From rxpgnews.com
Remote Detection Makes NMR Compatible with Microfluidics
By Lawrence Berkeley National Laboratory (Berkeley Lab) and the University of California, Berkeley,
Oct 11, 2005 - 12:47:38 AM
A breakthrough in the technology of nuclear magnetic resonance (NMR), one of the most powerful analytic tools known to science, is opening the door to new applications in microfluidic chips, devices for studying super-tiny amounts of fluids. A team of scientists with Lawrence Berkeley National Laboratory (Berkeley Lab) and the University of California, Berkeley, has demonstrated a means by which NMR can be made compatible with microfluidic lab-on-a-chip devices. Our novel methodology bypasses the long-standing problem of optimizing the two basic steps of NMR, signal encoding and detection, by physically separating them, and, at the same time, adds an important dimension to the study of fluid flow dynamics with the possibility of time-of-flight measurements, said Alexander Pines, one of the worlds leading authorities on NMR technology. Pines holds a joint appointment as a chemist with Berkeley Labs Materials Sciences Division and with UC Berkeley, where he is the Glenn T. Seaborg Professor of Chemistry.
The technique in which NMR signal encoding and detection are carried out independently (in a conventional NMR setup, the two actions take place within a single device) is called remote NMR detection. In a paper published in the online edition of the Proceedings of the National Academy of Sciences (PNAS), for the week of October 3, Pines and his collaborators describe the use of remote NMR to study the flow of gases through microfluidic devices.
Remote detection of the NMR signal overcomes the sensitivity limitation of NMR and enables spatially resolved imaging in addition to time-of-flight measurements, said chemist Christian Hilty, a member of Pines research group and the principal author of the PNAS paper. We can use it to measure microfluidic flow without the introduction of foreign tracer particles. This is important for the design and the operation of microfluidic devices.
The work is supported by the U.S. Department of Energys Basic Energy Sciences program in the Office of Science.
When a sample is exposed to a strong external magnetic field, these "bar magnets" attempt to align their axes along the lines of magnetic force. The alignment is not exact, resulting in a wobbly rotation about the magnetic field lines that is unique for each type of nuclei.
If, while exposed to the magnetic field, the nuclei in a sample are also subjected to a sequence of radiofrequency (rf) pulses, they will absorb and re-emit energy at characteristic frequencies. This is called the signal encoding phase of NMR. In the detection phase, the frequencies of these encoded signals are measured to obtain an NMR spectrum. While NMR has long been a powerful tool for studying the chemical composition of macroscopic samples, its application to microfluidic chip devices has been hampered by low sensitivity. Obtaining an NMR signal depends upon an excess of nuclei in a sample with spins pointing in one direction or the other, but the natural population difference in a typical fluid sample, even under a powerful magnetic field, is usually no more than one in 100,000 at room temperature.
To overcome this low spin polarization so they can measure gas flow, Pines and his research group have been injecting their samples with xenon whose atomic nuclei have been hyperpolarized by laser light. Hyperpolarized xenon boosts the NMR sensitivity of a sample by at least four orders of magnitude, and, xenon being inert, does not interfere with the other sample constituents as it is carried along in the flow.
When working with microfludic samples of gas, Pines and his collaborators apply their NMR encoding technique to the hyperpolarized xenon. With its long spin-relaxation time (several minutes), hyperpolarized xenon is well-suited for transporting the encoded NMR information to a separate site for detection. By staging the encoding and detection phases at separate sites, each site can be customized to obtain optimal results.
Xenons long spin-relaxation time (several minutes), make it an ideal carrier of an NMR signal for remote measurements of gas flow, said Hilty.
Microfluidic devices are essentially miniaturized chemistry laboratories, featuring a series of micrometer-sized channels etched into a chip in which nanoliter-sized samples of fluids can be analyzed. Using remote NMR instead offers several advantages.
With remote detection of NMR, we dont need the addition of markers that perturb the flow because we can use the spins of the hyperpolarized xenon nuclei, said Hilty. Also, when we apply the hyperpolarized xenon for the encoding step of remote detection, we can individually tag a fluid sample in any and all points within the device, whereas we can inject a fluorescent marker only at a devices inlet.
According to Hilty and Pines, their NMR remote detection technology is ready to be applied to any existing microfluidic device, so long as the fluid is transported to the detection site within the spin relaxation time of encoded NMR information.
In our PNAS paper, we describe an application in which we measure gas flow in microfluidic devices by remote detection of NMR, said Hilty. Pines and his research group are working on the development of alternative, less expensive means of detecting encoded NMR signals for example, a magnetometer. According to Hilty, preliminary results on this line of research have been promising.
All rights reserved by RxPG Medical Solutions Private Limited ( www.rxpgnews.com )
|
|