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Background: Many Mexican Ternstroemia species mainly inhabit the tropical montane cloud forest. These species have been misidentified in herbaria due to their morphological resemblance. Question: Are there foliar anatomical and micromorphological characters with diagnostic value that allow discriminating between the Mexican species of Ternstroemia? Study species: Ternstroemia sylvatica Schltdl. & Cham., and T. lineata DC. subsp. lineata (Pentaphylacaceae Engl.), 2018-2019. Study site and date: Tropical montane cloud forests at the Trans-Mexican Volcanic Belt and Sierra Madre Oriental. Methods: Botanical specimens were collected and removed from herbarium sheets. The leaves were prepared through cleared, dehydration and paraffin inclusion techniques to observe and describe them. Results: The Ternstroemia species showed specific features of plants in humid environments, such as thin cuticle, mesophyll with scarce parenchyma palisade, and abundant intercellular spaces in the spongy parenchyma, and specific pigments that help to capture light and serve as protection. The species share a festooned broquidodromous venation pattern, anomocytic stomata, and closed collateral vascular bundle surrounded by perivascular fibers. Both species are differentiated by leaf shape, abundance of collenchyma layers, lenght of palisade parenchyma, and number of stomata per square millimeter on the abaxial surface. Conclusions: We support and validate some features recorded for Ternstroemia species and reject some previous generalizations made worldwide to the genus. This research is the first attempt to study anatomy, architecture, and foliar micromorphology of Mexican Pentaphylacaceae.

This work reports the building of a low-cost experimental setup for high temporal resolution data acquisition. The setup is useful for different applications, especially for voltage data acquisition during electrochemical experiments. The proposed setup performed two hundred thousand measurements per second (5 µs time resolution) and revealed unknown curve characteristics during chronopotentiometry of the anodization of valve metals. This information can serve as a starting point for further investigations on the nature of voltage oscillations in the breakdown region during valve metal anodization.

El doble propósito de satisfacer las grandes necesidades habitacionales en las zonas intertropicales, sin comprometer aún más la estabilidad de sus ecosistemas, requiere de nuevos conceptos que contribuyan a solventar el divorcio existente entre los esquemas organizativos de los sistemas naturales y el de los artificiales. Apoyándose en la extensa información científica disponible acerca de los sistemas vivos (SV), se infieren en el presente trabajo algunos de los atributos que deben integrar los conceptos relativos a las funciones de acondicionamiento, contención y organización de actividades de aquellas edificaciones estrechamente vinculadas a los SV. Para ello se expone el concepto del Sistema Kiron (SK) –elemento que integra el actual desarrollo de la tesis Doctoral del autor– consistente en un nuevo nivel jerárquico de organización, semi-artificial, constituido por tres subsistemas (el ecosistema, el cuerpo humano en tanto organismo o biosistema y la edificación o sistema artificial) cuya función es, precisamente, contribuir a disolver la dicotomía entre la lógica organizativa de los sistemas naturales y la de los artificiales. Es en el seno del SK donde se modifican los conceptos de tales funciones. Los límites del Sistema Kiron vienen a constituir el nuevo continente dentro del cual la edificación o sistema artificial (SA) organiza y es organizada, contiene y es contenida, y donde su función de acondicionamiento ambiental es conceptuada como un transductor que compatibiliza las entradas y salidas entre el subsistema SE y el subsistema SB, posibilitando la constitución de una red híbrida de elementos naturales y artificiales, cuyo objetivo común es alcanzar su propia estabilidad dinámica y la del SK al que pertenecen.

El presente trabajo describe la estandarización de un ensayo diseñado para cuantificar la actividad hidrolítica de la enzima biotinidasa en muestras de suero humano, el cual se basa en el método de Wolf y colaboradores, que emplea el N-biotinil-p-aminobenzoico (BPABA) como sustrato. Con la adición de detergentes a la solución de nitrito de sodio, se eliminan las burbujas de nitrógeno formadas durante la reacción de diazotación y se mejora la precisión del ensayo. Se observó que la congelación-descongelación de las muestras de suero no afecta la actividad hidrolitica de la enzima biotinidasa. La evaluación de la interferencia de fármacos en el ensayo mostró que con el sulfametoxasol/trimetoprim y la procainal benzilpenicilina hay desarrollo de color en ausencia del sustrato BPABA. Los valores promedio de actividad hidrolitica de la biotinidasa, obtenidos en un grupo de 205 niños sanos, fue de 7,04 + 2,2 nmol/min/ml. No se encontraron diferencias estadísticamente significativas al evaluar la actividad de la enzima por sexo, raza y grupos de edad. Este ensayo se puede emplear en la determinación de la actividad hidrolítica de la enzima biotinidasa en muestras de suero humano y, específicamente, en la confirmación de los casos detectados por los programas de tamizaje neonatal para la deficiencia de biotinidasa.

