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Behavior, human observation

The following section describes protocols for evaluating both dependence and abuse. For reasons of homogeneity with the other procedures presented above, only protocols in the rat will be presented. Although results in the rat are generally similar to those obtained in non-human primates, the regulatory authorities, in particular the FDA, prefer primate studies for abuse evaluation because of a presumed increased predictability to man. The active doses and pharmacokinetics are likely to be closer between human and non-human primates, as are the kinds of overt behavioral effects observed. [Pg.49]

When the double bond of the 3-ene-l,5-diyne system is part of a benzene or a naphthalene ring, a lowered activity resulted, in agreement with the lower activity of benzo-fused enediynes already cited in Section 19.3.2. Finally, the activity both in vitro (human carcinoma KB cells) and in vivo (mice inoculated with murine P338 leukemia) of 87-89 was tested. Interestingly, while the phenyl carbamates have no detectable in vitro activity against plasmid DNA and were less cytotoxic in vitro than 87-89, an opposite behavior was observed in vivo. Thus the phenyl carbamates showed an interesting activity, while the sulfones showed little or no activity, probably due to the fact that they are quite unstable and they are not able to reach tumor cells before cycloaromatization begins. [Pg.474]

Senders, J. W., Elkind, J. E., Grignetti, M. C., Smallwood, R. P (1964). An investigation of visual sampling behavior of human observers (NASA R-434). Cambridge, MA Bolt, Beianek, Newman. [Pg.286]

Cognitive type This contemporary technique is used for supervisory control and decision making. Here, the focus is on the mental process behind human observable behavior in decision making or problem solving. This also forms part of HRA. [Pg.129]

Percutaneous penetration of [ H]DFP was tested in vitro with human and pig skin. In the test using full skin, the absorbed dose 24 h after depot was 15.6 1% in pig skin and 9.4 1.5% in human skin, with a ratio of 1.7 pigrhuman. The penetration rates between 0.5 and 4h were 3.22% and 1.63% dose per hour, with a ratio of 1.7 for pigrhuman skin. Similar behavior was observed using split-thickness skin. [Pg.862]

Usually 25-50 drugs can be screened by one person per week using a 32-channel trainer. Courtship behavior and aggression are the most common phenotypes used in social interaction assays. The recording of these social interaction phenotypes is difficult to automate and therefore requires a human observer. However, some important parts have been automated by video tracking software. Thus, locomotor activity, aggression, and courtship behavior can be analyzed simultaneously on 96 video channels [25, 26]. [Pg.136]

CI-979 (29) is a balanced muscarinic agonist having equal affinities for cloned ml and m2 receptors (144). However, unlike prototypical muscarinic compounds such as (25), (29) increases central muscarinic tone, as indicated by behavioral and electroencephalogram (EEG) parameters, at doses lower than those requited to produce gastrointestinal effects (144). CI-979 is well tolerated in humans up to a dose of 1 mg. Dose-limiting side effects such as stomach pain and emesis were observed at a dose of 2 mg. [Pg.99]

The term Task Analysis (TA) can be applied very broadly to encompass a wide variety of human factors techniques. Nearly all task analysis techniques provide, as a minimum, a description of the observable aspects of operator behavior at various levels of detail, together with some indications of the structure of the task. These will be referred to as action oriented approaches. Other techniques focus on the mental processes that imderlie observable behavior, for example, decision making and problem solving. These will be referred to as cognitive approaches. [Pg.161]


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