Sentence examples for quantitative dosing from inspiring English sources

For styrene, we used sorbent tubes, the aspiration flows and times, and the analytical procedure for the gas chromatographic quantitative dosing as described in National Institute for Occupational Safety and Health (NIOSH) method 1501 (NIOSH 1994c).

For total and respirable dusts, the use of filters, aspiration flows and times, and the analytical procedure for gravimetric quantitative dosing were in compliance with NIOSH Method 500 (NIOSH 1994a) and Method 600 (NIOSH 1994b), respectively.

In addition, data sets for quantitative dose-response functions were extracted from published in vivo animal dosing experiments.

In this article, we analyze a clinically based two-dimensional (2D) quantitative dose comparison case using a wide range of new and old comparison tools.

Exposure to chlorpyrifos (CPF), an organophosphorus (OP) anticholinesterase insecticide, occurs typically in settings where multiple agents are present (e.g., agriculture) and quantitative dose measures may be absent (e.g., pesticide application).

These models express the relationship between a certain chemical property (e.g. fragment) and the effect (e.g. carcinogenicity) in a qualitative way (carcinogenic or noncarcinogenic), without assigning a continuous numerical value to the toxicity, such as a specific quantitative dose, which can have a wide range of values.

Quantitative dose-response relationships were found in the induction of extrafloral nectar production in Macaranga tanarius plants that were sprayed with JA [22].

The reviews of risk factors did not give sufficient information to derive quantitative dose-response relationships, and the findings from the studies that indicated a relationship between duration of computer use and pain complaints could not indicate a threshold value.

Quantitative dose response data (Figure 1B) indicate that both GluR1 and GluR2 surface expression are increased by corticosterone but that GluR2 is more sensitive and increases to a greater extent than GluR1.

The quantitative dose effect of these variables as shown in Figure 2 supports this conclusion, especially for the extreme groups such as those with pI>8 and/or EP score>2.

Our findings emphasize the importance of using a quantitative dose-dependent binding assay with recombinant HA in order to correlate biochemical glycan-binding affinity with molecular HA-glycan interactions.