ABSTRACT
Resumen La descentralización de laboratorios clínicos, se encuentra en desarrollo, lo anterior ha llevado a diseñar instrumentos que ofrecen resultados rápidos, confiables y al lado del paciente, esta tendencia se le conoce como prueba en el punto de atención (point of core testing POCT) y brinda la posibilidad de dar un seguimiento inmediato al padecimiento. El objetivo de esta investigación fue la implementación de un medidor de absorbancia, empleando la estructura de un microscopio óptico, al cual se le ha adaptado un filtro de luz, y una cámara digital. Lo anterior permite obtener valores de intensidad promedio de imágenes sólidas microscópicas de reacciones enzimáticas, y a partir de ellas estimar absorbancia o concentración. Como resultados se presentan rectas de calibración de absorbancia y mediciones de concentraciones para los casos de violeta de genciana, un kit de glucosa oxidasa y muestras problemas de pacientes voluntarios. Concluimos que existe un error de medición menor de ±1mg/dL comparados con las mediciones de un lector de placas de Elisa y un analizador de química sanguínea semiautomatizado. Teniendo en cuenta lo anterior el sistema resulta ser una alternativa viable para la estimación de absorbancia y aumenta la funcionalidad de microscopios ópticos en clínicas de salud.
Abstract The decentralization of clinical laboratories is under development, which has led to the design of instruments that offer fast, reliable and patient-side results, this trend is known as point of core testing (POCT) and It offers the possibility of giving an immediate follow-up to the disease. The objective of this investigation was the implementation of an absorbance meter, using the structure of an optical microscope, to which a light filter and a digital camera have been adapted. This allows to obtain values of average intensity of solid images of enzymatic reactions, and from them to estimate absorbance or concentration. As results, we present absorbance calibration lines and concentration measurements for cases of gentian violet, a glucose oxidase kit and samples of volunteer patients. We conclude that there is a measurement error of less than ± 1mg / dl compared with the measurements of an Elisa plate reader and a semi-automated blood chemistry analyzer. Taking into account the above, the system turns out to be a viable alternative for estimating absorbance and increasing the functionality of optical microscopes in health clinics.
ABSTRACT
Successive stimuli of constant intensity applied to Ia afferents produce spinal monosynaptic reflexes (MSRs) of variable amplitude. We recorded simultaneous MSRs in the left and right L7 (or L6) ventral roots of anesthetized cats. We analyzed the cross-covariance (CCV) between the amplitudes of bilateral MSRs. Long-time series (5 to 8 h) of these bilateral MSRs exhibited transitory changes in their covariations (as measured by the zero-lag peak of their CCV), thus suggesting the existence of certain neural sources contributing to produce these changes. The aim of the present study was to show that spinal centers producing negative spontaneous cord dorsum potentials (nSCDPs) contribute to maintain correlations in the amplitude of bilateral MSRs. After spinal cord transection at the L1 segment, no significant changes were observed in the correlation between the amplitude of bilateral nSCDPs versus the amplitude of bilateral MSRs. However, this correlation, as well as the peak at zero lag in the CCV between bilateral MSRs and the CCV between bilateral nSCDPs, respectively, were abolished after a subsequent longitudinal bisection at the L1-S2 spinal segments. These results suggest that lumbar spinal neurons (bilaterally interconnected) contribute to maintain the synchronous fluctuations of bilateral MSRs.
