Biomedical subjects

R Chesler

Publications and source records attributed to R Chesler.

4 recordsLinked to original sources

PubMed1992

Rationale for using multiple regression analysis with complex interferences.

Non-specificities and interferences may become complex when they involve the analyte as well as other interfering substances. These non-specificities and interferences are known as analyte-dependent and multi-interferent interferences. Multiple regression analysis has proven valuable in analysing this type of interference, but the theoretical foundation for using multiple regression analysis to study the basic mechanisms of interference has not been explicitly demonstrated. Graph theory can depict and model the basic mechanisms of interferences and the possible interactions. The relationship between the analyte, the interferents, and the response of the instrument to these entities can be approximated by a polymial of order three, which includes partial derivatives and cross-terms. The partial derivatives relate to the different interactions found with the graph theory model. Further, the partial derivatives can be associated with the coefficients in the multiple regression analysis when the respective values of the three variables (analyte, interferent one, and interferent two) are multiplied by one another. One can decide to retain or discard the coefficient of a variable, based on the statistical significance of the coefficient. The respective interactions in the graphic model can then be assembled and the framework of the interference mechanism established.

Bilirubin↗

PubMed1990

Effect of serum lyophilization on the rate constants of enzymatic methods for measuring cholesterol.

We determined the equilibrium absorbances and rate constants for two enzymatic methods, aca (DuPont) and RA-1000 (Technicon), used in determining cholesterol in reconstituted lyophilized serum. The lyophilized materials included two serum pools, three control materials, a College of American Pathologists' survey material, and Standard Reference Material no. 909. We calibrated the reagents with aca standards for cholesterol (DuPont). The difference in the mean concentrations of cholesterol (aca - RA-1000) was -0.09 g/L overall and was not statistically significant by analysis of variance. The mean rate constant for all materials was 0.23 min-1 for the aca and 1.42 min-1 for the RA-1000, significantly different (P less than 0.001). Lyophilization causes lower results for the aca method than for the Ra-1000, because the reaction rate for the aca method is slower and has not reached equilibrium when the final absorbance reading is made.

Cholesterol↗

PubMed1989

Effect of lyophilization on results of five enzymatic methods for cholesterol.

We studied the effect of lyophilization of serum pools on the determination of cholesterol with the enzymatic methods used in five automated analyzers: SMAC (Technicon), the RA-1000 (Technicon), the aca (Du Pont), the TDx (Abbott), and the Ektachem 700P (Kodak). We prepared two serum pools: pool A (2.2 g/L) and pool B (1.9 g/L). We separated each pool into three groups for treatment by lyophilizing or freezing at -20 and -70 degrees C. We determined cholesterol by the above methods at regular intervals during the next 270 days. For all methods, the measured concentration of cholesterol was less for the lyophilized serum than for frozen (P less than 0.007 by the paired-sample t-test). After adjusting for the dilutional effects of reconstitution, the decrease in original value was 0.7% for the SMAC, 1.7% for the RA-1000, 5.7% for the Ektachem, 9.4% for the TDx, and 14.3% for the aca. Lyophilization of cholesterol standards or serum samples may hamper the effective standardization of enzymatic methods and may be a source of apparent inaccuracy (bias) among enzymatic methods.

Autoanalysis↗

PubMed1986

Automated determination of urinary creatinine without sample dilution: theory and practice.

The rate of the Jaffé reaction depends on the concentration of sodium hydroxide; the pseudo-first-order rate constant of the reaction, at 37 degrees C in 10 mmol/L picrate solution, is 0.004 mmol/L. We formulated an automated method to determine urinary creatinine directly without manual sample dilution. The conditions are as follows: 10 mmol/L picrate and 60 mmol/L sodium hydroxide (final concentrations); ratio of sample to final volume, 1:41; temperature, 37 degrees C; wavelengths of measurement, 500 or 510 nm; interval of measurement, 30 to 90 s; and mode of measurement, kinetic. Determinations of creatinine in patients' samples by the new method compared favorably with those obtained with the AutoAnalyzer and aca. The run-to-run CVs were 3.6% or less, and the method was accurate for concentrations of creatinine up to 3000 mg/L. We recommend this method as a good replacement for the AutoAnalyzer or aca methods.

Autoanalysis↗