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Different Volumes (different + volume)
Terms modified by Different Volumes Selected AbstractsUsing translational medicine to understand clinical differences between botulinum toxin formulationsEUROPEAN JOURNAL OF NEUROLOGY, Issue 2006K. R. Aoki When using botulinum toxin-based products, the physician must decide the optimal location and dose required to alleviate symptoms and improve the patient's quality of life. To deliver effective treatment, the physician needs to understand the importance of accurate target muscle selection and localization and the implications of each product's migration properties when diluted in different volumes. Pre-clinical mouse models of efficacy and safety have been utilized to compare local and distal muscle relaxation effects following defined intramuscular administration. Data from the model allow the products to be ranked based on their propensity for local efficacy versus their distal migration properties. Using standardized dilutions, the non-parallel dose,response curves for the various formulations demonstrate that they have different efficacy profiles. Distal effects were also noted at different treatment doses, which are reflected in the different safety and/or therapeutic margins. Based on these pre-clinical data, the safety and therapeutic margin rankings are ordered, largest to smallest, as BOTOX®, Dysport® and Myobloc®. The results of subsequent clinical trials are variable and dose comparisons are inconclusive, thus supporting the regulatory position that the dose units of the individual preparations are unique and cannot be simply converted between products. [source] Thermal Conductivity of Cellular Metals Measured by the Transient Plane Source Method,ADVANCED ENGINEERING MATERIALS, Issue 6 2008E. Solórzano The thermal conductivity of a collection of cellular metals has been measured by the Transient Plane Source (TPS) method. Using this method, it has been possible to cover different volumes of selected samples and to study their in-homogeneities from their surface to their inner part. Additionally, these samples have been characterized by tomography. With the TPS method, in combination with tomography, it has been possible to analyse the in-homogeneity of the samples as well as to characterize the thermal conductivity of a single in-homogeneous sample as a complete collection of different porosity specimens. This is the corrected version of the paper by Solórzano et al., Adv. Eng. Mater.2008, 10, 371, which was unfortunately published in an uncorrected version. [source] Hyperpolarized 3He apparent diffusion coefficient MRI of the lung: Reproducibility and volume dependency in healthy volunteers and patients with emphysemaJOURNAL OF MAGNETIC RESONANCE IMAGING, Issue 4 2008Sandra Diaz MD Abstract Purpose To measure the apparent diffusion coefficient (ADC) of hyperpolarized (HP) 3He gas using diffusion weighted MRI in healthy volunteers and patients with emphysema and examine the reproducibility and volume dependency. Materials and Methods A total of eight healthy volunteers and 16 patients with emphysema were examined after inhalation of HP 3He gas mixed with nitrogen (N2) during breathhold starting from functional residual capacity (FRC) in supine position. Coronal diffusion-sensitized MR images were acquired. Each subject was imaged on three separate days over a seven-day period and received two different volumes (6% and 15% of total lung capacity [TLC]) of HP 3He each day. ADC maps and histograms were calculated. The mean and standard deviation (SD) of the ADC at different days and volumes were compared. Results The reproducibility of the mean ADC and SD over several days was good in both healthy volunteers and patients (SD range of 0.003,0.013 cm2/second and 0.001,0.009 cm2/second at 6% and 15% of TLC for healthy volunteers, and a SD range of 0.001,0.041 cm2/second and 0.001,0.011 cm2/second, respectively, for patients). A minor but significant increase in mean ADC with increased inhaled gas volume was observed in both groups. Conclusion Mean ADC and SD of HP 3He MRI is reproducible and discriminates well between healthy controls and patients with emphysema at the higher gas volume. This method is robust and may be useful to gain new insights into the pathophysiology and course of emphysema. J. Magn. Reson. Imaging 2008. © 2008 Wiley-Liss, Inc. [source] 34 In vivo tumour hypoxia and carbonic anhydrase IX expression in xenografted human renal cell carcinoma animal models using probes, 124I-G250 pet, biodistribution and immunohistochemistry immunobiodistribution, and oxygen studiesBJU INTERNATIONAL, Issue 2006N. LAWRENTSCHUK Introduction:, Hypoxia stimulates angiogenesis and has been demonstrated in tumours where it correlates with resistance to treatment and poor prognosis. We have previously demonstrated hypoxia in human Renal Cell Carcinoma (RCC). The purpose of animal models was to further evaluate oxygen levels within RCC whilst also focusing on expression of the protein carbonic anhydrase IX (CA IX). This protein is stimulated by hypoxia and involved in angiogenesis and may be a potential tumour target for imaging and future therapies. Methods:, Balb/c nude mice had human RCC (SK-RC-52) xenografted subcutaneously. Tumours were grown to different volumes with oxygen levels measured. Further groups then had the radiolabelled monoclonal antibody 124I-G250 (that binds to CA IX) injected intravenously and had Positron Emission Tomography (PET), gamma counting and oxygen studies performed on days 0,1,2,3,5,7,10 and 14 post injection. Immunohistochemistry and autoradiography was also performed. Results:, An inverse relationship between tumour volume and hypoxia within the model was established (P < 0.001). Furthermore, CA IX was expressed by tumours with maximal uptake of 124I-G250 on days 2/3 by distribution with gamma counting that could be correlated with uptake on PET imaging. Conclusions:, The xenograft model confirms human RCC are hypoxic. Also, that the level of hypoxia is inversely proportional to tumour sise. A correlation was made between PET scanning with 124I-G250 and biodistribution within tumours by gamma counting confirming CAIX as an imaging and potential therapeutic target in RCC. [source] |