306 research outputs found
Polydispersity Effects in Colloid-Polymer Mixtures
We study phase separation and transient gelation in a mixture consisting of
polydisperse colloids and non-adsorbing polymers, where the ratio of the
average size of the polymer to that of the colloid is approximately 0.063.
Unlike what has been reported previously for mixtures with somewhat lower
colloid polydispersity, the addition of polymers does not expand the
fluid-solid coexistence region. Instead, we find a region of fluid-solid
coexistence which has an approximately constant width but an unexpected
re-entrant shape. We detect the presence of a metastable gas-liquid binodal,
which gives rise to two-stepped crystallization kinetics that can be
rationalized as the effect of fractionation. Finally, we find that the
separation into multiple coexisting solid phases at high colloid volume
fractions predicted by equilibrium statistical mechanics is kinetically
suppressed before the system reaches dynamical arrest.Comment: 11 pages, 5 figure
Projected free energies for polydisperse phase equilibria
A `polydisperse' system has an infinite number of conserved densities. We
give a rational procedure for projecting its infinite-dimensional free energy
surface onto a subspace comprising a finite number of linear combinations of
densities (`moments'), in which the phase behavior is then found as usual. If
the excess free energy of the system depends only on the moments used, exact
cloud, shadow and spinodal curves result; two- and multi-phase regions are
approximate, but refinable indefinitely by adding extra moments. The approach
is computationally robust and gives new geometrical insights into the
thermodynamics of polydispersity.Comment: 4 pages, REVTeX, uses multicol.sty and epsf.sty, 1 postscript figure
include
Spinodal-assisted crystallization in polymer melts
Recent experiments in some polymer melts quenched below the melting temperature have reported spinodal kinetics in small-angle x-ray scattering before the emergence of a crystalline structure. To explain these observations we propose that the coupling between density and chain conformation induces a liquid-liquid binodal within the equilibrium liquid-crystalline solid coexistence region. A simple phenomenological theory is developed to illustrate this idea, and several experimentally testable consequences are discussed. Shear is shown to enhance the kinetic role of the hidden binodal
Predicting phase equilibria in polydisperse systems
Many materials containing colloids or polymers are polydisperse: They
comprise particles with properties (such as particle diameter, charge, or
polymer chain length) that depend continuously on one or several parameters.
This review focusses on the theoretical prediction of phase equilibria in
polydisperse systems; the presence of an effectively infinite number of
distinguishable particle species makes this a highly nontrivial task. I first
describe qualitatively some of the novel features of polydisperse phase
behaviour, and outline a theoretical framework within which they can be
explored. Current techniques for predicting polydisperse phase equilibria are
then reviewed. I also discuss applications to some simple model systems
including homopolymers and random copolymers, spherical colloids and
colloid-polymer mixtures, and liquid crystals formed from rod- and plate-like
colloidal particles; the results surveyed give an idea of the rich
phenomenology of polydisperse phase behaviour. Extensions to the study of
polydispersity effects on interfacial behaviour and phase separation kinetics
are outlined briefly.Comment: 48 pages, invited topical review for Journal of Physics: Condensed
Matter; uses Institute of Physics style file iopart.cls (included
Diffusive Evolution of Stable and Metastable Phases II: Theory of Non-Equilibrium Behaviour in Colloid-Polymer Mixtures
By analytically solving some simple models of phase-ordering kinetics, we
suggest a mechanism for the onset of non-equilibrium behaviour in
colloid-polymer mixtures. These mixtures can function as models of atomic
systems; their physics therefore impinges on many areas of thermodynamics and
phase-ordering. An exact solution is found for the motion of a single, planar
interface separating a growing phase of uniform high density from a
supersaturated low density phase, whose diffusive depletion drives the
interfacial motion. In addition, an approximate solution is found for the
one-dimensional evolution of two interfaces, separated by a slab of a
metastable phase at intermediate density. The theory predicts a critical
supersaturation of the low-density phase, above which the two interfaces become
unbound and the metastable phase grows ad infinitum. The growth of the stable
phase is suppressed in this regime.Comment: 27 pages, Latex, eps
Comparative Effectiveness of Guidelines for the Management of Hyperlipidemia and Hypertension for Type 2 Diabetes Patients
