High-throughput microcoil NMR of compound libraries using zero-dispersion segmented flow analysis

被引:61
作者
Kautz, RA
Goetzinger, WK
Karger, BL
机构
[1] Northeastern Univ, Barnett Inst Chem & Biol Anal, Boston, MA 02115 USA
[2] Arqule Inc, Woburn, MA 01801 USA
来源
JOURNAL OF COMBINATORIAL CHEMISTRY | 2005年 / 7卷 / 01期
关键词
D O I
10.1021/cc0498940
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An automated system for loading samples into a microcoil NMR probe has been developed using segmented flow analysis. This approach enhanced 2-fold the throughput of the published direct injection and flow injection methods, improved sample utilization 3-fold, and was applicable to high-field NMR facilities with long transfer lines between the sample handler and NMR magnet. Sample volumes of 2 muL (10-30 mM, similar to10 mug) were drawn from a 96-well microtiter plate by a sample handler, then pumped to a 0.5-muL microcoil NMR probe as a queue of closely spaced "plugs" separated by an immiscible fluorocarbon fluid. Individual sample plugs were detected by their NMR signal and automatically positioned for stopped-flow data acquisition. The sample in the NMR coil could be changed within 35 s by advancing the queue. The fluorocarbon liquid wetted the wall of the Teflon transfer line, preventing the DMSO samples from contacting the capillary wall and thus reducing sample losses to below 5% after passage through the 3-m transfer line. With a wash plug of solvent between samples, sample-to-sample carryover was <1%. Significantly, the samples did not disperse into the carrier liquid during loading or during acquisitions of several days for trace analysis. For automated high-throughput analysis using a 16-second acquisition time, spectra were recorded at a rate of 1.5 min/sample and total deuterated solvent consumption was <0.5 mL ($1) per 96-well plate.
引用
收藏
页码:14 / 20
页数:7
相关论文
共 22 条
[1]  
ADLER H, 1973, ADV AUTOMATED ANAL T, V9, P81
[2]  
Baldino CM, 1997, SYNLETT, P488
[3]   Limited-sample NMR using solenoidal microcoils perfluouocarbon plugs, and capillary spinning [J].
Behnia, B ;
Webb, AG .
ANALYTICAL CHEMISTRY, 1998, 70 (24) :5326-5331
[4]   A straightforward means of coupling preparative high-performance liquid chromatography and mass spectrometry [J].
Cai, H ;
Kiplinger, JP ;
Goetzinger, WK ;
Cole, RO ;
Laws, KA ;
Foster, M ;
Schrock, A .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (06) :544-554
[5]   Continuous segmented-flow polymerase chain reaction for high-throughput miniaturized DNA amplification [J].
Curcio, M ;
Roeraade, J .
ANALYTICAL CHEMISTRY, 2003, 75 (01) :1-7
[6]   High-throughput method for the production and analysis of large natural product libraries for drug discovery [J].
Eldridge, GR ;
Vervoort, HC ;
Lee, CM ;
Cremin, PA ;
Williams, CT ;
Hart, SM ;
Goering, MG ;
O'Neil-Johnson, M ;
Zeng, L .
ANALYTICAL CHEMISTRY, 2002, 74 (16) :3963-3971
[7]   Sample concentration and separation for nanoliter-volume NMR spectroscopy using capillary isotachophoresis [J].
Kautz, RA ;
Lacey, ME ;
Wolters, AM ;
Foret, F ;
Webb, AG ;
Karger, BL ;
Sweedler, JV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (13) :3159-3160
[8]   Direct-injection NMR (DI-NMR): A flow NMR technique for the analysis of combinatorial chemistry libraries [J].
Keifer, PA ;
Smallcombe, SH ;
Williams, EH ;
Salomon, KE ;
Mendez, G ;
Belletire, JL ;
Moore, CD .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2000, 2 (02) :151-171
[9]   Flow NMR applications in combinatorial chemistry [J].
Keifer, PA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2003, 7 (03) :388-394
[10]   Flow injection analysis NMR (FIA-NMR): a novel flow NMR technique that complements LC-NMR and direct injection NMR (DI-NMR) [J].
Keifer, PA .
MAGNETIC RESONANCE IN CHEMISTRY, 2003, 41 (07) :509-516