It has been recurring adulterations in fuels (such as gasoline, ethanol and diesel), being necessary the exploration of the use of more modern analytical techniques capable of controlling the quality of these fuels, since some regulated tests may be inefficient to detect the adulteration. Among them, it is highlighted proton nuclear magnetic resonance (1H NMR) spectroscopy, and portable near infrared spectroscopy (microNIR). In this work, it was studied the conformities of 115 samples of seized fuels (76 of gasoline, 23 of ethanol, and 16 of diesel) by means of standardized techniques with parameters established by the ANP. Results obtained were compared to photometer, MicroNIR and 1H NMR analyzes. The analyzes carried out by ANP showed four nonconforming samples (one of gasoline and three of ethanol). By the photometric technique, only 14 gasoline samples had ethanol content permitted by legislation (i.e ≈ 27 %v/v). By 1H NMR analysis, it was possible to verify nonconformities by presence of aromatics and olefins compounds in the gasoline and diesel samples as well as of methanol in fuel ethanol samples. It is also worth noting the efficiency of MicroNIR when combined with unsupervised chemometric methods to indicate nonconformities presented by 1H NMR and photometry techniques.

Quality of the sample and phenylalanine and 17-hydroxyprogesterone levels in neonatal screening. In the programs for neonatal screening many different analytes are quantified from dried blood on filter paper cards. Several factors affect the quality of the samples invalidating their employment in the laboratory: inadequate collection procedures, quality of the filter paper, the drying, storage and transportation under extreme environmental conditions. This article aims to show how the quality of the sample collection influences the phenylalanine (Phe) and 17-hydroxyprogesterone (17-OHP) levels. As such, samples of newborns on filter paper from Ramon Gonzalez Coro Hospital were collected and analyzed.The blood spots from a sample were classified according to their appearance, satisfactory spot (MV) or unsatisfactory spot (MNV). Phe and 17OHP levels were determinated by UMTEST PKU and UMELISA 17OH Progesterone NEONATAL, respectively. 19.5% of 3043 newborns samples exhibited unsatisfactory spots. Concordance correlations studies between MV y MNV showed the precision and accuracy were affected by quality of the samples. False positive and negative values (with concerning control sample) were detected from samples with MNV. The correct application of collection procedures for samples is essential in obtaining reliable results in screening neonatal laboratories.

Congenital hypothyroidism (CH) is one of the most common preventable causes of mental retardation. Newborn screening and thyroid therapy started within 2 weeks of age can normalize the cognitive and motor impairment caused by lack of thyroid hormone during the early postnatal phase of brain development. The availability of assays to determine thyroxin (T4) and thyroid stimulating hormone has allowed the establishment of newborn screening programs for CH. The Immunoassay Center (Cuba) developed the T4 Neonatal UMELISA(r) to determine neonatal T4 levels in dried blood on filter paper using 5 mm discs of samples, standards and controls. The number of diseases which can be diagnosed in Neonatal Screening Programs has increased, so it is necessary to make the maximum use of blood samples collected on filter paper. This work shows the standardization of the T4 Neonatal UMELISA(r) modified in order to use 3 mm discs. The assay was completed in 3 1/2 hours, with a measuring range of 25-400 nmol/L. The intra- and inter-assay coefficients of variation (CV) were 6-10 % and 7-12 % respectively, depending on the T4 concentrations. The recovery ranged from 91.8-115.1 %. The modified assay showed high Pearson correlation (r = 0.877) and concordance correlation (?c = 0.867) with the T4 Neonatal UMELISA(r). The performed modifications do not affect the sensitivity, precision and accuracy of the assay, permitting a more rational use of newborn blood samples and the possibility to increase the number of diseases included in the newborn screening programs.

Background: The long QT syndrome (LQTS) is an inherited arrhythmia syndrome with increased QT interval and risk of sudden death. Mutations in genes KCNQ1, KCNH2 and SCN5A account for 90% of cases with genotype determined, and genotyping is informative for genetic counseling and better disease management., Objective: Molecular investigation and computational analysis of gene variants of KCNQ1, KCNH2 and SCN5A associated with LQTS, in families with the disease., Methods: The coding regions of genes KCNQ1, KCNH2 and SCN5A in patients with LQTS and their family members were sequenced and analyzed using Geneious ProTM software., Results: Two families with clinical criteria for LQTS were investigated. The proband of Family A had QTC = 562 ms, Schwartz Score = 5.5. The genotyping identified the G1714A mutation in the KCNH2 gene. QTC = 521 ± 42 ms was observed in family members carrying the mutation against QTC = 391 ± 21 ms for non-carriers. The proband of Family B had QTc = 551 ms, Schwartz Score = 5.5. The genotyping identified the G1600T mutation, in the same gene. The analysis of family members revealed QTC = 497 ± 42 ms in mutation carriers, compared with QTC = 404 ± 29 ms in non-carriers., Conclusion: Two gene variants previously associated with LQTS were found in two families clinically diagnosed with LQTS. The prolongation of the QT interval was observed in all family members carrying the mutations. A strategy was developed to identify variants of genes KCNQ1, KCNH2 and SCN5A, making it possible to train technical staff for future application to diagnosis routine.