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K L Daniels

Publications and source records attributed to K L Daniels.

2 recordsLinked to original sources

Solid-phase radioimmunoassay and chemiluminoimmunoassay for somatostatin in unextracted rat plasma.

Measurement of somatostatin (SS) in small microliter volumes of rat plasma obtained from the hypophysial portal circulation would be aided by a sensitive and robust technique not dependent on extraction. We have developed radioimmunoassay (RIA) and chemiluminoimmunoassay (CIA) for SS in unextracted rat plasma from a previously described solid-phase method in human plasma. Plasma SS was captured by primary antibody bound to second antibody coated polystyrene bead. After incubation the bead was washed and [125I]Tyr1-SS added. Following overnight incubation and washing, the bead was counted. The sensitivity for 50 microliters plasma was 11 pg/ml. Parallel displacement with abdominal portal and hypophysial portal plasma was demonstrated. For direct CIA, SS was labeled with acridinium and purified using 2 sequential gradient elutions on reversed-phase HPLC. Labeled SS performed satisfactorily in solution CIA, but did not bind well in solid-phase CIA. Hence, an indirect CIA using biotinylated SS and quantitation by acridinium labeled streptavidin was established with equivalent performance to solid-phase RIA. In summary, we have developed and validated sensitive and robust solid-phase RIA and indirect CIA for SS in unextracted rat plasma. This solid-phase method could serve as a universal system for the measurement of other neuropeptides in rat plasma.

Animals↗

Statistical analysis of structure-activity relationships.

The relationship between organic structure and biological activity (toxicity) is examined by statistically comparing concentration-response regression lines among structurally related compounds. Response data from acute toxicity tests are initially transformed to the logistic function while concentration data are transformed to the logarithm base 10 before being fit to a linear model using a weighted least squares analysis. A sequential approach is presented that uses statistical models for testing differences among related compounds. The approach first tests for the overall equality of regression lines (slopes and intercepts). If the regression lines are found to be different, another set of tests are conducted to determine if the slopes of the lines are equal (i.e. parallel). If the slopes are equal, multiple comparisons are made using Scheffé's procedure for determining which compounds differ in their intercepts. Relative toxicities are then estimated for various concentrations of particular compounds.

Regression Analysis↗