connection with a conductance paste were used to accommodate the typical BIA frequencies and to facilitate accurate measurements. Use of mfBIA data to look into the effects of myofascial release treatment was also demonstrated. Our findings indicate that mfBIA provides a non-invasive, easily measurable and very precise assessment of the state of muscles in horses. This study also shows the potential of mfBIA as a diagnostic tool as well as a tool to monitor effects of treatment e.g. myofascial release therapy and metabolic diseases, respectively.