TY - JOUR
T1 - Rate of mixing controls rate and outcome of autocatalytic processes
T2 - Theory and microfluidic experiments with chemical reactions and blood coagulation
AU - Pompano, Rebecca R.
AU - LI, Hung Wing
AU - Ismagilov, Rustem F.
N1 - Funding Information:
This work was supported in part by ONR under Grant No. N00014-03-10482, the NIBIB under Grant No. ROI EB001903-04, and by the Camille Dreyfus Teacher-Scholar Awards Program. R.F.I. is a Cottrell Scholar of Research Corporation and an A. P. Sloan Research Fellow. Some of this work was performed at the MRSEC microfluidic facility (funded by the NSF). We thank Jessica M. Price for contributions in writing and editing this manuscript.
PY - 2008/8/1
Y1 - 2008/8/1
N2 - This article demonstrates that the rate of mixing can regulate the rate and outcome of both biological and nonbiological autocatalytic reaction systems that display a threshold response to the concentration of an activator. Plug-based microfluidics was used to control the timing of reactions, the rate of mixing, and surface chemistry in blood clotting and its chemical model. Initiation of clotting of human blood plasma required addition of a critical concentration of thrombin. Clotting could be prevented by rapid mixing when thrombin was added near the critical concentration, and mixing also affected the rate of clotting when thrombin was added at concentrations far above the critical concentration in two clinical clotting assays for human plasma. This phenomenon was modeled by a simple mechanism - local and global competition between the clotting reaction, which autocatalytically produces an activator, and mixing, which removes the activator. Numerical simulations showed that the Damköhler number, which describes this competition, predicts the effects of mixing. Many biological systems are controlled by thresholds, and these results shed light on the dynamics of these systems in the presence of spatial heterogeneities and provide simple guidelines for designing and interpreting experiments with such systems.
AB - This article demonstrates that the rate of mixing can regulate the rate and outcome of both biological and nonbiological autocatalytic reaction systems that display a threshold response to the concentration of an activator. Plug-based microfluidics was used to control the timing of reactions, the rate of mixing, and surface chemistry in blood clotting and its chemical model. Initiation of clotting of human blood plasma required addition of a critical concentration of thrombin. Clotting could be prevented by rapid mixing when thrombin was added near the critical concentration, and mixing also affected the rate of clotting when thrombin was added at concentrations far above the critical concentration in two clinical clotting assays for human plasma. This phenomenon was modeled by a simple mechanism - local and global competition between the clotting reaction, which autocatalytically produces an activator, and mixing, which removes the activator. Numerical simulations showed that the Damköhler number, which describes this competition, predicts the effects of mixing. Many biological systems are controlled by thresholds, and these results shed light on the dynamics of these systems in the presence of spatial heterogeneities and provide simple guidelines for designing and interpreting experiments with such systems.
UR - http://www.scopus.com/inward/record.url?scp=51049122628&partnerID=8YFLogxK
U2 - 10.1529/biophysj.108.129486
DO - 10.1529/biophysj.108.129486
M3 - Journal article
C2 - 18424502
AN - SCOPUS:51049122628
SN - 0006-3495
VL - 95
SP - 1531
EP - 1543
JO - Biophysical Journal
JF - Biophysical Journal
IS - 3
ER -