Using the dentinal fluid pressure system resulted in an adequate flow of dentinal fluid that allowed EndoSequence BC Sealer to set inside the root canal. Although the sealers tested were tricalcium silicate based, the hydration reaction and bioactivity in the presence of dentinal fluid were different to hydration in vitro. Thus, clinically, material bioactivity cannot be assumed.
Dielectric properties are the most important parameters determining energy deposition when biological tissues are exposed to radio frequency and microwave fields. Energy absorption is determined by the specific absorption rate (SAR). SAR distributions can be computed accurately only if the complex relative permittivity of the target tissue is known to a sufficiently high accuracy, and currently there is a lack of data on the dielectric properties of biological tissues at high frequencies. In this study, tissue dielectric properties are measured using an open-ended coaxial probe technique from 500 MHz up to 40 GHz. We present dielectric data for ex vivo bovine and porcine muscle and liver tissues at 37 °C. One-pole Cole-Cole model is used to fit the measured data as a function of frequency and the dispersion parameters are presented. This data is supported by an accurate study on reference liquids such as methanol and ethanediol.
In this article, we report on the characterization of the dielectric properties of in vivo rat liver at 36.4°C from 500 MHz up to 40 GHz with less than 5% uncertainty. The measured data were fitted to a Cole-Cole model and dielectric parameters are presented together with their respective 95% confidence interval. The root mean square error is 0.42. Moreover, ex vivo measurements were conducted in situ at 1, 2, 4 and 6 min after animal death and are compared to in vivo measurements. The results show that immediate changes in [Formula: see text]and [Formula: see text] are within experimental uncertainty, and therefore changes between in vivo and published ex vivo dielectric properties can be attributed to tissue hydration.
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The aim of this study was to characterize the hydration fractions of biological tissues and to model these accurately from mixture equations. Hydration fractions, better known as volume fractions, are based on quantification of tissue hydration and accurate knowledge about the physiological composition of tissue fluids. Data on weight loss percentages for excised muscle and adipose tissue from a previous study were utilized for this purpose. The Bruggeman and Maxwell Garnett equations were then used to characterize the dielectric properties of the tissues in terms of mixtures of dry biological constituents and physiological saline solutions. It is shown that these models are accurate in modelling in vivo and ex vivo tissue in different states of hydration. This is based on precise knowledge of the physiological composition of biological fluids and their corresponding percentage contents. RECEIVED
In this paper, the effects of coagulation and temperature on the dielectric properties of human blood are investigated over the frequency range of 400 MHz -20 GHz using freshly extracted blood samples. The dielectric properties are measured using blood in four different sample collection tubes (bottles): one containing pure whole blood, two containing different anticoagulant agents, and one containing clot activator and serum separator. The collected data indicates that additive agents can have a significant impact on the measured dielectric properties of blood, both immediately after the sample is taken, and over longer time periods. This is an important finding as it suggests that measurements of blood properties conducted on sample repositories, or tissue banks, may not be representative of natural blood properties. Further, the results demonstrate that the dielectric properties of normal blood vary over time due to coagulation. Different clotting rates lead to dielectric properties of female and male blood samples that vary distinctly over time. The results also show that the relative permittivity of the anti-coagulated blood decreases with increasing temperature, up to the cross-over point around 10 GHz where the trend reverses.
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