Microfluidic gradient generators are used to study the movement of living cells, lipid vesicles, and colloidal particles in response to spatial variations in their local chemical environment. Such gradient driven motions are often slow (less than 1 μm s −1 ) and therefore influenced or disrupted by fluid flows accompanying the formation and maintenance of the applied gradient. Even when external flows are carefully eliminated, the solute gradient itself can drive fluid motions due to combinations of gravitational body forces and diffusioosmotic surface forces. Here, we develop a microfluid gradient generator based on the in situ formation of biopolymer membranes and quantify the fluid flows induced by steady solute gradients. The measured velocity profiles agree quantitatively with those predicted by analytical approximations of relevant hydrodynamic models. We discuss how the speed of gradient-driven flows depends on system parameters such as the gradient magnitude, the fluid viscosity, the channel dimensions, and the solute type. These results are useful in identifying and mitigating undesired flows within microfluidic gradient systems.
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Convection Confounds Measurements of Osmophoresis for Lipid Vesicles in Solute Gradients
Lipid vesicles immersed in solute gradients are predicted to migrate from regions of high to low solute concentration due to osmotic flows induced across their semipermeable membranes. This process─known as osmophoresis─is potentially relevant to biological processes such as vesicle trafficking and cell migration; however, there exist significant discrepancies (several orders of magnitude) between experimental observations and theoretical predictions for the vesicle speed. Here, we seek to reconcile predictions of osmophoresis with observations of vesicle motion in osmotic gradients. We prepare quasi-steady solute gradients in a microfluidic chamber using density-matched solutions of sucrose and glucose to eliminate buoyancy-driven flows. We quantify the motions of giant DLPC vesicles and Brownian tracer particles in such gradients using Bayesian analysis of particle tracking data. Despite efforts to mitigate convective flows, we observe directed motion of both lipid vesicles and tracer particles in a common direction at comparable speeds of order 10 nm/s. These observations are not inconsistent with models of osmophoresis, which predict slower motion at ca. 1 nm/s; however, experimental uncertainty and the confounding effects of fluid convection prohibit a quantitative comparison. In contrast to previous reports, we find no evidence for anomalously fast osmophoresis of lipid vesicles when fluid convection is mitigated and quantified. We discuss strategies for enhancing the speed of osmophoresis using high permeability membranes and geometric confinement.
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- Award ID(s):
- 1804332
- PAR ID:
- 10502009
- Publisher / Repository:
- ACS
- Date Published:
- Journal Name:
- Langmuir
- Volume:
- 39
- Issue:
- 3
- ISSN:
- 0743-7463
- Page Range / eLocation ID:
- 942 to 948
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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