22 research outputs found
Holographic Scanning Laser Acoustic Microscopy (HOLOSLAM): A New QNDE Tool
Acoustic microscopy is the name given to high frequency, 10 MHz to 3 GHz ultrasonic visualization. The scanning laser acoustic microscopy (SLAM) is an important branch of acoustic microscopy which uses ultrasound in the frequency range of 10 to 200 MHz to produce high resolution ultrasonic images.1,2 In contrast to other visual observation techniques, SLAM provides direct access to the structural elastic properties of solid materials and biological tissues. By using this technique, valuable insight can be gained into mechanisms responsible for the changes of elastic architecture over areas tens of microns in diameter
Factors associated with HIV infection among children born to mothers on the prevention of mother to child transmission programme at Chitungwiza Hospital, Zimbabwe, 2008
Radiological images on personal computers: Introduction and fundamental principles of digital images
Tradeoff between Approximation Accuracy and Complexity for Range Analysis using Affine Arithmetic
Displaying radiologic images on personal computers: Image storage and compression—Part 2
Pharmacokinetic characteristics of vincristine sulfate liposomes in patients with advanced solid tumors
From East to West- Has the Twain Met? Linkages Between Context Sensitivity and Soft Systems Methodology
Seroprevalence of influenza A virus in pigs and low risk of acute respiratory illness among pig workers in Kenya
Vincristine Chemotherapy Trials and Pharmacokinetics in Tasmanian Devils with Tasmanian Devil Facial Tumor Disease
Extent: 7 p.Tasmanian Devil Facial Tumor Disease (DFTD) is a transmissible cancer threatening to cause the extinction of Tasmanian Devils in the wild. The aim of this study was to determine the susceptibility of the DFTD to vincristine. Escalating dosage rates of vincristine (0.05 to 0.136 mg/kg) were given to Tasmanian devils in the early stages of DFTD (n = 8). None of these dosage rates impacted the outcome of the disease. A dosage rate of 0.105 mg/kg, a rate significantly higher than that given in humans or domestic animals, was found to the highest dosage rate that could be administered safely. Signs of toxicity included anorexia, vomiting, diarrhea and neutropenia. Pharmacokinetic studies showed that, as with other species, there was a rapid drop in blood concentration following a rapid intravenous infusion with a high volume of distribution (1.96 L/ kg) and a relatively long elimination half life (11 h). Plasma clearance (1.8 ml/min/kg) was slower in the Tasmanian devil than in humans, suggesting that pharmacodynamics and not pharmacokinetics explain the Tasmanian devil’s ability to tolerate high dosage rates of vincristine. While providing base-line data for the use of vincristine in Tasmanian devils and possibly other marsupials with vincristine susceptible cancers, these findings strongly suggest that vincristine will not be effective in the treatment of DFTD.David N. Phalen, Angela Frimberger, Stephen Pyecroft, Sarah Peck, Colette Harmsen, Suzanneth Lola, Beatriz de Mello Mattos, Kong M. Li, Andrew J. McLachlan and Antony Moor
