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Biomedical subjects

D R Hoak

Publications and source records attributed to D R Hoak.

4 recordsLinked to original sources

An automated approach to characterize, in simple kinetic terms, the generation and inactivation of thrombin and the interaction of fibrinogen with thrombin.

Here, we used a fully automated, computer-directed centrifugal analyzer (which permitted simultaneous turbidimetry and calculation of results) and purified thrombin, fibrinogen, and various inhibitors to study clot formation. The Km and Vm for these reactions were useful in detecting and partly characterizing anticoagulants. We also explored the generation and inactivation of thrombin, using the two-stage prothrombin time and antithrombin activity tests. The amount of thrombin instantaneously generated and inactivated was monitored under artificially created pathological conditions. The pseudo-first-order rate constant for thrombin generation and inactivation and the instantaneous concentration of enzymatically active and inactive thrombin were used in the characterization of these conditions. We believe this approach is suitable for routine clinical use.

Algorithms↗

A fully automated immuno-turbidimetric determination of fibrin(ogen) degradation products.

A fully automated procedure for the determination of fibrin(ogen) degradation products was developed using the I. L. Multistat Centrifugal Analyzer (MCA). The assay is based on the turbidometric measurement of the interaction between antibodies to human fibrinogen and defibrinogenated specimens. The method allows, with high reproducibility, for the accurate quantitation of degradation products between 10 and 160 micrograms/ml. A comparative study of 100 normal and abnormal patient samples revealed an excellent correlation with the semi-quantitative manual procedure. The method can be adapted to existing automated coagulation procedures and can become part of coagulation panels.

Antibodies↗

A fully automated method for clot based coagulation panels using an MCA Multistat Centrifugal Analyzer.

Small modifications of the commercially available software of the I.L. Multistat Centrifugal Analyzer (MCA) enabled us to evaluate clot based prothrombin times (PT), activated partial thromboplastin times (APTT) and thrombin times (TT) simultaneously within one run. This imparted a great deal of flexibility to this procedure in that batches and/or panels of clot based and other types of turbidimetric tests can be performed concurrently in any combination. The PT and TT by this turbidimetric procedure correlated very well with those of the Fibrometer in normal specimens as well as in a wide variety of coagulation defects. The turbidimetric APTT procedure, however, often produced clotting times longer than those achieved with the Fibrometer. The discrepancy between the Fibrometer and turbidimetric APTT procedures was shown to be the consequence of greater sensitivity of the latter to detect low concentrations of heparin, elevated fibrinogen split products and mild factor deficiencies. The available clot based procedures are suitable for use in detecting specific factor deficiencies and the presence of coagulation inhibitors.

Autoanalysis↗