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Concentration of doses

Aldehydes, polycyclic aromatic compounds, benzene, ethene, organic acids some of them are known as potential respiratory, eye and skin irritants, others could mutate cells or cause cancer under specific conditions, dependent on concentration of dose... etc. - and, though there is considerable uncertainty as to the... [Pg.47]

Dosing. All animals must be dosed by gavage. All animals must receive the same concentration of dosing solution. They should also receive about the same volume of dosing solution, which should not exceed 4-5 ml. per animal. [Pg.153]

The experimental biological activities used in correlations are almost always logarithms of reciprocal of active concentrations of doses or of equilibrium constants, They will be denoted by A or — to mention explicitly the compound M to which they refer. The literature source for the experimental activities A used in correlations is usually not indicated it may be found in the bibliography of the cited QSAR-paper. The calculated activities, resulted from correlational equations will be denoted by A or... [Pg.2]

In laboratory tests, appHcation of DMAC to the skin of pregnant rats has caused fetal deaths when the dosages were close to the lethal dose level for the mother. Embryonal malformations have been observed at dose levels 20% of the lethal dose and higher. However, when male and female rats were exposed to mean DMAC concentrations of 31,101, and 291 ppm for 6 h per day over several weeks, no reproductive effects were observed (6). [Pg.85]

In thermoluminescence dating, a sample of the material is heated, and the light emitted by the sample as a result of the de-excitations of the electrons or holes that are freed from the traps at luminescence centers is measured providing a measure of the trap population density. This signal is compared with one obtained from the same sample after a laboratory irradiation of known dose. The annual dose rate for the clay is calculated from determined concentrations of radioisotopes in the material and assumed or measured environmental radiation intensities. [Pg.419]

The progestin doses necessary for effective cancer therapy are very high, reaching 1000-2000 mg/d. These high concentrations of progestins may... [Pg.223]

Once the steady-state concentration is known, the rate of dmg clearance determines how frequendy the dmg must be adininistered. Because most dmg elimination systems do not achieve saturation under therapeutic dosing regimens, clearance is independent of plasma concentration of the dmg. This first-order elimination of many dmgs means that a constant fraction of dmg is eliminated per unit time. In the simplest case, clearance can be deterrnined by the dose and the area under the curve (AUC) describing dmg concentration as a function of total time ... [Pg.271]

R = / -C H ), in low doses, exhibits the former behavior and is used primarily as an extradural agent in obstetrics. The lowest effective extradural concentration of etidocaine (21, X = CH, R = R = 2H, R = / -C H ), however, shows both adequate sensory and profound motor blockade so that it is useful in surgical situations where maximum neuromuscular blockade is necessary. In an isolated nerve preparation, bupivacaine blocks unmyelinated C fibers which are mainly responsible for pain perception at a much greater extent than the myelinated A fibers which carry motor impulses. It is postulated that absorption of bupivacaine by the vasculature at the site of injection, combined with the slow diffusion of this agent, results in an insufficient amount of the drug penetrating the large A fibers to cause motor conduction blockade. Clinically, motor block can be observed in some procedures. [Pg.414]

Florfenicol concentrations in tissues and body fluids of male veal calves were studied after 11 mg/kg intramuscular doses adininistered at 12-h intervals (42). Concentrations of florfenicol in the lungs, heart, skeletal muscle, synovia, spleen, pancreas, large intestine, and small intestine were similar to the corresponding semm concentrations indicating excellent penetration of florfenicol into these tissues. Because the florfenicol concentration in these tissues decreased over time as did the corresponding semm concentrations, it was deemed that florfenicol equiUbrated rapidly between these tissues and the blood. Thus semm concentrations of florfenicol can be used as an indicator of dmg concentrations in these tissues. [Pg.517]

Because the regions of the alimentary tract vary widely ia pH and chemical composition, many different commercial formulations of barium sulfate are available. The final preparations of varyiag viscosity, density, and formulation stabiUty levels are controlled by the different size, shape, uniformity and concentration of barium sulfate particles and the presence of additives. The most important additives are suspending and dispersiag agents used to maintain the suspension stabiUty. Commercial preparations of barium sulfate iaclude bulk and unit-dose powders and suspensions and principal manufacturers are E-Z-EM (Westbury, New York), Lafayette-Pharmacol, Inc. (Lafayette, Indiana), and Picker International, Inc. (Cleveland, Ohio). [Pg.469]

Nonetheless, these methods only estimate organ-averaged radiation dose. Any process which results in high concentrations of radioactivity in organs outside the MIRD tables or in very small volumes within an organ can result in significant error. In addition, the kinetic behavior of materials in the body can have a dramatic effect on radiation dose and models of material transport are constandy refined. Thus radiation dosimetry remains an area of significant research activity. [Pg.483]

Acute toxicity studies are often dominated by consideration of lethaUty, including calculation of the median lethal dose. By routes other than inhalation, this is expressed as the LD q with 95% confidence limits. For inhalation experiments, it is convenient to calculate the atmospheric concentration of test material producing a 50% mortaUty over a specified period of time, usually 4 h ie, the 4-h LC q. It is desirable to know the nature, time to onset, dose—related severity, and reversibiUty of sublethal toxic effects. [Pg.236]


See other pages where Concentration of doses is mentioned: [Pg.103]    [Pg.114]    [Pg.11]    [Pg.145]    [Pg.79]    [Pg.88]    [Pg.28]    [Pg.103]    [Pg.114]    [Pg.11]    [Pg.145]    [Pg.79]    [Pg.88]    [Pg.28]    [Pg.259]    [Pg.182]    [Pg.116]    [Pg.168]    [Pg.366]    [Pg.419]    [Pg.476]    [Pg.200]    [Pg.409]    [Pg.222]    [Pg.224]    [Pg.32]    [Pg.107]    [Pg.396]    [Pg.517]    [Pg.25]    [Pg.189]    [Pg.233]    [Pg.271]    [Pg.274]    [Pg.275]    [Pg.481]    [Pg.516]    [Pg.206]    [Pg.485]    [Pg.489]    [Pg.497]    [Pg.382]    [Pg.382]    [Pg.510]    [Pg.196]    [Pg.336]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.33 ]




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