A novel, rapid method to compare the therapeutic windows of oral anticoagulants using the Hill coefficient.

TitleA novel, rapid method to compare the therapeutic windows of oral anticoagulants using the Hill coefficient.
Publication TypeJournal Article
Year of Publication2016
AuthorsChang JB, Quinnies KM, Realubit R, Karan C, Rand JH, Tatonetti NP
JournalSci Rep
Volume6
Pagination29387
Date Published2016 07 21
ISSN2045-2322
KeywordsAdministration, Oral, Anticoagulants, Arginine, Blood Coagulation, Blood Platelets, Dose-Response Relationship, Drug, Fluorometry, Fondaparinux, Humans, Inhibitory Concentration 50, Pipecolic Acids, Plasma, Polysaccharides, Sulfonamides, Thrombin
Abstract

A central challenge in designing and administering effective anticoagulants is achieving the proper therapeutic window and dosage for each patient. The Hill coefficient, nH, which measures the steepness of a dose-response relationship, may be a useful gauge of this therapeutic window. We sought to measure the Hill coefficient of available anticoagulants to gain insight into their therapeutic windows. We used a simple fluorometric in vitro assay to determine clotting activity in platelet poor plasma after exposure to various concentrations of anticoagulants. The Hill coefficient for argatroban was the lowest, at 1.7 ± 0.2 (95% confidence interval, CI), and the Hill coefficient for fondaparinux was the highest, at 4.5 ± 1.3 (95% CI). Thus, doubling the dose of fondaparinux from its IC50 would decrease coagulation activity by nearly a half, whereas doubling the dose of argatroban from its IC50 would decrease coagulation activity by merely one quarter. These results show a significant variation among the Hill coefficients, suggesting a similar variation in therapeutic windows among anticoagulants in our assay.

DOI10.1038/srep29387
Alternate JournalSci Rep
PubMed ID27439480
PubMed Central IDPMC4954953
Grant ListR01 GM107145 / GM / NIGMS NIH HHS / United States
U54 CA209997 / CA / NCI NIH HHS / United States
Related Faculty: 
Jacob H. Rand, M.D.

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