@article {317,
	title = {NMR-based biosensing with optimized delivery of polarized Xe-129 to solutions},
	journal = {Analytical Chemistry},
	volume = {77},
	year = {2005},
	note = {Anal Chem942GLTimes Cited:30Cited References Count:37},
	month = {Jul 1},
	pages = {4008-4012},
	abstract = {<p>Laser-enhanced (LE) Xe-129 nuclear magnetic resonance (NMR) is an exceptional tool for sensing extremely small physical and chemical changes; however, the difficult mechanics of bringing polarized xenon and samples of interest together have limited applications, particularly to biological molecules. Here we present a method for accomplishing solution Xe-129 biosensing based on flow (bubbling) of LE Xe-129 gas through a solution in situ in the NMR probe, with pauses for data acquisition. This overcomes fundamental limitations of conventional solution-state LE Xe-129 NMR, e.g., the difficulty in transferring hydrophobic xenon into aqueous environments, and the need to handle the sample to refresh LE Xe-129 after an observation pulse depletes polarization. With this new method, we gained a factor of \&gt; 100 in sensitivity due to improved xenon transfer to the solution and the ability to signal average by renewing the polarized xenon. Polarized xenon in biosensors was detected at very low concentrations, \&lt;= 250 nanomolar, while retaining all the usual information from NMR. This approach can be used to simultaneously detect multiple sensors with different chemical shifts and is also capable of detecting signals from opaque, heterogeneous samples, which is a unique advantage over optical methods. This general approach is adaptable for sensing minute quantities of xenon in heterogeneous in vitro samples, in miniaturized devices and should be applicable to certain in-vivo environments.</p>
},
	keywords = {blood},
	isbn = {0003-2700},
	doi = {Doi 10.1021/Ac0500479},
	url = {<Go to ISI>://WOS:000230270800035},
	author = {Han, S. I. and Garcia, S. and Lowery, T. J. and Ruiz, E. J. and Seeley, J. A. and Chavez, L. and King, D. S. and Wemmer, D. E. and Pines, A.}
}
