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Time from symptom onset to blood sampling was calculated for all individual patients according to the actual sampling moment.
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The relative volumes of individual preparations against the original blood samples were calculated and are summarized in Table 1.
The ratios between T A and G C for each blood sample were calculated and were within 0.94 1.05 and 0.94 1.06, respectively.
WNV titers in the blood samples were calculated as the TCID50 per microliter of specimen by the method of Reed and Muench (9).
Absolute counts of lymphocyte subsets per blood sample were calculated by determining the ratio of the beads to the cell population and then multiplying this ratio by the number of beads in the tube.
Following typical procedures in pharmacokinetics [21], the area from t = 0 to t = x min (when the final blood sample was taken) was calculated using the trapezoidal rule.
The representative values of data in the blood and GCF samples were calculated as means in triplicate.
The homeostasis model assessment (HOMA-R) and plasma leptin-to-adiponectin ratio (L/A ratio), which are convenient IR indexes calculated from fasting blood sampling, were examined.
The population density (number of individuals per sampling area) of the blood cockles was calculated for each set of sampling data for late-January and mid-March.
The 99mTc mebrofenin liver-to-blood ratio was calculated using blood sampling points and corresponding liver activity from scintigraphic imaging data.
An average blood time activity curve was calculated from the pooled blood sample data of all seven patients (Fig. 2).
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