Diffusion characteristics of ethylene glycol in skeletal muscle

Part of the optical clearing study in biological tissues concerns the determination of the diffusion characteristics of water and optical clearing agents in the subject tissue. Such information is sufficient to characterize the time dependence of the optical clearing mechanisms—tissue dehydration and refractive index (RI) matching. We have used a simple method based on collimated optical transmittance measurements made from muscle samples under treatment with aqueous solutions containing different concentrations of ethylene glycol (EG), to determine the diffusion time values of water and EG in skeletal muscle. By representing the estimated mean diffusion time values from each treatment as a function of agent concentration in solution, we could identify the real diffusion times for water and agent. These values allowed for the calculation of the correspondent diffusion coefficients for those fluids. With these results, we have demonstrated that the dehydration mechanism is the one that dominates optical clearing in the first minute of treatment, while the RI matching takes over the optical clearing operations after that and remains for a longer time of treatment up to about 10 min, as we could see for EG and thin tissue samples of 0.5 mm.

Projecto de molde para peça para a indústria automóvel

A realização deste trabalho teve por base uma solicitação por parte de uma empresa dedicada ao projecto e fabrico de moldes, assim como à injecção de plásticos, no sentido de projectar um molde para a injecção de uma peça em plástico (PP-Polipropileno +20% ) para a indústria automóvel, segundo os requisitos de qualidade exigidos pelo cliente Assim, atendendo a esses requisitos, foi planeado e elaborado o projecto do respectivo molde para a injecção, tendo em consideração todos os factores que contribuem de forma activa para a obtenção das peças desejadas, com a qualidade exigida e com o tempo de vida desejado para o molde. Tendo início na definição das cavidades e movimentos do molde, passando pela selecção dos materiais mais adequados a cada um dos componentes do molde, selecção de componentes normalizados para o molde, simulação do enchimento e necessidades de arrefecimento, até à execução do molde e análise de possíveis não conformidades nas peças nele injectadas, o trabalho acompanhou todo o processo de criação do molde, desde a recepção das especificações emanadas pelo cliente, até ao teste e realização das correcções finais. Constatou-se que o molde, após ligeiras afinações finais, cumpriu com os objectivos inicialmente traçados, permitindo a obtenção de peças com o formato e qualidade exigidas pelo cliente final.

Detection of cardiac biomarker proteins using a disposable based on a molecularly imprinted polymer grafted onto graphite

A low-cost disposable was developed for rapid detection of the protein biomarker myoglobin (Myo) as a model analyte. A screen printed electrode was modified with a molecularly imprinted material grafted on a graphite support and incorporated in a matrix composed of poly(vinyl chloride) and the plasticizer o-nitrophenyloctyl ether. The protein-imprinted material (PIM) was produced by growing a reticulated polymer around a protein template. This is followed by radical polymerization of 4-styrenesulfonic acid, 2-aminoethyl methacrylate hydrochloride, and ethylene glycol dimethacrylate. The polymeric layer was then covalently bound to the graphitic support, and Myo was added during the imprinting stage to act as a template. Non-imprinted control materials (CM) were also prepared by omitting the Myo template. Morphological and structural analysis of PIM and CM by FTIR, Raman, and SEM/EDC microscopies confirmed the modification of the graphite support. The analytical performance of the SPE was assessed by square wave voltammetry. The average limit of detection is 0.79 μg of Myo per mL, and the slope is −0.193 ± 0.006 μA per decade. The SPE-CM cannot detect such low levels of Myo but gives a linear response at above 7.2 μg · mL−1, with a slope of −0.719 ± 0.02 μA per decade. Interference studies with hemoglobin, bovine serum albumin, creatinine, and sodium chloride demonstrated good selectivity for Myo. The method was successfully applied to the determination of Myo urine and is conceived to be a promising tool for screening Myo in point-of-care patients with ischemia.