We have used nuclear magnetic resonance (NMR) to obtain spatially and temporally resolved profiles of gas flow in microfluidic devices. Remote detection of the NMR signal both overcomes the sensitivity limitation of NMR and enables time-of-flight measurement in addition to spatially resolved imaging. Thus, detailed insight is gained into the effects of flow, diffusion, and mixing in specific geometries. The ability for noninvasive measurement of microfluidic flow, without the introduction of foreign tracer particles, is unique to this approach and is important for the design and operation of microfluidic devices. Although here we demonstrate an application to gas flow, extension to liquids, which have higher density, is implicit.hyperpolarization ͉ xenon ͉ magnetic resonance imaging M iniaturized fluid-handling devices have attracted considerable interest recently in many areas of science (1). Such microfluidic chips perform a variety of functions ranging from analysis of biological macromolecules (2, 3) to catalysis of reactions and sensing in the gas phase (4,5). To enable precise fluid handling, accurate knowledge of the flow properties within these devices is important. Because of low Reynolds numbers, laminar flow is usually assumed. However, either by design or unintentionally, the flow characteristic in small channels is often altered (e.g., by surface interactions, viscous and diffusional effects, or electrical potentials). Therefore, its prediction is not always straightforward (6-8). Currently, most microfluidic flow measurements rely on optical detection of markers (9, 10), requiring the injection of tracers and transparent devices. Here we show profiles of microfluidic gas flow in capillaries and chip devices obtained by NMR in the remote-detection modality (11,12). Through the transient measurement of dispersion (13), NMR is well adaptable for noninvasive yet sensitive determination of the flow field and provides a potentially more powerful tool to profile flow in capillaries and miniaturized flow devices.NMR remote detection separates the encoding of NMR information from the detection of the actual signal. Information about a stationary object of interest is encoded into spin polarization of a mobile sensor by using radiofrequency (rf) pulses and field gradients. The spin sensor is then physically transferred to a different location for detection, which leads to a decisive enhancement of signal whenever geometrical constraints prevent the use of a sensitive NMR coil for detection directly at the sample site (11,12). In the present work, we studied gas flow in model microfluidic devices by using hyperpolarized 129 Xe as a spin-carrying nucleus (14). Experimental ProceduresImage information was encoded with an rf coil that completely encompassed the microfluidic device (Fig. 1). Such a coil arrangement ideally allows NMR-image information to be obtained from the entire microfluidic device. For measuring flow, it provides a decisive advantage over localized detection, which is achievable, for example,...
We present a novel approach to perform high-sensitivity NMR imaging and spectroscopic analysis on microfluidic devices. The application of NMR, the most information rich spectroscopic technique, to microfluidic devices remains a challenge because the inherently low sensitivity of NMR is aggravated by small fluid volumes leading to low NMR signal, and geometric constraints resulting in poor efficiency for inductive detection. We address the latter by physically separating signal detection from encoding of information with remote detection. Thereby, we use a commercial imaging probe with sufficiently large diameter to encompass the entire device, enabling encoding of NMR information at any location on the chip. Because large-diameter coils 1 are too insensitive for detection, we store the encoded information as longitudinal magnetization and flow it into the outlet capillary. There, we detect the signal with optimal sensitivity using a solenoidal microcoil, and reconstruct the information encoded in the fluid. We present a generally applicable design for a detection-only microcoil probethat can be inserted into the bore of a commercial imaging probe. Using hyperpolarized 129 Xe gas, we show that this probe enables sensitive reconstruction of NMR spectroscopic information encoded by the large imaging probe while keeping the flexibility of a large coil.
Here we report on using NMR imaging and spectroscopy in conjunction with time-of-flight tracking to noninvasively tag and monitor nuclear spins as they flow through the channels of a microfluidic chip. Any species with resolvable chemical-shift signatures can be separately monitored in a single experiment, irrespective of the optical properties of the fluids, thereby eliminating the need for foreign tracers. This is demonstrated on a chip with a mixing geometry in which two fluids converge from separate channels, and is generally applicable to any microfluidic device through which fluid flows within the nuclear spin-lattice relaxation time.
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