Background: Several guidelines to reduce cardiovascular risk in diabetes patients exist in North America, Europe, and Australia. Their ability to achieve this goal efficiently is unclear. Methods and Findings: Decision analysis was used to compare the efficiency and effectiveness of international contemporary guidelines for the management of hypertension and hyperlipidemia for patients aged 40-80 with type 2 diabetes. Measures of comparative effectiveness included the expected probability of a coronary or stroke event, incremental medication costs per event, and number-needed-to-treat (NNT) to prevent an event. All guidelines are equally effective, but they differ significantly in their medication costs. The range of NNT to prevent an event was small across guidelines (6.5-7.6 for males and 6.5-7.5 for females); a larger range of differences were observed for expected cost per event avoided (ranges, 157,186 for males and 163,775 for females). Australian and U.S. guidelines result in the highest and lowest expected costs, respectively. Conclusions: International guidelines based on the same evidence and seeking the same goal are similar in their effectiveness; however, there are large differences in expected medication costs. © 2011 Shah et al
Power to identify a genetic predictor of antihypertensive drug response using different methods to measure blood pressure response
<p>Abstract</p> <p>Background</p> <p>To determine whether office, home, ambulatory daytime and nighttime blood pressure (BP) responses to antihypertensive drug therapy measure the same signal and which method provides greatest power to identify genetic predictors of BP response.</p> <p>Methods</p> <p>We analyzed office, home, ambulatory daytime and nighttime BP responses in hypertensive adults randomized to atenolol (N = 242) or hydrochlorothiazide (N = 257) in the Pharmacogenomic Evaluation of Antihypertensive Responses Study. Since different measured BP responses may have different predictors, we tested the "same signal" model by using linear regression methods to determine whether known predictors of BP response depend on the method of BP measurement. We estimated signal-to-noise ratios and compared power to identify a genetic polymorphism predicting BP response measured by each method separately and by weighted averages of multiple methods.</p> <p>Results</p> <p>After adjustment for pretreatment BP level, known predictors of BP response including plasma renin activity, race, and sex were independent of the method of BP measurement. Signal-to-noise ratios were more than 2-fold greater for home and ambulatory daytime BP responses than for office and ambulatory nighttime BP responses and up to 11-fold greater for weighted averages of all four methods. Power to identify a genetic polymorphism predicting BP response was directly related to the signal-to-noise ratio and, therefore, greatest with the weighted averages.</p> <p>Conclusion</p> <p>Since different methods of measuring BP response to antihypertensive drug therapy measure the same signal, weighted averages of the BP responses measured by multiple methods minimize measurement error and optimize power to identify genetic predictors of BP response.</p
Multi-Institutional Implementation of Clinical Decision Support for APOL1, NAT2, and YEATS4 Genotyping in Antihypertensive Management
(1) Background: Clinical decision support (CDS) is a vitally important adjunct to the implementation of pharmacogenomic-guided prescribing in clinical practice. A novel CDS was sought for the APOL1, NAT2, and YEATS4 genes to guide optimal selection of antihypertensive medications among the African American population cared for at multiple participating institutions in a clinical trial. (2) Methods: The CDS committee, made up of clinical content and CDS experts, developed a framework and contributed to the creation of the CDS using the following guiding principles: 1. medical algorithm consensus; 2. actionability; 3. context-sensitive triggers; 4. workflow integration; 5. feasibility; 6. interpretability; 7. portability; and 8. discrete reporting of lab results. (3) Results: Utilizing the principle of discrete patient laboratory and vital information, a novel CDS for APOL1, NAT2, and YEATS4 was created for use in a multi-institutional trial based on a medical algorithm consensus. The alerts are actionable and easily interpretable, clearly displaying the purpose and recommendations with pertinent laboratory results, vitals and links to ordersets with suggested antihypertensive dosages. Alerts were either triggered immediately once a provider starts to order relevant antihypertensive agents or strategically placed in workflow-appropriate general CDS sections in the electronic health record (EHR). Detailed implementation instructions were shared across institutions to achieve maximum portability. (4) Conclusions: Using sound principles, the created genetic algorithms were applied across multiple institutions. The framework outlined in this study should apply to other disease-gene and pharmacogenomic projects employing CDS
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